School of Medicine, University of North Carolina, Chapel Hill, NC, USA.
Division of Infectious Diseases, University of North Carolina, Chapel Hill, NC, USA.
Br J Haematol. 2019 Jan;184(2):246-252. doi: 10.1111/bjh.15651. Epub 2018 Nov 21.
Although renin-angiotensin-aldosterone system (RAAS) blocking agents decrease albuminuria in short-term studies, there is no evidence confirming their long-term efficacy in sickle cell disease (SCD). In a single-centre, retrospective study, we evaluated the long-term effect of RAAS blocking agents on proteinuria and declining estimated glomerular filtration rates (eGFR). Eighty-six patients on RAAS blocking agents for proteinuria, followed for a median of 2·28 years, were compared with 68 patients with proteinuria followed for 2·24 years who were not receiving such treatment. The log odds of proteinuria decreased over time in patients on RAAS blocking agents (β: -0·23, P = 0·03) and in the non-treatment group (β: -0·54, P < 0·0001), but was not statistically different between both groups (β: 0·31, P = 0·063). The eGFR declined over time in patients on RAAS blocking agents (β: -2·78, P < 0·0001) and in those not on such treatment (β: -4·7, P < 0·0001), and was statistically different between both groups (β: 1·9, P = 0·0002). Baseline eGFR was associated with mortality (Hazard rato: 0·97, P < 0·0001), but RAAS blocking agents had no significant effect on mortality. These data suggest that RAAS blockade may slow the loss of kidney function in SCD.
虽然肾素-血管紧张素-醛固酮系统(RAAS)阻滞剂可在短期研究中降低蛋白尿,但没有证据证实其在镰状细胞病(SCD)中的长期疗效。在一项单中心回顾性研究中,我们评估了 RAAS 阻滞剂对蛋白尿和估算肾小球滤过率(eGFR)下降的长期影响。86 例接受 RAAS 阻滞剂治疗蛋白尿的患者中位随访时间为 2.28 年,与 68 例接受相同治疗但未接受 RAAS 阻滞剂治疗的蛋白尿患者中位随访时间为 2.24 年进行比较。RAAS 阻滞剂组患者的蛋白尿对数优势随时间推移而降低(β:-0.23,P=0.03),而非治疗组患者(β:-0.54,P<0.0001)也是如此,但两组之间无统计学差异(β:0.31,P=0.063)。RAAS 阻滞剂组患者的 eGFR 随时间推移而下降(β:-2.78,P<0.0001),而非治疗组患者(β:-4.7,P<0.0001)也是如此,且两组之间有统计学差异(β:1.9,P=0.0002)。基线 eGFR 与死亡率相关(风险比:0.97,P<0.0001),但 RAAS 阻滞剂对死亡率无显著影响。这些数据表明,RAAS 阻断可能减缓 SCD 患者肾功能的丧失。