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Plasma GDF15 affects long-term dementia risk and alters neuro-immune signaling

Blew, C. O.; Duggan, M. R.; Tsitsipatis, D.; Gomez, G. T.; Hernandez Rodriguez, Z.; Pilling, L. C.; Chen, J.; Jacobsen, E.; Dark, H. E.; Lu, Y.; Drouin, S. M.; Joynes, C. M.; Yao, M.; Bilgel, M.; Moghekar, A.; Tian, Q.; Candia, J.; Kaileh, M.; Gupta, A.; Mazan-Mamczarz, K.; Gorospe, M.; Lyashkov, A.; Lukyanenko, Y.; Kivimaki, M.; Frank, P.; Jennings, L. L.; Gudmundsdottir, V.; Gudnason, V.; Launer, L. J.; Kaneko, N.; Kato, S.; Furuichi, M.; Shibayama, M.; Katsuno, M.; Hiraga, K.; Nishita, Y.; Otsuka, R.; Pike, J. R.; Rooney, M. R.; Schlosser, P.; Cui, Y.; Erus, G.; Davatzkios, C.; Gottesman, R

2025-07-21 neurology
10.1101/2025.07.18.25331297 medRxiv
Show abstract

Growth/differentiation factor-15 (GDF15) is a secreted peptide hormone and cytokine that is strongly associated with dementia risk. However, the extent to which plasma GDF15 represents a biomarker and driver of dementia risk remains unclear. Across multiple cohorts, we demonstrated that plasma GDF15 is associated with greater dementia risk over 15-to 25-year follow-up periods when measured in midlife, with stronger associations observed for vascular dementia compared to Alzheimers disease (AD). Two-sample Mendelian randomization supported plasma GDF15s mechanistic role in AD and related dementias, while cohort studies linked it to cerebral small vessel disease, diffuse neurodegeneration, phosphorylated tau, and a cerebrospinal fluid proteomic signature indicative of neuro-immune activation. Exposure of cultured myeloid cells to recombinant GDF15 altered biological pathways that we subsequently demonstrated are predictive of dementia risk, including interferon/antiviral responses, pyruvate metabolism, and scavenging of heme. These findings support circulating GDF15s role as an early biomarker - particularly for vascular dementia and neuroinflammation - and identify the mechanisms by which it may drive dementia risk.

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