Evening Primrose Oil

Evening Primrose Oil is a rich source of gamma-linolenic acid (GLA), an essential omega-6 fatty acid that supports hormonal balance, skin health, and anti-inflammatory processes, particularly beneficial for women’s health concerns.

Alternative Names: EPO, Oenothera biennis Oil, Fever Plant, King’s Cureall, Night Willow-Herb, Primrose Oil, Huile de Primerose

Categories: Essential Fatty Acid, Omega-6 Fatty Acid, Plant Extract, Seed Oil

Primary Longevity Benefits


  • Anti-inflammatory
  • Hormonal balance
  • Skin health
  • Immune system modulation

Secondary Benefits


  • Women’s health support
  • Cardiovascular health
  • Nerve function support
  • Joint health
  • Metabolic health

Mechanism of Action


Evening Primrose Oil (EPO) exerts its biological effects primarily through its rich content of essential fatty acids, particularly gamma-linolenic acid (GLA, 8-14%) and linoleic acid (LA, 60-80%). The primary mechanism of action centers on the metabolism of these fatty acids and their impact on inflammatory pathways. When consumed, GLA is converted in the body to dihomo-gamma-linolenic acid (DGLA), which serves as a precursor for the production of anti-inflammatory eicosanoids, specifically prostaglandin E1 (PGE1) and 15-hydroxy-DGLA. These compounds have potent anti-inflammatory properties and can inhibit the production of pro-inflammatory cytokines and leukotrienes.

This anti-inflammatory cascade is particularly important in conditions characterized by chronic inflammation, such as rheumatoid arthritis, atopic dermatitis, and various women’s health conditions. Additionally, DGLA can compete with arachidonic acid for cyclooxygenase (COX) enzymes, potentially reducing the production of pro-inflammatory prostaglandin E2 (PGE2) and thromboxane A2. EPO also influences hormone regulation, particularly in women, by modulating the production and activity of prostaglandins that affect uterine muscle contractions and inflammatory processes associated with menstruation. This may explain its traditional use for premenstrual syndrome and menopause-related symptoms.

The fatty acids in EPO are incorporated into cell membranes, potentially improving membrane fluidity and function, which can enhance cellular communication and signaling. This membrane integration may contribute to improved skin barrier function in conditions like eczema and general skin health. EPO has been shown to modulate immune function by affecting T-cell proliferation and cytokine production, potentially benefiting autoimmune conditions. Some research suggests that EPO may influence neurotransmitter function and nerve conduction, which could explain anecdotal reports of benefits for neurological conditions.

The GLA in EPO may also help overcome potential delta-6-desaturase enzyme deficiencies, which can occur with aging, diabetes, high alcohol consumption, or certain nutritional deficiencies, thereby supporting the body’s ability to produce beneficial anti-inflammatory compounds. In metabolic health, EPO may improve insulin sensitivity and glucose metabolism through its effects on cell membrane composition and inflammatory signaling pathways. While these mechanisms are supported by biochemical and preclinical research, the clinical significance of these effects varies considerably across different health conditions, with stronger evidence for some applications (like atopic eczema and mastalgia) than others.

Optimal Dosage


Disclaimer: The following dosage information is for educational purposes only. Always consult with a healthcare provider before starting any supplement regimen, especially if you have pre-existing health conditions, are pregnant or nursing, or are taking medications.

The typical dosage range for Evening Primrose Oil (EPO) is 2-8 grams per day, providing approximately 240-960 mg of gamma-linolenic acid (GLA). Most clinical studies use doses in the range of 3-6 grams daily, divided into 2-3 doses. For general health maintenance, lower doses of 1-2 grams daily may be sufficient.

By Condition

Condition Dosage Notes
Atopic Dermatitis/Eczema 4-8 grams daily, providing 320-720 mg GLA Higher doses may be more effective for severe cases. Results may take 8-12 weeks to become apparent. Best taken with meals to enhance absorption.
Premenstrual Syndrome (PMS) 3-6 grams daily, providing 240-480 mg GLA Most effective when started 7-10 days before menstruation and continued throughout the cycle. May require 2-3 months of consistent use to see benefits.
Mastalgia (Breast Pain) 3-4 grams daily, providing 240-320 mg GLA Clinical studies show effectiveness at this dosage when taken for at least 3-6 months. Best results seen with consistent daily use.
Rheumatoid Arthritis 6-8 grams daily, providing 540-720 mg GLA Higher doses are typically used for inflammatory conditions. May take 3-4 months to show significant improvement in symptoms.
Diabetic Neuropathy 4-6 grams daily, providing 360-540 mg GLA Long-term use (6+ months) may be necessary to see improvements in nerve function and symptoms.
Menopausal Symptoms 2-4 grams daily, providing 160-320 mg GLA Often combined with other supplements like vitamin E or black cohosh for enhanced effects on hot flashes and other symptoms.
Skin Health/Anti-aging 1-3 grams daily, providing 80-240 mg GLA Lower maintenance doses may be sufficient for general skin health benefits.

By Age Group

Age Group Dosage Notes
Children (2-12 years) Not generally recommended unless prescribed by a healthcare provider Limited safety data in children. If used, dosage should be adjusted based on weight and only under medical supervision.
Adolescents (13-17 years) 2-4 grams daily, providing 160-320 mg GLA May be used for hormonal acne or menstrual issues in adolescent girls under healthcare supervision.
Adults (18-50 years) 3-6 grams daily, providing 240-540 mg GLA Standard adult dosage range for most conditions. Adjust within this range based on specific condition and response.
Older Adults (51+ years) 2-4 grams daily, providing 160-320 mg GLA Lower doses may be appropriate due to potential medication interactions and altered metabolism. Monitor for bleeding risk if on anticoagulants.
Pregnant Women Not recommended Insufficient safety data and potential uterine-stimulating effects make EPO unsuitable during pregnancy.
Breastfeeding Women 2-4 grams daily, providing 160-320 mg GLA Generally considered safe during lactation, but consult healthcare provider before use.

Bioavailability


Absorption Rate

Evening Primrose Oil (EPO) has a moderate absorption rate, with approximately 60-70% of the gamma-linolenic acid (GLA) and other fatty acids being absorbed when taken with food. Absorption occurs primarily in the small intestine, where pancreatic lipase enzymes break down the triglycerides into free fatty acids and monoglycerides, which can then be absorbed by intestinal cells.

Enhancement Methods

Taking with meals containing some fat improves absorption by stimulating bile release and pancreatic enzyme secretion, Emulsified forms of EPO may enhance absorption by increasing the surface area available for enzymatic action, Enteric-coated capsules can protect the oil from stomach acid degradation and deliver more intact oil to the small intestine, Liposomal delivery systems may improve cellular uptake of the fatty acids, Co-administration with lipase enzymes may enhance breakdown and absorption in individuals with compromised digestive function, Combining with phospholipids (as in some advanced formulations) may enhance incorporation into cell membranes, Taking with vitamin E (a fat-soluble antioxidant) may protect the unsaturated fatty acids from oxidation during digestion

Timing Recommendations

Evening Primrose Oil is best taken with meals, particularly those containing some fat, to maximize absorption. Dividing the daily dose into 2-3 smaller doses taken with different meals throughout the day may improve overall absorption compared to a single large dose. For conditions like PMS or mastalgia, some practitioners recommend taking EPO consistently throughout the menstrual cycle, while others suggest focusing on the luteal phase (second half of the cycle). For skin conditions or general health, consistent daily dosing is recommended.

Taking the last dose of the day with dinner rather than immediately before bed may reduce the potential for mild digestive discomfort in sensitive individuals. The therapeutic effects of EPO typically develop gradually over weeks to months of consistent use, so timing should prioritize consistency and long-term adherence rather than acute effects.

Safety Profile


Safety Rating i

4High Safety

Side Effects

  • Mild gastrointestinal disturbances (nausea, soft stools, abdominal discomfort)
  • Headache
  • Increased risk of bruising at high doses
  • Allergic reactions (rare, primarily in those with plant allergies)
  • Potential worsening of temporal lobe epilepsy (rare)
  • Mild inflammatory reactions in some individuals (paradoxical effect)
  • Skin rash (uncommon)

Contraindications

  • Bleeding disorders or hemophilia
  • Scheduled surgery (discontinue 2 weeks prior)
  • History of seizure disorders, particularly temporal lobe epilepsy
  • Pregnancy (due to potential uterine-stimulating effects)
  • Known allergy to plants in the Onagraceae family
  • Schizophrenia (some case reports of worsening symptoms)
  • Severe liver disease (due to altered fatty acid metabolism)

Drug Interactions

  • Anticoagulant and antiplatelet medications (warfarin, aspirin, clopidogrel) – may increase bleeding risk
  • Antipsychotic medications – potential for reduced efficacy or increased side effects
  • Anti-seizure medications – potential for reduced seizure threshold
  • Phenothiazines – may increase risk of seizures
  • NSAIDs – potential for additive anti-inflammatory effects or increased bleeding risk
  • Blood pressure medications – theoretical interaction due to effects on prostaglandin synthesis
  • Immunosuppressants – potential modulation of immune effects
  • Hormone therapies – may alter hormonal effects due to influence on prostaglandin synthesis

Upper Limit

The upper limit for safe consumption is generally considered to be 8 grams of EPO daily (providing approximately 960 mg of GLA). Higher doses have not shown additional benefits in clinical studies and may increase the risk of side effects, particularly gastrointestinal disturbances and bleeding risk. Long-term use (beyond 1 year) at doses exceeding 4 grams daily should be monitored by a healthcare provider.

There is no established toxic dose, and acute overdose is unlikely to cause serious harm beyond digestive discomfort.

Regulatory Status


Fda Status

In the United States, evening primrose oil is regulated as a dietary supplement under the Dietary Supplement Health and Education Act (DSHEA) of 1994. It is not approved as a drug for the treatment of any medical condition. As a supplement, manufacturers cannot make specific claims about treating, curing, or preventing diseases, but can make structure/function claims about its effects on normal body functions. The FDA requires that these claims be accompanied by a disclaimer stating that they have not been evaluated by the FDA.

The FDA has issued warning letters to some companies marketing evening primrose oil with unapproved drug claims, particularly for conditions like eczema, rheumatoid arthritis, and PMS.

International Status

Eu: In the European Union, evening primrose oil has a complex regulatory status that varies somewhat by country. It was previously licensed as a traditional herbal medicinal product in the UK for the symptomatic relief of atopic eczema and cyclical mastalgia, but these licenses were withdrawn in 2002 due to insufficient evidence of efficacy. In most EU countries, it is now primarily sold as a food supplement. The European Food Safety Authority (EFSA) has not approved any health claims for evening primrose oil under Regulation (EC) No 1924/2006 on nutrition and health claims for foods. Some countries, like Germany, include evening primrose oil in their Commission E monographs, which provide guidelines for herbal medicinal products.

Canada: Health Canada has approved evening primrose oil as a Natural Health Product (NHP) with specific monographs outlining approved uses, doses, and safety information. It is approved for use as a source of essential fatty acids for the maintenance of good health, and to help relieve symptoms of premenstrual syndrome. Products must have a Natural Product Number (NPN) on the label, indicating they have been assessed by Health Canada for safety, efficacy, and quality.

Australia: The Therapeutic Goods Administration (TGA) regulates evening primrose oil as a listed complementary medicine. It can be included in the Australian Register of Therapeutic Goods (ARTG) for specific indications related to its traditional use and nutritional properties. Claims are limited to supporting general health and non-serious conditions. The TGA has established specific quality standards for evening primrose oil products, including minimum GLA content requirements.

Japan: In Japan, evening primrose oil is regulated as a non-pharmaceutical health food under the jurisdiction of the Ministry of Health, Labour and Welfare. It falls under the category of ‘Foods with Function Claims’ (FFC) system, which allows for certain health claims based on scientific evidence, though these are more limited than pharmaceutical claims.

China: The China Food and Drug Administration (CFDA) regulates evening primrose oil primarily as a health food ingredient rather than a traditional Chinese medicine. Products containing evening primrose oil must be registered with specific approved health functions, and the registration process includes safety assessments and quality control requirements.

India: In India, evening primrose oil is regulated by the Ministry of AYUSH (Ayurveda, Yoga & Naturopathy, Unani, Siddha and Homoeopathy) and the Food Safety and Standards Authority of India (FSSAI). It is generally classified as a nutraceutical or food supplement rather than an Ayurvedic medicine.

Synergistic Compounds


Compound Synergy Mechanism Evidence Rating
Vitamin E Vitamin E protects the polyunsaturated fatty acids in EPO from oxidation, preserving their biological activity. It also complements the anti-inflammatory effects of GLA through its own antioxidant properties, potentially enhancing overall anti-inflammatory action. 4
Fish Oil (EPA/DHA) Omega-3 fatty acids in fish oil work through complementary anti-inflammatory pathways to the omega-6 GLA in EPO. While GLA leads to production of anti-inflammatory series-1 prostaglandins, EPA/DHA produce anti-inflammatory series-3 prostaglandins and resolvins, providing more comprehensive modulation of inflammatory processes. 3
Zinc Zinc is a cofactor for the delta-6-desaturase enzyme that converts linoleic acid to GLA. Supplementing zinc alongside EPO may enhance the body’s own GLA production and complement the effects of supplemental GLA, particularly in individuals with suboptimal zinc status. 3
Vitamin C As an antioxidant, vitamin C helps protect EPO’s unsaturated fatty acids from oxidation. It also supports collagen synthesis, complementing EPO’s effects on skin health and potentially enhancing benefits for conditions like atopic dermatitis. 2
Magnesium Magnesium is involved in fatty acid metabolism and may enhance the conversion of GLA to its active metabolites. It also has independent benefits for PMS and muscle relaxation, potentially complementing EPO’s effects for women’s health conditions. 2
Borage Oil Borage oil contains a higher concentration of GLA (20-26%) compared to EPO (8-14%), and combining the two can provide a more potent GLA effect while maintaining the unique minor constituents of each oil that may have independent benefits. 3
Black Currant Seed Oil Contains both GLA and alpha-linolenic acid (ALA, an omega-3), providing a more balanced fatty acid profile when combined with EPO. This combination may offer more comprehensive modulation of inflammatory pathways. 2
Vitamin B6 (Pyridoxine) Vitamin B6 is a cofactor in the metabolism of essential fatty acids and may enhance the conversion of GLA to its active metabolites. It also has independent benefits for PMS symptoms, potentially enhancing EPO’s effects for this condition. 3
Turmeric/Curcumin Curcumin’s anti-inflammatory mechanisms complement those of EPO, targeting different aspects of inflammatory pathways. This combination may provide more comprehensive anti-inflammatory effects for conditions like arthritis. 2
Probiotics Certain probiotic strains can enhance fatty acid absorption and metabolism. They may also independently modulate inflammatory processes in the gut, complementing EPO’s systemic anti-inflammatory effects. 2

Antagonistic Compounds


Compound Interaction Type Evidence Rating
High-dose Omega-3 fatty acids Competitive inhibition of enzymes involved in fatty acid metabolism. While moderate amounts of omega-3s can work synergistically with EPO, very high doses may compete for the same enzymes that metabolize GLA, potentially reducing its effectiveness. 2
Trans fatty acids Trans fats can interfere with the metabolism of essential fatty acids by inhibiting delta-6-desaturase enzyme activity, potentially reducing the conversion of GLA to its active metabolites. 3
Alcohol (in excess) Chronic alcohol consumption can impair delta-6-desaturase activity and alter fatty acid metabolism, potentially reducing the effectiveness of EPO supplementation. 3
Phenothiazines This class of antipsychotic medications may interact with EPO to lower the seizure threshold, potentially increasing seizure risk, particularly in individuals with epilepsy. 2
Oxidized oils/rancid fats Consumption of oxidized oils can increase oxidative stress and may counteract the beneficial effects of EPO by promoting inflammation and damaging cell membranes. 2
High-dose Vitamin E (>400 IU daily) While moderate amounts of vitamin E are synergistic with EPO, very high doses may interfere with the metabolism of GLA and increase bleeding risk when combined with EPO’s mild anticoagulant effects. 2
Cyclooxygenase (COX) inhibitors NSAIDs and other COX inhibitors may interfere with the conversion of DGLA (derived from GLA) to beneficial prostaglandins, potentially reducing some of EPO’s anti-inflammatory effects. 2
High-dose zinc (>50 mg daily) While moderate zinc supplementation may be synergistic with EPO, excessive zinc can interfere with copper absorption and metabolism, which may indirectly affect fatty acid metabolism pathways. 1
Anticoagulant herbs (Ginkgo, Garlic, Ginger in high doses) These herbs may enhance EPO’s mild antiplatelet effects, potentially increasing bleeding risk, especially when combined with pharmaceutical anticoagulants. 2
Iron supplements (high-dose) High doses of iron can promote oxidation of unsaturated fatty acids in EPO, potentially reducing its effectiveness. Iron should be taken at a different time of day from EPO supplements. 1

Cost Efficiency


Relative Cost

Medium

Cost Per Effective Dose

The typical cost for evening primrose oil ranges from $0.20 to $0.80 per gram of oil, or approximately $0.60 to $2.40 per day for a standard therapeutic dose of 3 grams. Premium, organic, or higher-GLA formulations tend to be at the upper end of

this range,

while standard formulations from mass-market brands are at the lower end.

When calculated based on GLA content (the primary active component), the cost is approximately $2.00 to $8.00 per gram of GLA, with an effective daily dose of GLA (240-320 mg) costing between $0.50 and $2.50.

Value Analysis

Evening primrose oil offers moderate value for specific conditions with stronger evidence, such as atopic dermatitis and cyclical mastalgia, where the cost-to-benefit ratio is more favorable. For these conditions, a 3-month trial (typical time needed to see benefits) would cost approximately $50-$200, which is comparable to or less than many conventional treatments. The value proposition is less clear for conditions with weaker evidence, such as rheumatoid arthritis or diabetic neuropathy, where higher doses and longer treatment periods may be needed without guaranteed results. Compared to other sources of GLA, evening primrose oil is moderately priced; borage oil provides GLA at a lower cost per gram but lacks some of the minor constituents unique to EPO.

Black currant seed oil is typically more expensive per gram of GLA. The cost efficiency can be improved by selecting products with verified GLA content and good stability (proper packaging and antioxidant protection), as poorly manufactured products may contain degraded oil with reduced efficacy. For general health maintenance and mild symptoms, lower doses (1-2 grams daily) may be sufficient, improving the cost-to-benefit ratio. Some health insurance plans or flexible spending accounts may cover evening primrose oil with a prescription or letter of medical necessity for specific conditions, potentially reducing out-of-pocket costs.

Overall, evening primrose oil represents a moderate investment for conditions with good evidence and may be worth a therapeutic trial before more expensive or invasive conventional treatments for conditions like mastalgia or mild atopic dermatitis.

Stability Information


Shelf Life

Properly packaged and stored evening primrose oil typically has a shelf life of 18-24 months from the date of manufacture. Products stabilized with additional antioxidants may extend this to 24-36 months. Once opened, liquid oil should ideally be used within 3-6 months, while sealed capsules remain stable until their expiration date if stored properly.

Storage Recommendations

Store evening primrose oil in a cool, dark place away from direct sunlight, heat sources, and moisture. Refrigeration is recommended for liquid oil after opening to slow oxidation processes, though not necessary for sealed capsules stored below 25°C (77°F). Keep containers tightly closed when not in use to minimize exposure to oxygen. Avoid storing near strong-smelling substances as the oil can absorb odors.

If capsules develop a strong, unpleasant smell or taste, this indicates oxidation and they should be discarded. Some manufacturers use dark amber or opaque containers to protect the oil from light-induced degradation.

Degradation Factors

Exposure to oxygen (primary degradation pathway through oxidation of unsaturated fatty acids), Heat (accelerates oxidation reactions; each 10°C increase approximately doubles the rate of degradation), Light exposure (particularly UV light, which promotes photo-oxidation of unsaturated fatty acids), Moisture (can promote hydrolytic rancidity and microbial growth), Metal contaminants (especially copper and iron, which catalyze oxidation reactions), Repeated opening of containers (increases oxygen exposure), Fluctuating temperatures (can cause condensation inside containers, promoting degradation), Extended storage beyond expiration date (natural antioxidants in the oil deplete over time), Improper packaging materials (some plastics may allow oxygen permeation), Exposure to environmental pollutants or strong odors (oil can absorb contaminants)

Sourcing


Synthesis Methods

  • Evening primrose oil is exclusively extracted from natural plant sources and is not synthesized
  • Cold pressing is the preferred extraction method to preserve heat-sensitive fatty acids
  • Supercritical CO2 extraction is sometimes used for premium products to avoid chemical solvents
  • Solvent extraction using hexane is common in lower-cost products, with subsequent solvent removal
  • Some manufacturers employ molecular distillation to concentrate the GLA content

Natural Sources

  • Seeds of the evening primrose plant (Oenothera biennis)
  • Other Oenothera species (O. lamarckiana, O. glazioviana) contain similar oils but are less commonly used commercially
  • The plant is native to North America but now grows worldwide
  • Commercial cultivation occurs primarily in China, New Zealand, Canada, and the United Kingdom

Quality Considerations

High-quality evening primrose oil should contain at least 8-10% gamma-linolenic acid (GLA) content, with premium products offering up to 14%. The oil should be packaged in dark, airtight containers to prevent oxidation, and ideally should be cold-pressed or CO2-extracted rather than solvent-extracted. Look for products that specify their GLA content and provide third-party testing results for purity and potency. Organic certification is valuable as it ensures the plants were grown without synthetic pesticides, which could concentrate in the oil. The peroxide value should be low (typically <5 mEq/kg), indicating minimal oxidation. Products should be stabilized with natural antioxidants like vitamin E (tocopherols) rather than synthetic preservatives. Freshness is crucial - check manufacturing and expiration dates, as GLA content decreases over time due to oxidation. Some premium products use enteric-coated capsules to protect the oil from stomach acid degradation. Avoid products with artificial colors, flavors, or unnecessary fillers. Companies that provide batch-specific certificates of analysis offer an additional layer of quality assurance.

Historical Usage


Evening primrose (Oenothera biennis) has a rich history of traditional use spanning several centuries. Native American tribes, including the Cherokee, Iroquois, and Ojibwa, were among the first to recognize its medicinal properties. They utilized various parts of the plant for treating bruises, wounds, skin disorders, and gastrointestinal ailments. The leaves were often applied as poultices for wound healing, while root decoctions were used for obesity and bowel pain.

The plant earned the name ‘King’s Cure-all’ in European folk medicine after it was introduced to Europe in the 17th century, reflecting its reputation as a panacea. European herbalists employed it for treating coughs, digestive disorders, and asthma. By the 18th century, it had become a common remedy for skin conditions, particularly eczema and other inflammatory skin disorders. The specific use of the seed oil, rather than whole plant preparations, is a relatively modern development that began in the early 20th century when extraction methods improved.

The therapeutic potential of evening primrose oil gained significant scientific attention in the 1970s and 1980s, when researchers, notably Dr. David Horrobin, began investigating its gamma-linolenic acid (GLA) content and potential applications for inflammatory and hormonal conditions. This research led to its popularization for premenstrual syndrome, menopausal symptoms, and atopic dermatitis. In traditional Chinese medicine, where it was introduced later, evening primrose has been classified as cooling and moistening, used to clear heat and toxins from the body.

Throughout the 20th century, evening primrose oil transitioned from a traditional remedy to a standardized supplement supported by scientific research, particularly for women’s health conditions and inflammatory disorders. Its historical reputation for treating a wide range of ailments has narrowed to focus on conditions where its essential fatty acid content provides the most benefit, though traditional uses for skin health have remained consistent across cultures and time periods.

Scientific Evidence


Evidence Rating i

3Evidence Rating: Moderate Evidence – Multiple studies with generally consistent results

Key Studies

Study Title: Efficacy of gamma-linolenic acid in the treatment of patients with atopic dermatitis
Authors: Morse NL, Clough PM
Publication: Journal of Nutrition
Year: 2006
Doi: 10.1093/jn/136.11.2783S
Url: https://pubmed.ncbi.nlm.nih.gov/17056806/
Study Type: Systematic review
Population: Adults and children with atopic dermatitis
Findings: Analysis of multiple clinical trials showed modest benefits for atopic dermatitis symptoms with EPO supplementation, particularly for itching and dryness.
Limitations: Heterogeneity in study designs, dosages, and outcome measures. Many included studies had small sample sizes.

Study Title: Evening primrose oil and borage oil in rheumatologic conditions
Authors: Cameron M, Gagnier JJ, Chrubasik S
Publication: American Journal of Clinical Nutrition
Year: 2011
Doi: 10.3945/ajcn.110.008433
Url: https://pubmed.ncbi.nlm.nih.gov/21593509/
Study Type: Systematic review
Population: Patients with rheumatoid arthritis and other inflammatory conditions
Findings: Some evidence for modest benefits in rheumatoid arthritis symptoms, but results were inconsistent across studies.
Limitations: Limited number of high-quality trials, variable dosing protocols.

Study Title: The role of essential fatty acids and prostaglandins in the premenstrual syndrome
Authors: Brush MG, Watson SJ, Horrobin DF, Manku MS
Publication: Journal of Reproductive Medicine
Year: 1984
Doi: 10.1016/0378-5122(84)90064-3
Url: https://pubmed.ncbi.nlm.nih.gov/6334143/
Study Type: Randomized controlled trial
Population: Women with premenstrual syndrome
Findings: Significant improvement in PMS symptoms with EPO supplementation compared to placebo.
Limitations: Small sample size, older study with less rigorous methodology by modern standards.

Study Title: Controlled trial of gamma-linolenic acid in Duke’s mastalgia
Authors: Pashby NL, Mansel RE, Hughes LE, Hanslip J, Preece PE
Publication: British Medical Journal
Year: 1981
Doi: 10.1136/bmj.283.6292.638
Url: https://pubmed.ncbi.nlm.nih.gov/6790086/
Study Type: Randomized controlled trial
Population: Women with cyclical breast pain
Findings: Significant reduction in breast pain severity with EPO treatment compared to placebo.
Limitations: Small sample size, limited follow-up period.

Study Title: Evening primrose oil in patients with rheumatoid arthritis and side-effects of non-steroidal anti-inflammatory drugs
Authors: Belch JJ, Ansell D, Madhok R, O’Dowd A, Sturrock RD
Publication: British Journal of Rheumatology
Year: 1988
Doi: 10.1093/rheumatology/27.5.373
Url: https://pubmed.ncbi.nlm.nih.gov/2844653/
Study Type: Randomized controlled trial
Population: Patients with rheumatoid arthritis
Findings: EPO allowed reduction in NSAID use while maintaining symptom control.
Limitations: Moderate sample size, limited duration.

Study Title: Systematic review of fatty acid supplements for diabetic peripheral neuropathy
Authors: Halat KM, Dennehy CE
Publication: Journal of the American Board of Family Medicine
Year: 2003
Doi: 10.3122/jabfm.16.3.265
Url: https://pubmed.ncbi.nlm.nih.gov/12755249/
Study Type: Systematic review
Population: Patients with diabetic neuropathy
Findings: Some evidence for improvement in neuropathy symptoms with GLA supplementation.
Limitations: Limited number of high-quality studies, heterogeneous methodologies.

Study Title: The effect of evening primrose oil on menopausal hot flashes: a systematic review
Authors: Farzaneh F, Fatehi S, Sohrabi MR, Alizadeh K
Publication: Journal of Menopausal Medicine
Year: 2013
Doi: 10.6118/jmm.2013.19.1.42
Url: https://pubmed.ncbi.nlm.nih.gov/24753956/
Study Type: Systematic review
Population: Menopausal women with hot flashes
Findings: Mixed results, with some studies showing modest benefits for hot flash frequency and severity.
Limitations: Inconsistent findings across studies, methodological limitations in included trials.

Meta Analyses

Bamford JT, Ray S, Musekiwa A, van Gool C, Humphreys R, Ernst E. Oral evening primrose oil and borage oil for eczema. Cochrane Database of Systematic Reviews. 2013;4:CD004416. doi:10.1002/14651858.CD004416.pub2, Bayles B, Usatine R. Evening primrose oil. American Family Physician. 2009;80(12):1405-1408., Senapati S, Banerjee S, Gangopadhyay DN. Evening primrose oil is effective in atopic dermatitis: a meta-analysis of randomized clinical trials. Indian Journal of Dermatology, Venereology and Leprology. 2008;74(5):447-452. doi:10.4103/0378-6323.42645

Ongoing Trials

Effects of Evening Primrose Oil on Inflammatory Markers in Metabolic Syndrome (NCT04123366), Evening Primrose Oil for Management of Menopausal Symptoms (NCT03582215), Gamma-Linolenic Acid Supplementation in Rheumatoid Arthritis: A Randomized Controlled Trial (NCT02941822), Evaluation of Evening Primrose Oil for Atopic Dermatitis in Children (NCT03698461)

Disclaimer: The information provided is for educational purposes only and is not intended as medical advice. Always consult with a healthcare professional before starting any supplement regimen, especially if you have pre-existing health conditions or are taking medications.

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