Lack of Association between Interleukin 12 C(-1188)A Polymorphism and Irritable Bowel Syndrome

Barkhordari, Elham; Amirzargar, Ali Akbar; Ebrahimi-Daryani, Naser; Mahmoudi, Mahdi; Ansaripour, Bita; Alighardashi, Maryam; Ahmadi-Ashtiani, Hamid Reza; Bashashati, Mohammad; Rezaei, Nima

Lack of Association between Interleukin 12 C(-1188)A Polymorphism and Irritable Bowel Syndrome

Document Type : Short communication

Authors

Elham Barkhordari ¹

Ali Akbar Amirzargar ¹

Naser Ebrahimi-Daryani ²

Mahdi Mahmoudi ¹

Bita Ansaripour ¹

Maryam Alighardashi ¹

Hamid Reza Ahmadi-Ashtiani ³

Mohammad Bashashati ⁴

Nima Rezaei ⁵

¹ Molecular Immunology Research Center, Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

² Department of Gastroenterology and Hepatology, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran

³ Biochemistry and Nutrition Department, Zanjan University of Medical Sciences, Zanjan; and Clinical Biochemistry Department, School of Medical Science, Tarbiat Modarres University, Tehran, Iran

⁴ Gastrointestinal Research Group, University of Calgary, Calgary, Alberta, Canada

⁵ Molecular Immunology Research Center, Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children’s Me

Abstract

Irritable Bowel Syndrome (IBS) is a functional gastrointestinal disorder, characterized by recurrent abdominal pain and altered bowel habits. This study was performed to investigate the important role of interleukin-12 (IL-12) in intestinal inflammation. For this study seventy one patients with IBS and 140 controls were investigated. The allele and genotype frequencies of IL-12 C(-1188)A were determined using polymerase chain reaction with sequence-specific primers. The allele A was more common that the allele C in both groups of patients and controls. There was not any significant difference on IL-12 alleles and genotypes between patients and controls. The AA genotype was the most common genotypes, which was seen in 57.4% of the patients and 51.4% of the controls (p=0.53). Although frequency of the CC genotype in the control group was lower than the patient group, this difference was not significant (5.7% vs. 11.5%, respectively, p=0.16). Considering the lack of association between IL-12 C(-1188)A polymorphism and IBS, this cytokine gene polymorphism may not have significant role in the pathophysiology of disease.

Keywords

Genetic polymorphism

interleukin

Irritable bowel syndrome

Introduction

Irritable bowel syndrome (IBS) is a multi-factorial functional gastrointestinal disorder. The affected patients usually suffer from re-current abdominal pain and altered bowel habits (1,2). Although the exact etiology of IBS is still uncertain, several mechanisms have been proposed for the pathophysiology of disease (3-8). Genetic factors could have also a major role in this disease (9-11).
Interleukin-12 (IL-12), as a cytokine of T helper 1 (Th1)-mediated immunity in humans, can play an important role in intestinal in-flammation (12-14). IL-12 production is under genetic control and secretion of this cytokine could be affected by genetic polymorphisms (15,16). Genetic predisposition to produce high or low amounts of IL-12 may affect the dis-ease susceptibility and clinical outcome (17,18).
We previously showed that IL-6 and TNF-alpha proinflammatory cytokine gene poly-morphisms as well as IL-4 and IL-10 gene polymorphisms could affect individual’s sus-ceptibility to IBS (19,20). This study was per-formed in the group of patients with IBS to analyze the genotype and allele frequencies of a polymorphic gene coding for IL-12 compar-ed to healthy control subjects.

Materials and Methods

Seventy one unrelated Iranian patients with IBS (22 males, 49 females) were enrolled in this study. The diagnosis of IBS in this patient population was made based on the Rome III criteria, as described in our previous reports (19,20). One hundred and forty healthy control subjects were also enrolled in this study (21). This study was approved by the Ethics Com-mittee of Tehran University of Medical Sci-ences. Written informed consent was obtained from all subjects before sampling.
After DNA extraction from whole blood, using salting out method, cytokine genes typ-ing was performed by polymerase chain reac-tion with sequence-specific primers (PCR-SSP) assay (PCR-SSP kit, Heidelberg Univer-sity, Heidelberg, Germany) (19,20).
Amplification was done using a thermal cycler Techne Flexigene apparatus (Rosche, Cambridge, UK). The presence or absence of PCR products was visualized by 2% agarose gel electrophoresis. After electrophoresis, the gel was placed on a UV transilluminator and a picture for interpretation and documentation was taken.
The allele and genotype frequencies of IL-12 C(-1188)A were deter-mined and com-pared using the chi-square test. The odds ratio (OR) and 95% confidence intervals (95% CI) were calculated for allele/ genotype in the patient and control groups. P-value of less than 0.05 was considered significant.

Results

The allele A at position -1188 IL-12 was detected in 72.9% of the patients, similar to what was detected in the control group. There was not any significant difference on IL-12 alleles between the patient and the control groups (p=0.92).
The AA genotype was the most common genotype, which was seen in 57.4% of the patients and 51.4% of the controls (p=0.53, OR=1.27, 95% CI: 0.66-2.44). Although fre-quency of the CC genotype in the control group was lower than the patient group, this difference was not significant (5.7% vs. 11.5%, respectively, p=0.16, OR=2.14, 95% CI: 0.66-6.91). There was not any significant difference on IL-12 CA genotype between the patient and the control groups (31.1% vs. 42.9%, respectively, p=0.16, OR=0.60, 95% CI: 0.30-1.19).

Discussion

Cytokine gene polymorphisms could change the individual susceptibility to IBS and might have a role in the pathophysiology of disease. We have recently shown the asso-ciations of variety of cytokine gene poly-morphisms (IL-4, IL-10, IL-6, TNF-α) and IBS (19,20). In this study, we have genotyped a sample of IBS patients for IL-12.
It should be noted that there is no single pathophysiologic mechanism that explains the clinical manifestations of IBS. Although no active inflammation is expected in IBS, tran-sient mucosal inflammation could be an im-portant factor for the manifestation of IBS. Therefore, as cytokines are involved in the regulation of the immune and inflammatory reaction, their genetic polymorphisms, which could be associated with high or low cytokine production, may predispose individual to IBS, or affect its clinical manifestation (22).
IL-12 is secreted by antigen-presenting dendritic cells and phagocytes and activates CD4+ T cells to differentiate to Th1- and is associated with cellular immune responses (23). An A-to-C exchange has been found in the 3′-UTR of IL-12 gene, in position -1188 (24) that correlates with decreased protein secretion (14). A single nucleotide polymorphism situated at positions -1188 (A/C) in the promoter region of IL-12 gene was investigated in this study that did not showed any significant difference on IL-12 alleles and genotypes between pa-tients and controls. Although it was previous-ly reported that the ratio of IL-10 secretion to IL-12 was significantly lower in IBS patients compared to controls (25), there is not any evi-dence of the role of IL-12 gene polymorph-isms in IBS patients, to our best knowledge.

Conclusion

Considering lack of association between IL-12 C(-1188)A polymorphism and IBS, this cytokine gene polymorphism may not have significant role in the pathophysiology of disease.

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