“…Excess alcohol intake (pure alcohol consumption ≥30 g/day for more than 2 years), biliary lithiasis (presence of gallbladder, common bile duct lithiasis or sludge) [17,18], hypercalcemia (>3 mmol/l) [19], hypertriglyceridemia (>10 mmol/l) [20], drugs/medication causing acute pancreatitis, personal history of abdominal radiotherapy [21], autoimmune disease (personal history of autoimmune disease, dosing of gammaglobulin, immunoglobulin A, G (including subfraction IgG4) and M, Latex Waaler-Rose, anti-nuclear antibodies, anti-smooth muscle antibodies, anti-mitochondrial antibodies, anti-neutrophil cytoplasmic antibodies) [22], traumatic pancreatitis and duct obstruction (mainly due to tumor) were ruled out in all patients. Besides the search for CF mutations, a hereditary cause of pancreatitis was systematically ruled out by questioning patients about family history and by searching for cationic trypsinogen gene mutations [14,16,23,24,25]. Patients with SPINK1 mutations (n = 2), which are considered as ‘disease modifiers’ rather than a causative agent, were not excluded from the study.…”