饮食总抗氧化能力与染色体5q13-14位点的变体相互作用,影响肥胖成年人的心脏代谢危险因素。

Mahdieh Khodarahmi, Amir Sobhrakhshan Khah, Mahdieh Abbasalizad Farhangi, Goli Siri, Houman Kahroba
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引用次数: 0

摘要

背景:流行病学研究表明,可卡因和苯丙胺调节的转录物前肽基因(CARPT)与肥胖相关结果之间存在关联。然而,在饮食抗氧化潜力方面,缺乏关于CARPT基因与饮食相互作用的数据。因此,本研究旨在测试CARPT基因与饮食非酶抗氧化能力(NEAC)的相互作用对肥胖个体心脏代谢危险因素的影响。方法和材料:本横断面研究在288名20-50岁的明显健康肥胖成年人中进行。采用半定量食物频率问卷(FFQ),通过计算氧自由基吸收能力(ORAC)、铁还原抗氧化能力(FRAP)、总自由基捕获抗氧化参数(TRAP)和Trolox等效抗氧化能力(TEAC)来评估日粮的抗氧化能力。采用聚合酶链式反应-限制性片段长度多态性(PCR-RFLP)方法对CARTPT rs2239670多态性进行基因分型。结果:CARTPT rs2239670与膳食ORAC在BMI上存在显著的交互作用(P交互作用 = 0.048)和脂肪质量百分比(FM%)(P相互作用 = 0.008);在A等位基因携带者中,较高的膳食ORAC依从性与较低的BMI和FM%水平有关。并且,在FRAP指数和rs2239670之间观察到与HOMA相关的显著相互作用(P相互作用 = 0.049)和QUICKI(PInteraction = 0.048)。此外,rs2239670与TRAP存在显著的相互作用(P相互作用 = 0.029)和TEAC(P相互作用 = 0.034)对血糖水平的影响;AG基因型个体对TRAP摄入量的增加更有反应。结论:本研究表明,CARTPT rs2239670与肥胖及其相关代谢参数之间的关系取决于对膳食NEAC的坚持。需要进行大规模的前瞻性研究来证实我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dietary total antioxidant capacity interacts with a variant of chromosome 5q13-14 locus to influence cardio-metabolic risk factors among obese adults.

Dietary total antioxidant capacity interacts with a variant of chromosome 5q13-14 locus to influence cardio-metabolic risk factors among obese adults.

Dietary total antioxidant capacity interacts with a variant of chromosome 5q13-14 locus to influence cardio-metabolic risk factors among obese adults.

Dietary total antioxidant capacity interacts with a variant of chromosome 5q13-14 locus to influence cardio-metabolic risk factors among obese adults.

Background: The association between cocaine- and amphetamine-regulated transcript prepropeptide gene (CARTPT) and obesity-related outcomes has shown in the epidemiological studies. Nevertheless, there is lack of data regarding the CARTPT gene-diet interactions in terms of antioxidant potential of diet. So, this study aimed to test CARTPT gene-dietary non-enzymatic antioxidant capacity (NEAC) interactions on cardio-metabolic risk factors in obese individuals.

Methods and material: The present cross-sectional study was carried out among 288 apparently healthy obese adults within age range of 20-50 years. Antioxidant capacity of diet was estimated by calculating the oxygen radical absorbance capacity (ORAC), ferric reducing antioxidant power (FRAP), total radical-trapping antioxidant parameter (TRAP) and Trolox equivalent antioxidant capacity (TEAC) using a semiquantitative food frequency questionnaire (FFQ). Genotyping for CARTPT rs2239670 polymorphism was conducted by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method.

Results: A significant interaction was revealed between CARTPT rs2239670 and dietary ORAC on BMI (PInteraction = 0.048) and fat mass percent (FM%) (PInteraction = 0.008); in A allele carriers, higher adherence to the dietary ORAC was related to lower level of BMI and FM%. And, the significant interactions were observed between FRAP index and rs2239670 in relation to HOMA (PInteraction = 0.049) and QUICKI (PInteraction = 0.048). Moreover, there were significant interactions of rs2239670 with TRAP (PInteraction = 0.029) and TEAC (PInteraction = 0.034) on the serum glucose level; individuals with AG genotype were more respondent to higher intake of TRAP.

Conclusion: The present study indicated that the relationships between CARTPT rs2239670 and obesity and its-related metabolic parameters depend on adherence to the dietary NEAC. Large prospective studies are needed to confirm our findings.

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