Associations of early-onset coronary heart disease and genetic susceptibility with incident dementia and white matter hyperintensity: A prospective cohort study.

IF 7.8 Q2 BUSINESS The Journal of Prevention of Alzheimer's Disease Pub Date : 2025-02-01 Epub Date: 2025-01-01 DOI:10.1016/j.tjpad.2024.100041
Jie Liang, Yanyu Zhang, Wenya Zhang, Yang Pan, Darui Gao, Jingya Ma, Yuling Liu, Yiwen Dai, Mengmeng Ji, Wuxiang Xie, Fanfan Zheng
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Abstract

Background: 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.

Objectives: This study aimed to investigate whether observed and genetically predicted early-onset CHD were related to subsequent dementia and WMH volume.

Design: Prospective cohort study.

Setting: UK Biobank.

Participants: 500 671 individuals without dementia at baseline.

Measurements: 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.

Results: 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, Ptrend<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, Ptrend<0.001) and WMH volume (β for the highest quartile: 0.042, 95% CI: 0.017 to 0.068, Ptrend=0.002).

Conclusions: 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.

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早发冠心病和遗传易感性与痴呆症和白质高密度的关系:一项前瞻性队列研究。
背景:早发性冠心病(CHD)和遗传易感性与痴呆和脑白质高强度(WMH)的关系尚不清楚。阐明这一问题可以促进对早发性冠心病神经认知影响的认识,并为预防痴呆提供建议。目的:本研究旨在探讨观察到的和基因预测的早发性冠心病是否与随后的痴呆和WMH容量有关。设计:前瞻性队列研究。地点:英国生物银行。参与者:基线时无痴呆的500671人。指标:早发性冠心病(男性≤55岁;女性(≤65岁)根据住院病历确定。事件性痴呆包括全因痴呆、阿尔茨海默病和血管性痴呆,通过医院住院记录、死亡登记数据和自我报告数据来确定。通过脑磁共振成像(MRI)测量WMH体积。采用Cox比例风险模型和线性回归模型分析早发性冠心病与痴呆和WMH的相关性。随后,进行了多遗传风险评分(PRS)分析,以研究遗传预测的早发性冠心病与预后的关系。结果:500 671只个体中,女性272 669只,占54.5%;平均年龄:57.0±8.1岁),在13.8年的中位随访期间发生9294例痴呆。与非冠心病组相比,早发性冠心病组(n = 16 133)和晚发性冠心病组(n = 43 944)发生痴呆的风险均较高(风险比[HR]: 1.99, 95%可信区间[CI]: 1.81 ~ 2.19;晚发组HR: 1.20, 95% CI: 1.14 ~ 1.27)。在冠心病患者中,与晚发型冠心病患者相比,早发型冠心病患者发生痴呆的风险明显更高(HR: 1.56, 95% CI: 1.39 ~ 1.75)。在中位9.3年随访期间完成脑MRI扫描的40290名个体中,早发性冠心病参与者在三组(早发性冠心病、晚发性冠心病和非冠心病,Ptrendtrendtrend=0.002)中表现出最大的WMH体积。结论:早发性冠心病和遗传易感性与较高的痴呆发生率和较大的WMH体积相关。对早发性冠心病患者的神经认知状况应给予额外的关注。
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The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
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期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
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