| Literature DB >> 34781145 |
Daniel Valle-Millares1, Óscar Brochado-Kith1, Alicia Gómez-Sanz1, Luz Martín-Carbonero2, Pablo Ryan3, Ignacio De Los Santos4, Juan M Castro2, Jesús Troya3, Mario Mayoral-Muñoz2, Guillermo Cuevas3, Paula Martínez-Román1, Jesús Sanz-Sanz4, María Muñoz-Muñoz5, María Á Jiménez-Sousa1, Salvador Resino1, Verónica Briz6, Amanda Fernández-Rodríguez7.
Abstract
Gender-specific consequences after HCV eradication are unexplored. MicroRNAs (miRNAs) play a crucial role in the immune response against viral infections. However, few have highlighted miRNA role in sex-biased disease or therapy response. We aim to assess gender differences reflected in the miRNA expression of HIV/HCV-coinfected patients who achieve sustained virological response (SVR) with direct acting antivirals (DAAs). We conducted a prospective study of miRNA expression in PBMCs from 28 chronic HIV/HCV-coinfected patients (HIV/HCV) at baseline and after achieving SVR with DAAs. Sixteen HIV-monoinfected patients (HIV) and 36 healthy controls (HC) were used as controls. Identification of significant differentially expressed (SDE) miRNAs was performed with generalized linear model and mixed GLMs. We also explored putative dysregulated biological pathways. At baseline, the HIV/HCV patients showed differences in the miRNA profile concerning the HIV group (165 and 102 SDE miRNAs for males and females, respectively). Gender-stratified analysis of HIV/HCV group at baseline versus at SVR achievement showed higher differences in males (80 SDE miRNAs) than in females (55 SDE miRNAs). After SVR, HIV/HCV group showed similar values to HIV individuals, especially in females (1 SDE miRNA). However, ten miRNAs in males remained dysregulated, which were mainly involved in cancer, fatty acid, and inflammatory pathways. Taken together, our results show gender-biased dysregulation in the miRNA expression profile of PBMCs after HCV eradication with DAAs. These differences were normalized in females, while miRNA profile and their target-related pathways in males lack of normalization, which may be related to a high-risk of developing liver-related complications.Entities:
Keywords: DAAs; Gender; HCV; HIV; High throughput sequencing; MicroRNAs
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Year: 2021 PMID: 34781145 DOI: 10.1016/j.biopha.2021.112405
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529