Plasma amyloid beta 40/42, phosphorylated tau 181, and neurofilament light are associated with cognitive impairment and neuropathological changes among World Trade Center responders: A prospective cohort study of exposures and cognitive aging at midlife

Author:

Kritikos Minos1,Diminich Erica D.1,Meliker Jaymie1,Mielke Michelle2,Bennett David A.3,Finch Caleb E.4,Gandy Sam E.56,Carr Melissa A.7,Yang Xiaohua7,Kotov Roman8,Kuan Pei‐Fen9,Bromet Evelyn J.8,Clouston Sean A. P.1,Luft Benjamin J.7

Affiliation:

1. Program in Public Health and Department of Family Population, and Preventive Medicine Renaissance School of Medicine at Stony Brook University Stony Brook New York USA

2. Department of Epidemiology and Prevention Wake Forest University School of Medicine Winston‐Salem North Carolina USA

3. Rush Alzheimer's Disease Center Rush University Chicago Illinois USA

4. Leonard Davis School of Gerontology University of Southern California Los Angeles California USA

5. Department of Neurology Icahn School of Medicine at Mount Sinai New York New York USA

6. Department of Psychiatry and Mount Sinai Alzheimer's Disease Research Center Icahn School of Medicine, Mount Sinai New York New York USA

7. Department of Medicine Renaissance School of Medicine at Stony Brook University Stony Brook New York USA

8. Department of Psychiatry Renaissance School of Medicine at Stony Brook University Stony Brook New York USA

9. Department of Applied Mathematics Renaissance School of Medicine at Stony Brook University Stony Brook New York USA

Abstract

AbstractIntroductionWorld Trade Center (WTC) responders are experiencing a high risk of mild cognitive impairment (MCI) and dementia, though the etiology remains inadequately characterized. This study investigated whether WTC exposures and chronic post‐traumatic stress disorder (PTSD) were correlated with plasma biomarkers characteristic of Alzheimer's disease (AD) neuropathology.MethodsEligible participants included WTC‐exposed individuals with a baseline cognitive assessment and available plasma sample. We examined levels of the amyloid beta (Aβ)40/42 ratio, phosphorylated tau 181 (p‐tau181), and neurofilament light chain (NfL) and associations with a WTC exposures (duration on site ≥15 weeks, dust cloud), the PTSD Symptom Checklist for Diagnostic and Statistical Manual of Mental Disorders, 4th edition PTSD, and classification of amyloid/tau/neurodegeneration (AT[N]) profiles. Multinomial logistic regressions assessed whether biomarkers predicted increased risk of MCI or dementia.ResultsOf 1179 eligible responders, 93.0% were male, mean (standard deviation) age 56.6 years (7.8). Aβ40/42, p‐tau181, and NfL intercorrelated and increased with age. In subgroup analyses of responders with available neuroimaging data (n = 75), Aβ40/42 and p‐tau181 were further associated with decreased hippocampal volume (Spearman's ρ = −0.3). Overall, 58.08% of responders with dementia had ≥1 elevated biomarker, and 3.45% had elevations across all biomarkers. In total, 248 (21.05%) had MCI and 70 (5.94%) had dementia. Increased risk of dementia was associated with plasma AT(N) profile T+ or A+N+. Exposure on site ≥15 weeks was independently associated with T+ (adjusted risk ratio [aRR] = 1.03 [1.01−1.05], P = 0.009), and T+N+ profile (aRR = 2.34 [1.12−4.87]). The presence of PTSD was independently associated with risk of A+ (aRR = 1.77 [1.11−2.82]).DiscussionWTC exposures and chronic PTSD are associated with plasma biomarkers consistent with neurodegenerative disease.

Funder

National Institutes of Health

Centers for Disease Control and Prevention

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical)

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