Evans Jennifer R, Lawrenson John G
Cochrane Eyes and Vision, ICEH, London School of Hygiene & Tropical Medicine, Keppel Street, London, UK, WC1E 7HT.
Cochrane Database Syst Rev. 2017 Jul 31;7(7):CD000254. doi: 10.1002/14651858.CD000254.pub4.
It has been proposed that antioxidants may prevent cellular damage in the retina by reacting with free radicals that are produced in the process of light absorption. Higher dietary levels of antioxidant vitamins and minerals may reduce the risk of progression of age-related macular degeneration (AMD).
The objective of this review was to assess the effects of antioxidant vitamin or mineral supplementation on the progression of AMD in people with AMD.
We searched CENTRAL (2017, Issue 2), MEDLINE Ovid (1946 to March 2017), Embase Ovid (1947 to March 2017), AMED (1985 to March 2017), OpenGrey (System for Information on Grey Literature in Europe, the ISRCTN registry (www.isrctn.com/editAdvancedSearch), ClinicalTrials.gov (www.clinicaltrials.gov) and the WHO International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en). We did not use any date or language restrictions in the electronic searches for trials. We last searched the electronic databases on 29 March 2017.
We included randomised controlled trials (RCTs) that compared antioxidant vitamin or mineral supplementation (alone or in combination) to placebo or no intervention, in people with AMD.
Both review authors independently assessed risk of bias in the included studies and extracted data. One author entered data into RevMan 5; the other author checked the data entry. We graded the certainty of the evidence using GRADE.
We included 19 studies conducted in USA, Europe, China, and Australia. We judged the trials that contributed data to the review to be at low or unclear risk of bias.Nine studies compared multivitamins with placebo (7 studies) or no treatment (2 studies) in people with early and moderate AMD. The duration of supplementation and follow-up ranged from nine months to six years; one trial followed up beyond two years. Most evidence came from the Age-Related Eye Disease Study (AREDS) in the USA. People taking antioxidant vitamins were less likely to progress to late AMD (odds ratio (OR) 0.72, 95% confidence interval (CI) 0.58 to 0.90; 2445 participants; 3 RCTs; moderate-certainty evidence). In people with very early signs of AMD, who are at low risk of progression, this would mean that there would be approximately 4 fewer cases of progression to late AMD for every 1000 people taking vitamins (1 fewer to 6 fewer cases). In people at high risk of progression (i.e. people with moderate AMD) this would correspond to approximately 8 fewer cases of progression for every 100 people taking vitamins (3 fewer to 13 fewer). In one study of 1206 people, there was a lower risk of progression for both neovascular AMD (OR 0.62, 95% CI 0.47 to 0.82; moderate-certainty evidence) and geographic atrophy (OR 0.75, 95% CI 0.51 to 1.10; moderate-certainty evidence) and a lower risk of losing 3 or more lines of visual acuity (OR 0.77, 95% CI 0.62 to 0.96; 1791 participants; moderate-certainty evidence). Low-certainty evidence from one study of 110 people suggested higher quality of life scores (National Eye Institute Visual Function Questionnaire) in treated compared with the non-treated people after 24 months (mean difference (MD) 12.30, 95% CI 4.24 to 20.36). Six studies compared lutein (with or without zeaxanthin) with placebo. The duration of supplementation and follow-up ranged from six months to five years. Most evidence came from the AREDS2 study in the USA. People taking lutein or zeaxanthin may have similar or slightly reduced risk of progression to late AMD (RR 0.94, 95% CI 0.87 to 1.01; 6891 eyes; low-certainty evidence), neovascular AMD (RR 0.92, 95% CI 0.84 to 1.02; 6891 eyes; low-certainty evidence), and geographic atrophy (RR 0.92, 95% CI 0.80 to 1.05; 6891 eyes; low-certainty evidence). A similar risk of progression to visual loss of 15 or more letters was seen in the lutein and control groups (RR 0.98, 95% CI 0.91 to 1.05; 6656 eyes; low-certainty evidence). Quality of life (measured with Visual Function Questionnaire) was similar between groups in one study of 108 participants (MD 1.48, 95% -5.53 to 8.49, moderate-certainty evidence). One study, conducted in Australia, compared vitamin E with placebo. This study randomised 1204 people to vitamin E or placebo, and followed up for four years. Participants were enrolled from the general population; 19% had AMD. The number of late AMD events was low (N = 7) and the estimate of effect was uncertain (RR 1.36, 95% CI 0.31 to 6.05, very low-certainty evidence). There were no data on neovascular AMD or geographic atrophy.There was no evidence of any effect of treatment on visual loss (RR 1.04, 95% CI 0.74 to 1.47, low-certainty evidence). There were no data on quality of life. Five studies compared zinc with placebo. The duration of supplementation and follow-up ranged from six months to seven years. People taking zinc supplements may be less likely to progress to late AMD (OR 0.83, 95% CI 0.70 to 0.98; 3790 participants; 3 RCTs; low-certainty evidence), neovascular AMD (OR 0.76, 95% CI 0.62 to 0.93; 2442 participants; 1 RCT; moderate-certainty evidence), geographic atrophy (OR 0.84, 95% CI 0.64 to 1.10; 2442 participants; 1 RCT; moderate-certainty evidence), or visual loss (OR 0.87, 95% CI 0.75 to 1.00; 3791 participants; 2 RCTs; moderate-certainty evidence). There were no data reported on quality of life.Very low-certainty evidence was available on adverse effects because the included studies were underpowered and adverse effects inconsistently reported.
AUTHORS' CONCLUSIONS: People with AMD may experience some delay in progression of the disease with multivitamin antioxidant vitamin and mineral supplementation. This finding was largely drawn from one large trial, conducted in a relatively well-nourished American population. We do not know the generalisability of these findings to other populations. Although generally regarded as safe, vitamin supplements may have harmful effects. A systematic review of the evidence on harms of vitamin supplements is needed. Supplements containing lutein and zeaxanthin are heavily marketed for people with age-related macular degeneration but our review shows they may have little or no effect on the progression of AMD.
有人提出抗氧化剂可通过与光吸收过程中产生的自由基发生反应来预防视网膜细胞损伤。饮食中抗氧化剂维生素和矿物质水平较高可能会降低年龄相关性黄斑变性(AMD)进展的风险。
本综述的目的是评估补充抗氧化剂维生素或矿物质对患有AMD的人群中AMD进展的影响。
我们检索了Cochrane系统评价数据库(CENTRAL,2017年第2期)、MEDLINE(Ovid平台,1946年至2017年3月)、Embase(Ovid平台,1947年至2017年3月)、联合和补充医学数据库(AMED,1985年至2017年3月)、OpenGrey(欧洲灰色文献信息系统)、国际标准随机对照试验编号注册库(ISRCTN registry,网址:www.isrctn.com/editAdvancedSearch)、美国国立医学图书馆临床试验数据库(ClinicalTrials.gov,网址:www.clinicaltrials.gov)以及世界卫生组织国际临床试验注册平台(ICTRP,网址:www.who.int/ictrp/search/en)。在电子检索试验时,我们未使用任何日期或语言限制。我们最近一次检索电子数据库的时间是2017年3月29日。
我们纳入了将抗氧化剂维生素或矿物质补充剂(单独或联合使用)与安慰剂或不进行干预相比较的随机对照试验(RCT),受试者为患有AMD的人群。
两位综述作者独立评估纳入研究的偏倚风险并提取数据。一位作者将数据录入RevMan 5软件;另一位作者检查数据录入情况。我们使用GRADE方法对证据的确定性进行分级。
我们纳入了在美国、欧洲、中国和澳大利亚进行的19项研究。我们判断为综述提供数据的试验存在低或不明确的偏倚风险。9项研究比较了复合维生素与安慰剂(7项研究)或不治疗(2项研究)对早期和中度AMD患者的影响。补充和随访时间从9个月到6年不等;一项试验的随访时间超过2年。大多数证据来自美国的年龄相关性眼病研究(AREDS)。服用抗氧化剂维生素的人进展为晚期AMD的可能性较小(比值比(OR)0.72,95%置信区间(CI)0.58至0.90;2445名参与者;3项RCT;中等确定性证据)。对于AMD早期迹象且进展风险较低的人群,这意味着每1000名服用维生素的人中进展为晚期AMD的病例大约会减少4例(减少1例至6例)。对于进展风险较高的人群(即中度AMD患者),这相当于每100名服用维生素的人中进展病例大约会减少8例(减少3例至减少13例)。在一项针对1206人的研究中,新生血管性AMD(OR 0.62,95% CI 0.47至0.82;中等确定性证据)和地图状萎缩(OR 0.75,95% CI 0.51至1.10;中等确定性证据)的进展风险较低,视力下降3行或更多行的风险也较低(OR 0.77,95% CI 0.62至0.96;1791名参与者;中等确定性证据)。一项针对110人的研究提供的低确定性证据表明,治疗24个月后,与未治疗者相比,治疗组的生活质量评分(美国国立眼科研究所视觉功能问卷)更高(平均差(MD)12.30,95% CI 4.24至20.36)。6项研究比较了叶黄素(含或不含玉米黄质)与安慰剂。补充和随访时间从6个月到5年不等。大多数证据来自美国的AREDS2研究。服用叶黄素或玉米黄质的人进展为晚期AMD的风险可能相似或略有降低(风险比(RR)0.94,95% CI 0.87至1.01;6891只眼;低确定性证据),新生血管性AMD(RR 0.92,95% CI 0.84至1.02;6891只眼;低确定性证据)和地图状萎缩(RR 0.92,95% CI 0.80至1.05;6891只眼;低确定性证据)。叶黄素组和对照组中视力下降15个或更多字母的进展风险相似(RR 0.98,95% CI 0.91至1.05;6656只眼;低确定性证据)。在一项针对108名参与者的研究中,两组之间的生活质量(用视觉功能问卷测量)相似(MD 1.48,95% CI -5.53至8.49,中等确定性证据)。在澳大利亚进行的一项研究比较了维生素E与安慰剂。该研究将1204人随机分为维生素E组或安慰剂组,并随访4年。参与者来自普通人群;19%患有AMD。晚期AMD事件数量较少(N = 7),效应估计不确定(RR 1.36,95% CI 0.31至6.0