Sargen K, Demaine A G, Kingsnorth A N
Department of Surgery, Plymouth Postgraduate Medical School, Derriford Hospital. Plymouth, United Kingdom.
JOP. 2000 Jul;1(2):24-35.
Pro-inflammatory and regulatory cytokines play a key role in the pathogenesis of acute pancreatitis. Genetic loci encoding cytokines have been shown to be polymorphic, in some cases influencing protein expression.
To investigate if TNF and IL-10 gene loci are associated with the occurrence or severity of acute pancreatitis.
Acute surgical unit within large district hospital serving a population of 500,000. METHODS, Three TNF microsatellite loci (TNFa, TNFb, TNFc), the TNF-308 polymorphism, the IL-10.G microsatellite locus, and 3 i-allelic polymorphisms in the IL-10 5' region were typed using PCR in 135 acute pancreatitis patients and ethnically matched normal controls (n=107). Aetiology of disease was determined and patients grouped according to disease severity by assigning an organ failure score or classification according to the Atlanta system.
Allelic frequency of polymorphic loci in patients with different aetiology and disease course in acute pancreatitis.
No difference was noted in allelic frequency of any of the cytokine gene loci between groups stratified according to disease severity. When aetiology was studied again there was no significant difference in allelic frequency.
The cytokine gene polymorphisms studied play no part in determination of disease severity or susceptibility to acute pancreatitis.
促炎细胞因子和调节性细胞因子在急性胰腺炎的发病机制中起关键作用。编码细胞因子的基因座已被证明具有多态性,在某些情况下会影响蛋白质表达。
研究肿瘤坏死因子(TNF)和白细胞介素-10(IL-10)基因座是否与急性胰腺炎的发生或严重程度相关。
为50万人口服务的大型地区医院的急性外科病房。
使用聚合酶链反应(PCR)对135例急性胰腺炎患者和种族匹配的正常对照者(n = 107)进行三个TNF微卫星基因座(TNFa、TNFb、TNFc)、TNF - 308多态性、IL - 10.G微卫星基因座以及IL - 10 5'区域的3个二等位基因多态性的分型。确定疾病病因,并根据器官衰竭评分或按照亚特兰大系统进行分类,将患者按疾病严重程度分组。
急性胰腺炎不同病因和病程患者中多态性基因座的等位基因频率。
根据疾病严重程度分层的各组之间,任何细胞因子基因座的等位基因频率均无差异。再次研究病因时,等位基因频率也无显著差异。
所研究的细胞因子基因多态性在急性胰腺炎疾病严重程度的确定或易感性方面不起作用。