Why the study?
The study investigated the role of Apolipoprotein B polymorphisms (Ins/Del and EcoRI) and genotype interactions on lipid profiles and atherogenic indices in response to dietary total antioxidant capacity.
Does dietary total antioxidant capacity modify the effects of Apo-B polymorphisms on lipid profiles and atherogenic indices in diabetic patients?
Does dietary total antioxidant capacity modify the effects of Apo-B polymorphisms on lipid profiles and atherogenic indices in diabetic patients?
Apo-B polymorphisms interact with dietary antioxidant capacity to influence lipid profiles and atherogenic risk in diabetic patients.
DTAC may interact with Apo-B variants on lipids and adiposity in diabetes; hypothesis-generating and requires prospective trials before clinical consideration.
We aimed to study the role of Apolipoprotein B (Apo-B) polymorphisms (Ins/Del and EcoRI) and genotype interaction on lipid profiles and atherogenic indices in response to changes in dietary total antioxidant capacity (DTAC) of diet. This cross-sectional study consisted of 700 diabetic patients. Biochemical markers including total cholesterol (TC), low-density lipoprotein (LDL), high-density lipoprotein (HDL), triglyceride (TG), superoxide dismutase (SOD), C-reactive protein (CRP), total antioxidant capacity (TAC), interlukin-18 (IL-18), and Prostaglandin F2α (PGF2α) were measured based on standard protocols. Genotyping of the Apo-B polymorphisms was conducted by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Subjects with Ins/Ins genotype with higher DTAC intake had lower TG, AIP, and AC compared to Del-allele carriers. Moreover, A-allele carriers (EcoRI) with a higher median intake of DTAC had lower body mass index (BMI) and waist circumference (WC) compared to GG homozygotes. For combined genotypes, the EcoRI only variant (Ins/Ins and AA + AG) with higher DTAC intake had lower BMI and WC. Moreover, Ins/Del only variant (Ins/del + del/del and GG) with more adherence to DTAC had higher TG and AIP. Our study showed that Apo-B polymorphisms interact with the antioxidant capacity of diet to ameliorate the risk of cardio-metabolic diseases, especially atherosclerosis in the A carriers of EcoR1 and Ins/Ins homozygous of Ins/Del polymorphism.
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Abaj et al. (2025) studied this question.
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