International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: unknown, P. 136748 - 136748
Published: Oct. 1, 2024
Language: Английский
International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: unknown, P. 136748 - 136748
Published: Oct. 1, 2024
Language: Английский
International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(2), P. 637 - 637
Published: Jan. 14, 2025
Type 2 diabetes (T2D) is a heterogeneous disease influenced by both genetic and environmental factors. Recent studies suggest that T2D subtypes may exhibit distinct gene expression profiles. In this study, we aimed to identify cluster-specific miRNA signatures for the previously reported five clinical characterize underlying pathophysiology of long-standing T2D: severe insulin-resistant (SIRD), insulin-deficient (SIDD), mild age-related (MARD), obesity-related (MOD), early-onset (MEOD). We analyzed circulating microRNAs (miRNAs) in 45 subjects representing clusters 7 non-T2D healthy controls single-end small RNA sequencing. Bioinformatic analyses identified total 430 known miRNAs 13 unreported novel miRNAs. Of these, 71 were upregulated 37 downregulated either or individual clusters. Each subtype was associated with specific dysregulated profile, from controls. Specifically, 3 unique SIRD, 1 MARD, 9 MOD, 18 MEOD. Among miRNAs, 11 SIDD, Our study confirms heterogeneity T2D, represented distinguishable clinically epigenetically highlights potential as markers distinguishing subtypes.
Language: Английский
Citations
0Clinica Chimica Acta, Journal Year: 2025, Volume and Issue: unknown, P. 120178 - 120178
Published: Feb. 1, 2025
Language: Английский
Citations
0Functional & Integrative Genomics, Journal Year: 2025, Volume and Issue: 25(1)
Published: April 5, 2025
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: unknown, P. 136748 - 136748
Published: Oct. 1, 2024
Language: Английский
Citations
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