Nakayama Tomohiro, Asai Satoshi, Sato Naoyuki, Soma Masayoshi
Department of Advanced Medical Science, Nihon University School of Medicine, Ooyaguchi-kamimachi, 30-1 Itabashi-ku, Tokyo 173-8610, Japan.
Curr Med Chem. 2007;14(30):3171-8. doi: 10.2174/092986707782793871.
Stroke is thought to be a multifactorial disease that is affected by several environmental factors and genetic variants. In 2002, a candidate locus for stroke (STRK1) was identified with a significant logarithm of odds (LOD) score at 5q12 in Caucasians, and in 2003, the PDE4D gene was subsequently identified as a susceptibility gene at this locus. Some investigators have recently examined whether polymorphisms in the PDE4D gene are associated with stroke in population studies. Some of these studies have reported the polymorphisms to be associated with a risk of stroke, while others have reported the exact opposite. These discrepancies have been attributed to racial differences or differences in methodologies and analyses. In 2006, a powerful method for isolating the susceptibility region at 5q12 was reported in a haplotype-based case-control study. In the present paper, we review both current issues and progress in the isolation of susceptibility genes for ischemic stroke, with particular emphasis on the PDE4D gene in the STRK1 region of 5q12.
中风被认为是一种多因素疾病,受多种环境因素和基因变异影响。2002年,在白种人中,一个中风候选基因座(STRK1)在5q12被鉴定出具有显著的优势对数(LOD)分数,2003年,PDE4D基因随后被确定为该基因座的一个易感基因。最近,一些研究人员在人群研究中检验了PDE4D基因的多态性是否与中风相关。其中一些研究报告这些多态性与中风风险相关,而另一些研究则得出了相反的结论。这些差异归因于种族差异或方法和分析的不同。2006年,在一项基于单倍型的病例对照研究中报告了一种在5q12分离易感区域的有效方法。在本文中,我们综述了缺血性中风易感基因分离方面的当前问题和进展,特别强调了5q12的STRK1区域中的PDE4D基因。