Skip to main content

SYSTEMATIC REVIEW article

Front. Neurosci., 21 March 2024
Sec. Gut-Brain Axis
This article is part of the Research Topic Reviews in Gut-Brain Axis: Stress, dysregulation in gut-brain axis function and stress related disorders View all 7 articles

Bipolar disorder and the gut microbiota: a bibliometric analysis

  • 1Hangzhou First People’s Hospital, Hangzhou, China
  • 2Department of Psychiatry, Chaohu Hospital of Anhui Medical University, Hefei, China
  • 3School of Mental Health and Psychological Sciences, Anhui Medical University, Hefei, China

Background: Previous studies have explored the relationship between bipolar disorder and gut microbiota. However, there has been no bibliometric analysis to summarize and analyze these publications. Our objective was to perform a bibliometric analysis to investigate the current status and frontiers of the publications in the field of the association between bipolar disorder and the gut microbiota.

Methods: We retrieved publications concerning the interplay between the gut microbiota and bipolar disorder from the Web of Science Core Collection (WoSCC). The analysis was executed using WoSCC’s literature analysis tool and VOSviewer 1.6.16.

Results: In total, we identified 177 publications originating from 362 institutions across 39 countries/regions, and these articles were disseminated in 104 different journals. The most productive institutions, authors, countries/regions, and journals were Zhejiang University contributing 18 publications, Shaohua Hu authoring 12 publications, China with 53 publications, and Frontiers in Psychiatry with 11 publications. The first high-cited document was published in the Journal of Psychiatric Research in 2017, and authored by Evans. In this article, they found gut microbiome composition was associated with BD and its illness severity, and they concluded that targeting the gut microbiota may be helpful to develop the effective treatment for bipolar disorder. The top 5 keywords with the highest frequency except for bipolar disorder and gut microbiota were as follows: depression, inflammation, probiotic, gut-brain axis, and anxiety.

Conclusion: In conclusion, this is the first bibliometric analysis to explore the publications in the field of the association between bipolar disorder and the gut microbiota. The main research hotspots regarding this field were the characteristics, abundance, and diversity of gut microbiome in bipolar disorder, the role of treatment and gut microbiome in bipolar disorder, microbiome-brain connections in bipolar disorder, and interventions for bipolar disorder based on microbiota composition modification. The number of studies about the association between gut microbiota and bipolar disorder is relatively small, and more studies are needed to expand our understanding the association between gut microbiota and bipolar disorder.

Introduction

Bipolar disorder is a severe psychiatric disorder which is characterized by hypomanic states, manic episodes, and the interweaving or alternating occurrences of depressive episodes (Craddock and Sklar, 2013; Grande et al., 2016; Scott et al., 2017; Carvalho et al., 2020; McIntyre et al., 2020; Goes, 2023). It is estimated that the 12-month and lifetime prevalence for bipolar disorder is 1.5 and 2.4%, respectively. It was reported 6 to 7% of patients with bipolar disorder committed suicide (Carvalho et al., 2020). The treatment for bipolar disorder consists two aspects of acute management and long-term management (Goes, 2023). In the phase of acute management, antipsychotics and mood stabilizers are the mainstay of depression and bipolar mania. In addition, electroconvulsive therapy (ECT) is effective for treatment-resistant patients, particularly those with catatonic features or psychotic. For the phase of long-term management, the combinations of pharmacological, psychological, and lifestyle interventions should be used (Carvalho et al., 2020). More strategies should be explored to prevent and treat the bipolar disorder.

In recent years, the studies about bipolar disorder and the gut microbiome become more and more popular (Evans et al., 2017; Zheng et al., 2020; Li et al., 2022). The gut microbiota is a rapidly advancing biomedical frontier, which is associated with psychiatric diseases including schizophrenia (Samochowiec and Misiak, 2021; Yang et al., 2022), bipolar disorder (Li et al., 2022), depression (Zhu et al., 2021; Liu et al., 2023), and autism (Sharon et al., 2019; Lin et al., 2022). Gut microbiota, act as “metabolic machinery,” can influence many aspects of physiology through immunological hormonal, and neural pathways (Hu et al., 2019). The gut microbiota can influence host metabolism, and interact with the central nervous system by gut-brain axis (Basiji et al., 2023). Gut microbiota may influence the pathophysiology and etiology of bipolar disorder by disrupting homeostatic regulation (Li et al., 2022). Understanding the association between gut microbiota in bipolar disorder (BD) will be helpful to find new effective disease markers and treatment strategies (Fond et al., 2015; Nguyen et al., 2018). Bibliometric analysis is the most frequently used method to summarize the current status and predict developmental trends by analysis of many components such as authors, countries, institutions, and citations for overall studies in a specific field. By this method, previous studies have explored the association between gut microbiota and many psychiatric conditions including schizophrenia (Yang et al., 2022), depression (Zhu et al., 2021), and autism (Lin et al., 2022). However, there was no bibliometric study to explore the association between gut microbiota and bipolar disorder. Bibliometric analysis is a methodological approach used to quantitatively assess academic literature, providing a comprehensive overview of research trends, patterns, and networks in a specific field. It involves statistical analysis of various aspects of scientific publications, such as publication and citation counts, to gauge the impact and influence of research works, authors, or journals. This analysis also includes examining the relationships and collaborations between authors, institutions, and countries, as well as identifying dominant themes, emerging trends, and potential gaps in the research through content analysis. Conducting a bibliometric analysis of the relationship between BD and gut microbiota is crucial can provide a comprehensive overview of the research landscape, identifying pivotal studies, trends, and gaps in this emerging field. Therefore, our study aims to conduct a bibliometric analysis for the publications in the field of the association between gut microbiota and bipolar disorder, to determine the current status and frontiers in this field.

Materials and methods

In our study, all relevant publications were extracted from Web of Science Core Collection (WoSCC). The search terms were: (microbiome* OR microbiot* OR microflora OR microbiota OR microbiome) AND (intestin* OR intestinal OR gut OR gastro-intestin* OR gastrointestinal*) AND (“bipolar disorder” or “bipolar depression” or “bipolar disorders” or mania or “mood disorder” or “affective disorder” or “mood disorders” or “affective disorders”) from inception to 1 June 2023. Two reviewers (Lin and Wang) investigated each study according to inclusion criteria by screening the titles, abstracts, and full-text of publications. They discussed with the third author (Huang) if they could not reach an agreement about some publications.

After the selection process, we downloaded and imported the TXT format containing “Full Record and Cited References” into the VOSviewer software. Our analysis encompassed two stages, utilizing both the WoSCC literature analysis system and the VOSviewer 1.6.16 software. The WoSCC literature analysis system was used to analysis categories, publication years, document types, h-index and the distribution of institutions, countries/regions and authors. We summarized the leading 10 authors, institutions, countries/regions, and journals in terms of the number of publications, and provided the information of the 20 most highly cited publications. VOSviewer1.6.16 software was used to perform co-authorship of authors, organizations, and countries, co-occurrence of all keywords and co-citation of cited references. For co-occurrence analysis of keywords, we merge the synonyms of “gut microbiota,” “gut microbiome,” “fecal microbiota,” “gut-microbiota,” “intestinal microbiota,” “microbiota,” and “microbiome” into the term “gut microbiota”; “major depressive disorder” and “depression” into the term “depression.”

Results

Literature search and trends analysis

A total of 436 records were yielded in our primary database search. After screening titles, abstracts, and full text, a total of 177 publications were included in the analysis, which was shown in Figure 1. The total number of publications per year was listed in Figure 2. The documents can be classified into two phases: documents published before 2017 were in the first phase. In this phase, the number of documents was small annually. The second phase was 2017–2023, and in this phase, the number of documents was all beyond 10 publications per year. For subject area of documents, the top two subject categories were the psychiatry and neurosciences, accounting for 79 and 56 publications, respectively.

FIGURE 1
www.frontiersin.org

Figure 1. Search flowchart.

FIGURE 2
www.frontiersin.org

Figure 2. Annual publications quantitative distribution.

Country/region, institution and author analysis

In total, 394 institutions across 46 countries/regions were included. The most productive institution was Zhejiang University contributing 18 publications, which was followed by University of Toronto contributing 11 publications, and Baylor College of Medicine contributing 9 publications. The top 3 productive countries were China with 53 publications, USA with 42 publications, and Canada with 19 publications. For most productive authors, Shaohua Hu contributed the most publications with 12 documents, and Peifen Zhang, Caixi Xi, Jianbo Lai with 9 publications following him. The top 10 most productive organizations, authors, and countries/regions were shown in Table 1. In addition, the network visualization maps of co-authorship of countries, authors, and institutions were displayed in Figure 3, and the top 3 cooperative authors were Shaohua Hu (TLS = 118), Jianbo Lai (TLS = 113), and Caixi Xi (TLS = 89). For organizations, they were Zhejiang University (TLS = 47), Melbourne University (TLS = 30), and Deakin University (TLS = 30). For countries/regions, they were USA (TLS = 34), Australia (TLS = 25) and Canada (TLS = 22).

TABLE 1
www.frontiersin.org

Table 1. The top 10 productive authors, institutions and countries based on publications.

FIGURE 3
www.frontiersin.org

Figure 3. Visualization knowledge maps of authors, institutions, and countries/regions (A) The co-authorship map of authors (B) the co-authorship map of institutions (C) the co-authorship map of countries/regions.

Journal and high-cited publication analysis

All publications were distributed in 112 journals. Among them, Frontiers in Psychiatry was the most productive journal with 11 publications, and followed by Progress in Neuro-Psychopharmacology & Biological Psychiatry with 8 publications, and Journal of Affective Disorders with 5 publications. The top 10 most productive journals were summarized in Table 2. For the citation of publications, the first high-cited document was in Journal of Psychiatric Research in 2017, and authored by Evans et al. (2017). In this study, 115 patients with bipolar disorder and 64 control subjects were included and the stool microbiome were measured by the stool microbiome. They found gut microbiome compositions were associated with BD and its illness severity, and they concluded that targeting the gut microbiota may be helpful to develop effective treatment for bipolar disorder. The second high-cited document was in Brain Behavior and Immunity in 2017, and authored by Dickerson et al. (2017). In their article, they believed that the successful development of therapeutic agents which can alter gut microbiome and gastrointestinal inflammation in bipolar disorder will be helpful to develop novel effective strategies to prevent and treat it. The third high-cited document was in JAMA Psychiatry in 2021, and authored by Nikolova et al. (2021). In this article, they found that gut microbiome perturbations were related to the transdiagnostic pattern with bipolar disorder. The characteristics of top 20 most high-cited publications (Hornig, 2013; Fond et al., 2015; Alam et al., 2017; Dickerson et al., 2017; Evans et al., 2017; Flowers et al., 2017; Jacka, 2017; Rosenblat and McIntyre, 2017; Kim and Shin, 2018; Nguyen et al., 2018; Coello et al., 2019; Fries et al., 2019; Hu et al., 2019; Huang et al., 2019; Painold et al., 2019; Rong et al., 2019; Misiak et al., 2020; Zheng et al., 2020; Nikolova et al., 2021; McGuinness et al., 2022) were displayed in Table 3. The network visualization maps of citations of journals and documents were summarized in Figure 4. In addition, Figure 5 displayed the co-cited references, which are cited by more than one article in these 177 documents, and the top 3 co-cited references were consistent with the top three high-cited publications.

TABLE 2
www.frontiersin.org

Table 2. The top 10 productive journals based on publications.

TABLE 3
www.frontiersin.org

Table 3. The top 20 most high-cited references.

FIGURE 4
www.frontiersin.org

Figure 4. Visualization knowledge maps of journals and references (A) citation of journal; (B) citation of references.

FIGURE 5
www.frontiersin.org

Figure 5. The network visualization map of co-citation of references.

Keyword analysis

The map of the co-occurrence of keywords was displayed in Figure 6, and there were four research directions are also shown. The green cluster includes inflammation and brain. The red cluster includes gut microbiota, depression, and anxiety. The blue cluster includes bipolar disorder, schizophrenia, and probiotic. The yellow cluster includes gut-brain axis and stress. The top 5 keywords with the highest frequency except for bipolar disorder and gut microbiota were as follows: depression (N = 62), schizophrenia (n = 50), inflammation (N = 39), gut-brain axis (N = 25), and brain (N = 24).

FIGURE 6
www.frontiersin.org

Figure 6. Visualization of keyword co-occurrence analysis.

Discussion

General information

To the best of knowledge, it is the first bibliometric analysis of publications in the field of bipolar disorder and the gut microbiome. There were 177 documents from 362 organizations across 39 countries/regions, which were published in 104 journals. The most productive organizations, authors, countries/regions, and journals were Zhejiang University contributing 18 publications, Shaohua Hu authoring 12 publications, China with 53 publications, and Frontiers in Psychiatry with 11 publications. The first high-cited document was in Journal of Psychiatric Research in 2017, and authored by Evans et al. (2017). In this article, they found gut microbiome composition were associated with BD and its illness severity, and they concluded that targeting the gut microbiota may be helpful to develop effective treatment for bipolar disorder. The top 5 keywords with the highest frequency except for bipolar disorder and gut microbiota were as follows: depression, inflammation, probiotic, gut-brain axis, and anxiety. Most of the included publications were from China and USA (95/177, 53.7%), and the number of publications from other countries/regions should be improved.

Hotspots and frontiers

According to top 20 most high-cited documents and the core keywords, the research hotspots and frontiers were summarized as follows:

(1) The characteristics, abundance, and diversity of gut microbiome in bipolar disorder. In the top 20 most high-cited references, 11 publications (Evans et al., 2017; Flowers et al., 2017; Nguyen et al., 2018; Coello et al., 2019; Hu et al., 2019; Huang et al., 2019; Painold et al., 2019; Rong et al., 2019; Zheng et al., 2020; Nikolova et al., 2021; McGuinness et al., 2022) explored the characteristics abundance, and diversity of gut microbiome in bipolar disorder. Some systematic review and meta-analysis (Nguyen et al., 2021; Sublette et al., 2021; Vindegaard et al., 2021; McGuinness et al., 2022; Obi-Azuike et al., 2023) explored this topic, and they were summarized in Table 4. More and more studies have demonstrated disparities in gut microbiome, abundance, and diversity in BD (Chang et al., 2014; Evans et al., 2017; Flowers et al., 2017; Bengesser et al., 2018; Aizawa et al., 2019; Coello et al., 2019; Hu et al., 2019; Jiang et al., 2019; Lu et al., 2019; Painold et al., 2019; Rong et al., 2019; Vinberg et al., 2019; Lai et al., 2021; McIntyre et al., 2021). According to these systematic reviews (Nguyen et al., 2021; Sublette et al., 2021; Vindegaard et al., 2021; McGuinness et al., 2022; Obi-Azuike et al., 2023), it may be confirmed that there were reductions in overall microbial richness in BD. The findings about the α-diversity metrics including microbial richness were controversial. It seems that alterations in Ruminococcaceae, Faecalibacterium, Actinobacteria, Ruminococcus, Lachnospiraceae, and Bacteroidetes were most represented. In addition, the causation of alterations in the gut microbiota and bipolar disorder cannot be determined based on current studies since most of them are observational.

TABLE 4
www.frontiersin.org

Table 4. The systematic review and meta-analysis of the characteristics, abundance, and diversity of gut microbiome in bipolar disorder.

(2) The role of treatment and gut microbiome in bipolar disorder. A few studies explored the association between medication treatment for bipolar disorder and gut microbiome. For example, Flowers et al. (2017) found that the treatment of atypical antipsychotic (AAP) was associated with specific representation of gut bacterial families, and it is also is related to decreased species richness in female. Lai et al. (2022) focused on understanding the gut microbiota changes in bipolar disorder (BD) patients experiencing depressive episodes and the effects of quetiapine monotherapy. The research involved 62 BD patients and 60 healthy individuals, with fecal samples collected for metagenomic sequencing. The study found that BD patients had specific alterations in gut microbial diversity and composition, which were notably modified after 1 month of quetiapine treatment. A significant finding was the correlation of Clostridium bartlettii abundance with factors like patient age, baseline depression severity, and brain function, particularly in the hippocampus. The study also developed random forest models based on bacterial species, achieving reasonable accuracy in distinguishing between patients and controls, and between treatment responders and non-responders. These results suggest that gut microbiota alterations could serve as potential biomarkers for diagnosing BD and predicting treatment outcomes.

(3) Microbiome-brain connections in bipolar disorder. In the top 20 most high-cited references, 7 publications (Hornig, 2013; Alam et al., 2017; Dickerson et al., 2017; Rosenblat and McIntyre, 2017; Kim and Shin, 2018; Fries et al., 2019; Misiak et al., 2020) explored the microbiome-brain connections in bipolar disorder. For core keywords, inflammation in the green cluster, and gut-brain axis in the yellow cluster were related to this topic. Microbiome-brain connections in bipolar disorder may be associated with inflammation (Yuan et al., 2019; Jones et al., 2021; Lai et al., 2021), tryptophan metabolism (Barbuti et al., 2017; Wang and Miller, 2018; Wang et al., 2019), microglia (Cenit et al., 2017; Morais et al., 2021), the aryl hydrocarbon receptor (Reiter et al., 2018; Neamah et al., 2020; Tischkau, 2020; Barroso et al., 2021), and endocrine function (Perry et al., 2019; Anderson and Maes, 2020). A recent study (Li et al., 2022) used multi-omics analyses to explore microbiome-brain connections, and in this study, 109 unmedicated patients with BD and 40 controls were included. The serum metabolomics, fecal metagenomic, and neuroimaging were used to explore the characteristics of microbial-gut-brain axis in BD. The findings revealed the identification of BD-associated neuroactive microbes and metabolites, which emerged as potential markers linked to distinct features of brain network functional connectivity in BD. These markers suggested possible implications for disrupted cognitive functioning and emotional regulation. In a comprehensive analysis of over 12,000 measured metabolic features, a substantial divergence (73.54%) in serum metabolome profiles was observed between BD patients and healthy controls. This divergence pinpointed distinctively abundant microbial-derived neuroactive metabolites, encompassing various gamma-aminobutyric acid, kynurenic acid, B vitamins, and short-chain fatty acids. These identified metabolites demonstrated potential connections with the prevalence of specific gut microbiota species, each with corresponding biosynthetic capabilities. Notable among them were Akkermansia muciniphila, Citrobacter spp, Phascolarctobacterium spp, Yersinia spp, Enterobacter spp, and Flavobacterium spp. Some bacteria may play an important role as “psychobiotic” in the gut-brain axis connection between bipolar disorder and gut microbiome. This approach unveiled possible signaling pathways connecting the gut, the microbiome, and the brain, suggesting a potential contribution to the underlying mechanisms of BD.

(4) Interventions for bipolar disorder based on microbiota composition modification. In the top 20 most high-cited references, 5 publications mentioned the microbial-based interventions for bipolar disorder (Fond et al., 2015; Dickerson et al., 2017; Evans et al., 2017; Jacka, 2017; Rosenblat and McIntyre, 2017). For core words, the probiotic in the blue cluster was related to this topic. It may be a promising avenue to combine microbial-based interventions and standard therapy for improving certain parameters like hospitalization length, cognition, and metabolic side effects in bipolar disorder. For example, Reininghaus et al. (2018) conducted pilot study to analyze the effect of probiotic supplements on cognitive parameters in patients with bipolar disorder, and found that probiotic supplement might be helpful to improve the cognitive function in patients with bipolar disorder. Dickerson et al. (2018) conducted a trial to investigate whether the administration of probiotic supplement can prevent psychiatric rehospitalizations in individuals with BD, and in their study, 66 patients with BD were randomized to receive 6 months of adjunctive probiotics or adjunctive placebo. The results demonstrated that 8 rehospitalizations in the 33 patients who received the probiotics while 24 rehospitalizations in the 33 patients who received placebo (P = 0.009), and what’s more, probiotics was associated with a significant advantage (P = 0.007). They concluded that Probiotic supplementation may be associated with a lower rate of rehospitalization. A systematic review (Sublette et al., 2021) demonstrated that probiotic supplementation can lower patient rehospitalizations and improve cognitive impairments and depressive symptoms significantly in patients with BD. In addition, fecal microbial transplantation (FMT) may be a potentially effective strategy for the treatment of bipolar disorder.

Our study has some limitations that should be acknowledged. Firstly, we solely utilized the WoSCC database due to the constraints of the VOSviewer software, which prevented the analysis and visualization of co-citation maps from other databases such as Embase and PubMed. Secondly, the inclusion of publications from the year 2023 was incomplete due to our study’s cutoff date. In addition, there is a distinct role of gender in bipolar disorder. However, only few studies explored the gender differences between bipolar disorder and the gut microbiota (Flowers et al., 2019; Nikolova et al., 2021). Furthermore, the total number of publications in this specific domain remains relatively small, underscoring the necessity for further investigations to expand our understanding of the association between gut microbiota and bipolar disorder.

In conclusion, this is the first bibliometric analysis to investigate the publications in the field of the association between bipolar disorder and the gut microbiota. The main research hotspots regarding this field were the characteristics, abundance, and diversity of gut microbiome in bipolar disorder, the role of treatment and gut microbiome in bipolar disorder, microbiome-brain connections in bipolar disorder, and interventions for bipolar disorder based on microbiota composition modification. The number of studies about the association between gut microbiota and bipolar disorder is relatively small, and more studies are needed to expand our understanding of the link between gut microbiota and bipolar disorder.

Data availability statement

The original contributions presented in this study are included in this article/supplementary material, further inquiries can be directed to the corresponding authors.

Author contributions

XL: Data curation, Formal Analysis, Methodology, Project administration, Supervision, Writing – original draft. SW: Data curation, Funding acquisition, Methodology, Resources, Supervision, Writing – original draft, Writing – review & editing. JH: Formal Analysis, Funding acquisition, Project administration, Resources, Visualization, Writing – original draft, Writing – review & editing. KZ: Data curation, Supervision, Writing – original draft, Writing – review & editing.

Funding

The authors declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Aizawa, E., Tsuji, H., Asahara, T., Takahashi, T., Teraishi, T., Yoshida, S., et al. (2019). Bifidobacterium and Lactobacillus counts in the gut Microbiota of patients with bipolar disorder and healthy controls. Front. Psychiatry 9:730. doi: 10.3389/fpsyt.2018.00730

PubMed Abstract | Crossref Full Text | Google Scholar

Alam, R., Abdolmaleky, H., and Zhou, J. (2017). Microbiome, inflammation, epigenetic alterations, and mental diseases. Am. J. Med. Genet. B Neuropsychiatr. Genet. 174, 651–660.

Google Scholar

Anderson, G., and Maes, M. (2020). Gut dysbiosis dysregulates central and systemic homeostasis via suboptimal mitochondrial function: assessment, treatment and classification implications. Curr. Top. Med. Chem. 20, 524–539. doi: 10.2174/1568026620666200131094445

PubMed Abstract | Crossref Full Text | Google Scholar

Barbuti, M., Carvalho, A., Köhler, C., Murru, A., Verdolini, N., Guiso, G., et al. (2017). Thyroid autoimmunity in bipolar disorder: a systematic review. J. Affect. Disord. 221, 97–106.

Google Scholar

Barroso, A., Mahler, J., Fonseca-Castro, P., and Quintana, F. (2021). The aryl hydrocarbon receptor and the gut-brain axis. Cell Mol. Immunol. 18, 259–268.

Google Scholar

Basiji, K., Sendani, A., Ghavami, S., Farmani, M., Kazemifard, N., Sadeghi, A., et al. (2023). The critical role of gut-brain axis microbiome in mental disorders. Metab. Brain Dis. 38, 2547–2561.

Google Scholar

Bengesser, S., Reininghaus, E., Lackner, N., Birner, A., Fellendorf, F., Platzer, M., et al. (2018). Is the molecular clock ticking differently in bipolar disorder? Methylation analysis of the clock gene ARNTL. World J. Biol. Psychiatry 19, S21–S29. doi: 10.1080/15622975.2016.1231421

PubMed Abstract | Crossref Full Text | Google Scholar

Carvalho, A., Firth, J., and Vieta, E. (2020). Bipolar disorder. N. Engl. J. Med. 383, 58–66.

Google Scholar

Cenit, M., Sanz, Y., and Codoñer-Franch, P. (2017). Influence of gut microbiota on neuropsychiatric disorders. World J. Gastroenterol. 23, 5486–5498.

Google Scholar

Chang, P., Hao, L., Offermanns, S., and Medzhitov, R. (2014). The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition. Proc. Natl. Acad. Sci. U S A. 111, 2247–2252.

Google Scholar

Coello, K., Hansen, T., Sørensen, N., Munkholm, K., Kessing, L., Pedersen, O., et al. (2019). Gut microbiota composition in patients with newly diagnosed bipolar disorder and their unaffected first-degree relatives. Brain Behav. Immun. 75, 112–118. doi: 10.1016/j.bbi.2018.09.026

PubMed Abstract | Crossref Full Text | Google Scholar

Craddock, N., and Sklar, P. (2013). Genetics of bipolar disorder. Lancet 381, 1654–1662.

Google Scholar

Dickerson, F., Adamos, M., Katsafanas, E., Khushalani, S., Origoni, A., Savage, C., et al. (2018). Adjunctive probiotic microorganisms to prevent rehospitalization in patients with acute mania: a randomized controlled trial. Bipolar. Disord. 20, 614–621. doi: 10.1111/bdi.12652

PubMed Abstract | Crossref Full Text | Google Scholar

Dickerson, F., Severance, E., and Yolken, R. (2017). The microbiome, immunity, and schizophrenia and bipolar disorder. Brain Behav. Immun. 62, 46–52.

Google Scholar

Evans, S., Bassis, C., Hein, R., Assari, S., Flowers, S., Kelly, M., et al. (2017). The gut microbiome composition associates with bipolar disorder and illness severity. J. Psychiatr Res. 87, 23–29. doi: 10.1016/j.jpsychires.2016.12.007

PubMed Abstract | Crossref Full Text | Google Scholar

Flowers, S., Baxter, N., Ward, K., Kraal, A., McInnis, M., Schmidt, T., et al. (2019). Effects of atypical antipsychotic treatment and resistant starch supplementation on gut microbiome composition in a cohort of patients with bipolar disorder or Schizophrenia. Pharmacotherapy 39, 161–170.

Google Scholar

Flowers, S., Evans, S., Ward, K., McInnis, M., and Ellingrod, V. (2017). Interaction between atypical antipsychotics and the gut microbiome in a bipolar disease cohort. Pharmacotherapy 37, 261–267. doi: 10.1002/phar.1890

PubMed Abstract | Crossref Full Text | Google Scholar

Fond, G., Boukouaci, W., Chevalier, G., Regnault, A., Eberl, G., Hamdani, N., et al. (2015). The "psychomicrobiotic": targeting microbiota in major psychiatric disorders: a systematic review. Pathol. Biol. 63, 35–42.

Google Scholar

Fries, G., Walss-Bass, C., Bauer, M., and Teixeira, A. (2019). Revisiting inflammation in bipolar disorder. Pharmacol. Biochem. Behav. 177, 12–19.

Google Scholar

Goes, F. (2023). Diagnosis and management of bipolar disorders. BMJ 381:e073591.

Google Scholar

Grande, I., Berk, M., Birmaher, B., and Vieta, E. (2016). Bipolar disorder. Lancet 387, 1561–1572.

Google Scholar

Hornig, M. (2013). The role of microbes and autoimmunity in the pathogenesis of neuropsychiatric illness. Curr. Opin. Rheumatol. 25, 488–795.

Google Scholar

Hu, S., Li, A., Huang, T., Lai, J., Li, J., Sublette, M., et al. (2019). Gut microbiota changes in patients with bipolar depression. Adv. Sci. 6:1900752.

Google Scholar

Huang, T., Lai, J., Du, Y., Xu, Y., Ruan, L., and Hu, S. (2019). Current understanding of gut microbiota in mood disorders: an update of human studies. Front. Genet. 10:98. doi: 10.3389/fgene.2019.00098

PubMed Abstract | Crossref Full Text | Google Scholar

Jacka, F. (2017). Nutritional psychiatry: where to next? EBioMedicine 17, 24–29.

Google Scholar

Jiang, H., Xu, L., Zhang, X., Zhang, Z., and Ruan, B. (2019). The microbiome in bipolar depression: a longitudinal study of one pair of monozygotic twins. Bipolar. Disord. 21, 93–97. doi: 10.1111/bdi.12736

PubMed Abstract | Crossref Full Text | Google Scholar

Jones, G., Vecera, C., Pinjari, O., and Machado-Vieira, R. (2021). Inflammatory signaling mechanisms in bipolar disorder. J. Biomed. Sci. 28:45.

Google Scholar

Kim, Y., and Shin, C. (2018). The microbiota-gut-brain axis in neuropsychiatric disorders: pathophysiological mechanisms and novel treatments. Curr. Neuropharmacol. 16, 559–573.

Google Scholar

Lai, J., Li, A., Jiang, J., Yuan, X., Zhang, P., Xi, C., et al. (2022). Metagenomic analysis reveals gut bacterial signatures for diagnosis and treatment outcome prediction in bipolar depression. Psychiatry Res. 307:114326. doi: 10.1016/j.psychres.2021.114326

PubMed Abstract | Crossref Full Text | Google Scholar

Lai, W., Zhao, J., Xu, S., Deng, W., Xu, D., Wang, M., et al. (2021). Shotgun metagenomics reveals both taxonomic and tryptophan pathway differences of gut microbiota in bipolar disorder with current major depressive episode patients. J. Affect. Disord. 278, 311–319. doi: 10.1016/j.jad.2020.09.010

PubMed Abstract | Crossref Full Text | Google Scholar

Li, Z., Lai, J., Zhang, P., Ding, J., Jiang, J., Liu, C., et al. (2022). Multi-omics analyses of serum metabolome, gut microbiome and brain function reveal dysregulated microbiota-gut-brain axis in bipolar depression. Mol. Psychiatry 27, 4123–4135. doi: 10.1038/s41380-022-01569-9

PubMed Abstract | Crossref Full Text | Google Scholar

Lin, X., Zhou, R., Liang, D., Xia, L., Zeng, L., and Chen, X. (2022). The role of microbiota in autism spectrum disorder: a bibliometric analysis based on original articles. Front. Psychiatry 13:976827. doi: 10.3389/fpsyt.2022.976827

PubMed Abstract | Crossref Full Text | Google Scholar

Liu, L., Wang, H., Chen, X., Zhang, Y., Zhang, H., and Xie, P. (2023). Gut microbiota and its metabolites in depression: from pathogenesis to treatment. EBioMedicine 90:104527.

Google Scholar

Lu, Q., Lai, J., Lu, H., Ng, C., Huang, T., Zhang, H., et al. (2019). Gut microbiota in bipolar depression and its relationship to brain function: an advanced exploration. Front. Psychiatry 10:784. doi: 10.3389/fpsyt.2019.00784

PubMed Abstract | Crossref Full Text | Google Scholar

McGuinness, A., Davis, J., Dawson, S., Loughman, A., Collier, F., O’Hely, M., et al. (2022). A systematic review of gut microbiota composition in observational studies of major depressive disorder, bipolar disorder and schizophrenia. Mol. Psychiatry 27, 1920–1935. doi: 10.1038/s41380-022-01456-3

PubMed Abstract | Crossref Full Text | Google Scholar

McIntyre, R., Berk, M., Brietzke, E., Goldstein, B., López-Jaramillo, C., Kessing, L., et al. (2020). Bipolar disorders. Lancet 396, 1841–1856.

Google Scholar

McIntyre, R., Subramaniapillai, M., Shekotikhina, M., Carmona, N., Lee, Y., Mansur, R., et al. (2021). Characterizing the gut microbiota in adults with bipolar disorder: a pilot study. Nutr. Neurosci. 24, 173–180. doi: 10.1080/1028415X.2019.1612555

PubMed Abstract | Crossref Full Text | Google Scholar

Misiak, B., Łoniewski, I., Marlicz, W., Frydecka, D., Szulc, A., Rudzki, L., et al. (2020). The HPA axis dysregulation in severe mental illness: can we shift the blame to gut microbiota? Prog Neuropsychopharmacol Biol. Psychiatry 102:109951. doi: 10.1016/j.pnpbp.2020.109951

PubMed Abstract | Crossref Full Text | Google Scholar

Morais, L., Schreiber, H., and Mazmanian, S. (2021). The gut microbiota-brain axis in behaviour and brain disorders. Nat. Rev. Microbiol. 19, 241–255.

Google Scholar

Neamah, W., Busbee, P., Alghetaa, H., Abdulla, O., Nagarkatti, M., and Nagarkatti, P. (2020). AhR activation leads to alterations in the gut microbiome with consequent effect on induction of myeloid derived suppressor cells in a CXCR2-dependent manner. Int. J. Mol. Sci. 21:9613. doi: 10.3390/ijms21249613

PubMed Abstract | Crossref Full Text | Google Scholar

Nguyen, T., Hathaway, H., Kosciolek, T., Knight, R., and Jeste, D. (2021). Gut microbiome in serious mental illnesses: a systematic review and critical evaluation. Schizophr. Res. 234, 24–40. doi: 10.1016/j.schres.2019.08.026

PubMed Abstract | Crossref Full Text | Google Scholar

Nguyen, T., Kosciolek, T., Eyler, L., Knight, R., and Jeste, D. (2018). Overview and systematic review of studies of microbiome in schizophrenia and bipolar disorder. J. Psychiatr Res. 99, 50–61. doi: 10.1016/j.jpsychires.2018.01.013

PubMed Abstract | Crossref Full Text | Google Scholar

Nikolova, V., Smith, M., Hall, L., Cleare, A., Stone, J., and Young, A. (2021). Perturbations in gut microbiota composition in psychiatric disorders: a review and meta-analysis. JAMA Psychiatry 78, 1343–1354. doi: 10.1001/jamapsychiatry.2021.2573

PubMed Abstract | Crossref Full Text | Google Scholar

Obi-Azuike, C., Ebiai, R., Gibson, T., Hernandez, A., Khan, A., Anugwom, G., et al. (2023). A systematic review on gut-brain axis aberrations in bipolar disorder and methods of balancing the gut microbiota. Brain Behav. 13:e3037. doi: 10.1002/brb3.3037

PubMed Abstract | Crossref Full Text | Google Scholar

Painold, A., Mörkl, S., Kashofer, K., Halwachs, B., Dalkner, N., Bengesser, S., et al. (2019). A step ahead: exploring the gut microbiota in inpatients with bipolar disorder during a depressive episode. Bipolar Disord. 21, 40–49. doi: 10.1111/bdi.12682

PubMed Abstract | Crossref Full Text | Google Scholar

Perry, A., Roberts, G., Mitchell, P., and Breakspear, M. (2019). Connectomics of bipolar disorder: a critical review, and evidence for dynamic instabilities within interoceptive networks. Mol. Psychiatry 24, 1296–1318.

Google Scholar

Reininghaus, E., Wetzlmair, L., Fellendorf, F., Platzer, M., Queissner, R., Birner, A., et al. (2018). The impact of probiotic supplements on cognitive parameters in euthymic individuals with bipolar disorder: a pilot study. Neuropsychobiology Online ahead of print. doi: 10.1159/000492537

PubMed Abstract | Crossref Full Text | Google Scholar

Reiter, R., Tan, D., Rosales-Corral, S., Galano, A., Zhou, X., and Xu, B. (2018). Mitochondria: central organelles for melatonin’s antioxidant and anti-aging actions. Molecules 23:509. doi: 10.3390/molecules23020509

PubMed Abstract | Crossref Full Text | Google Scholar

Rong, H., Xie, X., Zhao, J., Lai, W., Wang, M., Xu, D., et al. (2019). Similarly in depression, nuances of gut microbiota: evidences from a shotgun metagenomics sequencing study on major depressive disorder versus bipolar disorder with current major depressive episode patients. J. Psychiatr. Res. 113, 90–99. doi: 10.1016/j.jpsychires.2019.03.017

PubMed Abstract | Crossref Full Text | Google Scholar

Rosenblat, J., and McIntyre, R. (2017). Bipolar disorder and immune dysfunction: epidemiological findings, proposed pathophysiology and clinical implications. Brain Sci. 7:144. doi: 10.3390/brainsci7110144

PubMed Abstract | Crossref Full Text | Google Scholar

Samochowiec, J., and Misiak, B. (2021). Gut microbiota and microbiome in schizophrenia. Curr. Opin. Psychiatry 34, 503–507.

Google Scholar

Scott, J., Murray, G., Henry, C., Morken, G., Scott, E., Angst, J., et al. (2017). Activation in bipolar disorders: a systematic review. JAMA Psychiatry 74, 189–196.

Google Scholar

Sharon, G., Cruz, N., Kang, D., Gandal, M., Wang, B., Kim, Y., et al. (2019). Human gut microbiota from autism spectrum disorder promote behavioral symptoms in mice. Cell 177, 1600–1618.e17. doi: 10.1016/j.cell.2019.05.004

PubMed Abstract | Crossref Full Text | Google Scholar

Sublette, M., Cheung, S., Lieberman, E., Hu, S., Mann, J., Uhlemann, A., et al. (2021). Bipolar disorder and the gut microbiome: a systematic review. Bipolar. Disord. 23, 544–564.

Google Scholar

Tischkau, S. (2020). Mechanisms of circadian clock interactions with aryl hydrocarbon receptor signalling. Eur. J. Neurosci. 51, 379–395.

Google Scholar

Vinberg, M., Ottesen, N., Meluken, I., Sørensen, N., Pedersen, O., Kessing, L., et al. (2019). Remitted affective disorders and high familial risk of affective disorders associate with aberrant intestinal microbiota. Acta Psychiatr. Scand. 139, 174–184. doi: 10.1111/acps.12976

PubMed Abstract | Crossref Full Text | Google Scholar

Vindegaard, N., Speyer, H., Nordentoft, M., Rasmussen, S., and Benros, M. (2021). Gut microbial changes of patients with psychotic and affective disorders: a systematic review. Schizophr. Res. 234, 1–10. doi: 10.1016/j.schres.2019.12.014

PubMed Abstract | Crossref Full Text | Google Scholar

Wang, A., and Miller, B. (2018). Meta-analysis of cerebrospinal fluid cytokine and tryptophan catabolite alterations in psychiatric patients: comparisons between Schizophrenia, bipolar disorder, and depression. Schizophr. Bull. 44, 75–83. doi: 10.1093/schbul/sbx035

PubMed Abstract | Crossref Full Text | Google Scholar

Wang, X., Sun, G., Feng, T., Zhang, J., Huang, X., Wang, T., et al. (2019). Sodium oligomannate therapeutically remodels gut microbiota and suppresses gut bacterial amino acids-shaped neuroinflammation to inhibit Alzheimer’s disease progression. Cell Res. 29, 787–803. doi: 10.1038/s41422-019-0216-x

PubMed Abstract | Crossref Full Text | Google Scholar

Yang, C., Lin, X., Wang, X., Liu, H., Huang, J., and Wang, S. (2022). The schizophrenia and gut microbiota: a bibliometric and visual analysis. Front. Psychiatry 13:1022472.

Google Scholar

Yuan, N., Chen, Y., Xia, Y., Dai, J., and Liu, C. (2019). Inflammation-related biomarkers in major psychiatric disorders: a cross-disorder assessment of reproducibility and specificity in 43 meta-analyses. Transl. Psychiatry 9:233. doi: 10.1038/s41398-019-0570-y

PubMed Abstract | Crossref Full Text | Google Scholar

Zheng, P., Yang, J., Li, Y., Wu, J., Liang, W., Yin, B., et al. (2020). Gut microbial signatures can discriminate unipolar from bipolar depression. Adv. Sci. 7:1902862. doi: 10.1002/advs.201902862

PubMed Abstract | Crossref Full Text | Google Scholar

Zhu, X., Hu, J., Deng, S., Tan, Y., Qiu, C., Zhang, M., et al. (2021). Bibliometric and visual analysis of research on the links between the gut microbiota and depression from 1999 to 2019. Front. Psychiatry 11:587670. doi: 10.3389/fpsyt.2020.587670

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: bipolar disorder, gut microbiota, a bibliometric analysis, gut-brain axis, interventions

Citation: Lin X, Huang J, Wang S and Zhang K (2024) Bipolar disorder and the gut microbiota: a bibliometric analysis. Front. Neurosci. 18:1290826. doi: 10.3389/fnins.2024.1290826

Received: 15 September 2023; Accepted: 18 January 2024;
Published: 21 March 2024.

Edited by:

Mingbang Wang, South China Hospital of Shenzhen University, China

Reviewed by:

Kiran Veer Sandhu, University College Cork, Ireland
Shaghayegh Baradaran Ghavami, Shahid Beheshti University of Medical Sciences, Iran

Copyright © 2024 Lin, Huang, Wang and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Xiaoxiao Lin, bGlueGlhb3hpYW9AemNtdS5lZHUuY24=; Shuai Wang, ZHJ3YW5nc2h1YWlAemp1LmVkdS5jbg==; Kai Zhang, emhhbmdrYWlAYWhtdS5lZHUuY24=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.