Impaired visceral sensitivity to acid reflux in patients with Barrett's esophagus. The role of esophageal motility

被引:28
作者
Byrne, PJ
Mulligan, ED
O'Riordan, J
Keeling, PWN
Reynolds, JV [1 ]
机构
[1] St James Hosp, Dept Surg, Trin Ctr Hlth Sci, Dublin 8, Ireland
[2] St James Hosp, Dept Med, Trin Ctr Hlth Sci, Dublin 8, Ireland
[3] Univ Dublin Trinity Coll, Dublin 2, Ireland
关键词
Barrett's; GERD; motility; pH-metry;
D O I
10.1046/j.1442-2050.2003.00328.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Patients with Barrett's esophagus have been reported to have impaired visceral sensitivity to acid perfusion and distension compared with non-Barrett's refluxers, but the mechanism is poorly understood. Esophageal motility and clearance mechanisms may be important, and this study explored the relationship of motility with symptoms. Seventy-four patients with Barrett's esophagus were compared with 216 patients with gastro-esophageal reflux disease (GERD) with abnormal acid reflux scores, and 50 symptomatic patients who had normal acid exposure. All patients had esophageal manometry and 24-h pH monitoring. Thirty-six Barrett's patients also had 24-h bile reflux monitoring. Symptoms were assessed by Symptom Index (SI) during 24-h pH monitoring. Barrett's patients with normal motility had a significantly lower SI than GERD patients for similar acid exposure (P < 0.001). Barrett's patients with abnormal motility had higher acid exposure than those with normal motility (P < 0.05), but the SI values for this group was not significantly different from the GERD patients. SI and Bile reflux in Barrett's esophagus was not significantly different in patient with normal or abnormal motility. Barrett's patients had less sensitivity than GERD patients for similar acid exposure. Normal motility in Barrett's esophagus is associated with the poorest sensitivity and the presence of increased acid exposure is required in order to achieve sensitivity levels comparable with GERD patients.
引用
收藏
页码:199 / 203
页数:5
相关论文
共 16 条
[1]
Twenty-four-hour pH monitoring is required to confirm acid reflux suppression in patients with Barrett's oesophagus undergoing anti-reflux surgery [J].
Booth, MI ;
Dehn, TCB .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2001, 13 (11) :1323-1326
[2]
AMBULATORY ESOPHAGEAL BILE REFLUX MONITORING IN BARRETTS-ESOPHAGUS [J].
CALDWELL, MTP ;
LAWLOR, P ;
BYRNE, PJ ;
WALSH, TN ;
HENNESSY, TPJ .
BRITISH JOURNAL OF SURGERY, 1995, 82 (05) :657-660
[3]
Predictive factors of Barrett esophagus - Multivariate analysis of 502 patients with gastroesophageal reflux disease [J].
Campos, GMR ;
DeMeester, SR ;
Peters, JH ;
Oberg, S ;
Crookes, PF ;
Hagen, JA ;
Bremner, CG ;
Sillin, LF ;
Mason, RJ ;
DeMeester, TR .
ARCHIVES OF SURGERY, 2001, 136 (11) :1267-1273
[4]
Increased esophageal chemoreceptor sensitivity to acid in patients after successful reversal of Barrett's esophagus [J].
Fass, R ;
Yalam, JM ;
Camargo, L ;
Johnson, C ;
Garewal, HS ;
Sampliner, RE .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (09) :1853-1858
[5]
BARRETTS-ESOPHAGUS - PH PROFILE [J].
GILLEN, P ;
KEELING, P ;
BYRNE, PJ ;
HENNESSY, TPJ .
BRITISH JOURNAL OF SURGERY, 1987, 74 (09) :774-776
[6]
Grade A, 1997, AM J GASTROENTEROL, V92, P2040
[7]
SYMPTOM INDEX AS A MARKER OF GASTROESOPHAGEAL REFLUX DISEASE [J].
JOHNSTON, BT ;
MCFARLAND, RJ ;
COLLINS, JSA ;
LOVE, AHG .
BRITISH JOURNAL OF SURGERY, 1992, 79 (10) :1054-1055
[8]
KATZKA DA, 1994, AM J GASTROENTEROL, V89, P989
[9]
Ineffective esophageal motility (IEM) - The primary finding in patients with nonspecific esophageal motility disorder [J].
Leite, LP ;
Johnston, BT ;
Barrett, J ;
Castell, JA ;
Castell, DO .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (09) :1859-1865
[10]
Vagal mechanoreceptors and chemoreceptors in mouse stomach and esophagus [J].
Page, AJ ;
Martin, CM ;
Blackshaw, LA .
JOURNAL OF NEUROPHYSIOLOGY, 2002, 87 (04) :2095-2103