遗传和非遗传因素对补充维生素D时总25(OH)D和生物可利用25(OH)D反应的影响

P. Yao, Liang Sun, Ling Lu, H. Ding, Xiafei Chen, Lixin Tang, Xinming Xu, Gang Liu, Yao Hu, Yiwei Ma, Feijie Wang, Q. Jin, He Zheng, H. Yin, R. Zeng, Yan Chen, F. Hu, Huaixing Li, Xu Lin
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Six common polymorphisms in vitamin D metabolism genes were genotyped. Results Between-arm net changes were +30.6 ± 1.7 nmol/L for 25(OH)D, +2.7 ± 0.2 nmol/L for 25(OH)DBio, and -5.2 ± 1.2 pg/mL for PTH, corresponding to 70% [95% confidence interval (CI), 62.8% to 77.2%] net reversion rate for vitamin D deficiency at week 20 (P < 0.001). Only 25(OH)DBio change was positively associated with calcium change (P < 0.001). Genetic factors (GC-rs4588/GC-rs7041, VDR-rs2228570, and CYP2R1-rs10741657; P ≤ 0.04) showed stronger influences on 25(OH)D or 25(OH)DBio responses than nongenetic factors, including baseline value, body mass index, and sex. An inverse association of PTH-25(OH)D was demonstrated only at 25(OH)D of <50.8 (95% CI, 43.6 to 59.0) nmol/L. Conclusions Supplemented 2000 IU/d vitamin D3 raised 25(OH)D and 25(OH)DBio but was unable to correct deficiency in 25% of Chinese participants, which might be partially attributed to the effect of genetic modification. 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引用次数: 55

摘要

关于遗传和非遗传因素如何改变非白人人群补充维生素D的反应,我们知之甚少。目的探讨维生素D3补充后25-羟基维生素D [25(OH)D]和生物可利用性25(OH)D [25(OH)DBio]反应的影响因素。在这项为期20周的随机、双盲、安慰剂对照试验中,448名维生素D缺乏症患者接受2000 IU/ D维生素D3或安慰剂治疗。主要观察指标测定血清25(OH)D、维生素D结合蛋白(VDBP)、甲状旁腺激素(PTH)和钙,并根据VDBP计算25(OH)DBio。对维生素D代谢基因的6个常见多态性进行了基因分型。结果25(OH)D组组间净变化为+30.6±1.7 nmol/L, 25(OH)DBio组组间净变化为+2.7±0.2 nmol/L, PTH组组间净变化为-5.2±1.2 pg/mL,第20周维生素D缺乏症组净逆转率为70%[95%可信区间(CI), 62.8% ~ 77.2%] (P < 0.001)。只有25(OH)DBio变化与钙变化呈正相关(P < 0.001)。遗传因素(GC-rs4588/GC-rs7041, VDR-rs2228570, CYP2R1-rs10741657;P≤0.04)对25(OH)D或25(OH)DBio反应的影响强于非遗传因素,包括基线值、体重指数和性别。PTH-25(OH)D仅在25(OH)D <50.8 (95% CI, 43.6 ~ 59.0) nmol/L时呈负相关。结论补充2000 IU/d维生素D3提高了25(OH) d和25(OH)DBio水平,但不能纠正25%的中国参与者的缺乏,这可能部分归因于基因修饰的作用。需要更多的研究来阐明亚洲人适当的维生素D推荐量以及25(OH)DBio的潜在临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Genetic and Nongenetic Factors on Total and Bioavailable 25(OH)D Responses to Vitamin D Supplementation
Context Little is known about how genetic and nongenetic factors modify responses of vitamin D supplementation in nonwhite populations. Objective To investigate factors modifying 25-hydroxyvitamin D [25(OH)D] and bioavailable 25(OH)D [25(OH)DBio] responses after vitamin D3 supplementation. Design, Setting, Participants, and Intervention In this 20-week, randomized, double-blinded, placebo-controlled trial, 448 Chinese with vitamin D deficiency received 2000 IU/d vitamin D3 or placebo. Main Outcome Measures Serum 25(OH)D, vitamin D-binding protein (VDBP), parathyroid hormone (PTH) and calcium were measured, and 25(OH)DBio was calculated based on VDBP levels. Six common polymorphisms in vitamin D metabolism genes were genotyped. Results Between-arm net changes were +30.6 ± 1.7 nmol/L for 25(OH)D, +2.7 ± 0.2 nmol/L for 25(OH)DBio, and -5.2 ± 1.2 pg/mL for PTH, corresponding to 70% [95% confidence interval (CI), 62.8% to 77.2%] net reversion rate for vitamin D deficiency at week 20 (P < 0.001). Only 25(OH)DBio change was positively associated with calcium change (P < 0.001). Genetic factors (GC-rs4588/GC-rs7041, VDR-rs2228570, and CYP2R1-rs10741657; P ≤ 0.04) showed stronger influences on 25(OH)D or 25(OH)DBio responses than nongenetic factors, including baseline value, body mass index, and sex. An inverse association of PTH-25(OH)D was demonstrated only at 25(OH)D of <50.8 (95% CI, 43.6 to 59.0) nmol/L. Conclusions Supplemented 2000 IU/d vitamin D3 raised 25(OH)D and 25(OH)DBio but was unable to correct deficiency in 25% of Chinese participants, which might be partially attributed to the effect of genetic modification. More studies are needed to elucidate appropriate vitamin D recommendations for Asians and the potential clinical implications of 25(OH)DBio.
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