Daniele A, Cammarata R, Pasanisi F, Finelli C, Salvatori G, Calcagno G, Bracale R, Labruna G, Nardelli C, Buono P, Sacchetti L, Contaldo F, Oriani G
Dipartimento di Scienze per la Salute, Università del Molise, Campobasso, Italy.
Ann Nutr Metab. 2008;53(3-4):155-61. doi: 10.1159/000172976. Epub 2008 Nov 14.
Severe obesity is a major worldwide public health concern affecting 0.5-5% of the adult population. Adiponectin (Acpr30), an adipokine secreted from adipocytes, shows pleiotropic beneficial effects on obesity and related disorders. In this study, sequence analysis of Acpr30 gene (ACDC) was performed in a highly selected population of severely obese young adult patients from Southern Italy to investigate the associations between polymorphisms in the ACDC gene and the development of severe obesity concomitantly with other features of the metabolic syndrome.
The ACDC gene was analyzed by direct sequencing in the severely obese patients (n=220) and compared to healthy controls (n=116). The associations between the ACDC gene single-nucleotide polymorphisms (SNPs) and the levels of serum Acpr30 as well as the correlation with the presence of severe obesity jointly associated with other features of the metabolic syndrome were also investigated. Total serum Acpr30 concentrations were measured by the ELISA method.
ACDC gene molecular screening revealed the presence of previously described SNPs and a new nucleotide alteration, c.355T>G, leading to a protein variant, p.L119V. Measurement of serum concentration of Acpr30 demonstrated lower levels of Acpr30 in the obese population compared to controls (30.5+/-28.3 vs. 43.9+/-35.7 microg/ml, p<0.01); in particular, significantly lower Acpr30 concentrations were observed in obese patients bearing c.-11377C>G SNP CG+GG genotypes than in those with CC genotype (22.9+/-20.5 vs. 33.1+/-29.4 microg/ml, p<0.05).
Our results confirmed that low serum levels of Acpr30 are related to severe obesity and a difference in protein expression is associated with variants in ACDC gene promoter region.
重度肥胖是一个全球性的重大公共卫生问题,影响着0.5%-5%的成年人口。脂联素(Acpr30)是一种由脂肪细胞分泌的脂肪因子,对肥胖及相关疾病具有多效性有益作用。在本研究中,对来自意大利南部的一组经过高度筛选的重度肥胖年轻成年患者进行了Acpr30基因(ACDC)的序列分析,以调查ACDC基因多态性与重度肥胖的发生以及代谢综合征其他特征之间的关联。
对重度肥胖患者(n=220)进行直接测序分析ACDC基因,并与健康对照(n=116)进行比较。还研究了ACDC基因单核苷酸多态性(SNP)与血清Acpr30水平之间的关联,以及与重度肥胖伴代谢综合征其他特征的相关性。采用酶联免疫吸附测定法(ELISA)测量血清总Acpr30浓度。
ACDC基因分子筛查发现了先前描述的SNP以及一个新的核苷酸改变,即c.355T>G,导致一种蛋白质变体p.L119V。与对照组相比,肥胖人群中Acpr30的血清浓度较低(30.5±28.3对43.9±35.7μg/ml,p<0.01);特别是,携带c.-11377C>G SNP CG+GG基因型的肥胖患者的Acpr30浓度明显低于CC基因型患者(22.9±20.5对33.1±29.4μg/ml,p<0.05)。
我们的结果证实,血清Acpr30水平低与重度肥胖有关,蛋白质表达差异与ACDC基因启动子区域的变体有关。