COL4A1和COL4A2变体的多器官表现及临床管理方案建议。

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY
Simone Gasparini, Simona Balestrini, Luigi Francesco Saccaro, Giacomo Bacci, Giorgia Panichella, Martino Montomoli, Gaetano Cantalupo, Stefania Bigoni, Giorgia Mancano, Simona Pellacani, Vincenzo Leuzzi, Nila Volpi, Francesco Mari, Federico Melani, Mara Cavallin, Tiziana Pisano, Giulio Porcedda, Augusto Vaglio, Davide Mei, Carmen Barba, Elena Parrini, Renzo Guerrini
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引用次数: 0

摘要

COL4A1/2 变异与多器官表现的高度可变性有关。描述 COL4A1/2 相关表现的整个临床谱具有挑战性,而且在管理和预防策略方面尚未达成共识。在对目前有关 COL4A1/2 相关疾病的证据进行系统回顾的基础上,我们编制了一份临床问卷,并对来自 23 个不同家族的 43 名携带致病变异体的患者进行了问卷调查。在这个队列中,我们将眼科和心脏科检查扩大到了无症状者和仅有一般人群中常见的有限或轻微、通常为非特异性临床症状的人(即少症状者)。文献综述和问卷调查中最常见的临床发现包括中风(203/685,29.6%)、癫痫发作或癫痫(199/685,29.0%)、智力障碍或发育迟缓(168/685,24.白内障(124/685,18.1%)、血尿(63/685,9.2%)和视网膜动脉迂曲(58/685,8.5%)。在少症状和无症状的携带者中,眼科检查发现了视网膜血管迂曲(5/13,38.5%)、前节发育不良(4/13,30.8%)和白内障(2/13,15.4%),而心脏检查除1/8(12.5%)人有轻度升主动脉异位外,其余均无异常。我们的多模式方法证实,COL4A1/2相关疾病的渗透性和表现性差异很大,甚至在家庭内部也是如此,神经系统受累是儿童和成人中最常见、最严重的病变。我们提出了基于个体化风险评估和定期多器官评估的预防和管理方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiorgan manifestations of COL4A1 and COL4A2 variants and proposal for a clinical management protocol.

COL4A1/2 variants are associated with highly variable multiorgan manifestations. Depicting the whole clinical spectrum of COL4A1/2-related manifestations is challenging, and there is no consensus on management and preventative strategies. Based on a systematic review of current evidence on COL4A1/2-related disease, we developed a clinical questionnaire that we administered to 43 individuals from 23 distinct families carrying pathogenic variants. In this cohort, we extended ophthalmological and cardiological examinations to asymptomatic individuals and those with only limited or mild, often nonspecific, clinical signs commonly occurring in the general population (i.e., oligosymptomatic). The most frequent clinical findings emerging from both the literature review and the questionnaire included stroke (203/685, 29.6%), seizures or epilepsy (199/685, 29.0%), intellectual disability or developmental delay (168/685, 24.5%), porencephaly/schizencephaly (168/685, 24.5%), motor impairment (162/685, 23.6%), cataract (124/685, 18.1%), hematuria (63/685, 9.2%), and retinal arterial tortuosity (58/685, 8.5%). In oligosymptomatic and asymptomatic carriers, ophthalmological investigations detected retinal vascular tortuosity (5/13, 38.5%), dysgenesis of the anterior segment (4/13, 30.8%), and cataract (2/13, 15.4%), while cardiological investigations were unremarkable except for mild ascending aortic ectasia in 1/8 (12.5%). Our multimodal approach confirms highly variable penetrance and expressivity in COL4A1/2-related conditions, even at the intrafamilial level with neurological involvement being the most frequent and severe finding in both children and adults. We propose a protocol for prevention and management based on individualized risk estimation and periodic multiorgan evaluations.

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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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