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DOI 10.1093/labmed/lmad066

Медицинская библиотека · Laboratory medicine · 2024

Insulin receptor substrate 2 gene Gly1057Asp polymorphism is a risk factor for nonalcoholic fatty liver disease.

Nouri Shadi, Mahmoudi Touraj, Hojjati Farzaneh, Najafabadi Zeinab Nourmohammadi, Shafiee Radmehr, Sayedsalehi Shiva, Dehghanitafti Atefeh, Ardalani Abbas, Kohansal Kiarash, Rezamand Gholamreza, Asadi Asadollah, Nobakht Hossein, Dabiri Reza, Farahani Hamid, Tabaeian Seidamir Pasha, Zali Mohammad Reza

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Аннотация

OBJECTIVE

Nonalcoholic fatty liver disease (NAFLD), which is an emerging global chronic liver disease, has a close association with insulin resistance. We aimed to determine whether the Gly1057Asp (rs1805097) polymorphism of the insulin receptor substrate 2 (IRS2) gene is associated with NAFLD.

METHODS

Using the polymerase chain reaction-restriction fragment length polymorphism method, 135 patients with biopsy-proven NAFLD and 135 controls underwent IRS2 genotype analysis.

RESULTS

Genotype and allele distributions of the IRS2 gene Gly1057Asp variant conformed to the Hardy-Weinberg equilibrium in both the case and control groups (P > .05). The Asp/Asp genotype of IRS2 gene Gly1057Asp polymorphism compared with Gly/Gly genotype was associated with a 2.1-fold increased risk for NAFLD after adjustment for confounding factors (P = .029; odds ratio = 2.10, 95% CI = 1.23-3.97).

CONCLUSION

Our findings revealed for the first time that the Gly1057Asp Asp/Asp genotype of the IRS2 gene is a marker of increased NAFLD susceptibility; however, studies in other populations are required to confirm the results.

Для цитирования: Nouri Shadi, Mahmoudi Touraj, Hojjati Farzaneh, Najafabadi Zeinab Nourmohammadi, Shafiee Radmehr, Sayedsalehi Shiva, Dehghanitafti Atefeh, Ardalani Abbas, Kohansal Kiarash, Rezamand Gholamreza, Asadi Asadollah, Nobakht Hossein, Dabiri Reza, Farahani Hamid, Tabaeian Seidamir Pasha, Zali Mohammad Reza. Insulin receptor substrate 2 gene Gly1057Asp polymorphism is a risk factor for nonalcoholic fatty liver disease.. Laboratory medicine. 2024. DOI: 10.1093/labmed/lmad066.

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