CSF biomarkers of immune activation and Alzheimer’s disease for predicting cognitive impairment risk in the elderly

Author:

Shue Francis1ORCID,White Launia J.2ORCID,Hendrix Rachel3ORCID,Ulrich Jason3ORCID,Henson Rachel L.3ORCID,Knight William3,Martens Yuka A.1ORCID,Wang Ni1,Roy Bhaskar1,Starling Skylar C.1,Ren Yingxue2,Xiong Chengjie4,Asmann Yan W.2ORCID,Syrjanen Jeremy A.5ORCID,Vassilaki Maria5ORCID,Mielke Michelle M.5ORCID,Timsina Jigyasha6ORCID,Sung Yun Ju6ORCID,Cruchaga Carlos6ORCID,Holtzman David M.3ORCID,Bu Guojun1ORCID,Petersen Ronald C.7ORCID,Heckman Michael G.2,Kanekiyo Takahisa1ORCID

Affiliation:

1. Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.

2. Division of Clinical Trials and Biostatistics, Department of Quantitative Health Sciences, Mayo Clinic, Jacksonville, FL 32224, USA.

3. Department of Neurology, Hope Center for Neurological Disorders, Knight Alzheimer’s Disease Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA.

4. Division of Biostatistics, Washington University School of Medicine, St. Louis, MO 93110, USA.

5. Department of Quantitative Health Sciences, Mayo Clinic, Rochester MN 55905, USA.

6. Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 93110, USA.

7. Departments of Neurology, Mayo Clinic, Rochester, MN 55905, USA.

Abstract

The immune system substantially influences age-related cognitive decline and Alzheimer’s disease (AD) progression, affected by genetic and environmental factors. In a Mayo Clinic Study of Aging cohort, we examined how risk factors like APOE genotype, age, and sex affect inflammatory molecules and AD biomarkers in cerebrospinal fluid (CSF). Among cognitively unimpaired individuals over 65 ( N = 298), we measured 365 CSF inflammatory molecules, finding age, sex, and diabetes status predominantly influencing their levels. We observed age-related correlations with AD biomarkers such as total tau, phosphorylated tau-181, neurofilament light chain (NfL), and YKL40. APOE4 was associated with lower Aβ42 and higher SNAP25 in CSF. We explored baseline variables predicting cognitive decline risk, finding age, CSF Aβ42, NfL, and REG4 to be independently correlated. Subjects with older age, lower Aβ42, higher NfL, and higher REG4 at baseline had increased cognitive impairment risk during follow-up. This suggests that assessing CSF inflammatory molecules and AD biomarkers could predict cognitive impairment risk in the elderly.

Publisher

American Association for the Advancement of Science (AAAS)

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