Is an MRI-derived anatomical measure of dementia risk also a measure of brain aging?

被引:4
作者
Casanova, Ramon [1 ]
Anderson, Andrea M. [1 ]
Barnard, Ryan T. [1 ]
Justice, Jamie N. [2 ]
Kucharska-Newton, Anna [3 ]
Windham, Beverly Gwen [4 ]
Palta, Priya [5 ]
Gottesman, Rebecca F. [6 ]
Mosley, Thomas H. [4 ]
Hughes, Timothy M. [2 ]
Wagenknecht, Lynne E. [7 ]
Kritchevsky, Stephen B. [2 ]
机构
[1] Wake Forest Sch Med, Dept Biostat & Data Sci, Winston Salem, NC 27101 USA
[2] Wake Forest Sch Med, Dept Internal Med, Winston Salem, NC 27101 USA
[3] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[4] Univ Mississippi, Med Ctr, Jackson, MS 39216 USA
[5] Columbia Univ, Sch Publ Hlth, New York, NY USA
[6] NIH, Bldg 10, Bethesda, MD 20892 USA
[7] Wake Forest Sch Med, Div Publ Hlth Sci, Winston Salem, NC 27101 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
Machine learning; Aging; Alzheimer's disease; Proteomics; Deficit accumulation index; Mortality; AGE; BIOMARKERS;
D O I
10.1007/s11357-022-00650-z
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Machine learning methods have been applied to estimate measures of brain aging from neuroimages. However, only rarely have these measures been examined in the context of biologic age. Here, we investigated associations of an MRI-based measure of dementia risk, the Alzheimer's disease pattern similarity (AD-PS) scores, with measures used to calculate biological age. Participants were those from visit 5 of the Atherosclerosis Risk in Communities Study with cognitive status adjudication, proteomic data, and AD-PS scores available. The AD-PS score estimation is based on previously reported machine learning methods. We evaluated associations of the AD-PS score with all-cause mortality. Sensitivity analyses using only cognitively normal (CN) individuals were performed treating CNS-related causes of death as competing risk. AD-PS score was examined in association with 32 proteins measured, using a Somalogic platform, previously reported to be associated with age. Finally, associations with a deficit accumulation index (DAI) based on a count of 38 health conditions were investigated. All analyses were adjusted for age, race, sex, education, smoking, hypertension, and diabetes. The AD-PS score was significantly associated with all-cause mortality and with levels of 9 of the 32 proteins. Growth/differentiation factor 15 (GDF-15) and pleiotrophin remained significant after accounting for multiple-testing and when restricting the analysis to CN participants. A linear regression model showed a significant association between DAI and AD-PS scores overall. While the AD-PS scores were created as a measure of dementia risk, our analyses suggest that they could also be capturing brain aging.
引用
收藏
页码:439 / 450
页数:12
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