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Published on: July 17, 2018
Polymorphism of CD36 gene, carbohydrate metabolism and plasma CD36 concentration in obese children. A preliminary
Monika E Rać1, Beata Krupa, Barbara Garanty-Bogacka
1Department of Biochemistry and Medical Chemistry Pomeranian Medical University, 70-111 Szczecin, Poland. carmon12@gmail.com
Insights
CD36 gene variations were not linked to carbohydrate metabolism issues in obese children. Further research is needed to understand the functional roles of these CD36 polymorphisms.
Area of Science:
- Genetics
- Metabolic Disorders
- Pediatrics
Background:
- CD36 is implicated in oxidized LDL removal, protein glycation, insulin resistance, and diabetic complications.
- Previous studies suggest a link between CD36 gene mutations and reduced macrophage expression in obese, hyperglycemic individuals.
- Investigating CD36 gene polymorphism in obese children is crucial for understanding its role in metabolic health.
Purpose of the Study:
- To investigate the association between CD36 gene polymorphism and carbohydrate metabolism disturbances in obese children.
- To examine the relationship between CD36 gene variants and plasma soluble CD36 concentrations in this population.
Main Methods:
- The study included 60 obese children (10-15 years) and 30 controls.
- Measurements included glycated hemoglobin, BMI, blood pressure, and oral glucose tolerance tests with insulin measurements.
- CD36 gene exons 4-6 were analyzed using DHPLC and sequencing, with plasma CD36 levels measured by ELISA.
Main Results:
- Two intronic alterations (rs3173798, rs3211892), one nonsynonymous substitution (rs183461468), and two synonymous transitions (rs5956, rs141680676) in the CD36 gene were identified.
- No significant differences were observed in biochemical or morphometric parameters across different genotype groups.
Conclusions:
- CD36 gene polymorphisms in the studied region are not associated with carbohydrate metabolism disturbances or soluble CD36 levels in obese children.
- Further investigation is required to elucidate the functional significance of these CD36 polymorphisms.
Introduction:
CD36 may play an important role in removal of oxidized LDLs from plasma, protein glycation, the pathogenesis of insulin resistance, type 2 diabetes, and diabetic micro- and macroangiopathy. Some reports have pointed to decreased expression of macrophages in association with mutations of the CD36 gene in hyperglycemic and obese subjects. The aim of the study was to search for an association between CD36 gene polymorphism and carbohydrate metabolism disturbances or variability of plasma soluble CD36 concentrations in obese children.
Material/Methods:
The study included 60 children aged 10 to 15 years: 30 with (study group) and 30 without (control group) obesity. Each patient's glycated hemoglobin, weight, height, waist and hip circumference, and systolic and diastolic blood pressure were measured, BMI, WHR and MAP were calculated, and oral glucose tolerance test was performed with glucose and insulin concentration measurements. Amplicons of exons 4-6 of CD36 were studied using DHPLC technique. The PCR products with alterations were bidirectionally sequenced. Plasma concentrations of human antigen CD36 was measured using a commercially available enzyme-linked immunosorbent assay (ELISA).
Results:
We found two intronic alterations: IVS3-6 T/C (rs3173798) and IVS4-10 G/A (rs3211892), one nonsynonymous substitution: G367A (Glu123Lys, rs183461468) in exon 5 and two synonymous transitions in exon 6: G573A (Pro191Pro, rs5956) and A591T (Thr197Thr, rs141680676). There were no significant differences in any biochemical or morphometric parameters between genotype groups.
Discussion:
The polymorphisms of the studied fragment of CD36 are not associated with carbohydrate metabolism disturbances or the variability of plasma soluble CD36 concentrations in obese children, but further research is necessary to assess their functional implications.
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