Department of Neurology and Neurosurgery, Rudolf Magnus Institute of Neuroscience, University Medical Centre Utrecht, Utrecht, The Netherlands.
Julius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht, Utrecht, The Netherlands.
Int J Stroke. 2015 Oct;10 Suppl A100:108-12. doi: 10.1111/ijs.12621.
Magnesium treatment did not improve outcome in patients with aneurysmal subarachnoid haemorrhage in the Magnesium in Aneurysmal Subarachnoid Haemorrhage II trial. We hypothesized that high glucose levels may have offset a potential beneficial effect to prevent delayed cerebral ischemia. We investigated if magnesium treatment led to less delayed cerebral ischemia and if glucose levels interacted with magnesium treatment in the Magnesium in Aneurysmal Subarachnoid Haemorrhage II trial.
To investigate the effect of magnesium treatment on occurrence of delayed cerebral ischemia and the interaction between glucose levels and magnesium treatment in subarachnoid hemorrhage patients.
The Magnesium in Aneurysmal Subarachnoid Haemorrhage was a phase III randomized placebo-controlled trial assessing the effect of magnesium sulphate on clinical outcome in aneurysmal subarachnoid hemorrhage patients. For the current study, we included only the patients admitted to the University Medical Centre-Utrecht. We calculated hazard ratios for occurrence of delayed cerebral ischemia in patients treated with magnesium vs. placebo for the entire study population, and separately in the subgroups of patients with high and low mean fasting and mean daily glucose levels until onset of delayed cerebral ischemia. We used the cross-product of magnesium and glucose in the regression analysis to evaluate whether an interaction between magnesium and glucose existed.
We included 616 patients: 307 received magnesium and 309 placebo; 156 patients had delayed cerebral ischemia. Hazard ratio for magnesium on occurrence of delayed cerebral ischemia was 1·0 (95% confidence interval: 0·7-1·4). Results were similar in patients with low or high fasting or daily glucose levels. We found no interactions between magnesium treatment and high fasting (P = 0·54) and daily glucose (P = 0·60).
Magnesium treatment did not reduce the risk of delayed cerebral ischemia in patients with aneurysmal subarachnoid hemorrhage, nor was there an interaction with glucose levels. It is therefore unlikely that glucose levels explain the failure of magnesium to prevent delayed cerebral ischemia and poor outcome after aneurysmal subarachnoid hemorrhage.
在“Magnesium in Aneurysmal Subarachnoid Haemorrhage II 试验”中,镁治疗并未改善蛛网膜下腔出血患者的预后。我们假设高血糖水平可能抵消了预防迟发性脑缺血的潜在有益作用。我们研究了镁治疗是否导致更少的迟发性脑缺血,以及血糖水平是否在“Magnesium in Aneurysmal Subarachnoid Haemorrhage II 试验”中与镁治疗相互作用。
研究镁治疗对蛛网膜下腔出血患者迟发性脑缺血发生的影响,以及血糖水平与镁治疗之间的相互作用。
“Magnesium in Aneurysmal Subarachnoid Haemorrhage”是一项评估硫酸镁对蛛网膜下腔出血患者临床结局影响的 III 期随机安慰剂对照试验。为了进行当前的研究,我们仅纳入了乌得勒支大学医学中心收治的患者。我们计算了接受镁治疗与安慰剂治疗的患者发生迟发性脑缺血的风险比,包括整个研究人群以及高血糖和低血糖患者的亚组。我们在回归分析中使用镁和血糖的乘积来评估镁和血糖之间是否存在相互作用。
我们纳入了 616 名患者:307 名接受镁治疗,309 名接受安慰剂治疗;156 名患者发生迟发性脑缺血。镁治疗发生迟发性脑缺血的风险比为 1.0(95%置信区间:0.7-1.4)。血糖水平低或高的患者结果相似。我们未发现镁治疗与高血糖的空腹(P=0.54)和日常血糖(P=0.60)之间存在相互作用。
镁治疗并未降低蛛网膜下腔出血患者迟发性脑缺血的风险,也与血糖水平无相互作用。因此,血糖水平不太可能解释镁未能预防迟发性脑缺血以及蛛网膜下腔出血后的不良预后。