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Multi-omics study of molecular and genetic bases of orthostatic hypotension

Title: Multi-omics study of molecular and genetic bases of orthostatic hypotension
Authors: Elena Zelenova; Veronika Daniel; Maria Bruttan; Lilya Artemieva; Ekaterina Spektor; Aleksandra Mamchur; Daria Kashtanova; Mikhail Ivanov; Gerel Abushinova; Lorena Matkava; Antonina Rumyantseva; Aleksey Ivashechkin; Pavel Grebnev; Liliya Golubnikova; Sergey Mitrofanov; Anna Akopyan; Olga Beloshevskaya; Tatiana Saliyeva; Irina Tarasova; Irina Strazhesko; Vladimir Yudin; Valentin Makarov; Anton Keskinov; Olga Tkacheva; Sergey Yudin; Veronika Skvortsova
Source: Clinical Epigenetics, Vol 17, Iss 1, Pp 1-17 (2025)
Publisher Information: BMC
Publication Year: 2025
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: Orthostatic hypotension; Geriatric syndromes; Older adults; DNA methylation; Genomics; Transcriptomics; Multi-omics technologies; Medicine; Genetics; QH426-470
Description: Orthostatic hypotension is a sharp decrease in blood pressure when an individual transitions from a supine to an upright position. OH affects at least 30% of older adults. It is attributed to the dysfunction of the autonomic innervation and decreased vascular bed capacity. Genomic (n = 2526), methylomic (n = 910), and transcriptomic (n = 391) data from centenarians aged 90 years and older were used to examine molecular and genetic factors for OH. No statistically significant genetic predictors of OH were identified. However, the study revealed numerous epigenetic markers of OH indicative of general aging, such as DNA hypomethylation. The predictive DNA methylation-based model for orthostatic hypotension demonstrated an average accuracy of 79%. The transcriptome analyses highlighted associations between OH and inflammation pathways, as well as other age-related biological processes. Integrated omics and clinical data have identified six key mechanisms associated with orthostatic hypotension: metabolic dysregulation, impaired muscle tone, altered cell proliferation, inflammation, humoral regulation, and neural regulation.
Document Type: article in journal/newspaper
Language: English
Relation: https://doi.org/10.1186/s13148-025-02019-3; https://doaj.org/toc/1868-7083; https://doaj.org/article/2f42ba78686a4ab4970f000373e218b2
DOI: 10.1186/s13148-025-02019-3
Availability: https://doi.org/10.1186/s13148-025-02019-3; https://doaj.org/article/2f42ba78686a4ab4970f000373e218b2
Accession Number: edsbas.2191F645
Database: BASE