Serum total tau, neurofilament light, and glial fibrillary acidic protein are associated with mortality in a population study

被引:1
|
作者
Halloway, Shannon [1 ]
Evans, Denis A. [2 ,3 ]
Desai, Pankaja [2 ,3 ]
Dhana, Klodian [2 ,3 ]
Beck, Todd [2 ,3 ]
Rajan, Kumar B. [2 ,3 ,4 ]
机构
[1] Univ Illinois, Coll Nursing, Dept Biobehav Nursing Sci, 845 S Damen Ave MC 820, Chicago, IL 60612 USA
[2] Rush Univ, Rush Inst Hlth Aging, Med Ctr, Chicago, IL USA
[3] Rush Univ, Med Ctr, Dept Internal Med, Chicago, IL USA
[4] Univ Calif Davis, Dept Neurol, Davis, CA USA
关键词
biomarkers; blood; cardiovascular; longevity; mortality; PHYSICAL FUNCTION; CHICAGO HEALTH; RISK; DISEASE; COMMUNITY; DECLINE;
D O I
10.1111/jgs.18632
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
Background: Total tau (t-tau), neurofilament light (NfL), and glial fibrillary acidic protein (GFAP) are neuronal cytoskeletal biomarkers that may indicate greater risk of poor outcomes in age-related conditions, including mortality. Health disparities experienced by some racial minority subgroups may influence biomarker expression and effects on longevity. We aimed to examine (a) associations of serum t-tau, NfL, and GFAP with overall and cardiovascular mortality and (b) differences in associations by racial background.Methods: Data came from 1327 older participants from the Chicago Health and Aging Project (CHAP), a longitudinal population-based study. Cox proportional hazards regression models were used to examine associations between concentrations of serum t-tau, NfL, and GFAP biomarker(s) and mortality (overall/cardiovascular mortality based on age at death). Interaction terms were used to examine differences between African-American and European-American participants. Models were adjusted for age, sex, education, the APOE-epsilon 4 allele, body mass index, chronic health conditions, and cognitive and physical functioning.Results: Models showed that fivefold higher concentrations of t-tau (HR = 1.46, 95% CI: 1.27, 1.68), NfL (HR = 2.13, 95% CI: 1.76, 2.58), and GFAP (HR = 1.43, 95% CI: 1.08, 1.90) were separately associated with increased risk of overall mortality, with higher risk in African Americans in t-tau or NfL. In models with all biomarkers, NfL (HR = 2.17, 95% CI: 1.65, 2.85) was associated with risk of overall mortality, with racial differences in t-tau. Higher concentrations of t-tau (HR = 1.32, 95% CI: 1.02, 1.70), NfL (HR = 1.95, 95% CI: 1.40, 2.72), and GFAP (HR = 1.87, 95% CI: 1.18, 2.98) were separately associated with risk of cardiovascular mortality, with racial differences in t-tau, NfL, or GFAP. In combined models, NfL (HR = 1.73, 95% CI: 1.08, 2.78) was associated with cardiovascular mortality.Conclusions: Serum t-tau, NfL, and GFAP may be early indicators for mortality outcomes among older adults, with racial differences among associations.
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收藏
页码:149 / 159
页数:11
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