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<p>Genome-wide association study of Parkinson’s disease (PD) identified common variants associated with lysosomal mechanism, including <i>TMEM175, SCARB2</i>, and <i>CTSB</i>. We investigated the association between common and rare variants across populations using cohorts from the Global Parkinson’s Genetics Program (GP2) (33,733 cases and 18,703 controls from ten ancestries). In the European cohort, we confirmed significant associations with PD risk for all known genetic risk variants across the three genes and <i>TMEM175</i> p. Met393Thr as an independent genome-wide significant signal. Additionally, a novel independent signal, <i>SCARB2</i> rs11547135, was detected. The burden analysis linked PD to <i>SCARB2</i> in African American, Ashkenazi Jewish and East Asian cohorts. Single variants-based tests identified rare missense variants in <i>SCARB2</i> in several populations. Our study reinforces the association of lysosomal genetic variants with PD risk, revealing genetic heterogeneity across populations.</p>

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TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations

  • 期刊论文

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  • 发表日期：

    2025年12月2日

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摘要

Genome-wide association study of Parkinson’s disease (PD) identified common variants associated with lysosomal mechanism, including TMEM175, SCARB2, and CTSB. We investigated the association between common and rare variants across populations using cohorts from the Global Parkinson’s Genetics Program (GP2) (33,733 cases and 18,703 controls from ten ancestries). In the European cohort, we confirmed significant associations with PD risk for all known genetic risk variants across the three genes and TMEM175 p. Met393Thr as an independent genome-wide significant signal. Additionally, a novel independent signal, SCARB2 rs11547135, was detected. The burden analysis linked PD to SCARB2 in African American, Ashkenazi Jewish and East Asian cohorts. Single variants-based tests identified rare missense variants in SCARB2 in several populations. Our study reinforces the association of lysosomal genetic variants with PD risk, revealing genetic heterogeneity across populations.