摘要
应用聚合酶链反应(PCR)技术研究了84例动脉硬化性血栓性脑梗塞(ATCI)患者和107例正常人的载脂蛋白B(apoB)基因的XbaI、EcoRI位点的多态性。结果ATCI组X-频率(0.827)低于对照组(0.916),ATCI组X+X-基因型频率增高,与对照组比较有显著性差异,而且X+X-基因型与血脂水平增高有相关性。提示,apoB基因的XbaI多态及连锁失衡可能作为动脉粥样硬化的遗传背景影响血脂质代谢,并参与ATCI的发病机制。
The polymorphic sites of the apolipoproteinB gene(apoB),the XbaI,EcoRI sites was examined by the polymerase chain reaction(PCR) technique in a sample of 84 patients with atherothrombotic cerebral infarction(ATCI) and 107 healthy agematched controls.Allele frequencies were compared between cases and controls,and their impact on lipid matabolism was also studied.The frequencies of X-alleles in ATCI cases were found as 0.827,which was lower than 0.916 in controls,and the differencies reached significance.Futhermore,the frequencies of X+X-genotypes(0.345) in group of ATCI cases was higher than 0.168 in controls,and the X+X-genotype associated with higher levels of Tch,LDLch,apoB.The date suggested that the variation in linkage disequilibrium with the XbaI of the apoB gene as a genetic background of atherosclerosis,may have correletion with the determination of lipid and apoB,and may contributed to the development of ATCI.
出处
《临床神经病学杂志》
CAS
1998年第1期3-6,共4页
Journal of Clinical Neurology
基金
卫生部科研基金