Jump to content
RemedySpot.com

Another possible nutrient reason for why nutriiveda is working

Rate this topic


Guest guest

Recommended Posts

Guest guest

Yesterday I brought up about the turmeric and vitamin D3 (the " sunshine

vitamin " ) and did a quick search to see if there were any links between D3 and

autism. More than a bit I'd say -this is quite long but thought it would be

good to share the entire thing for reference reasons. In general -may want to

read up on vitamin D3 (which is made naturally by the body from sunlight) One

of my best friends Dr. Ross who practices internal medicine out of

the Barnabas System in Jersey and was voted President of the Ocean County

Medical Association and on the board for her hospital has been telling me to

supplement with vitamin D for awhile. Sometimes when you hear things from

people you are close to you don't always listen. She's also the first doctor

friend years ago to tell me about fish oils too (she calls her patients " fish

deficient " ) so " Tree " (which is what I call her) is right again! Awesome friend

and awesome doctor...and can't wait to tell her that I don't have to supplement

with vitamin D3 because it's in my nutriiveda (and PS -not sure if she wants me

to share it so off the record not only is Tree using nutriiveda herself and

recommending to her patients -but like others I know has reduced the amount of

insulin she takes since being on it)

And look what else I found -vitamin D3 is not a vitamin it's a " metabolic

product " very interesting!

" Technically not a " vitamin, " vitamin D is in a class by itself. Its metabolic

product, calcitriol, is actually a secosteroid hormone that targets over 2000

genes (about 10% of the human genome) in the human body. Current research has

implicated vitamin D deficiency as a major factor in the pathology of at least

17 varieties of cancer as well as heart disease, stroke, hypertension,

autoimmune diseases, diabetes, depression, chronic pain, osteoarthritis,

osteoporosis, muscle weakness, muscle wasting, birth defects, periodontal

disease, and more. "

http://www.vitamindcouncil.org

For those that want to check this article against what is in nutriiveda in

regards to vitamin D3 or anything else -please visit

http://pursuitofresearch.org/ingredients.html They talk about the " other "

conditions below -from the same organization here's the theory of vitamin D and

autism:

Vitamin D Theory of Autism

Written by Dr. Cannell

Executive Director, The Vitamin D Council

www.vitamindcouncil.com

In addition to the current epidemic of vitamin D deficiency, say another

epidemic-an epidemic of autism-was upon our children? What if the autism

epidemic began at the same time the epidemic of vitamin D deficiency began? What

if both epidemics had worsened in unison? What if one theory explained all the

unexplained facts about autism? What if both epidemics had the same root cause:

sun avoidance? What if both were iatrogenic, that is, medical advice to avoid

the sun had caused both epidemics? Be warned, what follows is not light

reading-autism is not a light disease.

Does The Vitamin D Theory Best Explain Autism?

The theory that vitamin D deficiency, during pregnancy or childhood, causes

autism is just a theory. However, the theory has a plausible mechanism of

action, explains all the unexplained facts about autism, subsumes several other

theories, implies simple prevention, and is easily disprovable-all components of

a useful theory. A genetic lesion (abnormality) in some component of the vitamin

D system-a lesion vitamin D's unique pharmacology could overcome-would explain

why monozygotic (identical) twins are highly affected while fraternal twins are

not. Varying brain levels of activated vitamin D during later life would explain

why some identical twins get severe disease while others are barely affected.

Falling vitamin D levels over the last 20 years due to sun?avoidance explain

autism's rapid increase in incidence during that same time. The very different

effects estrogen and testosterone have on vitamin D metabolism may explain why

boys are much more likely to get it than girls are. Lower vitamin D levels in

blacks may explain their higher rates of autism. The vitamin D theory has

tenable explanations for all the epidemiological features of autism.

What's The Risk of Going In The Sun?

The window of opportunity to affect brain development is limited. Time is of the

essence if the vitamin D theory of autism is correct. Ask yourself, what is the

risk of taking your autistic child outside to play in the sun? What's the risk

of pregnant women sunbathing for a few minutes every day? Children always played

in the sun before the epidemic of autism; your pregnant grandmother spent time

in the sun as well. Physicians considered that sunshine was healthy before the

sun?scare, that is, before autism became an epidemic.

What Is Autism?

The Autism Society of America (http://www.autism-society.org) describes autism

as " a complex developmental disability that typically appears during the first

three years of life and is the result of a neurological disorder that affects

the normal functioning of the brain, impacting development in the areas of

social interaction and communication skills...One should keep in mind however,

that autism is a spectrum disorder, and it affects each individual differently

and to varying degrees. " They estimate that 1.5 million Americans and their

families are now affected, a national health crisis, costing about $35 billion

annually.

After exhaustive metabolic and genetic evaluations, more than 60% of individuals

with autism spectrum disorders are found to have idiopathic disease. 1 Even

after the most thorough medical evaluation possible, doctors simply cannot find

the cause for their autism.

What are autism's five unexplained features?

Any valid theory of autism must explain the following:

1. Significantly higher concordance (if one has it the other is likely to

have it) rates in identical, but not fraternal, twins.

2. Widely?varying symptoms, even among identical twins.

3. Striking 4:1 male to female sex ratio.

4. Increased rates in blacks.

5. Rapid increase in occurrence rates over the last 20 years.

Whatever its genetic roots, and they are strong, autism hardly follows classic

genetic inheritance. What is clear is that the genes that control autism confer

predisposition, not predestination.

Are autism rates increasing?

Multiple scientific groups have reported greatly increasing rates of autism over

the last 20 years. Dr. Hjordis Atladottir, of the University of Aarhus in

Denmark, recently reported that hyperactivity and Tourette's syndrome (two other

childhood neurodevelopmental disorders) have increased dramatically right along

with autism, while a third, childhood obsessive?compulsive disorder, has not

changed at all. Why would some childhood neurodevelopmental disorders increase

dramatically in such a short time, while another is entirely unchanged? Perhaps

something is harming our children's brains, and doing so with increasing

frequency. 2 3 4

Professor Gillian Baird, and his colleagues at Guy's and St. ' Foundation

Trust in England, recently discovered that about 1 in 88 English children will

eventually develop autism. Families caring for autistic children are under more

stress than those caring for a child with cystic fibrosis, a fatal illness. The

lifetime cost of autism is $3.2 million per case. Not only is autism epidemic,

it is catastrophic.

The Vitamin D Connection

Six years ago, Professor McGrath and his colleagues at the University of

Queensland in Australia, pointed out that vitamin D, " the neglected

neurosteroid, " was crucial for proper brain development. In the same paper, they

reported that activated vitamin D increases nerve growth factor in the brain and

the vitamin D receptor appears in a wide variety of brain tissue quite early in

the development of the baby. These two facts alone led them to conclude that

vitamin D deficiency " should be examined in more detail as a candidate risk

factor for neurodevelopmental...disorders. " 5

In 2006, Dr. Alan Kalueff and his colleagues went further, suggesting vitamin D

offers " neuroprotection, possible interplay with several brain neurotransmitter

system and hormones, as well as regulation of behaviors. " In 2007, Dr. Kalueff,

now at the National Institutes of Mental Health, reviewed the nootropic

(brain?enhancing) properties of vitamin D in even more detail and concluded that

the scientific data stress the importance of the mother having enough vitamin D

while she is pregnant and the child having enough vitamin D after birth for

" normal brain functioning. " There is no doubt vitamin D affects the brain, and

does so profoundly. 6 7

Predisposition - What Gene Should We Be Looking For?

Given what we know about neurosteroids, in our search for the genetics of autism

it is reasonable to search for a gene which:

* is environmentally responsive.

* codes for a systemic steroid that is also a potent neurosteroid.

* profoundly affects brain development

* has had its levels decrease over the same time that autism has increased.

* is affected differently by estrogen and testosterone.

* has levels that are much lower in blacks than in whites.

* explains all the bizarre epidemiology of autism.

A tall order indeed.

Two clues: rare genetic malformations of the vitamin D system

An inborn error of metabolism that causes a rare form of rickets, pseudo?vitamin

D deficiency rickets, involves the defective manufacture of activated vitamin D.

While no one has assessed afflicted children for signs of autism, these children

clearly display autistic markers such as hypotonia (flabby muscles), decreased

activity, developmental motor delay, listlessness, and failure to thrive.

Much more interesting is the fact that children with Syndrome (rare

congenital disorder due to a missing piece of chromosome seven) often have

greatly elevated activated vitamin D levels for several months in early life.

They usually present in later life with remarkable sociability,

overfriendliness, empathy, and willingness to initiate social

interaction-strikingly the opposite personality of autistic children. 8 9

So, abnormally?low activated vitamin D levels produce infants with symptoms of

autism while abnormally?high levels produce children with personalities the

exact opposite of autism.

What is the role of the vitamin D receptor in autism?

Variations in the DNA sequence of vitamin D receptor are common and called

vitamin D receptor (VDR) polymorphisms (many shaped receptors). No one has

studied them in autism, but a highly significant association exists between one

VDR polymorphism and larger head size. Larger head sizes are common in autism,

especially in childhood. 10

The Role of Sunlight

Vitamin D intake-are children and pregnant women getting as much as they used

to?

No, because sun exposure is much less common today. Furthermore, perhaps because

the term, vitamin D, contains the word " vitamin, " many people mistakenly assume

it is a vitamin. Vitamin D is the only known precursor for a steroid hormone

system that, until recent sun?avoidance, always began in the skin, not the

mouth. Before the sun?scare, 90% of human vitamin D stores came from skin

production, not diet. Large populations of pregnant women and autistic children

ingesting small amounts orally, instead of generating large amounts through the

skin, are novel to human brain development. 11 12

Obviously, if people are going to put it in their mouths, rather than make it in

their skin, oral intake must be adequate enough to make up for decreased skin

production. However, the skin's production of vitamin D is rapid and robust,

easily exceeding usual dietary sources by a factor of 10. For example, when

fair?skinned adults sunbathe in the summer (one, full?body, exposure to

ultraviolet light, enough to turn the skin slightly pink) they make about 20,000

units of vitamin D in 20 minutes. A pregnant woman would have to drink 200

glasses of milk or take 50 prenatal multivitamins to do the same. An autistic

boy who plays inside the house, instead of outside, would have to take several

thousand units of vitamin D to make up for what his skin would have produced had

he played outside that day. Holick MFHigh prevalence of vitamin D inadequacy and

implications for health. 13 13a

When did medical organizations first tell us to avoid the sun?

In 1989, around the time autism began to rise, the American Medical

Association's (AMA) Council on Scientific Affairs first warned about the dangers

of sun exposure, advising mothers to " keep infants out of the sun as much as

possible. " In 1999, when autism rates really exploded, the American Academy of

Pediatrics went further, advising mothers always to keep infants out of direct

sunlight, use sun?protective clothes and sunblock, and make sure children's

activities minimize sunlight exposure. Quite inexplicably, they said there was

" no evidence " such " rigorous sun protection " would affect vitamin D levels. By

2002, the Centers for Disease Control (CDC) reported such efforts were quite

successful: " protection from sun exposure is reported for a high proportion of

children. " 14 15 16

Did authorities recommend compensatory vitamin D intakes?

Medical organizations did not plan for the vitamin D deficiency such sun

avoidance would predictably induce. For example, when the AMA warned about the

dangers of sunlight, they did not even mention that sunlight triggers the

formation of vitamin D. Furthermore, medical recommendations for infants,

children, young women, and pregnant women, did not change during the decades of

sun avoidance: 200 units/day for all infants, children, pregnant women, and

young adults-regardless of weight. That is, they did, and still do, recommend

the same 200 daily units for a 5?pound infant as they do for a 200?pound

pregnant woman. In fact, in 2003, the American Academy of Pediatrics cut their

long?standing 400 units/day recommendation in half-apparently to comply with

government recommendations-and did so despite warnings from a prominent

University of Wisconsin professor of pediatrics, Dr. Greer, and despite

their own advice four years earlier that infants and children should avoid

sunlight. 17

Have vitamin D levels fallen as autism has increased?

Yes they have, although no linear studies of vitamin D levels over the last 20

years exist. That is, we don't know how successful sun avoidance campaigns have

been in lowering vitamin D levels. However, if one assumes that some Americans

do follow their government's and physician's advice, then at least some must

have had declining vitamin D levels over the last 20 years-unless they took

enough supplemental vitamin D to make up for lack of sun exposure.

Unfortunately, few take the thousands of daily units needed to do that. What we

do know is that vitamin D deficiency, like autism, is now an epidemic.

About Vitamin D

How is vitamin D unique?

Among the body's steroid hormone systems, vitamin D certainly is unique. Unlike

other steroids, the body cannot create the activated vitamin D it needs directly

from cholesterol; all of the body's activated vitamin D must come from simple

vitamin D-either made in the skin or taken orally. Besides its endocrine role in

maintaining blood calcium, activated vitamin D has multiple independent hormonal

functions, if enough of its precursor is available. Like all steroid hormones,

activated vitamin D binds to a member of the nuclear hormone receptor

superfamily where the complex then acts as a molecular switch to signal its

target genes. So far, we know 200 genes (about 0.5% of the human genome) are

primary targets of activated vitamin D, and the list is steadily growing. If

adequate precursor is available, most organs in the human body produce their own

activated vitamin D, have a vitamin D receptor, and regulate their own needs

independently. Thus, they do not depend on blood supply of activated vitamin D

from the kidney. 18 19

Does human behavior determine vitamin D levels?

The pharmacology contained in this paragraph may be a bit confusing to some, but

it is vitally important in understanding vitamin D. It is so important that

Professor Reinhold Vieth, of the University of Toronto, wrote an entire chapter

about its implications in the most current textbook of vitamin D. Unlike any

other steroid hormone, substrate (precursor) concentrations are absolutely

rate?limiting for activated vitamin D production. The enzyme that first

metabolizes vitamin D in the liver and the enzyme in tissue where activated

vitamin D is made both operate below their respective is?Menten constants

throughout the full range of their normal substrate concentrations, i.e. the

reactions follow first?order, mass?action, kinetics. In English, this means the

more vitamin D made in the skin or taken by mouth, the more vitamin D in your

blood, and the more vitamin D in your blood, the more activated vitamin D in

your brain. That is, levels of activated vitamin D during brain development

directly depend on the mother's vitamin D levels, which in turn, directly depend

on the amount of vitamin D the mother makes in her skin or ingests orally. That

is, the rate?limiting step for the production of activated vitamin D is totally

dependent on human behavior, a situation that is unique among all steroids.

Brain concentrations of activated vitamin D literally depend on one's

behavior-be it the step into the sun, to the supplements, into the shade, or to

the sunscreen.

Vitamin D and the Brain

Is vitamin D required for normal brain development?

Yes, Professor McGrath and Dr. Darryl Eyles of the University of Queensland

in Australia have repeatedly warned us that normal brain development depends on

adequate amounts of activated vitamin D to orchestrate the cellular architecture

of the brain. Both the vitamin D receptor and the enzyme necessary to make

activated vitamin D are present in a wide?variety of human brain tissues very

early in pregnancy. 20 21

Production of the vitamin D receptor in the developing mammalian brain rises

steadily beginning several weeks after conception where activated vitamin D

induces the expression of nerve growth factor and stimulates brain cell growth.

22 23

Does maternal vitamin D deficiency injure the developing brain?

We do not know what vitamin D deficiency during pregnancy does to human brains,

but we know what it does to rat brains and it is not good. In a series of recent

animal experiments, Professor McGrath, Dr. Darryl Eyles and their

Australian group found severe maternal vitamin D deficiency in mother rats

produced babies with abnormal apoptosis (normal cell death) and abnormal brain

cell proliferation, reduced production of proteins involved in nerve structure,

and baby rats who have subtle abnormalities in both learning and memory. 24 25

26 27

Several months ago, Dr. Almeras, Professor Feron, and their group at the

University of the Mediterranean in Marseilles found developmental vitamin D

deficiency disrupts 36 proteins involved in mammalian brain development. Severe

maternal vitamin D deficiency leads to rat pups with increased brain size and

enlarged ventricles (chambers in the brain), abnormalities very similar to those

found in autistic children. 28 29

Is autism an ongoing, destructive, inflammatory disease process?

Abnormal inflammation is associated with both autism and vitamin D deficiency.

For example, autistic individuals show increases in cytokines (inflammatory

mediators) that show a striking similarity to the immune processes regulated by

vitamin D. 30 31

Both the brain and the blood of autistic individuals show evidence of ongoing

chronic inflammation and oxidative stress. That is, the autistic disease process

is progressive and probably increasingly destructive. If this ongoing

inflammation could be interrupted, the symptoms might improve. Hope for a

vitamin D treatment effect lies in activated vitamin D's powerful

anti?inflammatory properties. Its administration decreases production of

inflammatory cytokines in the brain, which have consistently been associated

with brain impairment. Activated vitamin D stimulates neurotrophin release

(neurotrophins induce the survival of nerve cells), reduces toxic calcium levels

in the brain, and inhibits the production of nitrous oxide (nitrous oxide

destroys brain cells). Besides reducing inflammatory cytokines, vitamin D does

one more thing: it increases concentrations of glutathione-the brain's master

antioxidant. 32 33 34 35 36

Do brains function better with higher vitamin D?

At least five studies have found significant associations between higher vitamin

D levels and better intellectual functioning, but they all studied adults.

However, a recent report found a very high incidence of vitamin D deficiency

among 337 younger individuals with intellectual disabilities. The obvious

explanation is that intellectually impaired individuals do not go outdoors as

often as higher functioning individuals and thus have lower vitamin D levels.

Two groups found the association after controlling for outdoor activities,

making it likely that low vitamin D levels per se impair intellectual ability.

37 38 39 40 41 42

Does vitamin D explain the role of vaccines, mercury, and heavy metals?

Vitamin D's role in increasing glutathione levels may explain the link between

mercury and other heavy metals, oxidative stress, and autism. For example,

activated vitamin D lessens heavy metal induced oxidative injuries in rat brain.

The primary route for brain toxicity of most heavy metals is through depletion

of glutathione. Besides its function as a master antioxidant, glutathione acts

as a chelating (binding) agent to remove heavy metals, like mercury. Autistic

individuals have difficulty excreting heavy metals, like mercury. If brain

levels of activated vitamin D are too low to employ glutathione properly, and

thus unable to remove heavy metals, they may be damaged by heavy metal loads

normal children easily excrete. That is, the mercury in Thiomerosol vaccines may

have injured vitamin D deficient children while normal children would have

easily bound the mercury and excreted it. These studies offer further hope that

sun?exposure or vitamin D supplements may help autistic children by increasing

glutathione and removing heavy metals. Not only do we have more clues that

vitamin D is involved in autism, the vitamin D theory just did something else:

it explained two other theories of autism, the mercury accumulation theory and

the oxidative stress theory. 43 44 45

It bears repeating that the amount of activated vitamin D in the brain directly

depends on the amount of vitamin D made in the skin or ingested orally.

Vitamin D Deficiency's Role In Autism

Do children with common rickets show signs of autism?

If vitamin D deficiency caused autism, then children with vitamin D deficient

rickets would be at greater risk for the disease. To the best of my knowledge,

no studies have looked at the psychiatric profiles of children with vitamin D

deficient rickets to look for evidence of autism. However, children with rickets

are more likely to be hypotonic (flabby muscle tone), display decreased

activity, and have developmental motor delays. Hypotonia is common in children

with autism, as is decreased activity, and developmental motor delays are the

rule. 46 47 48 49

Does vitamin D explain autism's frequent infections?

Vitamin D deficiency in childhood is associated with an increased risk of

infections so the vitamin D theory of autism predicts autistic children would be

more prone to infections. A recent study found that children who went on to

develop autism were not prone to increased infection in the first two years of

their life but they looked at infection rates before the child was diagnosed

with autism, not afterwards. Three earlier studies found an increased incidence

of infections in children with autism. A Japanese study found a very strong

positive correlation between the prevalence of infantile autism in 1?year birth

cohorts (groups) and the total number of children hospitalized for pneumonia and

bronchiolitis during that cohort's birth year. 50 51 52 53 54 55

Drugs that interfere with vitamin D metabolism-do they cause autism?

The vitamin D theory predicts medications that lower vitamin D levels, if taken

during pregnancy, would increase the risk for autism. While little is known

about the drugs that interfere with vitamin D metabolism, sodium valproate

(Depakote) is one drug that lowers vitamin D levels and the drug has been

associated with autism. 56 57

Does vitamin D explain seizures, which are common in autism?

Seizures are very common in autism and activated vitamin D increases the seizure

threshold, making brain tissue less likely to seize. A controlled study found

vitamin D reduced the incidence of seizures in patients with intractable

seizures. 58 59

Vitamin D Explains Autism

Why are boys at higher risk?

The reason for the striking 4:1 sex difference is totally unknown. However,

there is a clue or two. Estrogen and testosterone have very different effects on

vitamin D metabolism. In mid?pregnancy, when brains are rapidly developing, boy

brains bathe in testosterone and girl brains bathe in estrogen. The majority of

studies have found estrogen has multiple enhancing effects on vitamin D

metabolism while testosterone does not. For example, in Feldman's massive

textbook on vitamin D, Dr. Epstein and Dr. Schneider report, " the majority of

studies have found a positive effect of estrogen on activated vitamin D levels. "

Yet, after reviewing similar studies on testosterone they conclude that " it is

unlikely that testosterone is a major controlling factor in vitamin D

metabolism. " If estrogen potentiates activated vitamin D, but testosterone does

not, the differences in sex steroids during brain development may mean that

estrogen protects developing female brains from vitamin D deficiencies, while

testosterone exposes male brains to those same deficiencies. This is important

because any good theory must be parsimonious (explain all known facts). 60

Does vitamin D?rich fish prevent autism?

The vitamin D theory of autism predicts that eating vitamin D?rich fatty ocean

fish during pregnancy would improve the offspring's mental abilities-that is as

long as that fish did not contain a lot of mercury. Higher fish consumption

during pregnancy was associated with better infant cognition, with the greatest

effect for infants whose mothers consumed the most fish. Very recently in a

Lancet article, Dr. ph Hibbeln and colleagues at the National Institutes of

Health found low maternal seafood consumption was associated with infants with

an increased?risk of lower verbal IQs and poor outcomes for social behaviors,

fine motor skills, communication, and social development-outcomes eerily similar

to autism. We don't know what in ocean fish helped, omega?3 or vitamin D, but

this evidence from a completely different source could support the vitamin D

theory of autism. 61 62

Is autism less?common at the equator?

If vitamin D played a role in autism, the disorder should be less common at

latitudes closer to the equator, at least before modern sun?avoidance. Dr.

Grant of SUNARC (http://www.sunarc.org) found a strong positive

association between latitude and the prevalence of autism in children born in

various countries born before 1985, but not after. Recently, the Centers for

Disease Control (CDC) in Atlanta reported the autism rates from 14 states. The

state with the highest prevalence, New Jersey, is the second most northern

state. Alabama, with the lowest prevalence, is the most southern of the 14

states surveyed. Studies of season?of?birth and autism are contradictory, as

would be expected if activated vitamin D deficiencies can impair brain

development during either pregnancy or in early childhood. However, most studies

show excessive autism births in the winter-especially March-when vitamin D

levels are at their lowest. 63 64 65

Sunscreen-Does It Increase Risk?

If prenatal or postnatal vitamin D deficiency caused autism, then parents who

rigorously used sun protection, during pregnancy and for their children, would

be more likely to have children with autism. Richer parents are more likely to

apply sunscreen to their children, as are parents with a higher education.

Although numerous studies, especially early ones, linked higher social class

with autism, a certain kind of statistical problem (called ascertainment bias)

confuses such associations. Despite identifying the source of the bias, Dr.

Bhasin at the CDC recently again found wealthier parents and more highly

educated parents were at higher risk for having an autistic child. It was not at

all clear that ascertainment bias explained all her findings. It appears that

people who bought into the sun?scare are more likely to have an autistic child.

66 67 68

Why do children first develop signs around the age of weaning?

If children can develop autism after birth, and it's not entirely a genetic

brain injury before birth, then autism should be rare before weaning as infant

formula contains significant amounts of vitamin D when calculated on a per?pound

basis and breast fed babies are supposed to be supplemented with vitamin D. The

disease should rapidly progress after weaning, unless the child takes vitamin D

supplements or drinks significant amounts of vitamin D fortified milk. A recent

prospective study (the only such prospective study in the medical literature) of

87 children, some at high?risk for autism and some not, found that the children

who later developed autism appeared entirely normal at 6 months of age. However,

around the age of weaning, the children who later developed autism first showed

signs of the disease with rapid additional impairments occurring between 14

months-24 months-the same age many toddlers stop drinking vitamin D?enriched

formula or milk and begin consuming lots of sodas and juice, which usually

contain no vitamin D. 69

Evidence Autism Responds To Sunlight and Vitamin D

Do vitamin D?containing multivitamins help children's brains?

Evidence that vitamin D affects mental abilities comes from a series of 14

controlled studies

(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & amp;cmd=Retrieve & amp;do\

pt=AbstractPlus & amp;list_uids=10706232) evaluating the effect of vitamin

D?containing multivitamins on childhood intelligence. All 14 studies they

reviewed reported small (1-2%) to modest (5-6%) improvements, usually in

nonverbal IQ. Lancet published the first study in 1988. More interestingly, most

studies showed no effect on the majority of children but very significant

effects (15% gains) in about 20% of children, perhaps the vitamin D?deficient

subgroup. Something in the multivitamins helped some of the children's brains

quite a bit. Was it the vitamin D? 70

Does autism improve in the summer?

If vitamin D was involved in autism, then symptoms might improve in the summer,

when vitamin D levels are the highest. To the best of my knowledge, no

controlled studies of such seasonality exist. A case study reported dramatic

improvements in both sleep and behavioral problems in an autistic Japanese boy

in the summer. Others reported significant improvements in autistic behaviors

during a summer camp program that included swimming, hiking, boating, and other

activities that would increase brain levels of activated vitamin D. 71 72

Can autistic children get better?

We don't know although most do not. However, if vitamin D is involved in autism

then young autistic children, whose brains have not been irreparably damaged,

may improve if they move to sunnier latitudes, increase their sun exposure, or

start consuming more vitamin D in their diet. Consistent with the theory, not

all children diagnosed with autism keep that diagnosis in adulthood and a few

children either improve spontaneously or improve after one of the numerous

treatment programs available. Naturally, any reports of improvement generate

suspicion that the initial diagnosis was incorrect-an obvious possibility. A

controlled 3?month study of 20 autistic children found that multivitamins with

even low doses of vitamin D (150 units) improved symptoms compared to placebo.

What would physiological doses of vitamin D do?

The Black Community: A Tragic Injustice

Is autism more common in dark?skinned people?

Vitamin D deficiency discriminates based on race, or more precisely, the amount

of melanin (pigment) in the skin, which is an effective and ever?present

sunscreen. The vitamin D theory of autism predicts that autism is more common in

children born to darker?skinned mothers. Such studies are difficult as they

raise sensitive social issues although 3 of 4 recent U.S. studies found a higher

incidence of autism in black children, sometimes appreciably higher. 73 74 75 76

In Europe, autism rates are higher in children of dark?skinned immigrants. Dr.

Gillberg and colleagues reported that the incidence of autism in Sweden for

children born to mothers who emigrated from Uganda was 15%-almost 200 times

higher than the general population. 77 78 79

The Centers for Disease Control in Atlanta and others report black children have

significantly higher rates of mild mental retardation than white children do and

socioeconomic factors cannot explain the differences. 80 81

Do Blacks have a higher risk of pregnancy problems?

Several studies indicate black mothers are more likely to give birth to infants

who weigh less and low birth weight is a clear risk factor for autism. 82 83 84

85

Black babies have lower Apgar scores. (Apgar tests are ten point examinations

done shortly after birth.) Low Apgar scores are associated with both poor

vitamin D intake and with autism. 86 87 88

Are black, pregnant women more likely to be vitamin D deficient?

Recent studies of vitamin D deficiency during pregnancy show striking racial

inequities in maternal vitamin D levels. Professor Bodnar of the University

of Pittsburg and her colleagues found that only 37% of white women, but only 4%

of black women, in the northern United States were vitamin D sufficient in early

pregnancy. That is, 96% of pregnant black women and 63% of pregnant white women

did not have adequate vitamin D blood levels. Their infants fared little better

and showed the same racial inequity. 45% of the pregnant black women and only 2%

of the pregnant white women were severely deficient. Prenatal vitamins,

virtually all of which contain only 400 IU of vitamin D, offered little

protective effect for mother or infant; 90% of the women in the study reported

taking them, to little or no effect. 89

Unless infants take enough vitamin D after birth-either via direct

supplementation or enriched formula-infant vitamin D levels are remarkably low,

with black infants at highest risk. 78% of unsupplemented, breast?fed, Iowa

infants had levels less than 11 ng/mL during winter. For those who wonder how

vitamin D could be important for brain development-given its very low levels in

breast milk-Professors Hollis and Wagner of the Medical University of South

Carolina discovered that breast milk is a source of vitamin D that is rich

enough to maintain healthy levels in infants-provided the mothers took at least

4,000 units/day. Pregnant women who do not go out into the sun need more vitamin

D than is in their prenatal vitamin-much more. 90 91

Are black children at a disadvantage, right from conception?

In 2002, Dr. Shanna Nesby?O'Dell and her colleagues at the CDC found that almost

50% of young, black women of childbearing age had vitamin D levels lower than 15

ng/mL. 12% of black women had levels less than 10 ng/mL, compared to 0.5% of

white women. While it is unknown if such low levels approach those seen in the

brain?injury animal studies reviewed above, the levels in these young black

women are close to undetectable. It may be that white children have a huge,

developmental advantage over black children-an advantage that begins immediately

after conception. One that has nothing to do with innate ability and everything

to do with environment.

What Should We Do Right Now?

That is, what do we do while we wait for all the hundreds of studies that need

to be done to see if the vitamin D theory is correct? The studies will take

years. If we do nothing but just wait, we are continuing an unplanned

naturalistic experiment on pregnant women, the brains of their unborn children,

and upon autistic individuals. A risk/benefit analysis tells us the risk of

doing nothing is potentially great while the risk of treating vitamin D

deficiency is minimal, simply good medicine, and the better choice.

So until we know for sure, pregnant women, infants, children,

everyone-especially autistic children-should receive sensible sun exposure

daily: around noon or 1:00 p.m., expose as much skin as possible, 10-30 minutes

duration-depending on how easily one sunburns. In the winter, use a suntan

parlor once a week, with the same precautions, or better yet, purchase an

ultraviolet vitamin D lamp (http://sperti.com/) for home use.

I prefer to avoid sunlight, what should I do?

You and your child should have a vitamin D blood test, called a

25?hydroxyvitamin D . Then take enough vitamin D to achieve adequate (natural

summertime) levels. Given what we do know, adequate 25(OH)D levels are now

thought to be somewhere above 40 ng/mL (100 nmol/L) and probably closer 50 ng/mL

(125 nmol/L). Ideal levels are unknown but they are probably close to levels

that were present when the human genome evolved. Natural levels (levels found in

humans who live or work in the sun) are around 50-70 ng/mL (125-175 nmol/L).

These levels are obtained by only a small fraction of modern humans. 92 93

How much vitamin D should I take?

The Food and Nutrition Board set the current Upper Limit for

medically?unsupervised intake by infants and babies (up to the age of 1

years?old) at 1,000 units/day. This means the government says it is safe to give

infants and babies up to 1,000 units a day without getting a blood test. Of

course, with correct sun exposure in the summer this is not necessary, but it

will be in winter. Children over 1 years of age, according to the Food and

Nutrition Board, may safely take 2,000 units/day-again, without requiring a

blood test.

For adolescents, pregnant women, and other adults, the government's Upper Limits

are a problem. While a 2,000 unit Upper Limit is entirely appropriate for

younger children, such limits in heavier adolescents, adults, and pregnant women

limit effective treatment of vitamin D deficiency. However, these limits no more

impair a physician's ability to treat vitamin D deficiency with higher doses

than comparable Upper Limits for calcium or magnesium impair their ability to

treat calcium or magnesium deficiencies with higher doses, should those

deficiencies be diagnosed. 94

In the absence of sun exposure and in winter, heavier children, adults, and

pregnant women may require doses above 2,000 units daily (depending on

pre?existing blood levels, body weight, degree of skin pigmentation, age, and

latitude of residence) in order to obtain and maintain levels of 50-70 ng/mL.

For example, Professor Heaney at Creighton University has estimated that about

3,000 units/day is required simply to assure that 97% of adult Americans obtain

levels greater than 35 ng/mL. Healthy adult men utilize up to 5,000 units of

vitamin D per day, if present in the body. Professors Bruce Hollis and Carol

Wagner, in South Carolina, have been giving pregnant women 4,000 units/day for

years. Professor Vieth, at the University of Toronto, found that actual vitamin

D toxicity, with systemic symptoms, is exceedingly rare and requires much higher

doses than those discussed above. When exceeding the Upper Limit, periodic serum

25(OH)D and calcium levels will reassure both physician and patient that such

amounts are safe as well as convince all concerned that the government should

revise their ten?year?old (yet most current) recommendations-the sooner the

better. 95 96 97 98

Is Autism Iatrogenic?

If the vitamin D theory of autism is correct, then to the extent it is correct,

the current plague of autism is an iatrogenic disease, caused by modern

sun?avoidance and the organizations that promulgated it. Long before we

worshipped our current gods, primitive humans venerated an older god, the sun.

Much as we have shunned our modern gods, 20 years ago we shunned the sun, hiding

from it under buildings, cars, shade, and sunblock. We told the sun she was

damaging us, and banished her from our lives-and from the lives of our pregnant

women and our children. Tragically, we relied on medical knowledge instead of

human traditions, government recommendations instead of common sense, the latest

science instead of basic instincts. The ancient Greeks, who loved the sun, knew

the gods seldom reward such hubris.

References:

1. Schaefer GB, Lutz RE. Diagnostic yield in the clinical genetic evaluation of

autism spectrum disorders. Genet Med. 2006 Sep;8(9):549-56.

2. Kippes C, Garrison CB. Are we in the midst of an autism epidemic? A review of

prevalence data. Mo Med. 2006 Jan-Feb;103(1):65-8.

3. Newschaffer CJ, Falb MD, Gurney JG. National autism prevalence trends from

United States special education data. Pediatrics. 2005 Mar;115(3):e277-82.

4. Atladottir HO, et al. Time trends in reported diagnoses of childhood

neuropsychiatric disorders: a Danish cohort study. Arch Pediatr Adolesc Med.

2007 Feb;161(2):193-8.

5. McGrath J, Feron F, Eyles D, Mackay?Sim A. Vitamin D: the neglected

neurosteroid? Trends Neurosci. 2001 Oct;24(10):570-2.

6. Kalueff AV, et al. The vitamin D neuroendocrine system as a target for novel

neurotropic drugs. CNS Neurol Disord Drug Targets. 2006 Jun;5(3):363-71.

7. Kalueff AV, Tuohimaa P. Neurosteroid hormone vitamin D and its utility in

clinical nutrition. Curr Opin Clin Nutr Metab Care. 2007 Jan;10(1):12-9.

8. Knudtzon J, Aksnes L, Akslen LA, Aarskog D. Elevated 1,25?dihydroxyvitamin D

and normocalcaemia in presumed familial syndrome. Clin Genet. 1987

Dec;32(6):369-74.

9. Mervis CB, Klein?Tasman BP. syndrome: cognition, personality, and

adaptive behavior. Ment Retard Dev Disabil Res Rev. 2000;6(2):148-58.

10. Handoko HY, et al. Polymorphisms in the vitamin D receptor and their

associations with risk of schizophrenia and selected anthropometric measures. Am

J Hum Biol. 2006 May-Jun;18 (3):415-7.

11. Poskitt EM, Cole TJ, Lawson DE. Diet, sunlight, and 25?hydroxyvitamin D in

healthy children and adults. Br Med J. 1979 Jan 27;1(6158):221-3.

12. Holick MF. Photosynthesis of vitamin D in the skin: effect of environmental

and life?style variables. Federation Proceedings 1987; 46:1876-1882.

13. Mayo Clinic Proceedings 2006; 81: 297-299.

13a. Hollis BW. Circulating 25?hydroxyvitamin D levels indicative of vitamin D

sufficiency: implications for establishing a new effective dietary intake

recommendation for vitamin D. J Nutr. 2005 Feb;135(2):317-22.

14. Guercio?Hauer C, Macfarlane DF, Deleo VA. Photodamage, photoaging and

photoprotection of the skin. Am Fam Physician. 1994 Aug;50(2):327-32, 334.

15. No authors listed. Harmful effects of ultraviolet radiation. Council on

Scientific Affairs. JAMA. 1989 Jul 21;262(3):380-4.

16. Hall HI, et al. Protection from sun exposure in US white children ages 6

months to 11 years. Public Health Rep. 2001 Jul-Aug;116(4):353-61.

17. Greer FR. Issues in establishing vitamin D recommendations for infants and

children. Am J Clin Nutr. 2004 Dec;80(6 Suppl):1759S-62S.

18. Lips P Vitamin D physiology. Prog Biophys Mol Biol. 2006 Sep;92(1):4-8. Epub

2006 Feb 28.

19. Dusso AS, Brown AJ, Slatopolsky E. Vitamin D. Am J Physiol Renal Physiol.

2005 Jul;289(1):F8-28.

20. Eyles D, Brown J, Mackay?Sim A, McGrath J, Feron F. Vitamin D3 and brain

development. Neuroscience. 2003;118(3):641-53.

21. Eyles DW, S, Kinobe R, Hewison M, McGrath JJ. Distribution of the

vitamin D receptor and 1 alpha?hydroxylase in human brain. J Chem Neuroanat.

2005 Jan;29(1):21-30.

22. McGrath JJ, Feron FP, Burne TH, Mackay?Sim A, Eyles DW. Vitamin

D3-implications for brain development. J Steroid Biochem Mol Biol. 2004

May;89-90(1-5):557-60.

23. Brachet P, et al. Vitamin D, a neuroactive hormone: from brain development

to pathological disorders. In Feldman D, Pike JW, Glorieux FH, eds. Vitamin D.

San Diego: Elsevier, 2005.

24. Ko P, Burkert R, McGrath J, Eyles D. Maternal vitamin D3 deprivation and

the regulation of apoptosis and cell cycle during rat brain development. Brain

Res Dev Brain Res. 2004 Oct 15;153(1):61-8.

25. Feron F, et al. Developmental Vitamin D3 deficiency alters the adult rat

brain. Brain Res Bull. 2005 Mar 15;65(2):141-8.

26. Burne TH, et al. Transient prenatal Vitamin D deficiency is associated with

hyperlocomotion in adult rats. Behav Brain Res. 2004 Oct 5;154(2):549-55.

27. Becker A, et al. Transient prenatal vitamin D deficiency is associated with

subtle alterations in learning and memory functions in adult rats. Behav Brain

Res. 2005 Jun 20;161(2):306-12.

28. Almeras L, et al. Developmental vitamin D deficiency alters brain protein

expression in the adult rat: implications for neuropsychiatric disorders.

Proteomics. 2007 Mar;7(5):769-80.

29. Piven J, et al. An MRI study of brain size in autism. Am J Psychiatry. 1995

Aug;152(8):1145-9.

30. Ashwood P, Wills S, Van de Water J. The immune response in autism: a new

frontier for autism research. J Leukoc Biol. 2006 Jul;80(1):1-15. Epub 2006 May

12.

31. Cantorna MT, Zhu Y, Froicu M, Wittke A. Vitamin D status,

1,25?dihydroxyvitamin D3, and the immune system. Am J Clin Nutr. 2004 Dec;80(6

Suppl):1717S-20S.

32. ME, Piazza A, McCartney Y, Lynch MA. Evidence that vitamin D3 reverses

age?related inflammatory changes in the rat hippocampus. Biochem Soc Trans. 2005

Aug;33(Pt 4):573-7.

33. Cohen?Lahav M, Shany S, Tobvin D, Chaimovitz C, Douvdevani A. Vitamin D

decreases NFkappaB activity by increasing IkappaBalpha levels. Nephrol Dial

Transplant. 2006 Apr;21 (4):889-97. Epub 2006 Feb 2.

34. Kalueff AV, Eremin KO, Tuohimaa P. Mechanisms of neuroprotective action of

vitamin d(3). Biochemistry (Mosc). 2004 Jul;69(7):738-41.

35. Garcion E, et al. New clues about vitamin D functions in the nervous system.

Trends Endocrinol Metab. 2002 Apr;13(3):100-5.

36. Chen KB, Lin AM, Chiu TH. Systemic vitamin D3 attenuated oxidative injuries

in the locus coeruleus of rat brain. Ann N Y Acad Sci. 2003 May;993:313-24;

discussion 345-9.

37. Dhesi JK, Bearne LM, Moniz C, Hurley MV, SH, Swift CG, Allain TJ.

Neuromuscular and psychomotor function in elderly subjects who fall and the

relationship with vitamin D status. J Bone Miner Res. 2002 May;17(5):891-7.

38. Kenny AM, Biskup B, Robbins B, Marcella G, Burleson JA. Effects of vitamin D

supplementation on strength, physical function, and health perception in older,

community?dwelling men. J Am Geriatr Soc. 2003 Dec;51(12):1762-7.

39. Kipen E, Helme RD, Wark JD, Flicker L. Bone density, vitamin D nutrition,

and parathyroid hormone levels in women with dementia. J Am Geriatr Soc. 1995

Oct;43(10):1088-91.

40. Vanlint S, Nugent M. Vitamin D and fractures in people with intellectual

disability. J Intellect Disabil Res. 2006 Oct;50(Pt 10):761-7.

41. Flicker L, Mead K, MacInnis RJ, Nowson C, Scherer S, Stein MS, x J,

Hopper JL, Wark JD. Serum vitamin D and falls in older women in residential care

in Australia. J Am Geriatr Soc. 2003 Nov;51(11):1533-8.

42. Przybelski RJ, Binkley NC. Is vitamin D important for preserving cognition?

A positive correlation of serum 25?hydroxyvitamin D concentration with cognitive

function. Arch Biochem Biophys. 2007 Apr 15;460(2):202-5. Epub 2007 Jan 8.

43. Lin AM, Chen KB, Chao PL. Antioxidative effect of vitamin D3 on zinc?induced

oxidative stress in CNS. Ann N Y Acad Sci. 2005 Aug;1053:319-29.

44. Valko M, H, Cronin MT. Metals, toxicity and oxidative stress. Curr

Med Chem. 2005;12(10):1161-208.

45. Kern JK, AM. Evidence of toxicity, oxidative stress, and neuronal

insult in autism. J Toxicol Environ Health B Crit Rev. 2006 Nov-Dec;9(6):485-99.

46. Pettifor JM. Vitamin D deficiency and nutritional rickets in children.

Unpublished manuscript.

47. Ming X, Brimacombe M, Wagner GC. Prevalence of motor impairment in autism

spectrum disorders. Brain Dev. 2007 Apr 27; [Epub ahead of print].

48. Zwaigenbaum L, et al. Behavioral manifestations of autism in the first year

of life. Int J Dev Neurosci. 2005 Apr-May;23(2-3):143-52.

49. Provost B, BR, Heimerl S. A comparison of motor delays in young

children: autism spectrum disorder, developmental delay, and developmental

concerns. J Autism Dev Disord. 2007 Feb;37(2):321-8.

50. Wayse V, Yousafzai A, Mogale K, Filteau S. Association of subclinical

vitamin D deficiency with severe acute lower respiratory infection in Indian

children under 5 y. Eur J Clin Nutr. 2004 Apr;58(4):563-7.

51. Rosen NJ, Yoshida CK, Croen LA. Infection in the first 2 years of life and

autism spectrum disorders. Pediatrics. 2007 Jan;119(1):e61-9.

52. Konstantareas MM, Homatidis S. Ear infections in autistic and normal

children. J Autism Dev Disord. 1987 Dec;17(4):585-94.

53. Rosenhall U, et al. Autism and hearing loss. J Autism Dev Disord. 1999

Oct;29(5):349-57.

54. Deykin EY, MacMahon B. Viral exposure and autism. Am J Epidemiol. 1979

Jun;109(6):628-38.

55. Tanoue Y, Oda S, Asano F, Kawashima K. Epidemiology of infantile autism in

southern Ibaraki, Japan: differences in prevalence in birth cohorts. J Autism

Dev Disord. 1988 Jun;18 (2):155-66.

56. Nicolaidou P, et al. Effects of anticonvulsant therapy on vitamin D status

in children: prospective monitoring study. J Child Neurol. 2006 Mar;21(3):205-9.

57. Rasalam AD, et al. Characteristics of fetal anticonvulsant syndrome

associated autistic disorder. Dev Med Child Neurol. 2005 Aug;47(8):551-5.

58. Rossi PG, et al. EEG features and epilepsy in patients with autism. Brain

Dev. 1995 May-Jun;17(3):169-74.

59. Siegel A, et al. Administration of 1,25?dihydroxyvitamin D3 results in the

elevation of hippocampal seizure threshold levels in rats. Brain Res. 1984 Apr

23;298(1):125-9.

60. Epstein S, Schneider AE. Drug and hormone effects on vitamin D metabolism.

In Feldman D, Pike JW, Glorieux FH, eds. Vitamin D. San Diego: Elsevier, 2005.

61. Oken E, et al. Maternal fish consumption, hair mercury, and infant cognition

in a U.S. Cohort. Environ Health Perspect. 2005 Oct;113(10):1376-80.

62. Hibbeln JR, et al. Maternal seafood consumption in pregnancy and

neurodevelopmental outcomes in childhood (ALSPAC study): an observational cohort

study. Lancet. 2007 Feb 17;369(9561):578-85.

63. Grant WB, Soles CM. Epidemiological evidence for supporting the role of

maternal vitamin D deficiency as a significant risk factor for the development

of infantile autism in those born prior to 1985. Unpublished manuscript.

64. Centers for Disease Control and Prevention. Prevalence of autism spectrum

disorders-autism and developmental disabilities monitoring network, 14 sites,

United States, 2002. MMWR Surveill Summ. 2007 Feb 9;56(1):12-28.

65. s MC, Fein DH, Waterhouse LH. Season of birth effects in autism. J

Clin Exp Neuropsychol. 2000 Jun;22(3):399-407.

66. JK, Rigel DS, Amonette RA. Summertime sun protection used by adults

for their children. J Am Acad Dermatol. 2000 May;42(5 Pt 1):746-53.

67. Hall HI, et al. Protection from sun exposure in US white children ages 6

months to 11 years. Public Health Rep. 2001 Jul-Aug;116(4):353-61.

68. Bhasin TK, Schendel D. Sociodemographic Risk Factors for Autism in a US

Metropolitan Area. J Autism Dev Disord. 2007 Apr;37(4):667-77.

69. Landa R, Garrett?Mayer E. Development in infants with autism spectrum

disorders: a prospective study. J Child Psychol Psychiatry. 2006

Jun;47(6):629-38.

70. Benton D, G. Effect of vitamin and mineral supplementation on

intelligence of a sample of schoolchildren. Lancet. 1988 Jan 23;1(8578):140-3.

71. Hayashi E, et al. Seasonal changes in sleep and behavioral problems in a

pubescent case with autism. Psychiatry Clin Neurosci. 2001 Jun;55(3):223-4.

72. Hung DW, Thelander MJ. Summer camp treatment program for autistic children.

Except Child. 1978 Apr;44(7):534-6.

73. Bhasin TK, Schendel D. Sociodemographic Risk Factors for Autism in a US

Metropolitan Area. J Autism Dev Disord. 2007 Apr;37(4):667-77.

74. Croen LA, et al. The changing prevalence of autism in California. J Autism

Dev Disord. 2002 Jun;32(3):207-15.

75. Hillman RE, et al. Prevalence of autism in Missouri: changing trends and the

effect of a comprehensive state autism project. Mo Med. 2000 May;97(5):159-63.

76. Yeargin?Allsopp M, et al. Prevalence of autism in a US metropolitan area.

JAMA. 2003 Jan 1;289(1):49-55.

77. Goodman R, s H. Child and adolescent psychiatric presentations of

second?generation Afro?Caribbeans in Britain. Br J Psychiatry. 1995

Sep;167(3):362-9.

78. Gillberg C, Schaumann H, Gillberg IC. Autism in immigrants: children born in

Sweden to mothers born in Uganda. J Intellect Disabil Res. 1995 Apr;39 ( Pt

2):141-4.

79. Newschaffer CJ, et al. The Epidemiology of Autism Spectrum Disorders (*).

Annu Rev Public Health. 2007 Apr 21;28:235-258.

80. Yeargin?Allsopp M, Drews CD, Decoufle P, CC. Mild mental retardation

in black and white children in metropolitan Atlanta: a case?control study. Am J

Public Health. 1995 Mar;85(3):324-8.

81. Drews CD, Yeargin?Allsopp M, Decoufle P, CC. Variation in the

influence of selected sociodemographic risk factors for mental retardation. Am J

Public Health. 1995 Mar;85(3):329-34.

82. Shiao SY, s CM, Helmreich RJ. Maternal race/ethnicity and predictors

of pregnancy and infant outcomes. Biol Res Nurs. 2005 Jul;7(1):55-66.

83. GR, et al. Racial differences in birthweight for gestational age

and infant mortality in extremely?low?risk US populations. Paediatr Perinat

Epidemiol. 1999 Apr;13(2):205-17.

84. GR, et al. US birth weight/gestational age?specific neonatal

mortality: 1995-1997 rates for whites, hispanics, and blacks. Pediatrics. 2003

Jan;111(1):e61-6.

85. Kolevzon A, Gross R, Reichenberg A. Prenatal and perinatal risk factors for

autism: a review and integration of findings. Arch Pediatr Adolesc Med. 2007

Apr;161(4):326-33.

86. Hegyi T, et al. The apgar score and its components in the preterm infant.

Pediatrics. 1998 Jan;101(1 Pt 1):77-81.

87. Sabour H, et al. Relationship between pregnancy outcomes and maternal

vitamin D and calcium intake: A cross?sectional study. Gynecol Endocrinol. 2006

Oct;22(10):585-9.

88. Larsson HJ, et al. Risk factors for autism: perinatal factors, parental

psychiatric history, and socioeconomic status. Am J Epidemiol. 2005 May

15;161(10):916-25; discussion 926-8.

89. Bodnar LM, et al. High prevalence of vitamin D insufficiency in black and

white pregnant women residing in the northern United States and their neonates.

J Nutr. 2007 Feb;137(2):447-52.

90. Ziegler EE, Hollis BW, SE, Jeter JM. Vitamin D deficiency in

breastfed infants in Iowa. Pediatrics. 2006 Aug;118(2):603-10.

91. Hollis BW, Wagner CL. Vitamin D requirements during lactation: high?dose

maternal supplementation as therapy to prevent hypovitaminosis D for both the

mother and the nursing infant. Am J Clin Nutr. 2004 Dec;80(6 Suppl):1752S-8S.

92. Heaney RP. The Vitamin D requirement in health and disease. J Steroid

Biochem Mol Biol. 2005 Jul 15; [Epub ahead of print]

93. Vieth R. What is the optimal vitamin D status for health? Prog Biophys Mol

Biol. 2006 Sep;92(1):26-32.

94. Hathcock JN, et al. Risk assessment for vitamin D. Am J Clin Nutr. 2007

Jan;85(1):6-18.

95. Hollis BW, Wagner CL. Vitamin D deficiency during pregnancy: an ongoing

epidemic. Am J Clin Nutr. 2006 Aug;84(2):273.

96. Heaney RP. The Vitamin D requirement in health and disease. J Steroid

Biochem Mol Biol. 2005; 97:13-19.

97. Heaney RP, et al. Human serum 25?hydroxycholecalciferol response to extended

oral dosing with cholecalciferol. Am J Clin Nutr. 2003 Jan;77(1):204-10.

98. Vieth R. Vitamin D supplementation, 25?hydroxyvitamin D concentrations, and

safety. Am J Clin Nutr. 1999 May;69(5):842-56.

~~~~~~~~~~~~~~~~~~~~~~

=====

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...