Hu Bang-Chuan, Chu Shao-Li, Wang Gu-Liang, Gao Ping-Jin, Zhu Ding-Liang, Wang Ji-Guang
Department of Hypertension and Centre for Epidemiological Studies and Clinical Trials, Ruijin Hospital, Shanghai Institute of Hypertension, Shanghai Jiao Tong University Medical School, Shanghai, China.
Clin Exp Hypertens. 2008 Feb;30(2):121-31. doi: 10.1080/10641960801931907.
Genetic variants of transforming growth factor (TGF) beta1 have been reported to be associated with diabetic nephropathy. Few studies investigated polymorphisms in the TGF-beta1 and TGF-beta3 genes in relation to renal dysfunction in non-diabetic subjects. In all, 601 non-diabetic Chinese were genotyped for the TGF-beta1 T869C and TGF-beta3 IVS3-98G>A polymorphisms by PCR-restriction fragment length polymorphism and real-time allele-specific PCR, respectively. Renal dysfunction was defined as a predicted glomerular filtration rate (GFR) of 60mL/min/1.73m(2) or less. 24-hour urinary albumin excretion was measured by an immunonephelometric assay in 352 hypertensive subjects. Our study sample included 184 (30.6%) women, 396 (65.9%) hypertensive patients (65.9%), and 94 (15.6%) patients with renal dysfunction. In men but not women, the TGF-beta1 TC genotype was significantly (p = 0.0005) overrepresented in patients with renal dysfunction (52.2% vs 36.8% in subjects with normal renal function). Accordingly, in men, with adjustment for age, body mass index, and systolic and diastolic blood pressure, serum creatinine concentration was significantly (p < or = 0.03) higher in the TC heterozygotes than TT and CC homozygotes. Furthermore, in 231 male hypertensive patients, with similar adjustments applied, 24-hour urinary albumin excretion was significantly (p = 0.02) higher in the IVS3-98 AA homozygotes than G allele carriers. In further multivariate regression analysis, only in men, TGF-beta1 and TGF-beta3 genotypes as independent predictors had statistically significant effect on serum creatinine (p = 0.007) and urinary albumin excretion (p = 0.022), respectively. Our study demonstrated the associations of genetic variants in the TGF-beta genes with renal dysfunction and albuminuria in non-diabetic Han Chinese men but not women.
据报道,转化生长因子(TGF)β1的基因变异与糖尿病肾病有关。很少有研究调查非糖尿病患者中TGF-β1和TGF-β3基因的多态性与肾功能障碍的关系。总共601名非糖尿病中国人分别通过聚合酶链反应-限制性片段长度多态性和实时等位基因特异性聚合酶链反应对TGF-β1 T869C和TGF-β3 IVS3-98G>A多态性进行基因分型。肾功能障碍定义为预测肾小球滤过率(GFR)为60mL/(min·1.73m²)或更低。通过免疫比浊法对352名高血压患者进行24小时尿白蛋白排泄量测定。我们的研究样本包括184名(30.6%)女性、396名(65.9%)高血压患者(65.9%)和94名(15.6%)肾功能障碍患者。在男性而非女性中,肾功能障碍患者中TGF-β1 TC基因型显著(p = 0.0005)过多(肾功能正常者中为36.8%,肾功能障碍患者中为52.2%)。因此,在男性中,校正年龄、体重指数以及收缩压和舒张压后,TC杂合子的血清肌酐浓度显著(p≤0.03)高于TT和CC纯合子。此外,在231名男性高血压患者中,进行类似校正后,IVS3-98 AA纯合子的24小时尿白蛋白排泄量显著(p = 0.02)高于G等位基因携带者。在进一步的多变量回归分析中,仅在男性中,TGF-β1和TGF-β3基因型作为独立预测因子分别对血清肌酐(p = 0.007)和尿白蛋白排泄量(p = 0.022)有统计学显著影响。我们的研究表明,TGF-β基因的基因变异与非糖尿病汉族男性而非女性的肾功能障碍和蛋白尿有关。