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钙和维生素 D 增加绝经前妇女的骨密度。

Calcium and vitamin D for increasing bone mineral density in premenopausal women.

机构信息

Clinical Epidemiology Unit, Children's Hospital of Mexico Federico Gomez-Faculty of Medicine UNAM, Mexico City, Mexico.

Cochrane Mexico UNAM (Universidad Nacional Autónoma de México), Cochrane Mexico, Mexico City, Mexico.

出版信息

Cochrane Database Syst Rev. 2023 Jan 27;1(1):CD012664. doi: 10.1002/14651858.CD012664.pub2.

Abstract

BACKGROUND

Osteoporosis is a condition where bones become fragile due to low bone density and impaired bone quality. This results in fractures that lead to higher morbidity and reduced quality of life. Osteoporosis is considered a major public health concern worldwide. For this reason, preventive measurements need to be addressed throughout the life course. Exercise and a healthy diet are among the lifestyle factors that can help prevent the disease, the latter including intake of key micronutrients for bone, such as calcium and vitamin D. The evidence on whether supplementation with calcium and vitamin D improves bone mineral density (BMD) in premenopausal women is still inconclusive. In this age group, bone accrual is considered to be the goal of supplementation, so BMD is relevant for the future stages of life.

OBJECTIVES

To evaluate the benefits and harms of calcium and vitamin D supplementation, alone or in combination, to increase the BMD, reduce fractures, and report the potential adverse events in healthy premenopausal women compared to placebo.

SEARCH METHODS

We used standard, extensive Cochrane search methods. The latest search was 12 April 2022.

SELECTION CRITERIA

We included randomised controlled trials in healthy premenopausal women (with or without calcium or vitamin D deficiency) comparing supplementation of calcium or vitamin D (or both) at any dose and by any route of administration versus placebo for at least three months. Vitamin D could have been administered as cholecalciferol (vitamin D) or ergocalciferol (vitamin D).

DATA COLLECTION AND ANALYSIS

We used standard Cochrane methods. Outcomes included total hip bone mineral density (BMD), lumbar spine BMD, quality of life, new symptomatic vertebral fractures, new symptomatic non-vertebral fractures, withdrawals due to adverse events, serious adverse events, all reported adverse events and additional withdrawals for any reason.

MAIN RESULTS

We included seven RCTs with 941 participants, of whom 138 were randomised to calcium supplementation, 110 to vitamin D supplementation, 271 to vitamin D plus calcium supplementation, and 422 to placebo. Mean age ranged from 18.1 to 42.1 years. Studies reported results for total hip or lumbar spine BMD (or both) and withdrawals for various reasons, but none reported fractures or withdrawals for adverse events or serious adverse events. Results for the reported outcomes are presented for the three comparisons: calcium versus placebo, vitamin D versus placebo, and calcium plus vitamin D versus placebo. In all comparisons, there was no clinical difference in outcomes, and the certainty of the evidence was moderate to low. Most studies were at risk of selection, performance, detection, and reporting biases. Calcium versus placebo Four studies compared calcium versus placebo (138 participants in the calcium group and 123 in the placebo group) with mean ages from 18.0 to 47.3 years. Calcium supplementation may have little to no effect on total hip or lumbar spine BMD after 12 months in three studies and after six months in one study (total hip BMD: mean difference (MD) -0.04 g/cm, 95% confidence interval (CI) -0.11 to 0.03; I = 71%; 3 studies, 174 participants; low-certainty evidence; lumbar spine BMD: MD 0 g/cm, 95% CI -0.06 to 0.06; I = 71%; 4 studies, 202 participants; low-certainty evidence). Calcium alone supplementation does not reduce or increase the withdrawals in the trials (risk ratio (RR) 0.78, 95% CI 0.52 to 1.16; I = 0%; 4 studies, 261 participants: moderate-certainty evidence). Vitamin D versus placebo Two studies compared vitamin D versus placebo (110 participants in the vitamin D group and 79 in the placebo group), with mean ages from 18.0 to 32.7 years. These studies reported lumbar spine BMD as a mixture of MDs and percent of change and we were unable to pool the results. In the original studies, there were no differences in lumbar BMD between groups. Vitamin D alone supplementation does not reduce or increase withdrawals for any reason between groups (RR 0.74, 95% CI 0.46 to 1.19; moderate-certainty evidence). Calcium plus vitamin D versus placebo Two studies compared calcium plus vitamin D versus placebo (271 participants in the calcium plus vitamin D group and 270 in the placebo group; 220 participants from Woo 2007 and 50 participants from Islam 2010). The mean age range was 18.0 to 36 years. These studies measured different anatomic areas, one study reported total hip BMD and the other study reported lumbar spine BMD; therefore, data were not pooled for this outcome. The individual studies found no difference between groups in percent of change on total hip BMD (-0.03, 95% CI -0.06 to 0; moderate-certainty evidence), and lumbar spine BMD (MD 0.01, 95% CI -0.01 to 0.03; moderate-certainty evidence). Calcium plus vitamin D supplementation may not reduce or increase withdrawals for any reason (RR 0.82, 95% CI 0.29 to 2.35; I = 72%; 2 studies, 541 participants; low-certainty evidence).

AUTHORS' CONCLUSIONS: Our results do not support the isolated or combined use of calcium and vitamin D supplementation in healthy premenopausal women as a public health intervention to improve BMD in the total hip or lumbar spine, and therefore it is unlikely to have a benefit for the prevention of fractures (vertebral and non-vertebral). The evidence found suggests that there is no need for future studies in the general population of premenopausal women; however, studies focused on populations with a predisposition to diseases related to bone metabolism, or with low bone mass or osteoporosis diagnosed BMD would be useful.

摘要

背景

骨质疏松症是一种由于骨密度低和骨质量受损导致骨骼脆弱的疾病。这会导致骨折,从而导致更高的发病率和降低生活质量。骨质疏松症被认为是全球主要的公共卫生问题。因此,需要在整个生命过程中采取预防措施。运动和健康饮食是可以预防疾病的生活方式因素之一,后者包括摄入钙和维生素 D 等关键的微量营养素。关于补充钙和维生素 D 是否能提高绝经前妇女的骨矿物质密度 (BMD) 的证据仍不明确。在这个年龄组中,骨积累被认为是补充的目标,因此 BMD 与生命的后期阶段有关。

目的

评估单独或联合补充钙和维生素 D 以增加 BMD、减少骨折,并报告与安慰剂相比,健康绝经前妇女的潜在不良事件。

检索方法

我们使用标准的、广泛的 Cochrane 检索方法。最新的检索日期是 2022 年 4 月 12 日。

选择标准

我们纳入了比较健康绝经前妇女(有或没有钙或维生素 D 缺乏)补充任何剂量和任何途径的钙或维生素 D(或两者)与安慰剂至少三个月的随机对照试验。维生素 D 可以是胆钙化醇(维生素 D)或麦角钙化醇(维生素 D)。

数据收集和分析

我们使用标准的 Cochrane 方法。结局包括全髋骨矿物质密度 (BMD)、腰椎 BMD、生活质量、新的有症状性椎体骨折、新的有症状性非椎体骨折、因不良事件退出、严重不良事件、所有报告的不良事件以及任何原因的额外退出。

主要结果

我们纳入了 7 项 RCT,共 941 名参与者,其中 138 人被随机分配到钙补充组,110 人被随机分配到维生素 D 补充组,271 人被随机分配到维生素 D 加钙补充组,422 人被随机分配到安慰剂组。平均年龄为 18.1 至 42.1 岁。研究报告了全髋或腰椎 BMD(或两者)以及各种原因的退出结果,但均未报告骨折或不良事件或严重不良事件的退出。报告结局的结果呈现了三种比较:钙与安慰剂、维生素 D 与安慰剂、钙加维生素 D 与安慰剂。在所有比较中,结果均无临床差异,证据的确定性为中等到低。大多数研究都存在选择、表现、检测和报告偏倚的风险。

钙与安慰剂

四项研究比较了钙与安慰剂(钙组 138 人,安慰剂组 123 人),平均年龄为 18.0 至 47.3 岁。在三项研究中,经过 12 个月和一项研究经过 6 个月后,钙补充剂对全髋或腰椎 BMD 的影响可能很小或没有(全髋 BMD:平均差值 (MD) -0.04 g/cm,95%置信区间 (CI) -0.11 至 0.03;I = 71%;3 项研究,174 名参与者;低确定性证据;腰椎 BMD:MD 0 g/cm,95% CI -0.06 至 0.06;I = 71%;4 项研究,202 名参与者;低确定性证据)。钙单独补充不会减少或增加试验中的退出(风险比 (RR) 0.78,95% CI 0.52 至 1.16;I = 0%;4 项研究,261 名参与者:中等确定性证据)。

维生素 D 与安慰剂:两项研究比较了维生素 D 与安慰剂(维生素 D 组 110 人,安慰剂组 79 人),平均年龄为 18.0 至 32.7 岁。这些研究报告了腰椎 BMD 的 MD 和百分比变化的混合物,我们无法对结果进行合并。在原始研究中,两组之间的腰椎 BMD 没有差异。维生素 D 单独补充不会减少或增加任何原因导致的组间退出(RR 0.74,95% CI 0.46 至 1.19;中等确定性证据)。

钙加维生素 D 与安慰剂:两项研究比较了钙加维生素 D 与安慰剂(钙加维生素 D 组 271 人,安慰剂组 270 人;220 人来自 Woo 2007 年的研究,50 人来自 Islam 2010 年的研究)。平均年龄范围为 18.0 至 36 岁。这些研究测量了不同的解剖区域,一项研究报告了全髋 BMD,另一项研究报告了腰椎 BMD;因此,对于该结局,数据无法合并。两项研究均发现,组间全髋 BMD 的百分比变化(-0.03,95% CI -0.06 至 0;中等确定性证据)和腰椎 BMD(MD 0.01,95% CI -0.01 至 0.03;中等确定性证据)无差异。钙加维生素 D 补充剂可能不会减少或增加任何原因导致的退出(RR 0.82,95% CI 0.29 至 2.35;I = 72%;2 项研究,541 名参与者;低确定性证据)。

作者结论

我们的结果不支持绝经前健康女性单独或联合使用钙和维生素 D 补充剂作为改善全髋或腰椎 BMD 的公共卫生干预措施,因此不太可能对预防骨折(椎体和非椎体)有益。发现的证据表明,一般绝经前女性人群不需要进一步研究;然而,针对有疾病易感性的人群(如与骨代谢相关的疾病、低骨量或骨质疏松症诊断的 BMD)的研究将是有用的。

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