内蒙古医科大学学报
內矇古醫科大學學報
내몽고의과대학학보
Journal of Inner Mongolia Medical University
2014年
3期
226-229,234
,共5页
周静%莫殿军%孙文阁%牛丽丽
週靜%莫殿軍%孫文閣%牛麗麗
주정%막전군%손문각%우려려
载脂蛋白(a)%五核苷酸重复序列%蒙古族%冠心病%脂蛋白(a)
載脂蛋白(a)%五覈苷痠重複序列%矇古族%冠心病%脂蛋白(a)
재지단백(a)%오핵감산중복서렬%몽고족%관심병%지단백(a)
apolipoprotein(a)%pentanucleotide repeat%CHD%Mongolian%lipoprotein(a)
目的:研究载脂蛋白(a)5忆调控区(TTTTA)n五核苷酸重复序列(PNR)基因多态性在内蒙古地区蒙古族健康人群及冠心病( CHD)病人中的分布特点。方法:采用PCR-聚丙烯酰胺凝胶电泳方法检测66例蒙古族健康人群及71例蒙古族冠心病病人的apo( a)的PNR基因多态性。结果:冠心病病人血浆Lp( a)、TG水平高于正常对照组,而HDL-C水平则低于正常对照组;冠心病病人组检测出( TTTTA)序列重复次数为5、8、9共3种等位基因,并检测出5/8、5/9、8/8、8/9、9/9共5种基因型。正常对照组检测出( TTTTA)序列重复次数为5、7、8、9共4种等位基因,检测出5/8、5/5、7/9、8/8、8/9、9/9共6种基因型。两组人群均以重复次数为8和基因型8/8分布频率最高;冠心病病人与正常对照apo( a) PNR比较发现各等位基因及基因型频率间均无显著性差异;冠心病病人基因型8/8与8/9间的血浆脂蛋白( a)水平比较无显著性差异。结论:蒙古族人群apo( a) PNR基因多态性可能与冠心病发生的不存在直接的相关性。
目的:研究載脂蛋白(a)5憶調控區(TTTTA)n五覈苷痠重複序列(PNR)基因多態性在內矇古地區矇古族健康人群及冠心病( CHD)病人中的分佈特點。方法:採用PCR-聚丙烯酰胺凝膠電泳方法檢測66例矇古族健康人群及71例矇古族冠心病病人的apo( a)的PNR基因多態性。結果:冠心病病人血漿Lp( a)、TG水平高于正常對照組,而HDL-C水平則低于正常對照組;冠心病病人組檢測齣( TTTTA)序列重複次數為5、8、9共3種等位基因,併檢測齣5/8、5/9、8/8、8/9、9/9共5種基因型。正常對照組檢測齣( TTTTA)序列重複次數為5、7、8、9共4種等位基因,檢測齣5/8、5/5、7/9、8/8、8/9、9/9共6種基因型。兩組人群均以重複次數為8和基因型8/8分佈頻率最高;冠心病病人與正常對照apo( a) PNR比較髮現各等位基因及基因型頻率間均無顯著性差異;冠心病病人基因型8/8與8/9間的血漿脂蛋白( a)水平比較無顯著性差異。結論:矇古族人群apo( a) PNR基因多態性可能與冠心病髮生的不存在直接的相關性。
목적:연구재지단백(a)5억조공구(TTTTA)n오핵감산중복서렬(PNR)기인다태성재내몽고지구몽고족건강인군급관심병( CHD)병인중적분포특점。방법:채용PCR-취병희선알응효전영방법검측66례몽고족건강인군급71례몽고족관심병병인적apo( a)적PNR기인다태성。결과:관심병병인혈장Lp( a)、TG수평고우정상대조조,이HDL-C수평칙저우정상대조조;관심병병인조검측출( TTTTA)서렬중복차수위5、8、9공3충등위기인,병검측출5/8、5/9、8/8、8/9、9/9공5충기인형。정상대조조검측출( TTTTA)서렬중복차수위5、7、8、9공4충등위기인,검측출5/8、5/5、7/9、8/8、8/9、9/9공6충기인형。량조인군균이중복차수위8화기인형8/8분포빈솔최고;관심병병인여정상대조apo( a) PNR비교발현각등위기인급기인형빈솔간균무현저성차이;관심병병인기인형8/8여8/9간적혈장지단백( a)수평비교무현저성차이。결론:몽고족인군apo( a) PNR기인다태성가능여관심병발생적불존재직접적상관성。
Objective:To investigate the relationship between pentanucleotide repeat ( PNR ) polymorphism of apolipoprotein(a)gene and Mongolian coronary heart disease(CHD). Methods:PNR polymorphism of the apo( a) gene from 66 controls and 71 patients of CHD were analyzed by polymerase chain reaction( PCR)-polyacrylamide gel electrophoresis-silver stain. Results:The concentrations of Lp( a) ,TG in CHD patients were elevated in comparison with that in normal subjects,however,HDL-C was decreased;There were 3 alleles, which were 5,8 and 9 repeats in CHD patients. Moreover, we detected 5 apo(a)PNR genetypes,which were 5/8,5/9,8/8,8/9,9/9 In control group,4 alleles were detected,namely,5,7,8,9. At the same time,we found 6 genetypes,they were 5/8,5/5,7/9,8/8,8/9,9/9. Among them,8 repeats and genetypes 8/8 were the most frequency distributions;The frequency of apo( a) PNR alleles and genetypes had no significant difference between CHD patients and controls.Conclusion:Apo( a) PNR polymorphism had no direct relationship with CHD in Mongolian.