Serum and Colonic Mucosal Immune Markers in Irritable Bowel Syndrome

被引:121
作者
Chang, Lin [1 ]
Adeyemo, Mopelola [1 ]
Karagiannidis, Iordanis [2 ]
Videlock, Elizabeth J. [1 ]
Bowe, Collin [2 ]
Shih, Wendy [3 ]
Presson, Angela P. [3 ]
Yuan, Pu-Qing [1 ,2 ,4 ]
Cortina, Galen [5 ]
Gong, Hua [6 ]
Singh, Sharat [6 ]
Licudine, Arlene [1 ]
Mayer, Minou [1 ]
Tache, Yvette [1 ,2 ,4 ]
Pothoulakis, Charalabos [2 ]
Mayer, Emeran A. [1 ,7 ,8 ,9 ]
机构
[1] Univ Calif Los Angeles, Ctr Neurobiol Stress, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Med, Ctr Inflammatory Bowel Dis, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Biostatist, Los Angeles, CA 90095 USA
[4] VA GLA Healthcare Syst, Los Angeles, CA USA
[5] Univ Calif Los Angeles, Dept Pathol, Los Angeles, CA 90095 USA
[6] Prometheus Labs, San Diego, CA USA
[7] Univ Calif Los Angeles, Dept Physiol, Los Angeles, CA 90095 USA
[8] Univ Calif Los Angeles, Dept Psychiat & Behav Sci, Los Angeles, CA 90095 USA
[9] Univ Calif Los Angeles, Brain Res Inst, David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
CORTICOTROPIN-RELEASING HORMONE; SEROTONIN REUPTAKE TRANSPORTER; MAST-CELLS; INTESTINAL INFLAMMATION; ENTEROCHROMAFFIN CELL; PROTEASE ACTIVITY; HUMAN COLONOCYTES; ABDOMINAL-PAIN; ACTIVATION; EXPRESSION;
D O I
10.1038/ajg.2011.423
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Low-grade colonic mucosal inflammation has been postulated to have an important role in the pathophysiology of irritable bowel syndrome (IBS). The objectives of this study were (i) to identify serum and tissue-based immunological and neuroendocrine markers associated with mucosal inflammation in male (M) and female (F) patients with non-post-infectious IBS (non-PI-IBS) compared with healthy controls and (ii) to assess possible correlations of such markers with IBS symptoms. METHODS: Sigmoid mucosal biopsies were obtained from 45 Rome II positive IBS patients without a history of PI-IBS (26 F, 35.5% IBS-C, 33.3% IBS-D, 31.1% IBS-A/M) and 41 healthy controls (22 F) in order to measure immunological markers (serum cytokine levels, colonic mucosal mRNA levels of cytokines, mucosal immune cell counts) and neuroendocrine markers associated with mucosal inflammation (corticotropin releasing factor-and neurokinin (NK)-related ligands and receptors, enterochromaffin cells). Symptoms were measured using validated questionnaires. RESULTS: Of all the serum and mucosal cytokines measured, only interleukin-10 (IL-10) mRNA expression showed a group difference, with female, but not male, patients showing lower levels compared with female controls (18.0+/-2.9 vs. 29.5+/-4.0, P=0.006). Mucosal mRNA expression of NK-1 receptor was significantly lower (1.15+/-0.19 vs. 2.66+/-0.56, P=0.008) in female, but not male, patients compared with healthy controls. No other significant differences were observed. CONCLUSIONS: Immune cell counts and levels of cytokines and neuropeptides that are associated with inflammation were not significantly elevated in the colonic mucosa of non-PI-IBS patients, and did not correlate with symptoms. Thus, these findings do not support that colonic mucosal inflammation consistently has a primary role in these patients. However, the finding of decreased IL-10 mRNA expression may be a possible biomarker of IBS and warrants further investigation.
引用
收藏
页码:262 / 272
页数:11
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