Wang Angela Yee Moon, Yu Alex Wai Yin, Lam Christopher Wai Kei, Yu Ly Mee, Li Philip Kam Tao, Goh Juliana, Lui Siu Fai
Department of Medicine, Center of Clinical Trials and Epidemiological Research, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, NT, Hong Kong.
Am J Kidney Dis. 2002 Mar;39(3):600-8. doi: 10.1053/ajkd.2002.31404.
Both angiotensin-converting enzyme inhibitors and angiotensin II receptor antagonists reduce hemoglobin (Hb) levels in patients with posttransplantation erythrocytosis (PTE). However, their effects in transplant recipients without PTE are not certain, and the mechanism by which they reduce Hb levels in patients with PTE remains unclear. This study evaluated the effects of losartan and enalapril on Hb levels in relation to serum erythropoietin (EPO) and insulin-like growth factor-1 (IGF-1) levels in 8 patients with PTE and 10 patients without PTE. All 18 patients were treated sequentially with 24 weeks of losartan therapy, followed by 24 weeks of enalapril therapy; the two treatment phases were separated by a washout period. Patients with PTE showed significantly greater baseline Hb and IGF-1 concentrations compared with patients without PTE before both losartan and enalapril treatments. Baseline serum EPO levels were similar for patients with and without PTE. Baseline Hb level correlated significantly with IGF-1 level (r = 0.517; P = 0.002), but not with EPO level. Treatment with enalapril, 5 mg, reduced Hb levels more markedly than treatment with losartan, 50 mg, in patients with PTE. In patients without PTE, enalapril, 5 mg, mildly reduced Hb levels, whereas losartan, 50 mg, had no significant Hb-lowering effect. The reduction in Hb levels with enalapril therapy in patients with PTE was associated with a significant reduction in circulating IGF-1 levels, but not EPO levels, whereas losartan reduced Hb levels with no significant change in circulating IGF-1 and EPO levels. In patients without PTE, no significant change was noted in serum EPO and IGF-1 levels with either treatment. The differential Hb-lowering effect with losartan and enalapril treatment in patients with and without PTE suggests that the pathogenesis for PTE is complex and heterogeneous. Different erythropoietic mechanisms may be involved in patients with and without PTE. Further large-scale study is needed to determine the exact interaction between the renin-angiotensin system and regulation of IGF-1 and EPO synthesis and define the exact mechanism by which losartan and enalapril reduce Hb levels.
血管紧张素转换酶抑制剂和血管紧张素II受体拮抗剂均可降低移植后红细胞增多症(PTE)患者的血红蛋白(Hb)水平。然而,它们对无PTE的移植受者的影响尚不确定,且它们降低PTE患者Hb水平的机制仍不清楚。本研究评估了氯沙坦和依那普利对8例PTE患者和10例无PTE患者的Hb水平以及血清促红细胞生成素(EPO)和胰岛素样生长因子-1(IGF-1)水平的影响。所有18例患者依次接受24周的氯沙坦治疗,随后接受24周的依那普利治疗;两个治疗阶段之间有洗脱期。在氯沙坦和依那普利治疗前,PTE患者的基线Hb和IGF-1浓度显著高于无PTE的患者。有PTE和无PTE患者的基线血清EPO水平相似。基线Hb水平与IGF-1水平显著相关(r = 0.517;P = 0.002),但与EPO水平无关。在PTE患者中,5mg依那普利治疗比50mg氯沙坦治疗更显著地降低Hb水平。在无PTE的患者中,5mg依那普利轻度降低Hb水平,而50mg氯沙坦对Hb水平无显著降低作用。依那普利治疗PTE患者时Hb水平的降低与循环IGF-1水平的显著降低相关,但与EPO水平无关,而氯沙坦降低Hb水平时循环IGF-1和EPO水平无显著变化。在无PTE的患者中,两种治疗均未使血清EPO和IGF-1水平发生显著变化。氯沙坦和依那普利治疗对有PTE和无PTE患者的Hb降低作用不同,提示PTE的发病机制复杂且异质性。有PTE和无PTE的患者可能涉及不同的红细胞生成机制。需要进一步的大规模研究来确定肾素-血管紧张素系统与IGF-1和EPO合成调节之间的确切相互作用,并确定氯沙坦和依那普利降低Hb水平的确切机制。