Haerian Batoul Sadat, Sha'ari Hidayati Mohd, Fong Choong Yi, Tan Hui Jan, Wong Sau Wei, Ong Lai Choo, Raymond Azman Ali, Tan Chong Tin, Mohamed Zahurin
Pharmacogenomics Laboratory, Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Pharmacogenomics Laboratory, Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
J Neuroimmunol. 2015 Jan 15;278:137-43. doi: 10.1016/j.jneuroim.2014.12.016. Epub 2014 Dec 20.
Neuroinflammation can damage the brain and plays a critical role in the pathophysiology of epilepsy. Tissue inhibitor of metalloproteinase 4 (TIMP4) is an inflammation-induced apoptosis and matrix turnover factor involved in several neuronal disorders and inflammatory diseases. Evidence has shown linkage disequilibrium between rs3755724 (-55C/T) of this gene with synapsin 2 (SYN2) rs3773364 and peroxisome proliferator-activated G receptor (PPARG) rs2920502 loci, which contribute to epilepsy in Caucasians. The aim of this study was to examine the association of these loci alone or their haplotypes with the risk of epilepsy in the Malaysian population. Genomic DNA of 1241 Malaysian Chinese, Indian, and Malay subjects (670 patients with epilepsy and 571 healthy individuals) was genotyped for the candidate loci by using the Sequenom MassArray method. Allele and genotype association of rs3755724 with susceptibility to epilepsy was significant in the Malaysian Chinese with focal epilepsy under codominant and dominant models (C vs. T: 1.5 (1.1-2.0), p=0.02; CT vs. TT: 1.8 (1.2-2.8), p=0.007 and 1.8 (1.2-2.7), p=0.006, respectively). The T allele and the TT genotype were more common in patients than in controls. No significant association was found between rs2920502 and rs3773364-rs3755724-rs2920502 haplotypes for susceptibility to epilepsy in each ethnicity. This study provides evidence that the promoter TIMP4 rs3755724 is a new focal epilepsy susceptibility variant that is plausibly involved in inflammation-induced seizures in Malaysian Chinese.
神经炎症会损害大脑,并在癫痫的病理生理学中起关键作用。金属蛋白酶组织抑制剂4(TIMP4)是一种炎症诱导的凋亡和基质转换因子,参与多种神经元疾病和炎症性疾病。有证据表明,该基因的rs3755724(-55C/T)与突触结合蛋白2(SYN2)的rs3773364以及过氧化物酶体增殖物激活受体γ(PPARG)的rs2920502位点之间存在连锁不平衡,这些位点在高加索人中与癫痫有关。本研究的目的是检查这些位点单独或其单倍型与马来西亚人群癫痫风险的关联。采用Sequenom MassArray方法对1241名马来西亚华裔、印度裔和马来裔受试者(670例癫痫患者和571名健康个体)的基因组DNA进行候选位点基因分型。在共显性和显性模型下,rs3755724的等位基因和基因型与癫痫易感性的关联在患有局灶性癫痫的马来西亚华裔中具有显著性(C与T:1.5(1.1 - 2.0),p = 0.02;CT与TT:1.8(1.2 - 2.8),p = 0.007和1.8(1.2 - 2.7),p = 0.006)。T等位基因和TT基因型在患者中比在对照组中更常见。在每个种族中,rs2920502以及rs3773364 - rs3755724 - rs2920502单倍型与癫痫易感性之间未发现显著关联。本研究提供了证据表明,TIMP4启动子rs3755724是一个新的局灶性癫痫易感变异体,可能参与马来西亚华裔炎症诱导的癫痫发作。