Journals / Turkish Journal of Medical Sciences / 2019 / Cilt: 49 - Sayı: 4

Association between PPARGC1A single nucleotide polymorphisms and increased risk of nonalcoholic fatty liver disease among Iranian patients with type 2 diabetes mellitus

Pages
1089–1094
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Gly482Ser polymorphism genotyping was done using the amplification refractory mutation system-polymerase chainreaction (ARMS-PCR) technique.Results: The results showed a significant difference between the PPARGC1A Gly482Ser polymorphism in NAFLD patients and thehealthy controls.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background/aim: Environmental and genetic factors may play a major role in the development of nonalcoholic fatty liver disease(NAFLD) among people with obesity and type 2 diabetes mellitus.
📊
Key Findings & Data:Based on the fact that PGC-1α, as the protein encoded by thePPARGC1A gene, plays a key role in energy metabolism pathways, it has been hypothesized that polymorphisms within the PPARGC1Agene may be associated with increased risks of NAFLD.
💡
Conclusion & Impact:Gly482Ser polymorphism genotyping was done using the amplification refractory mutation system-polymerase chainreaction (ARMS-PCR) technique.Results: The results showed a significant difference between the PPARGC1A Gly482Ser polymorphism in NAFLD patients and thehealthy controls.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background/aim: Environmental and genetic factors may play a major role in the development of nonalcoholic fatty liver disease(NAFLD) among people with obesity and type 2 diabetes mellitus. Based on the fact that PGC-1α, as the protein encoded by thePPARGC1A gene, plays a key role in energy metabolism pathways, it has been hypothesized that polymorphisms within the PPARGC1Agene may be associated with increased risks of NAFLD. Thus, this study was designed to evaluate the Gly482Ser polymorphism(rs8192678) within the PPARGC1A gene and its association with the increased risk of NAFLD in Iranian patients with type 2 diabetes.Materials and methods: A total of 145 NAFLD patients with a history of type 2 diabetes and 145 healthy control subjects were includedin the study. Gly482Ser polymorphism genotyping was done using the amplification refractory mutation system-polymerase chainreaction (ARMS-PCR) technique.Results: The results showed a significant difference between the PPARGC1A Gly482Ser polymorphism in NAFLD patients and thehealthy controls. Accordingly, the AA genotype and A allele were increased in the NAFLD patients when compared to the healthycontrols. However, no significant correlation was observed between the Gly482Ser polymorphism and the physiological and biochemicalparameters.Conclusion: Based on the results, the AA genotype, which is associated with the insertion of Ser, can be considered as a risk factor forthe development of NAFLD in Iranian patients with diabetes type 2.

🔖

Cite This Article

HOSSEINI-KHAH, Z., SALTANATPOUR, Z., HOSSEINZADEH, H., LOTFIPANAH, S., MOHAMMADI, M., JOHARI, B., SAREMI, L. (2022). Association between PPARGC1A single nucleotide polymorphisms and increased risk of nonalcoholic fatty liver disease among Iranian patients with type 2 diabetes mellitus. Turkish Journal of Medical Sciences, Cilt: 49 - Sayı: 4, 1089–1094. https://ajindex.com/articles/610079

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (11)

  1. Milic S, Mikolasevic I, Krznaric-Zrnic I, Stanic M, Poropat G et al. Nonalcoholic steatohepatitis: emerging targeted therapies to optimize treatment options. Drug Design, Development and Therapy 2015
  2. doi: 10.2147/DDDT.S64877 2. Moley KH, Colditz GA. Effects of obesity on hormonally driven cancer in women. Science Translational Medicine 2016
  3. 8 (323): 323ps3. doi: 10.1126/scitranslmed.aad8842 3. Targher G, Bertolini L, Padovani R, Rodella S, Zoppini G et al. Relations between carotid artery wall thickness and liver histology in subjects with nonalcoholic fatty liver disease. Diabetes Care 2006
  4. 29 (6): 1325-1330. doi: 10.2337/dc06-0135 4. Saremi L, Lotfipanah S, Mohammadi M, Hosseinzadeh H, Sayad A et al. Association of HFE gene mutations with nonalcoholic fatty liver disease in the Iranian population. Cellular and Molecular Biology (Noisy-le-Grand) 2016
  5. 62 (12): 123-128. doi: 10.14715/cmb/2016.62.12.2 5. Saremi L, Lotfipanah S, Mohammadi M, Hosseinzadeh H, Fathi-Kazerooni M et al. The Pro12Ala polymorphism in the PPAR-γ2 gene is not associated with an increased risk of NAFLD in Iranian patients with type 2 diabetes mellitus. 2019
  6. doi: 10.1186/s11658-019-0138-0 6. Dongiovanni P, Rametta R, Fracanzani AL, Benedan L, Borroni V et al. Lack of association between peroxisome proliferatoractivated receptors alpha and gamma2 polymorphisms and progressive liver damage in patients with non-alcoholic fatty liver disease: a case control study. BMC Gastroenterology 2010
  7. 10 (102): 102. doi: 10.1186/1471-230X-10-102 7. Portillo-Sanchez P, Cusi K. Treatment of nonalcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes mellitus. Clinical Diabetes and Endocrinology 2016
  8. 2 (9): 9. doi: 10.1186/s40842-016-0027-7 8. Bugianesi E, Leone N, Vanni E, Marchesini G, Brunello F et al. Expanding the natural history of nonalcoholic steatohepatitis: from cryptogenic cirrhosis to hepatocellular carcinoma. Gastroenterology 2002
  9. 123 (1): 134-140. doi: 10.1053/ gast.2002.34168 9. Adams LA, Lymp JF, St Sauver J, Sanderson SO, Lindor KD et al. The natural history of nonalcoholic fatty liver disease: a population-based cohort study. Gastroenterology 2005
  10. 129 (1): 113-121. doi: 10.1053/j.gastro.2005.04.014 10. Yoneda M, Hotta K, Nozaki Y, Endo H, Uchiyama T et al. Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD). BMC Gastroenterolgy 2008
  11. 8 (27): 27. doi: 10.1186/1471-230X-8-27 11. Burgueno A