α-Synuclein Gene Hypomethylation in LRRK2 Parkinson's Disease Patients.

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Tác giả: Ana Cámara, Lorena de Mena, Mario Ezquerra, Manel Fernández, Rubén Fernández-Santiago, Alicia Garrido, María-José Martí, Guillem Parés, Jesica Pérez, Daniel F Pilco-Janeta, Eduardo Tolosa, Francesc Valldeoriola

Ngôn ngữ: eng

Ký hiệu phân loại: 305.568 +Alienated and excluded classes

Thông tin xuất bản: United States : Movement disorders : official journal of the Movement Disorder Society , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 720460

BACKGROUND: α-Synuclein (SNCA) gene hypomethylation was reported in idiopathic Parkinson's disease (iPD). Based on a high clinical resemblance between iPD and leucine-rich repeat kinase 2 (LRRK2)-driven Parkinson's disease (L2PD), we investigated the epigenetic status of SNCA in an extensive LRRK2 clinical cohort from Spain. METHODS: We assessed the methylation levels of 23 CpG sites in the SNCA promoter region using peripheral blood DNA from L2PD patients (n = 151), LRRK2 nonmanifesting carriers (n = 55), iPD patients (n = 115), and healthy control subjects (n = 154) (total: N = 475). RESULTS: Compared with control subjects, we found significant SNCA hypomethylation in 11 of 23 CpGs in L2PD (48%), whereas 22 CpGs (96%) were hypomethylated in iPD. In line with a healthy status, asymptomatic mutation carriers had similar SNCA methylation profiles to control subjects. CONCLUSIONS: This study shows for the first time that SNCA hypomethylation occurs in patients with L2PD. Further studies addressing SNCA methylation status in additional worldwide LRRK2 cohorts are warranted. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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