Genotypes of Pain and Analgesia in a Randomized Trial of Irritable Bowel Syndrome.

genome-wide association study genotype irritable bowel syndrome pain randomized controlled trial

Journal

Frontiers in psychiatry
ISSN: 1664-0640
Titre abrégé: Front Psychiatry
Pays: Switzerland
ID NLM: 101545006

Informations de publication

Date de publication:
2022
Historique:
received: 23 12 2021
accepted: 22 02 2022
entrez: 11 4 2022
pubmed: 12 4 2022
medline: 12 4 2022
Statut: epublish

Résumé

Irritable bowel syndrome (IBS) is a highly prevalent chronic pain disorder with multiple underlying mechanisms and few treatments that have been demonstrated to be effective in placebo controlled trials. One potential reason may be the use of composite outcomes, such as the IBS Symptom Severity Scale (IBS-SSS) which includes descriptive items related to pain frequency and pain intensity as well as bowel dysfunction and bloating. We investigated if different features of IBS pain have distinct genetic associations and if these may be moderated by sex hormones. Adult outpatients with moderately severe IBS (>175 on IBS-SSS) enrolled in a clinical trial reported IBS-SSS at baseline and after 6 weeks of therapy. Fixed effects modeling was used to test the effect of A total of 212 participants (74% female) were included. The Previously reported association between

Sections du résumé

Background UNASSIGNED
Irritable bowel syndrome (IBS) is a highly prevalent chronic pain disorder with multiple underlying mechanisms and few treatments that have been demonstrated to be effective in placebo controlled trials. One potential reason may be the use of composite outcomes, such as the IBS Symptom Severity Scale (IBS-SSS) which includes descriptive items related to pain frequency and pain intensity as well as bowel dysfunction and bloating. We investigated if different features of IBS pain have distinct genetic associations and if these may be moderated by sex hormones.
Participants and Setting UNASSIGNED
Adult outpatients with moderately severe IBS (>175 on IBS-SSS) enrolled in a clinical trial reported IBS-SSS at baseline and after 6 weeks of therapy.
Methods UNASSIGNED
Fixed effects modeling was used to test the effect of
Results UNASSIGNED
A total of 212 participants (74% female) were included. The
Conclusions UNASSIGNED
Previously reported association between

Identifiants

pubmed: 35401282
doi: 10.3389/fpsyt.2022.842030
pmc: PMC8983929
doi:

Types de publication

Journal Article

Langues

eng

Pagination

842030

Subventions

Organisme : NHLBI NIH HHS
ID : K01 HL130625
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK119584
Pays : United States

Informations de copyright

Copyright © 2022 Vollert, Wang, Regis, Yetman, Lembo, Kaptchuk, Cheng, Nee, Iturrino, Loscalzo, Hall and Silvester.

Déclaration de conflit d'intérêts

AL owns stock in Bristol Myer Squibb and Johnson & Johnson and receives income from Vibrant and Mylan. JL is the scientific co-founder of Scipher Medicine, Inc. JN consults for World Clinical Care. JS has received consultancy fees from Alimentiv, Mozart Therapeutics, Takeda Pharmaceuticals, and Teva Pharmaceuticals. JV has received consultancy fees from Vertex Pharmaceuticals and Embody Orthopedics outside the submitted work. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Jan Vollert (J)

Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Department of Neurology, University Hospital of Schleswig-Holstein, Kiel, Germany.
Department of Anesthesiology, Intensive Care and Pain Medicine, University Hospital Muenster, Muenster, Germany.
Mannheim Center of Translational Neuroscience, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Ruisheng Wang (R)

Department of Medicine, Brigham Women's Hospital, Boston, MA, United States.
Department of Medicine, Harvard Medical School, Boston, MA, United States.

Stephanie Regis (S)

Division of Gastroenterology, Boston Children's Hospital, Boston, MA, United States.

Hailey Yetman (H)

Department of Medicine, Brigham Women's Hospital, Boston, MA, United States.

Anthony J Lembo (AJ)

Department of Medicine, Harvard Medical School, Boston, MA, United States.
Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, MA, United States.

Ted J Kaptchuk (TJ)

Department of Medicine, Harvard Medical School, Boston, MA, United States.
Program in Placebo Studies, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Department of General Medicine Primary Care, Beth Israel Deaconess Medical Center, Boston, MA, United States.

Vivian Cheng (V)

Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, MA, United States.

Judy Nee (J)

Department of Medicine, Harvard Medical School, Boston, MA, United States.
Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, MA, United States.

Johanna Iturrino (J)

Department of Medicine, Harvard Medical School, Boston, MA, United States.
Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, MA, United States.

Joseph Loscalzo (J)

Department of Medicine, Brigham Women's Hospital, Boston, MA, United States.
Department of Medicine, Harvard Medical School, Boston, MA, United States.

Kathryn T Hall (KT)

Department of Medicine, Brigham Women's Hospital, Boston, MA, United States.
Department of Medicine, Harvard Medical School, Boston, MA, United States.

Jocelyn A Silvester (JA)

Department of Medicine, Harvard Medical School, Boston, MA, United States.
Division of Gastroenterology, Boston Children's Hospital, Boston, MA, United States.
Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, MA, United States.

Classifications MeSH