摘要
应用聚合酶链反应(PCR),检测了106例正常汉族人及33例缺血性脑血管病(ICVD)病人的apoB基因xbaⅠ酶切位点限制性片段长度多态性(RFLPs)及其与血脂的关系。结果表明,ICVDtaxbaⅠ酶切位,走上x+的等位基因频率明显高于正常对照组(P<0.005);LVD组中具X+X-基因型者的血浆HDL-C较X-X-基因型者明显降低(P<0.05),而TC明显增高(P<0.05)。提示apoB基因多态分析结合血浆脂蛋白测定更能有效地检测ICVD易患人群。
estrictive fragment length Polymorphisms(RFLPs)of the apolipoprotein B(apoB)gene-xba Iwas examined in a sample of 33 patients with ischaemic cerebrovascular disease(ICVD)and 106 heaIthyindividuals.The relation between xba I RFLPs of apoB gene and plasma lipid level was also studied.It was demonstrated that the frequency of X+ llele gene(presence of xba I cutting site)was signifli-cantly higher in ICVD patients than that in controls. The patienls with genotype·of X+ X- had signifi-cantly lower HDL-C level and higher TC level than those with genotype of X- X- in the ICVD group.The results indicate that RFLPs of apoB gene and plasma lipid levels analysis are of great importance indetermining risk factors of ICVD;
出处
《中国医科大学学报》
CAS
CSCD
1996年第3期299-301,共3页
Journal of China Medical University
关键词
缺血性脑血管病
多态性
载脂蛋白
基因多态性
ischaemic cerebrovasuclar disease
gene
restrictine fragment length polymorphisms