From University of Minnesota, Minneapolis VA Health Care System, and HealthPartners, Minneapolis, Minnesota.
Ann Intern Med. 2018 Jan 2;168(1):52-62. doi: 10.7326/M17-1530. Epub 2017 Dec 19.
Optimal interventions to prevent or delay cognitive decline, mild cognitive impairment (MCI), or dementia are uncertain.
To summarize the evidence on efficacy and harms of over-the-counter (OTC) supplements to prevent or delay cognitive decline, MCI, or clinical Alzheimer-type dementia in adults with normal cognition or MCI but no dementia diagnosis.
Multiple electronic databases from 2009 to July 2017 and bibliographies of systematic reviews.
English-language trials of at least 6 months' duration that enrolled adults without dementia and compared cognitive outcomes with an OTC supplement versus placebo or active controls.
Extraction performed by a single reviewer and confirmed by a second reviewer; dual-reviewer assessment of risk of bias; consensus determination of strength of evidence.
Thirty-eight trials with low to medium risk of bias compared ω-3 fatty acids, soy, ginkgo biloba, B vitamins, vitamin D plus calcium, vitamin C or β-carotene, multi-ingredient supplements, or other OTC interventions with placebo or other supplements. Few studies examined effects on clinical Alzheimer-type dementia or MCI, and those that did suggested no benefit. Daily folic acid plus vitamin B12 was associated with improvements in performance on some objectively measured memory tests that were statistically significant but of questionable clinical significance. Moderate-strength evidence showed that vitamin E had no benefit on cognition. Evidence about effects of ω-3 fatty acids, soy, ginkgo biloba, folic acid alone or with other B vitamins, β-carotene, vitamin C, vitamin D plus calcium, and multivitamins or multi-ingredient supplements was either insufficient or low-strength, suggesting that these supplements did not reduce risk for cognitive decline. Adverse events were rarely reported.
Studies had high attrition and short follow-up and used a highly variable set of cognitive outcome measures.
Evidence is insufficient to recommend any OTC supplement for cognitive protection in adults with normal cognition or MCI.
Agency for Healthcare Research and Quality.
预防或延缓认知能力下降、轻度认知障碍(MCI)或痴呆的最佳干预措施仍不确定。
总结关于非处方(OTC)补充剂预防或延缓认知能力下降、MCI 或无痴呆诊断的临床阿尔茨海默型痴呆的疗效和危害的证据,这些补充剂用于认知正常或 MCI 的成年人。
2009 年至 2017 年 7 月的多个电子数据库和系统评价的参考文献。
至少持续 6 个月的英语试验,纳入无痴呆的成年人,并将认知结果与 OTC 补充剂与安慰剂或阳性对照进行比较。
由一名评审员进行提取,另一名评审员进行确认;对偏倚风险进行双重评审评估;共识确定证据强度。
38 项试验的偏倚风险低至中等,比较了 ω-3 脂肪酸、大豆、银杏叶、B 族维生素、维生素 D 加钙、维生素 C 或 β-胡萝卜素、多种成分补充剂或其他 OTC 干预与安慰剂或其他补充剂。很少有研究检查这些补充剂对临床阿尔茨海默型痴呆或 MCI 的影响,而那些研究表明没有益处。每日叶酸加维生素 B12 与一些客观测量的记忆测试的表现改善相关,这些改善具有统计学意义,但临床意义值得怀疑。中等强度的证据表明,维生素 E 对认知没有益处。关于 ω-3 脂肪酸、大豆、银杏叶、叶酸单独或与其他 B 族维生素、β-胡萝卜素、维生素 C、维生素 D 加钙以及多种维生素或多种成分补充剂的效果的证据不足或强度较低,表明这些补充剂并未降低认知能力下降的风险。不良事件很少报告。
研究的失访率和随访时间较短,且使用了一套高度可变的认知结果测量方法。
目前尚无足够证据推荐任何 OTC 补充剂用于认知正常或 MCI 成年人的认知保护。
医疗保健研究与质量局。