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Evening Primrose Oil

How It Works

Bottom Line: Evening primrose oil has not been shown to treat or prevent cancer.

Scientists have not figured out how exactly evening primrose oil exerts its effects, but theorize that it has anti-inflammatory activity. It may be beneficial for patients with mastalgia (breast pain). It may also help those with diabetes, heart disease, cancer, premenstrual syndrome, eczema, or high cholesterol conditions but there is no enough data to support such effects.

Purported Uses

  • To treat cancer
    Evening primrose oil had no effect on tumor size or survival in patients with liver cancer. In another study, patients with breast cancer who received GLA in addition to Tamoxifen had faster response to treatment than those who received Tamoxifen alone.
  • To treat diabetic neuropathy
    Studies in animals suggest that evening primrose oil can prevent or reverse diabetic neuropathy, and one clinical trial almost 20 years ago supported this use. However, more research is needed.
  • To treat eczema
    Clinical trials show conflicting results.
  • To treat gastrointestinal disorders such as colitis or irritable bowel syndrome
    One clinical trial has studied the effects of evening primrose oil on ulcerative colitis, showing weak effects. In general, there is little support for this use.
  • To reduce high cholesterol
    One small clinical trial suggested that evening primrose oil led to a decrease in LDL ("bad") cholesterol, but these findings have not been confirmed by additional studies.
  • To relieve breast pain (mastalgia)
    A handful of clinical trials support this use, especially for mastalgia associated with menstrual cycle.
  • To relieve menopausal symptoms
    One clinical trial found that evening primrose oil was no better than placebo at relieving menopausal hot flashes.
  • To prevent premenstrual syndrome (PMS)
    Results of clinical trials are inconsistent.
  • To reduce inflammation of rheumatoid arthritis
    Two clinical trials have shown an improvement in subjective symptoms of rheumatoid arthritis, but no changes in the actual disease process.

    • Research Evidence

      Premenstrual syndrome (PMS):
      A meta-analysis compiled and analyzed the results of seven clinical trials that used evening primrose oil to prevent premenstrual syndrome. Overall, evening primrose oil had no consistent effect on premenstrual syndrome. However, most of the clinical trials were small, so it may be the case that no effect was seen simply because there were too few patients. Nonetheless, on current evidence, evening primrose oil is of little value in the management of premenstrual syndrome.

      Mastalgia (breast pain):
      The results of several clinical trials and volunteer studies conducted in the United Kingdom were compiled to measure the effect of evening primrose oil on mastalgia (breast pain). Overall, evening primrose oil was found to have a similar level of effectiveness as bromocriptine (a drug used to treat mastalgia), having beneficial effects in 44% of women treated. However, this was less effective than treatment with danazol, another medication. Treatment with evening primrose oil was more effective in women with cyclical mastalgia than in women with non-cyclical pain. Another study found evening primrose oil no more effective than wheat-germ oil in the treatment of breast pain.

      Warnings

    • This product is regulated by the FDA as a dietary supplement. Unlike approved drugs, supplements are not required to be manufactured under specific standardized conditions. This product may not contain the labeled amount or may be contaminated. In addition, it may not have been tested for safety or effectiveness.

    • Do Not Take If

    • You are pregnant.
    • You are taking anticoagulants or antiplatelet agents (Evening primrose oil may enhance their effects.)
    • You are taking phenothiazines such as fluphenazine (Evening primrose oil may lower the seizure threshold and increase the risk of seizures in patients taking phenothiazines).

    • Side Effects

    • Headache
    • Stomach upset
    • Nausea
    • Increased risk of pregnancy complications

    • Scientific Name

      Oenothera biennis

      Common Name

      EPO, night willow herb, fever plant, king's cure-all

      Clinical Summary

      Derived from the plant Oenothera biennis, evening primrose oil (EPO) is used for rheumatoid arthritis, premenstrual syndrome, eczema, fatigue, diabetic neuropathy and mastalgia. EPO contains gamma-linolenic acid (GLA), a primary fixed oil that is converted to dihomo-gamma-linolenic-acid, a prostaglandin precursor (2) (3). One study showed GLA to be an effective adjunctive therapy for breast cancer (4). It may also prevent weight regain in individuals who recently experienced major weight loss (5).
      In vitro studies indicate that EPO may inhibit platelet aggregation (6) (7). Clinical efficacy data are inconsistent. EPO has been shown in small studies to be effective against atopic dermatitis (18) and 5-azacitidine-induced skin reactions in patients with myelodysplastic syndromes (MLD) (19). But conclusions from a meta analysis indicate that EPO is ineffective in treating mastalgia (1).
      Adverse reactions include headache and GI disturbances. EPO should not be taken during pregnancy (8).
      One study reported a reduced seizure threshold when EPO was combined with phenothiazine antipsychotics (9).
      Although EPO does not have intrinsic estrogenic properties, some commercial products combine EPO with phytoestrogens. Patients with hormone-sensitive cancer should use EPO products with caution.

      Purported uses

    • Cancer treatment
    • Diabetic neuropathy
    • Eczema
    • GI disorders
    • High cholesterol
    • Mastalgia
    • Menopausal symptoms
    • Premenstrual syndrome
    • Rheumatoid arthritis

    • Constituents

    • Fixed oils: Cis-Linoleic acid, cis-gammalinolenic acid (GLA), oleic acid, palmitic acid and stearic acid
      (10)

    • Mechanism of Action

      Theoretically, GLA can be converted directly to the prostaglandin, precursor dihomo-GLA. The administration of the oil might be beneficial to individuals unable to metabolize cis-linolenic acid to GLA and to produce subsequent intermediates of considerable metabolic significance, including prostaglandins.
      (2) (3)

      Pharmacokinetics

      Repeated oral administration of evening primrose oil (480 mg/day gamma-linoleic acid/day) to healthy volunteers resulted in mean Cmax of approximately 20.7-22.6 mcg/ml. Gamma-linoleic acid levels were approximately 4.5 times greater from baseline in all patients, but serum levels of other fatty acids did not change significantly from baseline. Gastric absorption and Tmax for morning doses was longer than Tmax for identical doses given in the evening.
      (11)

      Contraindications

      Pregnant women should not take evening primrose oil due to increased risk of pregnancy complications. (8)


      Adverse Reactions

      Reported: Headache, GI upset, nausea, and increased risk of pregnancy complications
      Petechiae and ecchymoses were observed in a neonate whose mother used raspberry leaf tea and evening primrose oil (vaginally and orally) 1 week before childbirth.
      (12)

      Herb-Drug Interactions

      Anticoagulants / Antiplatelets: May have additive effects and increase risk of bleeding.
      Phenothiazines (e.g. fluphenazine): Evening primrose oil may lower the seizure threshold and precipitate seizures in patients taking phenothiazines.
      (9)


      Literature Summary and Critique

      Blommers J, et al. Evening primrose oil and fish oil for severe chronic astalgia: a randomized, double-blind, controlled trial. Am J Obstet Gynecol. 2002 Nov;187(5):1389-94.
      This clinical trial involved one hundred and twenty premenopausal women to evaluate the effect of evening primrose oil and fish oil on mastalgia. The author concluded that primrose oil is no better than a placebo (wheat-germ oil) in treating breast pain.

      Srivastava A, et al. Evidence-based management of Mastalgia: a meta-analysis of randomised trials. Breast. Oct 2007;16(5):503-512.
      In a meta-analysis of commonly used treatments for mastalgia, including Evening primrose oil (EPO), Bromocriptine, Danazol, and Tamoxifen, previously reported randomized, placebo-controlled trials were analyzed. Three randomized, controlled trials of EPO were included along with 1 trial of gamma-linolenic acid. Although Bromocriptine, Danazol, and Tamoxifen improved mastalgia, EPO was ineffective and therefore should not be used for mastalgia relief.

      References

      1. Srivastava A, Mansel RE, Arvind N, et al. Evidence-based management of Mastalgia: a meta-analysis of randomised trials. Breast. Oct 2007;16(5):503-512.
      2. Belch JJ, Hill A. Evening primrose oil and borage oil in rheumatologic conditions. Am J Clin Nutr 2000;71:352S-6S.
      3. Tyler, V. Herbs of Choice, the Therapeutical Use of Phytomedicinals. Binghamton: Pharmaceutical Press; 1994.
      4. Kenny FS, et al. Gamma linolenic acid with Tamoxifen as primary therapy in breast cancer. Int J Cancer 2000; 85:643-8.
      5. Schirmer MA, Phinney SD. Gamma-linolenate reduces weight regain in formerly obese humans. J Nutr. Jun 2007;137(6):1430-1435.
      6. De La Cruz JP, Martin-Romero M, Carmona JA, et al. Effect of evening primrose oil on platelet aggregation in rabbits fed an atherogenic diet. Thromb Res. Jul 1 1997;87(1):141-149.
      7. Guivernau M, Meza N, Barja P, Roman O. Clinical and experimental study on the long-term effect of dietary gamma-linolenic acid on plasma lipids, platelet aggregation, thromboxane formation, and prostacyclin production. Prostaglandins Leukot Essent Fatty Acids. Nov 1994;51(5):311-316.
      8. Dove D, Johnson P. Oral evening primrose oil: its effect on length of pregnancy and selected intrapartum outcomes in low-risk nulliparous women. J Nurse Midwifery. 1999 May-Jun;44(3):320-4.
      9. Holman CP, et al. A trial of evening primrose oil in the treatment of chronic schizophrenia. J Orthomolecular Psychiatry 1983;12:302-4.
      10. Newall C. Herbal Medicines, A Guide for Health Care Professionals. London: Pharmaceutical Press; 1997.
      11. Martens-Lobenhoffer J, Meyer FP. Pharmacokinetic data of gamma-linoleic acid in healthy volunteers after the administration of evening primrose oil (Epogam). Int J Clin Pharmacology Therapeutics 1998;36:363-6.
      12. Wedig KE, Whitsett JA. Down the primrose path: petechiae in a neonate exposed to herbal remedy for parturition. J Pediatr. Jan 2008;152(1):140, 140 e141.
      13. Zurier RB, et al. Gamma-linolenic acid treatment of rheumatoid arthritis. A randomized, placebo-controlled trial. Arthritis Rheum 1996;39:1808-17.
      14. Budeiri D, et al. Is evening primrose oil of value in the treatment of premenstrual syndrome? Control Clin Trials 1996;17:60-8.
      15. Keen H, et al. Treatment of diabetic neuropathy with gamma-linolenic acid. Diabetes Care 1993;16:8-15.
      16. Pye JK, et al. Clinical experience of drug treatment for mastalgia. Lancet 1985;2:373-7.
      17. Blommers J, et al. Evening primrose oil and fish oil for severe chronic astalgia: a randomized, double-blind, controlled trial. Am J Obstet Gynecol. 2002 Nov;187(5):1389-94.
      18. Senapati S, Banerjee S, Gangopadhyay DN. Evening primrose oil is effective in atopic dermatitis: a randomized placebo-controlled trial. Indian J Dermatol Venereol Leprol. 2008 Sep-Oct;74(5):447-52.
      19. Platzbecker U, Aul C, Ehninger G, Giagounidis A. Reduction of 5-azacitidine induced skin reactions in MDS patients with evening primrose oil. Ann Hematol. 2009 Aug 28. [Epub ahead of print]

      Last Updated: Dec. 4, 2009
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