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Ensayo controlado aleatorizado1992Financiación no declarada

Treatment of ulcerative colitis with fish oil supplementation: a prospective 12 month randomised controlled trial

Hawthorne AB, Daneshmend TK, Hawkey CJ, Belluzzi A, Everitt SJ, Holmes GK, Malkinson C, Shaheen MZ, Willars JE

Gut · 187 citas

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Financiación no declarada

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
1992-07-01 · Gut · vol. 33 · número 7 · págs. 922–928
Editorial
BMJ
Citado
300 citas · más que el 96% de estudios similares · 5.3× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
36 trabajos
Acceso
Lectura gratuita
Áreas de investigación
Inflammatory Bowel Disease · Fatty Acid Research and Health · Inflammatory mediators and NSAID effects
Palabras clave
ulcerative colitis, fish oil supplementation, eicosapentaenoic acid, leukotriene B4, leukotriene B5, corticosteroid-sparing effect, remission, relapse, neutrophils, olive oil placebo, maintenance therapy
MeSH
humans, colitis, ulcerative, sulfasalazine, aminosalicylic acids, mesalamine, prednisolone, eicosapentaenoic acid, leukotriene b4, plant oils, drug therapy, combination, remission induction, prospective studies, adolescent, adult, aged, middle aged, female, male, olive oil

9 autores

  • A. Barney Hawthorne🇬🇧University of Nottingham
  • T K Daneshmend🇬🇧University of Nottingham
  • C J Hawkey🇬🇧University of Nottingham
  • Andrea Belluzzi🇬🇧University of Nottingham
  • S J Everitt🇬🇧University of Nottingham
  • G. K. T. Holmes🇬🇧University of Nottingham
  • C Malkinson🇬🇧University of Nottingham
  • M Z Shaheen🇬🇧University of Nottingham
  • J E Willars🇬🇧University of Nottingham

Resumen

El texto original del estudio, en el idioma en que se publicó.

The effect of fish oil on the course of ulcerative colitis was investigated in a randomised blinded controlled study. Eighty seven patients received supplements of 20 ml HiEPA fish oil as triglyceride (4.5 g of eicosapentaenoic acid) or olive oil placebo daily for one year. The oils were given in addition to standard drug therapy and trial entry was stratified for disease activity. Fish oil significantly increased the eicosapentaenoic acid content of rectal mucosa to 3.2% of total fatty acids at six months, compared with 0.63% for patients on olive oil. This was associated with increased synthesis of leukotriene B5, and 53% suppression of leukotriene B4 synthesis by ionophore--stimulated neutrophils. Leukotriene B4 suppression persisted for at least two months after treatment was stopped. Treatment with fish oil resulted in measurable, but only limited clinical benefit. For patients entering the trial in relapse (n = 53), there was a significant reduction in corticosteroid requirement after one and two months treatment. There was a trend towards achieving remission (off corticosteroids) faster in the patients on fish oil, although differences were not significant. For patients in remission at trial entry or during the trial (n = 69), there was no significant difference in the rate of relapse by log rank analysis. We conclude that fish oil supplementation produces a modest corticosteroid sparing effect in active disease, but there is no benefit in maintenance therapy.

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