Association of OBPIIa genetic variants with prodromal Parkinsonian phenotypes and dopaminergic biomarkers in the PPMI cohort.
Association of OBPIIa genetic variants with prodromal Parkinsonian phenotypes and dopaminergic biomarkers in the PPMI cohort.
Where did the research take place?
The study site has not been established. Author addresses may differ from where the research occurred.
Qingdao, CN · Author affiliation
Department of Neurology, Affiliated Hospital of Qingdao University, Qingdao, China; Cerebral Vascular Disease Institute, Affiliated Hospital of Qingdao University, Qingdao, China.Location evidence
Xinqiao, CN · Author affiliation
Department of Neurology, Xinqiao Hospital, Third Military Medical University (Army Medical University), Chongqing, China.Location evidence
Chongqing, CN · Author affiliation
Department of Neurology, Xinqiao Hospital, Third Military Medical University (Army Medical University), Chongqing, China.Location evidence
Weifang, CN · Author affiliation
Department of Neurology, Weifang People's Hospital, Weifang, China. Electronic address: liyaqingqy@126.com.Location evidence
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Original abstract
BACKGROUND: Odorant-binding protein IIa (OBPIIa) gene variants are linked to Parkinson's disease (PD)-related olfactory loss, but their role in clinical subtypes and mechanisms remains unclear. This study examined associations with clinical scales, neuroimaging, and cerebrospinal fluid (CSF) biomarkers. METHODS: Data from the Parkinson's Progression Markers Initiative (PPMI) cohort were analyzed. Multinomial logistic regression was employed to investigate the role of OBPIIa SNPs in PD prodromal or clinically established PD status. Additionally, the associations of OBPIIa SNPs with clinical scales, neuroimaging, and CSF biomarkers were evaluated using multiple linear or logistic regression models. RESULTS: Among the 1079 subjects (195 Healthy controls, 287 prodromal PD, and 597 clinically established PD), rs2590499 and rs2853652 were significantly associated with prodromal PD status, but not with clinically established PD diagnosis. Dopamine transporter (DAT)-SPECT imaging revealed divergent associations: rs3178137 was strongly linked to a higher DAT binding in the caudate, while rs504061 and rs2853652 exhibited a trend toward lower DAT binding. Concurrently, rs72766539 and rs3178137 were statistically significantly correlated to elevated levels of CSF DOPAC in females. In males, rs3178137 showed a trend toward milder non-motor symptoms, higher DAT binding, and higher levels of CSF tau proteins. No significant associations were found between OBPIIa variants and PD severity (H&Y stage). OBPIIa showed no longitudinal association with DAT or CSF progression. CONCLUSION: Our study showed that OBPIIa variants are associated with prodromal phenotypes and dopaminergic-related biomarker characteristics. These findings supported a potential link to early non-motor and biomarker features rather than clinically established PD.