Interleukin-10 promoter polymorphisms and asthma risk: A meta-analysis

Cytokine ◽  
2012 ◽  
Vol 60 (3) ◽  
pp. 849-855 ◽  
Author(s):  
Wei Nie ◽  
Zheng Fang ◽  
Bing Li ◽  
Qing-yu Xiu
Author(s):  
Danyal Imani ◽  
Navid Dashti ◽  
Arash Parvari ◽  
Sajad Shafiekhani ◽  
Fatemeh Alebrahim ◽  
...  

2020 ◽  
Vol 10 (4) ◽  
pp. e38-e38
Author(s):  
Gita Mishra ◽  
Sudeep Gautam ◽  
Thavanati Parvathi Kumara Reddy ◽  
Bhaskar VKS Lakkakula

Introduction: Diabetic nephropathy (DN) is a leading cause of chronic kidney disease (CKD) in diabetes patients. There is ample evidence that the inflammatory pathways are central to both diabetes and DN. Several studies that examined the link between the interleukin-10 (IL10) polymorphisms and DN risk yielded conflicting results. Objectives: The purpose of this meta-analysis is to evaluate the associations between IL10 promoter polymorphisms and DN risk. Methods: A bibliographic search was carried out on PubMed, Google scholar and Web of Science from the beginning until July 30, 2020. Association between IL10 promoter variants (-1082 A>G, -819 C>T and -592 C>A) and DN risk were assessed by considering diabetes without nephropathy (DWN) as well as healthy controls. Data were retrieved and the pooled odds ratio (OR) with 95% confidence interval (CI) was calculated. Results: For the IL10 -1082 A> G analysis, a total of 4 studies with DWN controls (682 cases and 529 controls) and 5 studies with healthy controls (1025 cases and 1625 controls) were considered. For the IL10 -819 C> T analysis, a total of three studies with DWN controls (9619 cases and 445 controls) and 5 studies with healthy controls (1005 cases and 1537 controls) were considered. For the IL10 -592 C> T analysis, a total of 5 studies with DWN controls (819 cases and 645 controls) and 5 studies with healthy controls (1005 cases and 1537 controls) were considered. In addition, there was no evidence of publication bias for IL10 promoter variants. No substantial association was observed between IL10 promoter variants and DN risk. Conclusion: Our study signifies that polymorphisms of IL10 -1082 A>G, -819 C>T and -592 C>A are not linked with DN risk.


Oncotarget ◽  
2017 ◽  
Vol 8 (37) ◽  
pp. 62382-62399 ◽  
Author(s):  
Ping Wang ◽  
Junling An ◽  
Yanfeng Zhu ◽  
Xuedong Wan ◽  
Hongzhen Zhang ◽  
...  

2016 ◽  
Vol 76 (2) ◽  
pp. 172-180 ◽  
Author(s):  
Duo Su ◽  
Yeye Zhang ◽  
Qingqin Wang ◽  
Jing Wang ◽  
Baoquan Jiao ◽  
...  

Author(s):  
Huan LIU ◽  
Yu Feng ◽  
Wei Zhang ◽  
Xiao-Dong Deng ◽  
Ying Ma ◽  
...  

Growing evidence indicated conflicting results that Interleukin-18 (IL-18) promoter polymorphisms rs1946518 (A-607C), rs187238 (G-137C) and rs549908 (A-105C) were associated with asthma risk. The aim of this study is to comprehensively evaluate the IL-18 polymorphisms and asthma by a systematic review and meta-analysis. A total of 12 studies testing the association between these polymorphisms and asthma were examined (8 studies for A-607C, 8 studies for G-137C, and 4 studies for A-105C) in the update meta-analysis, up to Dec 30, 2017. Summary odds ratios (ORs) and 95% confidence intervals (CI) were used to estimate the strength of association between each polymorphism and asthma using fixed- and random-effects models when appropriate. Heterogeneity and publication bias were evaluated. The meta-analysis results indicated that any allele frequencies of the IL-18 polymorphisms (A-607C, G-137C and A-105C) was not associated with asthma risk (p>0.05). And no statistically significant association was observed between genotype frequencies of these polymorphisms and asthma under different genetic models (p>0.05). Subgroup analysis results were similar to the main analysis by ethnicity, sample size, genotyping methods, matching criteria and quality score. There was no evidence of publication bias. The present meta-analysis suggests that IL-18 polymorphisms (A-607C, G-137C and A-105C) were unlikely to be associated with asthma risk.


Gene ◽  
2013 ◽  
Vol 515 (1) ◽  
pp. 49-55 ◽  
Author(s):  
Wei Fan ◽  
Shangwei Li ◽  
Qiong Chen ◽  
Zhongying Huang ◽  
Qianhong Ma ◽  
...  

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