Nand N, Mittal Atul
Senior Professor and Head of Department, Pt. B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana;*Corresponding Author.
Resident, Department of Medicine, Pt. B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana.
J Assoc Physicians India. 2018 Dec;66(12):29-32.
Thirty adult patients of end stage renal disease with erythropoietin hyporesponsiveness undergoing maintenance hemodialysis were included in the study. Patients were divided randomly into two groups of 15 patients each. Group A were given atorvastatin in a dose of 20 mg once daily for a period of 4 months along with erythropoietin 6000 IU S/C and IV iron 100mg twice weekly after each hemodialysis. Group B was given erythropoietin 6000 IU S/C and IV iron 100 mg twice weekly after each hemodialysis without addition of atorvastatin for 4 months. Hematological, renal parameters, inflammatory parameters such as erythrocyte sedimentation rate, highly sensitive C reactive protein, serum ferritin and erythropoietin resistance index were done at baseline and then two monthly intervals for 4 months.
At the end of study, in group A hemoglobin and haematocrit significantly increased (p <0.001 for both) while HsCRP, ESR and erythropoietin resistance index decreased significantly (p=0.001, 0.001 and <0.001 respectively). In group B, the increase in hemoglobin and haematocrit were not statistically significant (p >0.05) similarly fall in HsCRP and ERI were also not significant statistically (p >0.05). The mean rise in hemoglobin between subsequent months was higher in group A as compared to group B which was statically significant.
Statin can be used as an adjuvant to erythropoietin in management of anemia in patients of chronic kidney disease, who show hyporesponsiveness to increased doses of erythropoietin, by its anti-inflammatory properties.
本研究纳入了30例接受维持性血液透析且对促红细胞生成素反应低下的终末期肾病成年患者。患者被随机分为两组,每组15例。A组患者每天服用一次20mg阿托伐他汀,持续4个月,同时皮下注射促红细胞生成素6000IU,并在每次血液透析后每周两次静脉注射100mg铁剂。B组患者在每次血液透析后每周两次皮下注射促红细胞生成素6000IU和静脉注射100mg铁剂,不添加阿托伐他汀,持续4个月。在基线时以及之后的4个月内,每两个月检测一次血液学、肾脏参数、炎症参数,如红细胞沉降率、高敏C反应蛋白、血清铁蛋白和促红细胞生成素抵抗指数。
研究结束时,A组的血红蛋白和血细胞比容显著升高(两者p均<0.001),而高敏C反应蛋白、红细胞沉降率和促红细胞生成素抵抗指数显著降低(分别为p=0.001、0.001和<0.001)。B组中,血红蛋白和血细胞比容的升高无统计学意义(p>0.05),同样,高敏C反应蛋白和促红细胞生成素抵抗指数的下降也无统计学意义(p>0.05)。与B组相比,A组随后几个月血红蛋白的平均升高更高,具有统计学意义。
他汀类药物可通过其抗炎特性,作为促红细胞生成素的辅助药物,用于治疗对增加剂量促红细胞生成素反应低下的慢性肾病患者的贫血。