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老年非瓣膜性心房颤动患者血清Ⅰ型及Ⅲ型前胶原肽及血管紧张素转换酶基因多态性
引用本文:魏玲,孙林辉,李丽娟,刘斌,卢国良,张筱军,张亚林,杨晓华,刘绍华.老年非瓣膜性心房颤动患者血清Ⅰ型及Ⅲ型前胶原肽及血管紧张素转换酶基因多态性[J].中国心脏起搏与心电生理杂志,2008,22(4).
作者姓名:魏玲  孙林辉  李丽娟  刘斌  卢国良  张筱军  张亚林  杨晓华  刘绍华
作者单位:成都军区昆明总医院地方干部病房,云南昆明,650032
摘    要:目的探讨心肌纤维化与老年非瓣膜性心房颤动(简称房颤)的相关性及血管紧张素转换酶(ACE)基因插入/缺失多态性与心肌纤维化的关系。方法50例老年房颤患者及43例非房颤患者。用酶联免疫反应(ELISA)法测定心肌纤维化的指标Ⅰ型前胶原羧基端肽(PⅠP)、Ⅲ型前胶原氨基端肽(PⅢP)。用聚合酶链式反应(PCR)的方法检测ACE基因插入(I)/缺失(D)多态性、并比较不同基因型、不同等位基因的分布及其与PⅠP和PⅢP的关系。结果房颤组血清PⅠP、PⅢP水平均显著高于对照组(P<0.05)。其中房颤合并左室肥厚(LVH)较不合并LVH组PⅠP、PⅢP增高(P<0.05)。房颤合并左房扩大较不合并左房扩大组PⅠP、PⅢP高,但尚无统计学差异(P>0.05)。房颤组与对照组ACEI/D多态性缺失纯合型(DD型)、杂合子(DI型)、插入纯合型(Ⅱ型)基因型频率分别为32%,42%,26%和18.6%,42.2%,37.2%;D等位基因分布频率房颤组较对照组高(P<0.05);DD基因型PⅠP、PⅢP浓度高于DI型和Ⅱ型(P<0.05)。结论老年非瓣膜性房颤患者心肌纤维化指标显著升高;并与房颤伴LVH及左房扩大有关;ACEDD基因型可能是心肌纤维化及心脏重构的危险因素。

关 键 词:心血管病学  心房颤动  心房结构重构  ACE基因插入/缺失多态性  心肌纤维化

The association of polymorphisms in the angiotensin-converting enzyme insertion/deletion gene with nonvulvular atrial fibrillation
WEI Ling,SUN Lin-hui,LI Li-juan,LIU Bin,LU Guo-liang,ZANG Xiao-jun,ZHANG Ya-lin,YANG Xiao-hua,LIU Shao-hua.The association of polymorphisms in the angiotensin-converting enzyme insertion/deletion gene with nonvulvular atrial fibrillation[J].Chinese Journal of Cardiac Pacing and Electrophysiology,2008,22(4).
Authors:WEI Ling  SUN Lin-hui  LI Li-juan  LIU Bin  LU Guo-liang  ZANG Xiao-jun  ZHANG Ya-lin  YANG Xiao-hua  LIU Shao-hua
Abstract:Objective To explore the molecular mechanism of atrial fibrillation(AF) by investigating the effects of angiotensin-converting enzyme(ACE) insertion/deletion(I/D) gene polymorphisms in the structural remodeling of atrial myocardium. Methods Fifty patients with AF and 43 non-AF subjects were enrolled. The genotypes of ACE(I/D) gene were identified by polymerase chain reaction (PCR) and PCR-restricted fragment length polymorphism assay (RFLP-PCR). The serum concentration of carboxytermina propeptide of type I procollagen and aminotermianl propeptiden of type Ⅲ procollage were measured by ELISA. Result The frequency of the DD, ID,Ⅱ genotype of ACE in AF group and control group was 32%,42%,26%,and 18.6%,42.2%,37.2% respectively; Allele D genotype frequency was significantly different between AF and controls(P<0.05).The serum concentrations of PⅠP and PIIIP in AF group were higher than that in control group(P<0.05),and were also higher in DD genotype patients than that in DI genotype and IIgenotype(P<0.05); Conclusions The allele D may be the risk factor for AF. The DD genotype of ACE may have significant relationship with the structural remodeling of atrial myocardium.
Keywords:Cardiology  Atrial fibrillation  The structural remodeling of atrial myocardium  Angiotensin-concerting enzyme insertion/deletion genetic polymorphism  Atrial myocardium fibrosis
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