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A randomized, double-blind, placebo-controlled study to assess efficacy of mirtazapine for the treatment of diarrhea predominant irritable bowel syndrome

Bibliographic Data

ID19536799
AuthorsAlireza Khalilian (0000-0001-7463-1188, Hamedan University of Medical Sciences), Davoud Ahmadimoghaddam (0000-0003-3886-9935, Hamedan University of Medical Sciences), Shiva Saki (Hamedan University of Medical Sciences), Younes Mohammadi (0000-0001-7521-4909, Hamedan University of Medical Sciences), Maryam Mehrpooya (0000-0003-4119-1600, Hamedan University of Medical Sciences, corresponding author)
Year2021
Volume15
Issue1
Pages3-3
Publication date2021-12-01
Open AccessYes
TypeARTICLE
VenueBioPsychoSocial Medicine (JOURNAL)
Journal identifiersISSN: 1751-0759 • E-ISSN: 1751-0759
PublisherSpringer Science and Business Media LLC (PUBLISHER)
DOI10.1186/s13030-021-00205-2
PMID33536043
OpenAlexW3126749097
LanguageEN
References cited54

BACKGROUND: receptor antagonist property. This study, therefore, was undertaken to investigate whether compared to placebo, mirtazapine would be efficacious and safe in the treatment of patients with IBS-D. METHODS: From November 2019 until July 2020, 67 patients meeting Rome IV criteria for IBS-D were randomized in a double-blind fashion into either the mirtazapine treatment group (n = 34) or the placebo treatment group (n = 33). Patients started with mirtazapine 15 mg/day at bedtime for one-week; after which the dose was increased to 30 mg/day for an additional 7-week. Outcomes included changes in the total IBS symptom severity score (IBS-SSS), Hospital anxiety and depression scale score (HADS), and IBS Quality of Life. Additionally, changes in the diary-based symptoms scores including pain, urgency of defecation, bloating, stool frequency, and stool consistency based on the 7-point Bristol Stool Form Scale (BSFS), and a number of days per week with pain, urgency, diarrhea, or bloating, once during the 1-week run-in period, and once during the last week of treatment were recorded. RESULTS: All analyses were performed on an Intention-to-Treat (ITT) analysis data set. The results showed compared to placebo, mirtazapine is more efficacious in decreasing the severity of IBS symptoms (P-value = 0.002). Further, at the end of the treatment period, all diary-derived symptoms except bloating showed significantly more improvement in the mirtazapine-treated subjects compared to the placebo-treated subjects. While was well-tolerated, mirtazapine also significantly improved the patients' quality of life (P-value = 0.04) and anxiety symptoms (P-value = 0.005). CONCLUSIONS: Overall, mirtazapine seems to have a potential benefit in the treatment of patients with IBS-D, particularly those with concomitant psychological symptoms. However, further studies are warranted to determine whether these findings are replicated. TRIAL REGISTRATION: Trial registration: Registration number at Iranian Registry of Clinical Trials: IRCT20120215009014N311 . Registration date: 2019-10-21

Antidepressant · Bloating · Defecation · Diarrhea · Irritable bowel syndrome · Mirtazapine · Placebo · Randomized controlled trial · Tegaserod · Gastrointestinal motility and disorders · Inflammatory Bowel Disease · Medicine · Microscopic Colitis · Gastroenterology · Internal Medicine

  • The Hospital Anxiety and Depression Scale

    Open Access•A S Zigmond, R P Snaith•Acta Psychiatrica Scandinavica•1983

Highly citedNo

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