Proteomics identifies potential immunological drivers of postinfection brain atrophy and cognitive decline

痴呆 神经退行性变 萎缩 疾病 认知功能衰退 免疫学 生物 医学 蛋白质组学 病理 基因 遗传学
作者
Michael R. Duggan,Zhongsheng Peng,Pyry N. Sipilä,Joni V. Lindbohm,Jingsha Chen,Yifei Lü,Christos Davatzikos,Güray Erus,Timothy J. Hohman,Shea J. Andrews,Julián Candia,Toshiko Tanaka,Cassandra M Joynes,Chelsea X. Alvarado,Mike A. Nalls,Jenifer Cordon,Gulzar N. Daya,Timothy J. Hohman,Alexandria Lewis,Abhay Moghekar,Priya Palta,Josef Coresh,Luigi Ferrucci,Mika Kivimäki,Keenan A. Walker
出处
期刊:Nature Aging 被引量:1
标识
DOI:10.1038/s43587-024-00682-4
摘要

Abstract Infections have been associated with the incidence of Alzheimer disease and related dementias, but the mechanisms responsible for these associations remain unclear. Using a multicohort approach, we found that influenza, viral, respiratory, and skin and subcutaneous infections were associated with increased long-term dementia risk. These infections were also associated with region-specific brain volume loss, most commonly in the temporal lobe. We identified 260 out of 942 immunologically relevant proteins in plasma that were differentially expressed in individuals with an infection history. Of the infection-related proteins, 35 predicted volumetric changes in brain regions vulnerable to infection-specific atrophy. Several of these proteins, including PIK3CG, PACSIN2, and PRKCB, were related to cognitive decline and plasma biomarkers of dementia (Aβ 42/40 , GFAP, NfL, pTau-181). Genetic variants that influenced expression of immunologically relevant infection-related proteins, including ITGB6 and TLR5, predicted brain volume loss. Our findings support the role of infections in dementia risk and identify molecular mediators by which infections may contribute to neurodegeneration.
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