Munshi Anjana, Das Satrupa, Kaul Subhash
Centre for Human Genetics, School of Health Sciences, Central University of Punjab, Bathinda, Punjab, India.
Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad 500016, India; Dr. NTR University of Health Sciences, Vijayawada, Andhra Pradesh, India.
Gene. 2015 Jan 25;555(2):250-9. doi: 10.1016/j.gene.2014.11.015. Epub 2014 Nov 12.
Stroke is a global health problem and a leading cause of disability worldwide. There have been numerable studies undertaking research on different aspects of ischaemic stroke employing various epidemiological, clinical and molecular parameters. Nevertheless ischaemic stroke being a complex disorder with different subtypes demands equal attention towards its subtypes too. Since there has been enough evidence that disposition to certain subtype is genetically determined and there is a distinct mechanism that influences its development, association studies should focus on subtypes simultaneously while studying specific genes. Data from such studies will thus provide better and intricate findings with regard to heterogenous ischaemic stroke. In the present review we discuss the genes studied by our group over a period of seven years in association with stroke subtypes in a South Indian population and correlate the findings with similar genetic studies from other populations so as to provide an overview of various genes involved in the pathogenesis of ischaemic stroke subtypes.
中风是一个全球性的健康问题,也是全球残疾的主要原因。已经有无数的研究采用各种流行病学、临床和分子参数对缺血性中风的不同方面进行研究。然而,缺血性中风作为一种具有不同亚型的复杂疾病,其亚型也需要同样的关注。由于有足够的证据表明,某些亚型的易感性是由基因决定的,并且存在影响其发展的独特机制,因此关联研究在研究特定基因时应同时关注亚型。这些研究的数据将因此提供关于异质性缺血性中风的更好和更复杂的发现。在本综述中,我们讨论了我们小组在七年时间里在南印度人群中与中风亚型相关研究的基因,并将这些发现与其他人群的类似基因研究进行关联,以便概述参与缺血性中风亚型发病机制的各种基因。