From the Departments of Pediatrics (van de Wouw, Wang, Vaghef-Mehrabani, Dewey, Tomfohr-Madsen, Giesbrecht) and Psychology (Tomfohr-Madsen, Giesbrecht), University of Calgary; Alberta Children's Hospital Research Institute (ACHRI) (Dewey, Reimer, Tomfohr-Madsen, Giesbrecht); and Department of Community Health Sciences (Dewey, Giesbrecht), UCVM Bioinformatics, Faculty of Veterinary Medicine (Workentine), Faculty of Kinesiology (Reimer), and Department of Biochemistry and Molecular Biology, Cumming School of Medicine (Reimer), University of Calgary, Calgary, Alberta, Canada.
Psychosom Med. 2022;84(2):159-169. doi: 10.1097/PSY.0000000000001026.
Emerging evidence points toward a connection between mental health and the gut microbiota and its metabolites (e.g., short-chain fatty acids). It is unknown whether the gut microbiota is associated with the development of mental health problems (e.g., internalizing or externalizing behaviors) in preschool children. The objective of this study was to evaluate associations between the gut microbiota and internalizing and externalizing behaviors in preschool-aged children.
A community sample of 248 typically developing children (3-5 years of age) provided a stool sample for gut microbiota and SCFA analysis. Parents reported child internalizing and externalizing behaviors using the Child Behavior Checklist. Associations between child behaviors and gut microbiota measures were analyzed using Spearman correlations followed by an adjustment for multiple testing, with subanalysis conducted in children clinically "at risk" for behavioral problems compared with those who were not.
There was a correlation between Shannon alpha diversity with internalizing behaviors (rs = -0.134, p = .035) and its subscale somatic complaints (rs = -0.144, p = .023). In addition, children clinically "at risk" for internalizing problems had decreased alpha diversity (U = 551, p = .017). Internalizing behaviors correlated with valerate and isobutyrate (rs = -0.147, p = .021; rs = -0.140, p = .028, respectively). Furthermore the somatic complaints subscale additionally correlated with acetate and butyrate (rs = -0.219, p = .001; rs = -0.241, p < .001, respectively). These findings were also present in children "at risk" for internalizing problems (U = 569, p = .026; U = 571, p = .028) and somatic complaints (U = 164, p = .004; U = 145, p = .001).
These analyses reveal novel associations between internalizing behaviors and the gut microbiota in preschool children. Furthermore, a relationship between somatic complaints and acetate and butyrate was identified, indicating that interventions that increase SCFA production warrant future investigation.
越来越多的证据表明,心理健康与肠道微生物群及其代谢物(如短链脂肪酸)之间存在关联。目前尚不清楚肠道微生物群是否与学龄前儿童心理健康问题(如内化或外化行为)的发展有关。本研究旨在评估肠道微生物群与学龄前儿童内化和外化行为之间的关系。
对 248 名典型发育儿童(3-5 岁)进行社区样本采集,以获取肠道微生物群和 SCFA 分析。父母使用儿童行为检查表报告儿童的内化和外化行为。使用 Spearman 相关分析和多重检验调整后分析儿童行为与肠道微生物群测量值之间的关系,对临床“有行为问题风险”的儿童与无行为问题的儿童进行亚组分析。
Shannon 多样性与内化行为呈负相关(rs = -0.134,p =.035),与躯体抱怨呈负相关(rs = -0.144,p =.023)。此外,临床“有内化问题风险”的儿童 alpha 多样性降低(U = 551,p =.017)。内化行为与戊酸盐和异丁酸呈负相关(rs = -0.147,p =.021;rs = -0.140,p =.028)。此外,躯体抱怨子量表还与乙酸盐和丁酸盐呈负相关(rs = -0.219,p =.001;rs = -0.241,p <.001)。这些发现也存在于有内化问题风险的儿童中(U = 569,p =.026;U = 571,p =.028)和躯体抱怨(U = 164,p =.004;U = 145,p =.001)。
这些分析揭示了学龄前儿童内化行为与肠道微生物群之间的新关联。此外,还发现了躯体抱怨与乙酸盐和丁酸盐之间的关系,表明增加 SCFA 产生的干预措施值得进一步研究。