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遗传学主流化:英国遗传性心血管疾病临床服务的比较综述

Mainstreaming genetics: a comparative review of clinical services for inherited cardiovascular conditions in the UK.

作者信息

Burton Hilary, Alberg C, Stewart A

机构信息

Foundation for Genomics and Population Health, Cambridge, UK.

出版信息

Public Health Genomics. 2010;13(4):235-45. doi: 10.1159/000279625. Epub 2010 Apr 15.

DOI:10.1159/000279625
PMID:20395692
Abstract

Inherited cardiovascular conditions (ICCs) are a group of monogenic disorders caused by mutations in the components of the electrical and contractile system of the heart or its vasculature. ICCs include arrhythmias, cardiomyopathies, inherited arteriopathies such as Marfan syndrome, muscular dystrophies, and familial hypercholesterolaemia. Epidemiological data on ICCs are sparse but a survey of the available literature suggests that there are approximately 340,000 prevalent cases of these conditions in the UK (population 61 million). As a result of dramatic advances in understanding of the molecular pathology of ICCs, more than 50 ICCs have been recognised, and diagnostic genetic tests are increasingly available. As part of a needs assessment and review of provision of ICC services, a survey of all UK ICC services was undertaken focusing on both quantitative and qualitative aspects. Service provision was found to be highly inequitable, with typically a 10-20-fold variation in referral and genetic testing rates between different UK regions. Service levels per million population are much higher in London than in all but one of the regions. The review concluded that capacity of services is inadequate to meet current or future demand and many services lack the critical mass to provide the full range of services. Recommendations are made for the development of services appropriate for the future. Services should be led by cardiology but have close links with clinical genetics services, which should provide support with specialist genetics advice and cascade testing. Finally, the international relevance of this review is considered.

摘要

遗传性心血管疾病(ICCs)是一组单基因疾病,由心脏或其脉管系统的电传导和收缩系统成分的突变引起。ICCs包括心律失常、心肌病、遗传性动脉病(如马凡综合征)、肌肉萎缩症和家族性高胆固醇血症。关于ICCs的流行病学数据稀少,但对现有文献的一项调查表明,在英国(人口6100万)约有34万例这些疾病的流行病例。由于对ICCs分子病理学的理解取得了巨大进展,已识别出50多种ICCs,并且诊断性基因检测越来越普及。作为对ICCs服务提供情况进行需求评估和审查的一部分,对英国所有ICCs服务进行了一项调查,重点关注定量和定性方面。结果发现服务提供极不均衡,英国不同地区之间的转诊率和基因检测率通常相差10至20倍。伦敦每百万人口的服务水平比除一个地区外的所有其他地区都高得多。审查得出结论,服务能力不足以满足当前或未来的需求,许多服务缺乏提供全方位服务的规模。针对未来适合的服务发展提出了建议。服务应由心脏病学主导,但应与临床遗传学服务密切联系,临床遗传学服务应提供专业遗传学建议和级联检测方面的支持。最后,考虑了本审查的国际相关性。

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