Abstract

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.

Highlights

  • Lowering of blood lipid concentrations is a major target in both the primary and secondary prevention of Cardiovascular disease (CVD), but high interindividual variability exists in response to any given dietary intervention [5]

  • Genome-wide association studies (GWAS) have identified numerous single nucleotide polymorphisms (SNPs) that are associated with the variability of fasting blood cholesterol concentrations

  • A greater part of the variability in blood lipid concentrations could be explained by the additive effects of several SNPs, which, taken individually, may only have small, and barely significant, effects [10,11]

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Summary

Introduction

Genome-wide association studies (GWAS) have identified numerous single nucleotide polymorphisms (SNPs) that are associated with the variability of fasting blood cholesterol concentrations These genetic variations have been estimated to explain about 30% of total variance [6,7]. Several clinical trials have investigated the relationship between dietary interventions and blood lipid concentrations, considering the genetic characteristics of the participants By design, they usually only focus on individual SNPs, resulting in a relatively low explained genetic variance [8,9]. While numerous studies have reported SNPs that are significantly associated with blood cholesterol concentrations in response to various diets [8], there is a need to review additional data generated in this field. Looking at the sum of evidence accumulated in the field enables discussion of what is still missing in order to put this knowledge into practice

Search Process and Criteria
Study Design
SNPs in Genes Encoding Transporters Involved in Cholesterol Absorption
SNPs in Genes Encoding Apolipoproteins
Combinatory Patterns of SNPs Influencing Changes in Blood Cholesterol
Findings
Conclusions
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