Ingelsson Erik, Bennet Louise, Ridderstråle Martin, Söderström Marianne, Råstam Lennart, Lindblad Ulf
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
BMC Cardiovasc Disord. 2008 Dec 11;8:37. doi: 10.1186/1471-2261-8-37.
The Gly482Ser polymorphism in peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PPARGC1A) has been demonstrated to be associated with diabetes, obesity and hypertension, all of which are important risk factors for left ventricular diastolic dysfunction.
The PPARGC1A Gly482Ser polymorphism was genotyped in a community-based cohort of 499 men and 533 women, who also underwent an echocardiographic examination to determine their left ventricular diastolic function. The association between the polymorphism and the presence of diastolic dysfunction was evaluated using logistic regression models.
The Ser allele of the PPARGC1A Gly482Ser polymorphism was significantly associated with a lower risk of diastolic dysfunction in men, but not in women. In a model adjusting for potential confounders (age, body mass index, leisure time physical activity, hypertension and diabetes) the results were still significant and substantial (odds ratio 0.13, 95% confidence interval 0.03-0.54, p for trend = 0.004). The results were consistent in a series of models, and they imply a multiplicative, protective effect of the Ser allele, with lower risk of diastolic dysfunction for each copy of the allele.
The Ser allele of the PPARGC1A Gly482Ser polymorphism was associated with decreased risk of diastolic left ventricular dysfunction in men, but not in women, in our large community-based sample. It was associated with a substantially decreased risk, even after adjustment for potential confounders. The clinical importance of the findings has to be established in further studies.
过氧化物酶体增殖物激活受体γ辅激活因子-1α(PPARGC1A)基因的Gly482Ser多态性已被证明与糖尿病、肥胖和高血压相关,而这些都是左心室舒张功能障碍的重要危险因素。
对一个基于社区的队列中的499名男性和533名女性进行PPARGC1A Gly482Ser多态性基因分型,这些人还接受了超声心动图检查以确定其左心室舒张功能。使用逻辑回归模型评估该多态性与舒张功能障碍存在之间的关联。
PPARGC1A Gly482Ser多态性的Ser等位基因与男性舒张功能障碍风险较低显著相关,但与女性无关。在调整了潜在混杂因素(年龄、体重指数、休闲时间体力活动、高血压和糖尿病)的模型中,结果仍然显著且具有实质性意义(优势比0.13,95%置信区间0.03 - 0.54,趋势p值 = 0.004)。在一系列模型中结果一致,这意味着Ser等位基因具有相乘的保护作用,每一份该等位基因可降低舒张功能障碍的风险。
在我们这个基于社区的大样本中,PPARGC1A Gly482Ser多态性的Ser等位基因与男性左心室舒张功能障碍风险降低相关,但与女性无关。即使在调整潜在混杂因素后,它仍与风险大幅降低相关。这些发现的临床重要性有待进一步研究确定。