Efficacy of n-3 fatty acid supplementation on rheumatoid arthritis' disease activity indicators: a systematic review and meta-analysis of randomized placebo-controlled trials.
Konstantinos GkiourasMaria G GrammatikopoulouIoannis MyrogiannisTheodora PapamitsouEirini I RigopoulouLazaros I SakkasDimitrios Petros BogdanosPublished in: Critical reviews in food science and nutrition (2022)
Theoretical evidence and previous studies suggest that oralnutrient supplementation (ONS) with n-3 fatty acids for rheumatoid arthritis (RA) has the potential to lower disease activity indicators and non-steroidal anti-inflammatory drug (NSAID) uptake. A systematic search was conducted on five databases/registries from inception until May 23, 2021 with the aim to identify randomized placebo-controlled trials comparing n-3 supplements to placebo on disease-specific outcomes. A total of 23 studies matched the criteria (PROSPERO: CRD42019137041). Pooled analyses revealed that n-3 ONS provided a small effect in reducing pain [standardized mean difference (SMD): -0.16, 95% confidence intervals (CI): -0.40 to 0.09], and tender (SMD: -0.20, 95% CI: -0.46 to 0.05) and swollen joint count (SMD: -0.10, 95% CI: -0.28 to 0.07). In sensitivity analyses, there was a small effect in the reduction of NSAIDs intake (SMD: -0.22, 95% CI: -0.90 to 0.46), and c-reactive protein was reduced only by 0.21 mg/dL (95% CI: -0.75 to 0.33). Similar findings were observed regarding other objective/subjective outcomes. The certainty of the evidence was mostly of "very low/low" quality. Overall, n-3 ONS in RA might have a limited clinical benefit. Previous findings suggesting a reduction in NSAID intake may have been biased from the inadequate blinding of interventions.
Keyphrases
- disease activity
- placebo controlled
- rheumatoid arthritis
- double blind
- phase iii
- fatty acid
- systemic lupus erythematosus
- rheumatoid arthritis patients
- ankylosing spondylitis
- phase ii
- clinical trial
- juvenile idiopathic arthritis
- phase ii study
- study protocol
- anti inflammatory
- interstitial lung disease
- chronic pain
- case control
- open label
- squamous cell carcinoma
- depressive symptoms
- single cell
- anti inflammatory drugs
- weight gain
- randomized controlled trial
- peripheral blood
- spinal cord
- radiation therapy
- big data
- climate change
- machine learning
- spinal cord injury
- artificial intelligence
- emergency department
- risk assessment