Liang Jie, Zhang Yanyu, Zhang Wenya, Pan Yang, Gao Darui, Ma Jingya, Liu Yuling, Dai Yiwen, Ji Mengmeng, Xie Wuxiang, Zheng Fanfan
School of Nursing, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Department of Endocrinology, Peking University First Hospital, Beijing, China; Clinical Research Institute, Institute of Advanced Clinical Medicine, Peking University, Beijing, China; Key Laboratory of Epidemiology of Major Diseases (Peking University), Ministry of Education, Beijing, China.
J Prev Alzheimers Dis. 2025 Feb;12(2):100041. doi: 10.1016/j.tjpad.2024.100041. Epub 2025 Jan 1.
The associations of early-onset coronary heart disease (CHD) and genetic susceptibility with incident dementia and brain white matter hyperintensity (WMH) remain unclear. Elucidation of this problem could promote understanding of the neurocognitive impact of early-onset CHD and provide suggestions for the prevention of dementia.
This study aimed to investigate whether observed and genetically predicted early-onset CHD were related to subsequent dementia and WMH volume.
Prospective cohort study.
UK Biobank.
500 671 individuals without dementia at baseline.
Early-onset CHD (male ≤55 years; female ≤65 years) was ascertained using hospital inpatient records. Incident dementia including all-cause dementia, Alzheimer's disease, and vascular dementia was ascertained using hospital inpatient records, mortality register data, and self-reported data. WMH volume was measured through brain magnetic resonance imaging (MRI). Cox proportional hazards models and linear regression models were used to analyze the associations of early-onset CHD with incident dementia and WMH. Subsequently, a polygenetic risk score (PRS) analysis was conducted to investigate the associations of genetically predicted early-onset CHD with outcomes.
Among 500 671 individuals (female: 272 669, 54.5%; mean age: 57.0 ± 8.1 years), 9 294 dementia occurred during a median follow-up of 13.8 years. Compared with the non-CHD group, both early-onset (n = 16 133) and late-onset CHD (n = 43 944) groups had higher risks of developing dementia (hazard ratio [HR]: 1.99, 95% confidence interval [CI]: 1.81 to 2.19 for early-onset group; HR: 1.20, 95% CI: 1.14 to 1.27 for late-onset group). Among CHD participants, early-onset CHD was associated with a significantly higher risk of incident dementia, compared with late-onset CHD (HR: 1.56, 95% CI: 1.39 to 1.75). In a subset of 40 290 individuals who completed brain MRI scans during a median follow-up of 9.3 years, participants with early-onset CHD exhibited the largest WMH volume among the three groups (early-onset CHD, late-onset CHD, and non-CHD, P<0.001). The PRS analysis supported the associations of early-onset CHD with dementia (odds ratio [OR] for the highest quartile: 1.37, 95% CI: 1.28 to 1.46, P<0.001) and WMH volume (β for the highest quartile: 0.042, 95% CI: 0.017 to 0.068, P=0.002).
Early-onset CHD and genetic susceptibility are associated with a higher risk of incident dementia and a larger WMH volume. Additional attention should be paid to the neurocognitive status of individuals with early-onset CHD.
早发性冠心病(CHD)及遗传易感性与新发痴呆症和脑白质高信号(WMH)之间的关联尚不清楚。阐明这一问题有助于增进对早发性冠心病神经认知影响的理解,并为痴呆症的预防提供建议。
本研究旨在调查观察到的和基因预测的早发性冠心病是否与随后发生的痴呆症和WMH体积有关。
前瞻性队列研究。
英国生物银行。
500671名基线时无痴呆症的个体。
使用医院住院记录确定早发性冠心病(男性≤55岁;女性≤65岁)。使用医院住院记录、死亡率登记数据和自我报告数据确定新发痴呆症,包括全因痴呆症、阿尔茨海默病和血管性痴呆。通过脑磁共振成像(MRI)测量WMH体积。使用Cox比例风险模型和线性回归模型分析早发性冠心病与新发痴呆症和WMH之间的关联。随后,进行多基因风险评分(PRS)分析,以研究基因预测的早发性冠心病与结局之间的关联。
在500671名个体(女性:272669名,占54.5%;平均年龄:57.0±8.1岁)中,在中位随访13.8年期间发生了9294例痴呆症。与非冠心病组相比,早发性冠心病组(n = 16133)和晚发性冠心病组(n = 43944)发生痴呆症的风险更高(风险比[HR]:早发性冠心病组为1.99,95%置信区间[CI]:1.81至2.19;HR:晚发性冠心病组为1.20,95%CI:1.14至1.27)。在冠心病参与者中,与晚发性冠心病相比,早发性冠心病发生新发痴呆症的风险显著更高(HR:1.56,95%CI:1.39至1.75)。在中位随访9.3年期间完成脑MRI扫描的40290名个体的子集中,早发性冠心病参与者的WMH体积在三组(早发性冠心病、晚发性冠心病和非冠心病)中最大(P<0.001)。PRS分析支持早发性冠心病与痴呆症(最高四分位数的优势比[OR]:1.37,95%CI:1.28至1.46,P<0.001)和WMH体积(最高四分位数的β:0.042,95%CI:0.017至0.068,P = 0.002)之间的关联。
早发性冠心病和遗传易感性与新发痴呆症风险较高和WMH体积较大有关。应额外关注早发性冠心病个体的神经认知状态。