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Assessing the possible association between MTHFR (rs1801133) and GPx-1 (rs1050450) polymorphisms with the risk of type 2 diabetes, diabetic neuropathy, and diabetic retinopathy.
Asadi, Soheila; Rahimi, Zohreh; Kohsari, Maryam; Babajani, Fatemeh; Amiri, Mohammad; Jalilian, Nazanin; Naseri, Rozita; Haghnazari, Lida.
Afiliação
  • Asadi S; Department of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran. sohila.asadi75@yahoo.com.
  • Rahimi Z; Department of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Kohsari M; Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Babajani F; Department of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Amiri M; Department of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Jalilian N; Department of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Naseri R; Department of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Haghnazari L; Department of Internal Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Mol Biol Rep ; 51(1): 583, 2024 Apr 29.
Article em En | MEDLINE | ID: mdl-38683407
ABSTRACT

PURPOSE:

Oxidative stress in chronic hyperglycemia could injure the tissues and onset of diabetes-related complications like retinopathy and neuropathy. This study investigates the association between methylenetetrahydrofolate reductase (MTHFR) and glutathione peroxidase (GPx) genetic variants with these complications.

METHODS:

In this case-control study, 400 individuals, including 100 healthy subjects and 300 patients with type 2 diabetes mellitus (T2DM) in three subgroups with retinopathy(n = 100), with neuropathy(n = 100), and without complication (n = 100) from West Iran, were studied. MTHFR (rs1801133) and GPx-1 (rs1050450) variants were identified by the PCR-RFLP method. The plasma levels of GPx activity, glutathione, malondialdehyde (MDA), total antioxidant capacity (TAC), and total oxidative stress (TOS) were measured by chemical methods.

RESULTS:

Higher BMI, TOS and MDA levels were observed in patients with neuropathy compared to other patients and controls. Diabetic patients with neuropathy had lower levels of glutathione (7.8 ± 4.5; P < 0.001), GPx activity (39.5 ± 8.5; P < 0.001), and TAC (703.1 ± 129.1; P = 0.0001) in comparison with other groups. The patients without complication and retinopathic patients had higher plasma levels of glutathione (12.2 ± 2.4; p = 0.02) and TAC (793.4 ± 124.6; P < 0.001), respectively. MTHFR TT genotype significantly correlated with lower levels of TOS (3.5 ± 1.1; P < 0.001) and OSI (0.0050 ± 0.001; P < 0.001). Subjects with the GPx-1 TT genotype had higher levels of MDA (6.8 ± 2.5; P = 0.02) and lower levels of TOS (3.7 ± 1.6; P < 0.001), which is statistically significant. TT genotype of MTHFR was associated with 3.9 fold (95% CI 1.04-4.76; P = 0.0436) increased risk of neuropathy. Also, GPx-1 CT genotype increased the risk of retinopathy [OR = 2.7 (95% CI = 1.38-5.44; P = 0.0039)].

CONCLUSION:

The MTHFR TT genotype increased the risk of neuropathy in diabetic patients significantly. The GPx-1 CT genotype is related to increased retinopathy risk among diabetic patients. Both MTHFR and Gpx-1 TT genotypes were associated with higher BMI levels.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Metilenotetra-Hidrofolato Redutase (NADPH2) / Diabetes Mellitus Tipo 2 / Neuropatias Diabéticas / Retinopatia Diabética / Glutationa Peroxidase GPX1 / Glutationa Peroxidase Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Metilenotetra-Hidrofolato Redutase (NADPH2) / Diabetes Mellitus Tipo 2 / Neuropatias Diabéticas / Retinopatia Diabética / Glutationa Peroxidase GPX1 / Glutationa Peroxidase Idioma: En Ano de publicação: 2024 Tipo de documento: Article