Gut feelings: the relations between depression, anxiety, psychotropic drugs and the gut microbiome

广泛性焦虑症 重性抑郁障碍 焦虑 肠易激综合征 精神科 萧条(经济学) 微生物群 惊恐障碍 双相情感障碍 临床心理学 心理学 生物信息学 生物 心情 经济 宏观经济学
作者
Siobhan Brushett,Ranko Gaćeša,Arnau Vich Vila,Milla F. Brandao Gois,Sergio Andreu‐Sánchez,J. Casper Swarte,Marjolein A. Y. Klaassen,Valerie Collij,Trishla Sinha,Laura A. Bolte,Jing Wu,Morris A. Swertz,Marlou L. A. de Kroon,Sijmen A. Reijneveld,Cisca Wijmenga,Rinse K. Weersma,Jingyuan Fu,Hanna M. van Loo,Alexander Kurilshikov,Alexandra Zhernakova
出处
期刊:Gut microbes [Landes Bioscience]
卷期号:15 (2): 2281360-2281360 被引量:35
标识
DOI:10.1080/19490976.2023.2281360
摘要

The gut microbiome is involved in the bi-directional relationship of the gut - brain axis. As most studies of this relationship are small and do not account for use of psychotropic drugs (PTDs), we explored the relations of the gut microbiome with several internalizing disorders, while adjusting for PTDs and other relevant medications, in 7,656 Lifelines participants from the Northern Netherlands (5,522 controls and 491 participants with at least one internalizing disorder). Disorders included dysthymia, major depressive disorder (MDD), any depressive disorder (AnyDep: dysthymia or MDD), generalized anxiety disorder (GAD) and any anxiety disorder (AnyAnx: GAD, social phobia and panic disorder). Compared to controls, 17 species were associated with depressive disorders and 3 were associated with anxiety disorders. Around 90% of these associations remained significant (FDR <0.05) after adjustment for PTD use, suggesting that the disorders, not PTD use, drove these associations. Negative associations were observed for the butyrate-producing bacteria Ruminococcus bromii in participants with AnyDep and for Bifidobacterium bifidum in AnyAnx participants, along with many others. Tryptophan and glutamate synthesis modules and the 3,4-Dihydroxyphenylacetic acid synthesis module (related to dopamine metabolism) were negatively associated with MDD and/or dysthymia. After additional adjustment for functional gastrointestinal disorders and irritable bowel syndrome, these relations remained either statistically (FDR <0.05) or nominally (P < 0.05) significant. Overall, multiple bacterial species and functional modules were associated with internalizing disorders, including gut - brain relevant components, while associations to PTD use were moderate. These findings suggest that internalizing disorders rather than PTDs are associated with gut microbiome differences relative to controls.
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