Bustamante M, Nogués X, Mellibovsky L, Agueda L, Jurado S, Cáceres E, Blanch J, Carreras R, Díez-Pérez A, Grinberg D, Balcells S
Department of Genetics, University of Barcelona, Barcelona, Spain.
Eur J Endocrinol. 2007 Nov;157(5):677-84. doi: 10.1530/EJE-07-0389.
Osteoporosis and obesity are complex diseases with a strong genetic component. Bone mineral density (BMD) and body mass index (BMI) linkage studies identified a locus at 1q21-23, where the interleukin-6 receptor (IL6R) gene is located. The IL6R and the gp130 receptors are the mediators of IL6 action. Serum levels of IL6 and sIL6R (the soluble form of IL6R) are higher in several diseases such as osteoporosis or obesity. Variants at IL6R have been associated with BMI and obesity. However, IL6R is an as-yet-unexplored osteoporosis candidate gene.
In the present study we analysed two polymorphisms in the IL6R promoter, -1435 C/T (rs3887104) and -208 G/A (rs4845617), and the Asp358Ala polymorphism (rs8192284), in relation to both BMD and BMI in a cohort of 559 postmenopausal Spanish women.
The promoter polymorphisms, -1435 C/T and -208 G/A were associated with femoral neck (FN) BMD (P=0.011 and P=0.025 respectively). The C-A and T-G promoter haplotypes were also associated with FN BMD. Additionally, the Asp358Ala variant was associated with lumbar spine BMD (P=0.038). Finally, the -208 G/A polymorphism and the C-G and C-A haplotypes were associated with BMI and obesity, where GG was the risk genotype (P=0.033 for BMI; P=0.010 for obesity).
These data suggest that variants in the IL6R gene are not only involved in the determination of BMI but also relevant for the determination of BMD. The IL6R gene may belong to the growing list of genes known to be involved in both phenotypes.
骨质疏松症和肥胖症是具有强大遗传成分的复杂疾病。骨密度(BMD)和体重指数(BMI)连锁研究确定了位于1q21 - 23的一个基因座,白细胞介素6受体(IL6R)基因位于该基因座。IL6R和gp130受体是IL6作用的介质。在骨质疏松症或肥胖症等几种疾病中,血清IL6和sIL6R(IL6R的可溶性形式)水平较高。IL6R的变异与BMI和肥胖症有关。然而,IL6R是一个尚未被探索的骨质疏松症候选基因。
在本研究中,我们分析了559名西班牙绝经后女性队列中IL6R启动子的两个多态性,即 - 1435 C/T(rs3887104)和 - 208 G/A(rs4845617),以及Asp358Ala多态性(rs8192284)与BMD和BMI的关系。
启动子多态性 - 1435 C/T和 - 208 G/A与股骨颈(FN)骨密度相关(分别为P = 0.011和P = 0.025)。C - A和T - G启动子单倍型也与FN骨密度相关。此外,Asp358Ala变异与腰椎骨密度相关(P = 0.038)。最后, - 208 G/A多态性以及C - G和C - A单倍型与BMI和肥胖症相关,其中GG是风险基因型(BMI为P = 0.033;肥胖症为P = 0.010)。
这些数据表明,IL6R基因的变异不仅参与BMI的决定,而且与BMD的决定也相关。IL6R基因可能属于已知参与这两种表型的不断增加的基因列表。