Jang Y, Kim O Y, Lee J H, Koh S J, Chae J S, Kim J Y, Park S, Cho H, Lee J E, Ordovas J M
Division of Cardiology, Cardiovascular Genome Center, Yonsei Medical Institute, Yonsei University, Seoul, Korea.
Int J Obes (Lond). 2006 Nov;30(11):1601-8. doi: 10.1038/sj.ijo.0803312. Epub 2006 Apr 4.
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.
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.
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.
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.
perilipin(PLIN)是一类存在于脂肪细胞中包裹脂质小滴的蛋白质。我们旨在研究PLIN基因座常见单核苷酸多态性(SNP)与体重减轻后循环游离脂肪酸(FFA)及腹部脂肪分布之间的关联。
非糖尿病/超重肥胖的韩国人(n = 177)参加了一项为期12周的热量限制(-300千卡/天)计划。检测了7个SNP(6209T>C、10076C>G、10171A>T、11482G>A、13042A>G、13048C>T和14995A>T)、腹部脂肪面积(第1腰椎和第4腰椎水平的内脏/皮下脂肪面积)、血脂、血糖、胰岛素、FFA、氧化型低密度脂蛋白(LDL)和尿8-表前列腺素F(2α)(PGF(2α))。
单核苷酸多态性10076C>G/10171A>T显示出最强的正连锁不平衡(LD)(D' = 0.923,R(2) = 0.839,P < 0.001),SNP 11482G>A/14995A>T显示出中等程度的正LD(D' = 0.824,R(2) = 0.578,P < 0.001)。热量限制导致体重减轻4.6%,腹部脂肪显著减少。在体重减轻后,SNP 10076C>G/10171A>T处nCA/nCA单倍型的受试者FFA水平下降幅度大于CA/CA单倍型受试者(CA/CA:SNP 10076处为C/C,SNP 10171处为A/A,nCA:非CA单倍型携带者)。另一方面,SNP 11482G>A/14995A>T处nGA/nGA单倍型的受试者腹部脂肪快速减少的同时FFA水平升高,而GA/GA单倍型携带者FFA水平下降。在调整年龄、性别和BMI后,这些结果仍然显著。GA/GA单倍型携带者的前列腺素F(2α)和氧化型LDL也比nGA单倍型携带者降低得更多。在调整基线水平、年龄、性别和BMI后,这种效应仍然显著。矛盾的是,nGA单倍型携带者体重减轻后尿PGF(2α)水平升高。
超重肥胖受试者适度体重减轻后空腹血浆FFA的变化受PLIN基因座遗传变异的影响。此外,循环FFA的变化而非身体脂肪本身可能决定脂质过氧化物如尿PGF(2α)和氧化型LDL的变化。