Bell D R, Woods R L, Levi J A
Eur J Cancer Clin Oncol. 1985 Mar;21(3):287-90. doi: 10.1016/0277-5379(85)90127-0.
Hypomagnesemia is a well-recognised complication of cis-diamminedichloroplatinum (DDP) treatment. We prospectively evaluated 50 patients with advanced malignant disease receiving DDP for the development of hypomagnesemia. Urinary magnesium excretion was measured in 24 patients. The mean serum magnesium fell from 0.79 mmol/l (normal 0.7-1.1 mmol/l) prior to therapy to 0.55 mmol/l 3 months after commencing DDP. All 50 patients had become hypomagnesemic by this time and 10% were symptomatic, requiring oral magnesium supplementation. At 6 weeks after commencing DDP only four patients had restricted urinary magnesium excretion to less than 1.0 mmol/day. The other patients clearly had inappropriately high levels of urinary magnesium excretion, suggesting that DDP may induce a renal tubular defect in magnesium conservation. Hypomagnesemia is a common complication of DDP therapy which in many patients is asymptomatic. Further, more detailed studies of renal magnesium handling are necessary to determine fully the effect of DDP on urinary magnesium excretion.
低镁血症是顺二氯二氨铂(DDP)治疗中一种公认的并发症。我们前瞻性地评估了50例接受DDP治疗的晚期恶性疾病患者低镁血症的发生情况。对其中24例患者测量了尿镁排泄量。血清镁均值从治疗前的0.79 mmol/L(正常范围0.7 - 1.1 mmol/L)降至开始使用DDP 3个月后的0.55 mmol/L。此时所有50例患者均出现低镁血症,10%有症状,需要口服补充镁剂。开始使用DDP 6周时,只有4例患者尿镁排泄量限制在每天1.0 mmol以下。其他患者明显存在尿镁排泄量过高的情况,提示DDP可能导致肾小管对镁的重吸收出现缺陷。低镁血症是DDP治疗的常见并发症,在许多患者中无症状。此外,需要进行更详细的肾脏镁代谢研究,以全面确定DDP对尿镁排泄的影响。