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首页> 外文期刊>The American Journal of the Medical Sciences >Changes in urinary albumin excretion, inflammatory and oxidative stress markers in ADPKD patients with hypertension.
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Changes in urinary albumin excretion, inflammatory and oxidative stress markers in ADPKD patients with hypertension.

机译:ADPKD高血压患者尿白蛋白排泄,炎症和氧化应激指标的变化。

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BACKGROUNDS: Autosomal dominant polycystic kidney disease (ADPKD) progresses more quickly to end-stage renal disease in patients with hypertension than in their normotensive counterparts. The authors investigated the effect of telmisartan versus enalapril on systolic and diastolic blood pressure (SBP and DBP), urinary albumin excretion (UAE), serum high mobility group box-1 protein (HMGB1), serum interleukin (IL)-6 and urinary 8-hydroxydeoxyguanosine (8-OHdG) levels in patients with hypertensive ADPKD. METHODS: Twenty patients with hypertensive ADPKD with good renal function were randomly assigned to 1 of 2 treatments: telmisartan 80 mg once daily (n = 10) or enalapril 10 mg once daily (n = 10). Treatment lasted 12 months. SBP, DBP, serum creatinine, UAE, HMGB1, IL-6 and urinary 8-OHdG levels were measured before and 6 and 12 months after treatment. RESULTS: Both SBP and DBP were significantly reduced after treatment (P < 0.001) in both groups. Serum creatinine changed little during the experimental period in either group. UAE, serum HMGB1, serum IL-6 and urinary 8-OHdG levels were significantly decreased after treatment (UAE, HMGB1 and IL-6, P < 0.001; and 8-OHdG, P < 0.01 versus baseline levels) in both groups. However, the decreases in UAE, serum HMGB1 and serum IL-6 were significantly greater in the telmisartan group than in the enalapril group at 6 months (P < 0.05, P < 0.01 and P < 0.01, respectively) and 12 months (all, P < 0.05). CONCLUSIONS: Telmisartan seems to be equivalent to enalapril in lowering BP, but telmisartan has more potent renoprotective, anti-inflammatory and antioxidative effects than enalapril in patients with hypertensive ADPKD.
机译:背景:高血压患者的常染色体显性遗传性多囊肾病(ADPKD)进展为终末期肾病的速度要快于正常血压的同行者。作者研究了替米沙坦与依那普利对收缩压和舒张压(SBP和DBP),尿白蛋白排泄(UAE),血清高迁移率族box-1蛋白(HMGB1),血清白介素(IL)-6和尿液8的影响高血压ADPKD患者的-羟基脱氧鸟苷(8-OHdG)水平。方法:将20例肾功能良好的高血压ADPKD患者随机分配至2种治疗方法中的1种:替米沙坦每天80 mg(n = 10)或依那普利10 mg每天1(n = 10)。治疗持续了12个月。在治疗前和治疗后6个月和12个月测量SBP,DBP,血清肌酐,UAE,HMGB1,IL-6和尿中的8-OHdG水平。结果:两组治疗后SBP和DBP均显着降低(P <0.001)。两组的实验期间血清肌酐变化不大。两组治疗后的UAE,血清HMGB1,血清IL-6和尿液8-OHdG水平均显着降低(UAE,HMGB1和IL-6,P <0.001;和8-OHdG,P <0.01,相对于基线水平)。但是,替米沙坦组在6个月(分别为P <0.05,P <0.01和P <0.01)和12个月(分别为: P <0.05)。结论:替米沙坦在降低血压方面似乎与依那普利相当,但对于高血压ADPKD患者,替米沙坦比依那普利具有更强的肾脏保护,抗炎和抗氧化作用。

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