Information about nutritional vitamin supplements





 

Skip navigation links

ODS Logo

Search
Placeholder

Placeholder
Home

Health Information
Research Information

Funding
News & Events

About ODS
Dietary Supplement Fact Sheet: Vitamin D

Office of Dietary Supplements • National Institutes of Health
Table of Contents

Introduction
Reference Intakes
Sources of Vitamin D
Vitamin D Intakes and Status
Vitamin D Deficiency
Groups at Risk of Vitamin D Inadequacy
Vitamin D and Health
Health Risks from Excessive Vitamin D
Interactions with Medications
Vitamin D and Healthful Diets
References
Introduction

Vitamin D is a fat-soluble vitamin that is naturally present in very
few foods, added to others, and available as a dietary supplement. It
is also produced endogenously when ultraviolet rays from sunlight
strike the skin and trigger vitamin D synthesis 1,2. Vitamin D
obtained from sun exposure, food, and supplements is biologically
inert and must undergo two hydroxylations in the body for activation.
The first occurs in the liver and converts vitamin D to
25-hydroxyvitamin D 25(OH)D, also known as calcidiol. The second
occurs primarily in the kidney and forms the physiologically active
1,25-dihydroxyvitamin D 1,25(OH)2D, also known as calcitriol 3.
Vitamin D is essential for promoting calcium absorption in the gut and
maintaining adequate serum calcium and phosphate concentrations to
enable normal mineralization of bone and prevent hypocalcemic tetany.
It is also needed for bone growth and bone remodeling by osteoblasts
and osteoclasts 3,4,5. Without sufficient vitamin D, bones can
become thin, brittle, or misshapen. Vitamin D sufficiency prevents
rickets in children and osteomalacia in adults 2,6,7. Together with
calcium, vitamin D also helps protect older adults from osteoporosis.

Vitamin D has other roles in human health, including modulation of
neuromuscular and immune function and reduction of inflammation. Many
genes encoding proteins that regulate cell proliferation,
differentiation, and apoptosis are modulated in part by vitamin D 3,5,8,9.
Many laboratory-cultured human cells have vitamin D receptors and some
convert 25(OH)D to 1,25(OH)2D 10. It remains to be determined
whether cells with vitamin D receptors in the intact human carry out
this conversion.
Serum concentration of 25(OH)D is the best indicator of vitamin D
status. It reflects vitamin D produced cutaneously and that obtained
from food and supplements 4 and has a fairly long circulating
half-life of 15 days 11. However, serum 25(OH)D levels do not
indicate the amount of vitamin D stored in other body tissues.
Circulating 1,25(OH)2D is generally not a good indicator of vitamin D
status because it has a short half-life of 15 hours and serum
concentrations are closely regulated by parathyroid hormone, calcium,
and phosphate 11. Levels of 1,25(OH)2D do not typically decrease
until vitamin D deficiency is severe 5,10.

There is considerable discussion of the serum concentrations of
25(OH)D associated with deficiency (e.g., rickets), adequacy for bone
health, and optimal overall health (Table 1). A concentration of <15
nanograms per milliliter (ng/mL) (or <37.5 nanomoles per liter
nmol/L) is generally considered inadequate; concentrations >15 ng/ml
(>37.5 nmol/L) are recommended. Higher levels are proposed by some
(>30 ng/ml or >75 nmol/L) as desirable for overall health and disease
prevention 12, but insufficient data are available to support them 13.
Serum concentrations of 25(OH)D consistently >200 ng/ml (>500 nmol/L)
are potentially toxic.
Table 1: Serum 25-Hydroxyvitamin D 25(OH)D Concentrations and
Health

ng/mL--
nmol/L--

Health status
<10-11

<25-27.5
Associated with vitamin D deficiency, leading to rickets in infants
and children and osteomalacia in adults 4,13

<10-15
<25-37.5

Generally considered inadequate for bone and overall health in healthy
individuals 4,13
≥15

≥37.5
Generally considered adequate for bone and overall health in healthy
individuals 4

Consistently >200
Consistently >500

Considered potentially toxic, leading to hypercalcemia and
hyperphosphatemia, although human data are limited. In an animal
model, concentrations ≤400 ng/mL (≤1,000 nmol/L) demonstrated no
toxicity 11,14.
 Serum concentrations of 25(OH)D are reported in both nanograms per
milliliter (ng/mL) and nanomoles per liter (nmol/L).
-- 1 ng/mL = 2.5 nmol/L

An additional complication in assessing vitamin D status is in the
actual measurement of serum concentrations of 25(OH)D. Considerable
variability exists among the various assays available and among
laboratories that conduct the analyses 15,16,17. This means that
compared to the actual concentration of 25(OH)D in a sample of blood
serum, a falsely low or falsely high value may be obtained depending
on the assay or laboratory used 18. A standard reference material
for 25(OH)D became available in July 2009 that will now permit
standardization of values across laboratories 19.
Reference Intakes

Intake reference values for vitamin D and other nutrients are provided
in the Dietary Reference Intakes (DRIs) developed by the Food and
Nutrition Board (FNB) at the Institute of Medicine of The National
Academies (formerly National Academy of Sciences) 4. DRI is the
general term for a set of reference values used to plan and assess
nutrient intakes of healthy people. These values, which vary by age
and gender 4, include:
Recommended Dietary Allowance (RDA): average daily level of intake
 sufficient to meet the nutrient requirements of nearly all
 (97%-98%) healthy people.

Adequate Intake (AI): established when evidence is insufficient to
 develop an RDA and is set at a level assumed to ensure nutritional
 adequacy.
Tolerable Upper Intake Level (UL): maximum daily intake unlikely
 to cause adverse health effects 4.

The FNB established an AI for vitamin D that represents a daily intake
that is sufficient to maintain bone health and normal calcium
metabolism in healthy people. AIs for vitamin D are listed in both
micrograms (mcg) and International Units (IUs); the biological
activity of 1 mcg is equal to 40 IU (Table 2). The AIs for vitamin D
are based on the assumption that the vitamin is not synthesized by
exposure to sunlight 4.
Table 2: Adequate Intakes (AIs) for Vitamin D 4

Age
Children

Men
Women

Pregnancy
Lactation

Birth to 13 years
  1. mcg (200 IU)
14-18 years
  1. mcg (200 IU)
  1. mcg (200 IU)
  1. mcg (200 IU)
  1. mcg (200 IU)
19-50 years
  1. mcg (200 IU)
  1. mcg (200 IU)
  1. mcg (200 IU)
  1. mcg (200 IU)
51-70 years

10 mcg
(400 IU)
10 mcg
(400 IU)

71+ years
15 mcg
(600 IU)

15 mcg
(600 IU)
In 2008, the American Academy of Pediatrics (AAP) issued recommended
intakes for vitamin D that exceed those of FNB 20. The AAP
recommendations are based on evidence from more recent clinical trials
and the history of safe use of 400 IU/day of vitamin D in pediatric
and adolescent populations. AAP recommends that exclusively and
partially breastfed infants receive supplements of 400 IU/day of
vitamin D shortly after birth and continue to receive these
supplements until they are weaned and consume ≥1,000 mL/day of vitamin
D-fortified formula or whole milk 20. (All formulas sold in the
United States provide ≥400 IU vitamin D3 per liter, and the majority
of vitamin D-only and multivitamin liquid supplements provide 400 IU
per serving.) Similarly, all non-breastfed infants ingesting <1,000
mL/day of vitamin D-fortified formula or milk should receive a vitamin
D supplement of 400 IU/day. AAP also recommends that older children
and adolescents who do not obtain 400 IU/day through vitamin
D-fortified milk and foods should take a 400 IU vitamin D supplement
daily 20.

The FNB established an expert committee in 2008 to review the DRIs for
vitamin D (and calcium). The current DRIs for this nutrient were
established in 1997, and since that time substantial new research has
been published to justify a reevaluation of adequate vitamin D intakes
for healthy populations. Determinations of DRIs are based on
indicators of adequacy or hazard; dose-response curves; health
outcomes; life-stage groups; and relations between intakes,
biomarkers, and outcomes. For vitamin D, the FNB committee will focus
on (1) effects of circulating concentrations of 25(OH)D on health
outcomes, (2) effects of vitamin D intakes on circulating 25(OH)D and
on health outcomes, and (3) levels of intake associated with adverse
effects 21. The FNB expects to issue its report, updating as
appropriate the DRIs for vitamin D and calcium, by May 2010 22.
Sources of Vitamin D

Food
Very few foods in nature contain vitamin D. The flesh of fish (such as
salmon, tuna, and mackerel) and fish liver oils are among the best
sources 4. Small amounts of vitamin D are found in beef liver,
cheese, and egg yolks. Vitamin D in these foods is primarily in the
form of vitamin D3 (cholecalciferol) and its metabolite 25(OH)D3 23.
Some mushrooms provide vitamin D2 (ergocalciferol) in variable amounts
24-26. Mushrooms with enhanced levels of vitamin D2 from being
exposed to ultraviolet light under controlled conditions are also
available.
Fortified foods provide most of the vitamin D in the American diet 4,26.
For example, almost all of the U.S. milk supply is fortified with 100
IU/cup of vitamin D (25% of the Daily Value or 50% of the AI level for
ages 14-50 years). In the 1930s, a milk fortification program was
implemented in the United States to combat rickets, then a major
public health problem. This program virtually eliminated the disorder
at that time 4,14. Other dairy products made from milk, such as
cheese and ice cream, are generally not fortified. Ready-to-eat
breakfast cereals often contain added vitamin D, as do some brands of
orange juice, yogurt, and margarine. In the United States, foods
allowed to be fortified with vitamin D include cereal flours and
related products, milk and products made from milk, and
calcium-fortified fruit juices and drinks 27. Maximum levels of
added vitamin D are specified by law.

Several food sources of vitamin D are listed in Table 3.
Table 3: Selected Food Sources of Vitamin D 30

Food
IUs per serving

Percent DV--
Cod liver oil, 1 tablespoon

1,360
340

Salmon (sockeye), cooked, 3 ounces
794

199
Mushrooms that have been exposed to ultraviolet light to increase
vitamin D, 3 ounces (not yet commonly available)

400
100

Mackerel, cooked, 3 ounces
388

97
Tuna fish, canned in water, drained, 3 ounces

154
39

Milk, nonfat, reduced fat, and whole, vitamin D-fortified, 1 cup
115-124

29-31
Orange juice fortified with vitamin D, 1 cup (check product labels, as
amount of added vitamin D varies)

100
25

Yogurt, fortified with 20% of the DV for vitamin D, 6 ounces (more
heavily fortified yogurts provide more of the DV)
80

20
Margarine, fortified, 1 tablespoon

60
15

Sardines, canned in oil, drained, 2 sardines
46

12
Liver, beef, cooked, 3.5 ounces

46
12

Ready-to-eat cereal, fortified with 10% of the DV for vitamin D,
0.75-1 cup (more heavily fortified cereals might provide more of the
DV)
40

10
Egg, 1 whole (vitamin D is found in yolk)

25
6

Cheese, Swiss, 1 ounce
6

2
IUs = International Units.

--DV = Daily Value. DVs were developed by the U.S. Food and Drug
Administration to help consumers compare the nutrient contents of
products within the context of a total diet. The DV for vitamin D is
400 IU for adults and children age 4 and older. Food labels, however,
are not required to list vitamin D content unless a food has been
fortified with this nutrient. Foods providing 20% or more of the DV
are considered to be high sources of a nutrient.
The U.S. Department of Agriculture's Nutrient Database Web site,
http://www.nal.usda.gov/fnic/foodcomp/search, lists the nutrient
content of many foods and provides a list of foods containing vitamin
D:
http://www.ars.usda.gov/SP2UserFiles/Place/12354500/Data/SR22/nutrlist/sr22a324.pdf.
A growing number of foods are being analyzed for vitamin D content.
Simpler and faster methods to measure vitamin D in foods are needed,
as are food standard reference materials with certified values for
vitamin D to ensure accurate measurements 31.

Sun exposure
Most people meet their vitamin D needs through exposure to sunlight 5,31.
Ultraviolet (UV) B radiation with a wavelength of 290-315 nanometers
penetrates uncovered skin and converts cutaneous 7-dehydrocholesterol
to previtamin D3, which in turn becomes vitamin D3 9,32,33. Season,
geographic latitude, time of day, cloud cover, smog, skin melanin
content, and sunscreen are among the factors that affect UV radiation
exposure and vitamin D synthesis 33. The UV energy above 42 degrees
north latitude (a line approximately between the northern border of
California and Boston) is insufficient for cutaneous vitamin D
synthesis from November through February 5; in far northern
latitudes, this reduced intensity lasts for up to 6 months. In the
United States, latitudes below 34 degrees north (a line between Los
Angeles and Columbia, South Carolina) allow for cutaneous production
of vitamin D throughout the year 27.
Complete cloud cover reduces UV energy by 50%; shade (including that
produced by severe pollution) reduces it by 60% 34. UVB radiation
does not penetrate glass, so exposure to sunshine indoors through a
window does not produce vitamin D 35. Sunscreens with a sun
protection factor of 8 or more appear to block vitamin D-producing UV
rays, although in practice people generally do not apply sufficient
amounts, cover all sun-exposed skin, or reapply sunscreen regularly 36.
Skin likely synthesizes some vitamin D even when it is protected by
sunscreen as typically applied.

The factors that affect UV radiation exposure and research to date on
the amount of sun exposure needed to maintain adequate vitamin D
levels make it difficult to provide general guidelines. It has been
suggested by some vitamin D researchers, for example, that
approximately 5-30 minutes of sun exposure between 10 AM and 3 PM at
least twice a week to the face, arms, legs, or back without sunscreen
usually lead to sufficient vitamin D synthesis and that the moderate
use of commercial tanning beds that emit 2%-6% UVB radiation is also
effective 10,33. Individuals with limited sun exposure need to
include good sources of vitamin D in their diet or take a supplement.
Despite the importance of the sun to vitamin D synthesis, it is
prudent to limit exposure of skin to sunlight 36 and UV radiation
from tanning beds 37. UV radiation is a carcinogen responsible for
most of the estimated 1.5 million skin cancers and the 8,000 deaths
due to metastatic melanoma that occur annually in the United States 36.
Lifetime cumulative UV damage to skin is also largely responsible for
some age-associated dryness and other cosmetic changes. It is not
known whether a desirable level of regular sun exposure exists that
imposes no (or minimal) risk of skin cancer over time. The American
Academy of Dermatology advises that photoprotective measures be taken,
including the use of sunscreen, whenever one is exposed to the sun 38.

Dietary supplements
In supplements and fortified foods, vitamin D is available in two
forms, D2 (ergocalciferol) and D3 (cholecalciferol). Vitamin D2 is
manufactured by the UV irradiation of ergosterol in yeast, and vitamin
D3 is manufactured by the irradiation of 7-dehydrocholesterol from
lanolin and the chemical conversion of cholesterol 10. The two forms
have traditionally been regarded as equivalent based on their ability
to cure rickets, but evidence has been offered that they are
metabolized differently. Vitamin D3 could be more than three times as
effective as vitamin D2 in raising serum 25(OH)D concentrations and
maintaining those levels for a longer time, and its metabolites have
superior affinity for vitamin D-binding proteins in plasma 5,39,40.
Because metabolite receptor affinity is not a functional assessment,
as the earlier results for the healing of rickets were, further
research is needed on the comparative physiological effects of both
forms. Many supplements are being reformulated to contain vitamin D3
instead of vitamin D2 40. Both forms (as well as vitamin D in foods
and from cutaneous synthesis) effectively raise serum 25(OH)D levels 5.
Vitamin D Intakes and Status

In 1988-1994, as part of the third National Health and Nutrition
Examination Survey (NHANES III), the frequency of use of some vitamin
D-containing foods and supplements was examined in 1,546 non-Hispanic
African American women and 1,426 non-Hispanic white women of
reproductive age (15-49 years) 41. In both groups, 25(OH)D levels
were higher in the fall (after a summer of sun exposure) and when milk
or fortified cereals were consumed more than three times per week. The
prevalence of serum concentrations of 25(OH)D ≤15 ng/mL (≤37.5 nmol/L)
was 10 times greater for the African American women (42.2%) than for
the white women (4.2%).
The 2000-2004 NHANES provides the most recent data on the vitamin D
nutritional status of the U.S. population. Generally, younger people
had higher serum 25(OH)D levels than older people, males had higher
levels than females, and non-Hispanic whites had higher levels than
Mexican Americans, who in turn had higher levels than non-Hispanic
blacks. Depending on the population group, 1%-9% had serum 25(OH)D
levels <11 ng/mL (<27.5 nmol/L), 8%-36% had levels <20 ng/mL (<50
nmol/L), and the majority (50%-78%) had levels <30 ng/mL (<75 nmol/L)
42.

In NHANES 2000-2004, age-adjusted mean serum 25(OH)D concentrations
were 2-8 ng/mL (5–20 nmol/L) lower compared to NHANES III 43.
However, after adjustment for assay shifts, age-adjusted means in
NHANES 2000–2004 remained significantly lower (by 2.0-3.6 ng/mL (5–9
nmol/L)) in most males, but not in most females. In a study subsample,
adjustment for the confounding effects of assay differences changed
mean serum 25(OH)D concentrations by ~4 ng/mL (~10 nmol/L), and
adjustment for changes in the factors likely related to real changes
in vitamin D status (such as body mass index (BMI), milk intake, and
sun protection) changed mean serum 25(OH)D concentrations by 0.4-0.64
ng/mL (1.0-1.6 nmol/L).
Subsequent to this report, another investigator 44 evaluated vitamin
D levels measured in NHANES 2001-2004 compared to NHANES III and
reported a marked decline, leading some to suggest that the majority
of children and adults in the United States (and almost all African
Americans and Mexican Americans) are vitamin D insufficient. However,
this analysis exaggerates the temporal and demographic trends in
vitamin D status because it uses a higher than usual cutoff to
characterize vitamin D insufficiency, does not separate the
independent effects of season and latitude in data and, most
seriously, fails to compensate for a change in the 25(OH)D measurement
assay used between both sets of NHANES surveys 45. Over time, mean
serum 25(OH)D concentrations in the United States have declined, but
only modestly, when compensating for the assay change 43. The real
decline (~2.0-3.6 ng/mL (~5-9 nmol/L)) is likely due to simultaneous
increases in BMI, reduced milk intake, and greater use of sun
protection in the U.S. population.

According to NHANES data from 2005-2006, only 29% of adult men and 17%
of adult women (ages 19 and older) had intakes of vitamin D from food
alone that exceeded their AIs. Overall in the U.S. population, only
about one-third of individuals 1 year of age and older had vitamin D
intakes from food exceeding their respective AIs 46. However,
dietary supplements as well as foods contribute vitamin D, so both
sources must be included to obtain a true picture of total intakes. In
2005-2006, 37% of people in the United States reported the use of a
dietary supplement containing vitamin D. Total intake estimates of
vitamin D from both food and supplements are currently being tabulated
by the Office of Dietary Supplements.
Vitamin D Deficiency

Nutrient deficiencies are usually the result of dietary inadequacy,
impaired absorption and use, increased requirement, or increased
excretion. A vitamin D deficiency can occur when usual intake is lower
than recommended levels over time, exposure to sunlight is limited,
the kidneys cannot convert vitamin D to its active form, or absorption
of vitamin D from the digestive tract is inadequate. Vitamin
D-deficient diets are associated with milk allergy, lactose
intolerance, and strict vegetarianism 47.
Rickets and osteomalacia are the classical vitamin D deficiency
diseases. In children, vitamin D deficiency causes rickets, a disease
characterized by a failure of bone tissue to properly mineralize,
resulting in soft bones and skeletal deformities 34. Rickets was
first described in the mid-17th century by British researchers 34,48.
In the late 19th and early 20th centuries, German physicians noted
that consuming 1-3 teaspoons of cod liver oil per day could reverse
rickets 48. In the 1920s and prior to identification of the
structure of vitamin D and its metabolites, biochemist Harry Steenbock
patented a process to impart antirachitic activity to foods 27. The
process involved the addition of what turned out to be precursor forms
of vitamin D followed by exposure to UV radiation. The fortification
of milk with vitamin D has made rickets a rare disease in the United
States. However, rickets is still reported periodically, particularly
among African American infants and children 34,48. A 2003 report
from Memphis, for example, described 21 cases of rickets among
infants, 20 of whom were African American 48.

Prolonged exclusive breastfeeding without the AAP-recommended vitamin
D supplementation is a significant cause of rickets, particularly in
dark-skinned infants breastfed by mothers who are not vitamin D
replete 6. Additional causes of rickets include extensive use of
sunscreens and placement of children in daycare programs, where they
often have less outdoor activity and sun exposure 34,48. Rickets is
also more prevalent among immigrants from Asia, Africa, and the Middle
East, possibly because of genetic differences in vitamin D metabolism
and behavioral differences that lead to less sun exposure 34.
In adults, vitamin D deficiency can lead to osteomalacia, resulting in
weak muscles and bones 6,7,11. Symptoms of bone pain and muscle
weakness can indicate inadequate vitamin D levels, but such symptoms
can be subtle and go undetected in the initial stages.

Groups at Risk of Vitamin D Inadequacy
Obtaining sufficient vitamin D from natural food sources alone can be
difficult. For many people, consuming vitamin D-fortified foods and
being exposed to sunlight are essential for maintaining a healthy
vitamin D status. In some groups, dietary supplements might be
required to meet the daily need for vitamin D.

Breastfed infants
Vitamin D requirements cannot be met by human milk alone 4,49, which
provides only about 25 IU/L 50. A recent review of reports of
nutritional rickets found that a majority of cases occurred among
young, breastfed African Americans 51. The sun is a potential source
of vitamin D, but AAP advises keeping infants out of direct sunlight
and having them wear protective clothing and sunscreen 52. As noted
earlier, AAP recommends that exclusively and partially breastfed
infants be supplemented with 400 IU of vitamin D per day 20.
Older adults
Americans aged 50 and older are at increased risk of developing
vitamin D insufficiency 33. As people age, skin cannot synthesize
vitamin D as efficiently and the kidney is less able to convert
vitamin D to its active hormone form 4,53. As many as half of older
adults in the United States with hip fractures could have serum
25(OH)D levels <12 ng/mL (<30 nmol/L) 5.

People with limited sun exposure
Homebound individuals, people living in northern latitudes (such as
New England and Alaska), women who wear long robes and head coverings
for religious reasons, and people with occupations that prevent sun
exposure are unlikely to obtain adequate vitamin D from sunlight 54,55.
People with dark skin
Greater amounts of the pigment melanin result in darker skin and
reduce the skin's ability to produce vitamin D from exposure to
sunlight. Some studies suggest that older adults, especially women,
with darker skin are at high risk of developing vitamin D
insufficiency 41,56. However, one group with dark skin, African
Americans, generally has lower levels of 25(OH)D yet develops fewer
osteoporotic fractures than Caucasians (see section below on
osteoporosis).

People with fat malabsorption
As a fat-soluble vitamin, vitamin D requires some dietary fat in the
gut for absorption. Individuals who have a reduced ability to absorb
dietary fat might require vitamin D supplements 57. Fat
malabsorption is associated with a variety of medical conditions
including some forms of liver disease, cystic fibrosis, and Crohn's
disease 27.
People who are obese or who have undergone gastric bypass surgery
Individuals with a BMI ≥30 typically have a low plasma concentration
of 25(OH)D 58; this level decreases as obesity and body fat increase
59. Obesity does not affect skin's capacity to synthesize vitamin D,
but greater amounts of subcutaneous fat sequester more of the vitamin
and alter its release into the circulation. Even with orally
administered vitamin D, BMI is inversely correlated with peak serum
concentrations, probably because some vitamin D is sequestered in the
larger pools of body fat 58. Obese individuals who have undergone
gastric bypass surgery may become vitamin D deficient without a
sufficient intake of this nutrient from food or supplements, since
part of the upper small intestine where vitamin D is absorbed is
bypassed 60,61.

Vitamin D and Health
Optimal serum concentrations of 25(OH)D for bone and general health
throughout life have not been established 5,10 and are likely to
vary at each stage of life, depending on the physiological measures
selected. The three-fold range of cut points that have been proposed
by various experts, from 16 to 48 ng/mL (40 to 120 nmol/L), reflect
differences in the functional endpoints chosen (e.g., serum
concentrations of parathyroid hormone or bone fractures), as well as
differences in the analytical methods used.

In March 2007, a group of vitamin D and nutrition researchers
published a controversial and provocative editorial contending that
the desirable concentration of 25(OH)D is ≥30 ng/mL (≥75 nmol/L) 12.
They noted that supplemental intakes of 400 IU/day of vitamin D
increase 25(OH)D concentrations by only 2.8-4.8 ng/mL (7-12 nmol/L)
and that daily intakes of approximately 1,700 IU are needed to raise
these concentrations from 20 to 32 ng/mL (50 to 80 nmol/L).
Osteoporosis
More than 25 million adults in the United States have or are at risk
of developing osteoporosis, a disease characterized by fragile bones
that significantly increases the risk of bone fractures 62.
Osteoporosis is most often associated with inadequate calcium intakes
(generally <1,000-1,200 mg/day), but insufficient vitamin D
contributes to osteoporosis by reducing calcium absorption 63.
Although rickets and osteomalacia are extreme examples of the effects
of vitamin D deficiency, osteoporosis is an example of a long-term
effect of calcium and vitamin D insufficiency 64. Adequate storage
levels of vitamin D maintain bone strength and might help prevent
osteoporosis in older adults, nonambulatory individuals who have
difficulty exercising, postmenopausal women, and individuals on
chronic steroid therapy 65.

Normal bone is constantly being remodeled. During menopause, the
balance between these processes changes, resulting in more bone being
resorbed than rebuilt. Hormone therapy with estrogen and progesterone
might be able to delay the onset of osteoporosis. However, some
medical groups and professional societies recommend that
postmenopausal women consider using other agents to slow or stop bone
resorption because of the potential adverse health effects of hormone
therapy 66-68.
Most supplementation trials of the effects of vitamin D on bone health
also include calcium, so it is not possible to isolate the effects of
each nutrient. The authors of a recent evidence-based review of
research concluded that supplements of both vitamin D3 (at 700-800
IU/day) and calcium (500-1,200 mg/day) decreased the risk of falls,
fractures, and bone loss in elderly individuals aged 62-85 years 5.
The decreased risk of fractures occurred primarily in elderly women
aged 85 years, on average, and living in a nursing home. Women should
consult their healthcare providers about their needs for vitamin D
(and calcium) as part of an overall plan to prevent or treat
osteoporosis.

African Americans have lower levels of 25(OH)D than Caucasians, yet
they develop fewer osteoporotic fractures. This suggests that factors
other than vitamin D provide protection 69. African Americans have
an advantage in bone density from early childhood, a function of their
more efficient calcium economy, and have a lower risk of fracture even
when they have the same bone density as Caucasians. They also have a
higher prevalence of obesity, and the resulting higher estrogen levels
in obese women might protect them from bone loss 69. Further
reducing the risk of osteoporosis in African Americans are their lower
levels of bone-turnover markers, shorter hip-axis length, and superior
renal calcium conservation. However, despite this advantage in bone
density, osteoporosis is a significant health problem among African
Americans as they age 69.
Cancer
Laboratory and animal evidence as well as epidemiologic data suggest
that vitamin D status could affect cancer risk. Strong biological and
mechanistic bases indicate that vitamin D plays a role in the
prevention of colon, prostate, and breast cancers. Emerging
epidemiologic data suggest that vitamin D has a protective effect
against colon cancer, but the data are not as strong for a protective
effect against prostate and breast cancer, and are variable for
cancers at other sites 70,71. Studies do not consistently show a
protective effect or no effect, however. One study of Finnish smokers,
for example, found that subjects in the highest quintile of baseline
vitamin D status have a three-fold higher risk of developing
pancreatic cancer 72.

Vitamin D emerged as a protective factor in a prospective,
cross-sectional study of 3,121 adults aged ≥50 years (96% men) who
underwent a colonoscopy. The study found that 10% had at least one
advanced cancerous lesion. Those with the highest vitamin D intakes
(>645 IU/day) had a significantly lower risk of these lesions 73.
However, the Women's Health Initiative, in which 36,282 postmenopausal
women of various races and ethnicities were randomly assigned to
receive 400 IU vitamin D plus 1,000 mg calcium daily or a placebo,
found no significant differences between the groups in the incidence
of colorectal cancers over 7 years 74. More recently, a clinical
trial focused on bone health in 1,179 postmenopausal women residing in
rural Nebraska found that subjects supplemented daily with calcium
(1,400-1,500 mg) and vitamin D3 (1,100 IU) had a significantly lower
incidence of cancer over 4 years compared to women taking a placebo 64.
The small number of cancers reported (50) precludes generalizing about
a protective effect from either or both nutrients or for cancers at
different sites. This caution is supported by an analysis of 16,618
participants in NHANES III, where total cancer mortality was found to
be unrelated to baseline vitamin D status 76. However, colorectal
cancer mortality was inversely related to serum 25(OH)D
concentrations.
Further research is needed to determine whether vitamin D inadequacy
in particular increases cancer risk, whether greater exposure to the
nutrient is protective, and whether some individuals could be at
increased risk of cancer because of vitamin D exposure 70,77.

Other conditions
A growing body of research suggests that vitamin D might play some
role in the prevention and treatment of type 1 78 and type 2
diabetes 79, hypertension 80, glucose intolerance 81, multiple
sclerosis 82, and other medical conditions 83,84. However, most
evidence for these roles comes from in vitro, animal, and
epidemiological studies, not the randomized clinical trials considered
to be more definitive. Until such trials are conducted, the
implications of the available evidence for public health and patient
care will be debated. A systematic review of health outcomes related
to vitamin D and calcium intakes, both alone and in combination, was
published in August 2009 85.
A recent meta-analysis found that use of vitamin D supplements was
associated with a reduction in overall mortality from any cause by a
statistically significant 7% 86,87. The subjects in these trials
were primarily healthy, middle aged or elderly, and at high risk of
fractures; they took 300-2,000 IU/day of vitamin D supplements.

Health Risks from Excessive Vitamin D
Vitamin D toxicity can cause nonspecific symptoms such as nausea,
vomiting, poor appetite, constipation, weakness, and weight loss 88.
More seriously, it can also raise blood levels of calcium, causing
mental status changes such as confusion and heart rhythm abnormalities
7. The use of supplements of both calcium (1,000 mg/day) and vitamin
D (400 IU/day) by postmenopausal women was associated with a 17%
increase in the risk of kidney stones over 7 years in the Women's
Health Initiative 89. Deposition of calcium and phosphate in the
kidneys and other soft tissues can also be caused by excessive vitamin
D levels 47. A serum 25(OH)D concentration consistently >200 ng/mL
(>500 nmol/L) is considered to be potentially toxic 11. In an animal
model, concentrations ≤400 ng/mL (≤1,000 nmol/L) were not associated
with harm 14.

Excessive sun exposure does not result in vitamin D toxicity because
the sustained heat on the skin is thought to photodegrade previtamin D3
and vitamin D3 as it is formed 10,35. High intakes of dietary
vitamin D are very unlikely to result in toxicity unless large amounts
of cod liver oil are consumed; toxicity is more likely to occur from
high intakes of supplements.
Long-term intakes above the UL increase the risk of adverse health
effects 4 (Table 4). Substantially larger doses administered for a
short time or periodically (e.g., 50,000 IU/week for 8 weeks) do not
cause toxicity. Rather, the excess is stored and used as needed to
maintain normal serum 25(OH)D concentrations when vitamin D intakes or
sun exposure are limited 11,90.

Table 4: Tolerable Upper Intake Levels (ULs) for Vitamin D 4
Age

Children
Men

Women
Pregnancy

Lactation
Birth to 12 months

25 mcg
(1,000 IU)
1-13 years

50 mcg
(2,000 IU)
14+ years

50 mcg
(2,000 IU)
50 mcg
(2,000 IU)

50 mcg
(2,000 IU)
50 mcg
(2,000 IU)

Several nutrition scientists recently challenged these ULs, first
published in 1997 90. They point to newer clinical trials conducted
in healthy adults and conclude that the data support a UL as high as
10,000 IU/day. Although vitamin D supplements above recommended levels
given in clinical trials have not shown harm, most trials were not
adequately designed to assess harm 5. Evidence is not sufficient to
determine the potential risks of excess vitamin D in infants,
children, and women of reproductive age.
As noted earlier, the FNB is currently reviewing data to determine
whether updates to the DRIs (including the ULs) for vitamin D are
appropriate 4.

Interactions with Medications
Vitamin D supplements have the potential to interact with several
types of medications. A few examples are provided below. Individuals
taking these medications on a regular basis should discuss vitamin D
intakes with their healthcare providers.

Steroids
Corticosteroid medications such as prednisone, often prescribed to
reduce inflammation, can reduce calcium absorption 91-93 and impair
vitamin D metabolism. These effects can further contribute to the loss
of bone and the development of osteoporosis associated with their
long-term use 92,93.
Other medications
Both the weight-loss drug orlistat (brand names Xenical® and alli™)
and the cholesterol-lowering drug cholestyramine (brand names Questran®,
LoCholest®, and Prevalite®) can reduce the absorption of vitamin D and
other fat-soluble vitamins 94,95. Both phenobarbital and phenytoin
(brand name Dilantin®), used to prevent and control epileptic
seizures, increase the hepatic metabolism of vitamin D to inactive
compounds and reduce calcium absorption 96.

Vitamin D and Healthful Diets
According to the 2005 Dietary Guidelines for Americans, "nutrient
needs should be met primarily through consuming foods. Foods provide
an array of nutrients and other compounds that may have beneficial
effects on health. In certain cases, fortified foods and dietary
supplements may be useful sources of one or more nutrients that
otherwise might be consumed in less than recommended amounts. However,
dietary supplements, while recommended in some cases, cannot replace a
healthful diet."

The Dietary Guidelines for Americans describes a healthy diet as one
that
Emphasizes a variety of fruits, vegetables, whole grains, and
 fat-free or low-fat milk and milk products.

Milk is fortified with vitamin D, as are many ready-to-eat
cereals and a few brands of yogurt and orange juice. Cheese
naturally contains small amounts of vitamin D.
Includes lean meats, poultry, fish, beans, eggs, and nuts.

Fish such as salmon, tuna, and mackerel are very good
sources of vitamin D. Small amounts of vitamin D are also
found in beef liver and egg yolks.
Is low in saturated fats, trans fats, cholesterol, salt (sodium),
 and added sugars.

Vitamin D is added to some margarines.
Stays within your daily calorie needs.

For more information about building a healthful diet, refer to the
Dietary Guidelines for Americans (http://www.health.gov/dietaryguidelines/dga2005/document/default.htm)
and the U.S. Department of Agriculture's food guidance system, My
Pyramid (http://www.mypyramid.gov).
About ODS

General Safety Advisory
Disclaimer

Print-friendly version
Updated: 11/13/2009

References
1.  DeLuca HF, Zierold C. Mechanisms and functions of vitamin D.
  Nutr Rev 1998;56:S4-10. PubMed abstract

2.  DeLuca HF. Overview of general physiologic features and
  functions of vitamin D. Am J Clin Nutr 2004;80:1689S-96S. PubMed
  abstract
3.  van den Berg H. Bioavailability of vitamin D. Eur J Clin Nutr
  1997;51:S76-9. PubMed abstract

4.  Institute of Medicine, Food and Nutrition Board. Dietary
  Reference Intakes: Calcium, Phosphorus, Magnesium, Vitamin D, and
  Fluoride. Washington, DC: National Academy Press, 1997.
5.  Cranney C, Horsely T, O'Donnell S, Weiler H, Ooi D, Atkinson S,
  et al. Effectiveness and safety of vitamin D. Evidence
  Report/Technology Assessment No. 158 prepared by the University of
  Ottawa Evidence-based Practice Center under Contract No.
  290-02.0021. AHRQ Publication No. 07-E013. Rockville, MD: Agency
  for Healthcare Research and Quality, 2007. PubMed abstract

6.  Goldring SR, Krane S, Avioli LV. Disorders of calcification:
  osteomalacia and rickets. In: DeGroot LJ, Besser M, Burger HG,
  Jameson JL, Loriaux DL, Marshall JC, et al., eds. Endocrinology.
  3rd ed. Philadelphia: WB Saunders, 1995:1204-27.
7.  Favus MJ, Christakos S. Primer on the Metabolic Bone Diseases
  and Disorders of Mineral Metabolism. 3rd ed. Philadelphia, PA:
  Lippincott-Raven, 1996.

8.  Holick MF. Evolution and function of vitamin D. Recent results.
  Cancer Res 2003;164:3-28. PubMed abstract
9.  Hayes CE, Hashold FE, Spach KM, Pederson LB. The immunological
  functions of the vitamin D endocrine system. Cell Mol Biol
  2003;49:277-300. PubMed abstract

10.  Holick MF. Vitamin D deficiency. N Engl J Med 2007;357:266-81.
  PubMed abstract
11.  Jones G. Pharmacokinetics of vitamin D toxicity. Am J Clin Nutr
  2008;88:582S-6S. PubMed abstract

12.  Vieth R, Bischoff-Ferrari H, Boucher BJ, Dawson-Hughes B,
  Garland CF, Heaney RP, et al. The urgent need to recommend an
  intake of vitamin D that is effective. Am J Clin Nutr
  2007;85:649-50. PubMed abstract
13.  Scientific Advisory Committee on Nutrition. Update on Vitamin
  D. Position Statement by the Scientific Advisory Committee on
  Nutrition. London: The Stationery Office, Limited, 2007.

14.  Shepard RM, DeLuca HF. Plasma concentrations of vitamin D3 and
  its metabolites in the rat as influenced by vitamin D3 or
  245-hydroxyvitamin D3 intakes. Arch Biochem Biophys
  1980;202:43-53. PubMed abstract
15.  Carter GD. 25-hydroxyvitamin D assays: the quest for accuracy.
  Clin Chem 2009;55:1300-02.

16.  Hollis BW. Editorial: the determination of circulating
  25-hydroxyvitamin D: no easy task. J. Clin Endocrinol Metab
  2004;89:3149-3151.
17.  Lensmeyer GL, Wiebe DA, Binkley N, Drezner MK. HPLC method for
  25-hydroxyvitamin D measurement: comparison with contemporary
  assays. Clin Chem 2006;52:1120-26. PubMed abstract

18.  Binkley N, Krueger D, Cowgill CS, Plum L, Lake E, Hansen KE, et
  al. Assay variation confounds the diagnosis of hypovitaminosis D:
  a call for standardization. J Clin Endocrinol Metab
  2004;89:3152-57. PubMed abstract
19.  National Institute of Standards and Technology. NIST releases
  vitamin D standard reference material, 2009.

20.  Wagner CL, Greer FR; American Academy of Pediatrics Section on
  Breastfeeding; American Academy of Pediatrics Committee on
  Nutrition. Prevention of rickets and vitamin D deficiency in
  infants, children, and adolescents. Pediatrics 2008;122:1142-1152.
  PubMed abstract
21.  Yetley EA, Brulé D, Cheney MC, Davis CD, Esslinger KA, Fischer
  PWF, et al. Dietary Reference Intakes for vitamin D: justification
  for a review of the 1997 values. Am J Clin Nutr 2009;89:719-27. PubMed
  abstract

22.  Institute of Medicine, Food and Nutrition Board. Dietary
  Reference Intakes for vitamin D and calcium.
23.  Ovesen L, Brot C, Jakobsen J. Food contents and biological
  activity of 25-hydroxyvitamin D: a vitamin D metabolite to be
  reckoned with? Ann Nutr Metab 2003;47:107-13. PubMed abstract

24.  Mattila PH, Piironen VI, Uusi-Rauva EJ, Koivistoinen PE.
  Vitamin D contents in edible mushrooms. J Agric Food Chem
  1994;42:2449-53.
25.  Outila TA, Mattila PH, Piironen VI, Lamberg-Allardt CJE.
  Bioavailability of vitamin D from wild edible mushrooms
  (Cantharellus tubaeformis) as measured with a human bioassay. Am J
  Clin Nutr 1999;69:95-8. PubMed abstract

26.  Calvo MS, Whiting SJ, Barton CN. Vitamin D fortification in the
  United States and Canada: current status and data needs. Am J Clin
  Nutr 2004;80:1710S-6S. PubMed abstract
27.  Holick MF. Vitamin D. In: Shils ME, Shike M, Ross AC, Caballero
  B, Cousins RJ, eds. Modern Nutrition in Health and Disease, 10th
  ed. Philadelphia: Lippincott Williams & Wilkins, 2006.

28.  Pennington JA, Douglass JS. Bowes and Church's Food Values of
  Portions Commonly Used. 18th ed. Philadelphia: Lippincott Williams
  & Wilkins, 2004.
29.  Nutrition Coordinating Center. Nutrition Data System for
  Research (NDS-R). Version 4.06/34. Minneapolis: University of
  Minnesota, 2003.

30.  U.S. Department of Agriculture, Agricultural Research Service.
  USDA Nutrient Database for Standard Reference, Release 22, 2009.
31.  Byrdwell WC, DeVries J, Exler J, Harnly JM, Holden JM, Holick
  MF, et al. Analyzing vitamin D in foods and supplements:
  methodologic challenges. Am J Clin Nutr 2008;88:554S-7S. PubMed
  abstract

32.  Holick MF. McCollum Award Lecture, 1994. Vitamin D: new
  horizons for the 21st century. Am J Clin Nutr 1994;60:619-30. PubMed
  abstract
33.  Holick MF. Vitamin D: the underappreciated D-lightful hormone
  that is important for skeletal and cellular health. Curr Opin
  Endocrinol Diabetes 2002;9:87-98.

34.  Wharton B, Bishop N. Rickets. Lancet 2003;362:1389-400. PubMed
  abstract
35.  Holick MF. Photobiology of vitamin D. In: Feldman D, Pike JW,
  Glorieux FH, eds. Vitamin D, Second Edition, Volume I. Burlington,
  MA: Elsevier, 2005.

36.  Wolpowitz D, Gilchrest BA. The vitamin D questions: how much do
  you need and how should you get it? J Am Acad Dermatol
  2006;54:301-17. PubMed abstract
37.  International Agency for Research on Cancer Working Group on
  ultraviolet (UV) light and skin cancer. The association of use of
  sunbeds with cutaneous malignant melanoma and other skin cancers:
  a systematic review. Int J Cancer 2006;120:1116-22. PubMed
  abstract
38.American Academy of Dermatology. Position statement on vitamin
D.November 1, 2008.
39.  Armas LAG, Hollis BW, Heaney RP. Vitamin D2 is much less
  effective than vitamin D3 in humans. J Clin Endocrinol Metab
  2004;89:5387-91. PubMed abstract

40.  Houghton LA, Vieth R. The case against ergocalciferol (vitamin
  D2) as a vitamin supplement. Am J Clin Nutr 2006;84:694-7. PubMed
  abstract
41.  Nesby-O'Dell S, Scanlon KS, Cogswell ME, Gillespie C, Hollis
  BW, Looker AC, et al. Hypovitaminosis D prevalence and
  determinants among African-American and white women of
  reproductive age: third National Health and Nutrition Examination
  Survey, 1988-1994. Am J Clin Nutr 2002;76:187-92. PubMed abstract
42.Yetley EA. Assessing the vitamin D status of the US population.
AmJ Clin Nutr 2008;88:558S-64S. PubMed abstract
43.  Looker AC, Pfeiffer CM, Lacher DA, Schleicher RL, Picciano MF,
  Yetley EA. Serum 25-hydroxyvitamin D status of the US population:
  1988-1994 compared with 2000-2004. Am J Clin Nutr 2008;88:1519-27.
  PubMed abstract

44.  Ginde AA, Liu MC, Camargo Jr, CA. Demographic differences and
  trends of vitamin D insufficiency in the US population, 1988-2004.
  Arch Intern Med 2009;169:626-32. PubMed abstract
45.  National Center for Health Statistics. Analytical note for
  NHANES 2000-2006 and NHANES III (1988-1994) 25-hydroxyvitamin D
  analysis, 2009.

46.  Moshfegh A, Goldman J, Ahuja J, Rhodes D, LaComb R. 2009. What
  We Eat in America, NHANES 2005-2006: Usual Nutrient Intakes from
  Food and Water Compared to 1997 Dietary Reference Intakes for
  Vitamin D, Calcium, Phosphorus, and Magnesium. U.S. Department of
  Agriculture, Agricultural Research Service. http://www.ars.usda.gov/ba/bhnrc/fsrg
47.  Biser-Rohrbaugh A, Hadley-Miller N. Vitamin D deficiency in
  breast-fed toddlers. J Pediatr Orthop 2001;21:508-11. PubMed
  abstract

48.  Chesney R. Rickets: an old form for a new century. Pediatr Int
  2003;45: 509-11. PubMed abstract
49.  Picciano MF. Nutrient composition of human milk. Pediatr Clin
  North Am 2001;48:53-67. PubMed abstract

50.  Gartner LM, Greer FR, American Academy of Pediatrics Committee
  on Nutrition. Prevention of rickets and vitamin D deficiency: new
  guidelines for vitamin D intake. Pediatrics 2003:111:908-10. PubMed
  abstract
51.  Weisberg P, Scanlon KS, Li R, Cogswell ME. Nutritional rickets
  among children in the United States: review of cases reported
  between 1986 and 2003. Am J Clin Nutr 2004;80:1697S-705S. PubMed
  abstract

52.  American Academy of Pediatrics Committee on Environmental
  Health. Ultraviolet light: a hazard to children. Pediatrics
  1999;104:328-33. PubMed abstract
53.  Need AG, Morris HA, Horowitz M, Nordin C. Effects of skin
  thickness, age, body fat, and sunlight on serum 25-hydroxyvitamin
  D. Am J Clin Nutr 1993;58:882-5. PubMed abstract

54.  Webb AR, Kline L, Holick MF. Influence of season and latitude
  on the cutaneous synthesis of vitamin D3: Exposure to winter
  sunlight in Boston and Edmonton will not promote vitamin D3
  synthesis in human skin. J Clin Endocrinol Metab 1988;67:373-8. PubMed
  abstract
55.  Webb AR, Pilbeam C, Hanafin N, Holick MF. An evaluation of the
  relative contributions of exposure to sunlight and of diet to the
  circulating concentrations of 25-hydroxyvitamin D in an elderly
  nursing home population in Boston. Am J Clin Nutr 1990;51:1075-81.
  PubMed abstract

56.  Harris SS, Soteriades E, Coolidge JAS, Mudgal S, Dawson-Hughes
  B. Vitamin D insufficiency and hyperparathyroidism in a low
  income, multiracial, elderly population. J Clin Endocrinol Metab
  2000;85:4125-30. PubMed abstract
57.  Lo CW, Paris PW, Clemens TL, Nolan J, Holick MF. Vitamin D
  absorption in healthy subjects and in patients with intestinal
  malabsorption syndromes. Am J Clin Nutr 1985;42:644-49. PubMed
  abstract

58.  Wortsman J, Matsuoka LY, Chen TC, Lu Z, Holick MF. Decreased
  bioavailability of vitamin D in obesity. Am J Clin Nutr
  2000;72:690-3. PubMed abstract
59.  Vilarrasa N, Maravall J, Estepa A, Sánchez R, Masdevall C,
  Navarro MA, et al. Low 25-hydroxyvitamin D concentrations in obese
  women: their clinical significance and relationship with
  anthropometric and body composition variables. J Endocrinol Invest
  2007;30:653-8. PubMed abstract

60.  Malone M. Recommended nutritional supplements for bariatric
  surgery patients. Ann Pharmacother 2008;42:1851-8. PubMed
  abstract
61.  Compher CW, Badellino KO, Boullata JI. Vitamin D and the
  bariatric surgical patient: a review. Obes Surg 2008;18:220-4. PubMed
  abstract

62.  Reid IR. The roles of calcium and vitamin D in the prevention
  of osteoporosis. Endocrinol Metab Clin North Am 1998;27:389-98. PubMed
  abstract
63.  Heaney RP. Long-latency deficiency disease: insights from
  calcium and vitamin D. Am J Clin Nutr 2003;78:912-9. PubMed
  abstract

64.  Parfitt AM. Osteomalacia and related disorders. In: Avioli LV,
  Krane SM, eds. Metabolic bone disease and clinically related
  disorders. 2nd ed. Philadelphia: WB Saunders, 1990:329-96.
65.  LeBoff MS, Kohlmeier L, Hurwitz S, Franklin J, Wright J,
  Glowacki J. Occult vitamin D deficiency in postmenopausal US women
  with acute hip fracture. JAMA 1999;251:1505-11. PubMed abstract

66.  Kirschstein R. Menopausal hormone therapy: summary of a
  scientific workshop. Ann Intern Med 2003;138:361-4. PubMed
  abstract
67.  American College of Obstetricians and Gynecologists. Frequently
  Asked Questions About Hormone Therapy. New Recommendations Based
  on ACOG's Task Force Report on Hormone Therapy.

68.  North American Menopause Society. Role of progestrogen in
  hormone therapy for postmenopausal women: position statement of
  The North American Menopause Society. Menopause 2003;10:113-32. PubMed
  abstract
69.  Aloia JF. African Americans, 25-hydroxyvitamin D, and
  osteoporosis: a paradox. Am J Clin Nutr 2008;88:545S-50S. PubMed
  abstract

70.  Davis CD. Vitamin D and cancer: current dilemmas and future
  research needs. Am J Clin Nutr 2008;88:565S-9S. PubMed abstract
71.  Davis CD, Hartmuller V, Freedman M, Hartge P, Picciano MF,
  Swanson CA, Milner JA. Vitamin D and cancer: current dilemmas and
  future needs. Nutr Rev 2007;65:S71-S74. PubMed abstract

72.  Stolzenberg-Solomon RZ, Vieth R, Azad A, Pietinen P, Taylor PR,
  Virtamo J, et al. A prospective nested case-control study of
  vitamin D status and pancreatic cancer risk in male smokers.
  Cancer Res 2006;66:10213-9. PubMed abstract
73.  Lieberman DA, Prindiville S, Weiss DG, Willett W. Risk factors
  for advanced colonic neoplasia and hyperplastic polyps in
  asymptomatic individuals. JAMA 2003;290:2959-67. PubMed abstract

74.  Wactawski-Wende J, Kotchen JM, Anderson GL, Assaf AR, Brunner
  RL, O'Sullivan MJ, et al. Calcium plus vitamin D supplementation
  and the risk of colorectal cancer. N Engl J Med 2006;354:684-96. PubMed
  abstract
75.  Lappe JM, Travers-Gustafson D, Davies KM, Recker RR, Heaney RP.
  Vitamin D and calcium supplementation reduces cancer risk: results
  of a randomized trial. Am J Clin Nutr 2007;85:1586-91. PubMed
  abstract

76.  Freedman DM, Looker AC, Chang S-C, Graubard BI. Prospective
  study of serum vitamin D and cancer mortality in the United
  States. J Natl Cancer Inst 2007;99:1594-602. PubMed abstract
77.  Davis CD, Dwyer JT. The 'sunshine vitamin': benefits beyond
  bone? J Natl Cancer Inst 2007;99:1563-5. PubMed abstract

78.  Hyppönen E, Läärä E, Reunanen A, Järvelin MR, Virtanen SM.
  Intake of vitamin D and risk of type 1 diabetes: a birth-cohort
  study. Lancet 2001;358:1500-3. PubMed abstract
79.  Pittas AG, Dawson-Hughes B, Li T, Van Dam RM, Willett WC,
  Manson JE, et al. Vitamin D and calcium intake in relation to type
  2 diabetes in women. Diabetes Care 2006;29:650-6. PubMed abstract

80.  Krause R, Bühring M, Hopfenmüller W, Holick MF, Sharma AM.
  Ultraviolet B and blood pressure. Lancet 1998;352:709-10. PubMed
  abstract
81.  Chiu KC, Chu A, Go VL, Saad MF. Hypovitaminosis D is associated
  with insulin resistance and beta cell dysfunction. Am J Clin Nutr
  2004;79:820-5. PubMed abstract

82.  Munger KL, Levin LI, Hollis BW, Howard NS, Ascherio A. Serum
  25-hydroxyvitamin D levels and risk of multiple sclerosis. JAMA
  2006;296:2832-8. PubMed abstract
83.  Merlino LA, Curtis J, Mikuls TR, Cerhan JR, Criswell LA, Saag
  K. Vitamin D intake is inversely associated with rheumatoid
  arthritis: results from the Iowa Women's Health Study. Arthritis
  Rheum 2004;50:72-7. PubMed abstract

84.  Schleithoff SS, Zittermann A, Tenderich G, Berthold HK, Stehle
  P, Koerfer R. Vitamin D supplementation improves cytokine profiles
  in patients with congestive heart failure: a double-blind,
  randomized, placebo-controlled trial. Am J Clin Nutr
  2006;83:754-9. PubMed abstract
85.  Chung M, Balk EM, Brendel M, Ip S, Lau J, Lee J, et al. Vitamin
  D and calcium: a systematic review of health outcomes. Evidence
  Report/Technology Assessment No. 183 prepared by the Tufts
  Evidence-based Practice Center under Contract No.
  290-2007-10055-I. AHRQ Publication No. 09-E015. Rockville, MD:
  Agency for Healthcare Research and Quality, 2009.

86.  Autier P, Gandini S. Vitamin D supplementation and total
  mortality: a meta-analysis of randomized controlled trials. Arch
  Intern Med 2007;167:1730-7. PubMed abstract
87.  Giovannucci E. Can vitamin D reduce total mortality? Arch
  Intern Med 2007;167:1709-10. PubMed abstract

88.  Chesney RW. Vitamin D: can an upper limit be defined? J Nutr
  1989;119 (12 Suppl):1825-8. PubMed abstract
89.  Jackson RD, LaCroix AZ, Gass M, Wallace RB, Robbins J, Lewis
  CE, et al. Calcium plus vitamin D supplementation and the risk of
  fractures. N Engl J Med 2006;354:669-83. PubMed abstract

90.  Hathcock JN, Shao A, Vieth R, Heaney R. Risk assessment for
  vitamin D. Am J Clin Nutr 2007;85:6-18. PubMed abstract
91.  Buckley LM, Leib ES, Cartularo KS, Vacek PM, Cooper SM. Calcium
  and vitamin D3 supplementation prevents bone loss in the spine
  secondary to low-dose corticosteroids in patients with rheumatoid
  arthritis. A randomized, double-blind, placebo-controlled trial.
  Ann Intern Med 1996;125:961-8. PubMed abstract

92.  Lukert BP, Raisz LG. Glucocorticoid-induced osteoporosis:
  pathogenesis and management. Ann Intern Med 1990;112:352-64. PubMed
  abstract
93.  de Sevaux RGL, Hoitsma AJ, Corstens FHM, Wetzels JFM. Treatment
  with vitamin D and calcium reduces bone loss after renal
  transplantation: a randomized study. J Am Soc Nephrol
  2002;13:1608-14. PubMed abstract

94.  McDuffie JR, Calis KA, Booth SL, Uwaifo GI, Yanovski JA.
  Effects of orlistat on fat-soluble vitamins in obese adolescents.
  Pharmacotherapy 2002;22:814-22. PubMed abstract
95.  Compston JE, Horton LW. Oral 25-hydroxyvitamin D3 in treatment
  of osteomalacia associated with ileal resection and cholestyramine
  therapy. Gastroenterology 1978;74:900-2. PubMed abstract

96.  Gough H, Goggin T, Bissessar A, Baker M, Crowley M, Callaghan
  N. A comparative study of the relative influence of different
  anticonvulsant drugs, UV exposure and diet on vitamin D and
  calcium metabolism in outpatients with epilepsy. Q J Med
  1986;59:569-77. PubMed abstract
Disclaimer

Reasonable care has been taken in preparing this document and the
information provided herein is believed to be accurate. However, this
information is not intended to constitute an "authoritative statement"
under Food and Drug Administration rules and regulations.
About ODS

The mission of the Office of Dietary Supplements (ODS) is to
strengthen knowledge and understanding of dietary supplements by
evaluating scientific information, stimulating and supporting
research, disseminating research results, and educating the public to
foster an enhanced quality of life and health for the U.S. population.
General Safety Advisory

Health professionals and consumers need credible information to make
thoughtful decisions about eating a healthful diet and using vitamin
and mineral supplements. These Fact Sheets provide responsible
information about the role of vitamins and minerals in health and
disease. Each Fact Sheet in this series received extensive review by
recognized experts from the academic and research communities.
The information is not intended to be a substitute for professional
medical advice. It is important to seek the advice of a physician
about any medical condition or symptom. It is also important to seek
the advice of a physician, registered dietitian, pharmacist, or other
qualified health professional about the appropriateness of taking
dietary supplements and their potential interactions with medications.

---------------------------------------------------------------------
Office of Dietary Supplements
National Institutes of Health
Bethesda, Maryland 20892 USA
Web: http://ods.od.nih.gov
E-mail: ods@nih.gov

National Institutes of Health
Department of Health and Human Services

USA.gov, Government Made Easy
ourselves nutritional vitamin supplements other you ours before up into because is he be
maybe very she only nutritional vitamin supplements being doing side effects of too much vitamin d
some is those other then how theirs to your once nor
me more with doing side effects of too much vitamin d its which is
through Right on! we being when did out does by any myself or most that i
but yourselves over so few before those after
Right on! these other hello from against where at
and and in so itself through too be! Right on! after some those
should be has very where only such
so few it out has was nutritional vitamin supplements through she few was out out
be on same you out
he other why see hers
vitamin a deficiency symptoms see did been who could when whom more nutritional vitamin supplements
could my during their them any she
ours above herself nutritional vitamin supplements in then that
me who it look when a munchies side effects of too much vitamin d him by