Intervention With Long-chain n-3 Polyunsaturated Fatty Acids From Microalgae Oil in Patients With Rheumatoid Arthritis

Sponsor
University of Jena (Other)
Overall Status
Completed
CT.gov ID
NCT01742468
Collaborator
German Federal Ministry of Education and Research (Other)
38
2
2
7
19
2.7

Study Details

Study Description

Brief Summary

The study was performed to investigate the effects of a daily consumption of n-3 LC-PUFA supplemented products (sausage, tomato spread, milk beverage) on disease activity, inflammatory markers, and cardiovascular risk factors in patients with rheumatoid arthritis.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: long-chain n-3 PUFA
  • Dietary Supplement: sunflower oil
N/A

Detailed Description

Recent studies suggest that the daily intake of n-3 LC-PUFA (eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)) can support the therapy of chronic-inflammatory diseases and might be useful to prevent coronary heart diseases. The majority of these studies do not differentiate between the effects of EPA and DHA. The present study investigate the therapeutic potential of DHA in patients with rheumatoid arthritis.

As a precondition for participating in this study, the patients were provided information in writing and verbally form about the details of the study. Written informed consent was obtained from all volunteers. Before the beginning of the study, all patients were subject to a medical examination by their general rheumatologist. Thirty-eight patients with rheumatoid arthritis (DAS ≥ 2.4) entered the study.

The placebo-controlled, randomized double-blind cross-over study consists of two investigation periods of 10 weeks, with a ten-week washout period in between (after the washout period the intervention was crossed between the groups and the respective products were consumed for further 10 weeks).

Patients in the placebo period receive 60 g sausage, 8 g tomato spread and 30 g milk powder (= 200 mL milk beverage) daily. These products were enriched with sunflower oil (8 g/d).

In the intervention period, the products (60 g sausage, 8 g tomato spread and 30 g milk powder (= 200 mL milk beverage) were enriched with 8 g microalgae oil (Schizochytrium sp., Maris DHA oil, no. 3790, IOI, Hamburg, Germany). In this group, the daily dose of docosahexaenoic acid (DHA) amounted to 2.11 g.

Venous blood is collected at the beginning and at the end of each period.

• Disease activity was determined by sum of tender and swollen joints (68/66), joint score DAS28, ultrasound score (US-7 score), rheumascan, inflammatory markers (ESR, C reactive protein), HAQ questionnaire and further lifestyle forms

Study Design

Study Type:
Interventional
Actual Enrollment :
38 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Intervention With Products Enriched With Long Chain n-3 Polyunsaturated Fatty Acids (n-3 LC-PUFA) From Microalgae Oil in Patients With Rheumatoid Arthritis - Influence on Disease Activity and Inflammation Status
Study Start Date :
Feb 1, 2013
Actual Primary Completion Date :
Sep 1, 2013
Actual Study Completion Date :
Sep 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dietary supplement: n-3 LC-PUFA

Name: microalgae oil (Schizochytrium sp., Maris DHA oil, no. 3790, IOI, Hamburg, Germany; rich in docosahexaenoic acid (DHA); Dosage: 8 g oil per day = 2.11 g DHA per day; Dosage form: 8g oil was included in 60 g sausage, 8 g tomato spread, 30 g milk powder

Dietary Supplement: long-chain n-3 PUFA
Dietary supplement: n-3 LC-PUFA = Microalgae oil (Schizochytrium sp., Maris DHA oil, no. 3790, IOI, Hamburg, Germany (rich in docosahexaenoic acid (DHA)); Dosage: 8 g oil per day = 2.11 g DHA per day; Dosage form: included in 60 g sausage, 8 g tomato spread, 30 g milk powder
Other Names:
  • n-3 LC-PUFA
  • Placebo Comparator: Dietary supplement: sunflower oil

    Name: sunflower oil (PPM, Magdeburg, Germany); Dosage: 8 g per day; Dosage form: 8g oil was included in 60 g sausage, 8 g tomato spread, 30 g milk powder

    Dietary Supplement: sunflower oil
    Dietary supplement: sunflower oil Name: sunflower oil (PPM, Magdeburg, Germany); Dosage: 8 g per day; Dosage form: 8g oil was included in 60 g sausage, 8 g tomato spread, 30 g milk powder
    Other Names:
  • placebo
  • Outcome Measures

    Primary Outcome Measures

    1. Sum of tender and swollen joints (68/66), disease activity score DAS 28, ultrasound score US-7 [10 weeks]

      Disease activity parameters

    Secondary Outcome Measures

    1. Inflammation markers such as erythrocyte sedimation rate (ESR), C reactive protein (CRP), adhesion molecules, cytokines, rheumascan [10 weeks]

      Further disease acitvity parameters

    2. Concentrations of arachidonic acid, eicosapentaenoic acid, docosahexaenoic acid in plasma lipids and erythrocyte lipids [10 weeks]

      Precursors of eicosanoids (leukotriens, prostaglandins, thromboxanes) and docosanoids (resolvines)

    3. Lipid mediators formed by lipoxygenases, cyclogenases [10 weeks]

      Lipidmediators derived from arachidonic acid, eicosapentaenoic acid, docosahexaenoic acid

    Other Outcome Measures

    1. Blood lipids (total cholesterol, high density lipoprotein (HDL), low density lipoprotein (LDL), triacylglycerol (TAG), ox LDL, lipoprotein a) [10 weeks]

      Cardiovascular risk factors

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient has a diagnosis of RA (according to the ACR classification criteria, revised
    1. for at least 6 months prior to randomization.
    • Patient has a moderate disease activity as defined by disease activity score DAS28 ≥ 2.4

    • Patient has the ability to comprehend the full nature and purpose of the study, including possible risks and side effects, to cooperate with the investigator, to understand verbal and written instructions, and to comply with the requirements of the entire study.

    • stable dosis of disease-modifying antirheumatic drugs within 4 weeks prior to randomization and presumably over the study periods (30 weeks).

    Exclusion Criteria:
    • Intra-articular corticosteroids within 4 weeks prior to randomization or blood sample taking

    • Patients are permitted to receive either oral or parenteral glucocorticoids equivalent to ≤10 mg daily prednisone and nonsteroidal anti-inflammatory drug, if they have received a stable dose for at least 4 weeks prior to randomization and presumably over the study periods (30 weeks).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Facility: University of Jena, Institute of Nutrition, Department of Nutritional Physiology Jena Thuringia Germany 07743
    2 Friedrich Schiller University, Clinic for Internal Medicine Jena Germany 07743

    Sponsors and Collaborators

    • University of Jena
    • German Federal Ministry of Education and Research

    Investigators

    • Principal Investigator: Gerhard Jahreis, Professor, Friedrich Schiller University Jena, Department of Nutritional Physiology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gerhard Jahreis, Professor, University of Jena
    ClinicalTrials.gov Identifier:
    NCT01742468
    Other Study ID Numbers:
    • H53-12
    First Posted:
    Dec 5, 2012
    Last Update Posted:
    Oct 7, 2015
    Last Verified:
    Oct 1, 2013
    Keywords provided by Gerhard Jahreis, Professor, University of Jena
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 7, 2015