Association between Modifiable Risk Factors and Levels of Blood-Based Biomarkers of Alzheimer's and Related Dementias in the Look AHEAD Cohort.

JAR life Pub Date : 2024-01-05 eCollection Date: 2024-01-01 DOI:10.14283/jarlife.2024.1
K M Hayden, M M Mielke, J K Evans, R Neiberg, D Molina-Henry, M Culkin, S Marcovina, K C Johnson, O T Carmichael, S R Rapp, B C Sachs, J Ding, H Shappell, L Wagenknecht, J A Luchsinger, M A Espeland
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Abstract

Background: Emerging evidence suggests that a number of factors can influence blood-based biomarker levels for Alzheimer's disease (AD) and Alzheimer's related dementias (ADRD). We examined the associations that demographic and clinical characteristics have with AD/ADRD blood-based biomarker levels in an observational continuation of a clinical trial cohort of older individuals with type 2 diabetes and overweight or obesity.

Methods: Participants aged 45-76 years were randomized to a 10-year Intensive Lifestyle Intervention (ILI) or a diabetes support and education (DSE) condition. Stored baseline and end of intervention (8-13 years later) plasma samples were analyzed with the Quanterix Simoa HD-X Analyzer. Changes in Aβ42, Aβ40, Aβ42/Aβ40, ptau181, neurofilament light chain (NfL), and glial fibrillary acidic protein (GFAP) were evaluated in relation to randomization status, demographic, and clinical characteristics.

Results: In a sample of 779 participants from the Look AHEAD cohort, we found significant associations between blood-based biomarkers for AD/ADRD and 15 of 18 demographic (age, gender, race and ethnicity, education) and clinical characteristics (APOE, depression, alcohol use, smoking, body mass index, HbA1c, diabetes duration, diabetes treatment, estimated glomerular filtration rate, hypertension, and history of cardiovascular disease) .

Conclusions: Blood-based biomarkers of AD/ADRD are influenced by common demographic and clinical characteristics. These factors should be considered carefully when interpreting these AD/ADRD blood biomarker values for clinical or research purposes.

Look AHEAD 群体中可改变的风险因素与阿尔茨海默氏症及相关痴呆症血液生物标志物水平之间的关系。
背景:新的证据表明,一些因素会影响阿尔茨海默病(AD)和阿尔茨海默病相关痴呆症(ADRD)的血液生物标志物水平。我们对患有 2 型糖尿病和超重或肥胖症的老年临床试验队列进行了观察,研究了人口统计学特征和临床特征与 AD/ADRD 血液生物标志物水平之间的关系:年龄在 45-76 岁之间的参与者被随机分配到为期 10 年的强化生活方式干预 (ILI) 或糖尿病支持和教育 (DSE) 条件中。用Quanterix Simoa HD-X分析仪分析储存的基线和干预结束(8-13年后)血浆样本。评估Aβ42、Aβ40、Aβ42/Aβ40、ptau181、神经丝蛋白轻链(NfL)和胶质纤维酸性蛋白(GFAP)的变化与随机化状态、人口统计学和临床特征的关系:在 Look AHEAD 队列的 779 名参与者样本中,我们发现 AD/ADRD 的血液生物标志物与 18 个人口统计学特征(年龄、性别、种族和民族、教育程度)和临床特征(APOE、抑郁、饮酒、吸烟、体重指数、HbA1c、糖尿病病程、糖尿病治疗、估计肾小球滤过率、高血压和心血管疾病史)中的 15 个存在显著关联:基于血液的注意力缺失症/注意力缺失性痴呆症生物标志物受到常见人口统计学和临床特征的影响。在出于临床或研究目的解释这些 AD/ADRD 血液生物标志物值时,应仔细考虑这些因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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