首页> 外文期刊>Gut: Journal of the British Society of Gastroenterology >A loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders.
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A loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders.

机译:日本胰腺疾病患者的阴离子胰蛋白酶原(PRSS2)基因中功能丧失的p.G191R变体。

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摘要

OBJECTIVE: There is a concept that pancreatitis results from an imbalance of proteases and their inhibitors within the pancreatic parenchyma. It has been recently shown that a loss-of-function variant, c.571G>A (p.G191R), in the anionic trypsinogen (PRSS2) gene protects against chronic pancreatitis in European populations. Here we examined the association of the p.G191R variant with pancreatic disorders in Japan. METHODS: Genomic DNA was prepared from 378 healthy controls and 604 patients with pancreatic disorders (241 patients with chronic pancreatitis, 174 with acute pancreatitis, and 189 with pancreatic neoplasm). Mutational analysis of the PRSS2 gene was performed by polymerase chain reaction-restriction fragment length polymorphism and direct sequencing. RESULTS: The heterozygous p.G191R variant was found in three of 241 (1.2%) patients with chronic pancreatitis, in seven of 174 (4.0%) patients with acute pancreatitis, and in 12 of 189 (6.3%) patients with pancreatic neoplasm. The p.G191R variant was found in 25 (two were homozygous and 23 were heterozygous) of 378 (6.6%) healthy controls. The p.G191R frequency in patients with chronic pancreatitis was lower than that in healthy controls (p = 0.001; odds ratio (OR) 0.178; 95% confidence interval (CI) = 0.057 to 0.561). The p.G191R frequency was lower in patients with alcoholic (0.9%; p = 0.015; OR, 0.132; 95% CI, 0.022 to 0.779) and idiopathic (1.0%; p = 0.025; OR, 0.144; 95% CI, 0.025 to 0.851) chronic pancreatitis than that in healthy controls. There were no statistical differences in the p.G191R frequency between healthy controls and patients with acute pancreatitis or with pancreatic neoplasm. Patients with alcoholic acute pancreatitis (n = 59) had no variant carrier, and the p.G191R frequency was lower than that in healthy controls (p = 0.035). CONCLUSION: The p.G191R variant protected against alcoholic and idiopathic chronic pancreatitis as well as alcoholic acute pancreatitis in Japan.
机译:目的:有一个概念认为胰腺炎是由胰腺实质内蛋白酶及其抑制剂的失衡引起的。最近显示,阴离子胰蛋白酶原(PRSS2)基因中的功能丧失型变体c.571G> A(p.G191R)可预防欧洲人群中的慢性胰腺炎。在这里,我们研究了p.G191R变体与日本胰腺疾病的关系。方法:从378名健康对照者和604名胰腺疾病患者(241名慢性胰腺炎患者,174名急性胰腺炎患者和189名胰腺肿瘤患者)中制备基因组DNA。 PRSS2基因的突变分析是通过聚合酶链反应-限制性片段长度多态性和直接测序进行的。结果:241例慢性胰腺炎患者中有3例(1.2%)发现了p.G191R杂合子,174例(4.0%)急性胰腺炎患者中有7例,189例胰腺癌患者(6.3%)中发现了12例(6.3%)。在378名(6.6%)健康对照者中,有25名(两个是纯合子,23个是杂合子)发现了p.G191R变体。慢性胰腺炎患者的p.G191R频率低于健康对照组(p = 0.001;优势比(OR)0.178; 95%置信区间(CI)= 0.057至0.561)。酒精中毒(0.9%; p = 0.015; OR,0.132; 95%CI,0.022至0.779)和特发性(1.0%; p = 0.025; OR,0.144; 95%CI,0.025)患者的p.G191R频率较低至0.851)慢性胰腺炎要比健康对照者高。健康对照组和急性胰腺炎或胰腺肿瘤患者之间的p.G191R频率无统计学差异。酒精性急性胰腺炎患者(n = 59)没有变异携带者,p.G191R频率低于健康对照者(p = 0.035)。结论:p.G191R变体可预防日本的酒精性和特发性慢性胰腺炎以及酒精性急性胰腺炎。

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