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Effects of MSM on exercise-induced muscle and joint pain: a pilot study

Background

Participants in organized running commonly experience muscle and joint pain while training for and competing in distance events. Many runners report pain as a major influence on changes or breaks in training regimens, and as a common deterrent for returning to exercise after a break. Methylsulfonylmethane (MSM) is a sulfur-based nutritional supplement shown through several clinical trials to be effective in reducing pain associated with osteoarthritis, and to exhibit anti-inflammatory properties. To further investigate the role of MSM in pain management, this randomized, double-blind, placebo-controlled study evaluated the effects of MSM supplementation on exercise-induced muscle and joint pain.

Methods

Twenty-two healthy females (n = 17) and males (n = 5) (33.7 ± 6.9 yrs.) were recruited from the 2014 Portland Half-Marathon registrant pool. Participants were randomized to take either MSM (OptiMSM®) (n = 11), or a placebo (n = 11) at 3g/day for 21 days prior to the race and two days after (23 total). Pain was recorded using a 100 mm Visual Analogue Scale (VAS) for both muscle pain (MP) and joint pain (JP) on a single questionnaire. Participants completed the questionnaire at five time points. Baseline levels (T0) were recorded approximately one month prior to the race. Post-race pain levels were recorded at 15 minutes (T1), 90 minutes (T2), 1 Day (T3), and 2 days (T4) after race finish. Data were analyzed using linear mixed models controlled for baseline, with time point as a repeated factor. Simple contrasts compared post-race time points to baseline, and Student's t-tests assessed between-group time point comparisons.

Results

Half-marathon completion resulted in significant time effects for increased pain in both MP (p < 0.001) and JP (p < 0.001). Mean MP at T0 (14.7mm) significantly increased at T1 (38.4mm; p < 0.001), T2 (33.5mm; p = 0.001), and T3 (36.3mm; p = 0.001), and fell to non-significant levels at T4 (20.9mm; p = 0.330). Mean JP at T0 (8.4mm) significantly increased at T1 (33.5mm; p < 0.001), T2 (31.5mm; p < 0.001), and T3 (24.8mm; p = 0.004), and fell to non-significant levels at T4 (16.1 mm; p = 0.198). The results showed a trend of lower pain levels in the MSM group. However, time-by-treatment effects did not reach significance in either MP or JP. Compared to placebo, MSM supplementation resulted in nearly significantly lower MP at T1 (MSM = 27.3mm vs. placebo = 49.8mm, p = 0.063), and lower MP at T2 (27.1mm vs. 40.0mm; p = 0.300), and T3 (30.0mm vs. 41.9mm; p = 0.306). Similar results were seen for JP at T1 (24.2mm vs. 42.4mm; p = 0.156), T2 (22.7mm vs 39.3mm; p = 0.204), and T3 (15.4mm vs. 32.2mm; p = 0.152).

Conclusion

Exercise-induced muscle pain and joint pain increase within 15 minutes of completing a half-marathon, continue through the following day, and diminish approximately two days post-race. Three weeks of MSM supplementation at 3g/day attenuated post-exercise muscle and joint pain at clinically significant levels compared to placebo. However, the pain reductions did not reach statistical significance, warranting further research on MSM and post-exercise pain among larger samples.

Acknowledgements

Eric D Withee is employed part-time at Bergstrom Nutrition (Vancouver, WA), manufacturers of MSM (OptiMSMâ„¢).

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Correspondence to Eric D Withee.

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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Withee, E.D., Tippens, K.M., Dehen, R. et al. Effects of MSM on exercise-induced muscle and joint pain: a pilot study. J Int Soc Sports Nutr 12 (Suppl 1), P8 (2015). https://doi.org/10.1186/1550-2783-12-S1-P8

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  • DOI: https://doi.org/10.1186/1550-2783-12-S1-P8