A pilot randomized, placebo-controlled clinical trial to investigate the efficacy and safety of an extract of Artemisia annua administered over 12 weeks, for managing pain, stiffness, and functional limitation associated with osteoarthritis of the hip and knee

Abstract

The objective of this study was to investigate the safety and efficacy of a dietary supplement, Arthrem, containing an extract from the medicinal plant Artemisia annua, on pain, stiffness, and functional limitation in osteoarthritis (OA) of the hip or knee. Forty-two patients were randomized to one of three groups (n = 14 in each group): 150-mg Artemisia annua extract (ART) twice daily (BD) (ART low dose), 300-mg ART BD (ART high dose), or placebo BD administered over 12 weeks. Efficacy was assessed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC®) and visual analog scale (VAS) for pain. Participants treated with ART low dose demonstrated significant improvement in WOMAC total scores from baseline to 12 weeks (mean change, −12.2; standard deviation, [SD] 13.84; p = 0.0159); improvement was not shown in the placebo group (mean change, −7.8; SD, 19.80; p = 0.1029). Statistically significant reductions were seen from baseline in the ART low-dose group for individual WOMAC components stiffness and physical function. VAS pain scores were statistically significantly reduced from baseline to 12 weeks in the ART low-dose group (mean change, −21.4 mm; SD, 23.48 mm; p = 0.0082) but not the placebo group (mean change, −11.5 mm; SD, 28.97 mm, p = 0.1757). No statistically significant changes occurred from baseline in the placebo or ART high-dose groups for any parameter. ART low dose was well tolerated. ART has potential as an anti-inflammatory/analgesic in OA. Treatment with ART 150 mg BD is associated with clinically relevant reductions in pain over 12 weeks. Further studies are warranted.

This is a preview of subscription content, log in to check access.

Fig. 1
Fig. 2
Fig. 3

References

  1. 1.

    Graziose R, Lila MA, Raskin I (2010) Merging traditional Chinese medicine with modern drug discovery technologies to find novel drugs and functional foods. Curr Drug Discov Technol 7:2–12

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  2. 2.

    Miller LH, Su X (2011) Artemisinin: discovery from the Chinese herbal garden. Cell 146:855–8

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  3. 3.

    Nosten F, White NJ (2007) Artemisinin-based combination treatment of falciparum malaria. Am J Trop Med Hyg 77:181–92

    CAS  PubMed  Google Scholar 

  4. 4.

    Bellamy N, Brooks PM (1986) Current practice in antimalarial drug prescribing in rheumatoid arthritis. J Rheumatol 13:551–5

    CAS  PubMed  Google Scholar 

  5. 5.

    Hunt S, Yoshida M, Davis CE, Greenhill NS, Davis PF (2015) An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils. J Inflamm Res 8:9–14

    Article  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Roberts E, Delgado Nunes V, Buckner S, Latchem S, Constanti M, Miller P et al (2015) Paracetamol: not as safe as we thought? A systematic literature review of observational studies. Ann Rheum Dis. doi:10.1136/annrheumdis-2014-206914

    PubMed Central  Google Scholar 

  7. 7.

    Makris UE, Abrams RC, Gurland B, Reid MC (2014) Management of persistent pain in the older patient: a clinical review. JAMA 312:825–36

    Article  PubMed  PubMed Central  Google Scholar 

  8. 8.

    Ernst E (1998) Usage of complementary therapies in rheumatology: a systematic review. Clin Rheumatol 17:301–5

    CAS  Article  PubMed  Google Scholar 

  9. 9.

    De Silva V, El-Metwally A, Ernst E, Lewith G, Macfarlane GJ (2011) Arthritis Research UK Working Group on Complementary and Alternative Medicines. Evidence for the efficacy of complementary and alternative medicines in the management of osteoarthritis: a systematic review. Rheumatology (Oxford) 50:911–20

    Article  Google Scholar 

  10. 10.

    Bellamy N, Buchanan WW, Goldsmith CH, Campbell J, Stitt LW (1988) Validation study of WOMAC®: a health status instrument for measuring clinically important patient relevant outcomes to antirheumatic drug therapy in patients with osteoarthritis of the hip or knee. J Rheumatol 15:1833–40

    CAS  PubMed  Google Scholar 

  11. 11.

    Krishnan E, Sokka T, Häkkinen A, Hubert H, Hannonen P (2004) Normative values for the Health Assessment Questionnaire disability index: benchmarking disability in the general population. Arthritis Rheum 50:953–60

    Article  PubMed  Google Scholar 

  12. 12.

    Doherty M, Dieppe P (2009) The “placebo” response in osteoarthritis and its implications for clinical practice. Osteoarthr Cartil 17:1255–62

    CAS  Article  PubMed  Google Scholar 

  13. 13.

    Todd KH (1996) Clinical versus statistical significance in the assessment of pain relief. Ann Emerg Med 27:439–41

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Hawker GA, Stewart L, French MR, Cibere J, Jordan JM, March L et al (2008) Understanding the pain experience in hip and knee osteoarthritis—an OARSI/OMERACT initiative. Osteoarthr Cartil 16:415–22

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Shou-zhong Y (1997) The Divine Farmer’s Materia Medica: a translation of the Shen Nong Ben Cao Jing. Blue Poppy Press, Boulder

    Google Scholar 

  16. 16.

    Zhang YX, Sun HX (2009) Immunosuppressive effect of ethanol extract of Artemisia annua on specific antibody and cellular responses of mice against ovalbumin. Immunopharmacol Immunotoxicol 31:625–30

    Article  PubMed  Google Scholar 

  17. 17.

    Cuzzocrea S, Saadat F, Di Paola R, Mirshafiey A (2005) Artemether: a new therapeutic strategy in experimental rheumatoid arthritis. Immunopharmacol Immunotoxicol 27:615–30

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Wang JX, Tang W, Zhou R, Wan J, Shi LP, Zhang Y et al (2008) The new water-soluble artemisinin derivative SM905 ameliorates collagen-induced arthritis by suppression of inflammatory and Th17 responses. Br J Pharmacol 153:1303–10

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  19. 19.

    Ferreira JF, Luthria DL, Sasaki T, Heyerick A (2010) Flavonoids from Artemisia annua L. as antioxidants and their potential synergism with artemisinin against malaria and cancer. Molecules 15:3135–70

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Rasoanaivo P, Wright CW, Willcox ML, Gilbert B (2011) Whole plant extracts versus single compounds for the treatment of malaria: synergy and positive interactions. Malar J 10(Suppl 1):S4

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

The authors thank Liam Harker MSc (Research Scientist, Promisia Ltd) for data management and study monitoring and Liz English (Bellbird Editing) for editorial assistance.

Author information

Affiliations

Authors

Corresponding author

Correspondence to Simon Stebbings.

Ethics declarations

Compliance with ethical standards

The study was conducted according to the principals of good clinical practice, which protects the rights, safety, and well-being of trial subjects in accordance with the principles of the Declaration of Helsinki. All patients provided written informed consent before any study-related procedures. The study received ethical approval from the Health and Disability Ethics Committee New Zealand (14/NTB/11).

Disclosures and conflict of interest

The study was funded by Promisia Ltd., the manufacturer of the extract of Artemisia used in the study. S Hunt and E Beattie are employees of Promisia Ltd.

Dr Hunt provided assistance in the design of the study. The interpretation of data and writing of the manuscript was performed by Dr Stebbings. Dr Hunt had input into the manuscript. Ms Beattie performed all statistical analysis and randomization. The final decision to publish lay solely with Dr Stebbings.

Dr Stebbings has no financial interests or other conflicts of interest in association with Promisia Ltd, including stock ownership, honoraria, paid expert testimony, or personal relationships, which may inappropriately influence the conduct of the trial.

There are no conflicts of interest for D McNamara.

Additional information

ACTRN12614000259640

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Stebbings, S., Beattie, E., McNamara, D. et al. A pilot randomized, placebo-controlled clinical trial to investigate the efficacy and safety of an extract of Artemisia annua administered over 12 weeks, for managing pain, stiffness, and functional limitation associated with osteoarthritis of the hip and knee. Clin Rheumatol 35, 1829–1836 (2016). https://doi.org/10.1007/s10067-015-3110-z

Download citation

Keywords

  • Anti-inflammatory agents
  • Artemisia annua
  • Dietary supplements
  • Herbal medicine
  • Osteoarthritis
  • Randomized controlled trial