Zoe Cormier A study of two ancient hominins from South Africa suggests that changes in the shape and size of the middle ear occurred early in our evolution. Such alterations could have profoundly changed what our ancestors could hear — and perhaps how they could communicate. Palaeoanthropologist Rolf Quam of Binghamton University in New York state and his colleagues recovered and analysed a complete set of the three tiny middle-ear bones, or ossicles, from a 1.8-million-year-old specimen of Paranthropus robustus and an incomplete set of ossicles from Australopithecus africanus, which lived from about 3.3 million to around 2.1 million years ago. The ossicles are the smallest bones in the human body, and are rarely preserved intact in hominin fossils, Quam says. In both specimens, the team found that the malleus (the first in the chain of the three middle-ear bones) was human-like — smaller in proportion compared to the ones in our ape relatives. Its size would also imply a smaller eardrum. The similarity between the two species points to a “deep and ancient origin” of this feature, Quam says. “This could be like bipedalism: a defining characteristic of hominins.” It is hard to draw conclusions about hearing just from the shape of the middle-ear bones because the process involves so many different ear structures, as well as the brain itself. However, some studies have shown that the relative sizes of the middle-ear bones do affect what primates can hear2. Genomic comparisons with gorillas have indicated that changes in the genes that code for these structures might also demarcate humans from apes3. © 2013 Nature Publishing Group

Keyword: Hearing; Evolution
Link ID: 18151 - Posted: 05.14.2013

by Michael Balter Researchers debate when language first evolved, but one thing is sure: Language requires us not only to talk but also to listen. A team of scientists now reports recovering the earliest known complete set of the three tiny middle ear bones—the malleus ("hammer"), incus ("anvil"), and stapes ("stirrup")—in a 2.0-million-year-old skull of Paranthropus robustus, a distant human relative found in South Africa (see photo). Reporting online today in the Proceedings of the National Academy of Sciences, the researchers found that the malleus of P. robustus, as well one found earlier in the early human relative Australopithecus africanus, is similar to that of modern humans, whereas the two other ear bones most closely resemble existing African and Asian great apes. The team is not entirely sure what this precocious appearance of a human-like malleus means. But since the malleus is attached directly to the eardrum, the researchers suggest that it might be an early sign of the high human sensitivity to middle-range acoustic frequencies between 2 and 4 kilohertz—frequencies critical to spoken language, but which apes and other primates are much less sensitive to. © 2010 American Association for the Advancement of Science

Keyword: Hearing; Evolution
Link ID: 18150 - Posted: 05.14.2013

By DAVID DOBBS In the autistic person, it seems, hums a vital and distinctive essence — but one whose nature is obscured by thick layers of behavior and perception. Or, as Temple Grandin puts it, “two panes of glass.” For a quarter century, Dr. Grandin — the brainy, straight-speaking, cowboy-shirt-wearing animal scientist and slaughterhouse designer who at 62 is perhaps the world’s most famous autistic person — has been helping people break through the barriers separating autistic from nonautistic experience. Like Dr. Sacks, who made her famous as the title figure in his 1995 collection “An Anthropologist on Mars,” Dr. Grandin has helped us understand autism not just as a phenomenon, but as a different but coherent mode of existence that otherwise confounds us. In her own books and public appearances, she excels at finding concrete examples that reveal the perceptual and social limitations of autistic and “neurotypical” people alike. In “The Autistic Brain,” her latest book, written with the science author Richard Panek, she shows this talent most vividly in a middle chapter that looks at the sensory world of autism. It is a world filled with anomalies, in which everyday sensations can be overwhelming: A school bell can feel like a dentist’s drill, a scratchy shirt like a swarm of fire ants. In other cases the autistic person may feel so little sensation that she’ll try to fill the vacuum and create some sort of order — hence the rocking, twirling, hand-flapping, noisemaking behaviors that can discomfit and alienate onlookers. © 2013 The New York Times Company

Keyword: Autism
Link ID: 18149 - Posted: 05.14.2013

By Melanie Tannenbaum Imagine that you’re an infant monkey, and you’ve just been thrown into a cage after several hours in isolation. You’ve been deprived of food, so you’re starving. Facing you are two adult-looking (fake) monkeys, designed to look like each one could potentially be your mother. On the left is a “wire mother,” equipped with a bottle and feeding tube so you can cling to her and fill your belly with milk. On the right is a “cloth mother,” with no bottle, but with a fuzzy terrycloth exterior that will allow for hours of soft, warm snuggles. You can only run to one of the monkeys. Which one will you choose? Six or seven decades ago, many psychologists would have claimed that any affection that we experience towards our parental figures is a purely behaviorist response. After many instances of conditioning a sense of “positive affect” after receiving life-sustaining food from mothers, children associate that positive emotion with these caregivers, an association that serves as the sole explanation for why people “love” their mothers. But that’s not what Harry Harlow thought. Harlow, a psychologist working at the University of Wisconsin – Madison during the 1960s, believed that there was something more important underlying our affection for Mom and Dad than our primal need to eat and survive. He believed that there was an additional factor: Comfort. What Harlow did to test this hypothesis was arguably ingenious, though inarguably cruel.1 Harlow deprived monkeys of food, making them desperately hungry, and then stuck them into a cage where they had a choice of two “mother figures” to run towards. On the left was a wire mother – cold and uncomfortable, yet equipped with a bottle that would feed the baby with life-sustaining nutrients. On the right was a cloth mother – warm, soft, and comfortable, yet unable to provide the infant with any food. If the only reason why we “love” our mothers (and fathers) is based on a conditioned response to our need for food, then the infant monkeys should run to the wire mothers who can feed them every time. © 2013 Scientific American

Keyword: Sexual Behavior; Development of the Brain
Link ID: 18148 - Posted: 05.14.2013

By ANDREW C. REVKIN Twenty-two months ago, I interrupted my nonstop reporting about paths toward a sustainable future for our species to focus on sustaining myself. The hiatus was not by choice, but was mandated by a stroke — the out-of-the-blue variant, the rare kind of “brain attack” (the term preferred by some neurologists) that is most often seen in otherwise healthy, youngish middle-aged people. It’s Fourth of July weekend, 2011 — a beautiful, if hot, morning for a run in the Hudson Valley woods with my son Daniel, back from brief service in the Israeli army. I’m eager to be pushed hard. I’m not even a lapsed middle-aged athlete; I’m truly negligent when it comes to exercise. We’re jogging up a steep path, and my breathing gets deeper and faster. At a particularly tough turn, I pause, hands on knees. “Come on, keep it up, Dad.” I’m panting but don’t want to disappoint. We press on. But I stop again, this time insisting that Daniel run ahead. I rest in the mottled shade and sunlight of the woods until he returns. Then I realize that through my left eye, the world appears paisley — as if I were looking through a patterned curtain. Something is really wrong. We make it back to the car. Daniel takes the wheel. Back home, I take a shower, thinking that cooling off will help. For the first time, a thought flickers. Could this be a stroke? Almost unconsciously, I take half a dozen baby aspirin. I know enough about aspirin’s blood-thinning properties to think this can’t hurt. Copyright 2013 The New York Times Company

Keyword: Stroke
Link ID: 18147 - Posted: 05.14.2013

By ANAHAD O'CONNOR The nation’s largest cardiovascular health organization has a new message for Americans: Owning a dog may protect you from heart disease. The unusual message was contained in a scientific statement published on Thursday by the American Heart Association, which convened a panel of experts to review years of data on the cardiovascular benefits of owning a pet. The group concluded that owning a dog, in particular, was “probably associated” with a reduced risk of heart disease. People who own dogs certainly have more reason to get outside and take walks, and studies show that most owners form such close bonds with their pets that being in their presence blunts the owners’ reactions to stress and lowers their heart rate, said Dr. Glenn N. Levine, the head of the committee that wrote the statement. But most of the evidence is observational, which makes it impossible to rule out the prospect that people who are healthier and more active in the first place are simply more likely to bring a dog or cat into their home. “We didn’t want to make this too strong of a statement,” said Dr. Levine, a professor at the Baylor College of Medicine. “But there are plausible psychological, sociological and physiological reasons to believe that pet ownership might actually have a causal role in decreasing cardiovascular risk.” Nationwide, Americans keep roughly 70 million dogs and 74 million cats as pets. Copyright 2013 The New York Times Company

Keyword: Emotions; Neuroimmunology
Link ID: 18146 - Posted: 05.11.2013

By Puneet Kollipara Identical twin mice sharing the same mazelike environment develop distinct personalities based on how much they explore their surroundings, researchers report in the May 10 Science. After death, those differences were reflected in the animals’ brains. The study “highlights something for which we had some intuition before, but actually quantifies it,” says Fred Gage, a neuroscientist at the Salk Institute for Biological Studies in La Jolla, Calif. Some character and biological differences between identical twins may originate as early as pregnancy. But twins become more and more different as life goes on, even when they grow up together. Scientists have recognized that having distinct experiences within the same environment might boost such personality differences, but that’s difficult to test in humans. Studying it in animals has multiple benefits. “You can keep the genes constant and also keep the environment constant,” says Gerd Kempermann of the Center for Regenerative Therapies Dresden in Germany. “It’s much more controlled than in a human situation.” Researchers led by Kempermann put 40 genetically identical female mice in an elaborate cage and observed their behavior. The cage had multiple levels linked together by tubes and contained toys and other features that the animals could explore. The researchers equipped each mouse with a microchip that tracked its location, using the animals’ movements as a measure of exploratory behavior. Initially, the mice differed only slightly in their tendency to roam. As they grew older, all tended to explore more often, but the differences among the mice grew more pronounced. © Society for Science & the Public 2000 - 2013

Keyword: Epigenetics; Genes & Behavior
Link ID: 18145 - Posted: 05.11.2013

Heidi Ledford Nassir Ghaemi, director of the Mood Disorders Program at Tufts Medical Center in Boston, Massachusetts, has felt shackled by the Diagnostic and Statistical Manual of Mental Disorders (DSM), often called the bible of psychiatry. Some of his depressed patients occasionally show manic behaviour but do not fulfil the DSM’s criteria for a diagnosis of bipolar disorder. Ghaemi is interested in whether such patients might respond better to drugs for bipolar disorder than for depression. But his colleagues warned him against straying from the DSM when he applied for funding at the US National Institute of Mental Health (NIMH), because peer reviewers tended to insist on research that hewed to DSM categories. Ghaemi held off from applying. If NIMH director Thomas Insel has his way, Ghaemi and other mental-health researchers will no longer feel the weight of the DSM. “NIMH will be re-orienting its research away from DSM categories,” Insel wrote in a blog entry on 29 April. The latest edition, the DSM-5, will be unveiled on 22 May at the annual meeting of the American Psychiatric Association in San Francisco, California. Like many psychiatrists, Insel questions whether the DSM’s categories accurately reflect the way the brain works. He is pushing a project that aims to create a new framework that classifies mental-health disorders according to their biological roots. “Going forward, we will be supporting research projects that look across current categories — or sub-divide current categories — to begin to develop a better system,” Insel wrote. The blog post made waves in the media and rattled some psychiatric clinicians and researchers. But Insel says that he has been talking about the issue since 2008. “The word was just still not out there,” he says. Insel says that he has increasingly received complaints from grant applicants who have tried to follow his guidance, only to be shot down by peer reviewers for eschewing DSM scripture. © 2013 Nature Publishing Group

Keyword: Schizophrenia; Depression
Link ID: 18144 - Posted: 05.11.2013

by Claudia M Gold It seems that the National Institute of Mental Health (NIMH) may have dealt a death blow to the recently published Diagnostic and Statistical Manual of Mental Disorders (DSM 5) when the organization declared they would no longer fund research based on the DSM system of diagnosis. The views of NIMH director Thomas Insel were referenced in the recent New York Times article on the subject. His goal was to reshape the direction of psychiatric research to focus on biology, genetics and neuroscience so that scientists can define disorders by their causes, rather than their symptoms. I am no fan of the DSM system, which reduces complex experience to lists of symptoms; focusing on the "what" rather than the "why." However, the NIMH model has limits as well. There seems to be a wish to study mental illness in the same way we study cancer or diabetes. While I certainly have great respect for the complexity of the pancreas, or the process of malignant transformation of cells, trying to understand the brain/mind in an analogous way seems to be an unnecessary and even undesirable reduction of human experience. What is missing from both paradigms is recognition of the relational and historical context of being human. Fortunately there seems to be awareness that neither paradigm is complete. The Times article goes on to say: Dr. Insel is one of a growing number of scientists who think that the field needs an entirely new paradigm for understanding mental disorders, though neither he nor anyone else knows exactly what it will look like. © 2013 NY Times Co.

Keyword: Schizophrenia; Depression
Link ID: 18143 - Posted: 05.11.2013

by Helen Thomson "I was sitting on the toilet. I suddenly felt an explosion in the left side of my head and ended up on the floor. I think the only thing that kept me conscious was that I didn't want to be found with my pants down. Then the other side of my head went bang! I woke up in hospital and looked out of the window to see the tree was sprouting numbers. 3, 6, 9. Then I started talking in rhyme…" Ten days after having a subarachnoid haemorrhage – a stroke caused by bleeding in and around the brain – Tommy McHugh, an ex-con who'd been in his fair share of scraps, became a new man, with a personality that nobody recognised. When he was a young man, Tommy did time in prison. But after his stroke at age 51, everything changed. "I could taste the femininity inside of myself," he said. "My head was full of rhymes and images and pictures." Not only did he feel a sudden urge to write poetry, but he also began to paint and draw obsessively for up to 19 hours a day. He was never artistic before – in fact, he joked that he'd never even been in an art gallery "except to maybe steal something". Desperate to find out what was going on, Tommy wrote to several neuroscientists and end up working closely with Alice Flaherty at Harvard Medical School and Mark Lythgoe at University College London. © Copyright Reed Business Information Ltd.

Keyword: Laterality; Stroke
Link ID: 18142 - Posted: 05.11.2013

By Ian Chant Most people make good decisions most of the time. But when drug addiction, disease or brain injury enters the picture, rational thinking can go awry. What if the damaged brain just needed a little reminder of how it feels to choose wisely? Enter the MIMO neural prosthesis, an array of electrodes implanted in the brain that make contact with eight neuron circuits in the prefrontal cor-tex, the brain's command center for decision making. The device can both record the brain activity associated with good choices and stimulate the relevant neurons to get the brain back on track. Although the implant can listen in only on a tiny subset of the neurons in this region, the scientists who developed it, based at Wake Forest Baptist Medical Center, were surprised to discover that they could still pick up signature patterns associated with correct choices, at least in the context of a simple task. The researchers tested the neural prosthesis on monkeys that were trained to move a cursor over a picture on a computer screen to get a food reward. The implant first recorded the brain activity associated with choosing the correct picture. Then the monkeys were given cocaine, and their performance plummeted. But when the implant was switched on to send electric current to the neurons that had earlier been associated with the correct answers, the monkeys immediately started selecting the right pictures again. Some of them did an even better job than they had before receiving cocaine. © 2013 Scientific American,

Keyword: Drug Abuse; Learning & Memory
Link ID: 18141 - Posted: 05.11.2013

By Bruce Bower Provocative evidence that certain memory exercises make people smarter has sparked the rise of online brain-training programs such as Lumosity. But at least one type of brain training may not work as advertised, a new study finds. As expected, practicing improved volunteers’ performance on tests of memory and the ability to locate items quickly in busy scenes, say psychologist Thomas Redick of Indiana University Purdue University Columbus and his colleagues. That improvement did not, however, translate into higher scores on tests of intelligence and multitasking, the researchers report in the May Journal of Experimental Psychology: General. Redick’s investigation is part of a growing scientific debate about brain training, which is promoted by some companies as having a variety of mental benefits. Some researchers say that extensive instruction and training on memory tasks can indeed fortify reasoning and problem solving. Others are skeptical that vigorous memory sessions produce such wide-ranging effects. The dispute feeds into a longstanding scientific controversy about whether enriched environments can increase intelligence, as measured on IQ tests. What’s not up for debate is that many people feel smarter after brain training. In the new study, 10 of 23 individuals who completed memory sessions said that the program helped them to think, multitask and focus better in daily life. But the scientists say that even if some participants performed daily tasks better after memory training, they may simply have tried harder or felt better about their efforts due to a belief that training had strengthened their minds. © Society for Science & the Public 2000 - 2013

Keyword: Learning & Memory
Link ID: 18140 - Posted: 05.11.2013

By John McCarthy Into brains of newborn mice, researchers implanted human “progenitor cells.” These mature into a type of brain cell called astrocytes (see below). They grew into human astrocytes, crowding out mouse astrocytes. The mouse brains became chimeras of human and mouse, with the workhorse mouse brain cells – neurons – nurtured by billions of human astrocytes. Neuroscience is only beginning to discover what astrocytes do in brains. One job that is known is that they help neurons build connections (synapses) with other neurons. (Firing neurotransmitter molecules across synapses is how neurons communicate.) Human astrocytes are larger and more complex than those of other mammals. Humans’ unique brain capabilities may depend on this complexity. Human astrocytes certainly inspired the mice. Their neurons did indeed build stronger synapses. (Perhaps this was because human astrocytes signal three times faster than mouse astrocytes do.) Mouse learning sharpened, too. On the first try, for instance, altered mice perceived the connection between a noise and an electric shock (a standard learning test in mouse research). Normal mice need a few repetitions to get the idea. Memories of the doctored mice were better too: they remembered mazes, object locations, and the shock lessons longer. The reciprocal pulsing of billions of human and mouse brain cells inside a mouse skull is a little creepy. Imagine one of these hybrid mice exploring your living room. Would you feel like a Stone Age tribesman observing a toy robot? Does the thing think? © 2013 Scientific American

Keyword: Glia; Learning & Memory
Link ID: 18139 - Posted: 05.11.2013

Roberta Kwok Sitting motionless in her wheelchair, paralysed from the neck down by a stroke, Cathy Hutchinson seems to take no notice of the cable rising from the top of her head through her curly dark hair. Instead, she stares intently at a bottle sitting on the table in front of her, a straw protruding from the top. Her gaze never wavers as she mentally guides a robot arm beside her to reach across the table, close its grippers around the bottle, then slowly lift the vessel towards her mouth. Only when she finally manages to take a sip does her face relax into a luminous smile. This video of 58-year-old Hutchinson illustrates the strides being taken in brain-controlled prosthetics1. Over the past 15 years, researchers have shown that a rat can make a robotic arm push a lever2, a monkey can play a video game3 and a person with quadriplegia — Hutchinson — can sip from a bottle of coffee1, all by simply thinking about the action. Improvements in prosthetic limbs have been equally dramatic, with devices now able to move individual fingers and bend at more than two dozen joints. But Hutchinson's focused stare in that video also illustrates the one crucial feature still missing from prosthetics. Her eyes could tell her where the arm was, but she could not feel what it was doing. Nor could she sense when the grippers touched the bottle, or whether it was slipping out of their grasp. Without this type of sensory feedback, even the simplest actions can be slow and clumsy, as Igor Spetic of Madison, Ohio, knows well. Fitted with a prosthetic after his right hand was crushed in an industrial accident in 2010, Spetic describes breaking dishes, grabbing fruit too hard and bruising it and dropping a can when trying to pick it up at the local shop. Having a sense of touch would be “tremendous”, he says. “It'd be one step closer to having the hand back.” © 2013 Nature Publishing Group,

Keyword: Pain & Touch; Robotics
Link ID: 18138 - Posted: 05.09.2013

Ed Yong Many moths have evolved sensitive hearing that can pick up the ultrasonic probes of bats that want to eat them. But one species comes pre-adapted for anything that bats might bring to this evolutionary arms race. Even though its ears are extremely simple — a pair of eardrums on its flanks that each vibrate four receptor cells — it can sense frequencies up to 300 kilohertz, well beyond the range of any other animal and higher than any bat can squeak. “A lot of previous work has suggested that some bats have evolved calls that are out of the hearing range of the moths they are hunting. But this moth can hear the calls of any bat,” says James Windmill, an acoustical engineer at the University of Strathclyde, UK, who discovered the ability in the greater wax moth (Galleria mellonella). His study is published in Biology Letters1. Windmill's collaborator Hannah Moir, a bioacoustician now at the University of Leeds, UK, played sounds of varying frequencies to immobilized wax moths. As the insects “listened”, Moir used a laser to measure the vibrations of their eardrums, and electrodes to record the activity of their auditory nerves. The moths were most sensitive to frequencies of around 80 kilohertz, the average frequency of their courtship calls. But when exposed to 300 kilohertz, the highest level that the team tested, the insects' eardrums still vibrated and their neurons still fired. © 2013 Nature Publishing Group

Keyword: Hearing; Evolution
Link ID: 18137 - Posted: 05.09.2013

By NICHOLAS BAKALAR Two studies have found that depression and the use of certain antidepressants are both associated with increased risk for Clostridium difficile infection, an increasingly common cause of diarrhea that in the worst cases can be fatal. Researchers studied 16,781 men and women, average age 68, using hospital records and interviews to record cases of the infection, often called C. diff, and diagnoses of depression. The interviews were conducted biennially from 1991 to 2007 to gather self-reports of feelings of sadness and other emotional problems. There were 404 cases of C. difficile infection. After adjusting for other variables, the researchers found that the risk of C. diff infection among people with a history of depression or depressive symptoms was 36 to 47 percent greater than among people without depression. A second study, involving 4,047 hospitalized patients, average age 58, found a similar association of infection with depression. In addition, it found an association of some antidepressants — Remeron, Prozac and trazodone — with C. diff infection. There was no association with other antidepressants. “We have known for a long time that depression is associated with changes in the gastrointestinal system,” said the lead author, Mary A.M. Rogers, a research assistant professor at the University of Michigan, “and this interaction between the brain and the gut deserves more study.” Both reports appeared in the journal BMC Medicine. Copyright 2013 The New York Times Company

Keyword: Depression; Neuroimmunology
Link ID: 18136 - Posted: 05.09.2013

By James Gallagher Health and science reporter, BBC News Flu during pregnancy may increase the risk of the unborn child developing bipolar disorder later in life, research suggests. A study of 814 expectant women, published in JAMA Psychiatry, showed that infection made bipolar four times more likely. The overall risk remained low, but it echoes similar findings linking flu and schizophrenia. Experts said the risks were small and women should not worry. Bipolar leads to intense mood swings, which can last months, ranging from depression and despair to manic feelings of joy, overactivity and loss of inhibitions. Researchers at the Columbia University Medical Center identified a link between the condition, often diagnosed during late teens and twenties, and experiences in the womb. In their study looking at people born in the early 1960s, bipolar disorder was nearly four times as common in people whose mothers caught flu during pregnancy. The condition affects about one in 100 people. The lead researcher, Prof Alan Brown, estimated that influenza infection during pregnancy could lead to a 3-4% chance of bipolar disorder in the resulting children. However, in the vast majority of cases of bipolar disorder there would no history of flu. BBC © 2013

Keyword: Schizophrenia; Development of the Brain
Link ID: 18135 - Posted: 05.09.2013

By Ben Thomas Horror isn’t the only film genre that specializes in dread. War movies like Apocalypse Now, sci-fi mysteries like Brazil and Blade Runner, and dramas like Melancholia and Requiem for a Dream all masterfully evoke a less violent, more subtle and pervasive sense that something is unwell with the world – that somewhere along the line, something went deeply wrong and now normality itself is unraveling before our eyes. The director David Lynch has arguably built his entire career on directing these kinds of films. In Lynch’s universe, even the most banal moments are still somehow suffused with unnerving suspense. In films like Blue Velvet and Mulholland Drive, disturbing surprises erupt into scene after scene of buried tension, until every ordinary conversation feels like a trap waiting to spring. And then there’s the infamous Eraserhead, where family life itself is transformed into an onslaught of surreal and nauseating images. It’s hard to come away from these movies without feeling that a little of Lynch’s unease has rubbed off on you. So when a team of researchers at the University of British Columbia set out to describe and treat an ancient biological alarm system buried deep within the human brain, they turned to Lynch’s films as an analogy for – and a set of examples of – the feeling of omnipresent yet maddeningly vague “wrongness” that seems to underlie many anxiety disorders. © 2013 Scientific American

Keyword: Emotions
Link ID: 18134 - Posted: 05.09.2013

By Nathan Seppa Multiple sclerosis, long considered a disease of white females, has affected more black women in recent years, a new study finds. Hispanic and Asian women, who have previously seemed to be at less risk of MS, remain so, researchers report May 7 in Neurology. The findings bolster a theory that vitamin D deficiency, which is common in people with dark skin in northern latitudes, contributes to MS. MS is a debilitating condition in which the protective coatings on nerves in the central nervous system get damaged, resulting in a loss of motor control, muscle weakness, vision complications and other problems. The National Multiple Sclerosis Society estimates that 2.1 million people worldwide have the condition. The researchers scanned medical information from 3.5 million people who were members of the health maintenance organization Kaiser Permanente Southern California and found that 496 people received diagnoses of MS from 2008 through 2010. Of these patients, women comprised 70 percent, not an unusual fraction for people with MS. Surprisingly, the patients included 84 black women. That means the annual incidence of MS in black women was 10.2 cases per 100,000 people. That’s not a great risk for an individual, but it was higher than the annual rates for white, Hispanic and Asian women, which were 6.9, 2.9 and 1.4 per 100,000 people, respectively. Among blacks, women had three times the incidence as men; in the other racial and ethnic groups, the MS rate in women was roughly double that of men. © Society for Science & the Public 2000 - 2013

Keyword: Multiple Sclerosis; Neuroimmunology
Link ID: 18133 - Posted: 05.09.2013

By Ingrid Wickelgren I have seen the invisible arms of multiple sclerosis, a potentially devastating disease of the nervous system, touch friends, relatives and acquaintances. They perturbed the personality of a father of a close friend and left him unable to keep a job and support the family. They forced a young woman I met years ago to walk tentatively, watching her step. They put one beloved member of my extended family with two small children in a wheelchair and took away his voice. Nowadays, many people with MS find that new medications can mitigate the progression of their disease (see “New Treatments Tackle Multiple Sclerosis,” by James D. Bowen, Scientific American Mind, July/August 2013). But many mysteries remain about the cause of the disorder and no one knows how to prevent or cure it. About a decade ago, a technology entrepreneur named Art Mellor, who was diagnosed with MS in 2000, founded an organization called Accelerated Cure Project based in Waltham, Massachusetts to help speed progress on solving these mysteries, in part through greater collaboration among scientists. In one of its efforts, it maintains a repository of thousands of blood samples from patients who visited any of 10 U.S. clinics. The samples are made available to anyone willing to share their data with the Project. Scientists have used these samples in more than 70 different studies into the causes of MS and how to diagnose and treat it. A number of these experiments involve trying to identify molecular signs of the disease in the blood, in hopes of developing a simple blood test for the disorder. Such a test might reduce the time and cost of an MS diagnosis. The primary tool for spotting MS today is magnetic resonance imaging (MRI), which can reveal inflammation in the brain characteristic of the disorder. © 2013 Scientific American

Keyword: Multiple Sclerosis
Link ID: 18132 - Posted: 05.08.2013