Saeed Anum, Chang Yuefang, Swanson Justin, Vu Michael, Mapstone Mark, Villemagne Victor L, Snitz Beth E, Royse Sarah K, Wang Hongtian, Lopresti Brian, Aizenstein Howard J, Wu Minjie, Kip Kevin, Reis Steven E, Lopez Oscar, Cohen Ann
University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, USA.
J Alzheimers Dis Rep. 2025 Jan 15;9:25424823241299297. doi: 10.1177/25424823241299297. eCollection 2025 Jan-Dec.
Atherosclerotic cardiovascular disease (ASCVD) risk factors in mid-life are associated with cognitive decline and late-life dementia. However, the role of these risk factors in Alzheimer's disease (AD) pathology remains elusive.
We investigated the association of mid-life 10-year ASCVD risk with late-life amyloid, tau, neurodegeneration [AT(N)] measures and white matter hyperintensities (WMHs).
Participants enrolled in the Heart Strategies Concentrating on Risk Evaluation (Heart SCORE) study between 2003-2005 (mid-life) and underwent brain MRI and PET scans in 2018-2022 (age >65 years, late-life) to detect and quantify amyloid (A, PiB-PET) and tau (T, Flortaucipir (FTP) PET) deposition, cortical thickness (N) and WMHs. Mid-life ASCVD risk was categorized as; borderline (5%-7.4%), intermediate (7.5%-<15%), or high (≥15%). Association of mid-life ASCVD risk HR (95% CI) was assessed using logistic and linear regressions with A, T, or N and chi square beta coefficients for WMH in late life.
Over a ∼16 years follow up, in 135 participants (mean age 73 years), mid-life ASCVD risk categories had a graded association with neurodegeneration (OR 6.98 [2.44-19.95]; p < 0.05) driven primarily by self-identified Black race and age, while none with A and T. ASCVD risk score was also associated with WMHs ((β=0.42 ± 0.22; p = 0.05).
In this asymptomatic, diverse cohort, 10-year ASCVD risk was predictive of late-life neurodegeneration and WMHs but not amyloid or tau. Further mechanistic studies can elucidate whether midlife ASCVD risk factors associated neurodegeneration initiates brain vulnerability leading to AD in late life.
中年时期的动脉粥样硬化性心血管疾病(ASCVD)风险因素与认知能力下降和晚年痴呆症相关。然而,这些风险因素在阿尔茨海默病(AD)病理过程中的作用仍不明确。
我们研究了中年时期10年ASCVD风险与晚年淀粉样蛋白、tau蛋白、神经退行性变[AT(N)]指标及白质高信号(WMH)之间的关联。
参与者于2003年至2005年(中年时期)参加了聚焦风险评估的心脏策略(Heart SCORE)研究,并于2018年至2022年(年龄>65岁,晚年时期)接受了脑部MRI和PET扫描,以检测和量化淀粉样蛋白(A,PiB-PET)和tau蛋白(T,氟代脱氧葡萄糖(FTP)PET)沉积、皮质厚度(N)和WMH。中年ASCVD风险分为:临界(5%-7.4%)、中等(7.5%-<15%)或高(≥15%)。使用逻辑回归和线性回归评估中年ASCVD风险HR(95%CI)与A、T或N的关联,并使用卡方β系数评估晚年WMH的关联。
在约16年的随访中,135名参与者(平均年龄73岁)中,中年ASCVD风险类别与神经退行性变存在分级关联(OR 6.98[2.44-19.95];p<0.05),主要由自我认定的黑人种族和年龄驱动,而与A和T无关。ASCVD风险评分也与WMH相关((β=0.42±0.22;p=0.05)。
在这个无症状的多样化队列中,10年ASCVD风险可预测晚年神经退行性变和WMH,但不能预测淀粉样蛋白或tau蛋白。进一步的机制研究可以阐明中年ASCVD风险因素相关的神经退行性变是否会引发大脑易损性,从而导致晚年患AD。