Davies Julie M, Teh Jing Jie, Ewais Tatjana, Begun Jakob
Mater Research-The University of Queensland, Woolloongabba, QLD, Australia.
Frazer Institute, The University of Queensland, Woolloongabba QLD, Australia.
Inflamm Bowel Dis. 2024 Dec 5;30(12):2428-2439. doi: 10.1093/ibd/izae121.
Patients with inflammatory bowel diseases (IBDs) are more likely to have depression and anxiety symptoms compared with healthy individuals and those with other chronic illnesses. Previous studies have shown a link between the microbiome composition and depression symptoms; however, many antidepressant medications have antibacterial activity confounding cross-sectional studies of these populations. Therefore, we aimed to determine whether we could detect longitudinal changes in the microbiome of a subset of patients who participated in a previously published mindfulness-based cognitive therapy (MBCT) study to improve depression symptoms in adolescents and young adults with IBD.
Stool samples were collected at baseline and 8 weeks (n = 24 participants, 37 total samples, 13 paired samples). During this time, some participants achieved a 50% reduction in their depression symptoms either through MBCT or treatment as usual with their mental health team (responders). The microbiome composition and function of responders were compared with participants who did not improve their depression scores (nonresponders). Depression scores were determined using the depression, anxiety, and stress score (DASS-21), and metagenomic sequencing of stool samples was performed.
No difference in alpha diversity was found between responders and nonresponders. Beta diversity measures were similarly unchanged. Clinical features including fecal calprotectin, C-reactive protein, and serum IL-6 levels were unchanged.
In this small longitudinal study, we were not able to detect longitudinal changes in the microbiome associated with improvement in depression scores. Follow-up studies that are sufficiently powered to detect changes in the microbiome are required to confirm our results.
与健康个体及患有其他慢性疾病的人相比,炎症性肠病(IBD)患者更易出现抑郁和焦虑症状。既往研究表明微生物组组成与抑郁症状之间存在关联;然而,许多抗抑郁药物具有抗菌活性,这使得对这些人群的横断面研究结果存在混淆。因此,我们旨在确定能否在参与一项先前发表的基于正念的认知疗法(MBCT)研究的部分患者的微生物组中检测到纵向变化,该研究旨在改善患有IBD的青少年和青年的抑郁症状。
在基线和8周时收集粪便样本(n = 24名参与者,共37个样本,13对配对样本)。在此期间,一些参与者通过MBCT或与心理健康团队进行常规治疗使抑郁症状减轻了50%(反应者)。将反应者的微生物组组成和功能与抑郁评分未改善的参与者(无反应者)进行比较。使用抑郁、焦虑和压力评分(DASS - 21)确定抑郁评分,并对粪便样本进行宏基因组测序。
反应者和无反应者之间在α多样性上未发现差异。β多样性指标同样未发生变化。包括粪便钙卫蛋白、C反应蛋白和血清IL - 6水平在内的临床特征未改变。
在这项小型纵向研究中,我们未能检测到与抑郁评分改善相关的微生物组纵向变化。需要开展有足够效力检测微生物组变化的后续研究来证实我们的结果。