Uni-leaflet mitral valve in adults: a systematic review of case reports and case series.

IF 1.1 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Future cardiology Pub Date : 2026-05-01 Epub Date: 2026-04-16 DOI:10.1080/14796678.2026.2659088
Martina Mookadam, Safiyya A Mookadam, Michael Morris, Sandip Pradhan, Farouk Mookadam
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引用次数: 0

Abstract

Introduction: Uni-leaflet mitral valve (ULMV) is a rare congenital anomaly historically considered incompatible with long-term survival, yet increasing reports describe diagnosis in adulthood. We conducted a systematic review to characterize clinical presentation, anatomy, imaging findings, management, and outcomes in adults with ULMV.

Methods: Following PRISMA guidelines, major databases were searched from 1960 through January 2024. Eligible studies reported adult patients with confirmed ULMV. Data were extracted on demographics, valve morphology, symptoms, associated anomalies, imaging modalities, interventions, and outcomes.

Results: Thirty-six publications comprising 40 adult patients met inclusion criteria. Mean age at diagnosis was 50.5 years, with female predominance. Posterior leaflet hypoplasia or agenesis accounted for 97.5% of cases. Most patients were symptomatic, commonly with dyspnea or heart failure, and over half had moderate or greater mitral regurgitation. Atrial fibrillation, atrial septal defects, and aortic valve abnormalities were frequent comorbidities. Transthoracic echocardiography was used universally, with transesophageal and three-dimensional imaging providing incremental anatomical detail. Approximately one-third underwent mitral valve repair or replacement, with generally favorable outcomes.

Conclusions: Adult ULMV demonstrates marked clinical and anatomical heterogeneity and may represent a developmental spectrum rather than a single entity. Standardized definitions and prospective registries are needed to improve risk stratification and guide management.

Protocol registration: http://www.crd.york.ac.uk/prospero identifier is CRD420251083213.

成人单叶二尖瓣:病例报告和病例系列的系统回顾。
单叶二尖瓣(ULMV)是一种罕见的先天性异常,历来被认为与长期生存不相容,但越来越多的报道描述了成年期的诊断。我们对成人ULMV的临床表现、解剖、影像学表现、治疗和结局进行了系统回顾。方法:根据PRISMA指南,检索1960年至2024年1月期间的主要数据库。符合条件的研究报告了确诊ULMV的成年患者。我们提取了人口统计学、瓣膜形态、症状、相关异常、成像方式、干预措施和结果方面的数据。结果:36篇出版物包括40例成人患者符合纳入标准。平均诊断年龄50.5岁,以女性为主。后小叶发育不全占97.5%。大多数患者有症状,通常有呼吸困难或心力衰竭,一半以上有中度或更严重的二尖瓣反流。房颤、房间隔缺损和主动脉瓣异常是常见的合并症。经胸超声心动图普遍使用,经食管和三维成像提供了更多的解剖细节。大约三分之一的患者接受了二尖瓣修复或置换术,总体效果良好。结论:成人ULMV表现出明显的临床和解剖学异质性,可能代表了一个发育谱系,而不是单一的实体。需要标准化定义和前瞻性登记来改进风险分层和指导管理。协议注册:http://www.crd.york.ac.uk/prospero标识为CRD420251083213。
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来源期刊
Future cardiology
Future cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.80
自引率
5.90%
发文量
87
期刊介绍: Research advances have contributed to improved outcomes across all specialties, but the rate of advancement in cardiology has been exceptional. Concurrently, the population of patients with cardiac conditions continues to grow and greater public awareness has increased patients" expectations of new drugs and devices. Future Cardiology (ISSN 1479-6678) reflects this new era of cardiology and highlights the new molecular approach to advancing cardiovascular therapy. Coverage will also reflect the major technological advances in bioengineering in cardiology in terms of advanced and robust devices, miniaturization, imaging, system modeling and information management issues.
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