Drug treatment options for irritable bowel syndrome - Managing for success

被引:17
作者
Dunphy, RC [1 ]
Verne, GN [1 ]
机构
[1] Univ Florida, Dept Med, Div Gastroenterol Hepatol & Nutr, Gainesville, FL USA
关键词
D O I
10.2165/00002512-200118030-00005
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
Irritable bowel syndrome (IBS) is a functional gut disorder the diagnosis of which is based on clinical symptoms as set forth by the Rome criteria. As the population ages, especially with the population of patients >75 years of age expanding greatly over the next 10 years, IBS is becoming one of the most common diseases of the elderly. Thus far, developing treatment strategies for patients with IBS has been difficult because of the lack of pharmacological targets and the wide range of symptomatology. Additionally, demonstration of a therapeutic benefit is difficult in the presence of a high placebo response observed regardless of the therapy employed. Fibre, antidiarrhoeals and antispasmodics all play some role in the symptomatic treatment of IBS. With the evolution of IBS as a disorder of visceral hypersensitivity, new drugs have been developed that target the enteric nervous system. Tricyclic antidepressants (TCAs) have been found to target the enteric neurons and play a role in pain modulation. Currently, the TCAs are recommended only for severe cases of IBS pain. The newest class of drugs to be approved for use in IBS are the serotonin (5-hydroxytryptamine; 5-HT) antagonists. Specifically, the 5-HT3 receptor antagonists have been shown to decrease symptoms in female patients with IBS. A related class of drugs, the 5-HT4 receptor agonists, is being developed for the treatment of constipation-predominant IBS. Further investigation into the role of spinal afferent neurons in visceral hypersensitivity is at the forefront of IBS research. Several experimental drug therapies for IBS are also discussed in this review including N-methyl-D-aspartate receptor antagonists, neurokinin-1 receptor antagonists, octreotide, clonidine and the selective M3 receptor antagonist, zamifenacin.
引用
收藏
页码:201 / 211
页数:11
相关论文
共 61 条
[1]
*AM GASTR ASS, 1997, GASTROENTEROLOGY, V112, P2118
[2]
Treatment of irritable bowel syndrome with Chinese herbal medicine - A randomized controlled trial [J].
Bensoussan, A ;
Talley, NJ ;
Hing, M ;
Menzies, R ;
Guo, A ;
Ngu, M .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (18) :1585-1589
[3]
Selective stimulation of colonic transit by the benzofuran 5HT4 agonist, prucalopride, in healthy humans [J].
Bouras, EP ;
Camilleri, M ;
Burton, DD ;
McKinzie, S .
GUT, 1999, 44 (05) :682-686
[4]
BURKITT DP, 1972, LANCET, V1, P1408
[5]
Irritable bowel syndrome [J].
Camilleri, M ;
Choi, MG .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 1997, 11 (01) :3-15
[6]
THE IRRITABLE-BOWEL-SYNDROME - MECHANISMS AND A PRACTICAL APPROACH TO MANAGEMENT [J].
CAMILLERI, M ;
PRATHER, CM .
ANNALS OF INTERNAL MEDICINE, 1992, 116 (12) :1001-1008
[7]
Camilleri M, 1999, ALIMENT PHARM THERAP, V13, P48
[8]
Camilleri M, 1999, ALIMENT PHARM THERAP, V13, P1149
[9]
Insights into the pathophysiology and mechanisms of constipation, irritable bowel syndrome, and diverticulosis in older people [J].
Camilleri, M ;
Lee, JS ;
Viramontes, B ;
Bharucha, AE ;
Tangalos, EG .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2000, 48 (09) :1142-1150
[10]
ROLE OF LOPERAMIDE AND PLACEBO IN MANAGEMENT OF IRRITABLE BOWEL SYNDROME (IBS) [J].
CANN, PA ;
READ, NW ;
HOLDSWORTH, CD ;
BARENDS, D .
DIGESTIVE DISEASES AND SCIENCES, 1984, 29 (03) :239-247