Department of Neurology The Johns Hopkins University School of Medicine Baltimore MD.
Division of Epidemiology and Community Health, School of Public Health University of Minnesota Minneapolis MN.
J Am Heart Assoc. 2022 Aug 16;11(16):e025646. doi: 10.1161/JAHA.121.025646. Epub 2022 Aug 10.
Background The contribution of atrial cardiopathy to dementia risk is uncharacterized. We aimed to evaluate the association of atrial cardiopathy with incident dementia and potential mediation by atrial fibrillation (AF) and stroke. Methods and Results We conducted a prospective cohort analysis of participants in the ARIC (Atherosclerosis Risk in Communities) study attending visit 5 (2011-2013). We used Cox regression to determine the association between atrial cardiopathy and risk of dementia. Structural equation modeling methods were used to determine potential mediation by AF and/or stroke. Atrial cardiopathy was defined if ≥1 of the following at visit 5: P-wave terminal force >5000 mV·ms in ECG lead V1, NT-proBNP (N-terminal pro-brain natriuretic peptide) >250 pg/mL or left atrial volume index ≥34 mL/m by transthoracic echocardiography. We repeated our analysis necessitating ≥2 markers to define atrial cardiopathy. The prevalence of atrial cardiopathy was 34% in the 5078 participants (mean age 75 years, 59% female, 21% Black adults), with 763 participants developing dementia. Atrial cardiopathy was significantly associated with dementia (adjusted HR, 1.35 [95% CI, 1.16-1.58]), with strengthening of the effect estimate when necessitating ≥2 biomarkers (adjusted HR, 1.54 [95% CI, 1.25-1.89]). There was an increased risk of dementia among those with atrial cardiopathy when excluding those with AF (adjusted HR, 1.31 [95% CI, 1.12-1.55]) or stroke (adjusted HR, 1.28 [95% CI, 1.09-1.52]). The proportion of the effect mediated by AF was 4% (=0.005), and 9% was mediated by stroke (=0.048). Conclusions Atrial cardiopathy was significantly associated with an increased risk of dementia, with only a small percent mediation of the effect by AF or stroke.
心房心脏病对痴呆风险的影响尚不清楚。我们旨在评估心房心脏病与痴呆症发病的相关性,并探讨心房颤动(AF)和中风的潜在中介作用。
我们对参加 ARIC(社区动脉粥样硬化风险)研究的参与者进行了前瞻性队列分析,该研究在第 5 次访视(2011-2013 年)中进行。我们使用 Cox 回归来确定心房心脏病与痴呆风险之间的关联。结构方程模型方法用于确定 AF 和/或中风的潜在中介作用。如果在第 5 次访视时满足以下 1 种或多种标准,则定义为心房cardiopathy:心电图 V1 导联 P 波终末力>5000 mV·ms,NT-proBNP(N 末端脑利钠肽前体)>250 pg/mL 或经胸超声心动图左心房容积指数≥34 ml/m。我们重复了我们的分析,需要≥2 个标记物来定义心房心脏病。在 5078 名参与者(平均年龄 75 岁,59%为女性,21%为黑人成年人)中,有 34%患有心房心脏病,有 763 名参与者发生了痴呆。心房心脏病与痴呆症显著相关(调整后的 HR,1.35 [95%CI,1.16-1.58]),当需要≥2 种生物标志物时,效应估计值会增强(调整后的 HR,1.54 [95%CI,1.25-1.89])。在排除 AF(调整后的 HR,1.31 [95%CI,1.12-1.55])或中风(调整后的 HR,1.28 [95%CI,1.09-1.52])患者后,患有心房心脏病的患者发生痴呆的风险增加。AF 介导的效应比例为 4%(=0.005),9%由中风介导(=0.048)。
心房心脏病与痴呆风险增加显著相关,AF 或中风仅对效应有较小程度的介导作用。