Small Ubiquitin-Like Modifier 4 (SUMO4) Gene M55V Polymorphism and Type 2 Diabetes Mellitus: A Meta-analysis Including 6,823 Subjects
Many studies suggest that the M55V gene polymorphism (rs237025) may be associated with an increased risk of type 2 diabetes mellitus (T2DM). However, due to other conflicting results, a clear consensus is lacking in the matter. A meta-analysis consisting of 6,823 subjects from 10 studies was conduct...
Saved in:
Published in | Frontiers in endocrinology (Lausanne) Vol. 8; p. 303 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
02.11.2017
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Many studies suggest that the
M55V gene polymorphism (rs237025) may be associated with an increased risk of type 2 diabetes mellitus (T2DM). However, due to other conflicting results, a clear consensus is lacking in the matter.
A meta-analysis consisting of 6,823 subjects from 10 studies was conducted to elucidate relationship between the
M55V gene polymorphism and T2DM. Depending on the heterogeneity of the data, either a fixed or random-effects model would be used to assess the combined odds ratio (ORs) and their corresponding 95% confidence interval (CI).
gene M55V polymorphism was significantly associated with T2DM in the whole population under allelic (OR: 1.18, 95% CI: 1.10-1.28,
= 1.63 × 10
), recessive (OR: 1.59, 95% CI: 1.14-2.23,
= 0.006), dominant (OR: 0.815, 95% CI: 0.737-0.901,
= 6.89 × 10
), homozygous (OR: 1.415, 95% CI: 1.170-1.710,
= 0.0003), heterozygous (OR: 1.191, 95% CI: 1.072-1.323,
= 0.001), and additive genetic models (OR: 1.184, 95% CI: 1.097-1.279,
= 1.63 × 10
). In our subgroup analysis, a significant association was found again in the Chinese population, but not in Japanese or Iranian population.
gene M55V polymorphism may correlate with increased T2DM risk. Chinese carriers of the V allele of the
gene M55V polymorphism may be predisposed to developing T2DM. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Specialty section: This article was submitted to Genomic Endocrinology, a section of the journal Frontiers in Endocrinology Reviewed by: Sinan Tanyolac, Istanbul University, Turkey; Marta Letizia Hribal, Magna Græcia University, Italy These authors have contributed equally to this work. Edited by: Antonio Brunetti, Magna Græcia University, Italy |
ISSN: | 1664-2392 1664-2392 |
DOI: | 10.3389/fendo.2017.00303 |