Department of Nutrition, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences (TUMS), P.O. Box:14155-6117, Tehran, Iran.
BMC Endocr Disord. 2022 Sep 1;22(1):221. doi: 10.1186/s12902-022-01132-1.
Cardiovascular disease (CVD) is the leading cause of death in women globally. Recent studies have reported that the minor allele (C allele) for melanocortin 4 receptor (MC4R) rs17782313 may be related to the incidence of obesity and the risk of CVD. Therefore, the present study aimed to investigate the interactions between the modified Nordic-style diet score (MND) and MC4R gene variant on markers of CVD.
The current cross-sectional study was conducted on 282 Iranian women, aged 18-48 years, with a body mass index (BMI) ≥ 25. MND score was assessed using a 147 items food frequency questionnaire (FFQ). Genotyping of the MC4R (rs17782313) was conducted by the PCR method. The anthropometric measurements and serum profiles were assessed by standard protocols.
The means and standard deviation (SD) of age, weight, and BMI of individuals were 36.67 ± 9.10 years, 81.29 ± 12.43 kg, and 31.26 ± 4.29 kg/m, respectively. The overall prevalence of rs17782313 genotypes was 30.1%, 24.8%, and 45.1% for TT, TC, and CC, respectively. Our results showed significant negative interactions between high MND score and rs17782313 SNP in terms of visceral fat level (VFL) (β: -10.84, 95% CI: -20.64 to -1.04, P = 0.03) and total cholesterol (β: -24.24, 95% CI: -49.87 to 1.38, P = 0.06) in the crude model. After adjusting confounders, the interaction between high MND scores and VFL remained significant.
In conclusion, the results of the present study suggest that diet, gene variants, and their interaction should be considered in metabolic disease risk assessment. Further studies are needed to confirm these data and better elucidate the interaction.
心血管疾病(CVD)是全球女性死亡的主要原因。最近的研究报告称,黑素皮质素 4 受体(MC4R)rs17782313 的次要等位基因(C 等位基因)可能与肥胖的发生率和 CVD 的风险有关。因此,本研究旨在探讨改良北欧饮食评分(MND)与 MC4R 基因变异对 CVD 标志物的相互作用。
本横断面研究纳入了 282 名年龄在 18-48 岁、BMI≥25 的伊朗女性。使用 147 项食物频率问卷(FFQ)评估 MND 评分。通过 PCR 法检测 MC4R(rs17782313)的基因分型。采用标准方案评估人体测量学指标和血清谱。
个体的年龄、体重和 BMI 的平均值和标准差(SD)分别为 36.67±9.10 岁、81.29±12.43kg 和 31.26±4.29kg/m2。rs17782313 基因型的总体发生率分别为 TT、TC 和 CC 基因型的 30.1%、24.8%和 45.1%。我们的结果表明,在未调整模型中,高 MND 评分与 rs17782313 SNP 之间存在显著的负交互作用,表现在内脏脂肪水平(VFL)(β:-10.84,95%CI:-20.64 至-1.04,P=0.03)和总胆固醇(β:-24.24,95%CI:-49.87 至 1.38,P=0.06)方面。在调整混杂因素后,高 MND 评分与 VFL 之间的交互作用仍然显著。
总之,本研究结果表明,在评估代谢性疾病风险时,应考虑饮食、基因变异及其相互作用。需要进一步的研究来证实这些数据并更好地阐明相互作用。