Osiecka Zuzanna, Fausto Bernadette A, Gills Joshua L, Sinha Neha, Malin Steven K, Gluck Mark A
Aging and Brain Health Alliance, Center for Molecular and Behavioral Neuroscience, Rutgers University-Newark, Newark, NJ, United States.
Department of Kinesiology and Health, School of Arts and Sciences, Rutgers University, New Brunswick, NJ, United States.
Front Aging Neurosci. 2023 Sep 4;15:1239727. doi: 10.3389/fnagi.2023.1239727. eCollection 2023.
Excess body weight and Alzheimer's disease (AD) disproportionately affect older African Americans. While mid-life obesity increases risk for AD, few data exist on the relationship between late-life obesity and AD, or how obesity-based and genetic risk for AD interact. Although the APOE-ε4 allele confers a strong genetic risk for AD, it is unclear if late-life obesity poses a greater risk for APOE-ε4 carriers compared to non-carriers. Here we assessed: (1) the influence of body mass index (BMI) (normal; overweight; class 1 obese; ≥ class 2 obese) on cognitive and structural MRI measures of AD risk; and (2) the interaction between BMI and APOE-ε4 in older African Americans.
Seventy cognitively normal older African American participants (M = 69.50 years; M = 31.01 kg/m; 39% APOE-ε4 allele carriers; 86% female) completed anthropometric measurements, physical assessments, saliva collection for APOE-ε4 genotyping, cognitive testing, health and lifestyle questionnaires, and structural neuroimaging [volume/surface area (SA) for medial temporal lobe subregions and hippocampal subfields]. Covariates included age, sex, education, literacy, depressive symptomology, and estimated aerobic fitness.
Using ANCOVAs, we observed that individuals who were overweight demonstrated better hippocampal cognitive function (generalization of learning: a sensitive marker of preclinical AD) than individuals with normal BMI, = 0.016, η2 = 0.18. However, individuals in the obese categories who were APOE-ε4 non-carriers had larger hippocampal subfield cornu Ammonis region 1 (CA1) volumes, while those who were APOE-ε4 carriers had smaller CA1 volumes, = 0.003, η2 = 0.23.
Thus, being overweight by BMI standards may preserve hippocampal function, but obesity reduces hippocampal structure and function in older African Americans with the APOE-ε4 Alzheimer's disease risk allele.
超重和阿尔茨海默病(AD)对老年非裔美国人的影响尤为严重。虽然中年肥胖会增加患AD的风险,但关于晚年肥胖与AD之间的关系,或者AD的肥胖相关风险和遗传风险如何相互作用的数据却很少。尽管APOE-ε4等位基因赋予了很强的AD遗传风险,但尚不清楚晚年肥胖对APOE-ε4携带者是否比非携带者构成更大的风险。在此,我们评估了:(1)体重指数(BMI)(正常;超重;1级肥胖;≥2级肥胖)对AD风险的认知和结构MRI测量指标的影响;以及(2)老年非裔美国人中BMI与APOE-ε4之间的相互作用。
70名认知正常的老年非裔美国参与者(平均年龄 = 69.50岁;平均BMI = 31.01 kg/m²;39%为APOE-ε4等位基因携带者;86%为女性)完成了人体测量、身体评估、用于APOE-ε4基因分型的唾液采集、认知测试、健康和生活方式问卷以及结构神经成像[内侧颞叶亚区域和海马亚区的体积/表面积(SA)]。协变量包括年龄、性别、教育程度、识字率、抑郁症状和估计的有氧适能。
使用协方差分析,我们观察到超重个体的海马认知功能(学习泛化:临床前AD的一个敏感标志物)比BMI正常的个体更好,F = 0.016,η² = 0.18。然而,APOE-ε4非携带者的肥胖类别个体海马亚区海马角1(CA1)体积更大,而APOE-ε4携带者的CA1体积更小,F = 0.003,η² = 0.23。
因此,按照BMI标准超重可能会保留海马功能,但肥胖会降低携带APOE-ε4阿尔茨海默病风险等位基因的老年非裔美国人的海马结构和功能。