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CFTR 的 IVS8-5T 等位基因是慢性胰腺炎的危险因素,尤其是特发性慢性胰腺炎。

IVS8-5T Allele of CFTR is the Risk Factor in Chronic Pancreatitis, Especially in Idiopathic Chronic Pancreatitis.

机构信息

Medical Scientific Research Center, Guangxi Medical University, Nanning, Guangxi, China.

Scientific Research Center, Guilin Medical University, Nanning, Guilin, China.

出版信息

Am J Med Sci. 2020 Jul;360(1):55-63. doi: 10.1016/j.amjms.2020.04.019. Epub 2020 Apr 25.

Abstract

BACKGROUND

Cystic fibrosis transmembrane conductance regulator IVS8-5T gene variation appears to be associated with a higher risk of chronic pancreatitis (CP); however, there is inconsistency between previous reported studies. Here, we performed a meta-analysis to investigate this relationship.

MATERIALS AND METHODS

PubMed and WANFANG databases were searched for the case-control studies that contained Patients with CP with IVS8-5T variation. Odd ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the relevance of IVS8-5T gene variation and CP.

RESULTS

Analysis showed that the frequency of the 5T allele was significantly higher in CP subjects than that in control subjects (OR = 1.43, 95% CI: 1.13-1.81, I = 1.2%). Based on the subgroup analysis stratified by etiology, the 5T allele was associated with a higher risk of idiopathic chronic pancreatitis (ICP) (OR = 1.80, 95% CI: 1.18-2.76, I = 0.0%) and not alcoholic CP (OR = 2.14, 95% CI: 0.98-4.66, I = 0.0%). Further study indicated that the 5T allele was related to higher ICP prevalence in the European population (OR = 1.79, 95% CI: 1.06-3.03, I = 0.0%). In contrast, there was no significant difference between ICP subjects and healthy controls within the Asian population (OR = 1.84, 95% CI: 0.91-3.72, I = 38.0%).

CONCLUSIONS

Cystic fibrosis transmembrane conductance regulator IVS8-5T is a risk factor in patients with CP. IVS8-5T variation may play a significant role in the occurrence of ICP, especially in the European population.

摘要

背景

囊性纤维化跨膜电导调节因子 IVS8-5T 基因突变似乎与慢性胰腺炎(CP)的风险增加有关;然而,之前的报道研究结果并不一致。在这里,我们进行了一项荟萃分析来研究这种关系。

材料和方法

检索了包含 IVS8-5T 变异的 CP 患者的病例对照研究的 PubMed 和万方数据库。使用比值比(ORs)和 95%置信区间(CIs)来评估 IVS8-5T 基因变异与 CP 的相关性。

结果

分析表明,CP 组中 5T 等位基因的频率明显高于对照组(OR=1.43,95%CI:1.13-1.81,I=1.2%)。基于病因学的亚组分析,5T 等位基因与特发性慢性胰腺炎(ICP)的风险增加相关(OR=1.80,95%CI:1.18-2.76,I=0.0%),但与酒精性 CP 无关(OR=2.14,95%CI:0.98-4.66,I=0.0%)。进一步的研究表明,5T 等位基因与欧洲人群中较高的 ICP 患病率相关(OR=1.79,95%CI:1.06-3.03,I=0.0%)。相比之下,亚洲人群中 ICP 患者与健康对照组之间没有显著差异(OR=1.84,95%CI:0.91-3.72,I=38.0%)。

结论

囊性纤维化跨膜电导调节因子 IVS8-5T 是 CP 患者的一个危险因素。IVS8-5T 变异可能在 ICP 的发生中起重要作用,特别是在欧洲人群中。

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