Why the study?
Evidence suggests lncRNAs are involved in diabetes mellitus pathogenesis, but results regarding lncRNA expression in DM patients remain inconclusive.
Are specific lncRNAs consistently dysregulated in patients with diabetes mellitus compared to controls?
Are specific lncRNAs consistently dysregulated in patients with diabetes mellitus compared to controls?
Six specific lncRNAs are consistently dysregulated in diabetes mellitus, highlighting their potential role as biomarkers and involvement in metabolism-related pathways.
Supports lncRNA biomarker validation in diabetes; confirms consistent dysregulation across studies while leaving clinical adoption open.
Long non-coding RNAs (lncRNAs) are non-coding transcripts that have emerged as one of the largest and diverse RNA families that regulate gene expression. Accumulating evidence has suggested a number of lncRNAs are involved in diabetes mellitus (DM) pathogenesis. However, results about lncRNA expressions in DM patients are still inconclusive. Thus, we performed a systematic review of the literature on the subject followed by bioinformatics analyses to better understand which lncRNAs are dysregulated in DM and in which pathways they act. Pubmed, Embase, and Gene Expression Omnibus (GEO) repositories were searched to identify studies that investigated lncRNA expression in cases with DM and non-diabetic controls. LncRNAs consistently dysregulated in DM patients were submitted to bioinformatics analysis to retrieve their target genes and identify potentially affected signaling pathways under their regulation. Fifty-three eligible articles were included in this review after the application of the inclusion and exclusion criteria. Six hundred and thirty-eight lncRNAs were differentially expressed between cases and controls in at least one study. Among them, six lncRNAs were consistently dysregulated in patients with DM ( Anril , Hotair , Malat1 , Miat , Kcnq1ot1 , and Meg3 ) compared to controls. Moreover, these six lncRNAs participate in several metabolism-related pathways, evidencing their importance in DM. This systematic review suggests six lncRNAs are dysregulated in DM, constituting potential biomarkers of this disease.
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Dieter et al. (2021) studied this question.
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