Bicik Zerrin, Gönen Sevim, Bahçebasi Talat, Reis Kadriye, Arinsoy Turgay, Sindel Sükrü
Department of Nephrology, Medical Faculty, Abant lzzet Baysal University, Düzce, Turkey.
Department of Nephrology, Medical Faculty, Gazi University, Ankara,Turkey.
Curr Ther Res Clin Exp. 2005 Jul;66(4):266-78. doi: 10.1016/j.curtheres.2005.08.003.
Many studies have shown that transforming growth factor(TGF)-β has a major role in renal scarring in many renal diseases and hypertension.
The primary aim of this study was to investigate both the relationship between hypertension and serum and urinary levels of TGF-β2 (a more sensitive isoform for glomeruli than TGF-β1), and the effects of combination therapy with perindopril + indapamide on microalbuminuria, which becomes an early indicator of hypertensive benign nephropathy, and serum and urinary TGF-β2 levels in patients with mild to moderate essential hypertension. In addition, we examined the possible relationship between TGF-β2 gene polymorphism and essential hypertension.
This study was conducted at the Department of Nephrology, Medical Faculty, Gazi University, Ankara, Turkey. Patients aged ≥18 years with newly diagnosed mild to moderate essential hypertension (systolic/diastolic blood pressure [SBP/DBP] >120/>80 mm Hg) who had not previously received antihypertensive treatment were included in the study. Patients with stage I hypertension received perindopril 2 mg + indapamide 0.625 mg (tablet), and patients with stage lI hypertension received perindopril 4 mg + indapamide 1.125 mg (tablet). All study drugs were given OD (morning) PO with food for 6 months. Serum and urinary TGF-β2 and creatinine levels and serum and urinary albumin levels were measured before and after perindopril + indapamide administration. Amplified DNA fragments of the TGF-β2 primer region were screened using amplification refractory mutation system polymerase chain reaction analysis, and the number of ACA repeats was confirmed by DNA sequencing. Genetic studies were performed using a commercial TGF-β2 kit.
Forty patients were enrolled in the study, and 38 patients (27 women, 11 men; mean [SD] age, 46.3 [6.5] years) completed it. SBP and DBP were significantly decreased from baseline with perindopril/indapamide (both, P < 0.001). Microalbuminuria and urinary TGF-β2 levels also decreased significantly from baseline (P = 0.04 and P < 0.001, respectively), whereas the serum TGF-β2 level did not change significantly. Three patients, all of whom were found to have TGF-β2 gene mutations, had increased urinary TGF-β2 levels despite good blood pressure control.
The results of this study in patients with mild to moderate hypertension suggest that, despite good clinical control of blood pressure, the persistence of microalbuminuria and high urinary TGF-β2 levels might predict renal impairment. When treating these patients, genetic tendencies and possible polymorphisms on the TGF-β2 locus should be kept in mind.
许多研究表明,转化生长因子(TGF)-β在多种肾脏疾病和高血压的肾脏瘢痕形成中起主要作用。
本研究的主要目的是探讨高血压与血清及尿液中TGF-β2(一种比TGF-β1对肾小球更敏感的异构体)水平之间的关系,以及培哚普利+吲达帕胺联合治疗对微量白蛋白尿(高血压良性肾病的早期指标)、血清和尿液TGF-β2水平在轻度至中度原发性高血压患者中的影响。此外,我们还研究了TGF-β2基因多态性与原发性高血压之间的可能关系。
本研究在土耳其安卡拉加齐大学医学院肾脏病科进行。纳入年龄≥18岁、新诊断为轻度至中度原发性高血压(收缩压/舒张压[SBP/DBP]>120/>80 mmHg)且此前未接受过抗高血压治疗的患者。I期高血压患者服用培哚普利2 mg+吲达帕胺0.625 mg(片剂),II期高血压患者服用培哚普利4 mg+吲达帕胺1.125 mg(片剂)。所有研究药物均于早餐时口服,每日一次,共服用6个月。在培哚普利+吲达帕胺给药前后测定血清和尿液中的TGF-β2、肌酐水平以及血清和尿液中的白蛋白水平。使用扩增阻滞突变系统聚合酶链反应分析筛选TGF-β2引物区域的扩增DNA片段,并通过DNA测序确认ACA重复序列的数量。使用商用TGF-β2试剂盒进行基因研究。
40例患者纳入本研究,38例患者(27例女性,11例男性;平均[标准差]年龄,46.3[6.5]岁)完成研究。培哚普利/吲达帕胺治疗后SBP和DBP较基线显著降低(均P<0.001)。微量白蛋白尿和尿液TGF-β2水平也较基线显著降低(分别为P = 0.04和P<0.001),而血清TGF-β2水平无显著变化。3例患者均检测到TGF-β2基因突变,尽管血压控制良好,但尿液TGF-β2水平仍升高。
本研究在轻度至中度高血压患者中的结果表明,尽管血压在临床上得到良好控制,但微量白蛋白尿和尿液TGF-β2水平持续升高可能预示肾脏损害。在治疗这些患者时,应考虑TGF-β2基因位点的遗传倾向和可能的多态性。