Gaman Alexandru, Bucur Maria Cristina, Kuo Braden
Massachusetts General Hospital, Gastrointestinal Unit, Harvard Medical School, Boston, MA, USA.
Therap Adv Gastroenterol. 2009 May 1;2(3):169-181. doi: 10.1177/1756283X08103656.
Reported prevalence rates of irritable bowel syndrome (IBS) are between 8% to 20% in the US general population with an average medical expenditure of US$1.35 billion direct and US$205 million indirect costs. Current pathophysiologic theories are based on abnormalities of both the brain and gut, thus setting a new stage for current and future therapeutic approaches. There are numerous treatment options in IBS acting centrally and peripherally by influencing motility and visceral sensitivity. Clinical evidence is variable; however, newer emerging treatments are being evaluated using better-designed clinical trials. Accurate assessment of IBS drug efficacy is still hampered by heterogeneity of the IBS population. Novel methods such as pharmacogenomics or brain imaging may be helpful in the future to better understand and characterize IBS patient subtypes, and this in turn will lead to more specific and efficient therapeutic options. Patient subpopulation measurement of side effects is also a clinical challenge and further understanding could improve treatment efficacy enhancing the patient compliance.
在美国普通人群中,肠易激综合征(IBS)的报告患病率在8%至20%之间,直接医疗费用平均为13.5亿美元,间接费用为2.05亿美元。当前的病理生理理论基于大脑和肠道的异常,从而为当前和未来的治疗方法开启了新的阶段。IBS有多种治疗选择,通过影响动力和内脏敏感性在中枢和外周发挥作用。临床证据参差不齐;然而,正在使用设计更优的临床试验对新出现的治疗方法进行评估。IBS人群的异质性仍然阻碍着对IBS药物疗效的准确评估。诸如药物基因组学或脑成像等新方法未来可能有助于更好地理解和描述IBS患者亚型,这反过来将带来更具体、更有效的治疗选择。对副作用进行患者亚组测量也是一项临床挑战,进一步了解可能会提高治疗效果,增强患者的依从性。