Faculty of Health, University of Newcastle, Callaghan, New South Wales, Australia.
Gut. 2012 Sep;61(9):1284-90. doi: 10.1136/gutjnl-2011-300474. Epub 2012 Jan 10.
Psychological factors are known to be associated with functional gastrointestinal disorders (FGIDs) including irritable bowel syndrome (IBS) and functional dyspepsia (FD). No prospective studies have evaluated whether it is the brain (eg, via anxiety) that drives gut symptoms, or whether gut dysfunction precipitates the central nervous system features such as anxiety. In a 12-year longitudinal, prospective, population-based study, we aimed to determine the directionality of the brain-gut mechanism in FGIDs.
Participants (n=1775) were a random population sample from Australia who responded to a survey on FGIDs in 1997 and agreed to be contacted for future research; 1002 completed the 12-year follow-up survey (response rate =60%), with 217, 82 and 45 people meeting Rome II for new onset FGIDs, IBS and FD, respectively. Anxiety and depression were measured using the Delusions Symptom States Inventory at baseline and follow-up.
Among people free of a FGID at baseline, higher levels of anxiety (OR 1.11; 95% CI 1.03 to 1.19, p=0.006) but not depression at baseline was a significant independent predictor of developing new onset FGIDs 12 years later. Among people who did not have elevated levels of anxiety and depression at baseline, those with a FGID at baseline had significantly higher levels of anxiety and depression at follow-up (mean difference coefficient 0.76, p<0.001 and 0.30, p=0.01 for anxiety and depression, respectively). In IBS higher levels of anxiety and depression at baseline were predictive of IBS at follow-up, while only depression was predictive of FD at follow-up.
The central nervous system and gut interact bidirectionally in FGIDs.
已知心理因素与功能性胃肠疾病(FGIDs)有关,包括肠易激综合征(IBS)和功能性消化不良(FD)。没有前瞻性研究评估是大脑(例如,通过焦虑)驱动肠道症状,还是肠道功能障碍引发焦虑等中枢神经系统特征。在一项为期 12 年的纵向、前瞻性、基于人群的研究中,我们旨在确定 FGIDs 中大脑-肠道机制的方向性。
参与者(n=1775)是来自澳大利亚的随机人群样本,他们在 1997 年对 FGIDs 进行了调查,并同意接受未来研究的联系;1002 人完成了 12 年的随访调查(应答率=60%),分别有 217、82 和 45 人符合罗马 II 标准,新出现 FGIDs、IBS 和 FD。基线和随访时使用错觉症状状态量表测量焦虑和抑郁。
在基线时无 FGID 的人群中,基线时较高水平的焦虑(OR 1.11;95%CI 1.03 至 1.19,p=0.006)但无抑郁是 12 年后新出现 FGIDs 的独立显著预测因素。在基线时没有焦虑和抑郁升高的人群中,基线时患有 FGID 的人在随访时焦虑和抑郁水平明显更高(平均差异系数 0.76,p<0.001 和 0.30,p=0.01 分别用于焦虑和抑郁)。在 IBS 中,基线时较高的焦虑和抑郁水平预测随访时的 IBS,而只有抑郁预测随访时的 FD。
中枢神经系统和肠道在 FGIDs 中相互作用。