Original scientific paper
Effects of Lipoprotein Lipase and Peroxisome Proliferator-Activated Receptor-g Gene Variants on Metabolic Syndrome Traits
Tamara Božina
; University of Zagreb, School of Medicine, Department of Medical Chemistry, Biochemistry and Clinical Chemistry, Zagreb, Croatia
Iveta Šimić
; University of Zagreb, University Hospital Center Zagreb, School of Medicine, Department of Internal Medicine, Zagreb, Croatia
Jasna Lovrić
; University of Zagreb, School of Medicine, Department of Medical Chemistry, Biochemistry and Clinical Chemistry, Zagreb, Croatia
Ivan Pećin
; University of Zagreb, University Hospital Center Zagreb, School of Medicine, Department of Internal Medicine, Zagreb, Croatia
Bojan Jelaković
; University of Zagreb, University Hospital Center Zagreb, School of Medicine, Department of Internal Medicine, Zagreb, Croatia
Jadranka Sertić
; University of Zagreb, School of Medicine, Department of Medical Chemistry, Biochemistry and Clinical Chemistry, Zagreb, Croatia
Željko Reiner
; University of Zagreb, University Hospital Center Zagreb, School of Medicine, Department of Internal Medicine, Zagreb, Croatia
Abstract
Peroxisome proliferator activated receptor-g (PPARG) and lipoprotein lipase (LPL) play important role in lipid ho- meostasis, insulin resistance and adipogenesis, and their gene variability could be considered as predictive genetic mar- kers for metabolic syndrome (MetSy). The aim of the study was to estimate possible associations of PPARG (Pro12Ala) and LPL PvuII (+/–) polymorphisms with MetSy and its traits. Study included 527 subjects. According to the modified National Cholesterol Education Program Adult Treatment Panel III definitions, subjects were classified into the meta- bolic syndrome group and control group. Genotyping was performed using polymerase chain reaction-restriction frag- ment length polymorphism methods. In the total sample, LPL variants were associated with waist circumference (c 2 = 7.263, d.f.=2, p=0.026) and with BMI (c 2 =6.549, d.f.=2, p=0.038), where PvuII (+/+) genotype carriers had the highest risk for increased waist circumference (specific PvuII (+/+) vs. others analysis c 2 =7.033, p=0.008) and increased BMI (specific Pvu II(+/+) vs. others analysis c 2 =5.154, p=0.023). LPL gene variants were also associated with HDL-C levels (c 2 =6.901, d.f.=2, p=0.032), where PvuII (–/–) genotype carriers had higher HDL-C values in comparison to others (spe- cific Pvu (+/+) vs. others analysis c 2 =6.504, p=0.011). Furthermore, PvuII (–) allele carriers had significantly lower glucose (allele based analysis Add Value=–0.0878, c 2 =5.878, d.f.=1, p=0.015). Significant interaction was detected be- tween PPARG and LPL that affected HDL-C levels in male population (c 2 =11.790, d.f.=1, p=0.0006) in the manner that Ala/PvuII(+) contributed to the lowest HDL-C values (Specific Ala/ Pvu(+) vs. others analysis was c 2 =11.750, p= 0.0006). According to obtained results LPL and PPARG gene variants could be susceptibility factors of obesity and lipid status, contributing to development of MetSy, particularly in males. Because of antiatherogenic function of HDL-C, the identification of genetic variants associated with HDL-C can provide useful information related to genotype-phenotype relationships. Since the interplay between PPARG and LPL gene and gender seems to be significant it could point to the personalized behavioural recommendations for prevention of metabolic and cardiovascular diseases.
Keywords
metabolic syndrome; genetic polymorphisms; peroxisome proliferator-activated receptor g gene; lipoprotein lipase gene
Hrčak ID:
118222
URI
Publication date:
30.9.2013.
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