Feifei Ge , Bo Song , Xixi Wang , Minjie Tian , Xingjian Lin , Jingping Shi , Xing Ye
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引用次数: 0
Abstract
Background:
The link between thyroid autoimmunity and Alzheimer’s disease (AD) biomarkers in euthyroid individuals is poorly understood. We investigated the independent and interactive effects of thyroid peroxidase antibodies (TPOAb) and thyroglobulin antibodies (TgAb) on core cerebrospinal fluid (CSF) biomarkers of AD pathology.
Methods:
We analyzed CSF biomarkers (A1–42, A1–40, T-tau, and P-tau181) measured using validated ELISA assays (Fujirebio) in 114 euthyroid, amyloid-positive participants stratified by antibody status. Associations were assessed using multiple linear regression and four-group cross-classification analyses, adjusting for age and gender.
Results:
TPOAb positivity was independently associated with a significantly lower CSF A1-42/A1-40 ratio (mean ± SD: 0.04 ± 0.01 vs. 0.05 ± 0.02; adjusted p=0.022; Cohen’s d = −0.65), indicating more advanced amyloid pathology. Importantly, we identified a novel interaction modulating tau pathology: isolated positivity for either TPOAb or TgAb was linked to elevated P-tau181, but this effect was significantly attenuated in subjects positive for both antibodies (interaction p=0.037).
Conclusion:
Thyroid autoimmunity is associated with AD neuropathological changes independent of thyroid hormone status. The specific association of TPOAb with amyloid pathology and the complex interplay between antibodies on tau pathology highlight previously unrecognized mechanisms. These findings, pending validation in longitudinal studies, suggest thyroid antibody screening in elderly euthyroid individuals may aid in identifying those at higher risk for Alzheimer’s pathology, potentially facilitating earlier detection and intervention.
期刊介绍:
The Journal of Neuroimmunology affords a forum for the publication of works applying immunologic methodology to the furtherance of the neurological sciences. Studies on all branches of the neurosciences, particularly fundamental and applied neurobiology, neurology, neuropathology, neurochemistry, neurovirology, neuroendocrinology, neuromuscular research, neuropharmacology and psychology, which involve either immunologic methodology (e.g. immunocytochemistry) or fundamental immunology (e.g. antibody and lymphocyte assays), are considered for publication.