Maryland University of Integrative Health, Laurel, MD, USA.
Department of Psychiatry, Oregon Health & Science University, Portland, OR, USA.
Cochrane Database Syst Rev. 2024 May 9;5(5):CD014914. doi: 10.1002/14651858.CD014914.pub2.
The common cold is an acute, self-limiting viral respiratory illness. Symptoms include nasal congestion and mucus discharge, sneezing, sore throat, cough, and general malaise. Given the frequency of colds, they are a public health burden and a significant cause of lost work productivity and school absenteeism. There are no established interventions to prevent colds or shorten their duration. However, zinc supplements are commonly recommended and taken for this purpose.
To assess the effectiveness and safety of zinc for the prevention and treatment of the common cold.
We searched CENTRAL, MEDLINE, Embase, CINAHL, and LILACS to 22 May 2023, and searched Web of Science Core Collection and two trials registries to 14 June 2023. We also used reference checking, citation searching, and contact with study authors to identify additional studies.
We included randomised controlled trials (RCTs) in children or adults that tested any form of zinc against placebo to prevent or treat the common cold or upper respiratory infection (URTI). We excluded zinc interventions in which zinc was combined with other minerals, vitamins, or herbs (e.g. a multivitamin, or mineral supplement containing zinc).
We used the Cochrane risk of bias tool to assess risks of bias, and GRADE to assess the certainty of the evidence. We independently extracted data. When necessary, we contacted study authors for additional information. We assessed zinc (type and route) with placebo in the prevention and treatment of the common cold. Primary outcomes included the proportion of participants developing colds (for analyses of prevention trials only), duration of cold (measured in days from start to resolution of the cold), adverse events potentially due to zinc supplements (e.g. unpleasant taste, loss of smell, vomiting, stomach cramps, and diarrhoea), and adverse events considered to be potential complications of the common cold (e.g. respiratory bacterial infections).
We included 34 studies (15 prevention, 19 treatment) involving 8526 participants. Twenty-two studies were conducted on adults and 12 studies were conducted on children. Most trials were conducted in the USA (n = 18), followed by India, Indonesia, Iran, and Turkey (two studies each), and Australia, Burkina Faso, Colombia, Denmark, Finland, Tanzania, Thailand, and the UK (one study each). The 15 prevention studies identified the condition as either common cold (n = 8) or URTI (n = 7). However, almost all therapeutic studies (17/19) focused on the common cold. Most studies (17/34) evaluated the effectiveness of zinc administered as lozenges (3 prevention; 14 treatment) in acetate, gluconate, and orotate forms; gluconate lozenges were the most common (9/17). Zinc gluconate was given at doses between 45 and 276 mg/day for between 4.5 and 21 days. Five (5/17) lozenge studies gave acetate lozenges and two (2/17) gave both acetate and gluconate lozenges. One (1/17) lozenge study administered intranasal (gluconate) and lozenge (orotate) zinc in tandem for cold treatment. Of the 17/34 studies that did not use lozenges, 1/17 gave capsules, 3/17 administered dissolved powders, 5/17 gave tablets, 4/17 used syrups, and 4/17 used intranasal administration. Most studies were at unclear or high risk of bias in at least one domain. There may be little or no reduction in the risk of developing a cold with zinc compared to placebo (risk ratio (RR) 0.93, 95% CI 0.85 to 1.01; I = 20%; 9 studies, 1449 participants; low-certainty evidence). There may be little or no reduction in the mean number of colds that occur over five to 18 months of follow-up (mean difference (MD) -0.90, 95% CI -1.93 to 0.12; I = 96%; 2 studies, 1284 participants; low-certainty evidence). When colds occur, there is probably little or no difference in the duration of colds in days (MD -0.63, 95% CI -1.29 to 0.04; I² = 77%; 3 studies, 740 participants; moderate-certainty evidence), and there may be little or no difference in global symptom severity (standardised mean difference (SMD) 0.04, 95% CI -0.35 to 0.43; I² = 0%; 2 studies, 101 participants; low-certainty evidence). When zinc is used for cold treatment, there may be a reduction in the mean duration of the cold in days (MD -2.37, 95% CI -4.21 to -0.53; I² = 97%; 8 studies, 972 participants; low-certainty evidence), although it is uncertain whether there is a reduction in the risk of having an ongoing cold at the end of follow-up (RR 0.52, 95% CI 0.21 to 1.27; I² = 65%; 5 studies, 357 participants; very low-certainty evidence), or global symptom severity (SMD -0.03, 95% CI -0.56 to 0.50; I² = 78%; 2 studies, 261 participants; very low-certainty evidence), and there may be little or no difference in the risk of a change in global symptom severity (RR 1.02, 95% CI 0.85 to 1.23; 1 study, 114 participants; low-certainty evidence). Thirty-one studies reported non-serious adverse events (2422 participants). It is uncertain whether there is a difference in the risk of adverse events with zinc used for cold prevention (RR 1.11, 95% CI 0.84 to 1.47; I = 0%; 7 studies, 1517 participants; very low-certainty evidence) or an increase in the risk of serious adverse events (RR 1.67, 95% CI 0.78 to 3.57; I = 0%; 3 studies, 1563 participants; low-certainty evidence). There is probably an increase in the risk of non-serious adverse events when zinc is used for cold treatment (RR 1.34, 95% CI 1.15 to 1.55; I = 44%; 2084 participants, 16 studies; moderate-certainty evidence); no treatment study provided information on serious adverse events. No study provided clear information about adverse events considered to be potential complications of the common cold.
AUTHORS' CONCLUSIONS: The findings suggest that zinc supplementation may have little or no effect on the prevention of colds but may reduce the duration of ongoing colds, with an increase in non-serious adverse events. Overall, there was wide variation in interventions (including concomitant therapy) and outcomes across the studies, as well as incomplete reporting of several domains, which should be considered when making conclusions about the efficacy of zinc for the common cold.
普通感冒是一种急性、自限性的病毒性呼吸道疾病。症状包括鼻塞和黏液分泌、打喷嚏、喉咙痛、咳嗽和全身不适。由于感冒的频率很高,它们是公共卫生的负担,也是导致工作生产力下降和学校缺勤的一个重要原因。目前还没有确定的干预措施可以预防感冒或缩短其持续时间。然而,锌补充剂通常被推荐用于此目的。
评估锌在预防和治疗普通感冒方面的有效性和安全性。
我们检索了截至 2023 年 5 月 22 日的 CENTRAL、MEDLINE、Embase、CINAHL 和 LILACS,并检索了 2023 年 6 月 14 日的 Web of Science 核心合集和两个试验注册库,以确定其他研究。我们还使用参考文献检查、引文搜索和与研究作者的联系来确定其他研究。
我们纳入了在儿童或成人中测试任何形式的锌与安慰剂对照以预防或治疗普通感冒或上呼吸道感染(URTI)的随机对照试验(RCT)。我们排除了锌干预措施,其中锌与其他矿物质、维生素或草药(例如多种维生素或含有锌的矿物质补充剂)联合使用。
我们使用 Cochrane 偏倚风险工具评估偏倚风险,并使用 GRADE 评估证据的确定性。我们独立提取数据。必要时,我们会与研究作者联系以获取更多信息。我们评估了锌(类型和途径)与安慰剂在预防和治疗普通感冒方面的作用。主要结局包括参与者发生感冒的比例(仅用于预防试验的分析)、感冒持续时间(从开始到感冒缓解的天数)、可能因锌补充剂引起的不良事件(例如不愉快的味道、嗅觉丧失、呕吐、腹痛和腹泻),以及被认为是普通感冒潜在并发症的不良事件(例如呼吸道细菌感染)。
我们纳入了 34 项研究(15 项预防,19 项治疗),涉及 8526 名参与者。22 项研究在成年人中进行,12 项研究在儿童中进行。大多数试验在美国(n = 18)进行,其次是印度、印度尼西亚、伊朗和土耳其(各有两项研究),以及澳大利亚、布基纳法索、哥伦比亚、丹麦、芬兰、坦桑尼亚、泰国和英国(各有一项研究)。15 项预防研究将病情确定为普通感冒(n = 8)或 URTI(n = 7)。然而,几乎所有的治疗研究(17/19)都集中在普通感冒上。大多数研究(34/34)评估了锌作为含片(3 项预防;14 项治疗)的有效性,以醋酸盐、葡萄糖酸盐和柠檬酸盐形式给药;葡萄糖酸盐含片最常见(17/19)。锌葡萄糖酸盐的剂量在 45 至 276 毫克/天之间,持续时间为 4.5 至 21 天。五项(17/19)含片研究给予醋酸盐含片,两项(17/19)给予醋酸盐和葡萄糖酸盐含片。一项(17/19)研究同时给予鼻腔内(葡萄糖酸盐)和含片(柠檬酸盐)锌治疗感冒。在不使用含片的 17/34 项研究中,1/17 给予胶囊,1/17 给予溶解粉末,3/17 给予片剂,4/17 给予糖浆,4/17 给予鼻腔内给药。大多数研究在至少一个领域存在高或中度偏倚风险。与安慰剂相比,锌补充剂可能对预防感冒的效果很小或没有(风险比(RR)0.93,95%置信区间(CI)0.85 至 1.01;I = 20%;9 项研究,1449 名参与者;低确定性证据)。在五到 18 个月的随访中,锌补充剂可能对发生的感冒次数没有明显减少(平均差异(MD)-0.90,95%CI-1.93 至 0.12;I = 96%;2 项研究,1284 名参与者;低确定性证据)。当感冒发生时,锌对感冒持续时间的影响可能很小或没有差异(平均差异(MD)-0.63,95%CI-1.29 至 0.04;I² = 77%;3 项研究,740 名参与者;中等确定性证据),并且锌对整体症状严重程度的影响可能很小或没有差异(标准化平均差异(SMD)0.04,95%CI-0.35 至 0.43;I² = 0%;2 项研究,101 名参与者;低确定性证据)。当锌用于感冒治疗时,感冒持续时间可能会缩短(MD-2.37,95%CI-4.21 至-0.53;I² = 97%;8 项研究,972 名参与者;低确定性证据),尽管尚不确定是否能减少随访结束时持续感冒的风险(RR 0.52,95%CI 0.21 至 1.27;I² = 65%;5 项研究,357 名参与者;非常低确定性证据)或整体症状严重程度(SMD-0.03,95%CI-0.56 至 0.50;I² = 78%;2 项研究,261 名参与者;非常低确定性证据),并且锌对整体症状严重程度变化的风险可能没有差异(RR 1.02,95%CI 0.85 至 1.23;1 项研究,114 名参与者;低确定性证据)。31 项研究报告了非严重不良事件(2422 名参与者)。尚不确定锌用于预防感冒的不良事件风险是否存在差异(RR 1.11,95%CI 0.84 至 1.47;I = 0%;7 项研究,1517 名参与者;非常低确定性证据)或严重不良事件风险增加(RR 1.67,95%CI 0.78 至 3.57;I = 0%;3 项研究,1563 名参与者;低确定性证据)。当锌用于治疗感冒时,非严重不良事件的风险可能会增加(RR 1.34,95%CI 1.15 至 1.55;I = 44%;2084 名参与者,16 项研究;中等确定性证据);没有治疗研究提供有关严重不良事件的信息。没有研究提供有关普通感冒潜在并发症的不良事件的明确信息。
研究结果表明,锌补充剂可能对预防感冒的效果很小或没有,但可能会缩短正在发生的感冒的持续时间,并增加非严重不良事件的风险。总体而言,研究之间在干预措施(包括伴随疗法)和结局方面存在很大差异,并且报告的多个领域不完整,在得出关于锌对普通感冒疗效的结论时应考虑这些因素。