National Report on Biochemical Indicators of Diet and
Nutrition in the U.S. Population 1999-2002 Fat-Soluble Vitamins &
Micronutrients: Vitamin D Vitamin D (calciferol) comprises a group of fat
soluble seco-sterols found naturally only in a few foods, such as fish-liver
oils, fatty fish, mushrooms, egg yolks, and liver. The two major
physiologically relevant forms of vitamin D are D2 (ergocalciferol) and D3
(cholecalciferol). Vitamin D3 is photosynthesized in the skin of vertebrates by
the action of solar ultraviolet (UV) B radiation on 7-dehydrocholesterol
(Fieser 1959). Vitamin D2 is produced by UV irradiation of ergosterol, which
occurs in molds, yeast, and higher-order plants. Under conditions of regular
sun exposure, dietary vitamin D intake is of minor importance. However,
latitude, season, aging, sunscreen use, and skin pigmentation influence the
production of vitamin D3 by the skin (Institute of Medicine 1997). Most of the
dietary intake of vitamin D comes from fortified milk products and other
fortified foods such as breakfast cereals and orange juice (Institute of
Medicine 1997). Both vitamin D2 and D3 are used in nonprescription vitamin D supplements,
but vitamin D2 is the form available by prescription in the United States
(Holick 2007). Vitamin D without a subscript represents either D2 or D3 or both
and is biologically inert. Vitamin D from the skin or diet is only short-lived
in circulation (with a half-life of 1–2 days), as it is either stored in fat
cells or metabolized in the liver (Mawer 1972). In circulation, vitamin D is
bound to vitamin D-binding protein and transported to the liver, where it is
converted to 25-hydroxyvitamin D [25(OH)D] (DeLuca 1984). This major
circulating form of vitamin D is a good reflection of cumulative effects of
exposure to sunlight and dietary intake of vitamin D (Haddad 1973; Holick 1995)
and is therefore used by clinicians to determine vitamin D status. To be
biologically activated at physiologic concentrations, 25(OH)D must be converted
in the kidneys to 1,25-dihydroxyvitamin D [1,25(OH)2 D], which is thought to be
responsible for most, if not all, of the biologic functions of vitamin D
(DeLuca 1988; Reichel 1989). The production of 25(OH)D in the liver and of
1,25(OH)2 D in the kidney is tightly regulated. In the liver, vitamin
D-25-hydroxylase is down-regulated by vitamin D and its metabolites, thereby
limiting any increase in the circulating concentration of 25(OH)D following
intakes or following production of vitamin D after exposure to sunlight. In the
kidney, in response to serum calcium and phosphorus concentrations, the
production of 1,25(OH)2 D is regulated through the action of parathyroid hormone
(PTH) (DeLuca 1988; Reichel 1989). 2 Fat-Soluble Vitamins & Micronutrients
61 Active vitamin D functions as a hormone, and its main biologic function in
people is to maintain serum calcium and phosphorus concentrations within the
normal range by enhancing the efficiency of the small intestine to absorb these
minerals from the diet (DeLuca 1988; Reichel 1989). When dietary calcium intake
is inadequate to satisfy the body’s calcium requirement, 1,25(OH)2 D, along
with PTH, mobilizes calcium stores from the bone. In the kidney, 1,25(OH)2 D
increases calcium reabsorption by the distal renal tubules. Apart from these
traditional calcium-related actions, 1,25(OH)2 D and its synthetic analogs are
increasingly recognized for their potent antiproliferative, prodifferentiative,
and immunomodulatory activities (Nagpal 2005). Vitamin D deficiency is
characterized by inadequate mineralization or by demineralization of the
skeleton. Among children, vitamin D deficiency is a common cause of bone
deformities known as rickets. Vitamin D deficiency in adults leads to a
mineralization defect in the skeleton, causing osteomalacia, and induces
secondary hyperparathyroidism with consequent bone loss and osteoporosis.
Potential roles for vitamin D beyond bone health, such as effects on muscle
strength, the risk for cancer and for type 2 diabetes, are currently being
studied. The Agency for Healthcare Research and Quality recently reviewed the
effectiveness and safety of vitamin D on outcomes related to bone health
(Cranney 2007). The report suggests that vitamin D supplementation has positive
effects on bone health in postmenopausal women and older men. Still, what
constitutes the optimal intake of vitamin D remains a matter of some
disagreement. Current recommendations from the Institute of Medicine (1997)
call for 200 international units (IU) [5.0 micrograms (µg)] of vitamin D daily
from birth through age 50, 400 IU (10 µg) for those aged 51–70 years, and 600
IU (15 µg) for those older than 70 years. According to the Dietary Guidelines
for Americans (U.S. Department of Health and Human Services and U.S. Department
of Agriculture 2005) older adults, people with dark skin, and people exposed to
insufficient UV B radiation should consume extra vitamin D from vitamin
D-fortified foods or supplements. The American Cancer Society Guidelines on
Nutrition and Physical Activity for Cancer Prevention echo this recommendation
(Kushi 2006). Some experts say that optimal amounts for all adults are closer
to 800–1000 IU (20–25 µg) daily (Vieth 2007; BischoffFerrari 2006;
Dawson-Hughes 2005). The tolerable upper intake level for vitamin D is 2000 IU
(50 µg) per day in North America and in Europe; however, some scientists are
calling for an upward revision (Hathcock 2007; Vieth 2006). Some clinical laboratories
use conventional units for 25(OH)D (nanogram per milliliter [ng/mL]) whereas
other laboratories use international system (SI) units (nanomole per liter
[nmol/L]). The conversion factor to SI units is: 1 ng/mL = 2.496 nmol/L. No
common definition exists for adequate vitamin D status measured as 25(OH)D
serum concentrations (Dawson-Hughes 2005). The Institute of Medicine (1997)
defined vitamin D deficiency as serum 25(OH)D concentrations of less than 11
ng/mL (27.5 nmol/L) for neonates, infants, and young children. Because the
lower limit of the normal range can be as low as 8 ng/mL (20 nmol/L) and as
high as 15 ng/mL (37.5 nmol/L), depending on the geographic location, vitamin D
deficiency has been 62 National Report on Biochemical Indicators of Diet and
Nutrition in the U.S. Population 1999-2002 defined as a concentration of less
than 12 ng/mL (mid-range between 8 and 15 ng/ mL) for adults (Institute of
Medicine 1997). More recently, some scientists have suggested that the criteria
used to define adequate status should be revised upwards; serum 25(OH)D
concentrations between 20 ng/mL (50 nmol/L) and 32 ng/mL (80 nmol/L) have been
defined as sufficient (Hollis 2005; Dawson-Hughes 2005; Bischoff-Ferrari 2006;
Norman 2007). A common definition for high serum vitamin D concentrations is
also lacking. The Institute of Medicine (1997) used serum calcium
concentrations greater than 11 milligrams per deciliter (mg/dL) for assessing
the potential for increased risk of harm associated with high vitamin D intakes.
To date, however, no evidence has surfaced of adverse effects with serum
25(OH)D concentrations as high as 56 ng/mL (140 nmol/L) in healthy individuals
(Vieth 1999). Different assays measure serum 25(OH)D, and at times large
variations occur among methods and even between laboratories using the same
method (Singh 2008; Binkley 2004; Carter 2004). Standard reference materials
(SRMs) for serum 25(OH)D are currently under development by the U.S. National
Institute of Standards and Technology (U.S. NIST) (http://www.cstl.nist.gov/projects/
fy06/food0683904.pdf ). Improvement in the agreement between laboratories and
methods is expected as laboratories begin to use the SRMs. For more information
about vitamin D, see the Institute of Medicine’s Dietary Reference Intake
reports (Institute of Medicine 1997), fact sheets from the National Institutes
of Health, Office of Dietary Supplements
(http://ods.od.nih.gov/Health_Information/Information_About_Individual_Dietary_
Supplements.aspx), as well as information from the American Society for
Nutrition (http:// jn.nutrition.org/nutinfo/). Since 1988, NHANES has monitored
the vitamin D status of the U.S. population. By design, this survey collects
information and biological samples in the summer from people living at higher
latitudes and in the winter from people living at lower latitudes. Because the
different racial and ethnic groups are not evenly distributed across all
geographic regions in the United States, the season-latitude structure of the
survey can affect comparisons by race or ethnicity. In two seasonal
subpopulations from NHANES III (1988–1994), Looker et al. (2002) showed that in
the winter and lower latitude subpopulation, 1–5 percent and 25–57 percent had
25(OH)D concentrations less than 10 ng/mL (25 nmol/L) and less than 25 ng/mL
(62.5 nmol/L), respectively. In the summer and higher latitude subpopulation,
1–3 percent and 21–49 percent had 25(OH)D concentrations below these cutoffs.
Mean Medical technologist checks samples for vitamin D analysis. 2 Fat-Soluble
Vitamins & Micronutrients 63 25(OH)D concentrations were highest in
non-Hispanic whites, intermediate in Mexican Americans, and lowest in
non-Hispanic blacks. Nesby-O’Dell et al. (2002) restricted the analysis of
NHANES III data to African-American and white women of reproductive age and
found the prevalence of hypovitaminosis [25(OH)D concentrations < 15 ng/mL
(37.5 nmol/L)] to be 42.2 percent among African Americans and 4.2 percent among
whites. Selected Observations and Highlights The following sample observations
and figures are taken from the tables of 2001–2002 data contained in this
report. Statements about categorical differences between demographic groups
noted below are based on non-overlapping confidence limits from univariate
analysis without adjusting for demographic variables (e.g., age, sex,
race/ethnicity) or other determinants of these blood concentrations (e.g.,
dietary intake, supplement usage, smoking, BMI). A multivariate analysis may
alter the size and statistical significance of these categorical differences.
Furthermore, additional significant differences of smaller magnitude may be
present despite their lack of mention here (e.g., if confidence limits slightly
overlap or if differences are unobservable before covariate adjustment has
occurred). For a selection of citations of descriptive NHANES papers related to
these biochemical indicators of diet and nutrition, see Appendix E. General
Observations • Serum 25(OH)D concentrations are similar throughout all age
groups, except that children 6–11 years of age have higher concentrations than
do people in other age groups. • Non-Hispanic whites have higher concentrations
of 25(OH)D than do Mexican Americans, who themselves have higher concentrations
than do non-Hispanic blacks. • Approximately 10 percent of the population has
concentrations of 25(OH)D that are less than 11 ng/mL. The values at the 10th
percentile vary greatly by racial-ethnic group, with non-Hispanic blacks having
the highest prevalence of low 25(OH)D concentrations. 64 National Report on
Biochemical Indicators of Diet and Nutrition in the U.S. Population 1999-2002
Highlights Because of the current disagreement regarding appropriate criteria
by which to define adequate status on the basis of serum 25(OH)D concentrations,
the figure below presents prevalence estimates for older people (≥ 60 years)
for three cut-off values: 11 ng/mL, 20 ng/mL, and 30 ng/mL. Regardless of the
cut-off value, nonHispanic blacks have the highest prevalence of low serum
25(OH)D concentrations (Fig. 2.a). Figure 2.a Prevalence estimates (95 percent
confidence intervals) of serum 25-hydroxyvitamin D among U.S. persons 60 years
and older by race/ethnicity, National Health and Nutrition Examination Survey,
2001–2002. Prevalence estimates shown here are not part of the tables displayed
in this report; rather, the data were analyzed separately to generate this
figure. 2 Fat-Soluble Vitamins & Micronutrients 65 Table 2.9.a. Serum
25-hydroxyvitamin D: Total population Geometric mean and selected percentiles
of serum concentrations (in ng/mL) for the total U.S. population aged 6 years
and older, National Health and Nutrition Examination Survey, 2001–2002.
Geometric mean (95% conf. interval) Selected percentiles (95% conf. interval)
Sample 10th 50th 90th size Males and Females Total, 6 years and older 21.9
(21.0-22.7) 11.0 (11.0-12.0) 22.0 (22.0-23.0) 35.0 (33.0-36.0) 7807 6–11 years
25.5 (24.2-26.9) 17.0 (16.0-19.0) 26.0 (24.0-27.0) 35.0 (32.0-39.0) 991 12–19
years 22.0 (21.0-23.1) 13.0 (11.0-14.0) 23.0 (22.0-24.0) 35.0 (33.0-35.0) 2167
20–39 years 21.6 (20.7-22.6) 11.0 (11.0-12.0) 22.0 (22.0-24.0) 35.0 (33.0-38.0)
1691 40–59 years 21.6 (20.6-22.6) 11.0 (11.0-13.0) 22.0 (22.0-23.0) 34.0
(32.0-36.0) 1449 60 years and older 21.0 (20.0-22.1) 12.0 (10.0-12.0) 22.0
(21.0-24.0) 33.0 (32.0-34.0) 1509 Males Total, 6 years and older 22.6
(21.8-23.4) 13.0 (13.0-14.0) 24.0 (23.0-24.0) 34.0 (33.0-36.0) 3782 6–11 years
26.1 (24.5-27.9) 18.0 (17.0-20.0) 26.0 (24.0-27.0) 38.0 (33.0-44.0) 497 12–19
years 23.1 (21.9-24.3) 13.0 (11.0-16.0) 24.0 (22.0-25.0) 35.0 (34.0-37.0) 1068
20–39 years 22.2 (21.4-23.1) 13.0 (11.0-14.0) 23.0 (21.0-24.0) 34.0 (32.0-37.0)
709 40–59 years 22.3 (21.2-23.5) 12.0 (11.0-14.0) 22.0 (22.0-23.0) 33.0
(32.0-37.0) 762 60 years and older 21.5 (20.7-22.5) 13.0 (11.0-14.0) 22.0
(21.0-24.0) 32.0 (31.0-33.0) 746 Females Total, 6 years and older 21.2
(20.2-22.2) 10.0 (9.00-12.0) 23.0 (22.0-23.0) 34.0 (33.0-36.0) 4025 6–11 years
24.9 (23.6-26.3) 17.0 (15.0-19.0) 26.0 (24.0-27.0) 35.0 (32.0-37.0) 494 12–19
years 21.0 (20.0-22.0) 11.0 (9.00-13.0) 22.0 (20.0-22.0) 33.0 (32.0-35.0) 1099
20–39 years 21.1 (19.9-22.4) 10.0 (9.00-12.0) 22.0 (21.0-24.0) 37.0 (32.0-40.0)
982 40–59 years 20.8 (19.6-22.1) 10.0 (9.00-12.0) 23.0 (21.0-24.0) 34.0
(32.0-35.0) 687 60 years and older 20.6 (19.3-22.0) 11.0 (10.0-12.0) 22.0
(20.0-23.0) 34.0 (33.0-36.0) 763 Table 2.9.b. Serum 25-hydroxyvitamin D:
Mexican Americans Geometric mean and selected percentiles of serum
concentrations (in ng/mL) for Mexican Americans in the U.S. population aged 6
years and older, National Health and Nutrition Examination Survey, 2001–2002.
Geometric mean (95% conf. interval) Selected percentiles (95% conf. interval)
Sample 10th 50th 90th size Males and Females Total, 6 years and older 19.6
(18.5-20.7) 11.0 (10.0-12.0) 20.0 (19.0-22.0) 29.0 (28.0-32.0) 1961 6–11 years
22.6 (21.7-23.6) 17.0 (15.0-17.0) 22.0 (22.0-24.0) 30.0 (28.0-32.0) 283 12–19
years 19.7 (18.5-21.0) 12.0 (11.0-14.0) 20.0 (18.0-21.0) 29.0 (27.0-32.0) 687
20–39 years 19.5 (18.2-20.9) 12.0 (10.0-13.0) 20.0 (18.0-21.0) 31.0 (27.0-33.0)
452 40–59 years 18.1 (16.5-19.8) 10.0 (8.00-11.0) 20.0 (18.0-21.0) 28.0
(24.0-33.0) 286 60 years and older 18.3 (15.9-21.1) 10.0 (8.00-11.0) 18.0
(16.0-21.0) 29.0 (24.0-36.0) 253 Males Total, 6 years and older 20.6 (19.4-21.8)
13.0 (11.0-13.0) 21.0 (19.0-22.0) 30.0 (27.0-32.0) 942 6–11 years 22.8
(21.8-23.9) 17.0 (15.0-18.0) 22.0 (22.0-24.0) 28.0 (26.0-31.0) 138 12–19 years
21.1 (19.7-22.7) 13.0 (11.0-15.0) 21.0 (19.0-24.0) 29.0 (27.0-33.0) 323 20–39
years 20.1 (18.7-21.7) 12.0 (10.0-13.0) 20.0 (19.0-22.0) 31.0 (26.0-34.0) 208
40–59 years 19.9 (18.3-21.7) 12.0 (9.00-14.0) 21.0 (19.0-22.0) 28.0 (25.0-33.0)
148 60 years and older 19.5 (16.6-22.9) 9.00 (6.00-11.0) 21.0 (16.0-25.0) 31.0
(25.0-39.0) 125 Females Total, 6 years and older 18.6 (17.5-19.7) 10.0
(10.0-11.0) 18.0 (17.0-20.0) 29.0 (27.0-31.0) 1019 6–11 years 22.4 (21.4-23.5)
17.0 (15.0-18.0) 22.0 (20.0-23.0) 30.0 (28.0-33.0) 145 12–19 years 18.3
(17.0-19.6) 11.0 (9.00-14.0) 18.0 (17.0-20.0) 26.0 (25.0-28.0) 364 20–39 years
18.8 (17.3-20.4) 10.0 (9.00-12.0) 18.0 (17.0-21.0) 31.0 (27.0-33.0) 244 40–59
years 16.3 (14.5-18.3) 8.00 (7.00-10.0) 18.0 (14.0-20.0) 25.0 (22.0-33.0) 138
60 years and older 17.4 (14.7-20.7) 10.0 (7.00-12.0) 18.0 (16.0-21.0) 27.0
(22.0-30.0) 128 66 66 National Report on Biochemical Indicators of Diet and
Nutrition in the U.S. Population 1999–2002 Table 2.9.c. Serum 25-hydroxyvitamin
D: Non-Hispanic blacks Geometric mean and selected percentiles of serum
concentrations (in ng/mL) for non-Hispanic blacks in the U.S. population aged 6
years and older, National Health and Nutrition Examination Survey, 2001–2002.
Geometric mean (95% conf. interval) Selected percentiles (95% conf. interval)
Sample 10th 50th 90th size Males and Females Total, 6 years and older 13.0
(12.5-13.6) 7.00 (6.00-7.00) 13.0 (13.0-14.0) 22.0 (22.0-23.0) 1821 6–11 years
18.7 (17.7-19.8) 11.0 (10.0-14.0) 19.0 (18.0-19.0) 25.0 (24.0-27.0) 334 12–19
years 13.2 (12.4-14.0) 7.00 (7.00-8.00) 14.0 (13.0-14.0) 22.0 (20.0-23.0) 653
20–39 years 11.6 (11.0-12.2) 7.00 (6.00-7.00) 12.0 (11.0-12.0) 20.0 (17.0-22.0)
312 40–59 years 12.2 (11.4-13.0) 5.00 (5.00-6.00) 12.0 (11.0-14.0) 23.0
(21.0-24.0) 285 60 years and older 14.6 (13.4-15.9) 6.00 (6.00-7.00) 14.0
(13.0-17.0) 28.0 (24.0-29.0) 237 Males Total, 6 years and older 14.2
(13.4-15.0) 7.00 (7.00-8.00) 14.0 (13.0-15.0) 23.0 (22.0-25.0) 898 6–11 years
19.8 (18.5-21.2) 12.0 (10.0-15.0) 20.0 (18.0-21.0) 27.0 (26.0-29.0) 172 12–19
years 14.6 (13.5-15.7) 7.00 (6.00-9.00) 14.0 (13.0-16.0) 22.0 (22.0-25.0) 328
20–39 years 12.7 (11.6-13.8) 7.00 (7.00-8.00) 13.0 (11.0-15.0) 20.0 (19.0-23.0)
127 40–59 years 13.2 (12.1-14.5) 5.00 (5.00-6.00) 13.0 (11.0-15.0) 23.0
(21.0-24.0) 154 60 years and older 14.6 (13.7-15.6) 7.00 (6.00-9.00) 15.0
(13.0-17.0) 26.0 (22.0-29.0) 117 Females Total, 6 years and older 12.2
(11.5-12.8) 7.00 (6.00-7.00) 12.0 (12.0-13.0) 22.0 (22.0-24.0) 923 6–11 years
17.5 (16.1-19.1) 11.0 (9.00-14.0) 18.0 (16.0-19.0) 25.0 (23.0-26.0) 162 12–19
years 11.9 (11.1-12.8) 7.00 (5.00-7.00) 11.0 (11.0-12.0) 21.0 (18.0-24.0) 325
20–39 years 11.0 (10.2-11.7) 6.00 (3.00-7.00) 11.0 (10.0-11.0) 19.0 (16.0-23.0)
185 40–59 years 11.3 (10.2-12.5) 5.00 (5.00-6.00) 10.0 (9.00-12.0) 21.0
(17.0-26.0) 131 60 years and older 14.6 (12.5-17.0) 6.00 (3.00-7.00) 14.0 (12.0-17.0)
26.0 (21.0-31.0) 120 Table 2.9.d. Serum 25-hydroxyvitamin D: Non-Hispanic
whites Geometric mean and selected percentiles of serum concentrations (in
ng/mL) for non-Hispanic whites in the U.S. population aged 6 years and older,
National Health and Nutrition Examination Survey, 2001–2002. Geometric mean
(95% conf. interval) Selected percentiles (95% conf. interval) Sample 10th 50th
90th size Males and Females Total, 6 years and older 24.3 (23.5-25.2) 15.0
(14.0-16.0) 25.0 (24.0-25.0) 37.0 (34.0-38.0) 3416 6–11 years 28.5 (26.6-30.5)
21.0 (19.0-22.0) 28.0 (26.0-29.0) 39.0 (33.0-45.0) 294 12–19 years 25.8
(25.0-26.6) 17.0 (16.0-18.0) 25.0 (25.0-26.0) 36.0 (35.0-38.0) 648 20–39 years
25.2 (24.4-26.1) 17.0 (15.0-18.0) 26.0 (25.0-26.0) 38.0 (36.0-42.0) 766 40–59
years 23.7 (22.6-24.9) 13.0 (12.0-15.0) 25.0 (23.0-26.0) 36.0 (33.0-38.0) 768
60 years and older 22.0 (20.9-23.3) 13.0 (11.0-14.0) 23.0 (21.0-24.0) 34.0
(32.0-34.0) 940 Males Total, 6 years and older 24.8 (23.8-25.8) 15.0
(14.0-17.0) 26.0 (24.0-26.0) 37.0 (34.0-39.0) 1655 6–11 years 29.1 (26.9-31.4)
22.0 (19.0-24.0) 28.0 (26.0-31.0) 39.0 (35.0-46.0) 152 12–19 years 26.7
(25.4-28.1) 20.0 (17.0-20.0) 27.0 (25.0-28.0) 38.0 (35.0-41.0) 320 20–39 years
25.0 (24.0-26.0) 16.0 (14.0-18.0) 25.0 (23.0-26.0) 36.0 (33.0-39.0) 309 40–59
years 24.2 (22.9-25.7) 14.0 (14.0-16.0) 25.0 (22.0-26.0) 37.0 (33.0-38.0) 406
60 years and older 22.6 (21.6-23.7) 13.0 (12.0-15.0) 23.0 (23.0-25.0) 33.0
(31.0-34.0) 468 Females Total, 6 years and older 23.9 (23.0-24.9) 13.0 (13.0-15.0)
25.0 (24.0-25.0) 37.0 (34.0-39.0) 1761 6–11 years 27.8 (25.8-30.0) 21.0
(19.0-22.0) 27.0 (26.0-29.0) 38.0 (33.0-44.0) 142 12–19 years 25.0 (24.3-25.7)
16.0 (14.0-18.0) 26.0 (24.0-27.0) 36.0 (34.0-38.0) 328 20–39 years 25.5
(24.1-26.9) 15.0 (14.0-18.0) 25.0 (24.0-27.0) 39.0 (35.0-44.0) 457 40–59 years
23.1 (22.0-24.2) 12.0 (10.0-13.0) 25.0 (23.0-26.0) 34.0 (33.0-37.0) 362 60
years and older 21.6 (20.1-23.1) 11.0 (10.0-13.0) 23.0 (21.0-24.0) 35.0
(33.0-36.0) 472 2 Fat-Soluble Vitamins & Micronutrients 67 References
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;89:3152-7. Bischoff-Ferrari HA,
Giovannucci E, Willett WC, Dietrich T, Dawson-Hughes B. Estimation of optimal
serum concentrations of 25-hydroxyvitamin D for multiple health outcomes. Am J
Clin Nutr. 2006;84:18-28. Carter GD, Carter R, Jones J, Berry J. How accurate
are assays for 25-hydroxyvitamin D? Data from the international vitamin D
external quality assessment scheme. Clin Chem. 2004;50:2195-7. Cranney A,
Horsley T, O’Donnell S, Weiler HA, Puil L, Ooi DS, et al. Effectiveness and
safety of vitamin D in relation to bone health. Evid Rep Technol Assess (Full Rep).
2007;158:1-235. Dawson-Hughes B, Heaney RP, Holick MF, Lips P, Meunier PJ,
Vieth R. Estimates of optimal vitamin D status. Osteoporos Int. 2005;16:713-6.
DeLuca HF. The metabolism, physiology, and function of vitamin D. In: Kumar R,
editor. Vitamin D: basic and clinical aspects. Boston (MA): M. Nijhoff
Publishers; 1984. p. 1-68. DeLuca HF. The vitamin D story: a collaborative
effort of basic science and clinical medicine. FASEB J. 1988;2:224-36. Fieser
LF, Fieser M. Vitamin D. In: Steroids. 1st ed. New York: Reinhold Publishing
Corporation;1959. p. 90-168. Haddad JG, Hahn TJ. Natural and synthetic sources
of circulating 25-hydroxy-vitamin D in man. Nature. 1973;244:515-7. Hathcock
JN, Shao A, Vieth R, Heaney R. Risk assessment for vitamin D. Am J Clin Nutr.
2007;85:6-18. Holick MF. Vitamin D: photobiology, metabolism, and clinical
applications. In: DeGroot LJ, editor. Endocrinology, Vol 2, 3rd ed.
Philadelphia (PA): WB Saunders; 1995. p. 990-1013. Holick MF. Vitamin D
deficiency. N Engl J Med. 2007;357:266-81. 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;135:317-22. Institute of Medicine, Food and Nutrition Board. Dietary
Reference Intakes: calcium, phosphorus, magnesium, vitamin D and fluoride.
Washington, D.C.: National Academy Press; 1997. Kushi LH, Byers T, Doyle C,
Bandera EV, McCullough M, Gansler T, et al. American Cancer Society guidelines
on nutrition and physical activity for cancer prevention: reducing the risk of
cancer with healthy food choices and physical activity. CA Cancer J Clin.
2006;56:254-81. Looker AC, Dawson-Hughs B, Calvo MS, Gunter EW, Sayhoun NR.
Serum 25-hydroxyvitamin D status of adolescents and adults in two seasonal
subpopulations from NHANES III. Bone. 2002;30:771-7. Mawer EB, Blackhouse J,
Holman CA, Lumb GA, Stanbury DW. The distribution and storage of vitamin D and
its metabolites in human tissues. Clin Sci. 1972;43:413-31. Nagpal S, Na S,
Rathnachalam R. Noncalcemic actions of vitamin D receptor ligands. Endocr Rev.
2005;26:662-87. 68 National Report on Biochemical Indicators of Diet and
Nutrition in the U.S. Population 1999-2002 Nesby-O’Dell S, Scanlon KS, Cogswell
ME, Gillespie C, Hollis BW, Looker AC, et al. Hypovitaminosis D 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. Norman AW, Bouillon R, Whiting SJ, Vieth R, Lips P. 13th
Workshop consensus for vitamin D nutritional guidelines. J Steroid Biochem Mol
Biol. 2007;103:204-5. Reichel H, Koeffler HP, Norman AW. The role of vitamin D
endocrine system in health and disease. N Engl J Med. 1989;320:980-91. Singh
RJ. Are clinical laboratories prepared for accurate testing of 25-hydroxy
vitamin D? Clin Chem. 2008;54:221-2. U.S. Department of Health and Human
Services and U.S. Department of Agriculture. Dietary guidelines for Americans,
2005. 6th ed. Washington, D.C.: U.S. Government Printing Office; January 2005.
Vieth R. Vitamin D supplementation, 25-hydroxyvitamin D concentrations, and
safety. Am J Clin Nutr. 1999;69:842-56. Vieth R. Critique of the considerations
for establishing the tolerable upper intake level for vitamin D: critical need
for revision upwards. J Nutr. 2006;136:1117-22. Vieth R. The urgent need to
recommend an intake of vitamin D that is effective. Am J Clin Nutr.
2007;85:649-50. 2 Fat-Soluble Vitamins & Micronutrients 69

0 Comments