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作 者:陈能[1] 吴淑群[1] 张水堂[1] 刘仲熊[1] 田鸾英[1]
机构地区:[1]湖北医科大学附一院儿科
出 处:《中华医学遗传学杂志》1997年第6期358-361,共4页Chinese Journal of Medical Genetics
摘 要:为探讨apoB基因XbaⅠ多态性与新生儿、载脂蛋白水平的关系。应用多聚酶链反应(PCR)研究了31例有冠心病家族史(观察组)、92例无冠心病家族史(对照组)足月健康新生儿载脂蛋白B(apoB)基因XbaⅠ酶切位点的限制性片段长度多态性(RFLP)及其与血脂的关系。结果显示:两组间少见的X+等位基因频率无显著性差异,但具有X+X-基因型者,HDL-C水平低于X-X-基因型者(P<0.05),观察组与对照组血脂比较,前者apoB水平升高(P<0.01)。说明:X+等位基因与血脂改变有关,它是心血管疾病的一个危险因素,具有冠心病家族史及X+基因型的新生儿较其它新生儿更易罹患心血管疾病。Using the polymerase chain reaction(PCR),We studied the relation between the apolipoprotein B(apo B) gene XbaⅠpolymorphism and serum lipid,apolipoprotein levels in 31 healthy newborns with a grandparental history of coronary heart disease,92 newborns without such a history.The results showed that no significant difference was noted between the two groups in the frequency of rare X+ allele,but X+X- genotype was associated with lower level of HDLC,compared with X-X- genotype (P<005).The level of apo B in the group with coronary heart disease family history was significantly higher than that in the group without such a history (P<0001) The study demonstrates that X+ allele as one of the risk factors is associated with the change of serum lipid.Newborns who have cardiovascular disease family history and X+ allele are more liable to cardiovascular disease.
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