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Annals of the Rheumatic Diseases 2001;60:946-949; doi:10.1136/ard.60.10.946
Copyright © 2001 BMJ Publishing Group Ltd & European League Against Rheumatism.
Ann Rheum Dis 2001;60:946-949 ( October )

Extended report

Vitamin E is ineffective for symptomatic relief of knee osteoarthritis: a six month double blind, randomised, placebo controlled study C Branda, J Snaddonb, M Baileyb, F Cicuttinib

a Department of Rheumatology, Alfred Hospital, Prahran, Vic, Australia, b Department of Epidemiology and Preventive Medicine, Monash University Medical School, Alfred Hospital, Prahran, Vic, Australia

Correspondence to: Dr Brand hollandc{at}ocean.com.au

Accepted for publication 8 March 2000

OBJECTIVE---There is a putative role for antioxidant treatment in osteoarthritis (OA) based on animal, epidemiological, and human clinical studies. Vitamin E, a fat soluble vitamin, is one of the major dietary antioxidants. Short term clinical studies using vitamin E in the form of alpha -tocopherol suggested a benefit over placebo of similar dimension to that of diclofenac for relief of OA pain.
METHODS---A six month, double blind, randomised, placebo controlled study of vitamin E 500 IU/day was carried out. Primary outcome measures were pain, stiffness, and function. Statistical analysis was performed on an intention to treat basis.
RESULTS---77 patients were included in the study. Vitamin E showed no benefit over placebo at one month, three months, or six months for any of the outcome measures. The placebo group had higher pain levels (p=0.15) and body mass index (p=0.03) at baseline, and lower pain levels (p=0.02) at completion of the study. Radiological score, exercise score, age, or antioxidant intake at baseline or six months did not differ between the groups. The reasons for the better performance of the placebo group are uncertain but may relate to the initially higher pain score and subsequent regression to the mean.
CONCLUSIONS---Vitamin E shows no benefit for the management of symptomatic knee OA. The role of vitamin E in preventing OA progression is currently under investigation.


© 2001 by Annals of the Rheumatic Diseases

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