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Osteoporos Int
DOI 10.1007/s00198-010-1285-3

 POSITION PAPER



IOF position statement: vitamin D recommendations
for older adults
B. Dawson-Hughes & A. Mithal & J.-P. Bonjour &
S. Boonen & P. Burckhardt & G. E.-H. Fuleihan &
R. G. Josse & P. Lips & J. Morales-Torres & N. Yoshimura




Received: 9 March 2010 / Accepted: 16 April 2010
# International Osteoporosis Foundation and National Osteoporosis Foundation 2010


Abstract This position paper of the International Osteopo-            Introduction
rosis Foundation makes recommendations for vitamin D
nutrition in elderly men and women from an evidence-                  Vitamin D is important for bone and muscle development,
based perspective.                                                    function, and preservation. The serum 25OHD concentra-
                                                                      tion is the best available clinical indicator of vitamin D
Keywords Musculoskeletal health . Requirement .                       status. Until recently, optimal serum 25OHD concentration
Vitamin D                                                             was considered to be that level associated with maximal
                                                                      parathyroid hormone (PTH) suppression. Estimates of that
                                                                      threshold level have clustered around 32–50 nmol/L
                                                                      (12.8–20 ng/ml) and 68–75 nmol/L (27.2–30 ng/ml),
                                                                      depending upon analytical approach used [1]. In the last
                                                                      decade, however, the evidence base for older men and
                                                                      women has grown to include many randomized, controlled
This material is based in part upon work supported by the US          clinical trials (RCTs) with falls and fracture endpoints.
Department of Agriculture, Agricultural Research Service, under       Because the RCTs have for the most part been conducted in
agreement no. 58-1950-7-707. Any opinions, findings, conclusion,
                                                                      men and women over the age of 60 to 65 years, our
or recommendations expressed in this publication are those of the
author(s) and do not necessarily reflect the view of the US           recommendations are directed at this large and growing
Department of Agriculture, the Centers for Disease Control and        older segment of the adult population. Our objective is to
Prevention or the US Department of Health and Human Services.         use available evidence to support recommendations for
This statement has been endorsed by the IOF Committee of Scientific   optimal vitamin D status. We approach this by examining
Advisors
B. Dawson-Hughes (*)                                                  S. Boonen
Jean Mayer USDA Human Nutrition Research Center on Aging,             Centre for Metabolic Bone Diseases and Division of Geriatric
Tufts University,                                                     Medicine, University of Leuven,
711 Washington Street,                                                Herestraat 49,
Boston, MA 02111, USA                                                 3000 Leuven, Belgium
e-mail: bess.dawson-hughes@tufts.edu
                                                                      P. Burckhardt
A. Mithal
                                                                      Association Suisse contre l’Ostéoporose,
Indraprastha Apollo Hospitals, Sarita Vihar,
                                                                      Clinique Bois-Cerf,
Delhi-Mathura Road,
                                                                      Avenue d’Ouchy 31,
110044 New Delhi, India
                                                                      1006 Lausanne, Switzerland
J.-P. Bonjour
University Hospital, Division of Bone Diseases,                       G. E.-H. Fuleihan
University Hospitals and Faculty of Medicine,                         Calcium Metabolism and Osteoporosis Program,
Rue Micheli-du-Crest 24,                                              American University of Beirut-Medical Center,
1211 Geneva, Switzerland                                              Riad El Solh, PO BOX: 11-0236, 1107 2020 Beirut, Lebanon
Osteoporos Int


the efficacy of different vitamin D doses administered and      Falls
levels of 25OHD achieved in reducing risk of falls and
fractures. In this process, it is important to consider other   Vitamin D is thought to act on myocyte vitamin D receptors
factors that influence serum 25OHD levels and responses to      to exert its effect on muscle tissue. In prospective studies,
oral vitamin D supplementation.                                 lower serum 25OHD levels have been associated with
                                                                decreased grip strength and appendicular muscle mass in
                                                                older men and women [10, 11] Supplementation with
Determinants of serum 25OHD levels and of the serum             vitamin D has improved lower extremity muscle perfor-
25OHD response to oral vitamin D                                mance and reduced risk of falling in several high-quality
                                                                double blind RCTs [12]. These trials have employed doses
Vitamin D intake and effective sun exposure are the major       up to 25 μg (1,000 IU) of vitamin D per day, with and
determinants of the serum 25OHD level. Several factors          without calcium. Supplementation in amounts of 17.5 to
influence the increment in serum 25OHD in response to a         25 μg/day (700–1,000 IU/day) lowered risk of falling by
given dose of vitamin D3, including the starting level of       20% in older individuals, independent of their calcium
25OHD. At a dose of 2.5 μg (100 IU/d), the mean                 intake level. In contrast, supplementation with doses of
increment ranges from 2.75 nmol/l (1.1 ng/ml) at low            <17.5 μg/day (<700 IU/day) had no detectable effect on
starting 25OHD levels to 1.75 nmol/l (0.7 ng/ml) at higher      falls. From this meta-analysis of available data, it appears
(near optimal) starting levels [2]. The increment in 25OHD      that a mean serum 25OHD level of at least 60 nmol/L
in response to a given dose of vitamin D also varies with       (24 ng/ml) is needed for optimal fall risk reduction.
body size. It is smaller in subjects with high BMI than in      Observational studies suggest that there may be benefit to
individuals with normal BMI [3, 4]. Other factors affect        increasing serum 25OHD levels beyond 60 nmol/L
25OHD levels but have no known impact on 25OHD                  (24 ng/ml), but higher levels (and doses) have not been
responses to supplemental vitamin D. Estrogen use               evaluated in RCTs.
increases measured serum 25OHD levels by increasing
levels of vitamin D binding protein [5] but does not alter
the serum 25OHD increment achieved with supplementa-            Fractures
tion. Serum 25OHD levels decline with aging, but the
serum 25OHD response to a given dose of supplemental            Vitamin D affects fracture risk through its effects on bone
vitamin D3 is not affected by age [6]. Similarly, the dietary   metabolism and on risk of falling. Randomized controlled
calcium intake, within the range usually consumed, does         trials indicate that supplementation with vitamin D reduces
not affect the serum 25OHD response to vitamin D                rates of bone loss in older women [13]. The impact of
supplementation [7]. (The latter statement should not be        supplemental vitamin D on fracture risk has been examined
confused with the observations that the calcium require-        mainly in men and women age 65 and older. A recent meta-
ment may be dependent upon vitamin D status and that an         analysis revealed that vitamin D in doses in the range of
adequate calcium intake is important for bone health [8].)      more than 10 through 20 μg/day (>400–800 IU/day)
Finally, serum 25OHD levels vary widely across commonly         reduced risk of non-vertebral and hip fracture by approx-
used assays. Until this problem is addressed by widespread      imately 20% whereas doses up through 10 μg/day
use of standard reference material such as the NIST             (400 IU/day) had no evident effect [14]. Doses above
standards [9] and participation in the DEQAS quality            20 μg/day (800 IU/day) have not been studied. The mean
control program (www.deqas.org), assay variability will         serum 25OHD level associated with reduction in non-
continue to complicate the process of determining the           vertebral fracture risk was 66 nmol/L (26.4 ng/ml). Hip
desired 25OHD level and the impact of a given dose on           fracture risk reduction was observed at a mean 25OHD
serum 25OHD levels.                                             level of 74 nmol/L (29.6 ng/ml) and higher. Based on this

R. G. Josse                                                     J. Morales-Torres
Division of Endocrinology and Metabolism,                       Hospital Aranda de la Parra,
University of Toronto, St Michael’s Hospital Health Centre,     Hidalgo 329-704,
61 Queen Street East,                                           León 37000 GTO, Mexico
Toronto, ON M5C 2T2, Canada
                                                                N. Yoshimura
                                                                Department of Joint Disease Research,
P. Lips                                                         22nd Century Medical and Research Center,
Division of Internal Medicine, Endocrine Section,               University of Tokyo,
VU University Medical Center,                                   7-3-1 Hongo, Bunkyo-ku,
PO Box 7057, 1007MB Amsterdam, Netherlands                      Tokyo 113-8655, Japan
Osteoporos Int


and other evidence, eight of ten IOF Working Group               yvitamin D appears to mediate some of the non-classical
members felt that 75 nmol/L (30 ng/ml) is the appropriate        effects of vitamin D.
target level of serum 25OHD for older individuals; in
contrast, two members felt that the target should be 50 to
75 nmol/l (20 to 30 ng/ml). The estimate of 75 nmol/l            Recommendations
(30 ng/ml) is close to the higher cluster of 25OHD levels
associated with maximal PTH suppression [1].                     The estimated average vitamin D requirement for older adults
                                                                 to reach a serum 25OHD level of 75 nmol/L (30 ng/ml) is 20
                                                                 to 25 μg/day (800 to 1,000 IU/day). Considerably higher
Other potential benefits                                         doses would be needed to ensure that almost all older adults
                                                                 reached 75 nmol/l (30 ng/ml). Efficacy of doses higher than
Vitamin D insufficiency has been implicated as a contrib-        20 μg/day (800 IU/day) for fractures and 25 μg/day
uting factor in a growing number of important chronic            (1,000 IU/day) for falls however have not been evaluated in
diseases including type 2 diabetes, cardiovascular disease,      RCTs. It is therefore premature to recommend higher intakes
selected cancers, and autoimmune diseases as well as             for all older adults at this time.
infections, and also to increased mortality. RCTs are needed        The repletion dose will vary among individuals accord-
before causal relationships can be determined and optimal        ing to their starting level, their BMI, their effective sun
25OHD levels for prevention can be established. The doses        exposure, and other unidentified factors. An intake lower
and mean serum levels needed to achieve optimal impact           than 20 μg/day (800 IU/day) may be adequate for
on these non-classical outcomes are not clear.                   individuals with regular effective sun exposure. Intake
                                                                 may need to be adjusted upward to as much as 50 μg/day
                                                                 (2,000 IU/day) in individuals who are obese, and in those
Global vitamin D status                                          with osteoporosis, limited sun exposure (institutionalized,
                                                                 homebound), and malabsorption, and in non-European
Vitamin D insufficiency, whether defined as 25OHD levels         populations known to be at high risk for vitamin D
<75 or <50 nmol/L (<30 or <20 ng/ml), is prevalent               deficiency such as those in the Middle East and South
worldwide [15]. For instance, the prevalence of levels           Asia, or immigrants from such regions living in Europe. In
<75 nmol/L (<30 ng/ml) in postmenopausal women has               these and other high-risk individuals, we recommend
been reported to be approximately 50% in Thailand and            measuring the serum 25OHD level. The required dose to
Malaysia, 75% in the USA, and 90% in Japan and South             reach 75 nmol/L can be estimated from the measured level.
Korea. Vitamin D deficiency, defined as a level below            Each 2.5 μg (100 IU) of added vitamin D will increase the
25 nmol/L (10 ng/ml) is very common in the Middle East           serum 25OHD level by about 2.5 nmol/L (range 1.75–
and South Asia where mean levels range from 10 to                2.75 nmol/L) or 1.0 ng/ml (range 0.7 to 1.1 ng/ml) [2].
30 nmol/L (4 to 12 ng/ml) [15, 16]. The high prevalence of       Because of the variability in individual 25OHD responses
suboptimal 25OHD levels in older men and women around            to supplemental vitamin D, however, in high-risk individ-
the world raises the possibility that many falls and fractures   uals, the serum 25OHD levels should be retested after about
can be prevented with vitamin D supplementation.                 3 months of supplementation to confirm that the target
                                                                 25OHD level has been reached.

Vitamin D preparations
                                                                 Conflicts of interest None.
Vitamin D is available in two forms, vitamin D2 (ergo-
calciferol) and vitamin D3 (cholecalciferol). Some find that
the two forms are equally effective in raising the serum
25OHD level [17] whereas others find that vitamin D3             References
gives a larger increment [18]. We generally recommend that
vitamin D3 be used when available. In some parts of the           1. Durazo-Arvizu RA, Dawson-Hughes B, Sempos CT, Yetley EA,
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substitute for adequate vitamin D intake. Vitamin D is the           maximal suppression of parathyroid hormone by 25-
                                                                     hydroxyvitamin D in persons 65 years of age and older. J Nutr.
substrate for 25OHD and the circulating 25OHD level may              doi:10.3945/jm.109.116681
be important to support the non-renal production of 1,25-         2. Heaney RP, Davies KM, Chen TC, Holick MF, Barger-Lux MJ
dihydroxyvitamin D. Local production of 1,25-dihydrox-               (2003) Human serum 25-hydroxycholecalciferol response to
Osteoporos Int

      extended oral dosing with cholecalciferol. Am J Clin Nutr            11. Visser M, Deeg DJ, Lips P (2003) Low vitamin D and high
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      serum 25 hydroxy vitamin D response to oral supplements in               (2009) Fall prevention with supplemental and active forms of
      healthy older adults. J Am Coll Nutr 27:274–279                          vitamin D: a meta-analysis of randomised controlled trials. Br
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      contraceptive use with plasma 25-hydroxyvitamin D levels. J Am       13. Ooms ME, Roos JC, Bezemer PD, van der Vijgh WJ, Bouter LM,
      Coll Nutr 17:282–284                                                     Lips P (1995) Prevention of bone loss by vitamin D supplemen-
 6.   Harris SS, Dawson-Hughes B (2002) Plasma vitamin D and                   tation in elderly women: a randomized double-blind trial. J Clin
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      Clin Endocrinol Metab 92:1415–1423                                   16. El-Hajj Fuleihan G (2009) Vitamin D deficiency in the Middle
 9.   May W, Parris R, Beck C, Fassett J, Greenberg R, Guenther F,             East and its health consequences. Clin Rev Bone Miner Metab
      Kramer G, Wise S, Gills T, Colbert J, Gettings R, MacDonald B            7:77–93
      (2000) Definitions of terms and modes used at NIST for value-        17. Holick MF, Biancuzzo RM, Chen TC, Klein EK, Young A,
      assignment of reference materials for chemical measurements. In          Bibuld D, Reitz R, Salameh W, Ameri A, Tannenbaum AD (2008)
      Technology NIoSa (ed). US Government Printing Office,                    Vitamin D2 is as effective as vitamin D3 in maintaining
      Gaithersburg                                                             circulating concentrations of 25-hydroxyvitamin D. J Clin
10.   Flicker L, MacInnis RJ, Stein MS, Scherer SC, Mead KE,                   Endocrinol Metab 93:677–681
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Raccomandazioni della iof (international osteoporosis foundation) sull’impiego della vitamina d negli anziani

  • 1. Osteoporos Int DOI 10.1007/s00198-010-1285-3 POSITION PAPER IOF position statement: vitamin D recommendations for older adults B. Dawson-Hughes & A. Mithal & J.-P. Bonjour & S. Boonen & P. Burckhardt & G. E.-H. Fuleihan & R. G. Josse & P. Lips & J. Morales-Torres & N. Yoshimura Received: 9 March 2010 / Accepted: 16 April 2010 # International Osteoporosis Foundation and National Osteoporosis Foundation 2010 Abstract This position paper of the International Osteopo- Introduction rosis Foundation makes recommendations for vitamin D nutrition in elderly men and women from an evidence- Vitamin D is important for bone and muscle development, based perspective. function, and preservation. The serum 25OHD concentra- tion is the best available clinical indicator of vitamin D Keywords Musculoskeletal health . Requirement . status. Until recently, optimal serum 25OHD concentration Vitamin D was considered to be that level associated with maximal parathyroid hormone (PTH) suppression. Estimates of that threshold level have clustered around 32–50 nmol/L (12.8–20 ng/ml) and 68–75 nmol/L (27.2–30 ng/ml), depending upon analytical approach used [1]. In the last decade, however, the evidence base for older men and women has grown to include many randomized, controlled This material is based in part upon work supported by the US clinical trials (RCTs) with falls and fracture endpoints. Department of Agriculture, Agricultural Research Service, under Because the RCTs have for the most part been conducted in agreement no. 58-1950-7-707. Any opinions, findings, conclusion, men and women over the age of 60 to 65 years, our or recommendations expressed in this publication are those of the author(s) and do not necessarily reflect the view of the US recommendations are directed at this large and growing Department of Agriculture, the Centers for Disease Control and older segment of the adult population. Our objective is to Prevention or the US Department of Health and Human Services. use available evidence to support recommendations for This statement has been endorsed by the IOF Committee of Scientific optimal vitamin D status. We approach this by examining Advisors B. Dawson-Hughes (*) S. Boonen Jean Mayer USDA Human Nutrition Research Center on Aging, Centre for Metabolic Bone Diseases and Division of Geriatric Tufts University, Medicine, University of Leuven, 711 Washington Street, Herestraat 49, Boston, MA 02111, USA 3000 Leuven, Belgium e-mail: bess.dawson-hughes@tufts.edu P. Burckhardt A. Mithal Association Suisse contre l’Ostéoporose, Indraprastha Apollo Hospitals, Sarita Vihar, Clinique Bois-Cerf, Delhi-Mathura Road, Avenue d’Ouchy 31, 110044 New Delhi, India 1006 Lausanne, Switzerland J.-P. Bonjour University Hospital, Division of Bone Diseases, G. E.-H. Fuleihan University Hospitals and Faculty of Medicine, Calcium Metabolism and Osteoporosis Program, Rue Micheli-du-Crest 24, American University of Beirut-Medical Center, 1211 Geneva, Switzerland Riad El Solh, PO BOX: 11-0236, 1107 2020 Beirut, Lebanon
  • 2. Osteoporos Int the efficacy of different vitamin D doses administered and Falls levels of 25OHD achieved in reducing risk of falls and fractures. In this process, it is important to consider other Vitamin D is thought to act on myocyte vitamin D receptors factors that influence serum 25OHD levels and responses to to exert its effect on muscle tissue. In prospective studies, oral vitamin D supplementation. lower serum 25OHD levels have been associated with decreased grip strength and appendicular muscle mass in older men and women [10, 11] Supplementation with Determinants of serum 25OHD levels and of the serum vitamin D has improved lower extremity muscle perfor- 25OHD response to oral vitamin D mance and reduced risk of falling in several high-quality double blind RCTs [12]. These trials have employed doses Vitamin D intake and effective sun exposure are the major up to 25 μg (1,000 IU) of vitamin D per day, with and determinants of the serum 25OHD level. Several factors without calcium. Supplementation in amounts of 17.5 to influence the increment in serum 25OHD in response to a 25 μg/day (700–1,000 IU/day) lowered risk of falling by given dose of vitamin D3, including the starting level of 20% in older individuals, independent of their calcium 25OHD. At a dose of 2.5 μg (100 IU/d), the mean intake level. In contrast, supplementation with doses of increment ranges from 2.75 nmol/l (1.1 ng/ml) at low <17.5 μg/day (<700 IU/day) had no detectable effect on starting 25OHD levels to 1.75 nmol/l (0.7 ng/ml) at higher falls. From this meta-analysis of available data, it appears (near optimal) starting levels [2]. The increment in 25OHD that a mean serum 25OHD level of at least 60 nmol/L in response to a given dose of vitamin D also varies with (24 ng/ml) is needed for optimal fall risk reduction. body size. It is smaller in subjects with high BMI than in Observational studies suggest that there may be benefit to individuals with normal BMI [3, 4]. Other factors affect increasing serum 25OHD levels beyond 60 nmol/L 25OHD levels but have no known impact on 25OHD (24 ng/ml), but higher levels (and doses) have not been responses to supplemental vitamin D. Estrogen use evaluated in RCTs. increases measured serum 25OHD levels by increasing levels of vitamin D binding protein [5] but does not alter the serum 25OHD increment achieved with supplementa- Fractures tion. Serum 25OHD levels decline with aging, but the serum 25OHD response to a given dose of supplemental Vitamin D affects fracture risk through its effects on bone vitamin D3 is not affected by age [6]. Similarly, the dietary metabolism and on risk of falling. Randomized controlled calcium intake, within the range usually consumed, does trials indicate that supplementation with vitamin D reduces not affect the serum 25OHD response to vitamin D rates of bone loss in older women [13]. The impact of supplementation [7]. (The latter statement should not be supplemental vitamin D on fracture risk has been examined confused with the observations that the calcium require- mainly in men and women age 65 and older. A recent meta- ment may be dependent upon vitamin D status and that an analysis revealed that vitamin D in doses in the range of adequate calcium intake is important for bone health [8].) more than 10 through 20 μg/day (>400–800 IU/day) Finally, serum 25OHD levels vary widely across commonly reduced risk of non-vertebral and hip fracture by approx- used assays. Until this problem is addressed by widespread imately 20% whereas doses up through 10 μg/day use of standard reference material such as the NIST (400 IU/day) had no evident effect [14]. Doses above standards [9] and participation in the DEQAS quality 20 μg/day (800 IU/day) have not been studied. The mean control program (www.deqas.org), assay variability will serum 25OHD level associated with reduction in non- continue to complicate the process of determining the vertebral fracture risk was 66 nmol/L (26.4 ng/ml). Hip desired 25OHD level and the impact of a given dose on fracture risk reduction was observed at a mean 25OHD serum 25OHD levels. level of 74 nmol/L (29.6 ng/ml) and higher. Based on this R. G. Josse J. Morales-Torres Division of Endocrinology and Metabolism, Hospital Aranda de la Parra, University of Toronto, St Michael’s Hospital Health Centre, Hidalgo 329-704, 61 Queen Street East, León 37000 GTO, Mexico Toronto, ON M5C 2T2, Canada N. Yoshimura Department of Joint Disease Research, P. Lips 22nd Century Medical and Research Center, Division of Internal Medicine, Endocrine Section, University of Tokyo, VU University Medical Center, 7-3-1 Hongo, Bunkyo-ku, PO Box 7057, 1007MB Amsterdam, Netherlands Tokyo 113-8655, Japan
  • 3. Osteoporos Int and other evidence, eight of ten IOF Working Group yvitamin D appears to mediate some of the non-classical members felt that 75 nmol/L (30 ng/ml) is the appropriate effects of vitamin D. target level of serum 25OHD for older individuals; in contrast, two members felt that the target should be 50 to 75 nmol/l (20 to 30 ng/ml). The estimate of 75 nmol/l Recommendations (30 ng/ml) is close to the higher cluster of 25OHD levels associated with maximal PTH suppression [1]. The estimated average vitamin D requirement for older adults to reach a serum 25OHD level of 75 nmol/L (30 ng/ml) is 20 to 25 μg/day (800 to 1,000 IU/day). Considerably higher Other potential benefits doses would be needed to ensure that almost all older adults reached 75 nmol/l (30 ng/ml). Efficacy of doses higher than Vitamin D insufficiency has been implicated as a contrib- 20 μg/day (800 IU/day) for fractures and 25 μg/day uting factor in a growing number of important chronic (1,000 IU/day) for falls however have not been evaluated in diseases including type 2 diabetes, cardiovascular disease, RCTs. It is therefore premature to recommend higher intakes selected cancers, and autoimmune diseases as well as for all older adults at this time. infections, and also to increased mortality. RCTs are needed The repletion dose will vary among individuals accord- before causal relationships can be determined and optimal ing to their starting level, their BMI, their effective sun 25OHD levels for prevention can be established. The doses exposure, and other unidentified factors. An intake lower and mean serum levels needed to achieve optimal impact than 20 μg/day (800 IU/day) may be adequate for on these non-classical outcomes are not clear. individuals with regular effective sun exposure. Intake may need to be adjusted upward to as much as 50 μg/day (2,000 IU/day) in individuals who are obese, and in those Global vitamin D status with osteoporosis, limited sun exposure (institutionalized, homebound), and malabsorption, and in non-European Vitamin D insufficiency, whether defined as 25OHD levels populations known to be at high risk for vitamin D <75 or <50 nmol/L (<30 or <20 ng/ml), is prevalent deficiency such as those in the Middle East and South worldwide [15]. For instance, the prevalence of levels Asia, or immigrants from such regions living in Europe. In <75 nmol/L (<30 ng/ml) in postmenopausal women has these and other high-risk individuals, we recommend been reported to be approximately 50% in Thailand and measuring the serum 25OHD level. The required dose to Malaysia, 75% in the USA, and 90% in Japan and South reach 75 nmol/L can be estimated from the measured level. Korea. Vitamin D deficiency, defined as a level below Each 2.5 μg (100 IU) of added vitamin D will increase the 25 nmol/L (10 ng/ml) is very common in the Middle East serum 25OHD level by about 2.5 nmol/L (range 1.75– and South Asia where mean levels range from 10 to 2.75 nmol/L) or 1.0 ng/ml (range 0.7 to 1.1 ng/ml) [2]. 30 nmol/L (4 to 12 ng/ml) [15, 16]. The high prevalence of Because of the variability in individual 25OHD responses suboptimal 25OHD levels in older men and women around to supplemental vitamin D, however, in high-risk individ- the world raises the possibility that many falls and fractures uals, the serum 25OHD levels should be retested after about can be prevented with vitamin D supplementation. 3 months of supplementation to confirm that the target 25OHD level has been reached. Vitamin D preparations Conflicts of interest None. Vitamin D is available in two forms, vitamin D2 (ergo- calciferol) and vitamin D3 (cholecalciferol). Some find that the two forms are equally effective in raising the serum 25OHD level [17] whereas others find that vitamin D3 References gives a larger increment [18]. We generally recommend that vitamin D3 be used when available. In some parts of the 1. Durazo-Arvizu RA, Dawson-Hughes B, Sempos CT, Yetley EA, world, active metabolites are available for use in the Looker AC, Cao G, Harris SS, Burt VL, Carriquiry AL, Picciano treatment of osteoporosis. These metabolites are not a MF (2010) Three-phase model harmonizes estimates of the substitute for adequate vitamin D intake. Vitamin D is the maximal suppression of parathyroid hormone by 25- hydroxyvitamin D in persons 65 years of age and older. J Nutr. substrate for 25OHD and the circulating 25OHD level may doi:10.3945/jm.109.116681 be important to support the non-renal production of 1,25- 2. Heaney RP, Davies KM, Chen TC, Holick MF, Barger-Lux MJ dihydroxyvitamin D. Local production of 1,25-dihydrox- (2003) Human serum 25-hydroxycholecalciferol response to
  • 4. Osteoporos Int extended oral dosing with cholecalciferol. Am J Clin Nutr 11. Visser M, Deeg DJ, Lips P (2003) Low vitamin D and high 77:204–210 parathyroid hormone levels as determinants of loss of muscle 3. Wortsman J, Matsuoka LY, Chen TC, Lu Z, Holick MF (2000) strength and muscle mass (sarcopenia): the Longitudinal Decreased bioavailability of vitamin D in obesity. Am J Clin Nutr Aging Study Amsterdam. J Clin Endocrinol Metab 88:5766– 72:690–693 [erratum appears in Am J Clin Nutr. 2003 May;77 5772 (5):1342] 12. Bischoff-Ferrari HA, Dawson-Hughes B, Staehelin HB, Orav EJ, 4. Blum M, Dallal GE, Dawson-Hughes B (2008) Body size and Stuck AE, Theiler R, Wong JB, Egli A, Kiel DP, Henschkowski J serum 25 hydroxy vitamin D response to oral supplements in (2009) Fall prevention with supplemental and active forms of healthy older adults. J Am Coll Nutr 27:274–279 vitamin D: a meta-analysis of randomised controlled trials. Br 5. Harris SS, Dawson-Hughes B (1998) The association of oral Med J 339:b3692 contraceptive use with plasma 25-hydroxyvitamin D levels. J Am 13. Ooms ME, Roos JC, Bezemer PD, van der Vijgh WJ, Bouter LM, Coll Nutr 17:282–284 Lips P (1995) Prevention of bone loss by vitamin D supplemen- 6. Harris SS, Dawson-Hughes B (2002) Plasma vitamin D and tation in elderly women: a randomized double-blind trial. J Clin 25OHD responses of young and old men to supplementation with Endocrinolol Metab 80:1052–1058 vitamin D3. J Am Coll Nutr 21:357–362 14. Bischoff-Ferrari HA, Willett WC, Wong JB, Giovannucci E, 7. Goussous R, Song L, Dallal G, Dawson-Hughes B (2005) The Dietrich T, Dawson-Hughes B (2005) Fracture prevention by effect of calcium intake on the vitamin D requirement. J Clin vitamin D supplementation: a meta-analysis of randomized Endocrinol Metab 90:707–711 controlled trials. J Am Med Assoc 293:2257–2264 8. Boonen S, Lips P, Bouillon R, Bischoff-Ferrari HA, Vanderschue- 15. Mithal A, Wahl DA, Bonjour JP, Burckhardt P, Dawson-Hughes ren D, Haentjens P (2007) Need for additional calcium to reduce B, Eisman JA, El-Hajj Fuleihan G, Josse RG, Lips P, Morales- the risk of hip fracture with vitamin D supplementation: evidence Torres J (2009) Global vitamin D status and determinants of from a comparative metaanalysis of randomized controlled trials. J hypovitaminosis D. Osteoporos Int 20:1807–1820 Clin Endocrinol Metab 92:1415–1423 16. El-Hajj Fuleihan G (2009) Vitamin D deficiency in the Middle 9. May W, Parris R, Beck C, Fassett J, Greenberg R, Guenther F, East and its health consequences. Clin Rev Bone Miner Metab Kramer G, Wise S, Gills T, Colbert J, Gettings R, MacDonald B 7:77–93 (2000) Definitions of terms and modes used at NIST for value- 17. Holick MF, Biancuzzo RM, Chen TC, Klein EK, Young A, assignment of reference materials for chemical measurements. In Bibuld D, Reitz R, Salameh W, Ameri A, Tannenbaum AD (2008) Technology NIoSa (ed). US Government Printing Office, Vitamin D2 is as effective as vitamin D3 in maintaining Gaithersburg circulating concentrations of 25-hydroxyvitamin D. J Clin 10. Flicker L, MacInnis RJ, Stein MS, Scherer SC, Mead KE, Endocrinol Metab 93:677–681 Nowson CA, Thomas J, Lowndes C, Hopper JL, Wark JD 18. Trang HM, Cole DE, Rubin LA, Pierratos A, Siu S, Vieth R (2005) Should older people in residential care receive vitamin D (1998) Evidence that vitamin D3 increases serum 25- to prevent falls? Results of a randomized trial. J Am Geriatr Soc hydroxyvitamin D more efficiently than does vitamin D2. Am J 53:1881–1888 Clin Nutr 68:854–858