ω-3 fatty acids as an adjuvant therapy ameliorates methotrexate-induced hepatotoxicity in children and adolescents with acute lymphoblastic leukemia: A randomized placebo-controlled study

被引:46
作者
Elbarbary, Nancy Samir [1 ]
Ismail, Eman Abdel Rahman [2 ]
Farahat, Reham Kamel [3 ]
El-Hamamsy, Manal [3 ]
机构
[1] Ain Shams Univ, Fac Med, Dept Pediat, Cairo, Egypt
[2] Ain Shams Univ, Fac Med, Dept Clin Pathol, Cairo, Egypt
[3] Ain Shams Univ, Fac Pharm, Dept Clin Pharm, Cairo, Egypt
关键词
Acute lymphoblastic leukemia; Methotrexate; omega-3 fatty acids; Oxidative stress; Hepatotoxicity; FISH-OIL SUPPLEMENTATION; INDUCED LIVER-INJURY; OXIDATIVE STRESS; FATTY-ACIDS; CANCER-CHEMOTHERAPY; ANTIOXIDANT STATUS; COMBINATION; INFECTION; DISEASE; OMEGA-3;
D O I
10.1016/j.nut.2015.06.010
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objectives: Methotrexate (MTX)-induced hepatotoxicity is a significant clinical problem that may affect overall prognosis and disease outcome. Oxidative stress is a key player in its pathogenesis. The aim of this study was to investigate the role of omega-3 fatty acids as an adjuvant therapy in children and adolescents with acute lymphoblastic leukemia (ALL) during the maintenance phase of chemotherapy and the effect of omega-3 on MTX-induced hepatotoxicity. Methods: This randomized, double-blind, placebo-controlled trial included 70 patients with ALL who were in the maintenance phase. The participants were divided into two groups: group A received oral MTX and omega-3 fatty acids (1000 mg/d) and group B (received MTX and placebo). Both groups were followed-up for 6 mo with assessment of liver enzymes, total antioxidant capacity (TAC), uric acid, malondialdhyde, superoxide dismutase (SOD), and glutathione peroxidase. The trial was registered at ClinicalTrials.gov (NCT02373579). Results: Baseline clinical and laboratory parameters were consistent between the two groups (P > 0.05). After 6 mo, liver enzymes and malondialdhyde increased, whereas TAC, uric acid, SOD, and glutathione peroxidase decreased in group B (MTX and placebo) compared with baseline levels or with group A ALL patients receiving omega-3 fatty acids (P < 0.001). The addition of omega-3 to MTX maintained normal liver function and oxidant antioxidant levels among group A patients at the end of treatment compared with pretherapy levels (P > 0.05). No adverse reactions due to omega-3 supplementation were reported. ALT was inversely correlated to TAC and SOD in the MTX group. Conclusions: The study determined that omega-3 fatty acids ameliorated MTX-induced hepatotoxicity and could be safely used during the maintenance phase of ALL (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:41 / 47
页数:7
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