Osman Hamed M, Khamis Osama A, Elfeky Mohamed S, El Amin Ali Amani M, Abdelwahed Mostafa Y
Medical Physiology, Faculty of Medicine, AL-Azhar University, Cairo, Egypt.
Internal Medicine, Faculty of Medicine, AL-Azhar University, Cairo, Egypt.
Indian J Endocrinol Metab. 2017 Sep-Oct;21(5):724-730. doi: 10.4103/ijem.IJEM_462_16.
Insulin resistance (IR) is a known complication of end-stage kidney disease (ESKD). It may be an important therapeutic target in stages of chronic kidney disease.
The study was conducted to evaluate the effect of short-term treatment with recombinant human erythropoietin (rHuEpo) therapy on IR, serum leptin, and neuropeptide Y in ESKD patients on hemodialysis.
Thirty ESKD patients were enrolled in the study and were randomly assigned into two groups. Erythropoietin (rHuEpo) group consisted of 15 patients (7 females, 8 males, mean age 47.8 ± 9.3 years) treated with rHuEpo therapy after each session of dialysis. No-rHuEpo group consisted of 15 patients (7 females, 8 males, mean age 45.5 ± 8.6 years) not treated with rHuEpo. In addition to, control group consisted of 15 healthy controls (6 females, 9 males, mean age 48.8 ± 11 years).
The mean fasting insulin (11 ± 4.2 mU/L) and homeostatic model assessment of IR (HOMA-IR) test (2.6 ± 1.1) were significantly higher in ESKD patients than control group (6.6 ± 1.4 mU/L and 1.5 ± 0.3, respectively). There were significant decreases in glycated hemoglobin (HbA1c) (5.6 ± 1%), fasting insulin level (9.3 ± 3.1 μU/mL), HOMA-IR (2.2 ± 0.7), and serum leptin levels (17.4 ± 8.7 ng/mL) also significant increase in neuropeptide Y levels (113 ± 9.9 pg/mL) after 3 months of rHuEpo therapy, in addition to further significantly decrease fasting insulin levels (7.1 ± 2.1 μU/mL) and HOMA-IR (1.7 ± 6) after 6 months in rHuEpo group. In contrast, there were significantly increases in HbA1c% (5.9 ± 0.5%) and leptin levels (42.3 ± 25.3 ng/mL) in No-rHuEpo group throughout the study.
IR and hyperleptinemia are improved by recombinant human erythropoietin therapy.
胰岛素抵抗(IR)是终末期肾病(ESKD)的一种已知并发症。它可能是慢性肾病阶段的一个重要治疗靶点。
本研究旨在评估重组人促红细胞生成素(rHuEpo)短期治疗对接受血液透析的ESKD患者的胰岛素抵抗、血清瘦素和神经肽Y的影响。
30例ESKD患者纳入本研究,并随机分为两组。促红细胞生成素(rHuEpo)组由15例患者组成(7例女性,8例男性,平均年龄47.8±9.3岁),每次透析后接受rHuEpo治疗。非rHuEpo组由15例患者组成(7例女性,8例男性,平均年龄45.5±8.6岁),未接受rHuEpo治疗。此外,对照组由15名健康对照者组成(6例女性,9例男性,平均年龄48.8±11岁)。
ESKD患者的平均空腹胰岛素水平(11±4.2 mU/L)和胰岛素抵抗稳态模型评估(HOMA-IR)测试值(2.6±1.1)显著高于对照组(分别为6.6±1.4 mU/L和1.5±0.3)。rHuEpo治疗3个月后,糖化血红蛋白(HbA1c)(5.6±1%)、空腹胰岛素水平(9.3±3.1 μU/mL)、HOMA-IR(2.2±0.7)和血清瘦素水平(17.4±8.7 ng/mL)均显著下降,神经肽Y水平(113±9.9 pg/mL)也显著升高,此外,rHuEpo组6个月后空腹胰岛素水平(7.1±2.1 μU/mL)和HOMA-IR(1.7±6)进一步显著下降。相比之下,在整个研究过程中,非rHuEpo组的HbA1c%(5.9±0.5%)和瘦素水平(42.3±25.3 ng/mL)显著升高。
重组人促红细胞生成素治疗可改善胰岛素抵抗和高瘦素血症。