NADPH oxidase 5 is a novel susceptibility gene for type 2 diabetes mellitus
This pilot study investigated whether single nucleotide polymorphisms (SNP) in the NOX5 gene (NADPH oxidase 5) are associated with the type 2 diabetes (T2D) risk. A total of 1579 patients with T2D and 1627 age- and sex-matched healthy subjects were recruited for this study. Genotyping of common SNPs...
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Published in | Archives of Endocrinology and Metabolism Vol. 68; p. e230527 |
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Format | Journal Article |
Language | English |
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Sociedade Brasileira de Endocrinologia e Metabologia
01.01.2024
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Abstract | This pilot study investigated whether single nucleotide polymorphisms (SNP) in the NOX5 gene (NADPH oxidase 5) are associated with the type 2 diabetes (T2D) risk.
A total of 1579 patients with T2D and 1627 age- and sex-matched healthy subjects were recruited for this study. Genotyping of common SNPs, namely rs35672233, rs3743093, rs2036343, rs311886, and rs438866, was performed using the MassArray-4 system.
SNP rs35672233 was associated with an increased risk of T2D (OR = 1.67, 95% CI 1.29-2.17, FDR = 0.003). The H3 haplotype (rs35672233T-rs3743093G-rs2036343A-rs311886C-rs438866C) increased T2D risk (OR = 1.65, 95% CI 1.27-2.13, FDR = 0.001). The rs35672233 polymorphism and H3 haplotype were found to have an association with T2D risk only in subjects with a body mass index greater than 25 kg/m
(FDR < 0.01). Environmental risk factors, such as chronic psycho-emotional stress, sedentary lifestyle, high-calorie diet and SNP rs35672233 were jointly associated with T2D susceptibility. A haplotype comprising the allele rs35672233-C and conferring protection against T2D, was associated with elevated levels of antioxidants such as total glutathione and uric acid, as well as reduced levels of two-hour postprandial glucose in the plasma of patients. The NOX5 polymorphisms showed no associations with diabetic complications.
The present study is the first to establish associations between polymorphisms in NOX5 and the risk of type 2 diabetes mellitus, and provides a new line of evidence for the crucial role of oxidative stress-related genes in disease susceptibility. |
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AbstractList | This pilot study investigated whether single nucleotide polymorphisms (SNP) in the NOX5 gene (NADPH oxidase 5) are associated with the type 2 diabetes (T2D) risk.
A total of 1579 patients with T2D and 1627 age- and sex-matched healthy subjects were recruited for this study. Genotyping of common SNPs, namely rs35672233, rs3743093, rs2036343, rs311886, and rs438866, was performed using the MassArray-4 system.
SNP rs35672233 was associated with an increased risk of T2D (OR = 1.67, 95% CI 1.29-2.17, FDR = 0.003). The H3 haplotype (rs35672233T-rs3743093G-rs2036343A-rs311886C-rs438866C) increased T2D risk (OR = 1.65, 95% CI 1.27-2.13, FDR = 0.001). The rs35672233 polymorphism and H3 haplotype were found to have an association with T2D risk only in subjects with a body mass index greater than 25 kg/m
(FDR < 0.01). Environmental risk factors, such as chronic psycho-emotional stress, sedentary lifestyle, high-calorie diet and SNP rs35672233 were jointly associated with T2D susceptibility. A haplotype comprising the allele rs35672233-C and conferring protection against T2D, was associated with elevated levels of antioxidants such as total glutathione and uric acid, as well as reduced levels of two-hour postprandial glucose in the plasma of patients. The NOX5 polymorphisms showed no associations with diabetic complications.
The present study is the first to establish associations between polymorphisms in NOX5 and the risk of type 2 diabetes mellitus, and provides a new line of evidence for the crucial role of oxidative stress-related genes in disease susceptibility. ABSTRACT Objective This pilot study investigated whether single nucleotide polymorphisms (SNP) in the NOX5 gene (NADPH oxidase 5) are associated with the type 2 diabetes (T2D) risk. Subjects and methods A total of 1579 patients with T2D and 1627 age- and sex-matched healthy subjects were recruited for this study. Genotyping of common SNPs, namely rs35672233, rs3743093, rs2036343, rs311886, and rs438866, was performed using the MassArray-4 system. Results SNP rs35672233 was associated with an increased risk of T2D (OR = 1.67, 95% CI 1.29-2.17, FDR = 0.003). The H3 haplotype (rs35672233T-rs3743093G-rs2036343A-rs311886C-rs438866C) increased T2D risk (OR = 1.65, 95% CI 1.27-2.13, FDR = 0.001). The rs35672233 polymorphism and H3 haplotype were found to have an association with T2D risk only in subjects with a body mass index greater than 25 kg/m2 (FDR < 0.01). Environmental risk factors, such as chronic psycho-emotional stress, sedentary lifestyle, high-calorie diet and SNP rs35672233 were jointly associated with T2D susceptibility. A haplotype comprising the allele rs35672233-C and conferring protection against T2D, was associated with elevated levels of antioxidants such as total glutathione and uric acid, as well as reduced levels of two-hour postprandial glucose in the plasma of patients. The NOX5 polymorphisms showed no associations with diabetic complications. Conclusion The present study is the first to establish associations between polymorphisms in NOX5 and the risk of type 2 diabetes mellitus, and provides a new line of evidence for the crucial role of oxidative stress-related genes in disease susceptibility. |
Author | Polonikov, Alexey Klyosova, Elena Azarova, Valentina Azarova, Iuliia |
AuthorAffiliation | 3 Department of Biology Medical Genetics and Ecology Kursk State Medical University Kursk Russian Federation Department of Biology, Medical Genetics and Ecology, Kursk State Medical University, Kursk, Russian Federation 5 Laboratory of Statistical Genetics and Bioinformatics Research Institute for Genetic and Molecular Epidemiology Kursk State Medical University Kursk Russian Federation Laboratory of Statistical Genetics and Bioinformatics, Research Institute for Genetic and Molecular Epidemiology, Kursk State Medical University, Kursk, Russian Federation 1 Department of Biological Chemistry Kursk State Medical University Kursk Russian Federation Department of Biological Chemistry, Kursk State Medical University, Kursk, Russian Federation 4 Kursk Emergency Hospital Kursk Russian Federation Kursk Emergency Hospital, Kursk, Russian Federation 2 Laboratory of Biochemical Genetics and Metabolomics Research Institute for Genetic and Molecular Epidemiology Kursk State Medical University Kursk Ru |
AuthorAffiliation_xml | – name: 2 Laboratory of Biochemical Genetics and Metabolomics Research Institute for Genetic and Molecular Epidemiology Kursk State Medical University Kursk Russian Federation Laboratory of Biochemical Genetics and Metabolomics, Research Institute for Genetic and Molecular Epidemiology, Kursk State Medical University, Kursk, Russian Federation – name: 3 Department of Biology Medical Genetics and Ecology Kursk State Medical University Kursk Russian Federation Department of Biology, Medical Genetics and Ecology, Kursk State Medical University, Kursk, Russian Federation – name: 4 Kursk Emergency Hospital Kursk Russian Federation Kursk Emergency Hospital, Kursk, Russian Federation – name: 1 Department of Biological Chemistry Kursk State Medical University Kursk Russian Federation Department of Biological Chemistry, Kursk State Medical University, Kursk, Russian Federation – name: 5 Laboratory of Statistical Genetics and Bioinformatics Research Institute for Genetic and Molecular Epidemiology Kursk State Medical University Kursk Russian Federation Laboratory of Statistical Genetics and Bioinformatics, Research Institute for Genetic and Molecular Epidemiology, Kursk State Medical University, Kursk, Russian Federation |
Author_xml | – sequence: 1 givenname: Iuliia orcidid: 0000-0001-8098-8052 surname: Azarova fullname: Azarova, Iuliia – sequence: 2 givenname: Elena orcidid: 0000-0002-1543-9230 surname: Klyosova fullname: Klyosova, Elena – sequence: 3 givenname: Valentina orcidid: 0000-0002-4307-9228 surname: Azarova fullname: Azarova, Valentina – sequence: 4 givenname: Alexey orcidid: 0000-0001-6280-247X surname: Polonikov fullname: Polonikov, Alexey |
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Keywords | Type 2 diabetes NADPH oxidase 5 risk factors gene-environment interactions single nucleotide polymorphism oxidative stress |
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Snippet | This pilot study investigated whether single nucleotide polymorphisms (SNP) in the NOX5 gene (NADPH oxidase 5) are associated with the type 2 diabetes (T2D)... ABSTRACT Objective This pilot study investigated whether single nucleotide polymorphisms (SNP) in the NOX5 gene (NADPH oxidase 5) are associated with the type... |
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SubjectTerms | Adult Aged Body Mass Index Case-Control Studies Diabetes Mellitus, Type 2 - genetics Female gene-environment interactions Genetic Predisposition to Disease - genetics Genotype Haplotypes - genetics Humans Male Middle Aged NADPH oxidase 5 NADPH Oxidase 5 - genetics Original oxidative stress Pilot Projects Polymorphism, Single Nucleotide - genetics Risk Factors single nucleotide polymorphism Type 2 diabetes |
Title | NADPH oxidase 5 is a novel susceptibility gene for type 2 diabetes mellitus |
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