The -A2518G polymorphism in theMCP-1gene and inflammatory bowel disease risk: A meta-analysis

2015 ◽  
Vol 16 (4) ◽  
pp. 177-185 ◽  
Author(s):  
Yu Wen Li ◽  
Ci Qiu Yang ◽  
Ying Lian Xiao ◽  
Jie Li ◽  
Chen Xi Xie ◽  
...  
2016 ◽  
Vol 48 (12) ◽  
pp. 1425-1431 ◽  
Author(s):  
Qiang Wang ◽  
Ke-Qun Xu ◽  
Xiang-Rong Qin ◽  
Wen-Lu ◽  
Yan-Liu ◽  
...  

2015 ◽  
Vol 64 (10) ◽  
pp. 825-831 ◽  
Author(s):  
Peng-Bo Wu ◽  
Jin-Fen Dai ◽  
Qian Wang ◽  
Guo Zhang ◽  
Shi-Yun Tan ◽  
...  

2013 ◽  
Vol 14 (6) ◽  
pp. 11392-11401 ◽  
Author(s):  
Yongchun Shen ◽  
Shujin Guo ◽  
Ting Yang ◽  
Liuqun Jia ◽  
Lei Chen ◽  
...  

2014 ◽  
Vol 41 (4) ◽  
pp. 2679-2685 ◽  
Author(s):  
Jun Wang ◽  
Xufeng Guo ◽  
Shijie Yu ◽  
Jixiang Zhang ◽  
Jia Song ◽  
...  

Genes ◽  
2021 ◽  
Vol 12 (9) ◽  
pp. 1419
Author(s):  
Paweł Petryszyn ◽  
Robert Dudkowiak ◽  
Agnieszka Gruca ◽  
Ewa Jaźwińska-Tarnawska ◽  
Paweł Ekk-Cierniakowski ◽  
...  

P-glycoprotein encoded by the ABCB1 gene constitutes a molecular barrier in the small and large bowel epithelium, and its different expression may influence susceptibility to inflammatory bowel disease (IBD). We aimed to assess the contribution of the C3435T polymorphism to disease risk in the Polish population. A total of 100 patients (50 Crohn’s disease (CD), 50 ulcerative colitis (UC)) and 100 healthy controls were genotyped for the single nucleotide polymorphism (SNP) C3435T by using the PCR-RFLP method. Patients were classified on the basis of disease phenotype and the specific treatment used. A meta-analysis was carried out of our results and those from previously published Polish studies. There was no significant difference in allele and genotype frequencies in IBD patients compared with controls. For CD patients, a lower frequency of TT genotype in those with colonic disease, a lower frequency of T allele, and a higher frequency of C allele in those with luminal disease were observed, whereas for UC patients, a lower frequency of CT genotype was observed in those with left-sided colitis. A meta-analysis showed a tendency towards higher prevalence of CC genotype in UC cases. These results indicate that the C3435T variants may confer a risk for UC and influence disease behaviour.


2020 ◽  
Vol 26 ◽  
Author(s):  
Yang Zhang ◽  
Dandan Li ◽  
Heng Guo ◽  
Weina Wang ◽  
Xingang Li ◽  
...  

Background: Conflicting data exist regarding the influence of thiopurines exposure on adverse pregnancy outcomes in female patients with inflammatory bowel disease (IBD). Objective: The aim of this study was to provide an up-to-date and comprehensive assessment of the safety of thiopurines in pregnant IBD women. Methods: All relevant articles reporting pregnancy outcomes in women with IBD received thiopurines during pregnancy were identified from the databases (PubMed, Embase, Cochrane Library, and ClinicalTrials.gov) with the publication data up to April 2020. Data of included studies were extracted to calculate the relative risk (RR) of multiple pregnancy outcomes: congenital malformations, low birth weight (LBW), preterm birth, small for gestational age (SGA), and spontaneous abortion. The meta-analysis was performed using the random-effects model. Results: Eight studies matched with the inclusion criteria and a total of 1201 pregnant IBD women who used thiopurines and 4189 controls comprised of women with IBD received drugs other than thiopurines during pregnancy were included. Statistical analysis results demonstrated that the risk of preterm birth was significantly increased in the thiopurine-exposed group when compared to IBD controls (RR, 1.34; 95% CI, 1.00-1.79; p=0.049; I 2 =41%), while no statistically significant difference was observed in the incidence of other adverse pregnancy outcomes. Conclusion: Thiopurines’ use in women with IBD during pregnancy is not associated with congenital malformations, LBW, SGA, or spontaneous abortion, but appears to have an association with an increased risk of preterm birth.


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