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Título: | Genetics of neurogenic orthostatic hypotension in Parkinson’s disease, results from a cross-sectional in silico study | Autor: | Chevalier, Guenson Udovin, Lucas D. Otero Losada, Matilde Bordet, Sofía Capani, Francisco Luo, Sheng Goetz, Christopher Pérez Lloret, Santiago |
Palabras clave: | ENFERMEDAD DE PARKINSON; POLIMORFISMO DE NUCLEÓTIDO SIMPLE; ENFERMEDADES NEURODEGENERATIVAS; FISIOPATOLOGÍA; HIPOTENSIÓN ORTOSTÁTICA NEUROGÉNICA | Fecha de publicación: | 2023 | Editorial: | MDPI | Cita: | Pérez Lloret, S., Chevalier, G., Udovin, L., Otero Losada, M. Genetics of neurogenic orthostatic hypotension in Parkinson’s disease, results from a cross-sectional in silico study [en línea]. Brain Sciences. 2023, 13, 506. doi: 10.3390/brainsci13030506. Disponible en: https://repositorio.uca.edu.ar/handle/123456789/17348 | Resumen: | Abstract: The genetic basis of Neurogenic Orthostatic Hypotension (NOH) in Parkinson’s disease (PD) has been inadequately explored. In a cross-sectional study, we examined the association between NOH and PD-related single-nucleotide polymorphisms (SNPs) and mapped their effects on gene expression and metabolic and signaling pathways. Patients with PD, free from pathological conditions associated with OH, and not taking OH-associated medications were included. NOH was defined as per international guidelines. Logistic regression was used to relate SNPs to NOH. Linkage-disequilibrium analysis, expression quantitative trait loci, and enrichment analysis were used to assess the effects on gene expression and metabolic/signaling pathways. We included 304 PD patients in the study, 35 of whom had NOH (11.5%). NOH was more frequent in patients with SNPs in SNCA, TMEM175, FAM47E-STBD1, CCDC62, SCN3A, MIR4696, SH3GL2, and LZTS3/DDRGK1 and less frequent in those with SNPs in ITGA8, IP6K2, SIPA1L2, NDUFAF2. These SNPs affected gene expression associated with the significant hierarchical central structures of the autonomic nervous system. They influenced several metabolic/signaling pathways, most notably IP3/Ca++ signaling, the PKA-CREB pathway, and the metabolism of fatty acids. These findings provide new insights into the pathophysiology of NOH in PD and may provide targets for future therapies. | URI: | https://repositorio.uca.edu.ar/handle/123456789/17348 | ISSN: | 2076-3425 | Disciplina: | MEDICINA | DOI: | 10.3390/brainsci13030506 | Derechos: | Atribución-NoComercial-CompartirIgual 4.0 Internacional Acceso abierto |
Fuente: | Brain Sciences. 2023, 13, 506 |
Aparece en las colecciones: | Artículos |
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