Birks J
Hospital de Cantoblanco, Consejería de Sanidad, Carretera de Colmenar km 14.500, Madrid, Madrid, SPAIN, 28049.
Cochrane Database Syst Rev. 2001(1):CD000147. doi: 10.1002/14651858.CD000147.
Dementia is an age-related condition in which Alzheimer's disease (AD) and cerebrovascular disease account for the bulk of cases. The role played by calcium in regulating brain functions is well known - the calcium ion links membrane excitation to subsequent intracellular enzymatic response. Change in calcium homeostasis is one important effect of aging with repercussions on higher cortical functions. Nimodipine is an isopropyl calcium channel blocker which can easily cross the blood brain barrier. Its primary action is to reduce the number of open channels, thus restricting influx of calcium ions into the cell. The usefulness of nimodipine in patients with Alzheimer's disease and vascular dementia and unspecified dementia is still controversial with mixed results. In spite of the uncertainties about its efficacy in dementia, nimodipine is currently a frequently prescribed drug for cognitive impairment and dementia in several European countries. This review will be conducted in two phases; the current review is based on evidence from published data only. The second phase will be based on individual-patient data analysed centrally and added to this review in due course.
To determine the clinical efficacy of nimodipine for the symptoms of dementia, either unclassified or according to the major subtypes - Alzheimer's disease, vascular, or mixed Alzheimer's and vascular dementia.
The Cochrane Dementia Group Register of Clinical Trials was searched using the terms 'nimodipine' and 'isopropyl (2-methoxy-ethyl) 1,4-dihydro-2, 6-dimethyl-4-(3-nitrophenyl)-3, 5-pyridinedicarboxylate'.
All unconfounded, double-blind, randomised trials in which treatment with nimodipine was administered for more than a day and compared to placebo in patients with dementia, either unclassified or according to the major subtypes - Alzheimer's disease, vascular, or mixed Alzheimer's and vascular dementia.
Data were extracted independently by the reviewers and the odds ratio (95%CI) or the average difference (95%CI) were estimated. Both intention-to-treat and on-treatment results were extracted.
This review produced no clear results. Many of the data published were not capable of being sensibly pooled. The data were compatible with nimodipine producing improvement, no change or even harm for those with Alzheimer's disease, vascular dementia, or mixed Alzheimer's and vascular dementia. It was not possible to use many of the published results in a combined analysis. For measures of overall clinical improvement, the intention-to-treat analysis, based on one study only, failed to detect any difference between nimodipine and placebo (OR 0.53; 95%CI 0.25 - 1.13). An on-treatment analysis, based on one study only, produced a statistically significant difference in favour of nimodipine (SMD 4.4; 95%CI 3.9 - 5.0). For cognitive function, the effect of nimodipine was statistically significantly different from placebo for the Mini Mental State Examination score (0-30; high =good) (SMD 0.9; 95%CI 0.59 - 1.22) and there was a statistically significant effect in favour of treatment for the Wechsler Memory Scale (SMD 0.47; 95%CI 0.17 - 0.77). These analyses were based only on those who completed the study and not intention-to-treat analyses. There were no results presented in a form suitable for pooling for functional autonomy, behaviour, quality of life dependency (eg institutionalization), effect on carer, death, acceptability of treatment (as measured by withdrawal rate, safety (as measured by the incidence of adverse effects, including side effects, leading to withdrawal).
REVIEWER'S CONCLUSIONS: This review provides no convincing evidence that nimodipine is a useful treatment for the symptoms of dementia, either unclassified or according to the major subtypes - Alzheimer's disease, vascular, or mixed Alzheimer's and vascular dementia. However, as so few of the trials presented data in a format suitable for pooling, the results of this review may be modified when further data from all relevant trials are included. There is an urgent need for the independent evaluation of the data already existing in the trials but not accessible through published or grouped data. An independent meta-analysis of the individual patient data is required. Nimodipine cannot be currently recommended in patients with dementia. The results and conclusions of this update are unaltered by further searching as the additional studies do not add any further valid/eligible data.
痴呆是一种与年龄相关的病症,其中阿尔茨海默病(AD)和脑血管疾病占大多数病例。钙在调节脑功能中所起的作用是众所周知的——钙离子将膜兴奋与随后的细胞内酶反应联系起来。钙稳态的变化是衰老的一个重要影响,对高级皮质功能有影响。尼莫地平是一种异丙基钙通道阻滞剂,它可以很容易地穿过血脑屏障。其主要作用是减少开放通道的数量,从而限制钙离子流入细胞。尼莫地平在阿尔茨海默病、血管性痴呆和未明确类型痴呆患者中的有效性仍存在争议,结果不一。尽管其在痴呆治疗中的疗效存在不确定性,但尼莫地平目前在几个欧洲国家是治疗认知障碍和痴呆的常用处方药。本综述将分两个阶段进行;当前的综述仅基于已发表数据的证据。第二阶段将基于集中分析的个体患者数据,并在适当时候添加到本综述中。
确定尼莫地平对未分类痴呆或主要亚型(阿尔茨海默病、血管性痴呆或阿尔茨海默病与血管性痴呆混合型)痴呆症状的临床疗效。
使用术语“尼莫地平”和“异丙基(2 - 甲氧基乙基)1,4 - 二氢 - 2,6 - 二甲基 - 4 -(3 - 硝基苯基)- 3,5 - 吡啶二羧酸酯”检索Cochrane痴呆临床试验组注册库。
所有无混杂因素、双盲、随机试验,其中尼莫地平治疗持续超过一天,并与痴呆患者(未分类或主要亚型为阿尔茨海默病、血管性痴呆或阿尔茨海默病与血管性痴呆混合型)的安慰剂进行比较。
由评审人员独立提取数据,并估计比值比(95%置信区间)或平均差(95%置信区间)。提取意向性分析和实际治疗结果。
本综述未得出明确结果。许多已发表的数据无法合理合并。这些数据表明,尼莫地平对阿尔茨海默病、血管性痴呆或阿尔茨海默病与血管性痴呆混合型患者可能产生改善、无变化甚至有害的影响。无法将许多已发表的结果用于综合分析。对于总体临床改善的测量,仅基于一项研究的意向性分析未发现尼莫地平与安慰剂之间有任何差异(比值比0.53;95%置信区间0.25 - 1.13)。仅基于一项研究的实际治疗分析得出有利于尼莫地平的统计学显著差异(标准化均数差4.4;95%置信区间(3.9 - 5.0))。对于认知功能,尼莫地平对简易精神状态检查表评分(0 - 30分;高分 = 良好)的影响与安慰剂在统计学上有显著差异(标准化均数差0.9;95%置信区间0.59 - 1.22),并且对韦氏记忆量表有有利于治疗的统计学显著效果(标准化均数差0.47;95%置信区间0.17 - 0.77)。这些分析仅基于完成研究的患者,而非意向性分析。没有以适合合并的形式呈现关于功能自主性、行为、生活质量依赖性(如机构化)、对护理者的影响、死亡、治疗可接受性(以退出率衡量)、安全性(以不良反应发生率衡量,包括导致退出的副作用)的结果。
本综述没有提供令人信服的证据表明尼莫地平对未分类痴呆或主要亚型(阿尔茨海默病、血管性痴呆或阿尔茨海默病与血管性痴呆混合型)痴呆症状是一种有效的治疗方法。然而,由于很少有试验以适合合并的格式呈现数据,当纳入所有相关试验的更多数据时,本综述的结果可能会被修改。迫切需要对试验中已存在但无法通过已发表或汇总数据获取的数据进行独立评估。需要对个体患者数据进行独立的荟萃分析。目前不能推荐在痴呆患者中使用尼莫地平。本次更新的结果和结论不会因进一步检索而改变,因为额外的研究没有添加任何进一步有效的/符合条件的数据。