Kokot F, Wiecek A, Mesjasz J, Adamczak M, Spiechowicz U
Department of Nephrology, Endocrinology and Metabolic Diseases, Silesian University School of Medicine, Katowice, Poland.
Nephrol Dial Transplant. 1998 May;13(5):1200-5. doi: 10.1093/ndt/13.5.1200.
In patients with chronic renal failure, rHuEpo therapy ameliorates anaemia and improves wellbeing, exercise tolerance, and appetite. Both leptin and neuropeptide Y play an important role in regulation of appetite and energy balance in humans.
The present study aimed to assess the influence of 12 months rHuEpo therapy on plasma leptin and neuropeptide Y concentrations in 15 haemodialysed patients (HDP) (6F, 9M; mean age 40.8+/-2.9 years; mean BMI 23.6+/-1.1 kg/m2; mean duration of HD 3.3+/-0.6 months) (Epo group). A second group (No-Epo group) consisted of 17 HDP (9F, 8M; mean age 44+/-3.2 years; mean BMI 24.3+/-1.0 kg/m2; mean duration of HD 2.5+/-0.4 months) not treated with rHuEpo for 12 months. Basal plasma leptin and neuropeptide Y concentrations were estimated by RIA at the beginning and after 3, 6, 9 and 12 months of rHuEpo therapy (Epo group) or clinical observation (No-Epo group). The control group consisted of 30 healthy subjects (15 females, 15 males, mean age=38.2+/-1.7 years, mean BMI 24.5+/-0.7 kg/m2).
Baseline plasma leptin concentrations in HDP were higher, although statistically not significant than leptinaemia in healthy subjects. After 3, 6, and 12 months of rHuEpo therapy plasma leptin concentrations were significantly lower than at the beginning of the study. Baseline plasma neuropeptide Y concentrations in HDP did not differ significantly from controls. After 3 and 6 months of the study period plasma neuropeptide Y concentrations increased significantly in patients of both the Epo and No-Epo group. This increase was, however, significantly higher in rHuEpo-treated than in untreated patients.
(1) rHuEpo treatment in haemodialysed patients with chronic renal failure is followed by a significant decline of leptinaemia and disappearance of the physiological positive BMI/leptinaemia relationship. (2) Suppression of leptinaemia induced by rHuEpo may be of clinical relevance in haemodialysed patients with chronic renal failure.
在慢性肾衰竭患者中,重组人促红细胞生成素(rHuEpo)治疗可改善贫血,并提高健康状况、运动耐力和食欲。瘦素和神经肽Y在人体食欲和能量平衡调节中均发挥重要作用。
本研究旨在评估12个月的rHuEpo治疗对15例血液透析患者(HDP)(6名女性,9名男性;平均年龄40.8±2.9岁;平均体重指数23.6±1.1kg/m²;平均血液透析时间3.3±0.6个月)(促红细胞生成素组)血浆瘦素和神经肽Y浓度的影响。第二组(无促红细胞生成素组)由17例未接受rHuEpo治疗12个月的血液透析患者组成(9名女性,8名男性;平均年龄44±3.2岁;平均体重指数24.3±1.0kg/m²;平均血液透析时间2.5±0.4个月)。在rHuEpo治疗(促红细胞生成素组)或临床观察(无促红细胞生成素组)开始时以及3、6、9和12个月后,通过放射免疫分析法测定基础血浆瘦素和神经肽Y浓度。对照组由30名健康受试者组成(15名女性,15名男性,平均年龄=38.2±1.7岁,平均体重指数24.5±0.7kg/m²)。
血液透析患者的基线血浆瘦素浓度虽高于健康受试者,但无统计学意义。rHuEpo治疗3、6和12个月后,血浆瘦素浓度显著低于研究开始时。血液透析患者的基线血浆神经肽Y浓度与对照组无显著差异。在研究期3和6个月后,促红细胞生成素组和无促红细胞生成素组患者的血浆神经肽Y浓度均显著升高。然而,接受rHuEpo治疗患者的升高幅度显著高于未治疗患者。
(1)慢性肾衰竭血液透析患者接受rHuEpo治疗后,瘦素血症显著下降,生理上的正体重指数/瘦素血症关系消失。(2)rHuEpo诱导的瘦素血症抑制在慢性肾衰竭血液透析患者中可能具有临床意义。