Iron supplementation for unexplained fatigue in non-anaemic women: double blind randomised placebo controlled trial
Abstract Objective To determine the subjective response to iron therapy in non-anaemic women with unexplained fatigue. Design Double blind randomised placebo controlled trial. Setting Academic primary care centre and eight general practices in western Switzerland. Participants 144 women aged 18 to 5...
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Published in | BMJ Vol. 326; no. 7399; pp. 1124 - 1126 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
British Medical Journal Publishing Group
24.05.2003
British Medical Association BMJ Publishing Group LTD BMJ Publishing Group BMJ Publishing Group Ltd |
Edition | International edition |
Subjects | |
Online Access | Get full text |
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Summary: | Abstract Objective To determine the subjective response to iron therapy in non-anaemic women with unexplained fatigue. Design Double blind randomised placebo controlled trial. Setting Academic primary care centre and eight general practices in western Switzerland. Participants 144 women aged 18 to 55, assigned to either oral ferrous sulphate (80 mg/day of elemental iron daily; n=75) or placebo (n=69) for four weeks. Main outcome measures Level of fatigue, measured by a 10 point visual analogue scale. Results 136 (94%) women completed the study. Most had a low serum ferritin concentration; ≤ 20 μg/l in 69 (51%) women. Mean age, haemoglobin concentration, serum ferritin concentration, level of fatigue, depression, and anxiety were similar in both groups at baseline. Both groups were also similar for compliance and dropout rates. The level of fatigue after one month decreased by −1.82/6.37 points (29%) in the iron group compared with −0.85/6.46 points (13%) in the placebo group (difference 0.95 points, 95% confidence interval 0.32 to 1.62; P=0.004). Subgroups analysis showed that only women with ferritin concentrations ≤ 50 μg/l improved with oral supplementation. Conclusion Non-anaemic women with unexplained fatigue may benefit from iron supplementation. The effect may be restricted to women with low or borderline serum ferritin concentrations. |
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Bibliography: | ark:/67375/NVC-N7W03FK2-W PMID:12763985 href:bmj-326-1124.pdf ArticleID:bmj.326.7399.1124 local:bmj;326/7399/1124 istex:FEA51FA35EDB8B7F4AE68B123293A22B37DF0DCB Correspondence to: B Favrat ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 ObjectType-News-3 content type line 23 Funding: This study was sponsored by Robapharm. The sponsor was not involved in the analysis of the results nor in writing or correcting the manuscript. We thank M Burnier for his contribution to the electronic monitoring of patient compliance and for his critique of the manuscript and W Ghali (University of Calgary, Alberta, Canada) for his comments on the revised manuscript. Correspondence to: B Favrat bernard.favrat@hospvd.ch Competing interests: FV and BF received financial support from Robapharm for producing a preliminary report of the study. Ethical approval: The study was approved by the ethical review committee for clinical research of the Department of Internal Medicine, University of Lausanne. Contributors: FV, BB, CLF, and BF participated in the conception and design of the study, analysis and interpretation of data, drafting and revising the manuscript, and inclusion of patients for BF and FV. CB, MG, AM, TB, MdeV, J-PS, LH, CC, JT, and AP participated in the conception and design of the study, inclusion of patients, and drafting and revising the manuscript. BF will act as guarantor for the paper. |
ISSN: | 0959-8138 0959-8146 1468-5833 1756-1833 |
DOI: | 10.1136/bmj.326.7399.1124 |