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成人 GH 缺乏症诊断检测的准确性:系统评价和荟萃分析。

The accuracy of diagnostic tests for GH deficiency in adults: a systematic review and meta-analysis.

机构信息

Knowledge and Evaluation Research Unit, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

出版信息

Eur J Endocrinol. 2011 Dec;165(6):841-9. doi: 10.1530/EJE-11-0476. Epub 2011 Aug 19.

DOI:10.1530/EJE-11-0476
PMID:21856789
Abstract

CONTEXT

The diagnostic accuracy of tests used to diagnose GH deficiency (GHD) in adults is unclear.

OBJECTIVE

We conducted a systematic review and meta-analysis of studies that provided data on the available diagnostic tests.

DATA SOURCES

We searched electronic databases (MEDLINE, EMBASE, Cochrane CENTRAL, Web of Sciences, and Scopus) through April 2011.

STUDY SELECTION

Review of reference lists and contact with experts identified additional candidate studies. Reviewers, working independently and in duplicate, determined study eligibility.

DATA EXTRACTION

reviewers, working independently and in duplicate, determined the methodological quality of studies and collected descriptive, quality, and outcome data.

DATA SYNTHESIS

Twenty-three studies provided diagnostic accuracy data; none provided patient outcome data. Studies had fair methodological quality, used several reference standards, and included over 1100 patients. Several tests based on direct or indirect stimulation of GH release were associated with good diagnostic accuracy, although most were assessed in one or two studies decreasing the strength of inference due to small sample size. Serum levels of GH or IGF1 had low diagnostic accuracy. Pooled sensitivity and specificity of the two most commonly used stimulation tests were found to be 95 and 89% for the insulin tolerance test and 73 and 81% for the GHRH+arginine test respectively. Meta-analytic estimates for accuracy were associated with substantial heterogeneity.

CONCLUSION

Several tests with reasonable diagnostic accuracy are available for the diagnosis of GHD in adults. The supporting evidence, however, is at high risk of bias (due to heterogeneity, methodological limitations, and imprecision).

摘要

背景

用于诊断成人生长激素缺乏症(GHD)的检测方法的诊断准确性尚不清楚。

目的

我们对提供了可用诊断检测方法数据的研究进行了系统评价和荟萃分析。

数据来源

我们通过 2011 年 4 月检索了电子数据库(MEDLINE、EMBASE、Cochrane 中心、Web of Sciences 和 Scopus)。

研究选择

通过查阅参考文献和与专家联系,确定了其他候选研究。审查员独立地进行两次审查,以确定研究的合格性。

数据提取

审查员独立地进行两次审查,以确定研究的方法学质量并收集描述性、质量和结果数据。

数据综合

23 项研究提供了诊断准确性数据;没有提供患者结局数据。这些研究具有良好的方法学质量,使用了几种参考标准,且纳入了 1100 多名患者。一些基于 GH 释放的直接或间接刺激的检测方法具有较好的诊断准确性,尽管大多数检测方法仅在一项或两项研究中进行,由于样本量小,降低了推断的强度。GH 或 IGF1 的血清水平的诊断准确性较低。胰岛素耐量试验和 GHRH+精氨酸试验这两种最常用的刺激试验的汇总敏感性和特异性分别为 95%和 89%,73%和 81%。准确性的荟萃分析估计与很大的异质性相关。

结论

有几种具有合理诊断准确性的检测方法可用于诊断成人 GHD。但是,这些证据存在高偏倚风险(由于异质性、方法学局限性和不精确性)。

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