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Association between genetic variants in ZNF365 and inflammatory bowel disease risk in Caucasians: a meta-analysis and trial sequential analysis.
Wu, Peng-Bo; Zhang, Yu; Nie, Gang; Huang, Xu; Yu, Yuan-Jie; Yin, An-Ning; Zhou, Rui; He, Chun-Ping; Wang, Peng.
Afiliação
  • Wu PB; Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei China.
  • Zhang Y; Infrastructure Management Department, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
  • Nie G; Department of Dermatovenereology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong China.
  • Huang X; Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei China.
  • Yu YJ; Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei China.
  • Yin AN; Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei China.
  • Zhou R; Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei China.
  • He CP; Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei China.
  • Wang P; Department of Gastrointestinal Surgery, Renmin Hospital of Wuhan University, Wuhan Hubei Province, China.
Expert Rev Clin Immunol ; 17(8): 915-921, 2021 08.
Article em En | MEDLINE | ID: mdl-34092165
ABSTRACT

OBJECTIVE:

The published studies regarding the relationships between zinc finger 365 (ZNF365) polymorphisms and inflammatory bowel disease (IBD) risk in Caucasians have yielded conflicting results. Therefore, we performed a meta-analysis to clarify this issue.

METHODS:

The Electronic databases of PubMed, Web of Science, Wiley Online Library, and EMBASE were searched for eligible studies up to 31 November 2020. The quality of eligible studies was evaluated using the Newcastle-Ottawa Scale. The pooled odds ratios (ORs) with 95% confidence intervals (CIs) under different genetic models were calculated to assess the strength of associations.

RESULTS:

A total of 22 relevant case-control studies with 9542 ulcerative colitis (UC) patients and 13,886 controls, as well as 13,651 Crohn's disease (CD) patients and 15,256 controls, were involved in our meta-analysis. rs10761659 polymorphism significantly decreased CD and UC risk (except for the heterozygous model and the dominant model in UC), and rs10995271 polymorphism was significantly associated with UC (except for the heterozygous model and dominant model) rather than CD.

CONCLUSIONS:

The meta-analysis demonstrated that the rs10761659 polymorphism might be a protective factor for both UC and CD in Caucasians, while the rs10995271 polymorphism might be a risk factor for UC rather than CD in Caucasians.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Colite Ulcerativa / Doença de Crohn Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Colite Ulcerativa / Doença de Crohn Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article