Altered visceral perceptual and neuroendocrine response in patients with irritable bowel syndrome during mental stress
Background and aims: Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral sensory responses to stress in IBS patients. Subjects and methods: Eighteen IBS patients and 22 control subjects were assessed...
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Published in | Gut Vol. 53; no. 8; pp. 1102 - 1108 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and British Society of Gastroenterology
01.08.2004
BMJ BMJ Publishing Group LTD Copyright 2004 by Gut |
Subjects | |
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Abstract | Background and aims: Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral sensory responses to stress in IBS patients. Subjects and methods: Eighteen IBS patients and 22 control subjects were assessed using rectal balloon distensions before, during, and after mental stress. Ten controls and nine patients were studied in supplementary sessions. Rectal sensitivity (thresholds and intensity—visual analogue scale (VAS)) and perceived stress and arousal (VAS) were determined. Plasma levels of corticotropin releasing factor (CRF), adrenocorticotropic hormone (ACTH), cortisol, noradrenaline, and adrenaline were analysed at baseline, immediately after stress, and after the last distension. Heart rate was recorded continuously. Results: Thresholds were increased during stress in control subjects (p<0.01) but not in IBS patients. Both groups showed lower thresholds after stress (p<0.05). Repeated distensions without stress did not affect thresholds. Both groups showed increased heart rate (p<0.001) and VAS ratings for stress and arousal (p<0.05) during stress. Patients demonstrated higher ratings for stress but lower for arousal than controls. Basal CRF levels were lower in patients (p<0.05) and increased significantly during stress in patients (p<0.01) but not in controls. Patients also responded with higher levels of ACTH during stress (p<0.05) and had higher basal levels of noradrenaline than controls (p<0.01). Controls, but not patients, showed increased levels of adrenaline and noradrenaline in response to stress (p<0.05). Conclusions: Stress induced exaggeration of the neuroendocrine response and visceral perceptual alterations during and after stress may explain some of the stress related gastrointestinal symptoms in IBS. |
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AbstractList | Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral sensory responses to stress in IBS patients.BACKGROUND AND AIMSStress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral sensory responses to stress in IBS patients.Eighteen IBS patients and 22 control subjects were assessed using rectal balloon distensions before, during, and after mental stress. Ten controls and nine patients were studied in supplementary sessions. Rectal sensitivity (thresholds and intensity-visual analogue scale (VAS)) and perceived stress and arousal (VAS) were determined. Plasma levels of corticotropin releasing factor (CRF), adrenocorticotropic hormone (ACTH), cortisol, noradrenaline, and adrenaline were analysed at baseline, immediately after stress, and after the last distension. Heart rate was recorded continuously.SUBJECTS AND METHODSEighteen IBS patients and 22 control subjects were assessed using rectal balloon distensions before, during, and after mental stress. Ten controls and nine patients were studied in supplementary sessions. Rectal sensitivity (thresholds and intensity-visual analogue scale (VAS)) and perceived stress and arousal (VAS) were determined. Plasma levels of corticotropin releasing factor (CRF), adrenocorticotropic hormone (ACTH), cortisol, noradrenaline, and adrenaline were analysed at baseline, immediately after stress, and after the last distension. Heart rate was recorded continuously.Thresholds were increased during stress in control subjects (p<0.01) but not in IBS patients. Both groups showed lower thresholds after stress (p<0.05). Repeated distensions without stress did not affect thresholds. Both groups showed increased heart rate (p<0.001) and VAS ratings for stress and arousal (p<0.05) during stress. Patients demonstrated higher ratings for stress but lower for arousal than controls. Basal CRF levels were lower in patients (p<0.05) and increased significantly during stress in patients (p<0.01) but not in controls. Patients also responded with higher levels of ACTH during stress (p<0.05) and had higher basal levels of noradrenaline than controls (p<0.01). Controls, but not patients, showed increased levels of adrenaline and noradrenaline in response to stress (p<0.05).RESULTSThresholds were increased during stress in control subjects (p<0.01) but not in IBS patients. Both groups showed lower thresholds after stress (p<0.05). Repeated distensions without stress did not affect thresholds. Both groups showed increased heart rate (p<0.001) and VAS ratings for stress and arousal (p<0.05) during stress. Patients demonstrated higher ratings for stress but lower for arousal than controls. Basal CRF levels were lower in patients (p<0.05) and increased significantly during stress in patients (p<0.01) but not in controls. Patients also responded with higher levels of ACTH during stress (p<0.05) and had higher basal levels of noradrenaline than controls (p<0.01). Controls, but not patients, showed increased levels of adrenaline and noradrenaline in response to stress (p<0.05).Stress induced exaggeration of the neuroendocrine response and visceral perceptual alterations during and after stress may explain some of the stress related gastrointestinal symptoms in IBS.CONCLUSIONSStress induced exaggeration of the neuroendocrine response and visceral perceptual alterations during and after stress may explain some of the stress related gastrointestinal symptoms in IBS. Background and aims: Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral sensory responses to stress in IBS patients. Subjects and methods: Eighteen IBS patients and 22 control subjects were assessed using rectal balloon distensions before, during, and after mental stress. Ten controls and nine patients were studied in supplementary sessions. Rectal sensitivity (thresholds and intensity—visual analogue scale (VAS)) and perceived stress and arousal (VAS) were determined. Plasma levels of corticotropin releasing factor (CRF), adrenocorticotropic hormone (ACTH), cortisol, noradrenaline, and adrenaline were analysed at baseline, immediately after stress, and after the last distension. Heart rate was recorded continuously. Results: Thresholds were increased during stress in control subjects (p<0.01) but not in IBS patients. Both groups showed lower thresholds after stress (p<0.05). Repeated distensions without stress did not affect thresholds. Both groups showed increased heart rate (p<0.001) and VAS ratings for stress and arousal (p<0.05) during stress. Patients demonstrated higher ratings for stress but lower for arousal than controls. Basal CRF levels were lower in patients (p<0.05) and increased significantly during stress in patients (p<0.01) but not in controls. Patients also responded with higher levels of ACTH during stress (p<0.05) and had higher basal levels of noradrenaline than controls (p<0.01). Controls, but not patients, showed increased levels of adrenaline and noradrenaline in response to stress (p<0.05). Conclusions: Stress induced exaggeration of the neuroendocrine response and visceral perceptual alterations during and after stress may explain some of the stress related gastrointestinal symptoms in IBS. Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral sensory responses to stress in IBS patients. Eighteen IBS patients and 22 control subjects were assessed using rectal balloon distensions before, during, and after mental stress. Ten controls and nine patients were studied in supplementary sessions. Rectal sensitivity (thresholds and intensity-visual analogue scale (VAS)) and perceived stress and arousal (VAS) were determined. Plasma levels of corticotropin releasing factor (CRF), adrenocorticotropic hormone (ACTH), cortisol, noradrenaline, and adrenaline were analysed at baseline, immediately after stress, and after the last distension. Heart rate was recorded continuously. Thresholds were increased during stress in control subjects (p<0.01) but not in IBS patients. Both groups showed lower thresholds after stress (p<0.05). Repeated distensions without stress did not affect thresholds. Both groups showed increased heart rate (p<0.001) and VAS ratings for stress and arousal (p<0.05) during stress. Patients demonstrated higher ratings for stress but lower for arousal than controls. Basal CRF levels were lower in patients (p<0.05) and increased significantly during stress in patients (p<0.01) but not in controls. Patients also responded with higher levels of ACTH during stress (p<0.05) and had higher basal levels of noradrenaline than controls (p<0.01). Controls, but not patients, showed increased levels of adrenaline and noradrenaline in response to stress (p<0.05). Stress induced exaggeration of the neuroendocrine response and visceral perceptual alterations during and after stress may explain some of the stress related gastrointestinal symptoms in IBS. Background and aims: Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral sensory responses to stress in IBS patients. Subjects and methods: Eighteen IBS patients and 22 control subjects were assessed using rectal balloon distensions before, during, and after mental stress. Ten controls and nine patients were studied in supplementary sessions. Rectal sensitivity (thresholds and intensity—visual analogue scale (VAS)) and perceived stress and arousal (VAS) were determined. Plasma levels of corticotropin releasing factor (CRF), adrenocorticotropic hormone (ACTH), cortisol, noradrenaline, and adrenaline were analysed at baseline, immediately after stress, and after the last distension. Heart rate was recorded continuously. Results: Thresholds were increased during stress in control subjects (p<0.01) but not in IBS patients. Both groups showed lower thresholds after stress (p<0.05). Repeated distensions without stress did not affect thresholds. Both groups showed increased heart rate (p<0.001) and VAS ratings for stress and arousal (p<0.05) during stress. Patients demonstrated higher ratings for stress but lower for arousal than controls. Basal CRF levels were lower in patients (p<0.05) and increased significantly during stress in patients (p<0.01) but not in controls. Patients also responded with higher levels of ACTH during stress (p<0.05) and had higher basal levels of noradrenaline than controls (p<0.01). Controls, but not patients, showed increased levels of adrenaline and noradrenaline in response to stress (p<0.05). Conclusions: Stress induced exaggeration of the neuroendocrine response and visceral perceptual alterations during and after stress may explain some of the stress related gastrointestinal symptoms in IBS. |
Author | Björnsson, E S Simrén, M Abrahamsson, H Posserud, I Agerforz, P Ekman, R |
AuthorAffiliation | 2 Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden 1 Department of Internal Medicine, Sahlgrenska University Hospital, Göteborg, Sweden |
AuthorAffiliation_xml | – name: 2 Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden – name: 1 Department of Internal Medicine, Sahlgrenska University Hospital, Göteborg, Sweden |
Author_xml | – sequence: 1 givenname: I surname: Posserud fullname: Posserud, I organization: Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden – sequence: 2 givenname: P surname: Agerforz fullname: Agerforz, P organization: Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden – sequence: 3 givenname: R surname: Ekman fullname: Ekman, R organization: Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden – sequence: 4 givenname: E S surname: Björnsson fullname: Björnsson, E S organization: Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden – sequence: 5 givenname: H surname: Abrahamsson fullname: Abrahamsson, H organization: Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden – sequence: 6 givenname: M surname: Simrén fullname: Simrén, M organization: Institute of Clinical Neuroscience, Section of Neurochemistry, Sahlgrenska University Hospital, Göteborg, Sweden |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15969976$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/15247175$$D View this record in MEDLINE/PubMed https://gup.ub.gu.se/publication/57730$$DView record from Swedish Publication Index |
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ContentType | Journal Article |
Copyright | Copyright 2004 by Gut 2004 INIST-CNRS Copyright: 2004 Copyright 2004 by Gut Copyright © Copyright 2004 by Gut 2004 |
Copyright_xml | – notice: Copyright 2004 by Gut – notice: 2004 INIST-CNRS – notice: Copyright: 2004 Copyright 2004 by Gut – notice: Copyright © Copyright 2004 by Gut 2004 |
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Keywords | Human Response Irritable bowel syndrome Gastroenterology Digestive diseases Intestinal disease Stress |
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Notes | istex:9D6F03F8E9CDD469A5C94D400373A7752B8B6E4A Correspondence to: Dr M Simrén Section of Gastroenterology and Hepatology, Department of Internal Medicine, 41345 Göteborg, Sweden; magnus.simren@medicine.gu.se href:gutjnl-53-1102.pdf local:0531102 ark:/67375/NVC-8GB5JZFC-9 PMID:15247175 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Correspondence to: Dr M Simrén Section of Gastroenterology and Hepatology, Department of Internal Medicine, 41345 Göteborg, Sweden; magnus.simren@medicine.gu.se |
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References_xml | – reference: 11874556 - Neurogastroenterol Motil. 2002 Feb;14(1):75-82 – reference: 1624167 - Gut. 1992 Jun;33(6):825-30 – reference: 9374695 - Am J Physiol. 1997 Nov;273(5 Pt 1):G997-1006 – reference: 5328883 - Acta Psychol (Amst). 1966;25(1):36-93 – reference: 8497182 - Brain Res Mol Brain Res. 1993 May;18(3):195-200 – reference: 9334797 - Res Nurs Health. 1997 Oct;20(5):431-41 – reference: 4027486 - Br J Psychol. 1985 May;76 ( Pt 2):183-6 – reference: 3617051 - Tohoku J Exp Med. 1987 Apr;151(4):373-85 – reference: 8978344 - Gastroenterology. 1997 Jan;112(1):64-72 – reference: 12526949 - Am J Gastroenterol. 2003 Jan;98(1):135-43 – reference: 9137116 - Am J Psychiatry. 1997 May;154(5):624-9 – reference: 687885 - Br J Soc Clin Psychol. 1978 Sep;17(3):283-4 – reference: 10202204 - Can J Gastroenterol. 1999 Mar;13 Suppl A:18A-25A – reference: 8020671 - Gastroenterology. 1994 Jul;107(1):271-93 – reference: 7498641 - Gastroenterology. 1995 Dec;109(6):1772-80 – reference: 10784583 - Gastroenterology. 2000 May;118(5):842-8 – reference: 3965273 - Dig Dis Sci. 1985 Jan;30(1):40-4 – reference: 9052500 - Dig Dis Sci. 1997 Feb;42(2):223-41 – reference: 3315118 - Brain Res. 1987 Sep 29;422(1):154-7 – reference: 8697187 - Neurogastroenterol Motil. 1996 Mar;8(1):9-18 – reference: 9391250 - Gut. 1997 Oct;41(4):505-12 – reference: 10924807 - Pain. 2000 Aug;87(2):137-47 – reference: 3350284 - Gastroenterology. 1988 May;94(5 Pt 1):1150-6 – reference: 8143999 - Gastroenterology. 1994 Apr;106(4):945-50 – reference: 11076888 - Gut. 2000 Dec;47(6):861-9 – reference: 9691924 - Gut. 1998 Jun;42(6):845-9 – reference: 11254476 - Am J Physiol Gastrointest Liver Physiol. 2001 Apr;280(4):G519-24 – reference: 7657095 - Gastroenterology. 1995 Sep;109(3):671-80 – reference: 12544695 - Eur J Gastroenterol Hepatol. 2003 Jan;15(1):55-62 – reference: 6342467 - Anal Biochem. 1983 Feb 1;128(2):257-74 – reference: 2714679 - Gut. 1989 Apr;30(4):455-9 – reference: 6880820 - Acta Psychiatr Scand. 1983 Jun;67(6):361-70 – reference: 7875470 - Gastroenterology. 1995 Mar;108(3):680-6 – reference: 7797041 - Gastroenterology. 1995 Jul;109(1):40-52 – reference: 8496339 - J Neuroimmunol. 1993 Apr;44(1):7-13 – reference: 9247458 - Gastroenterology. 1997 Aug;113(2):415-22 – reference: 9430796 - Neurogastroenterol Motil. 1997 Dec;9(4):271-9 – reference: 8633579 - Am J Gastroenterol. 1996 May;91(5):906-13 – reference: 10918705 - JAMA. 2000 Aug 2;284(5):592-7 – reference: 10457044 - Gut. 1999 Sep;45 Suppl 2:II43-7 – reference: 8978343 - Gastroenterology. 1997 Jan;112(1):55-63 |
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Snippet | Background and aims: Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered... Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered neuroendocrine and visceral... Background and aims: Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered... BACKGROUND AND AIMS: Stress often worsens the symptoms of irritable bowel syndrome (IBS). We hypothesised that this might be explained by altered... |
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SubjectTerms | ACTH Adrenocorticotropic Hormone Adrenocorticotropic Hormone - blood Adult Aged alternating type IBS Anxiety Anxiety - physiopathology Arousal Arousal - physiology Biological and medical sciences blood constipation predominant irritable bowel syndrome corticotropin releasing factor Corticotropin-Releasing Hormone Corticotropin-Releasing Hormone - blood CRF Defecation diarrhoea predominant irritable bowel syndrome Epinephrine Epinephrine - blood Female Gastroenterologi och hepatologi Gastroenterology and Hepatology Gastroenterology. Liver. Pancreas. Abdomen HAD scale Heart Rate Heart Rate - physiology Hormones hospital anxiety and depression scale Humans Hydrocortisone Hydrocortisone - blood IBS IBS-A IBS-C IBS-D interquartile range IQR Irritable Bowel Syndrome Irritable Bowel Syndrome - physiopathology Irritable Bowel Syndrome - psychology Male Medical sciences Middle Aged Nervous system neuroendocrine response Norepinephrine Norepinephrine - blood Other diseases. Semiology Pain Pain - physiopathology Pathophysiology physiology physiopathology Psychological psychology rectal sensitivity Rectum Rectum - physiopathology Sensory Thresholds Sensory Thresholds - physiology Spielberger state trait anxiety inventory STAI Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Stress Stress response Stress, Psychological - physiopathology VAS visual analogue scale |
Title | Altered visceral perceptual and neuroendocrine response in patients with irritable bowel syndrome during mental stress |
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