by Ethan A. Huff, staff writer
(NaturalNews) A new study out of Oxford University pinpoints vitamin D deficiency as a culprit in serious illnesses like cancer and autoimmune disorders. According to the report, which was recently published online in the journal Genome Research, genetic receptors throughout the body need adequate vitamin D levels to prevent these and other serious illnesses from developing.
Multiple sclerosis, diabetes, rheumatoid arthritis, Chron's disease, leukemia -- these and many more diseases are often caused by a lack of vitamin D. Your genes literally have receptors that need vitamin D in order to properly express themselves. If there is not enough of the vitamin, serious illness is prone to develop.
The Oxford team made specific observations about the importance of vitamin D in the genome regions associated with autoimmune diseases and cancer, noting that the nutrient is absolutely vital in helping to prevent these diseases from forming.
"Considerations of vitamin D supplementation as a preventative measure for these diseases are strongly warranted," expressed Sreeram Ramagopalan, author of the study.
However, current recommendations for vitamin D intake are unacceptably low, and many nations are considering updating their guidelines. The U.S. Institute of Medicine, for example, recommends getting a mere 200 to 600 international units (IU) of vitamin D a day, an amount far too low to have much therapeutic effect.
Since summer sun exposure creates about 20,000 IU of vitamin D in the skin in just 15 minutes, supplementation with at least 5,000 to 10,000 IU of vitamin D daily, particularly during the winter, is preferable. Healthy blood levels of vitamin D are somewhere between 50 and 80 nanograms per milliliter (ng/ml), so many natural health professionals recommend having a "25 OH Vitamin D" blood test performed to check these levels.
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Too bad the authors of the speculative paper (as opposed to actual study) did not have access to the new Oxford study. The entire basis of their study was that there was insufficient evidence and in now way did they state that Vitamin D did not or could not hlep. But then the Oxford study would not have fit in well with their conclusion, would it? Might very well have ruined the whole paper.
Besides the speculative paper, the authors are also noted for collaborating on a mice study which they used to draw conclusions for humans, despite the fact that mice are largely nocturnal and have a different mechanism for producing vitamin D.
From the University of Oxford:
Gene study supports link between vitamin D deficiency and disease
The extent to which vitamin D deficiency may increase susceptibility to a wide range of diseases is highlighted in a new study led by Oxford University.
Scientists have mapped the points at which vitamin D interacts with our DNA – and identified over 200 genes directly influenced by vitamin D. The results are published in the journal Genome Research.
It is estimated that 1 billion people worldwide do not have sufficient vitamin D. This deficiency is thought to be largely due to insufficient exposure to the sun and in some cases to poor diet.
As well as being a well-known risk factor for rickets, there is a growing body of evidence that vitamin D deficiency also increases an individual's susceptibility to autoimmune conditions such as multiple sclerosis (MS), rheumatoid arthritis and type 1 diabetes, as well as certain cancers and even dementia.
The University of Oxford researchers have now shown the extent to which vitamin D interacts with our DNA.
They used new DNA sequencing technology to create a map of vitamin D receptor binding across the genome in a study funded by the Medical Research Council (MRC), the MS Society, the Wellcome Trust, the Canadian MS Foundation and others. The vitamin D receptor is a protein activated by vitamin D, which attaches itself to DNA and thus influences what proteins are made from our genetic code.
The researchers found 2,776 binding sites for the vitamin D receptor along the length of the genome. These were unusually concentrated near a number of genes associated with susceptibility to autoimmune conditions such as MS, Crohn’s disease, lupus and rheumatoid arthritis, and to cancers such as chronic lymphocytic leukaemia and colorectal cancer.
They also showed that vitamin D had a significant effect on the activity of 229 genes including IRF8, previously associated with MS, and PTPN2, associated with Crohn’s disease and type 1 diabetes.
‘Our study shows quite dramatically the wide-ranging influence that vitamin D exerts over our health,’ says Dr Andreas Heger from the MRC Functional Genomics Unit at Oxford University, one of the lead authors of the study.
There is now evidence supporting a role for vitamin D in susceptibility to a host of diseases.
Dr Sreeram Ramagopalan The first author of the paper, Dr Sreeram Ramagopalan from the Wellcome Trust Centre for Human Genetics at Oxford University, adds: ‘There is now evidence supporting a role for vitamin D in susceptibility to a host of diseases. Vitamin D supplements during pregnancy and the early years could have a beneficial effect on a child's health in later life. Some countries such as France have instituted this as a routine public health measure.’
The main source of vitamin D in the body comes from exposing the skin to sunlight, although a diet of oily fish can provide some of the vitamin. Research has previously suggested that lighter skin colour and hair colour evolved in populations moving to parts of the globe with less sun to optimise production of vitamin D in the body. A lack of vitamin D can affect bone development, leading to rickets; in pregnant mothers, poor bone health can be fatal to both mother and child at birth, hence there are selective pressures in favour of people who are able to produce adequate vitamin D.
This new study supports this hypothesis, having found a significant number of vitamin D receptor binding sites in regions of the genome with genetic changes more commonly found in people of European and Asian descent.
It is probable that skin lightening as humans migrated out of Africa resulted from the necessity to be able to make more vitamin D and prevent rickets: vitamin D deficiency led to pelvic contraction resulting in increased risk of fatality of both mother and unborn child, effectively ending maternal lineages unable to find ways of increasing availability of the vitamin.
‘Vitamin D status is potentially one of the most powerful selective pressures on the genome in relatively recent times,’ says Professor George Ebers, Action Medical Research Professor of Clinical Neurology at the University of Oxford, and one of the senior authors of the paper. ‘Our study appears to support this interpretation and it may be we have not had enough time to make all the adaptations we have needed to cope with our northern circumstances.’
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