Sleep disturbances are common in patients with inflammatory bowel disease (IBD) and are associated with increased disease activity and reduced quality of life. Melatonin, a hormone regulating circadian rhythms, has shown potential anti-inflammatory and sleep-promoting effects in preliminary studies. This study aimed to evaluate the efficacy of melatonin supplementation on sleep quality in IBD patients in clinical remission.
Inflammatory bowel disease (IBD) is a chronic inflammatory disorder of the gastrointestinal tract characterized by immune-mediated intestinal inflammation. IBD is broadly classified into two main types: ulcerative colitis (UC) and Crohn's disease (CD). In recent years, the incidence of IBD has been increasing in several countries across Asia.¹ The natural course of IBD is variable, with disease activity that may improve, remain stable, or worsen despite treatment. Patients typically experience alternating periods of disease remission and disease relapse.²-³ Consequently, considerable efforts have been made to investigate new therapeutic approaches aimed at prolonging remission and improving clinical outcomes in patients with IBD. Previous studies have shown that patients with IBD are more likely to experience sleep disturbances, including increased microarousals during sleep and insomnia, compared with healthy individuals. These findings have been demonstrated using home-based wireless polysomnography and electroencephalographic monitoring.⁴ Furthermore, patients with IBD have been found to have reduced sleep efficiency compared with healthy controls.⁴ Studies evaluating sleep disturbances in IBD patients using sleep quality questionnaires or wrist actigraphy have reported an overall prevalence ranging from 41-88%. Notably, sleep disturbances appear to be more common among patients with active disease, with reported prevalence ranging from 55-100%, compared with 13-77% among patients in disease remission.⁵-⁹ Poor sleep quality has also been associated with increased disease severity, a higher risk of disease relapse, and reduced quality of life.¹⁰-¹¹ Melatonin is a hormone primarily produced by the pineal gland during the nighttime and released into the bloodstream under the regulation of the circadian rhythm. Melatonin plays an important role in regulating sleep by promoting sleep initiation and inhibiting wake-promoting neural signals.¹²-¹³ Previous studies have suggested that patients with IBD, even during remission, may exhibit abnormal melatonin secretion, which may contribute to sleep disturbance.¹⁴ In addition to the pineal gland, melatonin can also be synthesized by enterochromaffin cells in the gastrointestinal tract.¹⁵ Experimental studies in animal models have demonstrated that melatonin may enhance intestinal epithelial barrier function,¹⁶-¹⁷ promote beneficial gut microbiota,¹⁸-²⁰ and exert antioxidant effects.²¹-²² These findings suggest that melatonin may play a protective role in intestinal inflammation. Moreover, melatonin has been shown to modulate both innate and adaptive immune responses, including suppression of pro-inflammatory cytokines and enhancement of anti-inflammatory cytokines.²³-²⁸ Given that decreased melatonin levels may contribute to poor sleep quality in patients with IBD and may potentially exacerbate intestinal inflammation, several studies have investigated the effects of melatonin supplementation in patients with both active disease and disease remission. These studies have suggested that melatonin supplementation may improve sleep quality and quality of life, reduce disease activity,29-30, 32 decrease inflammatory markers,²⁹-³⁰ and may also prolong the duration of disease remission.³¹ However, the available evidence remains limited, as most studies have involved small sample sizes. In particular, only one study evaluating sleep quality and quality of life included 20 patients and was reported as a preliminary study. Therefore, the present study aims to evaluate the effect of melatonin supplementation compared with placebo on sleep quality in IBD patients with clinical remission.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
90
2 mg of prolonged release melatonin was prescribed at a dose of one tablet daily, taken one hour before the participant's usual bedtime.
placebo were manufactured to be identical in appearance
Division of Gastroenterology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University 2 Wang Lang Rd
Bangkok Noi, Bangkok, Thailand
RECRUITINGPSQI (Pittsburgh Sleep Quality Index) score at 12th week of study
Comparison of sleep quality between the melatonin and placebo groups in patients with IBD in clinical remission
Time frame: 12 weeks
PSQI (Pittsburgh Sleep Quality Index) score at 6th week of study
Sleep quality at 6th week of study
Time frame: 6 weeks
Component of PSQI score
The PSQI comprises seven components: (1) subjective sleep quality, (2) sleep latency, (3) sleep duration, (4) habitual sleep efficiency, (5) sleep disturbances, (6) use of sleep medication, and (7) daytime dysfunction.
Time frame: 12 weeks
Inflammatory Bowel Disease Questionnaire (IBDQ) score
Inflammatory Bowel Disease Questionnaire (IBDQ) score
Time frame: 6-12 weeks
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