Polygenic risk for psychiatric disorders and its association with neuropsychiatric symptoms in dementia

Najar, Jenna; Rojas, Itziar de ; Dalmasso, Maria Carolina; Fernandez, Maria Victoria; Boer, Sterre C.M. de; Ramirez, Alfredo; Priller, Josef; Laske, Christoph; Kleineidam, Luca; Schneider, Anja; Wagner, Michael; Heilmann-Heimbach, Stefanie; Scherer, Martin; Froelich, Lutz; Peters, Oliver; Hellmann-Regen, Julian; Wiltfang, Jens; Düzel, Emrah; Buerger, Katharina; Perneczky, Robert ; Teipel, Stefan ; Jessen, Frank; Kornhuber, Johannes; Lemstra, Afina W.; Pijnenburg, Yolande A.L.; Lee, Sven J. van der und Reus, Lianne M. (2025): Polygenic risk for psychiatric disorders and its association with neuropsychiatric symptoms in dementia. In: International Review of Psychiatry, Bd. 37, Nr. 8: S. 816-826

Abstract

Neuropsychiatric symptoms are common in Alzheimer’s disease (AD), dementia with Lewy bodies (DLB), and frontotemporal dementia (FTD), yet their genetic underpinnings remain unclear. To gain insight into biological processes related to neuropsychiatric symptoms in dementia, we investigated whether polygenic risk scores (PRS) for psychiatric disorders – major depressive disorder (MDD), schizophrenia (SCZ), bipolar disorder (BD), and autism spectrum disorder (ASD) – are associated with neuropsychiatric symptoms in dementia. Data included genetic and neuropsychiatric data of 6240 AD patients, 428 FTD patients and 390 DLB patients from five European cohorts (ADC, GR@ACE, DELCODE, AgeCoDe, and DCN). PRS for MDD, BD, SCZ, and ASD were calculated using LDpred2. Neuropsychiatric symptoms were assessed using total scores from the Neuropsychiatric Inventory (NPI) (NPI-12 and NPI-Q) and Geriatric Depression scale (GDS). Associations between PRS and symptoms were examined using linear regression models, followed by meta-analyses. In FTD, higher SCZ-PRS associated with lower NPI scores in the meta-analysis (β = −0.12, p = .001). No associations were found in AD and DLB. This is the first study to show that genetic liability for SCZ associates with lower NPI in FTD, warranting further investigation.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin > Munich Cluster for Systems Neurology (SyNergy)
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• ISSN: 0954-0261
• Sprache: Englisch
• DFG: Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 390857198