Douglas R M, Hemilä H, Chalker E, Treacy B
Cochrane Database Syst Rev. 2007 Jul 18(3):CD000980. doi: 10.1002/14651858.CD000980.pub3.
The role of vitamin C (ascorbic acid) in the prevention and treatment of the common cold has been a subject of controversy for 60 years, but is widely sold and used as both a preventive and therapeutic agent.
To discover whether oral doses of 0.2 g or more daily of vitamin C reduces the incidence, duration or severity of the common cold when used either as continuous prophylaxis or after the onset of symptoms.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 4, 2006); MEDLINE (1966 to December 2006); and EMBASE (1990 to December 2006).
Papers were excluded if a dose less than 0.2 g per day of vitamin C was used, or if there was no placebo comparison.
Two review authors independently extracted data and assessed trial quality. 'Incidence' of colds during prophylaxis was assessed as the proportion of participants experiencing one or more colds during the study period. 'Duration' was the mean days of illness of cold episodes.
Thirty trial comparisons involving 11,350 study participants contributed to the meta-analysis on the relative risk (RR) of developing a cold whilst taking prophylactic vitamin C. The pooled RR was 0.96 (95% confidence intervals (CI) 0.92 to 1.00). A subgroup of six trials involving a total of 642 marathon runners, skiers, and soldiers on sub-arctic exercises reported a pooled RR of 0.50 (95% CI 0.38 to 0.66). Thirty comparisons involving 9676 respiratory episodes contributed to a meta-analysis on common cold duration during prophylaxis. A consistent benefit was observed, representing a reduction in cold duration of 8% (95% CI 3% to 13%) for adults and 13.6% (95% CI 5% to 22%) for children. Seven trial comparisons involving 3294 respiratory episodes contributed to the meta-analysis of cold duration during therapy with vitamin C initiated after the onset of symptoms. No significant differences from placebo were seen. Four trial comparisons involving 2753 respiratory episodes contributed to the meta-analysis of cold severity during therapy and no significant differences from placebo were seen.
AUTHORS' CONCLUSIONS: The failure of vitamin C supplementation to reduce the incidence of colds in the normal population indicates that routine mega-dose prophylaxis is not rationally justified for community use. But evidence suggests that it could be justified in people exposed to brief periods of severe physical exercise or cold environments.
60年来,维生素C(抗坏血酸)在预防和治疗普通感冒中的作用一直存在争议,但它作为预防和治疗药物仍被广泛销售和使用。
探讨每日口服0.2克或更多剂量的维生素C,无论是持续预防还是在症状出现后使用,是否能降低普通感冒的发病率、持续时间或严重程度。
我们检索了Cochrane对照试验中心注册库(CENTRAL)(《Cochrane图书馆》2006年第4期);MEDLINE(1966年至2006年12月);以及EMBASE(1990年至2006年12月)。
如果使用的维生素C剂量低于每日0.2克,或者没有安慰剂对照,则排除相关论文。
两位综述作者独立提取数据并评估试验质量。预防期间感冒的“发病率”被评估为在研究期间经历一次或多次感冒的参与者比例。“持续时间”是感冒发作的平均患病天数。
30项试验比较涉及11350名研究参与者,用于对服用预防性维生素C时患感冒的相对风险(RR)进行荟萃分析。汇总RR为0.96(95%置信区间(CI)0.92至1.00)。涉及总共642名马拉松运动员、滑雪者和进行亚北极训练的士兵的六项试验亚组报告的汇总RR为0.50(95%CI 0.38至0.66)。30项比较涉及9676次呼吸道发作,用于对预防期间普通感冒持续时间进行荟萃分析。观察到一致的益处,即成人感冒持续时间减少8%(95%CI 3%至13%),儿童减少13.6%(95%CI 5%至22%)。7项试验比较涉及3294次呼吸道发作,用于对症状出现后开始使用维生素C治疗期间的感冒持续时间进行荟萃分析。与安慰剂相比未发现显著差异。4项试验比较涉及2753次呼吸道发作,用于对治疗期间感冒严重程度进行荟萃分析,与安慰剂相比未发现显著差异。
补充维生素C未能降低正常人群感冒的发病率,这表明常规大剂量预防在社区使用中缺乏合理依据。但有证据表明,对于暴露于短期剧烈体育锻炼或寒冷环境的人群,补充维生素C可能是合理的。