Sydenham Emma, Dangour Alan D, Lim Wee-Shiong
Cochrane Injuries Group, London School of Hygiene & Tropical Medicine, London,
Cochrane Database Syst Rev. 2012 Jun 13;2012(6):CD005379. doi: 10.1002/14651858.CD005379.pub3.
Evidence from observational studies suggests that diets high in omega-3 long-chain polyunsaturated fatty acids (PUFA) may protect people from cognitive decline and dementia. The strength of this potential protective effect has recently been tested in randomised controlled trials.
To assess the effects of omega-3 PUFA supplementation for the prevention of dementia and cognitive decline in cognitively healthy older people.
We searched ALOIS - the Cochrane Dementia and Cognitive Improvement Group's Specialized Register on 6 April 2012 using the terms: "omega 3", PUFA, "fatty acids", "fatty acid", fish, linseed, eicosapentaenoic, docosahexaenoic.
Randomised controlled trials of an omega-3 PUFA intervention which was provided for a minimum of six months to participants aged 60 years and over who were free from dementia or cognitive impairment at the beginning of the study. Two review authors independently assessed all trials.
The review authors sought and extracted data on incident dementia, cognitive function, safety and adherence, either from published reports or by contacting the investigators for original data. Data were extracted by two review authors. We calculated mean difference (MD) or standardised mean differences (SMD) and 95% confidence intervals (CI) on an intention-to-treat basis, and summarised narratively information on safety and adherence.
Information on cognitive function at the start of a study was available on 4080 participants randomised in three trials. Cognitive function data were available on 3536 participants at final follow-up.In two studies participants received gel capsules containing either omega-3 PUFA (the intervention) or olive or sunflower oil (placebo) for six or 24 months. In one study, participants received margarine spread for 40 months; the margarine for the intervention group contained omega-3 PUFA. Two studies had cognitive health as their primary outcome; one study of cardiovascular disease included cognitive health as an additional outcome.None of the studies examined the effect of omega-3 PUFA on incident dementia. In two studies involving 3221 participants there was no difference between the omega-3 and placebo group in mini-mental state examination score at final follow-up (following 24 or 40 months of intervention); MD -0.07 (95% CI -0.25 to 0.10). In two studies involving 1043 participants, other tests of cognitive function such as word learning, digit span and verbal fluency showed no beneficial effect of omega-3 PUFA supplementation. Participants in both the intervention and control groups experienced either small or no cognitive declines during the studies.The main reported side-effect of omega-3 PUFA supplementation was mild gastrointestinal problems. Overall, minor adverse events were reported by fewer than 15% of participants, and reports were balanced between intervention groups. Adherence to the intervention was on average over 90% among people who completed the trials. All three studies included in this review are of high methodological quality.
AUTHORS' CONCLUSIONS: Direct evidence on the effect of omega-3 PUFA on incident dementia is lacking. The available trials showed no benefit of omega-3 PUFA supplementation on cognitive function in cognitively healthy older people. Omega-3 PUFA supplementation is generally well tolerated with the most commonly reported side-effect being mild gastrointestinal problems.Further studies of longer duration are required. Longer-term studies may identify greater change in cognitive function in study participants which may enhance the ability to detect the possible effects of omega-3 PUFA supplementation in preventing cognitive decline in older people.
观察性研究的证据表明,富含ω-3长链多不饱和脂肪酸(PUFA)的饮食可能会保护人们免受认知能力下降和痴呆症的影响。这种潜在保护作用的强度最近已在随机对照试验中得到检验。
评估补充ω-3多不饱和脂肪酸对认知健康的老年人预防痴呆症和认知能力下降的效果。
我们于2012年4月6日在ALOIS(Cochrane痴呆与认知改善小组的专业注册库)中进行检索,检索词为:“omega 3”、PUFA、“脂肪酸”、“脂肪酸”、鱼、亚麻籽、二十碳五烯酸、二十二碳六烯酸。
ω-3多不饱和脂肪酸干预的随机对照试验,干预时间至少为6个月,参与者年龄在60岁及以上,且在研究开始时无痴呆症或认知障碍。两位综述作者独立评估所有试验。
综述作者从已发表的报告中或通过联系研究者获取原始数据,来查找和提取关于新发痴呆症、认知功能、安全性和依从性的数据。数据由两位综述作者提取。我们在意向性分析的基础上计算平均差(MD)或标准化平均差(SMD)以及95%置信区间(CI),并对安全性和依从性信息进行叙述性总结。
在三项试验中随机分组的4080名参与者可获得研究开始时的认知功能信息。在最终随访时,3536名参与者可获得认知功能数据。在两项研究中,参与者接受含有ω-3多不饱和脂肪酸的软胶囊(干预组)或橄榄油或葵花籽油(安慰剂组),为期6个月或24个月。在一项研究中,参与者接受人造黄油涂抹物40个月;干预组的人造黄油含有ω-3多不饱和脂肪酸。两项研究将认知健康作为主要结局;一项心血管疾病研究将认知健康作为额外结局。没有一项研究考察ω-3多不饱和脂肪酸对新发痴呆症的影响。在两项涉及3221名参与者的研究中,在最终随访时(经过24个月或40个月的干预),ω-3组和安慰剂组在简易精神状态检查表得分上没有差异;平均差为 -0.07(95%置信区间为 -0.25至0.10)。在两项涉及1043名参与者的研究中,其他认知功能测试,如单词学习、数字广度和语言流畅性,未显示补充ω-3多不饱和脂肪酸有有益效果。在研究期间,干预组和对照组的参与者认知能力下降均较小或未出现下降。补充ω-3多不饱和脂肪酸报告的主要副作用是轻度胃肠道问题。总体而言,不到15%的参与者报告有轻微不良事件,且干预组之间报告情况均衡。完成试验的人中,干预的依从性平均超过90%。本综述纳入的所有三项研究方法学质量都很高。
缺乏关于ω-3多不饱和脂肪酸对新发痴呆症影响的直接证据。现有试验表明,补充ω-3多不饱和脂肪酸对认知健康的老年人的认知功能没有益处。补充ω-3多不饱和脂肪酸通常耐受性良好,最常报告的副作用是轻度胃肠道问题。需要进行持续时间更长的进一步研究。长期研究可能会发现研究参与者认知功能有更大变化,这可能会增强检测补充ω-3多不饱和脂肪酸预防老年人认知能力下降可能效果的能力。