The role of microRNAs in understanding sex-based differences in Alzheimer's disease

Author:

Llera-Oyola Jaime1,Carceller Héctor1,Andreu Zoraida2,Hidalgo Marta R.1,Soler-Sáez Irene1,Gordillo Fernando1,Gómez-Cabañes Borja1,Roson Beatriz3,Iglesia-Vayá Maria de la4,Mancuso Roberta5,Guerini Franca R.5,Mizokami Akiko6,Garcia Francisco Garcia1ORCID

Affiliation:

1. CIPF: Centro de Investigacion Principe Felipe

2. Fundación Instituto Valenciano de Oncologia: Fundacion Instituto Valenciano de Oncologia

3. Hospital Clínico Universitario: Hospital Clinico Universitario

4. FISABIO: Fundacio per al Foment de la Investigacio Sanitaria i Biomedica

5. Don Gnocchi Foundation: Fondazione Don Carlo Gnocchi Onlus

6. Kyushu University: Kyushu Daigaku

Abstract

Abstract Background: The incidence of Alzheimer's disease (AD) - the most frequent cause of dementia - is expected to increase as life expectancies rise across the globe. While sex-based differences in AD have previously been described, there remain uncertainties regarding any association between sex and disease-associated molecular mechanisms. Studying sex-specific expression profiles of regulatory factors such as microRNAs (miRNAs) could contribute to more accurate disease diagnosis and treatment. Methods: A systematic review identified five studies of microRNA expression in AD patients that incorporated information regarding the biological sex of samples in the Gene Expression Omnibus repository. A differential microRNA expression analysis was performed, considering disease status and patient sex. Subsequently, results were integrated within a meta-analysis methodology, with a functional enrichment of meta-analysis results establishing an association between altered miRNA expression and relevant Gene Ontology terms. Results: Meta-analyses of miRNA expression profiles in blood samples revealed the alteration of sixteen miRNAs in female and twenty-two miRNAs in male AD patients. We discovered nine miRNAs commonly overexpressed in both sexes, suggesting a shared miRNA dysregulation profile. Functional enrichment results based on miRNA profiles revealed sex-based differences in biological processes; most affected processes related to ubiquitination, regulation of different kinase activities, and apoptotic processes in males, but RNA splicing and translation in females. Meta-analyses of miRNA expression profiles in brain samples revealed the alteration of six miRNAs in female and four miRNAs in male AD patients. We observed a single underexpressed miRNA in female and male AD patients (hsa-miR-767-5p); however, the functional enrichment analysis for brain samples did not reveal any specifically affected biological process. Conclusions: Sex-specific meta-analyses supported the detection of differentially expressed miRNAs in female and male AD patients, highlighting the relevance of sex-based information in biomedical data. Further studies on miRNA regulation in AD patients should meet the criteria for comparability and standardization of information.

Publisher

Research Square Platform LLC

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