Non-Coding RNA Biomarkers in Male Infertility: From Discovery to Clinical Actionability-A Narrative Review.

IF 3.1 3区 生物学 Q2 GENETICS & HEREDITY
Genes Pub Date : 2026-09-06 DOI:10.3390/genes17091074
Aris Kaltsas, Eleftheria Markou, Athanasios Zachariou, Fotios Dimitriadis, Nikolaos Sofikitis
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引用次数: 0

Abstract

Non-coding RNAs (ncRNAs) are biologically plausible biomarkers in male infertility, but no assay is ready for routine use. This narrative review organizes human evidence by intended clinical decision and defines clinical actionability as a test's ability to inform a specified decision through analytical reliability, clinical validity, incremental value, decision-level benefit, and feasible implementation. Evidence is most developed for obstructive versus non-obstructive azoospermia (NOA) classification and sperm-retrieval prognosis. Most reports, however, use selected case-control samples, single-center development cohorts, or same-program evaluations. Mixed biospecimens, incompletely specified RNA isoforms and normalization, uncertain cohort independence, imperfect diagnostic references, and protocol-dependent retrieval outcomes limit transportability. No independent geographic validation of a locked ncRNA assay or prospective evaluation of ncRNA-guided management was identified within the retrieved sources. Current guidelines do not recommend routine ncRNA testing. Progress requires prespecified intended uses, locked assays, representative multicenter validation, same-patient comparison with contemporary care, calibrated risk estimates, decision-curve analysis, and patient-important, couple-centered outcomes.

男性不育症的非编码RNA生物标志物:从发现到临床可操作性
非编码rna (ncRNAs)是男性不育症生物学上可信的生物标志物,但目前还没有准备好常规使用的检测方法。这篇叙述性综述通过预期的临床决策来组织人类证据,并将临床可操作性定义为一项测试通过分析可靠性、临床有效性、增量价值、决策层面效益和可行实施来为特定决策提供信息的能力。梗阻性与非梗阻性无精子症(NOA)的分类和精子恢复预后的证据最为发达。然而,大多数报告使用选定的病例对照样本、单中心发展队列或同一项目评估。混合的生物标本、不完全指定的RNA异构体和标准化、不确定的队列独立性、不完善的诊断参考和依赖于方案的检索结果限制了可移植性。在检索到的来源中,没有确定锁定ncRNA检测的独立地理验证或ncRNA引导管理的前瞻性评估。目前的指南不推荐常规的ncRNA检测。进展需要预先指定的预期用途、锁定的检测、具有代表性的多中心验证、同患者与当代护理的比较、校准的风险估计、决策曲线分析以及患者重要的、以夫妇为中心的结果。
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来源期刊
Genes
Genes GENETICS & HEREDITY-
CiteScore
5.20
自引率
5.70%
发文量
1975
审稿时长
22.94 days
期刊介绍: Genes (ISSN 2073-4425) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to genes, genetics and genomics. It publishes reviews, research articles, communications and technical notes. There is no restriction on the length of the papers and we encourage scientists to publish their results in as much detail as possible.
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