Qi Lu, Zhang Cuilin, van Dam Rob M, Hu Frank B
Departments of Nutrition and Epidemiology, Harvard School of Public Health, and Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
J Clin Endocrinol Metab. 2007 Sep;92(9):3618-25. doi: 10.1210/jc.2007-0877. Epub 2007 Jul 10.
IL-6 (IL6) is an immune-modulating cytokine associated with obesity in humans.
Our objective was to assess the associations between the genetic variability of IL6 gene and adiposity and long-term changes.
We determined the linkage disequilibrium-tagging single-nucleotide polymorphisms of IL6 gene in 2255 healthy women and 980 healthy men from two prospective cohorts. We also conducted a metaanalysis on the associations between polymorphism -174G>C (rs1800795) and adiposity.
IL6 haplotype 222211 (possessing rs2069827, rs1800797, rs1800795, rs1554606, rs2069861, and rs1818879; 1 codes the common and 2 codes the minor alleles) was consistently and significantly associated with greater waist circumference (P = 0.009 in men; P = 0.0003 in women) and baseline body mass index (BMI) (P = 0.01 in men; P = 0.046 in women) compared with the most common haplotype 111112. Haplotype 222211 was also associated with significantly higher early-adulthood BMI in women (P = 0.007). The haplotype-associated difference in BMI persisted significantly during the follow-up. A 5' promoter polymorphism, rs2069827, was consistently associated with significantly higher early-adulthood BMI, baseline BMI, and waist circumference in men (carriers vs. noncarriers, P = 0.01, 0.007, and 0.008) and women (P = 0.01, 0.10, and 0.0016). The data from this study and a metaanalysis of 26,944 individuals did not support substantial relations between the best-studied polymorphism, -174G>C, and adiposity.
Our data from two independent cohorts indicate that the variability of the IL6 gene is significantly associated with adiposity. Such associations are less likely to be caused by polymorphism -174G>C.
白细胞介素-6(IL-6)是一种与人类肥胖相关的免疫调节细胞因子。
我们的目的是评估IL6基因的遗传变异性与肥胖及长期变化之间的关联。
我们在来自两个前瞻性队列的2255名健康女性和980名健康男性中确定了IL6基因的连锁不平衡标签单核苷酸多态性。我们还对多态性-174G>C(rs1800795)与肥胖之间的关联进行了荟萃分析。
与最常见的单倍型111112相比,IL6单倍型222211(包含rs2069827、rs1800797、rs1800795、rs1554606、rs2069861和rs1818879;1代表常见等位基因,2代表次要等位基因)与更大的腰围(男性中P = 0.009;女性中P = 0.0003)和基线体重指数(BMI)(男性中P = 0.01;女性中P = 0.046)始终且显著相关。单倍型222211还与女性更高的成年早期BMI显著相关(P = 0.007)。在随访期间,单倍型相关的BMI差异持续显著。一种5'启动子多态性rs2069827与男性(携带者与非携带者相比,P = 0.01、0.007和0.008)和女性(P = 0.01、0.10和0.0016)更高的成年早期BMI、基线BMI和腰围始终显著相关。本研究的数据以及对26944名个体的荟萃分析不支持研究最多的多态性-174G>C与肥胖之间的实质性关系。
我们来自两个独立队列的数据表明,IL6基因的变异性与肥胖显著相关。这种关联不太可能由多态性-174G>C引起。