Abstract

BackgroundCaveolin-1 (CAV-1) is a cholesterol-dependent essential component located in caveolae. Several studies have been CAV-1 related to cardio-metabolic parameters in animal models, however, there are few studies in humans. Importantly, there is no study has investigated the interaction between CAV-1 rs3807992 gene and dietary patterns (DPs) on cardio-metabolic risk factors.MethodsThe current cross-sectional study was conducted on 404 overweight and obese women. Dietary intake was obtained from FFQ with 147 items. The CAV-1 genotype was measured by the PCR-RFLP method. The anthropometric measurements, serum lipid profile, and inflammatory markers were measured by standard protocols.ResultsThere was a significant interaction between CAV-1 rs3807992 and healthy DP on high-density cholesterol (HDL) (P-interaction = 0.03), TC/HDL (P-interaction = 0.03) and high sensitivity C-reactive protein (hs-CRP) (P-interaction = 0.04); in A-allele carriers, higher following a healthy DP was related to a higher level of HDL and lower TC/HDL and hs-CRP. As well as, the significant interactions were observed between CAV-1 rs3807992 and unhealthy DP in relation to triglyceride (TG) (P-interaction = 0.001), aspartate aminotransferase (AST) (P-interaction = 0.01) and monocyte chemoattractant protein-1(MCP-1) (P-interaction = 0.01); A-allele carriers were more following the unhealthy DP had lower levels of TG, AST and MCP-1.ConclusionsOur study revealed a significant gene-diet interaction between rs3807992 SNPs and DPs in relation to cardio-metabolic risk factors; A-allele carriers might be more sensitive to dietary composition compared to GG homozygotes. Following a healthy DP in A-allele-carriers may be improved their genetic association with cardio-metabolic risk factors.

Highlights

  • Caveolin-1 (CAV-1) is a cholesterol-dependent essential component located in caveolae

  • There was a significant association between CAV-1 polymorphism and serum Low-density lipoprotein (LDL)-C, high-density cholesterol (HDL) in both unadjusted and adjusted models (P < 0.0001 and P = 0.006, P = 0.003 and P = 0.001, respectively), Total cholesterol (TC)/HDL in unadjusted model (P = 0.01) and TC in the adjusted model (P = 0.04)

  • Serum LDL-C, HDL-C, and TC concentration were significantly higher in GG homozygous compared to A-allele carriers

Read more

Summary

Introduction

Caveolin-1 (CAV-1) is a cholesterol-dependent essential component located in caveolae. There is no study has investigated the interaction between CAV-1 rs3807992 gene and dietary patterns (DPs) on cardio-metabolic risk factors. Obesity-induced dyslipidemia, high blood pressure (BP) and inflammation have a key role in the pathogenesis of CVDs [2, 3]. Modifiable factors such as dietary intake and physical activity and non-modifiable including age, gender, and genes associated with the etiology of CVDs [4]. CAV-1 and caveolae are known to interact with a variety of physiologic and biologics pathways, including insulin sensitivity, lipid regulation especially cellular cholesterol and glucose homeostasis, maybe most importantly, cell signaling and receptors [15]. The association of CAV-1 rs3807992 polymorphism with CVDs has not been reported up to now, present study is the first report to investigate this association

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call