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首页> 外文期刊>Vojnosanitetski Pregled >Angiotensin II type 1 receptor gene polymorphism could influence renoprotective response to losartan treatment in type 1 diabetic patients with high urinary albumin excretion rate
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Angiotensin II type 1 receptor gene polymorphism could influence renoprotective response to losartan treatment in type 1 diabetic patients with high urinary albumin excretion rate

机译:血管紧张素II 1型受体基因多态性可能影响尿白蛋白排泄率高的1型糖尿病患者对氯沙坦治疗的肾脏保护反应

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Background/Aim. Diabetic nephropathy (DN) is a clinical syndrome characterized by persistent albuminuria, increasing arterial blood pressure and progressive decline in glomerular filtration rate (GFR). When persistent albuminuria is established, antihypertensive treatment becomes most important factor in slowing the progression of diabetic glomerulopathy. The aim of this study was to examine if renoprotective response to a short-term losartan therapy depends on 1166 A/C gene polymorphism for its target receptor. Method. The study included 35 patients with diabetes mellitus type 1 and persistently high urinary albumin excretion rate (UAE: > 30 mg/24 h), genotyped for the 1166 A/C gene polymorphism for the angiotensin II type 1 receptor (AT1R). The participants were segregated into 3 genotype groups according to combinations of A or C allele: AA(16%), AC(15%) and CC(11%). The patients received losartan 50 mg daily for 4 weeks, following 100 mg daily for another 8 weeks. At baseline and after 12 weeks of the treatment period UAE, blood pressure, GFR and filtration fraction (FF) were determined. Results. After 12 weeks of the treatment with losartan, albuminuria was reduced from baseline by 9% [95% confidence interval (CI): 1-17, p = 0.039] in the AA genotype, and by 11% (95% CI: 6-17, p = 0.0001) in the AC genotype. Losartan treatment reduced albuminuria in the CC group by 5% (95%CI: -13-22, p = 0.47). Glomerular filtration rate remained unchanged in all genotype groups. Filtration fraction was significantly reduced from baseline by 0.018 ± 0.024 (p = 0.012) only in the AC genotype. In the AA genotype, FF was reduced from baseline by 0.017 ± 0.03 (p = 0.052), and in the CC genotype by 0.01 ± 0.008 (p = 0.092). In the AA group, systolic blood pressure declined from 136 ± 24 mmHg at baseline, to an average of 121 ± 18 mmHg at the end of the study (p = 0.001). The AC group achived reduction from 131 ± 10 mmHg at baseline to 115 ± 7 mmHg (p = 0.001) during the investigation period. In the AA genotype group losartan reduced diastolic blood pressure from 86 ± 13 mmHg at baseline to 78 ± 8 mmHg (p = 0.004), and in the AC genotype from 88 ± 5 mmHg at baseline to 11.7 ± 5.6 mmHg during the investigation period (p = 0.001). In the CC genotype diastolic blood pressure reduction remained nonsignificant (p = 0.066). Conclusion. The results of our small sample size study provide the evidence that 1166 A/C AT1R polymorphism could be associated with the renoprotective response to losartan therapy.
机译:背景/目标。糖尿病肾病(DN)是一种临床综合征,其特征在于持续性白蛋白尿,动脉血压升高和肾小球滤过率(GFR)逐渐下降。建立持续性白蛋白尿后,降压治疗成为减缓糖尿病肾小球疾病进展的最重要因素。这项研究的目的是检查对短期氯沙坦疗法的肾脏保护反应是否依赖于其靶受体的1166 A / C基因多态性。方法。该研究纳入了35例1型糖尿病且尿白蛋白排泄率持续较高(UAE:> 30 mg / 24 h)的患者,这些患者的1166 A / C基因多态性与1型血管紧张素II型受体(AT1R)的基因型有关。根据A或C等位基因的组合将参与者分为3个基因型组:AA(16%),AC(15%)和CC(11%)。患者每天接受50 mg氯沙坦治疗4周,之后连续8周每天接受100 mg氯沙坦治疗。在基线和治疗期12周后的阿联酋,测定血压,GFR和滤过分数(FF)。结果。氯沙坦治疗12周后,AA基因型的蛋白尿比基线降低了9%[95%置信区间(CI):1-17,p = 0.039],降低了11%(95%CI:6- 17,p = 0.0001)。氯沙坦治疗可使CC组的白蛋白尿减少5%(95%CI:-13-22,p = 0.47)。在所有基因型组中,肾小球滤过率均保持不变。仅在AC基因型中,过滤分数与基线相比显着降低了0.018±0.024(p = 0.012)。在AA基因型中,FF与基线相比降低了0.017±0.03(p = 0.052),在CC基因型中,与基线相比降低了0.01±0.008(p = 0.092)。在AA组中,收缩压从基线时的136±24 mmHg下降到研究结束时的平均121±18 mmHg(p = 0.001)。 AC组在研究期间从基线的131±10 mmHg降至115±7 mmHg(p = 0.001)。在AA基因型组中,氯沙坦将舒张压从基线时的86±13 mmHg降低到78±8 mmHg(p = 0.004),而AC基因型在研究期间从基线时的88±5 mmHg降低到11.7±5.6 mmHg( p = 0.001)。在CC基因型中,舒张压下降幅度不显着(p = 0.066)。结论。我们小样本研究的结果提供了证据,表明1166 A / C AT1R基因多态性可能与对氯沙坦治疗的肾保护反应有关。

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