为接受减肥手术的成人肥胖症患者口服维生素 D 补充剂。

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Marlene T Chakhtoura, Nancy F Nakhoul, Elie A Akl, Bassem Y Safadi, Christos S Mantzoros, Maria-Inti Metzendorf, Ghada El-Hajj Fuleihan
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引用次数: 0

摘要

背景:减肥手术后维生素 D 缺乏很常见,预计会对骨骼产生有害影响。然而,维生素 D 补充剂对这一人群的益处和最佳剂量目前尚不清楚。有关该主题的现有指南均来自专家意见,并非基于证据:目的:比较不同剂量的维生素 D 补充剂(低剂量(小于 600 国际单位/天)、中等剂量(600 国际单位/天至 3500 国际单位/天)、高剂量(大于 3500 国际单位/天))对接受减肥手术的肥胖症成人的影响:我们检索了 CENTRAL、MEDLINE、Embase、LILACS、两个试验登记处以及系统综述、文章和卫生技术评估报告的参考文献列表,没有语言限制。所有数据库的最后一次检索日期均为 2023 年 6 月 27 日,但 Embase 除外,我们于 2015 年 8 月 14 日对其进行了检索:我们纳入了关于减肥手术患者补充维生素D的随机对照试验或对照临床试验,这些试验对不同剂量进行了比较,或对维生素D与安慰剂进行了比较:我们采用了标准的 Cochrane 方法。主要结果为骨折和不良事件。次要结果为维生素 D 状态、全因死亡率、骨矿物质变化、继发性甲状旁腺功能亢进、健康相关生活质量和肌肉力量。我们使用 GRADE 评估了每项比较中每项结果的证据确定性:我们确定了五项试验,共有 314 名参与者。我们在定量分析中纳入了三项试验。中等剂量维生素 D 与安慰剂的比较 一项试验将中等剂量维生素 D(3200 IU/天)与安慰剂进行了比较。与安慰剂相比,中等剂量维生素 D 可改善维生素 D 状态,并可能导致甲状旁腺激素水平几乎没有差异(25-羟基维生素 D 水平:平均差 (MD) 13.60 纳克/毫升,95% 置信区间 (CI) 7.94 至 19.26;甲状旁腺激素水平:-6.60 皮克/毫升,95% CI -17.12 至 3.92;1 项研究,79 名参与者;低确定性证据)。该试验报告称,中等剂量维生素 D 组未出现不良事件,但未提供安慰剂组不良事件的任何信息。没有关于骨折、全因死亡率、骨密度变化、健康相关生活质量和肌肉力量的数据。高剂量维生素 D 与中等剂量维生素 D 的比较 在 Roux-en-Y 胃旁路术中进行的两项试验比较了中等剂量(等效剂量为 800 IU/ 天至 2000 IU/天)与高剂量(等效剂量为 5000 IU/ 天至 7943 IU/天)维生素 D。与中等剂量相比,大剂量维生素 D 可在 12 个月内提高 25- 羟维生素 D 水平,但证据非常不确定(MD 15.55 ng/mL,95% CI 3.50 至 27.61;I2 = 62%;2 项研究,73 名参与者;极低确定性证据)。与12个月的中等剂量相比,大剂量维生素D可能对甲状旁腺激素水平几乎没有影响,但证据非常不确定(MD 2.15 pg/mL,95% CI -21.31至17.01;I2 = 0%;2项研究,72名参与者;极低确定性证据)。高剂量维生素 D 对腰椎、髋部和前臂的死亡率和骨矿物质密度可能几乎没有影响,但证据非常不确定。没有关于骨折、健康相关生活质量或肌肉力量的数据:作者的结论:没有试验报告了骨折情况,关于不良事件的证据也很少。与安慰剂相比,中等剂量的维生素 D 可改善维生素 D 状态,但对甲状旁腺激素水平的改善作用微乎其微。与中等剂量相比,高剂量维生素D补充剂(大于3500 IU/天)可能会提高25-羟维生素D水平,对甲状旁腺激素水平的影响可能很小,甚至没有影响,但两者的证据都很不确定。目前现有的有限证据可能不会对实践产生重大影响。我们需要进一步研究维生素 D 补充剂对减肥手术患者骨折、不良事件和肌肉骨骼参数的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral vitamin D supplementation for adults with obesity undergoing bariatric surgery.

Background: Vitamin D deficiency following bariatric surgery is common and is expected to be associated with a deleterious impact on the skeleton. However, the benefits of vitamin D supplementation and the optimal dose in this population is currently unknown. The available guidelines on the topic are derived from experts' opinions, and are not evidence based.

Objectives: To compare the effects of different doses of vitamin D supplementation (low dose (less than 600 international units (IU)/day), moderate dose (600 IU/day to 3500 IU/day), high dose (greater than 3500 IU/day)) to each other or to placebo in adults living with obesity undergoing bariatric surgery.

Search methods: We searched CENTRAL, MEDLINE, Embase, LILACS, two trial registries, and the reference lists of systematic reviews, articles, and health technology assessment reports without language restrictions. The last search of all databases was 27 June 2023, except Embase, which we searched on 14 August 2015.

Selection criteria: We included randomised controlled trials or controlled clinical trials on vitamin D supplementation comparing different doses or comparing vitamin D to placebo in people undergoing bariatric surgery.

Data collection and analysis: We used standard Cochrane methods. Primary outcomes were fractures and adverse events. Secondary outcomes were vitamin D status, all-cause mortality, bone mineral change, secondary hyperparathyroidism, health-related quality of life, and muscle strength. We used GRADE to assess the certainty of the evidence for each outcome in each comparison.

Main results: We identified five trials with 314 participants. We included three trials in the quantitative analysis. Moderate-dose vitamin D compared to placebo One trial compared moderate-dose vitamin D (3200 IU/day) to placebo. Moderate-dose vitamin D, compared to placebo, may improve vitamin D status and may result in little to no difference in the achieved parathyroid hormone level (achieved 25-hydroxyvitamin D level: mean difference (MD) 13.60 ng/mL, 95% confidence interval (CI) 7.94 to 19.26; achieved parathyroid hormone level: -6.60 pg/mL, 95% CI -17.12 to 3.92; 1 study, 79 participants; low-certainty evidence). The trial reported no adverse events in the moderate-dose vitamin D arm, but did not provide any information on adverse events in the placebo arm. There were no data on fractures, all-cause mortality, bone density change, health-related quality of life, and muscle strength. High-dose vitamin D compared to moderate-dose vitamin D Two trials in Roux-en-Y gastric bypass compared moderate-dose (equivalent dose 800 IU/day to 2000 IU/day) to high-dose (equivalent dose 5000 IU/day to 7943 IU/day) vitamin D. The evidence of high-dose vitamin D on adverse events is very uncertain (risk ratio (RR) 5.18, 95% CI 0.23 to 116.56; 2 studies, 81 participants; very low-certainty evidence). High-dose vitamin D may increase 25-hydroxyvitamin D levels compared to a moderate dose at 12 months, but the evidence is very uncertain (MD 15.55 ng/mL, 95% CI 3.50 to 27.61; I2 = 62%; 2 studies, 73 participants; very low-certainty evidence). High-dose vitamin D may have little to no effect on parathyroid hormone levels compared to a moderate dose at 12 months, but the evidence is very uncertain (MD 2.15 pg/mL, 95% CI -21.31 to 17.01; I2 = 0%; 2 studies, 72 participants; very low-certainty evidence). High-dose vitamin D may have little to no effect on mortality and bone mineral density at the lumbar spine, hip, and forearm, but the evidence is very uncertain. There were no data on fractures, health-related quality of life, or muscle strength.

Authors' conclusions: No trials reported on fractures and the evidence available on adverse events is scarce. Moderate-dose vitamin D may improve vitamin D status and may result in little to no improvement in parathyroid hormone levels compared with placebo. High-dose vitamin D supplementation (greater than 3500 IU/day) may increase 25-hydroxyvitamin D levels, and may have little to no effect on parathyroid hormone levels, compared to a moderate dose, but the evidence for both is very uncertain. The currently available limited evidence may not have a significant impact on practice. Further studies are needed to explore the impact of vitamin D supplementation on fractures, adverse events, and musculoskeletal parameters in people undergoing bariatric surgery.

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来源期刊
CiteScore
10.60
自引率
2.40%
发文量
173
审稿时长
1-2 weeks
期刊介绍: The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.
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