Affective disorders impact prevalence of Flavonifractor and abundance of Christensenellaceae in gut microbiota

被引:32
作者
Coello, Klara [1 ]
Hansen, Tue Haldor [2 ,3 ]
Sorensen, Nikolaj [4 ]
Ottesen, Ninja Meinhard [5 ]
Miskowiak, Kamilla Woznica [1 ]
Pedersen, Oluf [2 ,5 ]
Kessing, Lars Vedel [1 ,5 ]
Vinberg, Maj [1 ,5 ,6 ]
机构
[1] Copenhagen Univ Hosp, Rigshosp, Copenhagen Affect Disorders Res Ctr CADIC, Psychiat Ctr Copenhagen, Copenhagen, Denmark
[2] Ctr Basic Metab Res, Novo Nordisk Fdn, Sect Metab Genet, Copenhagen, Denmark
[3] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen, Denmark
[4] Clin Microbi, Copenhagen, Denmark
[5] Copenhagen Univ Hosp Bispebjerg, Child & Adolescent Mental Hlth Ctr, Copenhagen, Denmark
[6] Copenhagen Univ Hosp, Psychiat Ctr North Zealand, Psychiat Res Unit, Hillerod, Denmark
关键词
Affective disorders; Bipolar disorder; Major depressive disorder; High risk; Unaffected relatives; Gut microbiota; MAJOR DEPRESSIVE DISORDER; BIPOLAR DISORDER; CARDIOVASCULAR-DISEASE; SCIENTIFIC STATEMENT; METABOLIC SYNDROME; OXIDATIVE STRESS; RATING-SCALE; METAANALYSIS; GENETICS; UNIPOLAR;
D O I
10.1016/j.pnpbp.2021.110300
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Affective disorders (AD) have been associated with a higher prevalence of the gut Flavonifractor genus and a lower abundance of the gut Christensenellaceae family. Objective and methods By pooling two independent study samples of patients with AD (n = 176), their unaffected first-degree relatives (n = 70) and healthy controls (n = 101) we aimed to replicate and extend our prior findings of differential Flavonifractor prevalence and Christensenellaceae abundance when comparing patients with AD and healthy controls. The gut microbiota was profiled using 16S rRNA gene amplicon sequencing. Results The pattern of higher prevalence of Flavonifractor and lower Centered Log-Ratio (CLR) abundance of Christensenellaceae was associated with AD. In generalized linear models the CLR abundance of Christensenellaceae was lower in patients with AD (p = 0.024), and in smokers (p = 1.9*10-4), and inversely associated with increasing waist circumference (p = 0.031). The prevalence of Flavonifractor was higher in patients with AD (p = 0.033) and in smokers (p = 0.036). No impact of psychotropic medication was found. The CLR abundance of Christensenellaceae (p = 0.041), but not the prevalence of Flavonifractor (p = 0.20) could distinguish nonsmoking patients with AD from non-smoking healthy controls, whereas no such associations were found in smokers. Unaffected relatives neither differed from patients with AD nor from healthy controls. Conclusion Compared with findings in healthy controls, AD was associated with a significantly lower CLR abundance of the health-linked Christensenellaceae and a significantly higher prevalence of Flavonifractor; findings that are associated with enhanced oxidative stress and systemic low-grade inflammation. If our observations are validated in future independent studies, they support the notion that parts of aberrant gut microbiota are shared by AD and states of dysmetabolism.
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