Alizadeh Hadadhania Marzie, Ghaffari Kazem, Absalan Abdorrahim, Eghbali Aygin, Rahimi Afzal Roghayeh, Ghasemi Ali, Eghbali Aziz
Department of Pediatrics, Amir Kabir Hospital, Arak University of Medical Sciences, Arak, Iran.
Department of Basic and Laboratory Sciences, Khomein University of Medical Sciences, Khomein, Iran.
Adv Biomed Res. 2023 Jan 27;12:11. doi: 10.4103/abr.abr_292_21. eCollection 2023.
Magnesium oxide may be effective in renal insufficiency prevention after carboplatin therapy. We have evaluated magnesium oxide impression on the serum creatinine (Cr) and blood urea nitrogen (BUN) levels plus glomerular filtration rate (GFR) in cancerous children.
A group of children with different cancers ( = 18) was treated with 250 mg/day magnesium oxide supplementation (MOS) and compared with a matched placebo-treated group ( = 18). After 2 weeks, carboplatin chemotherapy started. We compared serum Cr, BUN, and GFR values before and 3 and 7 days post intervention.
Serum Cr and BUN were increased significantly 3 and 7 days after intervention in both the groups. Serum Cr and BUN were not statistically different between the MOS and placebo groups before the intervention and 3 or 7 days after carboplatin administration ( > 0.05). Three days after the intervention, the GFR reduced from 101.38 ± 14.67 to 90.11 ± 10.52 mL/min/1.73 m in the MOS group. Furthermore, in the placebo group, 3 days after the intervention, the GFR was reduced from 97.5 ± 9.71 to 92.33 ± 10.61 mL/min/1.73 m. Further, in the MOS group, after 7 days of the intervention, the GFR was reduced to 84.11 ± 12.47 mL/min/1.73 m. In the placebo group, after 7 days of the intervention, the GFR was diminished to 85.38 ± 10.66 mL/min/1.73 m ( = 0.371).
The current study suggests that magnesium supplementation does not prevent carboplatin-induced nephrotoxicity in children with malignancies. Anyway, we propose magnesium oxide supplementation for this group of pediatrics because magnesium is an essential element for cell and tissue growth, maintenance, and metabolism.
氧化镁可能对预防卡铂治疗后的肾功能不全有效。我们评估了氧化镁对癌症患儿血清肌酐(Cr)、血尿素氮(BUN)水平及肾小球滤过率(GFR)的影响。
一组患有不同癌症的儿童(n = 18)接受每日250毫克氧化镁补充剂(MOS)治疗,并与匹配的接受安慰剂治疗的组(n = 18)进行比较。2周后开始卡铂化疗。我们比较了干预前以及干预后3天和7天的血清Cr、BUN和GFR值。
两组在干预后3天和7天血清Cr和BUN均显著升高。在干预前以及卡铂给药后3天或7天,MOS组和安慰剂组之间的血清Cr和BUN无统计学差异(P > 0.05)。干预后3天,MOS组的GFR从101.38 ± 14.67降至90.11 ± 10.52毫升/分钟/1.73平方米。此外,在安慰剂组中,干预后3天,GFR从97.5 ± 9.71降至92.33 ± 十.61毫升/分钟/1.73平方米。此外,在MOS组中,干预7天后,GFR降至84.11 ± 12.47毫升/分钟/1.73平方米。在安慰剂组中,干预7天后,GFR降至85.38 ± 10.66毫升/分钟/1.73平方米(P = 0.371)。
当前研究表明,补充镁不能预防恶性肿瘤患儿卡铂诱导的肾毒性。无论如何,我们建议为这组儿科患者补充氧化镁,因为镁是细胞和组织生长、维持及代谢所必需的元素。