Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.
Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.
Where did the research take place?
The study site has not been established. Author addresses may differ from where the research occurred.
Montréal, CA · Author affiliation
The Neuro (Montreal Neurological Institute-Hospital), McGill University, Montreal, QC, Canada.Location evidence
Bethesda, US · Author affiliation
Center for Alzheimer's and Related Dementias, National Institute on Aging, Bethesda, MD, USA Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.Location evidence
US · Author affiliation · country only
Data Tecnica International, Washington, DC, USA.Location evidence
New York City, US · Author affiliation
Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.Location evidence
Tel Aviv, IL · Author affiliation
Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Location evidence
Publication status: preprint
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Original abstract
OBJECTIVE: α-synucleinopathies are clinically and biologically heterogeneous disorders lacking reliable biomarkers to assist with early diagnosis, disease progression, patient stratification, and therapeutic targeting. Genetic variation is known to impact biomarker levels, influencing their utility and interpretation in research and clinical settings. We aimed to identify common genetic modulators of biomarker levels implicated in α-synucleinopathy pathogenesis. METHODS: Genome-wide association studies (GWASs) were conducted on 63 CSF, plasma, and urine biomarkers in 581 individuals from the Parkinson's Progression Markers Initiative (PPMI). Analyses were adjusted for age, sex, disease status, and principal components. PD- and DLB-risk loci associations were separately assessed for each GWAS. RESULTS: We confirm strong associations between urine bis(monoacylglycerol)phosphate (BMP) isoforms and the variants LRRK2 p.G2019S and GBA1 p.N370S, while providing support for BMPs use as a LRRK2-PD biomarker. CSF Aβ was significantly associated with an APOE ε4 allele, reinforcing its central role in amyloid regulation. Novel associations were detected between CSF ceramide isoforms the MCF2L2 and GMNN loci, and between CSF tau and the TP63 locus. Multiple PD risk loci, including MAPT, SIPA1L2, MCCC1, and RAB29, were associated with lysosomal lipid biomarkers, highlighting pathway-level convergence. INTERPRETATION: The present study reveals established and novel genetic modulators of potential α-synucleinopathy biomarkers, demonstrating that genetic background significantly shapes biomarker levels. These genetic influences should be accounted for when conducting biomarker-based research, clinical trials, or therapeutic development to ensure accurate interpretation and improve their translational relevance.