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The role of the TNF-α gene -308 G/A polymorphism in the development of diabetic nephropathy: An updated meta-analysis.

Authors :
Tiongco RE
Aguas IS
Cabrera FJ
Catacata M
Flake CC
Manao MA
Policarpio A
Source :
Diabetes & metabolic syndrome [Diabetes Metab Syndr] 2020 Nov-Dec; Vol. 14 (6), pp. 2123-2129. Date of Electronic Publication: 2020 Nov 06.
Publication Year :
2020

Abstract

Background and Aims: Several studies have tried to link the relationship of tissue necrosis factor-alpha (TNF-α) -308 G/A polymorphism with the development of diabetic nephropathy (DN). However, these studies failed to reach a consensus due to conflicting results. This meta-analysis was done to thoroughly investigate the correlation between the polymorphism and DN development.<br />Methods: To carry out the objective, patients with type 2 diabetes mellitus (T2DM) were used as controls, while patients who developed DN were utilized as cases. Eight studies (i.e., published between 2007 and 2018) were included in the present meta-analysis. Review Manager 5.3 was used to compute for the odds ratios (OR) and 95% confidence interval (CI) of the overall and post-outlier outcomes.<br />Results: Overall, an association between DN development and the -308 G/A polymorphism was observed. However, Galbraith's plot analysis (as analyzed using Meta-Essentials) led to the removal of two studies, which significantly reduced heterogeneity. Post-outlier outcomes show significant results in the allelic (OR: 1.23; 95% CI: 1.01-1.50; p = 0.04) and co-dominant (OR: 1.60; 95% CI: 1.02-2.51; p = 0.04) models.<br />Conclusion: T2DM individuals with the -308 G/A polymorphism in the TNF-α gene are more likely to develop DN.<br />Competing Interests: Declaration of competing interest The authors declare no conflict of interest.<br /> (Copyright © 2020 Diabetes India. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1878-0334
Volume :
14
Issue :
6
Database :
MEDLINE
Journal :
Diabetes & metabolic syndrome
Publication Type :
Academic Journal
Accession number :
33395772
Full Text :
https://doi.org/10.1016/j.dsx.2020.10.032