» Articles » PMID: 17485234

L-FABP T94A is Associated with Fasting Triglycerides and LDL-cholesterol in Women

Overview
Journal Mol Genet Metab
Specialty Endocrinology
Date 2007 May 9
PMID 17485234
Citations 34
Authors
Affiliations
Soon will be listed here.
Abstract

To determine the possible role of the common FABP1 T94A polymorphism in modulating susceptibility to traits of the metabolic syndrome, we analysed a random sample of 826 subjects from the European Prospective Investigation into Cancer and Nutrition (EPIC)-Potsdam cohort. Multivariate adjusted linear trend regression analysis of metabolic, anthropometric and blood pressure variables in FABP1 T94A genotypes were performed in both genders. In women, a significant trend of higher plasma triglyceride (P=0.01) and LDL-cholesterol (P=0.02) concentrations were seen for A-allele carriers after adjustment for age, menopausal status, hormone intake and Apo E genotype. Because elevated triglyceride and cholesterol levels are important risk factors of cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM), we additionally analysed the association of the T94A variant and disease risks in two studies enrolling 220 incident CVD and 192 incident T2DM patients of the EPIC-Potsdam cohort. After adjusting for age, sex, BMI and other covariates, we found no association between FABP1 T94A and CVD or T2DM. In conclusion, our study provides evidence for an association of the FABP1 T94A polymorphism and fasting triglycerides and LDL-cholesterol levels in females. These results support previous findings in fenofibrate-treated individuals and thereby provide some additional indication of the functional relevance of the FABP1 T94A SNP in hepatic fatty acid and lipid metabolism in humans.

Citing Articles

Polymorphism in genes encoding two fatty acid binding proteins increases risk of ischemic stroke in a Chinese Han population.

Cao M, Zhang Y, Chen D, Zhong J, Zhang X, Yang L Front Genet. 2023; 14:1056186.

PMID: 37091779 PMC: 10117902. DOI: 10.3389/fgene.2023.1056186.


From Congenital Disorders of Fat Malabsorption to Understanding Intra-Enterocyte Mechanisms Behind Chylomicron Assembly and Secretion.

Levy E, Beaulieu J, Spahis S Front Physiol. 2021; 12:629222.

PMID: 33584351 PMC: 7873531. DOI: 10.3389/fphys.2021.629222.


Distinct Alteration of Gene Expression Programs in the Small Intestine of Male and Female Mice in Response to Ablation of Intestinal Fabp Genes.

Chen Y, Agellon L Genes (Basel). 2020; 11(8).

PMID: 32824144 PMC: 7465894. DOI: 10.3390/genes11080943.


Liver fatty acid-binding protein might be a predictive marker of clinical response to systemic treatment in psoriasis.

Baran A, Kiluk P, Maciaszek M, Swiderska M, Flisiak I Arch Dermatol Res. 2019; 311(5):389-397.

PMID: 30993401 PMC: 6546856. DOI: 10.1007/s00403-019-01917-w.


Ablating both Fabp1 and Scp2/Scpx (TKO) induces hepatic phospholipid and cholesterol accumulation in high fat-fed mice.

Milligan S, Martin G, Landrock D, McIntosh A, Mackie J, Schroeder F Biochim Biophys Acta Mol Cell Biol Lipids. 2018; 1863(3):323-338.

PMID: 29307784 PMC: 5807141. DOI: 10.1016/j.bbalip.2017.12.013.