绝经后非裔美国女性补充维生素D的剂量反应。
Dose response to vitamin D supplementation among postmenopausal African American women.
作者信息
Talwar Sonia A, Aloia John F, Pollack Simcha, Yeh James K
机构信息
Bone Mineral Research Center, Winthrop University Hospital, Mineola, NY 11501, USA.
出版信息
Am J Clin Nutr. 2007 Dec;86(6):1657-62. doi: 10.1093/ajcn/86.5.1657.
BACKGROUND
Reports on the dose response to vitamin D are conflicting, and most data were derived from white men and women.
OBJECTIVE
The objective was to determine the response of serum 25-hydroxyvitamin D [25(OH)D] to oral vitamin D(3) supplementation in an African American population.
DESIGN
Healthy black postmenopausal women (n = 208) participated in a vitamin D(3) supplementation trial for a period of 3 y. Analyses were done in the vitamin D supplementation arm (n = 104) to quantify the response in serum 25-hydroxyvitamin D concentrations at a steady state vitamin D input. The participants received 20 microg/d (800 IU) oral vitamin D(3) for the initial 2 y and 50 microg/d (2000 IU) for the third year.
RESULTS
Supplementation with 20 microg/d (800 IU/d) vitamin D(3) raised the mean serum 25(OH)D concentration from a baseline of 46.9 +/- 20.6 nmol/L to 71.4 +/- 21.5 nmol/L at 3 mo. The mean (+/-SD) concentration of serum 25(OH)D was 87.3 +/- 27.0 nmol/L 3 mo after supplementation increased to 50 microg/d (2000 IU/d). All participants achieved a serum 25(OH)D concentration >35 nmol/L, 95% achieved a concentration >50 nmol/L, but only 60% achieved a concentration >75 nmol/L. All patients had concentrations <153 nmol/L. On the basis of our findings, an algorithm for prescribing vitamin D so that patients reach optimal serum concentrations was developed. The algorithm suggests a dose of 70 microg (2800 IU/d) for those with a concentration >45 nmol/L and a dose of 100 microg (4000 IU/d) for those with a concentration <45 nmol/L.
CONCLUSIONS
Supplementation with 50 microg/d (2000 IU/d) oral vitamin D(3) is sufficient to raise serum 25-hydroxyvitamin D concentrations to >50 nmol/L in almost all postmenopausal African American women. However, higher doses were needed to achieve concentrations >75 nmol/L in many women in this population.
背景
关于维生素D剂量反应的报告相互矛盾,且大多数数据来自白人男性和女性。
目的
本研究旨在确定非裔美国人中血清25-羟维生素D[25(OH)D]对口服维生素D3补充剂的反应。
设计
健康的绝经后黑人女性(n = 208)参与了一项为期3年的维生素D3补充试验。对维生素D补充组(n = 104)进行分析,以量化在维生素D输入稳定状态下血清25-羟维生素D浓度的反应。参与者在最初2年每天口服20μg(800IU)维生素D3,第3年每天口服50μg(2000IU)。
结果
补充20μg/d(800IU/d)维生素D3 3个月时,血清25(OH)D平均浓度从基线的46.9±20.6nmol/L升至71.4±21.5nmol/L。补充剂量增加到50μg/d(2000IU/d)3个月后,血清25(OH)D平均(±标准差)浓度为87.3±27.0nmol/L。所有参与者血清25(OH)D浓度均>35nmol/L,95%的参与者浓度>50nmol/L,但只有60%的参与者浓度>75nmol/L。所有患者浓度均<153nmol/L。基于我们的研究结果,制定了一种维生素D处方算法,以使患者达到最佳血清浓度。该算法建议,对于浓度>45nmol/L的患者,剂量为70μg(2800IU/d);对于浓度<45nmol/L的患者,剂量为100μg(4000IU/d)。
结论
每天补充口服50μg(2000IU)维生素D3足以使几乎所有绝经后非裔美国女性血清25-羟维生素D浓度升至>50nmol/L。然而,该人群中许多女性需要更高剂量才能使浓度>75nmol/L。