Affiliation:
1. From the Department of Neurology (M.D.), Klinikum Groβhadern, München, Germany; and Clinical Neuroscience (H.S.M.), St. George’s Hospital Medical School, London, UK.
Abstract
Background and Purpose—
A large number of candidate gene association studies have attempted to identify genes implicated in stroke, but there have been few replicable and robust associations reported.
Summary of Review—
The skantness of replicable associations partly relates to poor study design. Important methodological considerations include adequate sample size, the selection of appropriate controls, careful clinical phenotyping using standardized classification systems, and determining associations with stroke subtypes as well as stroke as a whole. The use of intermediate phenotypes, particularly carotid intima-media thickness and MRI white matter hyperintensities, appears promising. It is essential that positive associations are replicated in independent populations, and appropriate methodology is used in such studies. To be of use for others, association studies should meet certain standards. In particular, genetic association studies should enable replication studies and meta-analyses.
Conclusions—
This article discusses key methodological aspects and suggests standard criteria for candidate gene studies in stroke.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)
Cited by
125 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献