Francès F, Verdú F, Portolés O, Castelló A, Sorlí J V, Guillen M, Corella D
Department of Preventive and Legal Medicine, School of Medicine, University of Valencia, Valencia, Spain.
Clin Chim Acta. 2008 Dec;398(1-2):70-4. doi: 10.1016/j.cca.2008.08.011. Epub 2008 Aug 22.
Peroxisome Proliferator-Activated Receptors (PPARs) and its co-activators are regulatory elements of the cellular lipid homeostasis and have been associated with feeding behavior modulation. Animal models suggest that these genes may be involved in alcohol consumption regulation. However, no studies in humans exist. Our aim is to estimate the possible association between polymorphisms in the PPAR-alpha, PPAR-gamma and PPAR-gamma co-activator 1A (PGC-1A) genes and alcohol consumption in humans.
We have conducted a cross-sectional study between the PPAR-alpha L162V, PPAR-gamma P12A and PGC-1A G482S polymorphisms, and alcohol consumption in a general Mediterranean Spanish population (303 men and 443 women).
We have found an association between the L162V polymorphism and alcohol consumption in which, carriers of the V allele were more prevalent among alcohol consumers (19.4% vs. 9.8%; OR 2.69; 95% CI: 1.31-5.54, p=0.007). The G482S polymorphism showed a significantly higher frequency in the group of high alcohol drinkers than in non-high alcohol drinkers (33.4% vs. 20.6%; OR 2.28; 95% CI: 1.07-4.88, p=0.034). Mean alcohol consumption was higher as the number of G alleles increased (GG 8.6+/-12.8 g/day, GS 6.6+/-9.2 g/day, SS 5.6+/-7.8 g/day, p=0.003). These results remained statistically significant after covariate adjustment.
PPAR-alpha L162V and PGC-1A G482S polymorphisms are associated with alcohol consumption in the Mediterranean population.
过氧化物酶体增殖物激活受体(PPARs)及其共激活因子是细胞脂质稳态的调节元件,并与进食行为调节有关。动物模型表明,这些基因可能参与酒精摄入调节。然而,目前尚无关于人类的研究。我们的目的是评估PPAR-α、PPAR-γ和PPAR-γ共激活因子1A(PGC-1A)基因多态性与人类酒精摄入之间的可能关联。
我们在西班牙地中海地区的普通人群(303名男性和443名女性)中进行了一项关于PPAR-α基因L162V、PPAR-γ基因P12A和PGC-1A基因G482S多态性与酒精摄入的横断面研究。
我们发现L162V多态性与酒精摄入之间存在关联,其中V等位基因携带者在酒精消费者中更为普遍(19.4%对9.8%;比值比2.69;95%置信区间:1.31 - 5.54,p = 0.007)。G482S多态性在高酒精饮用者组中的频率显著高于非高酒精饮用者组(33.4%对20.6%;比值比2.28;95%置信区间:1.07 - 4.88,p = 0.034)。随着G等位基因数量的增加,平均酒精摄入量升高(GG型8.6±12.8克/天,GS型6.6±9.2克/天,SS型5.6±7.8克/天,p = 0.003)。在进行协变量调整后,这些结果仍具有统计学意义。
PPAR-α基因L162V和PGC-1A基因G482S多态性与地中海人群的酒精摄入有关。