Wednesday, December 16, 2015

Sunday Review New York Times.  

OPINION

How to Think About the Risk of Autism

By SAM WANG

STUDY published last week found that the brains of autistic children show abnormalities that are likely to have arisen before birth, which is consistent with a large body of previous evidence. Yet most media coverage focuses on vaccines, which do not cause autism and are given after birth. How can we help people separate real risks from false rumors?

Over the last few years, we’ve seen an explosion of studies linking autism to a wide variety of genetic and environmental factors. Putting these studies in perspective is an enormous challenge. In a database search of more than 34,000 scientific publications mentioning autism since its first description in 1943, over half have come since 2008.

As a statistically minded neuroscientist, I suggest a different approach that relies on a concept we are familiar with: relative odds. As a single common measuring stick to compare odds, I have chosen the “risk ratio,” a measure that allows the bigger picture to come into focus.

For a variety of studies I asked the same question: How large is the increased risk for autism? My standard for comparison was the likelihood in the general population of autism spectrum disorder. Here’s an example. Start from the fact that the recorded rate of autism is now 1 in 68, according to a report released last week by the Centers for Disease Control and Prevention. If babies born in purple farmhouses have a rate of autism of 2 in 68, this doubling means that the purple farmhouse carries a risk ratio of 2. However, correlation is not causation, and there is no need to repaint that farmhouse just yet.

We can improve our chances of finding true causes by looking before the age of 2, when it becomes possible to diagnose autism. The risk ratio can give perspective where isolated news stories don’t. Media reports have focused on the risk associated with becoming a mother or father in one’s late 30s or after. The story has obvious appeal: Delayed parenthood is common, and readers are understandably anxious. However, parents-to-be should consider that the individual risk to the child is only around 1.4. The risk associated with enhanced or accelerated labor in full-term babies is about 1.2, after other complications are taken into account. And of course, the risk from vaccination is slightly less than 1 — there is no added risk. Even worse, incorrect beliefs about vaccines come with a cost. The return of measles in communities with falling vaccination rates is one recent example.

One might argue that any added risk is too much. But it is essential to put risk into perspective. The early research in the 1950s that first linked smoking with lung cancer gave a risk ratio around 25 for a pack-a-day smoker. In the case of autism, the risk associated with parental age is dwarfed by the impact of inheritance.

Comparing twins who grow up in the same environment allows researchers to focus on the effects of shared genes. A majority of children with an autistic identical twin are likely to be diagnosed with autism as well for a risk ratio somewhere around 80. A lower risk ratio comes from sharing half of one’s genes, as for fraternal twins or siblings. For these reasons, researchers believe that autism’s roots are largely genetic.

The human genome is dotted with hundreds of autism risk genes. Individually, each gene is usually harmless, and is in fact essential for normal function. This suggests that autism is caused by combinations of genes acting together. Think of genes as being like playing cards, and think of autism outcomes as depending on the entire hand. New mutations can also arise throughout life, which might account for the slightly greater risk associated with older fatherhood.

Although autism has a gene-based beginning, growing brains are also influenced by their environment and external events. Looking at when these risks are greatest can provide clues about when the growing brain is most vulnerable. Based on a large body of evidence, the known hazards occur before birth and fall into three broad categories: prematurity, prenatal stress and brain development.

MANY known risks for autism occur during late pregnancy and birth. Premature birth is a risk for developmental disability, including autism. Notably, elective cesarean section is associated with an autism risk ratio of 1.9. Since a substantial proportion of early deliveries are elective, without a compelling medical reason, this risk is preventable.

A highly underappreciated prenatal risk is stress. For pregnant women who take the sometimes-wrenching step of emigrating to a new country, for example, the risk ratio is 2.3. In the fifth through ninth months of pregnancy, getting caught in a hurricane strike zonecarries a risk ratio of about 3. Maternal post-traumatic stress disorder during pregnancy is associated with a similar effect. These events are likely to trigger the secretion of stress hormones, which can enter the fetus’s bloodstream and affect the developing brain for a lifetime. Stressors may also lead to maternal illness, the immune response to which may interfere with brain development.

Stress might account for other findings as well. Recent news coverage has speculated on the influence of air pollutants, which carry risk ratios around 1.4. This risk might be caused by chemicals — or by the stress of living in a poor or crowded neighborhood, where pollution is worse. A larger risk comes from households that already have an older sibling under 1 year of age, where newly conceived children have a risk ratio for autism of 3.4. So sure, parents should avoid smog — but also might think about spacing their children at judiciously chosen intervals.

After birth, known risks diminish. But the baby’s brain acquires a new need: social experience. In one group of Romanian orphanage children, babies were nearly isolated from social contact, and some later showed autism-like symptoms. Developing brains go through sensitive periods during which they require a minimum level of normal experience. Extreme deprivation may affect a critical period of the brain’s social and emotional development.

Risk ratios are good not just for parents, but also for researchers, who can follow them to new areas for in-depth study. The statistics suggest a conceptual framework in which fetal brain development stays on track unless it is driven awry by genetic hits, by adversity in late pregnancy, or a combination of the two.

In my laboratory, risk ratios have led us to examine particular brain regions. Many brain regions in autistic people show abnormalities, but it is not known whether some malfunctioning regions cause other regions to go off track. In one study focusing on detailed long-term outcomes in 51 children, damage to the cerebellum at birth leads to a risk ratio of about 40. The cerebellum links information arriving from different senses and communicates with nearly all regions of the cerebral cortex. Many known risk genes for autism are turned on together in the cerebellum in early life. Although cerebellum injury is rare, we think the cerebellum might be important in using sensory experience to guide normal brain development.

Looking at the problem of autism in terms of relative odds can provide a conceptual framework for understanding autism. For example, odds might help us understand why more children are being classified as autistic. Are the diagnostic criteria changing, or is the population changing as a result of stress and other risk factors?

Scientists do not agree on the answer to this question, but parents don’t need to worry too much about it. For them, the bottom line is reminiscent of an old piece of folk wisdom: Reduce stresses to the mother. And when reading or watching the news, remember that scare stories are not always what they seem. In this respect, looking at the hard data can help parents keep a cool head.

Sunday, December 13, 2015

Traumatic Memories Inherited

New research from Emory University School of Medicine, in Atlanta, has shown that it is possible for some information to be inherited biologically through chemical changes that occur in DNA. During the tests they learned that that mice can pass on learned information about traumatic or stressful experiences – in this case a fear of the smell of cherry blossom – to subsequent generations.

According to the Telegraph, Dr Brian Dias, from the department of psychiatry at Emory University, said: ”From a translational perspective, our results allow us to appreciate how the experiences of a parent, before even conceiving offspring, markedly influence both structure and function in the nervous system of subsequent generations.

“Such a phenomenon may contribute to the etiology and potential intergenerational transmission of risk for neuropsychiatric disorders such as phobias, anxiety and post-traumatic stress disorder.”

This suggests that experiences are somehow transferred from the brain into the genome, allowing them to be passed on to later generations.

wtff

The researchers now hope to carry out further work to understand how the information comes to be stored on the DNA in the first place. They also want to explore whether similar effects can be seen in the genes of humans.

Professor Marcus Pembrey, a paediatric geneticist at University College London, said the work provided“compelling evidence” for the biological transmission of memory.

He added: “It addresses constitutional fearfulness that is highly relevant to phobias, anxiety and post-traumatic stress disorders, plus the controversial subject of transmission of the ‘memory’ of ancestral experience down the generations.

“It is high time public health researchers took human transgenerational responses seriously.”

“I suspect we will not understand the rise in neuropsychiatric disorders or obesity, diabetes and metabolic disruptions generally without taking a multigenerational approach.”

Professor Wolf Reik, head of epigenetics at the Babraham Institute in Cambridge, said, however, further work was needed before such results could be applied to humans.

He said: “These types of results are encouraging as they suggest that transgenerational inheritance exists and is mediated by epigenetics, but more careful mechanistic study of animal models is needed before extrapolating such findings to humans.”

May our DNA Carrying also spiritual and cosmic memories passed down in genes from our ancestors?

Thursday, August 6, 2015

Do Homeopathic Remedies Expire?

Homeopathic Remedies-Medicines: Expiration Dates-Do Homeopathic Remedies Expire?

Years ago, I was surprised to learn that homeopathic remedies made in the form of sublingual tablets do not deteriorate and do not expire. When I was having a homeopathic remedy made at our local homeopathic pharmacy, the pharmacist told me that homeopathic remedies last for decades and decades.

We are so accustomed to buying western drug company chemical medicines that do deteriorate and do lose their effectiveness and do expire that each of us have a difficult time adjusting to the reality that homeopathic remedies do not suffer the same fate as the chemical medicines that are produced by our western drug companies.

In fact, the FDA has issued a rule which specifically states that homeopathic remedies are exempt from having any required expiration date. Some manufacturers do place an expiration date on their remedies, but those dates are not required (and those non-required dates may be more for marketing or other purposes). The FDA ruling regarding homeopathic remedy expiration dates is discussed in the Q & A  from Hylands which appears below.   Hylands is one of the most prominent manufacturers of widely used homeopathic remedies.

“Do these tablets expire?

Our tablets do not expire. We don’t put expiration dates on the products, as they have been exempted from expiration dating guidelines by the FDA (CFR 211.137) The numbers that are imprinted on the edge of the labels are lot numbers – so we know exactly when the product was produced. We can track any product we made using that number.”


Sunday, November 16, 2014

LYME DISEASE


Healing Requests

LYME DISEASE: A PARKINSON’S IMITATOR?
JANUARY 14, 2014
Lyme disease and all of its co-infections cause many constant symptoms; consequently it easily mimics disorders, such as Parkinson’s, chronic fatigue syndrome, fibromyalgia, ALS, ADHD and even Alzheimer’s disease. A distinctive mark unique to Lyme disease is the “bull’s-eye” rash known as Erythema Migrans, a red rash with an expanding red ring around it and this occurs soon after the tick bite; however, it is NOT ALWAYS in the shape of a bulls-eye. After the tick bite clears up, this bull’s-eye rash is gone. Erythema Migrans is the only manifestation of Lyme disease in the United States that is sufficiently distinctive to allow clinical diagnosis in the absence of laboratory confirmation
The cases of Lyme disease reported to the CDC (300,000 cases) have been distressingly low. Less than half of all cases of Lyme can be traced to a tick bite, so this “bulls-eye” rash is absent in many of those infected.
How do you know if you have Lyme disease? Besides the rash, some of the first symptoms of Lyme disease may include a flu-like condition with fever, chills, headache, stiff neck, achiness and fatigue. Early treatment is crucial to help avoid chronic Lyme. If one doesn’t see the tick and remove it, it can progress to ailments like arthritis, facial palsy, nervous system and heart problems and a hundred other symptoms. For an extensive list of symptoms, refer to the Tick-Borne Disease Alliance7 (TBDA). Some of the more frequent symptoms include the following:
•            Muscle and joint pain
•            Neurological problems
•            Fatigue
•            Low grade fevers, “hot flashes” or chills
•            Night sweats
•            Sore throat
•            Swollen glands
•            Stiff neck
•            Migrating arthralgias, stiffness and frank arthritis
•            Myalgia
•            Chest pain and palpitations
•            Abdominal pain, nausea
•            Sleep disturbance
•            Poor concentration and memory loss
•            Irritability and mood swings
•            Depression
•            Back pain
•            Blurred vision and eye pain & Hearing Problems
•            Jaw pain
•            Cranial nerve disturbance (facial numbness, pain, tingling, palsy or optic neuritis)
•            Lightheadedness
•            Mysterious migrating symptoms that seem to come and go
•            Migraines
According to his personal email and several press reports, in August of 2013 the College of Charleston President George Benson was hospitalized for Lyme disease. He had been hospitalized for severe back pain, but no one was sure of the exact cause. Lyme is everywhere, “The Lyme disease bacterium has a quirky feature for survival. It can exist without iron, which most other living organisms require to make proteins and enzymes. Instead of iron, B. burgdorferi uses manganese, thus eluding immune system defenses that destroy pathogens by starving them of iron.”