Up-to-date Science Info
An apple a day may keep the doctor away and is a good idea title for a book, but it’s probably a bad premise for a scientific study. The other day, a friend of mine drew my attention to a headline in the UK Telegraph “Eating an apple a day improves women's sex lives, study shows.” Bad grammar not withstanding, I defied my better judgment and decided to read the article. The Telegraph doesn’t have the best track record of health reporting. Recently they wildly misreported a study about edible flowers and true to form they botched this one as well.
The article makes a number of claims. It says that that apples have “been show to be an aphrodisiac,” that “an apple a day can improve the sex lives of women” and that they “boost sexual pleasure in healthy women.” These are impressive attributes for a simple fruit, so I decided to read the actual study this report was based on.
The study was published in the Archives of Gynecology and Obstetrics. Essentially researchers took 731 women and asked them how many apples they ate every day and then asked them to fill out a questionnaire about their sex lives in areas such as desire, arousal, satisfaction, pain, etc. Researchers found an improvement in lubrication and consequently in the total score, but not in any other area of the questionnaire. Here is an actual quote from the study, “No significant differences between the two study groups were observed concerning desire, sexual arousal, satisfaction, pain and orgasm.” (Interestingly, the group that ate less apples had a slightly higher satisfaction score 4.5 vs. 4.3). This strikes me as fairly convincing that apples are don’t affect the quality of women’s sex lives at least in terms of the metrics that actually matter. Having read this study, I cannot for the life of me figure out how the Telegraph could have generated their headline. I can only assume they didn’t actually read it and just parroted the press release.
Even if you accepted their one single positive finding, the study has a lot wrong with it. First off, it is not a randomized clinical trial. Even though the newspaper story seemed to imply that it was, here researchers simply asked women how many apples they ate and did not actually conduct an experiment. It is easy to image why women who ate apples on a daily basis would be different than women who did not. They were likely more health conscious, probably exercised more, and probably had a better diet overall. Those who ate more apples probably ate more bananas, more oranges, more pears and more fruits in general. Researchers did not ask about other fruits and they likely could have just as easily shown an association with kiwis or pomegranates. So why apples? I guess the link to the biblical story of Adam and Eve was too good to pass up. Of course, the fruit of the tree of knowledge wasn’t actually an apple but why quibble on details.
The newspaper article also then makes a number of claims that the benefits of apples are due to phloridizin and polyphenols. This is pure speculation. This study, as I mentioned, did not measure any hormone levels or perform any tests on the apples themselves. It was purely the analysis of questionnaire sent out to women. Clearly, throwing in a few “sciency” terms (and adding the requisite photo of an alluring women biting into an apple) made the article more appealing to the newspaper editors.
Apples are unlikely to improve your sex life and, while we’re at it, neither will oysters, chocolate, or ginseng. An overall healthy lifestyle with regular exercise and a balanced diet is probably your best bet (but admittedly this would make for a lousy headline). So what can we conclude overall about eating an apple day? No effect on sexual desire or satisfaction, great title for a book, and (from my point of view) it’s bad for business.Read more
I’m accustomed to being forwarded all sorts of videos about miraculous cures that are being suppressed by the establishment. There’s usually some “maverick doctor” who has made an astounding, shocking discovery about curing every disease known to mankind with some revolutionary herbal treatment, exotic juice or dietary supplement. There are testimonials, “rock solid” money back guarantees, and warnings about the need to click on the “buy now” button right away because of the uncertainty of keeping the video on the web. Why? Because the “establishment” is making every effort to remove it so as to protect the sales of Big Pharma’s worthless drugs. The products being promoted are usually safe but useless. Some people may actually be satisfied with their purchase because of the power of the mind over the body. I’ve seen dozens of these scams but now I’ve come across something new, at least to me. “Dr. Sen’s Perfect Vision System.” Yes, anyone can have perfect vision. Forget short sightedness, forget far sightedness, in fact forget macular degeneration, glaucoma and all other visual problems. These are not due to genetics, we are told, they are not due to a physical problem with the eyeball, they are, get this, learned traits! Our visual problems are due to focusing too frequently on books, television screens and computers. And glasses are not the answer, nor are contacts. These are scams perpetrated by optometrists and they actually make our vision worse. And laser surgery, well not only does it not correct vision, it can make you blind! So what is the answer? Dr. Sen knows. He has made an eye-opening discovery. And of course it is all natural. Who is Dr. Sen? According to the video, he’s a retired Chinese optometrist who is now ready to reveal his secret for perfect vision for free. Why? Because he has taken the Hippocratic Oath and abides by the philosophy of doing good for his patients. He is tired of the eye care industry trying to suppress the easy solution to visual problems so they can keep digging into their endless goldmine. Actually optometrists are not physicians and do not take the Hippocratic Oath. And no trace of the mythical Dr. Sen can be found outside of this revolting video. We just hear about his miraculous eye training method from someone called Samantha Pearson who voices the video. We are given no details except that using Dr. Sen’s “somewhat unusual” eye exercises, anyone can achieve 20/20 vision in just fourteen days. A true miracle! Actually there is a miracle here. It is that there are actually people who buy into this scam. Some must, otherwise the video would not crop up so often. What we have here is a demonstration both of the gullibility of some people and of scientific illiteracy. If you order right now, the video informs us, you also get Dr. Sen’s guide about how certain popular medications can worsen your eyesight and you also get to learn the secret of how one unusual food can cure blurry eyes in hours. This is no snake oil, we are told. For just thirty seven dollars, you are guaranteed to throw away your glasses and contacts. Actually, I’ll guarantee that the only thing you will be throwing out is thirty seven dollars.Read more
You never know what you will come across when surfing TV channels late at night, hoping against hope that you will come across a Seinfeld episode you haven’t seen a hundred times. Last night I was shocked to come across the villanous Peter Popoff yet again milking the gullible in a shameless fashion with his offer of “miracle water.” Exactly what was to be done with the water was murky, but its effects were clear. Financial fortune would befall those who called the number on the screen to ask for a “free sample” of the water. There were testimonials galore from people who saw money mysteriously appear in their bank accounts and others who suddenly were able to purchase cars and houses. There is indeed wealth to be gained from the miracle water. By the crooked Popoff. When you call the number you are asked to provide your name and address. Within days a letter arrives with a plastic bag filled with the miracle water, but alas, it has to be activated. You have to quickly send in a check or money order for $27, as “seed” money to show that you have faith in God’s intent to dole out money.
This is the same Peter Popoff who was famously exposed by Randi as a fraud back in 1986 when he was shown to be receiving information from his wife via an earpiece during his faith healing act. She was backstage going through the “prayer cards” that members of the audience had submitted so that Peter could “divine” who needed what sort of healing. After the exposure Popoff went bankrupt, but like the Phoenix rose from the ashes to practice this new form of chicanery. This man is pure evil. He is not a misguided believer in some higher power, he knows full well what he is doing. He is a reverse Robin Hood, robbing the poor to give to the rich, namely himself. And he has recouped all his losses, and more. Drives ritzy cars and lives in a multi-million dollar home. If there is a hell, Peter Popoff has a room waiting. Hopefully equipped with a torture rack.
The program was on Vision Television, a channel that is dedicated to religion. The only thing Peter Popoff worships is money. Popoff’s antics were so disturbing that I had to wash them away with one of my favourite Seinfeld episodes that I had recorded. It was the one about George seeking advice about his tonsil from a kooky New Age healer equipped with a pyramid, wacky sayings and a concoction made of who the loony new age healer, with his pyramid, wacky sayings, and a tea made of “cramp bark,” “cleavers” and “couch grass.” Needless to say it made George gag. Which is just what Popoff does to any reasonable viewer.Read more
It's frustrating, but most scientific studies end with the line, "more research is needed." But not always. We have one of these rare cases in a study published in the New England Journal of Medicine about the use of niacin to improve cholesterol profile. Niacin is familiar to many as the B vitamin that prevents pellagra but when it is used to decrease LDL (the "bad" cholesterol) and increase HDL (the "good" cholesterol) it is given in far higher doses than the amount that prevents pellagra. At a dose of 1000 mg a day, niacin is a drug. It has been used for decades in people with cholesterol problems because it clearly does decrease LDL and increases HDL. But that is not the same as reducing cardiac events. Now we have a study that quite categorically shows that in spite of the impact on cholesterol levels, niacing does not reduce cardiac events. Furthermore, it complicates diabetes and results is an increased risk of gastrointestinal, musculoskeletal and dermatological problems.
This was a very well designed study of some 25,000 people who were taking statin drugs because of cardiac risk. They were properly randomized to take a placebo or time-released niacin in combination with laropripran, added to reduce the classic flushing side effect of niacin, After four years the results were definitive. No reduction in cardiac events and an increase in side effects. No doubt the "natural treatment" advocates will declare that this study was contrived by Big Pharma to show that natural therapies do not work. Of course at doses needed to alter blood cholesterol, niacin can hardly be called natural. We'll see how many of the websites that promote niacin for reducing cardiac risk will change their sales pitch. Will Dr. Agatston change his mind? How about Dr. Oz who also recommends taking 400 mg of niacin a day. And Joe Mercola, who wildly promoted niacin on Dr. Oz's show while telling people to stay away from statins? Will be interesting to see.Read more
I’ve long been fascinated by space travel. I think I was first turned onto the idea back around 1957 with one of the first television shows I remember watching. “Rocky Jones, Space Ranger” was a kind of space policeman who would blast off from Earth and travel to other heavenly bodies where wicked aliens needed to be taken care of. There was no explanation as to where these worlds were, or how it was that the aliens always spoke English. I think the only concession to science was that Rocky’s spaceship looked like a German V-2 rocket which was also the prototype for the Redstone rocket that allowed Alan Shepard to become the first American in space in 1961. By that time I was hooked on space travel and was riveted to the TV set as Shepard was launched into his suborbital flight.
Then in 1965 along came Lost in Space, a television series that actually had smidgens of science. The plot centered around a family who set out from an overpopulated Earth to colonize a planet circling the star Alpha Centauri. At the time the show was produced no planets outside the ones that orbit our sun had been discovered. But the show was actually set in 1997, which is interesting because the first planeting orbiting a sun other than our own was discovered in 1995. More than 300 “exoplanets” as they are called have been discovered since. The show also paid some attention to the huge distances involved in space travel by having the travelers be frozen in some sort of state of suspended animation, only to be reanimated when approaching their target which had been chosen because space probes had revealed that the planet possessed ideal conditions for human life.
Lost in Space overlapped with the most successful of the TV science fiction shows which of course was Star Trek, debuting in 1966. The show was set in the twenty-third century so as to allow for ample passage of time to have developed the scientific wonders like phasers, beamers and travel at warp speed. The latter was necessary because it allowed travel faster than the speed of light which would be needed to travel to the diverse planets visited by Captain Kirk and his crew. Watching all these shows was great fun. And still is. But how far are they from reality? Unfortunately very, very far. That’s because the distance that would have to be travelled to get to a planet outside our solar system is almost unimaginable. Tremendous publicity was given this year to the discovery of the first planet, Kepler-186f, that may be sort of a cousin to Earth because it may have liquid water. How far is it? About 490 light years away. So when we see Kepler-186f we are really seeing that planet as it was 490 years ago, that is how long it took for the light to reach us. And how far have we travelled in space? We have made it to the moon. That is 1.2 light seconds away! So visiting other planets or being visited by aliens that may be out there remains firmly entrenched in science fiction.Read more
Let’s face it, running on a treadmill isn’t one of life’s most exciting activities, but it does provide time to contemplate life and think about what is likely to extend it. There’s plenty of evidence that exercise will, which is why one plods away on the treadmill in the first place.
But should one gear up for short bursts of high-intensity exercise or scamper along at a slower pace for a longer time? The scientific literature is ambivalent on the issue, but it is one that I follow closely because I am sort of addicted to the treadmill. That’s why a New York Times blog with the headline “For Fitness, Push Yourself” accompanied by a photo of competitive runners obviously at full tilt got my attention.
“Intense exercise changes the body and muscles at a molecular level in ways that milder physical activity doesn’t match, according to an enlightening new study,” the article began.
Was there finally an answer to the exercise conundrum?
The study was enlightening all right, if you are a mouse. This is not a criticism of the research, which was carried out by a very reputable group at the Scripps Research Institute in Florida. But it is a criticism of the interpretation of the study, not only by the New York Times blog, but by many other media reports that concluded “to realize the greatest benefits from workouts, we probably need to push ourselves.” There were also quotes from one of the researchers involved in the study about “no pain, no gain.” Coming to such a conclusion based on a study involving specially-bred mice scuttling on a treadmill is way too adventurous.
The study’s basic goal was to examine how the hormones adrenalin and noradrenaline affect muscle structure. These hormones are released under stressful conditions and are known to prime muscles for “flight or fight.” Since intense exercise is also known to release these chemicals, it is reasonable to explore its potential to increase muscle strength. The effects of the stress hormones are thought to be manifested through the activation of a specific protein termed CRTC2, present in mice as well as in people. The Scripps researchers therefore bred mice that were genetically programmed to produce more of this protein, put them on a program of strenuous treadmill exercise and found that they developed larger muscles and were more efficient at releasing fat for use as fuel than control animals. Interesting, but genetically modified mice are a long way from humans and the study does not justify giving any sort of advice to people.
The researchers also talk about “searching for molecular therapeutics that will activate the CRTC2 protein so that even an average exercise routine could potentially be enhanced and made more beneficial.” Sounds like an attractive research project, but I suspect it won’t be long before an inventive marketer puts the cart before the horse and starts promoting some sort of “CRTC2 enhancer.”
In the anti-aging business, making more of reputable science than is warranted is par for the course. Consider these headlines: “Cocoa Extract Highly Effective in Protecting Against Alzheimer’s disease, Says New Study” or “Worried About Alzheimer’s? Go on a Chocolate Binge, Study Says.” Well, no. The study doesn’t say anything like that. The grossly exuberant headlines were prompted by a paper published in the Journal of Alzheimer’s disease titled “Cocoa extracts Reduce Oligomerization of Amyloid-beta: Implications for Cognitive Improvement in Alzheimer’s disease.”
Did the researchers from the Mount Sinai School of Medicine in New York carry out experiments with cocoa on Alzheimer’s patients? No. Did they feed cocoa to animals? No. What they did was study the effects of a specific type of cocoa extract on the activity of nerve cells in mouse brain tissue dosed with synthetic compounds thought to model Alzheimer’s disease.
One of the hallmarks of Alzheimer’s disease, which affects an estimated 36 million people worldwide and is expected to double by 2030, is the deposition of a protein known as amyloid-beta between nerve cells. This virtually gums up the workings of the brain by preventing neurotransmitters, the chemicals nerve cells use to communicate with each other, from crossing the synapse, the gap between nerve cells. Since amyloid proteins are formed from smaller fragments called peptides, any interference with the ability of peptides to aggregate into the troublesome proteins is worthy of investigation.
Flavanols are a class of compounds found in cocoa that have been proposed as candidates for interfering with the formation of the amyloid proteins. The Mount Sinai researchers decided to use an unfermented, lightly processed cocoa known as “Lavado” in their investigation because of its high flavanol content. Most commercial cocoa is “Dutched” and has undergone alkali treatment to reduce bitterness, a treatment that also significantly reduces flavanol content. As far as chocolates go, their flavanol content is minimal.
The experiment that generated all the publicity consisted of bathing brain slices from mice specially bred to be prone to Alzheimer’s disease in solutions of the amyloid precursor peptides mixed with different cocoa extracts. When the nerve cells in these tissues were electrically stimulated, transmission of information between them was enhanced with Lavado cocoa extracts.
While this is interesting research, it cannot be used to draw any conclusion about people consuming cocoa. There is no way to know how the amount of the cocoa extracts used in these experiments relate to amounts of flavanol that may make it to the brain from eating chocolate or drinking cocoa. And mouse brain slices in a lab are a long way from a functioning human brain. Although maybe not so far from the human brains that clutter the media implications for human health based on preliminary laboratory or animal experiments.
Needless to say, I won’t go out searching for Lavado cocoa, at least not until a proper randomized trial in humans shows a benefit. And as far as the treadmill goes, I have no idea what “intense” mouse exercise means in human terms, but on looking into the issue, I did come across a scientific paper that added some pep to my treadmilling. The title was “Physical Exercise Protects Against Alzheimer’s disease.” I won’t be shouting about it from rooftops, though. The study was on mice genetically modified to develop the disease.Read more
When it comes to health matters, scientists rarely make statements that do not begin with “may.” But here is one. Excessive exposure to sunlight causes skin cancer! There’s no “may” about it. And here is another one. Chemical protection can effectively reduce exposure. Uncertainties do, however, emerge when it comes to deciding on which specific chemicals to use. Activists claim that some sunscreens are unsafe and blame regulatory agencies for not looking after the welfare of the public while manufacturers profess that their products have been thoroughly tested for safety and efficacy. As usual, the public is left confused. Actually, when you blow away the superfluous blather emanating both from the alarmists and from industry, there is some simple advice to offer. Let’s work it out.
The challenge is clear. Find a chemical or mixture of chemicals that can be applied to the skin to reduce exposure to the full spectrum of ultraviolet light. Then make sure these chemicals do not degrade upon exposure to light, have no topical or systemic toxicity, are minimally absorbed into the body, are resistant to water, do not have a greasy feel, are cosmetically acceptable, do not stain clothing and can be incorporated into a “vehicle” that allows for easy spreading. Quite a list of demands.
The first commercial “sunscreens” appeared in the 1960s and were designed to filter out “UVB,” the shorter wavelengths of ultraviolet light (290-320 nanometers). These are the rays that cause sunburn, which was the main concern at the time. Slightly longer waves, those responsible for tanning, were deemed safe. Finding chemicals that absorb the nasty UVB rays was not particularly difficult, with para-aminobenzoic acid (PABA), octocrylene, phenylbenzimidazole sulfonic acid and various cinnamates and salicylates being up to the task.
Products with different concentrations of these ingredients were introduced for different skin types, each prominently featuring a “Sun Protection Factor (SPF),” basically a measure of the time it takes for skin to redden compared with having no protection. The SPF value is determined in the laboratory by applying 2 mg of product per square centimeter to the skin of volunteers. Using a product with an SPF of 15 means that a person who normally begins to burn in ten minutes can in theory stay in the sun for a hundred and fifty minutes before experiencing any visible effect on the skin.
It didn’t take long for this scenario to prove to be too simplistic. As a clear link between skin cancer and UVB emerged, the focus shifted from preventing sunburn to preventing skin cancer, resulting in an industry frenzy of products with higher and higher SPF values. In truth, an SPF of 15 already blocks 94% of UVB, only 3% less than one labeled as SPF 30. In any case, these numbers are only meaningful if the product is applied the same way as in the lab studies, which turns out not to be the case. Most people were applying far less than 2 mg per square centimeter and were not getting the protection they thought they were getting. What many were getting, though, were various skin reactions. And something else became apparent as well. The longer wavelengths of ultraviolet light, 320-400 nm, known as UVA, previously thought to be inoccuous, were found to be more deeply penetrating than UVB and responsible for premature wrinkling and aging of the skin (“photoaging”). Unlike UVB, they can even pass through glass. Furthermore, UVA also was found to be potentially carcinogenic.
Now there was a need for a novel class of products that would protect the skin both from UVB and UVA. Ideally, not one that would just absorb some wavelengths, but one that would reflect all ultraviolet light. Titanium dioxide and zinc oxide, both mineral pigments, fit the bill, but left a white residue on the skin. That was alright for lifeguards’ noses, but not for vane sunbathers. The search was on for cosmetically acceptable molecules capable of absorbing UVA. Oxybenzone and avobenzone (Parsol 1789) were up to this task, but as usual, there are some “buts.”
When oxybenzone absorbs ultraviolet light it becomes energized and some of this energy is dissipated through the production of free radicals. These are very active molecular species that have been linked to cancer. Oxybenzone also undergoes a reaction in the presence of ultraviolet light to form a compound called a semiquinone which in turn can inactivate some of the naturally occurring antioxidants in the skin, such as reduced glutathione. Not a good thing since antioxidants offer protection against free radicals. And if that weren't enough, it turns out that oxybenzone can also mimic the behaviour of estrogens, at least in fish exposed to high doses. It has therefore been labeled a potential "endocrine disruptor." Concern has been raised, mostly by the Environmental Working Group, an American activist organization, because surveys have shown that ozybenzone can be found in the blood of 97% of the population.
But, and a big but it is, there is no evidence reported in the scientific literature of oxybenzone being linked to any human health problem, except for photodermatitis, a skin reaction triggered by exposure to sunlight. There are hundreds and hundreds of compounds, both natural and synthetic, that if scrutinized the same way as oxybenzone, could be linked to problems. Phthalates, bisphenol A, soy extracts and various pesticides are estrogenic. We live in a world full of hormone-like substances and a complete analysis of our blood would reveal hundreds of these. All of this goes to say that the risks of oxybenzone as implied by the Environmental Working Group, I think, are overstated.
Avobenzone is cosmetically elegant, non-irritating, but becomes unstable after a couple of hours of exposure to ultraviolet light. However, its stability is increased when combined with oxybenzone, especially if another stabilizing agent known as diethylhexyl-2,6-napthalene (DEHN) is added. This combination, developed by Neutrogena, is known as Helioplex. An important question arises here. What happens to the UV energy that these chemicals absorb? The energy has to go somewhere, might it not have a damaging effect? DEHN takes the energy absorbed by avobenzone and transfers it to oxybenzone which then fluoresces it as harmless red light.
Another effective broad spectrum sunscreen is tetraphalydine dicamphor sulphonic acid, which goes by the trade name Mexoryl. It is stable, absorbs UV light and dissipates the energy as harmless heat. Mexoryl isn’t absorbed through the skin and so far there are no safety issues. And recently, excellent products using “micronized” titanium dioxide and zinc oxide have been developed which do not leave a tell-tale white residue. Presently it is difficult to judge exactly how much protection a product affords against UVA because there is no SPF-like system has yet been devised. But regulatory agencies are working on it.
There is one more “may” about sunscreens that has been converted to fact. We no longer have to say that sunscreens may prevent skin cancer, we can say they do. A study in Australia, where skin cancer is a huge concern, involved 1600 subjects who were given sunscreen to use every day for four and a half years. They developed 40% fewer squamous cell cancers than a control group who just maintained normal skin care without being given specific instructions about the use of sunscreens.
So there it is. Sunscreens can prevent skin cancer, which is not a rare disease. The World Health Organization estimates 48,000 deaths a year from melanoma (likely sun related but not conclusively proven) and 12,000 from other forms of skin cancer. What to do?
Look for a product with SPF 30 containing for avobenzone, Mexoryl, titanium oxide or zinc oxide. Apply fifteen minutes before going out in the sun, use a shot glass full for the body and half a teaspoon for the face. Reapply frequently. Forget terms like “waterproof,” “all day protection” and “sweatproof.” They’re meaningless. And if you are buying something that is “chemical-free,” you are not getting a good deal because you’re buying a vacuum. Sunscreens should not be used to prolong sun but rather to protect the skin when exposure is unavoidable. Above all, remember that unfortunately there is no such thing as a healthy tan.Read more
The incidence of Alzheimer’s Disease varies widely around the world. There are far more cases diagnosed in Europe and North America than in Africa, Asia or India. The question is why. Is it genetics? Some difference in lifestyle? Or is the disease just underreported in developing countries? India has a low rate of Alzheimer’s but with less access to physicians and fewer tests available it is possible that many cases of Alzheimer’s are not being recognized as such.
Genetics is not likely to account for the pattern of Alzheimer’s around the globe. For example, Asians who have grown up in North America have the same rate of Alzheimer’s as other Americans. Nigerians in the U.S. experience a higher rate than Nigerians in Africa. In Japan, a country that has traditionally had a low rate of dementia, Alzheimer’s has been increasing significantly. This obviously cannot be attributed to a change in genetics, so it seems that some sort of lifestyle factor that distinguishes poorer and wealthier countries is at play. Diet would seem to be a prime candidate because of significant differences in what people consume around the world. Rice is a staple in most developing countries and is far less widely consumed in the West. Meat, on the other hand, is a western institution. Could it be that the fat content, or the cholesterol, or the iron in meat somehow predispose to Alzheimer’s? In Japan, the incidence of the disease appears to have increased in step with a increase in meat consumption and a decrease in rice consumption. That could mean that rice has some protective factor, or that something in meat is a problem or it could mean nothing.
Epidemiological studies cannot distinguish between associations and cause and effect relationships. For example, there is a highly significant correlation between the divorce rate in the state of Maine and the per capita consumption of margarine. Interesting, but in all likelihood meaningless. There is also a correlation between strict hygiene and sanitation methods as practiced in wealthy countries and the prevalence of Alzheimer’s Disease. Could that be meaningful? In countries with access to clean drinking water the incidence of Alzheimer’s is increased and in countries with a low rate of infectious disease such as Switzerland or Iceland the rates of Alzheimer’s are higher by some 12% than in China and Ghana, both countries with high rates of infectious disease. Is this some spurious correlation or is it meaningful?
The “hygiene hypothesis” is gaining traction when it comes to allergies and asthma with the theory being that exposure to bacteria, viruses and worms early in life primes the development of a healthy immune system. In the absence of exposure to organisms that can actually cause disease, the immune system targets innocent bystanders such as certain food components. Maybe, some researchers suggest, the deposition of proteins in the nervous system, one of the hallmarks of Alzheimer’s, is a result of an immune system that has gone astray. Sounds pretty far fetched, but the absence of any proven cause of Alzheimer’s makes for all sorts of half-baked theories being hatched.Read more
I suspect we will soon be hearing a lot about "Souvenaid," a dietary supplement that is supposed to be of some help in the early stages of Alzheimer's Disease. It was developed by Dr. Richard Wurtman of MIT, a very reputable researcher and the formulation of Souvenaid is based on legitimate science, but unfortunately the evidence for its effectiveness is virtually negligible.
In Alzheimer’s there is a loss of synapses, the connections between nerve cells that form when protrusions develop in cell membranes and reach out towards neighbouring nerve cells. The theory is that providing nutrients needed for healthy cell membranes encourages the formation of new synapses to compensate for the experienced loss.
Souvenaid provides a range of nutrients that include including omega-3 fatty acids (EPA and DHA), phospholipids, choline, uridine monophosphate, vitamins E, C, B12, B6, folic acid and selenium based on the theory that these are needed for the synthesis of phosphatidylcholine, a major constituent of synaptic membranes. The more phosphatidylcholine in cell membranes, the greater the likelihood of synapse formation, at least so goes the theory. But a theory needs evidence to back it up if it is to evolve into practical recommendations. And that evidence is not forthcoming. It isn’t for lack of effort.
A number of studies have been carried out on Alzheimer’s patients with Souvenaid using standardized assessment scales. The results are disappointing. There is no evidence of decreasing the rate of cognitive decline or delaying the progression of the disease in any way, but one of the studies offered a slight glimmer of hope. In patients experiencing early Alzheimer’s Disease, who are not yet taking medication, there was an improvement in verbal recall. That isn’t much to hang a hat on, but at least the supplement was tolerated without side effects. Souvenaid is on the market in Europe and Australia but not yet in the US or Canada despite the low level of evidence that is required for selling dietary supplements. My guess is that Souveanaid will not be of much aid in Alzheimer’s Disease.Read more
The world of instrument making is a peculiar blend of tradition and innovation. Once a good design is found, it’s rare for major modifications to occur. The big names we have heard of, Stradivarius violins (or as Homer Simpson says, “Strada-who-vious?”), or Steinway grands, are physically quite similar to their ancestors - a quality openly sought by musicians who buy these makes. More often, the innovation occurs from within the constraints of the traditional form of the instrument. We’ve switched out the cat gut for more resilient plastics (though you can still find the purist who swears by the older string type), and moved away from wooden piano frames, which has resulted in much fewer pianos spontaneously collapsing, releasing their strings, bound so tightly they could cleanly remove a finger. It’s therefore rare to come across a trumpet that’s almost completely made of plastic.
The “tiger trumpet”, a plastic trumpet that comes in a variety of vibrant colours, is the latest in a trend of professional quality plastic instruments. Likely inspired by the “p-bone”, a plastic trombone, and the first (and arguably, simplest) of the brass instruments to depart from its metallurgical heritage, the tiger trumpet is the answer to the trumpeter with a penchant for ‘toys’, which if you know any trumpeters, is all of us. At the highly affordable price of $295, I was able to get my hands on a beautiful blue and yellow model and examine it.
The horn itself is almost entirely made of plastic. It seems like a cop out to begin by saying that plastic has its limitations, as the horn is truly quite impressive. However, the basis of function of the valves still requires a small amount of metal, and indeed, with exception to a thin layer of aluminum which coat the valves, and supply the mechanical energy in the springs, the tiger trumpet is all ABS plastic.
Acrylonitrile Butadiene Styrene - for the more seasoned chemists, or the well-informed consumer, this plastic may ring a bell. You’ve probably come across it in the form of the beloved (and sometimes painful) children’s toy Lego, but it’s used in a variety of other applications. The plastic is rigid through a large range of temperatures, and when molten can be coloured with a variety of dyes. The plastic does have a drawback, and this is best told by the tale of the world’s largest auto recall of which several million cars manufactured by GM were subject. As it would turn out, ABS is prone to photo oxidation, and the mechanism of the seat belts in several GM SUVs made roughly over a 10 year period contained this plastic, which degraded, and was the cause os several hundred car accidents. Beyond the inherent wastefulness in the manufacture of most plastics, which use impressive amounts of petroleum products for their synthesis, photo oxidation, and solvency in acetone (keep that nail polish remover away from your trumpet) are the principal causes for concern with an ABS trumpet.Read more
“As seen on the Dr. Oz Show” is a claim that is guaranteed to boost sales for any product. Like the “phytoceramides” glorified by a couple of plastic surgeons on the show. Incorporated into dietary supplements, these plant derived chemicals are supposed to rejuvenate the skin. There’s no magic pill, Dr. Leif Rogers commented, but “this is pretty close.” And after Dr. Oz wondered “why we haven’t used this earlier,” marketers went to work and quickly filled websites with advertisements about how you can “fake a facelift” with phytoceramides. As is often the case, some websites bleated about Dr. Oz’s “phytoceramide scam,” a common ploy to attract an audience to their site which claims that the product shown on the Oz Show is not as good as the “authentic one” that they are selling.
Perhaps the most impactive statement on the show was Dr. Rogers’ claim that phytoceramides had recently been approved by the FDA. This is totally misleading. In the U.S. dietary supplements do not need premarket approval by the FDA, all that is required is a “Dietary Ingredient Notification” describing what is in the product and why it is believed to be safe. That was not a problem in this case because not only do ceramides occur naturally in our skin, they also can be found in a variety of foods that include dairy products, eggs, soybeans, rice, millet, spinach and wheat. The term “phyto” means plant, so “phytoceramides” are ceramides found in plants.
Ceramides are a class of compounds, along with fatty acids, proteins and cholesterol found in the skin’s outer layer, that help retain moisture. By plumping up the skin, moisture can reduce the appearance of wrinkles. Topical ceramides have long been incorporated into moisturizing creams with positive effects but there are all sorts of substances that can be smeared on the skin to prevent moisture loss, ranging from Vaseline and Crisco to snail extracts. They all work in terms of retaining moisture, but the feel on the skin can be very different. The phytoceramide pills seek to circumvent the problem of finding the right topical moisturizer by delivering the ceramides into the skin directly from blood vessels.
Some studies have indeed shown that such delivery is possible but of course the critical question is whether taking phytoceramide supplements has a noticeable effect. There’s plenty of anecdotal evidence and pictures on the web that show spectacular changes but of course it isn’t hard to fake photos. Then there are claims of celebrities using the product, ranging from Ellen DeGeneres to Jennifer Aniston. We are told that they are not allowed to speak about their use pf phytoceramides because they have contracts with other cosmetic companies. Well, if that is the case, how would anyone know they use phytoceramides?
It is possible that these pills may have an effect, however it is doubtful it would be “near magical.” No surprise that Dr. Rogers uses that expression, given that he sells his own brand of phytoceramides, along with a host of other cosmetics., something that was not mentioned on the Oz Show. Dr. Rogers’ did manage to milk his appearance by prominently featuring “as seen on the Dr. Oz Show” on his website where he also promotes the product she sells. Highly unethical to say the least.Read more
That was the opinion of Sir William Osler, graduate of McGill University, professor of medicine at McGill, one of the founders of the Johns Hopkins University School of Medicine, and a man often called the Father of Modern Medicine.
Osler introduced the concept of clinical clerkship, insisting that third- and fourth-year medical students be exposed to hands-on experience with patients. He also pioneered the idea of a residency program for medical graduates, to further hone their skills. He reportedly asked for no other epitaph than that he taught medical students in the wards, something he considered his most useful and important work. By putting less emphasis on lectures and books, and more on practical skills, he fundamentally changed the way medicine was taught.
“Listen to your patient,” he told his students. “He’s telling you the diagnosis.”
Osler’s statement about man’s desire to take medicine, which was made in a lecture he delivered to the public, is widely quoted, but his follow-up sentence isn’t:
“Why this appetite should have developed, how it could have grown to its present dimensions, what it will ultimately reach, are interesting problems in psychology.”
He was expressing his concern that while physicians “have gradually emancipated ourselves from a routine administration of nauseous mixtures on every possible occasion, and when we are able to say that a little more exercise, a little less food, and a little less tobacco and alcohol, may possibly meet the indications of a case, you, the people should wander off after all manner of idols, and delight more and more in patent medicines and be more than ever at the hands of the advertising quacks.”
It isn’t surprising that Osler was critical of the use of medicines at the time, because most of them did not do much good.
“One of the first duties of the physician is to educate the masses not to take medicine,” he maintained, believing in the self-limiting nature of disease.
Osler himself prescribed relatively few drugs, his basic armamentarium consisting of quinine for malaria, digitalis for heart failure, opiates for pain and coughs, and iron and arsenic for anemia. Instead of drugs, he recommended bleeding the patient for a variety of conditions including pneumonia, stroke and mumps, and he suggested acupuncture for sciatica and neuralgia. He also thought that for nosebleeds there was no harm in trying the insertion of a cobweb into the nostril.
That, of course, sounds pretty curious to us, but throughout history people have resorted to every imaginable remedy for their ailments, from a toothache poultice made of “mashed mouse” to a whiff of flatulence stored in a jar to ward off the Black Plague.
Most of the treatments failed, but eventually, through trial and error, at the expense of much misery, some effective drugs did emerge. As early as 70 AD, Dioscorides described the use of the seeds of autumn crocus to treat gout. The active ingredient, colchicine, was not extracted and identified until 1820. Some drugs, penicillin being a classic example, were discovered by accident; others, such as Taxol, for cancer, by a meticulous search for physiologically active compounds found in nature.
Today, drug research focuses on molecular structure and known mechanisms of action. Gleevec (imatinib), a drug that dramatically increases the survival rate in chronic myelocytic leukemia (CLM), was developed based on the finding that CML patients produce an abnormal version of the enzyme tyrosine kinase, which in turn leads to an overproduction of white blood cells. Knowing the molecular structure of the enzyme, researchers were then able to design and synthesize a compound that would inhibit its action.
In some cases, the effectiveness of a drug for an ailment was discovered when it was being used for a different condition.
Antidepressants known as monoamine oxidase inhibitors (MAOI) are a classic example. In 1951, isoniazid was introduced as a treatment for tuberculosis with great success. But it wasn’t long before concerns about bacterial resistance arose, and when that happens, chemists begin to tinker with the molecular structure of the drug to develop a derivative that will help stave off resistance. Within a year, iproniazid was ready for testing in tuberculosis hospitals. While it turned out not to be effective against TB, the drug had a remarkable side effect. Doctors and nurses noted a significant improvement in patients’ mood, with some even taking to dancing in the hallways. Not a common sight in any hospital.
As it turned out, iproniazid inhibited the action of monoamine oxidase, an enzyme that normally degrades norepinephrine and serotonin, two compounds that control mood. Inhibition of the enzyme raises blood levels of both and leads to feelings of happiness. After favourable results were obtained on testing depressed patients, iproniazid hit the marketplace as Marsilid, only to be withdrawn in 1961 because of liver toxicity. But iproniazid had demonstrated the principle of antidepressant action, and opened the way to the introduction of other monoamine oxidase inhibitors, which are still in use, although they have mostly given way to the newer serotonin reuptake inhibitors (SSRIs).
Other drug actions that have been discovered in this fashion include sildenafil (Viagra), first introduced as an anti-anginal medication. However, it was its ability to elevate more than just mood that brought it fame and fortune.
Amphetamine was introduced as a treatment for congestion and asthma, but it was its stimulant side-effect that led to its use both by the Allies and the Germans during the Second World War as a performance-enhancing substance. A further surprise was when amphetamine, despite being a stimulant, proved to be effective in the treatment of attention deficit hyperactivity disorder (ADHD).
So then, is it really the desire to take medicine that distinguishes us from animals, as Osler opined?
I would suggest it is the making of medicines rather than taking them that sets us apart.
After all, chimps have been known to seek out certain plants when they feel ill, but only humans have the ability to isolate and identify and perhaps improve upon the active ingredient. Who knows, maybe our next drug will come from some sort of monkey business.Read more
It was one of those happy endings. Paul, albeit still frail, was now smiling, eating, and chatting with his family. When I first met him, as described in my last post, he couldn’t even breathe on his own. He had been lying listless in the Intensive Care Unit (ICU) bed for days, skin and bones, barely moving a muscle. It was New Year’s Day, and I couldn’t think of a better time to tell him that he was ready to be discharged home. Paul was one of my first patients on a medical volunteer trip to Haiti earlier this year at Bernard-Mevs Hospital. Paul had been admitted to the ICU for acute respiratory failure secondary to an exacerbation of chronic obstructive pulmonary disease. I had made it my personal project to find him the best treatment regimen with the very limited resources we had. Often, especially at night, I was the only physician covering triage, the emergency room, the inpatient unit and the ICU, and I had only my pocket medicine book to rely on. That, and my own judgment. It is pretty amazing how quickly a resident physician can grow when forced to think and act by herself without the usual close supervision of an attending, as is the usual case during residency. I remember my second night shift when, while all the volunteers went out to dinner, I was assigned to stay behind to woman the fort. With a mere one and a half years of experience in internal medicine under my belt, it was a tad daunting to be left in charge of the entire hospital. Lo and behold, an ambulance rolled in with blaring sirens, bringing in a young man who was in a motorcycle accident. Just as I was evaluating this patient, another ambulance pulled in, followed by another. Just like that, I was in the entrance of the hospital, surrounded by three ambulances and a crowd of spectators. Seeing as we had our hands full, the third ambulance was diverted to MSF (Médecins Sans Frontières) France which was about 15 minutes away. As I gave instructions to stabilize the motorcycle accident victim’s neck with a neck collar to prevent worsening of potential cervical spine injury, I tried to gather some history about my second patient. “He has high blood pressure” was all that I could obtain from the paramedics. He was a transfer from another hospital, and apparently they couldn’t handle him so sent him to Bernard-Mevs. No one could tell me what his latest set of vital signs were, or what symptoms he had, so I jumped into the ambulance to take a look for myself. Read more
“When there is substantial, credible evidence of danger to human or environmental health, protective action should be taken despite continuing scientific uncertainty.” That’s the “Precautionary Principle” stated in its simplest format. Sounds like motherhood and apple pie. How can there even be a discussion about its application? But there is. That’s because “substantial, credible evidence” is open to interpretation and different countries approach the issue in different ways. Europe has introduced REACH, which stands for Registration, Evaluation, Authorisation and Restriction of Chemicals, a program that requires manufacturers to submit toxicity data to the European Chemical Agency before a chemical can be approved.
In the U.S., chemicals are governed by the Toxic Substances Control Act which is now under revision but historically has required proof of harm before acting on controlling a chemical. In Canada, chemicals are subject to the Chemicals Management Plan which is not quite as stringent as Europe’s REACH, but caters less to industry than U.S. regulations. The basic problem with all these regulations is that when it comes to the population being exposed to small amounts of chemicals, the data is very difficult to interpret. Occupational exposure, animal experiments and laboratory studies can provide clues but how relevant these data are to everyday human exposure is unclear. The most reasonable approach would be to weigh the need to use a certain chemical against toxicity data.
Consider food dyes as an example. While the data are not particularly compelling, there is some evidence that synthetics such as Red Dye No. 40, Yellow Dyes No. 5 and 6 may cause behavioural problems in some children and animal data suggest possible carcinogenicity. But different countries come to different conclusions about what to do. The U.K. Belgium, Switzerland, Denmark and France do not allow Red Dye No. 40, while Canada and the U.S. do. Here is a case where the precautionary principle should prevail. Food dyes are unnecessary, do not add anything in terms of nutrition and often make nutritionally poor foods more appealing. We don’t need them.
Bromates are another interesting case. When added to flour potassium bromate improves the baking qualities but is a suspected carcinogen. Bromates are not allowed in Europe or Canada but can be used in the U.S. because FDA says that they are destroyed during baking and only trace amounts remain. But if the rest of the world can get by quite nicely without adding bromates to flour, why can’t the U.S.? Because bromates make for the soft white texture and white colour that Americans have been goaded into preferring. Here too one can apply the precautionary principle. Remove bromates from flour.
However, when it comes to chemicals like preservatives, decisions become more difficult because these have obvious benefits. Theoretical risks for something like butylated hydroxyl toluene (BHT) or sodium nitrite have to be weighed against their demonstrated effects at keeping fat from going rancid or preventing botulism. The precautionary principle should also ne applied to using the precautionary principle.Read more
“Botanicals” are dietary supplements derived from plant sources that have purported health benefits. Echinacea for the common cold, St. John’s Wort for depression, ginkgo biloba for memory improvement and ginseng for energy enhancement are typical examples. Generally such products are assumed to be safe because they are “natural.” Of course whether a substance is natural or not has nothing to do with its efficacy or toxicity. The only way to determine these is by experimentation. But when it comes to botanicals, such experimentation is not easy.
Contrary to prescription drugs which tend to be single chemical entities and are quite amenable to testing at different doses, botanicals are complex mixtures. Panax ginseng, for example, has been found to contain over five hundred different compounds! Different varieties of ginseng will have different chemical profiles and even for one specific variety the composition will depend on when it is harvested, how much sun exposure it has seen and how it is processed. Attempts are sometimes made at standardization, but that also presents problems. Take the case of St. Johns Wort. Dozens of compounds have been identified in this plantt with one, hypericin, usually being the subject of standardization because it is readily tested for. Hypericin does not have any anti-depressant activity but the thinking is that if a supplement contains a given dose of this compound, all the other compounds will be present in a fixed ratio. Actually, this is not the case.
The best candidate for the antidepressant effect of St. John’s Worth is hyperforin, a compound that boosts the activity of serotonin, norepinephrine and dopamine, all neurotransmitters that are associated with mood elevation. It turns out, however, that the amount of hyperforin in an extract of St. John’s Wort is unrelated to the amount of hypericin, so that different supplements may have significantly different activity even if they are standardized to 0.3% hypericin, which is commonly done. Obviously, standardization should be in terms of hyperforin.
But this is not the biggest problem with St. John’s Wort. The major concern is that it can cross react with other medications, enhancing or detracting from their effect. Since St. John’s Wort increases serotonin levels, it can result in “serotonin syndrome” if taken concurrently with drugs that have a similar effect, such as the serotonin reuptake inhibitors (SSRIs). Symptoms can range from tremor and diarrhea to very dangerous confusion, muscle stiffness, drop in body temperature, and possibly even death.
Another issue is that hyperforin can activate genes that code for the production of Cytochrome P450 3A4, an enzyme found mainly in the liver and in the small intestine that oxidizes small foreign organic molecules, such as toxins or drugs, so that they can be removed from the body. Digoxin, used to treat congestive heart failure, is an example of a drug that is eliminated from the body via reaction with this enzyme. If the enzyme levels are unusually high because of ingested hyperforin, the drug will be more quickly eliminated, reducing its efficacy. Dozens of prescription drugs are metabolized by the cytochrome P-450 enzymes, meaning that people taking them should stay away from St. John’s Wort. A number of “miracle babies” have been born to women who took St. John’s Wort while they were also taking the birth control pill.Read more
During the Civil War northern forces blocked a number of Confederate ports. One of the consequences of the blockade was a dire shortage of cinchona bark imported from South America. The bark was in great demand, being the first substance ever found to be an effective treatment for malaria. Quinine, first isolated in 1820 was the active ingredient. Because of a lack of quinine, word went out from the surgeon general of the Confederate army asking that a search be launched for any native plants that might have fever reducing properties similar to cinchona. An obvious starting point for such a search was plants that had been used by native North Americans for their supposed medicinal properties. One of these was goldenseal, long used as a snake bite remedy and health tonic by natives. Like quinine, goldenseal tasted very bitter, so it seemed a good candidate for testing against malaria. Unfortunately it didn’t work, but doctors noted that when they used goldenseal in combination with quinine, less quinine was needed. They didn’t understand why this was the case, but today we can offer an explanation thanks to ourknowledge about how drugs are metabolized. Our body regards drugs as foreign intruders and attempts to eliminate them. One common method is through the action of the Cytochrome P450 enzymes that have the ability to break down small molecules. Like any plant, goldenseal contains numerous compounds, but two, namely berberine and hydrastine, bind to these enzymes and inhibit their activity. The result is that drugs are not broken down, they stay in the bloodstream longer and therefore become more potent. This can be a problem. Many medications are metabolized by the Cytochrome P-450 enzymes meaning that inactivation of these enzymes leads to higher than desired blood levels of the drug. Some of the drugs that fall into this category include Prozac, Lopressor, Zyprexa, Halcion, Viagra along with many others. The best bet is not to use goldenseal in combination with any prescription drug, especially given the lack of evidence for any of goldenseal’s supposed benefits. The ailments it purportedly benefits include the common cold, digestive problems, diarrhea, constipation, hemorrhoids, flatulence, acne, dandruff, eye inflammation, chronic fatigue, gonorrhea and fever. In general, when such a cacophony of benefits are attributed to a substance, it is unlikely that any of them will pass scientific muster. One of the popular myths about goldenseal is that it can mask the presence of illegal drugs in the urine. This idea can be traced back to “Stringtown on the Pike,” a novel written by chemist John Uri Lloyd in 1901 in which a boy is convicted for poisoning his uncle with strychnine. The tragedy is that the chemist who testified about the strychnine poisoning made a mistake. Goldenseal root taken in the uncle’s morning tonic produced a false positive for strychnine and the uncle’s death was actually from natural causes. Utterly devastated, the chemist takes his life with “too dangerous a drug to be known through science to the public.” Lyoyd came up with this plot after having noted the “remarkable correspondence” between the actions of strychnine and the goldenseal compound hydrastis in his research. Somehow this gave rise to the myth that goldenseal can mask drugs in the urine. It can’t.Read more
Sir Winston Churchill said Alan Turing’s breaking of German codes for secret messages shortened the Second World War by two years. Computer scientists credit Turing with formulating the philosophical principles that power every computer and smartphone today. Researchers in artificial intelligence, meanwhile, label him the founder of their field. Chemists say Turning predicted the existence of reactions that change colour in a periodic fashion before these had ever been observed. Biologists say his theories of “morphogenesis,” the biological process that causes an organism to develop its shape, explain phenomena such as the stripes of a zebra by predicting the effects of the diffusion of two different chemical signals, one activating and one deactivating growth. The British government said Turing was a homosexual who needed to be chemically castrated. Police said his death was the result of suicide, probably by consuming a cyanide-laced apple. Steve Jobs said he wished the Apple logo had been devised in Turing’s honour, reflecting how everyone says that he was a computational genius. Few, however, know that Turing’s first scientific infatuation was with chemistry.
In 1924, at the age of 12, young Turing got his hands on Natural Wonders Every Child Should Know, by Edwin Brewster. He was totally taken by the book’s discussion of plants containing chemicals like strychnine and atropine, capable of killing or curing. He was also intrigued by how “carbon dioxide becomes in the blood ordinary cooking soda” and how “the blood carries the soda to the lungs where it changes to carbon dioxide again, exactly as it does when, as cooking soda you add it to flour and use it to raise cake.” He was overjoyed when, for Christmas, he was given a set of chemicals, crucibles and test tubes. He immediately put it to use to extract minute quantities of iodine from seaweed.
Knowing of his interest in iodine, Christopher Marcom, an older student with whom Alan had developed a friendship that bordered on infatuation, told him of an experiment involving solutions of iodates and sulphites that, when mixed, resulted in the formation of iodine. When starch was present in the solution, the formation of iodine was signalled by the sudden appearance of a deep blue colour, characteristic of a starch-iodine complex. Turing was intrigued by the concentration-dependent time delay in the appearance of the blue colour and was convinced that the proper use of mathematics could predict the results. Indeed, it was this little problem that may have launched him into an area where his genius would be prominently displayed, namely mathematics and computer logic.
After receiving an undergraduate degree in mathematics from the University of Cambridge, Turing obtained a PhD from Princeton University, where he developed a strong interest in cryptography, the science of writing messages in secret code. When Britain declared war on Germany in 1939, Turing was immediately offered a position as a code breaker. The Germans had developed the Enigma, a machine that used a combination of mechanical and electrical effects to transform a message typed on a keyboard into what seemed like an undecipherable jumble of letters until the code was run through another Enigma unit. With colleague Gordon Welchman, Turing developed early computers, called “bombes,” that were capable of breaking the code. The Allies now had the ability to decode messages sent to German U-boats about planned attacks on supply ships carrying supplies vital for the war effort.
After the war, Turing worked at the National Physical Laboratory designing computers and then in 1948 joined the mathematics department at the University of Manchester where, in 1950, he launched the concept of artificial intelligence with his paper that asked the question “Can Machines Think?” In it he also introduced the Turing Test, aimed at determining whether a human can detect if he is communicating via a keyboard with another human or with a machine. The emphasis is on how closely the answers to questions posed resemble typical human answers, not on whether the answers are correct. If at least 30 per cent of judges believe that they are talking to a human when they are actually speaking with a computer, the computer is said to have passed the Turing Test.
Now, for the first time ever, Eugene Goostman, which is the name of a computer program created by Vladimir Veselov of Russia and Eugene Demchenko of Ukraine, has managed to fool the required number of judges into believing that they were actually speaking with a 13-year-old Ukrainian boy. The historic event took place at the renowned Royal Society in London, poignantly on the 60th anniversary of Turing’s death.
The death is still mired in mystery. In 1952, Turing’s house was burgled and suspicion fell on a young male guest who had been staying with him. During the investigation, Turing’s homosexuality was revealed and since this was a criminal offence at the time, he was charged with “gross indecency.” The option, the judge explained, was either jail time or “chemical castration.”
Back in the 1940s, there had been speculation that homosexuality was caused by low levels of testosterone, the male sex hormone. But if anything, treatment with testosterone increased the sex drive. Researchers then turned to female hormones, hoping to counter the effects of testosterone and soon discovered that these did indeed reduce libido. To avoid prison, Turing agreed to undergo a year-long treatment with the synthetic estrogen diethylstilbestrol (DES), a regimen that he apparently managed with no significant problems, carrying on as usual with his work.
We can only guess at what this brilliant mind could have accomplished had it not been put out of commission by cyanide in 1954. The official verdict was suicide, with speculation that a half-eaten apple found at the bedside had been used to deliver the poison. The apple was never tested and Turing was in fact known to favour an apple at bedtime. Given that he had shown no signs of depression and had planned meetings for the next week, some contend that Turing accidentally poisoned himself with some of the cyanide he was using in gold-plating experiments in his small apartment. And then there are the conspiracy theorists who maintain he was assassinated because authorities were worried that homosexuals who possessed sensitive information were a security threat to Britain.
In 2013, Queen Elizabeth II signed an official pardon for Turing’s conviction for gross indecency. Indeed, the only indecency had been the appalling way in which one of the greatest minds of the 20th century was treated.Read more
Dr. Mehmet Oz was asked to testify in front of a U.S. Senate Transport, Commerce and Science subcommitte on fraudulent weight loss products. It is a subject he knows a fair bit about. After all he has promoted everything from raspberry ketone and green coffee bean extract to acai berries, garcinia cambogia, Yakin syrup, mango seed extract, sea buckthorn, forskolin, saffron extract, capsiberry and FBCx. What do these have in common? A lack of evidence of efficacy. Oz claims to have “passionately studied” the products but the documentation he studied must have been furnished by the promoters. Why was he called to testify in front of this committee instead of true experts on weight control? Because of the “Oz Effect,” which is very real. He has legions of quasi-religious followers who hang on his every word. But with such power comes the burden of responsibility. He has the pulpit. He does do some good things. But he much too readily dives into the abyss of nonsense.
Oz was really taken to task by Senator Clair McCaskill of Missouri over hyping supplements that promise the moon without evidence and then presenting himself as a champion dedicated to fighting the fraudsters. It is true that he did go after some fraudsters, not because they were promoting products that do not work, but because they were using his name to promote them. Of course his “whistleblowing” also made for good TV. Actually the fraudsters weren't saying anything other than what Oz himself had said on his show about "magical" green coffee bean extract or the "miracle" of garcinia cambogia. He defended his portrayal of these products by waving around some studies, an impressive TV moment. But if anyone cared to actually read the studies they would quickly see the absence of any miracle.
Oz made a big deal of the fact that he doesn't sell any supplements. That's true. But he has repeatedly had cranks like Joe Mercola and Mike Adams and a host of others who sell a bevy of supplements including the ones Oz talks about. Having these characters on the show endorses them and by association their antics as well. Oz claims that he uses flowery language to promote products because he regards himself as a cheerleader for weight loss, and while he admits none of his recommendations other than diet and exercise lead to long term weight loss, they can “jump start” a weight loss regimen. And where is the evidence for that? There isn't any.
He did introduce a humorous element into the discussion when he claimed the only mistake he had made was not giving a list of "reputable" companies that sell the products he has "researched." That in his view would undercut the fly-by-night operators who sell disreputable supplements. Really? His problem is that a supplement marketed as "raspberry ketone" may not actually contain this chemical, not that raspberry ketone just doesn't work for weight loss?
After much well deserved chastizing he promised to be a good boy and use less "flowery" language in the future. He also said he hadn't talked about miracles for two years at which point Senator McCaskill came out with a couple of recent examples including one about Oz talking about an "itzy bitzy pill that will flush fat right out of your body." Unfortunately the camera didn't show his face at this time. Finally Oz said that he would right his wrongs by publicizing a list of companies that can be trusted to sell supplements that meet his standards. And what dietary supplements are there that can actually cause weight loss? Ephedra was one and would have been alright had it not killed people. Now of course ephedra supplements are illegal. Other than that, perhaps some sort of fiber pill (FBCx is the one he promotes) but even here the evidence is poor. About as poor as Oz's performance in front of the Senate subcommittee. And they didn't even ask him about his penchant for "therapeutic touch" or his recommendation for "Derriere Diet Butt-Busting Brownies" or about fawning over guests on his show who claim to talk to the dead.Read more