PMID 23440782 Vitamin C for preventing and treating the common cold Meta-analysis (Cochrane) · Cochrane Database Syst Rev, 2013 29 trials, 11,306 people - no cold prevention in the general population (RR 0.97), only extreme-exercise groups halved (0.48); regular use cut duration 8% (adults), 14% (children).
Key summary
A CochraneAn international network that rigorously reviews and synthesizes evidence. review settling 70 years of debate on vitamin C for the common cold (only placeboAn inert dummy treatment used as the comparison baseline.-controlled trials at 0.2 g/day or more). In 10,708 people in general community trials, regular use did not reduce cold incidence (relative risk 0.97). By contrast, in 598 people under extreme exercise such as marathoners and soldiers, the risk was more than halved (0.48). Regular use shortened duration by 8% in adults and 14% in children and reduced severity, but therapeutic trials starting after symptom onset showed no consistent effect. The authors said routine supplementation is not justified, though given its low cost and safety, cold patients may test therapeutic use on an individual basis.
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BACKGROUND: Vitamin C (ascorbic acid) for preventing and treating the common cold has been a subject of controversy for 70 years. OBJECTIVES: To find out whether vitamin C reduces the incidence, the duration or severity of the common cold when used either as a continuous regular supplementation every day or as a therapy at the onset of cold symptoms. MAIN RESULTS: Twenty-nine trial comparisons involving 11,306 participants contributed to the meta-analysis on the risk ratio (RR) of developing a cold whilst taking vitamin C regularly over the study period. In the general community trials involving 10,708 participants, the pooled RR was 0.97 (95% confidence interval (CI) 0.94 to 1.00). Five trials involving a total of 598 marathon runners, skiers and soldiers on subarctic exercises yielded a pooled RR of 0.48 (95% CI 0.35 to 0.64). Thirty-one comparisons examined the effect of regular vitamin C on common cold duration (9745 episodes). In adults the duration of colds was reduced by 8% (3% to 12%) and in children by 14% (7% to 21%). In children, 1 to 2 g/day vitamin C shortened colds by 18%. The severity of colds was also reduced by regular vitamin C administration. Seven comparisons examined the effect of therapeutic vitamin C (3249 episodes). No consistent effect of vitamin C was seen on the duration or severity of colds in the therapeutic trials. AUTHORS' CONCLUSIONS: The failure of vitamin C supplementation to reduce the incidence of colds in the general population indicates that routine vitamin C supplementation is not justified, yet vitamin C may be useful for people exposed to brief periods of severe physical exercise. Regular supplementation trials have shown that vitamin C reduces the duration of colds, but this was not replicated in the few therapeutic trials that have been carried out. ※ The abstract text as collected and stored via the API by the pipeline. The key summary is written based solely on this text.
View original ↗ PMID 18997197 Vitamins E and C in the prevention of cardiovascular disease in men: the Physicians' Health Study II randomized controlled trial Randomized controlled trial · JAMA, 2008 14,641 men, 8 years - 500 mg/day vitamin C did not reduce major cardiovascular events (hazard ratio 0.99; MI, stroke, and CV death all non-significant).
Key summary
A randomized, double-blind, placeboAn inert dummy treatment used as the comparison baseline.-controlled trial (Physicians' Health Study II) in 14,641 male physicians (aged 50+) at low cardiovascular risk. Over a mean of eight years, 500 mg/day of vitamin C showed no difference from placebo in major cardiovascular events (nonfatal MI, stroke, CV death; hazard ratio 0.99, 95% CI 0.89 to 1.11). MI (1.04), stroke (0.89), and CV death (1.02) were each non-significant, and vitamin E likewise had no effect. Contrary to the expectation from observational studies, no cardiovascular benefit of vitamin C supplementation was confirmed.
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CONTEXT: Basic research and observational studies suggest vitamin E or vitamin C may reduce the risk of cardiovascular disease. OBJECTIVE: To evaluate whether long-term vitamin E or vitamin C supplementation decreases the risk of major cardiovascular events among men. DESIGN, SETTING, AND PARTICIPANTS: The Physicians' Health Study II was a randomized, double-blind, placebo-controlled factorial trial of vitamin E and vitamin C that began in 1997 and continued until its scheduled completion on August 31, 2007. There were 14,641 US male physicians enrolled, who were initially aged 50 years or older. INTERVENTION: Individual supplements of 400 IU of vitamin E every other day and 500 mg of vitamin C daily. RESULTS: During a mean follow-up of 8 years, there were 1245 confirmed major cardiovascular events. There also was no significant effect of vitamin C on major cardiovascular events (active and placebo vitamin E groups, 10.8 and 10.9 events per 1000 person-years, respectively; HR, 0.99 [95% CI, 0.89-1.11]; P = .91), as well as total myocardial infarction (HR, 1.04 [95% CI, 0.87-1.24]; P = .65), total stroke (HR, 0.89 [95% CI, 0.74-1.07]; P = .21), and cardiovascular mortality (HR, 1.02 [95% CI, 0.85-1.21]; P = .86). ※ The abstract text as collected and stored via the API by the pipeline. The key summary is written based solely on this text.
View original ↗ PMID 19066368 Vitamins E and C in the prevention of prostate and total cancer in men: the Physicians' Health Study II randomized controlled trial Randomized controlled trial · JAMA, 2009 14,641 men, 8 years - 500 mg/day vitamin C did not reduce total or prostate cancer (cancer hazard ratio 1.01, prostate 1.02).
Key summary
A randomized, double-blind trial examining cancer prevention in the same cohort (Physicians' Health Study II, 14,641 male physicians). Over a mean of eight years, 500 mg/day of vitamin C did not reduce total cancer (hazard ratio 1.01, 95% CI 0.92 to 1.10) or prostate cancer (1.02), and had no effect on colorectal, lung, or other site-specific cancers. Adjusting for adherence and excluding early follow-up did not change the results. The authors concluded there is no support for vitamin C or E supplementation to prevent cancer in middle-aged and older men.
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CONTEXT: Vitamins E and C are among the most common individual supplements. No previous trial in men at usual risk has examined vitamin C alone in the prevention of cancer. OBJECTIVE: To evaluate whether long-term vitamin E or C supplementation decreases risk of prostate and total cancer events among men. DESIGN, SETTING, AND PARTICIPANTS: The Physicians' Health Study II is a randomized, double-blind, placebo-controlled factorial trial of vitamins E and C that began in 1997 and continued until its scheduled completion on August 31, 2007. A total of 14,641 male physicians in the United States initially aged 50 years or older were enrolled. INTERVENTION: Individual supplements of 400 IU of vitamin E every other day and 500 mg of vitamin C daily. RESULTS: During a mean follow-up of 8.0 years, there were 1008 confirmed incident cases of prostate cancer and 1943 total cancers. There was also no significant effect of vitamin C on total cancer (active and placebo vitamin C groups, 17.6 and 17.5 events per 1000 person-years; HR, 1.01; 95% CI, 0.92-1.10; P = .86) or prostate cancer (active and placebo vitamin C groups, 9.4 and 9.2 cases per 1000 person-years; HR, 1.02; 95% CI, 0.90-1.15; P = .80). Neither vitamin E nor vitamin C had a significant effect on colorectal, lung, or other site-specific cancers. CONCLUSIONS: In this large, long-term trial of male physicians, neither vitamin E nor C supplementation reduced the risk of prostate or total cancer. These data provide no support for the use of these supplements for the prevention of cancer in middle-aged and older men. ※ The abstract text as collected and stored via the API by the pipeline. The key summary is written based solely on this text.
View original ↗ PMID 5411783 Autonomic reflexes and vascular reactivity in experimental scurvy in man Human experimental study · J Clin Invest, 1970 Depriving five normal adults of vitamin C for three months produced scurvyA deficiency disease from prolonged lack of vitamin C, causing bleeding gums, bruising, and slow wound healing. signs, which resolved to asymptomatic after four months of repletion - a human experiment directly showing deficiency causes scurvy and repletion reverses it.
Key summary
Although its primary aim was the effect of vitamin C deficiency on autonomic and vascular reactivity, this is a classic experiment that directly documents the deficiency-repletion relationship of scurvyA deficiency disease from prolonged lack of vitamin C, causing bleeding gums, bruising, and slow wound healing. in humans. Depriving five normal volunteers of vitamin C for three months produced the symptoms and signs of scurvy, with plasma ascorbic acid falling to 0.178 mg/100 mL. After four months of vitamin C repletion they became asymptomatic and plasma levels recovered to 1.68 mg/100 mL. In other words, the causal chain that stopping vitamin C produces scurvy and restoring it resolves scurvy was confirmed under controlled human conditions. (Incidentally, deficiency did not interrupt autonomic reflexes and reduced only vascular constrictor responsiveness.)
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Ascorbic acid is a required cofactor in the conversion of dopamine to norepinephrine in vitro, and the deficiency of this vitamin in guinea pigs is associated with degeneration of autonomic ganglion cells and with cardiac supersensitivity to norepinephrine. Because of these findings, we tested the hypothesis that ascorbic acid deficiency in man alters autonomic cardiovascular reflexes and vasomotor responses to adrenergic stimuli. We studied five normal volunteers who had been deprived of ascorbic acid for a period of 3 months; they had developed symptoms and signs of scurvy and their plasma levels of ascorbic acid averaged 0.178 +/-SE 0.07 mg/100 ml. We repeated the studies after giving the subjects vitamin C for a period of 4 months; they had become asymptomatic and their plasma ascorbic acid had increased to an average of 1.68 +/-0.151 mg/100 ml. The results suggest that the decreased vascular responsiveness to intra-arterial norepinephrine and tyramine and to lower body negative pressure during ascorbic acid deficiency is caused by a defect in the ability of resistance vessels to constrict in response to adrenergic stimuli. Ascorbic acid deficiency in man does not interrupt autonomic reflexes and does not appear to cause significant depletion of endogenous norepinephrine. ※ The abstract text as collected and stored via the API by the pipeline. The key summary is written based solely on this text.
View original ↗ FDA (openFDA) ASCOR (ascorbic acid injection) - drug label (scurvy indication; oxalate nephropathy and G6PD hemolysis warnings)
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View original ↗ USDA FoodData Central Peppers, sweet, red, raw (FDC 170108)
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View original ↗ USDA FoodData Central Oranges, raw, all commercial varieties (FDC 169097)
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