Abstract

Introduction: Acute pancreatitis is an inflammatory disease with a diverse aetiology and variableclinical course. The IL-l gene cluster has been implicated in this disease.Aims: The aims of the study were to investigate polymorphisms of the genes encoded within the IL-lgene cluster in patients with acute pancreatitis and normal controls and to determine therelationship between the polymorphisms and protein levels.Methods: Genotype and allele frequencies were determined in controls (n=217) and patients withacute pancreatitis (n=137) using the polymerase chain reaction (PCR) followed by digestion withrestriction endonucleases where applicable. Protein levels were determined using in vitrostimulation of PBMCs followed by Enzyme Linked Immunosorbent Assay (ELISA). Patients werecategorised according to severity, organ failure scores and aetiology.Results: Allele l of the VNTR86 polymorphism in the IL-l RN gene was significantly increased inthe severe group of patients compared to controls (81.9% vs 63.0%, x2=9.38, p=0.002, Pc=0.004)and in the idiopathic group compared to controls (82.4% vs 63.0%, x2=9.33, p=0.002, Pc=0.004).The polymorphisms within the genes and between the genes were strongly linked. Significantlymore of the Mspl-VLP-VNTR86-Sspl 2-3-2-2 haplotype was observed in the control (15.7% vs0.1%, x2 =2528.11, p<0.000000l, Pc<0.0000001) and patient (14.0% VS 0.1%, x2 =4368.10,p<0.000000l, Pc<0.0000004) populations than expected. Significantly more of the Pstl-Aval-Alul-Taql2-2-2-1 haplotype was observed in controls (27.7% vs 9.7%, x2 =31.39, p<0.000000l,Pc<0.0000005) and patients (12.5% vs 2.0%, x2=53.69, p<0.000000l, Pc=0.0000007) thanexpected. Preferential combinations of the genotypes existed within controls and patients. Themedian IL-lα and IL-lβ protein levels from unstimulated PBMCs were significantly increased inpatients compared to controls: median values (interquartile range). In the IL-lα study, significantdifferences were found at 24 hours: 193.5 (127.5-363.5) pg/ml vs 1.0 (0.0-3.0) pg/ml, p=0.005, 48hours: 256.5 (171.5-417.0) pg/ml vs 6.5 (2.0-16.0) pg/ml, p=0.006 and at 72 hours: 210.5 (138-427)pg/ml vs 0.5 (0-7) pg/ml, p=0.005. In the IL-l β study, significant differences were found at 24hours: 663 (507-782) pg/ml vs 12 (5-53) pg/ml, p=0.004, 48 hours: 620 (570-1080) pg/ml vs 14.5(11-36) pg/ml, p=0.004 and at 72 hours: 545.5 (442-771) pg/ml vs 12.5 (2-43) pg/ml, p=0.006.Conclusion: Polymorphisms of the IL-l gene cluster are associated with susceptibility to and/orseverity of the acute pancreatitis. Polymorphisms within the IL-l gene cluster are in linkagedisequilibrium. Unstimulated PBMCs from patients with acute pancreatitis secrete significantlymore IL-la and IL-IP protein levels compared to those from controls. The (AC)n, Alu I andVNTR86 polymorphisms do not correspond to differences in functional protein levels.

Document Type

Thesis

Publication Date

2001-01-01

DOI

10.24382/4891

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