优势比
GSTP1公司
单核苷酸多态性
医学
置信区间
急性胰腺炎
内科学
遗传倾向
病例对照研究
SNP公司
基因型
胃肠病学
生物信息学
生物
遗传学
基因
疾病
作者
Francisco d' Oliveira Martins,Bruno Costa Gomes,António Sebastião Rodrigues,José Rueff
出处
期刊:Pancreas
[Ovid Technologies (Wolters Kluwer)]
日期:2016-10-12
卷期号:46 (1): 71-76
被引量:15
标识
DOI:10.1097/mpa.0000000000000707
摘要
Genetic testing could play a critical role in diagnosis and prognosis of acute pancreatitis (AP) and guide effective therapeutic interventions. We hypothesized that genetic polymorphisms in apoptosis and oxidative stress genes could determine incidence or severity in AP.We conducted a hospital-based case-control study in a white Portuguese population (133 AP patients and 232 age- and sex-matched healthy controls) to evaluate the role of 15 gene polymorphisms (2 deletions and 13 single nucleotide polymorphisms [SNPs]) in oxidative stress (GSTM1, GSTT1, GSTP1) and apoptosis genes (CASP7, CASP8, CASP9, CASP10, LTA, TNFRSF1B, TP53) in AP. Criteria for AP were abdominal pain, hyperamylasemia, and contrast-enhanced computed tomography.The presence of GSTM1 is associated with increased susceptibility for AP, and the GSTP1 Val105Ile SNP is associated with an increased risk for AP in men. CASP9 Phe136Leu/Phe136Phe SNPs (heterozygotes) increases the risk for mild AP (odds ratio, 3.616; 95% confidence interval, 1.151-11.364; P < 0.05), whereas the homozygotic genotype of CASP9 Ala28Val decreases risk for mild AP (odds ratio, 0.296; 95% confidence interval, 0.091-0.963; P < 0.05).Our results suggest that variations in GSTM1, GSTP1, and CASP9 may influence risk for AP.
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