Yang Qiong, Guo Chao-Yu, Cupples L Adrienne, Levy Daniel, Wilson Peter W F, Fox Caroline S
Department of Biostatistics, Boston University School of Public Health, Boston, MA 02118, USA.
Metabolism. 2005 Nov;54(11):1435-41. doi: 10.1016/j.metabol.2005.05.007.
Serum uric acid levels are associated with hypertension, cardiovascular disease, and renal disease. Uric acid has been shown to be heritable; however, genome-wide linkage analyses have not been reported. Genome-wide multipoint variance components linkage analyses with 401 markers spaced at approximately 10 centimorgan (cM) were conducted on 1258 subjects of the Framingham Heart Study, using the average of two serum uric acid measurements obtained in examinations 1 and 2 around 1971 and 1979. Covariates in fully adjusted model included sex, age, body mass index (BMI), serum creatinine, alcohol consumption, diabetes, diuretic treatment, and triglycerides. To investigate possible pleiotropic effects between uric acid and covariates that may have a genetic component, bivariate linkage analyses of uric acid with BMI, triglycerides, and glucose were conducted at the uric acid linkage regions. The heritability of uric acid was 0.63. The highest multipoint log-of-the-odds (LOD) score was 3.3 at 50 cM on chromosome 15 for age-sex-adjusted uric acid, but decreased to 1.5 after multivariable adjustment. Additional evidence of linkage was seen on chromosomes 2 (LOD score 1.1 at 4 cM) and 8 (LOD score 1.7 at 6 cM) for multivariable-adjusted uric acid. Pleiotropic effects were only found between uric acid and glucose and BMI at chromosomes 8 and 15 linkage locations, respectively. We have identified several novel loci linked to uric acid. We found possible pleiotropic effects between uric acid and BMI and glucose. Further research is necessary to identify the genes involved in uric acid metabolism and their roles in hypertension, cardiovascular disease, and renal disease.
血清尿酸水平与高血压、心血管疾病及肾脏疾病相关。尿酸已被证明具有遗传性;然而,尚未有全基因组连锁分析的报道。利用1971年和1979年左右在第1次和第2次检查中获得的两次血清尿酸测量值的平均值,对弗雷明汉心脏研究的1258名受试者进行了全基因组多点方差成分连锁分析,分析使用了间距约为10厘摩(cM)的401个标记。完全调整模型中的协变量包括性别、年龄、体重指数(BMI)、血清肌酐、饮酒量、糖尿病、利尿剂治疗及甘油三酯。为研究尿酸与可能具有遗传成分的协变量之间可能的多效性作用,在尿酸连锁区域对尿酸与BMI、甘油三酯及葡萄糖进行了双变量连锁分析。尿酸的遗传度为0.63。对于年龄和性别调整后的尿酸,在15号染色体50 cM处的最高多点对数优势(LOD)得分为3.3,但在多变量调整后降至1.5。对于多变量调整后的尿酸,在2号染色体(4 cM处LOD得分为1.1)和8号染色体(6 cM处LOD得分为1.7)上发现了连锁的其他证据。多效性作用仅分别在8号和15号染色体的连锁位置上的尿酸与葡萄糖及BMI之间被发现。我们已鉴定出几个与尿酸相关的新位点。我们发现尿酸与BMI及葡萄糖之间可能存在多效性作用。有必要进行进一步研究以确定参与尿酸代谢的基因及其在高血压、心血管疾病和肾脏疾病中的作用。