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Family history of myocardial infarction increases risk of renal dysfunction in middle age

机译:心肌梗塞家族史增加中年人肾功能不全的风险

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Background/Aims: Chronic kidney disease (CKD) is common in the general population, may lead to end-stage renal disease, and is most frequently found among males. Familial clustering of kidney diseases has been observed. We aimed to study a potential association between the family history of myocardial infarction (MI) and renal dysfunction. Methods: 22,297 males and 10,828 females, aged 33-60 years, from a population-based cohort study were studied. Estimated glomerular filtration rate (eGFR) was assessed by the CKD-EPI creatinine equation. Every participant filled in a self-administered questionnaire including family history. Heredity for MI was defined as mother or father having had MI and/or died from MI, and/or brother or sister having had MI. Binary logistic regression and multiple linear regression were used in the analyses. Results: Multiple linear regression revealed a significantly increased risk of renal dysfunction in those with a positive heredity for MI (the whole cohort p = 0.01, males p = 0.000, females p = 0.169). Binary logistic regression showed that males with heredity for MI with a mean age of 43 years have a 2 times higher risk (p = 0.02) of belonging to the group with GFR 45 ml/min/1.73 m2 compared to those without heredity. For the whole cohort the increased risk was 1.6 times (p = 0.07). There was no significant association for females (p = 0.88). Conclusion: These findings demonstrate that a familial burden of MI is associated with renal dysfunction, in men, already in middle age. Genetic variants may underlie predisposition to CKD in those with heredity for MI.
机译:背景/目的:慢性肾脏病(CKD)在普通人群中很常见,可能导致晚期肾脏疾病,并且最常见于男性。已经观察到肾脏疾病的家族聚集。我们旨在研究心肌梗塞家族史与肾功能不全之间的潜在关联。方法:从一项基于人群的队列研究中,对22297例男性和10828例女性,年龄33-60岁进行了研究。通过CKD-EPI肌酐方程评估肾小球滤过率(eGFR)。每个参与者填写一份包括家族病史的自我管理调查表。 MI的遗传定义为患有MI和/或死于MI的母亲或父亲,和/或患有MI的兄弟或姐妹。在分析中使用二元逻辑回归和多元线性回归。结果:多元线性回归显示,MI阳性的人群肾功能异常的风险显着增加(整个队列p = 0.01,男性p = 0.000,女性p = 0.169)。二元logistic回归分析显示,平均年龄为43岁的有MI遗传的男性与没有遗传的男性相比,属于GFR <45 ml / min / 1.73 m2的男性的风险高(p = 0.02)2倍。对于整个队列,增加的风险是1.6倍(p = 0.07)。女性之间没有显着关联(p = 0.88)。结论:这些发现表明,已在中年的男性中,家族性MI负担与肾功能不全有关。遗传变异可能是患有MI遗传的人群中CKD易感性的基础。

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