TY - JOUR
T1 - Central and peripheral hypersensitivity in the irritable bowel syndrome
AU - Zhou, Qi Qi
AU - Fillingim, Roger B.
AU - Riley, Joseph L.
AU - Malarkey, William B.
AU - Verne, G. Nicholas
N1 - Funding Information:
This study was supported by an NIH Grant (NIH RO1-NS053090 ) to G.N. Verne and by a VA Merit Review Award to G.N. Verne from the Medical Research Service of the Department of Veterans Affairs. The authors have no financial or other relationship to report that might lead to a conflict of interest.
PY - 2010/3
Y1 - 2010/3
N2 - Previous investigations of somatic hypersensitivity in IBS patients have typically involved only a single stimulus modality, and little information exists regarding whether patterns of somatic pain perception vary across stimulus modalities within a group of patients with IBS. Therefore, the current study was designed to characterize differences in perceptual responses to a battery of noxious somatic stimuli in IBS patients compared to controls. A total of 78 diarrhea-predominant and 57 controls participated in the study. We evaluated pain threshold and tolerance and sensory and affective ratings of contact thermal, mechanical pressure, ischemic stimuli, and cold pressor stimuli. In addition to assessing perceptual responses, we also evaluated differences in neuroendocrine and cardiovascular responses to these experimental somatic pain stimuli. A subset of IBS patients demonstrated the presence of somatic hypersensitivity to thermal, ischemic, and cold pressor nociceptive stimuli. The somatic hypersensitivity in IBS patients was somatotopically organized in that the lower extremities that share viscerosomatic convergence with the colon demonstrate the greatest hypersensitivity. There were also changes in ACTH, cortisol, and systolic blood pressure in response to the ischemic pain testing in IBS patients when compared to controls. The results of this study suggest that a more widespread alteration in central pain processing in a subset of IBS patients may be present as they display hypersensitivity to heat, ischemic, and cold pressor stimuli.
AB - Previous investigations of somatic hypersensitivity in IBS patients have typically involved only a single stimulus modality, and little information exists regarding whether patterns of somatic pain perception vary across stimulus modalities within a group of patients with IBS. Therefore, the current study was designed to characterize differences in perceptual responses to a battery of noxious somatic stimuli in IBS patients compared to controls. A total of 78 diarrhea-predominant and 57 controls participated in the study. We evaluated pain threshold and tolerance and sensory and affective ratings of contact thermal, mechanical pressure, ischemic stimuli, and cold pressor stimuli. In addition to assessing perceptual responses, we also evaluated differences in neuroendocrine and cardiovascular responses to these experimental somatic pain stimuli. A subset of IBS patients demonstrated the presence of somatic hypersensitivity to thermal, ischemic, and cold pressor nociceptive stimuli. The somatic hypersensitivity in IBS patients was somatotopically organized in that the lower extremities that share viscerosomatic convergence with the colon demonstrate the greatest hypersensitivity. There were also changes in ACTH, cortisol, and systolic blood pressure in response to the ischemic pain testing in IBS patients when compared to controls. The results of this study suggest that a more widespread alteration in central pain processing in a subset of IBS patients may be present as they display hypersensitivity to heat, ischemic, and cold pressor stimuli.
KW - Cold pressor pain threshold and tolerance (CPTh and CPTo)
KW - Heat pain threshold and tolerance (HPTh and HPTo)
KW - Irritable bowel syndrome (IBS)
KW - Ischemic pain threshold and tolerance (IPTh and IPTo)
KW - Pressure (mechanical) pain threshold (PPT)
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U2 - 10.1016/j.pain.2009.12.005
DO - 10.1016/j.pain.2009.12.005
M3 - Article
C2 - 20074857
AN - SCOPUS:76349122200
SN - 0304-3959
VL - 148
SP - 454
EP - 461
JO - Pain
JF - Pain
IS - 3
ER -