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bioRxiv · 10.1101/2025.07.13.664610

Mapping the microRNA-mediated crosstalk between insulin resistance and Alzheimers disease : a computational genomic insight

Ahmed, T. F.·Ahmed, A.·Haque, Z.·Azmi, M. B.·Salam, J. U.·Hanif, F.
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Abstract

Insulin resistance (IR) and Alzheimers disease (AD) share overlapping molecular mechanisms, but the precise link between these conditions remains unclear. MicroRNAs, as post-transcriptional regulators of gene expression, may mediate this connection by targeting genes involved in both pathways. In this study, we employed a multi-step bioinformatics approach to identify microRNAs that simultaneously regulate genes associated with IR and AD. Twenty key IR-related genes were selected from the literature, and their microRNA regulators were predicted using five computational tools. These predictions were validated using experimentally supported databases (TarBase and miRTarBase), and each miRNA-gene interaction was scored. Sixteen high-confidence microRNAs were shortlisted based on cumulative prediction and validation scores. These microRNAs were then analyzed for their interactions with AD pathway genes via KEGG pathway analysis. The AD-related target genes were further processed through protein-protein interaction network analysis using STRING and hub gene identification via Cytoscape. Functional enrichment of these hub genes using Gene Ontology and KEGG analysis revealed their involvement in shared biological processes, including apoptosis, insulin signaling, glucose metabolism, and neuroinflammation. Prominent candidates such as miR-7-5p, miR-106b, miR-424-5p, and miR-15a were identified. These results suggest that a subset of microRNAs may serve as critical molecular links between IR and AD, offering potential targets for early diagnosis and intervention.

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Ahmed, T. F., Ahmed, A., Haque, Z., Azmi, M. B., Salam, J. U., Hanif, F.. 2025-07-18. Mapping the microRNA-mediated crosstalk between insulin resistance and Alzheimers disease : a computational genomic insight. https://doi.org/10.1101/2025.07.13.664610

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