Melatonin corrects reticuloendothelial blockade and iron status in haemodialysed patients

被引:7
作者
Labonia, W [1 ]
Rubio, D [1 ]
Arias, C [1 ]
机构
[1] Hosp Santojanni, Serv Nefrol, Buenos Aires, DF, Argentina
关键词
haemodialysis; inflammation; iron; melatonin;
D O I
10.1111/j.1440-1797.2005.00488.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aim: Treatment of anaemia in haemodialysed patients in the setting of inflammation usually displays high levels of serum ferritin (> 800 ng/mL) and low transferrin saturation (TSAT) (< 20%) despite i.v. iron supplementation, thus proving iron trapping in the reticuloendothelial system. Melatonin has been reported to reduce cytokine production and, in dialysis patients, to prevent oxidative stress resulting from iron and erythropoietin treatment. Method: In this study, we evaluated a group of 10 patients undergoing haemodialysis who displayed elevated serum ferritin (981 +/- 44.6 ng/mL) and TSAT < 20% (15.6 +/- 3.8%) after having received 1.2 g of i.v. iron dextran over a period of 8 weeks. These patients received oral melatonin, 6 mg/day at night for 30 days. Results: After this treatment, all of them markedly increased TSAT values, reaching 35.5 +/- 6.7% (P < 0.0001 vs basal values). In addition, ferritin values decreased to 754.4 +/- 263.7 ng/mL (P < 0.05), and serum iron dramatically increased in all of the patients under study (42.4 +/- 9.4 vs 109.7 +/- 24.3 mu g/dL; P < 0.0001). Values for haematocrit (28.6 +/- 2.7 vs 31.9 +/- 3.57%; P < 0.05) and haemoglobin (9.19 +/- 0.97 vs 10.04 +/- 1.29 g/dL; P < 0.05) were also improved. Measurements were then repeated 2 weeks after melatonin withdrawal, showing an impressive decrease in TSAT (16.4 +/- 5.3%; P < 0.00001) and serum iron (48 +/- 14.7 mu g/dL; P < 0.0001) values and an almost significant increase in ferritin values (954.4 +/- 86 ng/mL; P < 0.054). Conclusion: The present study demonstrates that melatonin may strongly correct the reticuloendothelial blockade seen in dialysis patients under an inflammatory status, thus allowing a better management of iron derangements and renal anaemia.
引用
收藏
页码:583 / 587
页数:5
相关论文
共 35 条
  • [21] Lissoni Paolo, 1999, Neuro Endocrinol Lett, V20, P343
  • [22] Ma JZ, 1999, J AM SOC NEPHROL, V10, P610
  • [23] Erythropoietin resistance: the role of inflammation and pro-inflammatory cytokines
    Macdougall, IC
    Cooper, AC
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2002, 17 : 39 - 43
  • [24] INHIBITION OF HUMAN ERYTHROID COLONY-FORMING-UNITS BY INTERLEUKIN-1 IS MEDIATED BY GAMMA-INTERFERON
    MEANS, RT
    DESSYPRIS, EN
    KRANTZ, SB
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 150 (01) : 59 - 64
  • [25] MEANS RT, 1992, BLOOD, V80, P1639
  • [26] Role of different dialysis membranes in the release of interleukin-6-soluble receptor in uremic patients
    Memoli, B
    Postiglione, L
    Cianciaruso, B
    Bisesti, V
    Cimmaruta, C
    Marzano, L
    Minutolo, R
    Cuomo, V
    Guida, B
    Andreucci, M
    Rossi, G
    [J]. KIDNEY INTERNATIONAL, 2000, 58 (01) : 417 - 424
  • [27] ROGERS J, 1994, ADV EXP MED BIOL, V356, P127
  • [28] ROGERS J, 1991, BLOOD S, V1, pA367
  • [29] TRANSLATIONAL ENHANCEMENT OF H-FERRITIN MESSENGER-RNA BY INTERLEUKIN-1-BETA ACTS THROUGH 5' LEADER SEQUENCES DISTINCT FROM THE IRON-RESPONSIVE ELEMENT
    ROGERS, JT
    ANDRIOTAKIS, JL
    LACROIX, L
    DURMOWICZ, GP
    KASSCHAU, KD
    BRIDGES, KR
    [J]. NUCLEIC ACIDS RESEARCH, 1994, 22 (13) : 2678 - 2686
  • [30] ROSENLOF K, 1995, CLIN NEPHROL, V43, P249