Malouf M, Grimley Evans J, Areosa Sastre A
Dept. of Clinical Geratology, Cochrane Dementia and Cognitive Improvement Group, Radcliffe Infirmary, Woodstock Road, Oxford, UK, OX2 6HE.
Cochrane Database Syst Rev. 2003(4):CD004514. doi: 10.1002/14651858.CD004514.
Folates are vitamins essential to the development of the central nervous system. Insufficient folate activity at the time of conception and early pregnancy can result in congenital neural tube defects. In adult life folate deficiency has been known for decades to produce a characteristic form of anaemia ("megaloblastic"). More recently degrees of folate inadequacy, not severe enough to produce anaemia, have been found to be associated with high blood levels of the amino acid homocysteine. Such degrees of folate inadequacy can arise because of insufficient folates in the diet or because of inefficient absorption or metabolic utilisation of folates due to genetic variations. Conventional criteria for diagnosing folate deficiency may be inadequate for identifying people capable of benefiting from dietary supplementation. High blood levels of homocysteine have been linked with the risk of arterial disease, dementia and Alzheimer's disease. There is therefore interest in whether dietary supplements of folic acid (an artificial chemical analogue of naturally occurring folates) can improve cognitive function of people at risk of cognitive decline associated with ageing or dementia, whether by affecting homocysteine metabolism or through other mechanisms. There is a risk that if folic acid is given to people who have undiagnosed deficiency of vitamin B12 it may lead to neurological damage. Vitamin B12 deficiency produces both an anaemia identical to that of folate deficiency but also causes irreversible damage to the central and peripheral nervous systems. Folic acid will correct the anaemia of vitamin B12 deficiency and so delay diagnosis but will not prevent progression to neurological damage. For this reason trials of folic acid supplements may involve simultaneous administration of vitamin B12. Apparent benefit from folic acid given in the combination would therefore need to be "corrected" for any effect of vitamin B12 alone. A separate Cochrane review of vitamin B12 and cognitive function is being prepared.
To examine the effects of folic acid supplementation, with or without vitamin B12, on elderly healthy and demented people, in preventing cognitive impairment or retarding its progress.
Trials were identified from a search of the Cochrane Dementia and Cognitive Improvement Specialized Register Group on 9 April 2003 using the terms: folic acid, folate, vitamin B9, leucovorin, methyltetrahydrofolate, vitamin B12, cobalamin, cyanocobalamin, dementia, cognitive function, cognitive impairment, Alzheimer's disease, vascular dementia, mixed dementia and controlled trials. MEDLINE and EMBASE (both all years) were searched for additional trials on healthy people.
All double-blind placebo-controlled randomized trials, in which supplements of folic acid with or without vitamin B12 were compared with placebo for elderly healthy people or people with any type of dementia or cognitive impairment.
The reviewers independently applied the selection criteria and assessed study quality. One reviewer extracted and analysed the data. In comparing intervention with placebo, weighted mean differences, and standardized mean difference or odds ratios were estimated.
Four randomized controlled trials fulfilled the inclusion criteria for this review. One trial (Bryan 2002) enrolled healthy women, and three (Fioravanti 1997; Sommer 1998; VITAL 2003) recruited people with mild to moderate cognitive impairment or dementia with or without diagnosed folate deficiency. Fioravanti 1997 enrolled people with mild to moderate cognitive impairment or dementia as judged by scores on the Mini-Mental State Examination (MMSE) and Global Deterioration Scale and with serum folate level<3ng/l. One trial (VITAL 2003) studied the effects of a combination of vitamin B12 and folic acid on patients with mild to moderate cognitive impairment due to Alzheimer's disease or mixed dementia. The analysis from the included trials found no benefit from folic acid with or without vitamin B12 in comparison with placebo on any measures of cognition and mood for healthy or cognitively impaired or demented people: Folic acid effect and healthy participants: there was no benefit from of oral 750 mcg folic acid per day for five weeks compared with placebo on measures of cognition and mood of 19 healthy women aged 65 to 92. Folic acid effect and people with mild to moderate cognitive decline or dementia: there were no statistically significant results in favour of folic acid with or without vitamin B12 on any measures of cognitive function. Scores on the Mini-Mental State Examination (MMSE) revealed no statistically significant benefit from 2 mg per day folic acid plus 1mg vitamin B12 for 12 weeks when compared with placebo (WMD 0.39, 95% CI -0.43 to 1.21, P=0.35). Cognitive scores on the Alzheimer's Disease Scale (ADAS-Cog) showed no statistically significant benefit from 2 mg /day folic acid plus 1 mg /day vitamin B12 for 12 weeks compared with placebo (WMD 0.41, 95% -1.25 to 2.07, P=4.63). The Bristol Activities of Daily Living Scale (BADL) revealed no benefit from 2mg per day of folic acid plus 1 mg vitamin B12 for 12 weeks in comparison with placebo (WMD -0.57, 95%CI -1.95 to 0.81, P=0.42). None of the sub tests of the Randt Memory Test (RMT) showed statistically significant benefit from 15 mg of folic acid orally per day for 9 weeks when compared with placebo. One trial (Sommer 1998) reported a significant decline compared with placebo in two cognitive function tasks in demented patients who had received high doses of folic acid (10 mg /day) for unspecified periods. One trial (VITAL 2003) showed that 2 mg folic acid plus 1 mg vitamin B12 daily for 12 weeks significantly lowered serum homocysteine concentrations (P <0.0001).
REVIEWER'S CONCLUSIONS: There was no beneficial effect of 750 mcg of folic acid per day on measures of cognition or mood in older healthy women. In patients with mild to moderate cognitive decline and different forms of dementia there was no benefit from folic acid on measures of cognition or mood. Folic acid plus vitamin B12 was effective in reducing the serum homocysteine concentrations. Folic acid was well tolerated and no adverse effects were reported. More studies are needed.
叶酸是中枢神经系统发育所必需的维生素。受孕时及孕早期叶酸活性不足会导致先天性神经管缺陷。在成年人中,叶酸缺乏会导致一种典型的贫血(“巨幼细胞性贫血”),这一情况已为人所知数十年。最近发现,叶酸不足程度尚未严重到引发贫血时,会与血液中高浓度的氨基酸同型半胱氨酸有关。这种叶酸不足程度可能是由于饮食中叶酸不足,或者由于基因变异导致叶酸吸收或代谢利用效率低下。传统的叶酸缺乏诊断标准可能不足以识别能从膳食补充剂中获益的人群。血液中高浓度的同型半胱氨酸与动脉疾病、痴呆和阿尔茨海默病风险有关。因此,人们关注膳食补充叶酸(天然叶酸的人工化学类似物)是否能改善有认知能力下降风险的人群(与衰老或痴呆相关)的认知功能,无论是通过影响同型半胱氨酸代谢还是通过其他机制。如果给未诊断出维生素B12缺乏的人补充叶酸,可能会导致神经损伤。维生素B12缺乏不仅会导致与叶酸缺乏相同的贫血,还会对中枢和周围神经系统造成不可逆转的损害。叶酸会纠正维生素B12缺乏导致的贫血,从而延迟诊断,但无法预防神经损伤的进展。因此,叶酸补充剂试验可能需要同时给予维生素B12。因此,联合使用叶酸时的明显益处需要针对维生素B12单独产生的任何影响进行“校正”。正在准备一项关于维生素B12与认知功能的Cochrane系统评价。
研究补充叶酸(无论是否联合维生素B12)对健康老年人和痴呆患者预防认知障碍或延缓其进展的效果。
通过2003年4月9日检索Cochrane痴呆与认知改善专业注册组,使用以下检索词识别试验:叶酸、叶素、维生素B9、亚叶酸钙、甲基四氢叶酸、维生素B12、钴胺素、氰钴胺素、痴呆、认知功能、认知障碍、阿尔茨海默病、血管性痴呆、混合性痴呆和对照试验。检索MEDLINE和EMBASE(所有年份)以查找关于健康人群的其他试验。
所有双盲安慰剂对照随机试验,其中将补充叶酸(无论是否联合维生素B12)与安慰剂用于健康老年人或患有任何类型痴呆或认知障碍的人群进行比较。
综述作者独立应用入选标准并评估研究质量。一名综述作者提取并分析数据。在将干预措施与安慰剂进行比较时,估计加权平均差、标准化平均差或比值比。
四项随机对照试验符合本综述的纳入标准。一项试验(Bryan,2002年)纳入健康女性,三项试验(Fioravanti,1997年;Sommer,1998年;VITAL,2003年)招募了有轻度至中度认知障碍或痴呆的人群,无论是否诊断出叶酸缺乏。Fioravanti 1997年纳入的人群根据简易精神状态检查表(MMSE)和整体衰退量表评分判断为有轻度至中度认知障碍或痴呆,且血清叶酸水平<3ng/l。一项试验(VITAL,2003年)研究了维生素B12和叶酸联合使用对患有阿尔茨海默病或混合性痴呆导致的轻度至中度认知障碍患者的影响。纳入试验的分析发现,与安慰剂相比,无论是否联合维生素B12,叶酸对健康、认知受损或痴呆人群的任何认知和情绪指标均无益处:叶酸对健康参与者的影响:与安慰剂相比,每天口服750 mcg叶酸持续五周,对19名65至92岁健康女性的认知和情绪指标无益处。叶酸对轻度至中度认知衰退或痴呆患者的影响:无论是否联合维生素B12,叶酸对任何认知功能指标均无统计学显著结果。与安慰剂相比,每天2 mg叶酸加1mg维生素B12持续12周,简易精神状态检查表(MMSE)评分无统计学显著益处(加权平均差0.39,95%置信区间 -0.43至1.21,P = 0.35)。阿尔茨海默病量表(ADAS - Cog)的认知评分显示,与安慰剂相比,每天2 mg /天叶酸加1 mg /天维生素B12持续十周无统计学显著益处(加权平均差0.41,95% -1.25至2.07,P = 4.63)。布里斯托尔日常生活活动量表(BADL)显示,与安慰剂相比,每天2mg叶酸加1mg维生素B12持续12周无益处(加权平均差 -0.57,95%置信区间 -1.95至0.81,P = 0.42)。与安慰剂相比,每天口服15mg叶酸持续九周,兰特记忆测试(RMT)的任何子测试均无统计学显著益处。一项试验(Sommer,1998年)报告,与安慰剂相比,接受高剂量叶酸(10mg /天)未指明时间段的痴呆患者在两项认知功能任务中有显著下降。一项试验(VITAL,2003年)显示,每天2mg叶酸加1mg维生素B12持续12周可显著降低血清同型半胱氨酸浓度(P <0.0001)。
每天750 mcg叶酸对老年健康女性的认知或情绪指标无有益影响。在轻度至中度认知衰退和不同形式痴呆患者中,叶酸对认知或情绪指标无益处。叶酸加维生素B12可有效降低血清同型半胱氨酸浓度。叶酸耐受性良好,未报告不良反应。需要更多研究。