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Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis

BACKGROUND: Linaclotide, a guanylate cyclase C agonist relieves irritable bowel syndrome with predominant constipation (IBS‐C) symptoms, but how it improves pain in humans is unknown. AIMS: To investigate the effects of linaclotide and placebo on the afferent and efferent gut‐brain‐gut signalling in...

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Autores principales: Rao, Satish S.C., Xiang, Xuelian, Yan, Yun, Rattanakovit, Kulthep, Patcharatrakul, Tanisa, Parr, Rachael, Ayyala, Deepak, Sharma, Amol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384154/
https://www.ncbi.nlm.nih.gov/pubmed/32406112
http://dx.doi.org/10.1111/apt.15772
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author Rao, Satish S.C.
Xiang, Xuelian
Yan, Yun
Rattanakovit, Kulthep
Patcharatrakul, Tanisa
Parr, Rachael
Ayyala, Deepak
Sharma, Amol
author_facet Rao, Satish S.C.
Xiang, Xuelian
Yan, Yun
Rattanakovit, Kulthep
Patcharatrakul, Tanisa
Parr, Rachael
Ayyala, Deepak
Sharma, Amol
author_sort Rao, Satish S.C.
collection PubMed
description BACKGROUND: Linaclotide, a guanylate cyclase C agonist relieves irritable bowel syndrome with predominant constipation (IBS‐C) symptoms, but how it improves pain in humans is unknown. AIMS: To investigate the effects of linaclotide and placebo on the afferent and efferent gut‐brain‐gut signalling in IBS‐C patients, in a randomised clinical trial. METHODS: Patients with IBS‐C (Rome III) and rectal hypersensitivity were randomised (2:1) to receive linaclotide (290 µg) or placebo for 10 weeks and undergo bi‐directional gut and brain axis assessment using anorectal electrical stimulations and transcranial/transspinal‐anorectal magnetic stimulations. Rectal sensations were examined by balloon distention. Assessments included abdominal pain, bowel symptoms and quality of life (QOL) scores. Primary outcomes were latencies of recto‐cortical and cortico‐rectal evoked potentials. RESULTS: Thirty‐nine patients participated; 26 received linaclotide and 13 received placebo. Rectal cortical evoked potentials latencies (milliseconds) were significantly prolonged with linaclotide compared to baseline (P1:Δ 19 ± 6, P < 0.005; N1:Δ 20 ± 7, P < 0.02) but not with placebo (P1:Δ 3 ± 5; N1:Δ 4.7 ± 5,P = 0.3) or between groups. The efferent cortico‐anorectal and spino‐anorectal latencies were unchanged. The maximum tolerable rectal volume (cc) increased significantly with linaclotide compared to baseline (P < 0.001) and placebo (Δ 29 ± 10 vs 4 ± 20, (P < 0.03). Abdominal pain decreased (P < 0.001) with linaclotide but not between groups. Complete spontaneous bowel movement frequency increased (P < 0.001), and IBS‐QOL scores improved (P = 0.01) with linaclotide compared to baseline and placebo. There was no difference in overall responders between linaclotide and placebo (54% vs 23%, P = 0.13). CONCLUSIONS: Linaclotide prolongs afferent gut‐brain signalling from baseline but both afferent and efferent signalling were unaffected compared to placebo. Linaclotide significantly improves rectal hypersensitivity, IBS‐C symptoms and QOL compared to placebo. These mechanisms may explain the effects of linaclotide on pain relief in IBS‐C patients. ClinicalTrials.Gov: Registered at Clinical trials.gov no NCT02078323.
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spelling pubmed-73841542020-07-28 Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis Rao, Satish S.C. Xiang, Xuelian Yan, Yun Rattanakovit, Kulthep Patcharatrakul, Tanisa Parr, Rachael Ayyala, Deepak Sharma, Amol Aliment Pharmacol Ther Randomised Clinical Trials BACKGROUND: Linaclotide, a guanylate cyclase C agonist relieves irritable bowel syndrome with predominant constipation (IBS‐C) symptoms, but how it improves pain in humans is unknown. AIMS: To investigate the effects of linaclotide and placebo on the afferent and efferent gut‐brain‐gut signalling in IBS‐C patients, in a randomised clinical trial. METHODS: Patients with IBS‐C (Rome III) and rectal hypersensitivity were randomised (2:1) to receive linaclotide (290 µg) or placebo for 10 weeks and undergo bi‐directional gut and brain axis assessment using anorectal electrical stimulations and transcranial/transspinal‐anorectal magnetic stimulations. Rectal sensations were examined by balloon distention. Assessments included abdominal pain, bowel symptoms and quality of life (QOL) scores. Primary outcomes were latencies of recto‐cortical and cortico‐rectal evoked potentials. RESULTS: Thirty‐nine patients participated; 26 received linaclotide and 13 received placebo. Rectal cortical evoked potentials latencies (milliseconds) were significantly prolonged with linaclotide compared to baseline (P1:Δ 19 ± 6, P < 0.005; N1:Δ 20 ± 7, P < 0.02) but not with placebo (P1:Δ 3 ± 5; N1:Δ 4.7 ± 5,P = 0.3) or between groups. The efferent cortico‐anorectal and spino‐anorectal latencies were unchanged. The maximum tolerable rectal volume (cc) increased significantly with linaclotide compared to baseline (P < 0.001) and placebo (Δ 29 ± 10 vs 4 ± 20, (P < 0.03). Abdominal pain decreased (P < 0.001) with linaclotide but not between groups. Complete spontaneous bowel movement frequency increased (P < 0.001), and IBS‐QOL scores improved (P = 0.01) with linaclotide compared to baseline and placebo. There was no difference in overall responders between linaclotide and placebo (54% vs 23%, P = 0.13). CONCLUSIONS: Linaclotide prolongs afferent gut‐brain signalling from baseline but both afferent and efferent signalling were unaffected compared to placebo. Linaclotide significantly improves rectal hypersensitivity, IBS‐C symptoms and QOL compared to placebo. These mechanisms may explain the effects of linaclotide on pain relief in IBS‐C patients. ClinicalTrials.Gov: Registered at Clinical trials.gov no NCT02078323. John Wiley and Sons Inc. 2020-05-13 2020-06 /pmc/articles/PMC7384154/ /pubmed/32406112 http://dx.doi.org/10.1111/apt.15772 Text en © 2020 The Authors. Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Randomised Clinical Trials
Rao, Satish S.C.
Xiang, Xuelian
Yan, Yun
Rattanakovit, Kulthep
Patcharatrakul, Tanisa
Parr, Rachael
Ayyala, Deepak
Sharma, Amol
Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis
title Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis
title_full Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis
title_fullStr Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis
title_full_unstemmed Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis
title_short Randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis
title_sort randomised clinical trial: linaclotide vs placebo—a study of bi‐directional gut and brain axis
topic Randomised Clinical Trials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384154/
https://www.ncbi.nlm.nih.gov/pubmed/32406112
http://dx.doi.org/10.1111/apt.15772
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