Département des sciences fondamentales, Université du Québec à Chicoutimi, Saguenay, Québec, Canada.
Obesity (Silver Spring). 2011 Jan;19(1):222-7. doi: 10.1038/oby.2010.125. Epub 2010 Jun 3.
The inflammatory component in obesity is now well established. The CX3CR1 gene encodes the fractalkine (CX3CL1) receptor and has two coding single-nucleotide polymorphisms, V249I and T280M, linked to a lower risk of other inflammatory diseases such as coronary artery disease (CAD) and asthma. To determine whether CX3CR1 is associated with obesity, we genotyped the V249I and T280M polymorphisms of the CX3CR1 gene in subjects with a BMI ≥30 kg/m² and nonobese controls with a BMI <30 kg/m². Binary logistic regression analyses revealed that the 280MM genotype was associated with obesity (P = 0.022). A gender-specific one-way ANOVA was also conducted to investigate mean BMI and waist circumference differences between genotypes of each polymorphism. For both polymorphisms independently, women carrying two copies of the minor allele had significant higher mean waist circumference than those carrying only one copy of the minor allele (MM > TM, P = 0.031; II > VI, P = 0.013) or those who were homozygous for the major allele (MM > TT, P = 0.005; II > VV, P = 0.006). We also observed significant higher mean waist circumference in men carrying one copy of the minor allele when compared to those who were homozygous for the major allele for the T280M polymorphism (TM > TT, P = 0.029). This study suggests that CX3CR1, a biomarker of obesity in this sample, constitutes a potential target for further investigation of the role of inflammation in the expression of obesity-related phenotypes.
肥胖中的炎症成分现在已经得到充分证实。CX3CR1 基因编码趋化因子(CX3CL1)受体,具有两个编码单核苷酸多态性,即 V249I 和 T280M,与其他炎症性疾病(如冠心病和哮喘)的风险降低相关。为了确定 CX3CR1 是否与肥胖有关,我们对 BMI≥30kg/m²的受试者和 BMI<30kg/m²的非肥胖对照者的 CX3CR1 基因 V249I 和 T280M 多态性进行了基因分型。二元逻辑回归分析显示,280MM 基因型与肥胖有关(P=0.022)。还进行了性别特异性单因素方差分析,以研究每个多态性的基因型之间平均 BMI 和腰围的差异。对于这两种多态性,女性携带两个次要等位基因的个体的平均腰围显著高于仅携带一个次要等位基因的个体(MM>TM,P=0.031;II>VI,P=0.013)或纯合主要等位基因的个体(MM>TT,P=0.005;II>VV,P=0.006)。我们还观察到,与 T280M 多态性的主要等位基因纯合个体相比,携带一个次要等位基因的男性的平均腰围显著更高(TM>TT,P=0.029)。这项研究表明,CX3CR1 作为本样本中肥胖的生物标志物,可能是进一步研究炎症在肥胖相关表型表达中的作用的潜在目标。