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Genetic variation at the perilipin locus is associated with changes in serum free fatty acids and abdominal fat following mild weight loss

 Y Jang  ;  O Y Kim  ;  J H Lee  ;  S J Koh  ;  J S Chae  ;  J Y Kim  ;  S Park  ;  H Cho  ;  J E Lee  ;  J M Ordovas 
 International Journal of Obesity, Vol.30(11) : 1601-1608, 2006 
Journal Title
 International Journal of Obesity 
Issue Date
Adult ; Caloric Restriction/methods ; Carrier Proteins ; Dinoprost/urine ; Fatty Acids, Nonesterified/blood* ; Female ; Gene Frequency ; Haplotypes/genetics ; Humans ; Intra-Abdominal Fat/pathology* ; Linkage Disequilibrium/genetics ; Lipoproteins, LDL/urine ; Locus Control Region/genetics ; Male ; Obesity/blood ; Obesity/genetics* ; Obesity/physiopathology ; Oxidative Stress/physiology ; Perilipin-1 ; Phosphoproteins/genetics* ; Polymorphism, Single ; Nucleotide/genetics* ; Subcutaneous Fat, Abdominal/pathology* ; Weight Loss/physiology*
OBJECTIVE: Perilipin (PLIN) is a class of protein-coating lipid droplets in adipocytes. We aimed to examine the association between common single-nucleotide polymorphisms (SNPs) at PLIN locus with circulating free fatty acid (FFA) and abdominal fat distribution in response to weight loss. METHODS: Non-diabetic/overweight-obese Koreans (n=177) participated in a 12-week calorie restriction (-300kcal/day) program. Seven SNPs (6209T>C, 10076C>G, 10171A>T, 11482G>A, 13042A>G, 13048C>T and 14995A>T), abdominal fat areas (visceral/subcutaneous fat areas at 1st lumbar and 4th lumbar levels), serum lipids, glucose, insulin, FFA, oxidized low-density lipoprotein (LDL) and urinary 8-epi-prostaglandin F(2alpha) (PGF(2alpha)) were examined. RESULTS: Single-nucleotide polymorphisms 10076C>G/10171A>T showed the strongest positive linkage disequilibrium (LD) (D'=0.923, R (2)=0.839, P<0.001) and SNPs11482G>A/14995A>T showed moderate positive LD (D'=0.824, R (2)=0.578, P<0.001). Calorie restriction induced 4.6% weight loss with significant abdominal fat reduction. In response to weight loss, subjects with nCA/nCA haplotypes at SNPs 10076C>G/10171A>T showed greater reduction in FFA levels than those with CA/CA haplotype (CA/CA: C/C at SNP 10076 and A/A at SNP 10171, nCA: non-CA haplotype carrier). On the other hand, subjects with nGA/nGA haplotype at SNPs 11482G>A/14995A>T had increased FFA levels with a rapid loss in abdominal fat, whereas GA/GA haplotype carriers had reduction in FFA levels. These results still remained significant after adjusting for age, gender and BMI. Prostaglandin F(2alpha) and oxidized LDL were also more reduced in GA/GA haplotype carriers than in nGA haplotype carriers. This effect remained significant after adjusting for baseline level, age, gender and BMI. Paradoxically, nGA haplotype carriers had increased levels of urinary PGF(2alpha) after weight reduction. CONCLUSION: Fasting plasma FFA changes following a modest weight loss in overweight-obese subjects are influenced by the genetic variability at the PLIN locus. Furthermore, circulating FFA changes rather than body fat itself may determine changes in lipid peroxides such as urinary PGF(2alpha) and oxidized LDL.
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1. Journal Papers (연구논문) > 1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실)
Yonsei Authors
박성하(Park, Sung Ha)
장양수(Jang, Yang Soo)
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