CAJ | 학술논문

目的分析中国汉族人群Gs蛋白α亚基基因（GNAS1）T393C单核苷酸多态性（SNP）与非瓣膜性房颤是否存在相关性。方法分别选取非瓣膜性房颤患者90例及正常对照90例，采用PCR-RFLP分析非瓣膜性房颤患者GNAS1基因T393C等位基因型及等位基因频率分布特点，并通过研究其与心率变异性（HRV）的关系，从而分析GNAS1基因T393C位点与非瓣膜性房颤患者自主神经活动规律的关系。结果GNAS1基因T393C多态性等位基因型频率和等位基因频率在两组间比较具有显著性差异（P<0.01），CC基因型及T393C等位基因的频率在病例组中显著增高；pNN50、LF、LF/HF在不同基因型间差异有统计学意义（P<0.05）。结论GNAS1基因T393C SNP可能与中国汉族人群非瓣膜性房颤的发生有明显的相关性。
목적분석중국한족인군Gs단백α아기기인（GNAS1）T393C단핵감산다태성（SNP）여비판막성방전시부존재상관성。방법분별선취비판막성방전환자90례급정상대조90례，채용PCR-RFLP분석비판막성방전환자GNAS1기인T393C등위기인형급등위기인빈솔분포특점，병통과연구기여심솔변이성（HRV）적관계，종이분석GNAS1기인T393C위점여비판막성방전환자자주신경활동규률적관계。결과GNAS1기인T393C다태성등위기인형빈솔화등위기인빈솔재량조간비교구유현저성차이（P<0.01），CC기인형급T393C등위기인적빈솔재병례조중현저증고；pNN50、LF、LF/HF재불동기인형간차이유통계학의의（P<0.05）。결론GNAS1기인T393C SNP가능여중국한족인군비판막성방전적발생유명현적상관성。
Objective To analyze the association between T393C single nucleotide polymorphism (SNP) of GNAS1 gene and non-valvular atrial fibrillation (AF) in Chinese Han patients. Methods Ninety patients with non-valvular AF and 90 healthy subjects were examined for T393C SNP of GNAS1 gene using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The allele genotypes and the distribution of allele frequencies were analyzed and compared between the two groups. The relationship between allele frequency distribution characteristics and the heart rate variability (HRV) were also studied for analysis of the association between T393C SNP of GNAS1 gene and the autonomic nervous activation in non-valvular AF. Results The two groups showed a significant difference in the frequencies of genotypes of T393C SNP of GNAS1 gene and allele frequencies (P<0.01). CC genotype and T393C allele frequency were significantly increased in the case group. pNN50, LF, or LF/HF showed no significant difference between different genotypes (P<0.05). Conclusion The T393C SNP of GNAS1 gene is closely associated with non-valvular AF in Chinese Han patients.