Evidence map›Paper›PMID 25424204›Full record

ArticleDigestive diseases and sciences2015

Associations Between CYP2B6 rs707265, rs1042389, rs2054675, and Hirschsprung Disease in a Chinese Population.

Chao Xu, Pingfa Chen, Hua Xie, Hairong Zhu, Dongmei Zhu, Peng Cai, Weiwei Huo, Yufeng Qin, Hongxing Li, Yankai Xia and 1 more

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Article in Digestive diseases and sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Chao XuDepartment of Pediatric Surgery, Nanjing Children's Hospital Affiliated Nanjing Medical University, Nanjing, 210008, China.
Pingfa Chen
Hua Xie
Hairong Zhu
Dongmei Zhu
Peng Cai
Weiwei Huo
Yufeng Qin
Hongxing Li
Yankai Xia
Weibing Tang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies suggested that cytochrome P450 participated in the tumor metastasis and migration. CYP2B6 also acts as an important enzyme which metabolize partially or primarily metabolism of drugs, environmental contaminants, and mutagens. The objective of this study was to investigate the influence of CYP2B6 polymorphism on susceptibility of Hirschsprung disease.

methodsTaqMan assay was performed to determine the genotypes of CYP2B6 rs707265, rs1042389, rs2054675 in 262 cases and 290 control subjects. Logistic regression was used to assess the associations between these polymorphisms and HSCR.

resultsWe observed a significant association of CYP2B6 rs707265 (G>A) polymorphism and HSCR susceptibility (p < 0.001). Besides, rs707265 A presented a significant risk of HSCR (p < 0.001).

conclusionsOur result suggested that CYP2B6 rs707265 modified the risk of HSCR.

Indexed as

Polymorphism, GeneticAsian PeopleCase-Control StudiesChinaCytochrome P-450 CYP2B6Gene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHirschsprung DiseaseHumansLogistic ModelsOdds RatioPhenotypeRisk FactorsCytochrome P-450 CYP2B6

Identifiers

PMID25424204
PMCPMC4427616

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