Irisin Levels in Cerebrospinal Fluid Correlate with Biomarkers and Clinical Dementia Scores in Alzheimer Disease

Author:

Dicarlo Manuela1,Pignataro Patrizia12,Zecca Chiara3,Dell'Abate Maria Teresa3,Urso Daniele3,Gnoni Valentina3,Giugno Alessia3,Borlizzi Francesco3,Zerlotin Roberta1,Oranger Angela1,Colaianni Graziana1,Colucci Silvia2ORCID,Logroscino Giancarlo3ORCID,Grano Maria1

Affiliation:

1. Department of Precision and Regenerative Medicine and Ionian Area University of Bari “A. Moro” Bari Italy

2. Department of Translational Biomedicine and Neuroscience University of Bari “A. Moro” Bari Italy

3. Center for Neurodegenerative Diseases and the Aging Brain University of Bari “A. Moro” at “Pia Fondazione Card G. Panico” Hospital Tricase Italy

Abstract

ObjectiveIrisin, released by muscles during exercise, was recently identified as a neuroprotective factor in mouse models of Alzheimer disease (AD). In a cohort of AD patients, we studied cerebrospinal fluid (CSF) and plasma irisin levels, sex interactions, and correlations with disease biomarkers.MethodsCorrelations between CSF and plasma irisin levels and AD biomarkers (amyloid β 1‐42, hyperphosphorylated tau, and total tau [t‐tau]) and Clinical Dementia Rating Scale Sum of Boxes (CDR‐SOB) were analyzed in a cohort of patients with Alzheimer dementia (n = 82), mild cognitive impairment (n = 44), and subjective memory complaint (n = 20) biologically characterized according to the recent amyloid/tau/neurodegeneration classification.ResultsCSF irisin was reduced in Alzheimer dementia patients (p < 0.0001), with lower levels in female patients. Moreover, CSF irisin correlated positively with Aβ42 in both female (r = 0.379, p < 0.001) and male (r = 0.262, p < 0.05) patients, and negatively with CDR‐SOB (r = −0.234, p < 0.05) only in female patients. A negative trend was also observed between CSF irisin and t‐tau levels in all patients (r = −0.144, p = 0.082) and in the female subgroup (r = −0.189, p = 0.084).InterpretationThe results highlight the relationship between irisin and biomarkers of AD pathology, especially in females. Our findings also offer perspectives toward the use of irisin as a marker of the AD continuum. ANN NEUROL 2024;96:61–73

Publisher

Wiley

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