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MicroRNAs in the Progress of Diabetic Nephropathy: A Systematic Review and Meta-Analysis
Li-Ping Wang1, Yu-Zhen Gao1, Bin Song2
1Department of Biobank, Clinical Medical College, Yangzhou University, Northern Jiangsu People's Hospital, Yangzhou, Jiangsu, China.
Background:
We conducted a systematic review and meta-analysis of existing literature to evaluate the different outcomes of microRNAs (miRNAs) in diabetic nephropathy (DN), including urinary albumin excretion rates, urinary albumin creatinine rates, glomerular filtration rate, HbAc1, and creatinine.
Methods:
Electronic databases including PUBMED, MEDLINE, and EMBASE were searched for eligible publications to July 2018. The following comparisons between treatment groups were included: normal group versus DN group; control group versus micro/macroalbuminuria group.
Results:
Twelve eligible studies that included 2500 participants were finally recruited in this meta-analysis. Fifteen miRNAs (miRNA-21, miRNA-181b, miRNA-194, miRNA-30, miRNA-215, and others) were upregulated whereas seven miRNAs (miRNA-26a, miRNA-126, miRNA-424, miRNA-574-3p, miR-223, miR-155, and miR-192) were downregulated in the DN group compared with control groups. The miR-133b, miR-342, miR-30, miR-192, miR-194, and miR-215 were significantly correlated in urinary albumin excretion rates (r=0.33, 95% CI= 0.26-0.39). miR-192, miR-217, miR-15b, miR-34a, and miR-636 were correlated with urinary albumin creatinine rates (r=0.69; 95% CI=0.12-0.92), while miR-133b, miR-345, miR-33, miR-326, miR-574-3p, miR-126, miR-217, miR-15b, miR-34a, and miR-636 were significantly correlated with HbAc1 (r =0.23, 95% CI = 0.15-0.31). There were twelve miRNAs that were closely related to the glomerular filtration rate (r=0.28, 95% CI =0.21-0.34). Creatinine (r=0.33, 95% CI = 0.22-0.40) was significantly different between normal and DN groups.
Conclusions:
The meta-analysis acquired the correlations between miRNAs and outcomes including UAER, UACR, eGFR, HbAc1, and creatinine in DN. It suggested that miRNAs may participate in the pathogenesis of DN process.
Insights
This meta-analysis reveals specific microRNAs (miRNAs) are altered in diabetic nephropathy (DN) and correlate with key disease markers. These findings suggest miRNAs play a role in DN development.
Area of Science:
- Nephrology
- Genetics
- Biochemistry
Background:
- Diabetic nephropathy (DN) is a major complication of diabetes.
- MicroRNAs (miRNAs) are implicated in various disease processes.
- Understanding miRNA roles in DN is crucial for developing new therapies.
Purpose of the Study:
- To systematically review and meta-analyze the association between miRNAs and clinical outcomes in DN.
- To identify specific miRNAs that are upregulated or downregulated in DN.
- To correlate miRNA levels with markers of kidney function and glycemic control.
Main Methods:
- Systematic review and meta-analysis of published literature.
- Searched PubMed, MEDLINE, and EMBASE databases up to July 2018.
- Included studies comparing normal, DN, and micro/macroalbuminuria groups.
Main Results:
- Twelve studies with 2500 participants were analyzed.
- Fifteen miRNAs were upregulated and seven were downregulated in DN.
- Several miRNAs showed significant correlations with urinary albumin excretion rates, albumin-to-creatinine ratio, HbA1c, glomerular filtration rate, and creatinine levels.
Conclusions:
- This meta-analysis establishes correlations between specific miRNAs and key outcomes in DN.
- The findings support the involvement of miRNAs in the pathogenesis of diabetic nephropathy.
- Further research into miRNA-based diagnostics and therapeutics for DN is warranted.
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