期刊
INTERNATIONAL JOURNAL OF OBESITY
卷 30, 期 11, 页码 1601-1608出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.ijo.0803312
关键词
PLIN variant; weight loss; free fatty acid; visceral fat and oxidative stress
资金
- NHLBI NIH HHS [HL54776] Funding Source: Medline
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-2 alpha (PGF(2 alpha)) 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-2 alpha 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(2 alpha) 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(2 alpha) and oxidized LDL.
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