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Effect of 5-hydroxytryptophan on fatigue in quiescent inflammatory bowel disease: a randomized controlled trial.

Authors :
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service de gastro-entérologie
Truyens, Marie
Lobatón, Triana
Ferrante, Marc
Bossuyt, Peter
Vermeire, Séverine
Pouillon, Lieven
Dewint, Pieter
Cremer, Anneline
Peeters, Harald
Lambrecht, Guy
Louis, Edouard
Rahier, Jean-François
Dewit, Olivier
Muls, Vinciane
Holvoet, Tom
Vandermeulen, Liv
Peeters, Anneleen
Gonzales, Gerard Bryan
Bos, Simon
Laukens, Debby
De Vos, Martine
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service de gastro-entérologie
Truyens, Marie
Lobatón, Triana
Ferrante, Marc
Bossuyt, Peter
Vermeire, Séverine
Pouillon, Lieven
Dewint, Pieter
Cremer, Anneline
Peeters, Harald
Lambrecht, Guy
Louis, Edouard
Rahier, Jean-François
Dewit, Olivier
Muls, Vinciane
Holvoet, Tom
Vandermeulen, Liv
Peeters, Anneleen
Gonzales, Gerard Bryan
Bos, Simon
Laukens, Debby
De Vos, Martine
Source :
Gastroenterology, Vol. 163, no. 5, p. 1294-1305 (2022)
Publication Year :
2022

Abstract

Fatigue is highly prevalent among patients suffering from inflammatory bowel disease (IBD) and only limited treatment options are available. Based on the hypothetical link between low serum tryptophan concentrations and fatigue, we determined the effect of 5-hydroxytryptophan supplementation on fatigue in patients with inactive IBD. A multicenter randomized controlled trial was performed at 13 Belgian hospitals, including 166 patients with IBD in remission but suffering from fatigue defined by a fatigue Visual Analog Scale (fVAS) ≥5. Patients were treated in a crossover manner with 100 mg oral 5-hydroxytryptophan or placebo twice daily for two consecutive periods of eight weeks. The primary endpoint was the proportion of patients reaching a ≥20% reduction in fVAS after eight weeks of intervention. Secondary outcomes included changes in serum tryptophan metabolites, FACIT-F, and scores for depression, anxiety, and stress. The effect of the intervention on the outcomes was evaluated by linear mixed modeling. During 5-hydroxytryptophan treatment a significant increase in serum 5-hydroxytryptophan (estimated mean difference 52.66 ng/ml [39.34; 65.98], P < 0.001) and serotonin (3.0 ng/ml [1.97; 4.03], P < 0.001) levels was observed compared with placebo. The proportion of patients reaching ≥20% reduction in fVAS was similar in placebo (37.6%) and 5-hydroxytryptophan (35.6%) treated patients (P = 0.830). Both the fVAS reduction (-0.18 [-0.81; 0.46], P = 0.581) and FACIT-F increase (0.68 [-2.37; 3.73], P = 0.660) were comparable between 5-hydroxytryptophan and placebo treatment, as well as changes in depression, anxiety, and stress scores. Despite a significant increase in serum 5-hydroxytryptophan and serotonin levels, oral 5-hydroxytryptophan did not modulate IBD-related fatigue better than placebo. Belgian Federal Agency for Medication and Health Products, EudraCT number: 2017-005059-10. gov: NCT03574948, https://clinicaltrials.gov/ct2/show/NCT03574948.

Details

Database :
OAIster
Journal :
Gastroenterology, Vol. 163, no. 5, p. 1294-1305 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372949059
Document Type :
Electronic Resource