Association of rs5742612 Polymorphism in the Promoter Region of IGF1 Gene with Nonalcoholic Fatty Liver Disease: A Case-Control Study

Author:

Nobakht Hossein1,Mahmoudi Touraj2,Rezamand Gholamreza34,Tabaeian Seidamir Pasha34,Jeddi Golnaz5,Asadi Asadollah6,Farahani Hamid7,Dabiri Reza1,Mansour-Ghanaei Fariborz8,Kaboli Seyed Alireza9,Derakhshan Faramarz2,Zali Mohammad Reza2

Affiliation:

1. Internal Medicine Department, Semnan University of Medical Sciences , Semnan , Iran

2. Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences , Tehran , Iran

3. Department of Internal Medicine, School of Medicine, Iran University of Medical Sciences , Tehran , Iran

4. Colorectal Research Center, Iran University of Medical Sciences , Tehran , Iran

5. Department of Biology, Faculty of Basic Sciences, East Tehran Branch (Ghiamdasht), Islamic Azad University , Tehran , Iran

6. Department of Biology, Faculty of Science, University of Mohaghegh Ardabili , Ardabil , Iran

7. Department of Physiology and Pharmacology, School of Medicine, Qom University of Medical Sciences , Qom , Iran

8. Division of Gastroenterology and Hepatology, Gastrointestinal and Liver Diseases Research Center (GLDRC), Guilan University of Medical Sciences , Rasht , Iran

9. Department of Gastroenterology, School of Medicine, Hamadan University of Medical Sciences , Hamadan , Iran

Abstract

Abstract Objective Nonalcoholic fatty liver disease (NAFLD) is an emerging global chronic liver disease encompassing a wide spectrum of disorders ranging from simple steatosis to nonalcoholic steatohepatitis, fibrosis, cirrhosis, and hepatocellular carcinoma. Considering the strong association between NAFLD and insulin resistance, and the vital role of insulin-like growth factor 1 (IGF1) in IR, we hypothesized that IGF1 gene polymorphism might be associated with NAFLD. Methods A total of 302 subjects, including 149 patients with biopsy-proven NAFLD and 153 controls, were enrolled in this case-control study. All the subjects were genotyped for the rs5742612 polymorphism of the IGF1 gene using the polymerase chain reaction-restriction fragment length polymorphism method. Results The distribution of IGF1 rs5742612 genotypes and alleles differed significantly between the cases with NAFLD and controls. The IGF1 rs5742612 CC genotype compared with the TT genotype or the TT+TC genotype occurred more frequently in the cases than the controls and the differences remained significant after adjustment for confounding factors such as age and body mass index (P = .011, OR = 2.71, 95%CI = 1.16-5.85; and P = .032, OR = 2.29, 95% CI = 1.10-5.24, respectively). Conclusion For the first time, this study uncovered that the IGF1 rs5742612 CC genotype compared with the TT genotype or the TT+TC genotype had a 2.71-fold or 2.29-fold increased risk for NAFLD, respectively.

Funder

Iran National Science Foundation

Shahid Beheshti University of Medical Sciences

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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