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成人慢性肾脏病基因检测的效用:一项系统评价与荟萃分析

Utility of Genetic Testing in Adults with CKD: A Systematic Review and Meta-Analysis.

作者信息

Schott Clara, Lebedeva Victoria, Taylor Cambrie, Abumelha Saeed, Roshanov Pavel S, Connaughton Dervla M

机构信息

Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.

Division of Nephrology, Department of Medicine, London Health Sciences Centre, London, Ontario, Canada.

出版信息

Clin J Am Soc Nephrol. 2025 Jan 1;20(1):101-115. doi: 10.2215/CJN.0000000000000564. Epub 2024 Sep 19.

Abstract

KEY POINTS

Diagnostic yield of genetic testing in adults with CKD is 40%. Risk factors including positive family history and extra-kidney features associate with higher diagnostic yield, although young age at testing did not. Seventeen percent of patients who received a genetic diagnosis were reclassified into a different phenotype after testing.

BACKGROUND

Clinical and pathological confirmation of the diagnosis for CKD has limitations, with up to one third of individuals remaining without a formal diagnosis. Increasingly, data suggest that these limitations can be overcome by genetic testing. The objective of this study was to estimate the diagnostic yield of genetic testing in adults with CKD.

METHODS

Cohort studies that report diagnostic yield of genetic testing in adults with CKD published in PubMed or Embase between January 1, 2005, and December 31, 2023, were included. The Joanna Briggs Institute critical appraisal tool for prevalence studies was used to assess bias. Duplicate independent data extraction and a meta-analysis of proportions using generalized linear mixed models were completed.

RESULTS

We included 60 studies with 10,107 adults with CKD who underwent genetic testing. We found a diagnostic yield of 40% (95% confidence interval, 33 to 46); yield varied by CKD subtype with the highest yield of 62% (95% confidence interval, 57 to 68) in cystic kidney disease. Positive family history and presence of extra-kidney features were associated with higher diagnostic yield. Reclassification of the before testing diagnosis after a positive genetic testing result occurred in 17% of the solved cohort. Six studies showed the clinical benefits of genetic testing including cascade testing for family members and treatment changes.

CONCLUSIONS

Overall, we show that genetic testing is informative in a high proportion of clinically selected adults with CKD. The study was limited by heterogeneity in reporting, testing technologies, and cohort characteristics.

CLINICAL TRIAL REGISTRY NAME AND REGISTRATION NUMBER

: International prospective register of systematic reviews (CRD42023386880).

摘要

要点

成年慢性肾脏病患者基因检测的诊断率为40%。包括家族史阳性和肾外特征在内的风险因素与较高的诊断率相关,不过检测时年龄较小者并非如此。17%接受基因诊断的患者在检测后被重新分类为不同的表型。

背景

慢性肾脏病诊断的临床和病理确认存在局限性,多达三分之一的个体仍未得到正式诊断。越来越多的数据表明,基因检测可以克服这些局限性。本研究的目的是评估成年慢性肾脏病患者基因检测的诊断率。

方法

纳入2005年1月1日至2023年12月31日期间发表在PubMed或Embase上、报告成年慢性肾脏病患者基因检测诊断率的队列研究。使用乔安娜·布里格斯研究所患病率研究的批判性评价工具来评估偏倚。完成了重复独立数据提取和使用广义线性混合模型的比例荟萃分析。

结果

我们纳入了60项研究,共10107名接受基因检测的成年慢性肾脏病患者。我们发现诊断率为40%(95%置信区间,33%至46%);诊断率因慢性肾脏病亚型而异,囊性肾病的诊断率最高,为62%(95%置信区间,57%至68%)。家族史阳性和存在肾外特征与较高的诊断率相关。在17%的已解决队列中,基因检测结果呈阳性后,检测前的诊断被重新分类。六项研究显示了基因检测的临床益处,包括对家庭成员的级联检测和治疗改变。

结论

总体而言,我们表明基因检测对很大一部分临床选择的成年慢性肾脏病患者具有参考价值。该研究受到报告、检测技术和队列特征异质性的限制。

临床试验注册名称和注册号

国际系统评价前瞻性注册库(CRD42023386880)。

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