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评估常规剂量补充维生素D3对中国维生素D不足育龄妇女的影响。

Assessment of the effect of routine-dose vitamin D3 supplementation in Chinese women of childbearing age with vitamin D insufficiency.

作者信息

Shan Xiaoyun, Wu Wenxuan, Yang Jingxin, Cao Yang, Li Yuting, Hu Yichun, Wang Rui, Yang Lichen

机构信息

Chinese Center for Disease Control and Prevention, National Institute for Nutrition and Health, Beijing, China.

Hunan Key Laboratory of Typical Environmental Pollution and Health Hazards, School of Public Health, Hengyang Medical School, University of South China, Hengyang, Hunan, China.

出版信息

Eur J Nutr. 2025 May 30;64(5):192. doi: 10.1007/s00394-025-03723-9.

Abstract

BACKGROUND

It was reported that vitamin D deficiency is common in Chinese women of childbearing age. Although most government dietary guidelines recommend routine-dose (400-800 IU/d), the evidence from intervention studies using routine-dose is quite limited.

OBJECTIVE

In this study, the effects of daily supplementation with routine-dose of vitamin D3 in women of childbearing age with vitamin D insufficiency on vitamin D nutritional status and bone metabolism markers were assessed by dynamic tracking, and the thresholds for appropriate levels of vitamin D in this population was also explored.

METHODS

Single-group repeated measures design was performed. Forty-five women of childbearing age (18-50 years) with vitamin D insufficiency [serum total 25(OH)D < 20 ng/mL] were recruited. A 26-week trial of oral vitamin D3 supplementation at 400 international units (IU)/day (n = 15) and 800 IU/day (n = 25) was conducted for subjects in the intervention group with a parallel observation group (n = 5). Trends in serum total 25(OH)D and parathyroid hormone (PTH) were observed at baseline, 2, 3, 4, 5, 6, 10, 12, 14, 16, and 26 weeks, while free and bioavailable 25(OH)D and bone turnover markers (BTMs) were dynamically tracked. The intervention effect was then further analyzed by subgroup including 400 IU/d + low PTH group (n = 7), 400 IU/d + high PTH group (n = 8), 800 IU/d + low PTH group (n = 12), and 800 IU/d + high PTH group (n = 13) based on baseline serum PTH concentration. The appropriate level of total 25(OH)D was defined as the thresholds at which serum PTH can be maximally suppressed or plateaued and was explored by polynomial comparison and Gaussian process regression.

RESULTS

A total of 44 out of 45 (97.8%) participants completed the intervention and follow-up. By dynamic tracking, serum total 25(OH)D increased rapidly in women of childbearing age with vitamin D insufficiency after supplementation both with 400 IU/d and 800 IU/d of vitamin D3 during the first 4 weeks. Serum vitamin D status improved greatly after 26 weeks, with significant increases in total 25(OH)D, free 25(OH)D and bioavailable 25(OH)D concentrations compared with baseline. There was no statistically significant difference in the effect of the intervention between the two dose groups. Serum PTH decreased during the first 6 weeks, after which it entered a plateau, especially in the group with higher baseline serum PTH. While BTMs were relatively stable. The range of thresholds obtained by polynomial comparison and Gaussian process regression were 20.24-23.95 ng/mL and 20.2-21.65 ng/mL, respectively.

CONCLUSION

Routine-dose of vitamin D3 supplementation was proved to be, an effective and compliant supplementation approach in women of childbearing age with vitamin D insufficiency. The average of the total 25(OH)D threshold predicted by Gaussian process regression for the high PTH groups was approximately 21 ng/mL, which could be recommended as the reference level for appropriate vitamin D in Chinese women of childbearing age. This trial was registered with the Chinese clinical trial registry as ChiCTR2200058290.

CLINICAL TRIAL REGISTRATION

ChiCTR2200058290. https://www.chictr.org.cn/showprojEN.html?proj=162610.

摘要

背景

据报道,维生素D缺乏在中国育龄妇女中很常见。尽管大多数政府膳食指南推荐常规剂量(400 - 800 IU/天),但使用常规剂量的干预研究证据相当有限。

目的

本研究通过动态跟踪评估了常规剂量维生素D3每日补充对维生素D不足的育龄妇女维生素D营养状况和骨代谢标志物的影响,并探索了该人群维生素D适宜水平的阈值。

方法

采用单组重复测量设计。招募了45名维生素D不足[血清总25(OH)D<20 ng/mL]的育龄妇女(18 - 50岁)。干预组受试者进行了为期26周、每天口服400国际单位(IU)(n = 15)和800 IU(n = 25)维生素D3的试验,同时设立平行观察组(n = 5)。在基线、第2、3、4、5、6、10、12、14、16和26周观察血清总25(OH)D和甲状旁腺激素(PTH)的变化趋势,同时动态跟踪游离和生物可利用的25(OH)D以及骨转换标志物(BTMs)。然后根据基线血清PTH浓度将干预效果进一步分析为400 IU/天 + 低PTH组(n = 7)、400 IU/天 + 高PTH组(n = 8)、800 IU/天 + 低PTH组(n = 12)和800 IU/天 + 高PTH组(n = 13)亚组。通过多项式比较和高斯过程回归探索将血清PTH最大程度抑制或趋于平稳时的总25(OH)D适宜水平阈值。

结果

45名参与者中有44名(97.8%)完成了干预和随访。通过动态跟踪,维生素D不足的育龄妇女在补充400 IU/天和800 IU/天维生素D3后的前4周血清总25(OH)D迅速升高。26周后血清维生素D状况显著改善,与基线相比,总25(OH)D、游离25(OH)D和生物可利用25(OH)D浓度显著增加。两个剂量组的干预效果无统计学显著差异。血清PTH在前6周下降,之后进入平稳期,尤其是基线血清PTH较高的组。而BTMs相对稳定。通过多项式比较和高斯过程回归得到的阈值范围分别为20.24 - 23.95 ng/mL和20.2 - 21.65 ng/mL。

结论

事实证明,常规剂量补充维生素D3对维生素D不足的育龄妇女是一种有效且依从性好的补充方法。高斯过程回归预测的高PTH组总25(OH)D阈值平均值约为21 ng/mL,可推荐作为中国育龄妇女维生素D适宜水平的参考值。本试验在中国临床试验注册中心注册为ChiCTR2200058290。

临床试验注册

ChiCTR2200058290。https://www.chictr.org.cn/showprojEN.html?proj=162610。

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