Northwestern University Feinberg School of Medicine, Chicago, USA.
Eur J Prev Cardiol. 2014 May;21(5):601-7. doi: 10.1177/2047487312462801. Epub 2012 Oct 1.
It is unclear if associations between a parental history of premature CVD (pCVD) and subclinical atherosclerosis are attenuated by adjustment for long-term risk factor levels through middle adulthood.
Prospective community-based cohort study.
CARDIA participants who attended the year-20 exam (n = 2283, mean age 45 years) were grouped by pCVD status: maternal only, paternal only, any parental, and no parental history (referent). We used separate logistic regression models, adjusted for average risk factor levels over a 20-year follow up to assess associations of parental pCVD and subclinical atherosclerosis in offspring.
White participants with any parental history of pCVD had a higher odds of coronary artery calcium (CAC) >0 than participants with no parental history (OR 1.55, 95% CI 1.01-2.37). This was largely driven by the association of a paternal history of pCVD with CAC >0 (OR 2.15, 95% CI 1.42-3.23), which was minimally attenuated by multivariable adjustment (OR 2.09, 95% CI 1.31-3.32). Similarly, adjusted associations between parental pCVD and intima-media thickness (IMT) >90% were observed in white participants with a paternal history of pCVD (OR 1.93, 95% CI 1.10-3.39) and any parental history pCVD (OR 1.67, 95% CI 1.02-2.74). No significant associations between a parental history of pCVD and the odds of subclinical atherosclerosis were observed in black participants.
Parental pCVD is independently associated with early development of subclinical atherosclerosis; these associations may be race-specific for participants in their fifth decade of life.
目前尚不清楚,如果通过中年时期的长期风险因素水平调整,父母早发心血管疾病(pCVD)史与亚临床动脉粥样硬化之间的关联是否会减弱。
前瞻性社区为基础的队列研究。
参加 20 年检查的 CARDIA 参与者(n = 2283,平均年龄 45 岁)按 pCVD 状态分组:母亲仅、父亲仅、任何父母史和无父母史(参照)。我们使用单独的逻辑回归模型,根据 20 年随访期间的平均风险因素水平进行调整,以评估父母 pCVD 和后代亚临床动脉粥样硬化之间的关联。
有任何父母 pCVD 史的白人参与者的冠状动脉钙(CAC)>0 的几率高于无父母史的参与者(OR 1.55,95%CI 1.01-2.37)。这主要是由于 pCVD 父系史与 CAC>0(OR 2.15,95%CI 1.42-3.23)之间的关联所致,这种关联在多变量调整后略有减弱(OR 2.09,95%CI 1.31-3.32)。同样,在有 pCVD 父系史的白人参与者(OR 1.93,95%CI 1.10-3.39)和任何父母史 pCVD(OR 1.67,95%CI 1.02-2.74)中,也观察到了父母 pCVD 与内膜中层厚度(IMT)>90%之间的调整后关联。在黑人参与者中,父母 pCVD 史与亚临床动脉粥样硬化的几率之间没有显著关联。
父母 pCVD 与亚临床动脉粥样硬化的早期发展独立相关;这些关联对于 50 多岁的参与者来说可能是种族特异性的。