Garrison Scott R, Korownyk Christina S, Kolber Michael R, Allan G Michael, Musini Vijaya M, Sekhon Ravneet K, Dugré Nicolas
Department of Family Medicine, University of Alberta, Edmonton, Canada.
Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, Canada.
Cochrane Database Syst Rev. 2020 Sep 21;9(9):CD009402. doi: 10.1002/14651858.CD009402.pub3.
Skeletal muscle cramps are common and often occur in association with pregnancy, advanced age, exercise or motor neuron disorders (such as amyotrophic lateral sclerosis). Typically, such cramps have no obvious underlying pathology, and so are termed idiopathic. Magnesium supplements are marketed for the prophylaxis of cramps but the efficacy of magnesium for this purpose remains unclear. This is an update of a Cochrane Review first published in 2012, and performed to identify and incorporate more recent studies.
To assess the effects of magnesium supplementation compared to no treatment, placebo control or other cramp therapies in people with skeletal muscle cramps. SEARCH METHODS: On 9 September 2019, we searched the Cochrane Neuromuscular Specialised Register, CENTRAL, MEDLINE, Embase, LILACS, CINAHL Plus, AMED, and SPORTDiscus. We also searched WHO-ICTRP and ClinicalTrials.gov for registered trials that might be ongoing or unpublished, and ISI Web of Science for studies citing the studies included in this review.
Randomized controlled trials (RCTs) of magnesium supplementation (in any form) to prevent skeletal muscle cramps in any patient group (i.e. all clinical presentations of cramp). We considered comparisons of magnesium with no treatment, placebo control, or other therapy.
Two review authors independently selected trials for inclusion and extracted data. Two review authors assessed risk of bias. We attempted to contact all study authors when questions arose and obtained participant-level data for four of the included trials, one of which was unpublished. We collected all data on adverse effects from the included RCTs.
We identified 11 trials (nine parallel-group, two cross-over) enrolling a total of 735 individuals, amongst whom 118 cross-over participants additionally served as their own controls. Five trials enrolled women with pregnancy-associated leg cramps (408 participants) and five trials enrolled people with idiopathic cramps (271 participants, with 118 additionally crossed over to control). Another study enrolled 29 people with liver cirrhosis, only some of whom suffered muscle cramps. All trials provided magnesium as an oral supplement, except for one trial which provided magnesium as a series of slow intravenous infusions. Nine trials compared magnesium to placebo, one trial compared magnesium to no treatment, calcium carbonate or vitamin B, and another trial compared magnesium to vitamin E or calcium. We judged the single trial in people with liver cirrhosis and all five trials in participants with pregnancy-associated leg cramps to be at high risk of bias. In contrast, we rated the risk of bias high in only one of five trials in participants with idiopathic rest cramps. For idiopathic cramps, largely in older adults (mean age 61.6 to 69.3 years) presumed to have nocturnal leg cramps (the commonest presentation), differences in measures of cramp frequency when comparing magnesium to placebo were small, not statistically significant, and showed minimal heterogeneity (I² = 0% to 12%). This includes the primary endpoint, percentage change from baseline in the number of cramps per week at four weeks (mean difference (MD) -9.59%, 95% confidence interval (CI) -23.14% to 3.97%; 3 studies, 177 participants; moderate-certainty evidence); and the difference in the number of cramps per week at four weeks (MD -0.18 cramps/week, 95% CI -0.84 to 0.49; 5 studies, 307 participants; moderate-certainty evidence). The percentage of individuals experiencing a 25% or better reduction in cramp rate from baseline was also no different (RR 1.04, 95% CI 0.84 to 1.29; 3 studies, 177 participants; high-certainty evidence). Similarly, no statistically significant difference was found at four weeks in measures of cramp intensity or cramp duration. This includes the number of participants rating their cramps as moderate or severe at four weeks (RR 1.33, 95% CI 0.81 to 2.21; 2 studies, 91 participants; moderate-certainty evidence); and the percentage of participants with the majority of cramp durations of one minute or more at four weeks (RR 1.83, 95% CI 0.74 to 4.53, 1 study, 46 participants; low-certainty evidence). We were unable to perform meta-analysis for trials of pregnancy-associated leg cramps. The single study comparing magnesium to no treatment failed to find statistically significant benefit on a three-point ordinal scale of overall treatment efficacy. Of the three trials comparing magnesium to placebo, one found no benefit on frequency or intensity measures, another found benefit for both, and a third reported inconsistent results for frequency that could not be reconciled. The single study in people with liver cirrhosis was small and had limited reporting of cramps, but found no difference in terms of cramp frequency or cramp intensity. Our analysis of adverse events pooled all studies, regardless of the setting in which cramps occurred. Major adverse events (occurring in 2 out of 72 magnesium recipients and 3 out of 68 placebo recipients), and withdrawals due to adverse events, were not significantly different from placebo. However, in the four studies for which it could be determined, more participants experienced minor adverse events in the magnesium group than in the placebo group (RR 1.51, 95% CI 0.98 to 2.33; 4 studies, 254 participants; low-certainty evidence). Overall, oral magnesium was associated with mostly gastrointestinal adverse events (e.g. diarrhoea), experienced by 11% (10% in control) to 37% (14% in control) of participants.
AUTHORS' CONCLUSIONS: It is unlikely that magnesium supplementation provides clinically meaningful cramp prophylaxis to older adults experiencing skeletal muscle cramps. In contrast, for those experiencing pregnancy-associated rest cramps the literature is conflicting and further research in this population is needed. We found no RCTs evaluating magnesium for exercise-associated muscle cramps or disease-state-associated muscle cramps (for example amyotrophic lateral sclerosis/motor neuron disease) other than a single small (inconclusive) study in people with liver cirrhosis, only some of whom suffered cramps.
骨骼肌痉挛很常见,常与怀孕、高龄、运动或运动神经元疾病(如肌萎缩侧索硬化症)相关。通常,此类痉挛没有明显的潜在病理状况,因此被称为特发性。镁补充剂被用于预防痉挛,但镁在此方面的疗效仍不明确。这是对2012年首次发表的Cochrane系统评价的更新,旨在识别并纳入更新的研究。
评估补充镁与不治疗、安慰剂对照或其他痉挛疗法相比,对骨骼肌痉挛患者的影响。
2019年9月9日,我们检索了Cochrane神经肌肉专业注册库、Cochrane系统评价数据库、医学期刊数据库、荷兰医学文摘数据库、拉丁美洲及加勒比地区卫生科学数据库、护理学与健康领域数据库、联合和补充医学数据库以及体育与运动科学数据库。我们还检索了世界卫生组织国际临床试验注册平台和美国国立医学图书馆临床试验数据库,以查找可能正在进行或未发表的注册试验,并检索科学引文索引数据库,以查找引用本综述中纳入研究的文献。
对任何患者群体(即所有痉挛临床表现)补充镁(任何形式)以预防骨骼肌痉挛的随机对照试验。我们考虑了镁与不治疗、安慰剂对照或其他疗法的比较。
两位综述作者独立选择纳入试验并提取数据。两位综述作者评估偏倚风险。出现问题时,我们试图联系所有研究作者,并获取了纳入试验中的四项试验的参与者水平数据,其中一项试验未发表。我们从纳入的随机对照试验中收集了所有不良反应数据。
我们识别出11项试验(9项平行组试验、2项交叉试验),共纳入735名个体,其中118名交叉试验参与者还作为自身对照。5项试验纳入了患有与妊娠相关腿部痉挛的女性(408名参与者),5项试验纳入了患有特发性痉挛的患者(271名参与者,其中118名还交叉作为对照)。另一项研究纳入了29名肝硬化患者,其中只有部分患者出现肌肉痉挛。除一项试验通过一系列缓慢静脉输注提供镁外,所有试验均提供口服镁补充剂。9项试验将镁与安慰剂进行比较,一项试验将镁与不治疗、碳酸钙或维生素B进行比较,另一项试验将镁与维生素E或钙进行比较。我们判定肝硬化患者的单项试验以及妊娠相关腿部痉挛参与者的所有5项试验存在高偏倚风险。相比之下,特发性静息痉挛参与者的5项试验中只有1项被评为高偏倚风险。对于特发性痉挛,主要是年龄较大的成年人(平均年龄61.6至69.3岁),推测患有夜间腿部痉挛(最常见的表现),比较镁与安慰剂时,痉挛频率测量指标的差异较小,无统计学意义,且异质性最小(I² = 0%至12%)。这包括主要终点,即四周时每周痉挛次数相对于基线的百分比变化(平均差(MD)-9.59%,95%置信区间(CI)-23.14%至3.97%;3项研究,177名参与者;中等确定性证据);以及四周时每周痉挛次数的差异(MD -0.18次痉挛/周,95% CI -0.84至0.49;5项研究,307名参与者;中等确定性证据)。痉挛率从基线降低25%或更多的个体百分比也无差异(风险比(RR)1.