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Common Genetic Variations Involved in the Inter-Individual Variability of Circulating Cholesterol Concentrations in Response to Diets: A Narrative Review of Recent Evidence

机译:循环胆固醇浓度的常见遗传变异涉及循环胆固醇浓度的响应饮食:近期证据的叙述综述

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摘要

The number of nutrigenetic studies dedicated to the identification of single nucleotide polymorphisms (SNPs) modulating blood lipid profiles in response to dietary interventions has increased considerably over the last decade. However, the robustness of the evidence-based science supporting the area remains to be evaluated. The objective of this review was to present recent findings concerning the effects of interactions between SNPs in genes involved in cholesterol metabolism and transport, and dietary intakes or interventions on circulating cholesterol concentrations, which are causally involved in cardiovascular diseases and established biomarkers of cardiovascular health. We identified recent studies (2014–2020) that reported significant SNP–diet interactions in 14 cholesterol-related genes (NPC1L1, ABCA1, ABCG5, ABCG8, APOA1, APOA2, APOA5, APOB, APOE, CETP, CYP7A1, DHCR7, LPL, and LIPC), and which replicated associations observed in previous studies. Some studies have also shown that combinations of SNPs could explain a higher proportion of variability in response to dietary interventions. Although some findings still need replication, including in larger and more diverse study populations, there is good evidence that some SNPs are consistently associated with differing circulating cholesterol concentrations in response to dietary interventions. These results could help clinicians provide patients with more personalized dietary recommendations, in order to lower their risk for cardiovascular disease.
机译:鉴定单核苷酸多态性(SNPS)调节血脂曲线响应于膳食干预的抗核苷酸多态性(SNPS)的营养研究数量在过去十年中具有很大增加。但是,支持该地区的基于证据的科学的稳健性仍有待评估。本综述的目的是提出最近关于在胆固醇代谢和运输中参与胆固醇代谢和运输中的基因之间的相互作用的影响,以及循环胆固醇浓度的膳食摄入或干预,这些胆固醇浓度有因而参与心血管疾病和成立的心血管健康的生物标志物。我们鉴定了最近的研究(2014-2020),报告了14个胆固醇相关基因中的显着的SNP - 饮食相互作用(NPC1L1,ABCA1,ABCG5,ABCG8,APOA1,APOA2,APOA5,APOB,APOE,CETP,CYP7A1,DHCR7,LPL和LIPC),并在先前的研究中观察到哪种复制的联想。有些研究还表明,响应饮食干预,SNP的组合可以解释更高的变异性比例。虽然一些发现仍需要复制,包括在更大和更多样化的研究人群中,但有良好的证据表明一些SNP与不同的循环胆固醇浓度持续有关膳食干预措施。这些结果可以帮助临床医生为患者提供更个性化的饮食建议,以降低其心血管疾病的风险。

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