血清促甲状腺激素浓度与骨矿物质密度之间的关系:综述

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引用次数: 0

摘要

摘要 引言 本研究旨在总结以往的研究结果,对数据进行标准化处理,并提出新的统计结果,以便为医生提供有关血清促甲状腺激素(TSH)浓度与骨矿物质密度(BMD)之间关系的具有临床意义的结果。 方法 为了进行本综述,我们进行了一次系统性检索,在 PubMed、Web of Science、Embase、Scopus、Cochrane Library 和 Google Scholar 等主要在线医学数据库中搜索了有关 TSH 对 BMD 影响的荟萃分析和系统性综述。此外,还对所有主要研究进行了统计分析筛选。 结果 本研究的统计结果基于 75,898 名患者的数据。亚临床甲状腺功能亢进症患者发生各种骨折的汇总风险比估计为 1.36 (95% CI: 1.18-1.56; p < 0.001)。据估计,接受左旋甲状腺素抑制治疗的男性患者桡骨远端 BMD 的 SMD 为-0.61(95% CI:-1.10-(-0.11);P = 0.02)。此外,接受左旋甲状腺素抑制疗法的患者发生任何骨折的汇总风险比估计为 1.98 (95% CI: 0.98 - 3.98; p = 0.06)。这些患者的 BMD 可能与未接受治疗的患者有显著差异。然而,这种差异取决于骨的类型。 结论 我们的数据证实,亚临床甲状腺机能亢进对骨骼有不利影响,导致 BMD 减少。根据所获得的结果,作者认为促甲状腺激素血清水平降低本身可能是与 BMD 降低相关的一个个体因素,因此也是导致骨折风险增加的一个个体因素。不过,需要注意的是,TSH 抑制疗法对不同部位的 BMD 评估效果不同。此外,研究结果表明,在某些特定领域,这一问题不仅与绝经后女性有关,也与男性患者有关。这些结论应有助于仔细考虑在所有患者中应用促甲状腺激素抑制疗法。应特别关注接受 DTC 治疗后的患者,同时应单独考虑实施左旋甲状腺素治疗的所有利弊。
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Association between serum TSH concentration and bone mineral density: an umbrella review

Abstract

Introduction

The aim of this study was to summarize the results of previous studies, standardize the data, and present new statistical results in order to provide physicians with clinically significant outcomes regarding the association between serum TSH concentration and bone mineral density (BMD).

Methods

To perform this umbrella review, a systematic search was conducted in which major online medical databases, such as PubMed, Web of Science, Embase, Scopus, Cochrane Library, and Google Scholar, were searched for meta-analyses and systematic reviews regarding the effect of TSH on BMD. Furthermore, all primary studies were screened for statistical analysis.

Results

The statistical outcomes of the present study were based on the data of 75,898 patients. The pooled risk ratio of any kind of fracture in patients with subclinical hyperthyroidism was estimated to be 1.36 (95% CI: 1.18—1.56; p < 0.001). The SMD for BMD in the distal radius in male patients receiving L-thyroxine suppression therapy was estimated to be -0.61 (95% CI: -1.10—(-0.11); p = 0.02). Furthermore, the pooled risk ratio of any fracture in patients receiving L-thyroxine suppression therapy was estimated to be 1.98 (95% CI: 0.98 – 3.98; p = 0.06). In these patients, the BMD may significantly differ from that in non-treated patients. However, the difference depends on the type of bone.

Conclusions

Our data confirmed that subclinical hyperthyroidism has a detrimental effect on bones, causing decreased BMD. Based on the obtained results, the authors suggest that a reduced TSH serum level itself may be an individual factor associated with decreased BMD and, thus, with a greater risk of bone fracture. Nevertheless, it should be noted that the effects of TSH suppression therapy differ between areas of interest for assessing BMD. Furthermore, the results have shown that this issue may, in specific areas, concern not only postmenopausal women but also male patients. These conclusions should contribute to a careful consideration of the application of TSH suppressive therapy in all patients. Particular attention should be given to patients after DTC, while all the advantages and disadvantages of implementing L-thyroxine therapy should be individually considered.

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