Department of Gastroenterology and Alimentary Tract Surgery, Tampere University Hospital, 33520 Tampere, Finland.
Faculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Int J Mol Sci. 2022 Dec 11;23(24):15726. doi: 10.3390/ijms232415726.
Only 3-5% of heavy alcohol users develop acute alcohol pancreatitis (AAP). This suggests that additional triggers are required to initiate the inflammatory process. Genetic susceptibility contributes to the development of AAP, and SPINK1 mutation is a documented risk factor. We investigated the prevalence of the SPINK1(N34S) mutation in patients with AAP compared to heavy alcohol users who had never suffered an episode of pancreatitis. Blood samples for the mutational analysis from patients with first episode ( = 60) and recurrent AAP ( = 43) and from heavy alcohol users without a history of AAP ( = 98) as well as from a control population ( = 1914) were obtained. SPINK1 mutation was found in 8.7% of the patients with AAP. The prevalence was significantly lower in healthy controls (3.4%, OR 2.72; 1.32-5.64) and very low in alcoholics without pancreatitis (1.0%, OR 9.29; 1.15-74.74). In a comparison adjusted for potential cofounders between AAP patients and alcoholics, SPINK1 was found to be an independent marker for AAP. The prevalence of the SPINK1 mutation is overrepresented in AAP patients and very low in alcoholics without pancreatitis. This finding may play a role in understanding the variable susceptibility to AAP found in heavy alcohol users.
仅有 3-5%的重度饮酒者会发展为急性酒精性胰腺炎(AAP)。这表明需要其他触发因素来启动炎症过程。遗传易感性促成了 AAP 的发生,而 SPINK1 突变是一个已证实的危险因素。我们研究了 AAP 患者中 SPINK1(N34S)突变的患病率,并与从未发生过胰腺炎的重度饮酒者进行了比较。从首次发作的 AAP 患者(n=60)、复发性 AAP 患者(n=43)、无 AAP 病史的重度饮酒者(n=98)以及对照人群(n=1914)中获得了用于突变分析的血液样本。在 AAP 患者中发现了 8.7%的 SPINK1 突变。在健康对照组中(3.4%,OR 2.72;1.32-5.64),其患病率显著降低,在无胰腺炎的酗酒者中(1.0%,OR 9.29;1.15-74.74)非常低。在调整了潜在混杂因素后,将 AAP 患者与酗酒者进行比较,发现 SPINK1 是 AAP 的独立标志物。SPINK1 突变的患病率在 AAP 患者中过高,而在无胰腺炎的酗酒者中非常低。这一发现可能有助于理解重度饮酒者中发现的对 AAP 的不同易感性。