Gut Microbiome Composition Linked to Inflammatory Factors and Cognitive Functions in First-Episode, Drug-Naive Major Depressive Disorder Patients

The microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive disorder (MDD). However, studies on the microbiota-inflammatory-cognitive function axis in MDD are lacking. The aim of the present study was to...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in neuroscience Vol. 15; p. 800764
Main Authors Liu, Penghong, Gao, Mingxue, Liu, Zhifen, Zhang, Yanyan, Tu, Hongwei, Lei, Lei, Wu, Peiyi, Zhang, Aixia, Yang, Chunxia, Li, Gaizhi, Sun, Ning, Zhang, Kerang
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Research Foundation 28.01.2022
Frontiers Media S.A
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive disorder (MDD). However, studies on the microbiota-inflammatory-cognitive function axis in MDD are lacking. The aim of the present study was to analyze the gut microbiota composition and explore the correlation between gut microbiota and inflammatory factors, cognitive function in MDD patients. Study participants included 66 first-episode, drug naïve MDD patients as well as 43 healthy subjects (HCs). The composition of fecal microbiota was evaluated using16S rRNA sequencing and bioinformatics analysis. The cytokines such as hs-CRP, IL-1β, IL-6, IL-10, and TNF-α in peripheral blood were detected enzyme linked immunosorbent assay (ELISA); assessment of cognitive functions was performed using the Color Trail Test (CTT), The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and the Stroop Color-Word Test (SCWT). We found that compared with HCs, MDD patients had cognitive impairments and showed different α-diversity and β-diversity of gut microbiota composition. LDA effect size (LEfSe) analysis found MDD have higher and lower and at family level. and was higher in the MDD group, however, , and were lower at genus level. Furthermore, In MDD patients, the and were both positively correlated with hsCRP, CCT1, CCT2. was positively correlated with IL-6, Word time, Color time, Word-Color time, Color-Word time and negatively correlated with Delayed Memory, Total score and Standardized score. and were both negatively correlated with IL-1β and IL-6. The present findings confirm that the gut microbiota in MDD patients have altered gut microbes that are closely associated with inflammatory factors and cognitive function in MDD patients.
AbstractList ObjectiveThe microbiota–gut–brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive disorder (MDD). However, studies on the microbiota-inflammatory-cognitive function axis in MDD are lacking. The aim of the present study was to analyze the gut microbiota composition and explore the correlation between gut microbiota and inflammatory factors, cognitive function in MDD patients.MethodStudy participants included 66 first-episode, drug naïve MDD patients as well as 43 healthy subjects (HCs). The composition of fecal microbiota was evaluated using16S rRNA sequencing and bioinformatics analysis. The cytokines such as hs-CRP, IL-1β, IL-6, IL-10, and TNF-α in peripheral blood were detected via enzyme linked immunosorbent assay (ELISA); assessment of cognitive functions was performed using the Color Trail Test (CTT), The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and the Stroop Color-Word Test (SCWT).ResultsWe found that compared with HCs, MDD patients had cognitive impairments and showed different α-diversity and β-diversity of gut microbiota composition. LDA effect size (LEfSe) analysis found MDD have higher Deinococcaceae and lower Bacteroidaceae, Turicibacteraceae, Clostridiaceae and Barnesiellaceae at family level. Deinococcus and Odoribacter was higher in the MDD group, however, Bacteroides, Alistipes, Turicibacter, Clostridium, Roseburia, and Enterobacter were lower at genus level. Furthermore, In MDD patients, the Bacteroidaceae and Bacteroides were both positively correlated with hsCRP, CCT1, CCT2. Alistipes was positively correlated with IL-6, Word time, Color time, Word-Color time, Color-Word time and negatively correlated with Delayed Memory, Total score and Standardized score. Turicibacteraceae and Turicibacter were both negatively correlated with IL-1β and IL-6.ConclusionThe present findings confirm that the gut microbiota in MDD patients have altered gut microbes that are closely associated with inflammatory factors and cognitive function in MDD patients.
The microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive disorder (MDD). However, studies on the microbiota-inflammatory-cognitive function axis in MDD are lacking. The aim of the present study was to analyze the gut microbiota composition and explore the correlation between gut microbiota and inflammatory factors, cognitive function in MDD patients.OBJECTIVEThe microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive disorder (MDD). However, studies on the microbiota-inflammatory-cognitive function axis in MDD are lacking. The aim of the present study was to analyze the gut microbiota composition and explore the correlation between gut microbiota and inflammatory factors, cognitive function in MDD patients.Study participants included 66 first-episode, drug naïve MDD patients as well as 43 healthy subjects (HCs). The composition of fecal microbiota was evaluated using16S rRNA sequencing and bioinformatics analysis. The cytokines such as hs-CRP, IL-1β, IL-6, IL-10, and TNF-α in peripheral blood were detected via enzyme linked immunosorbent assay (ELISA); assessment of cognitive functions was performed using the Color Trail Test (CTT), The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and the Stroop Color-Word Test (SCWT).METHODStudy participants included 66 first-episode, drug naïve MDD patients as well as 43 healthy subjects (HCs). The composition of fecal microbiota was evaluated using16S rRNA sequencing and bioinformatics analysis. The cytokines such as hs-CRP, IL-1β, IL-6, IL-10, and TNF-α in peripheral blood were detected via enzyme linked immunosorbent assay (ELISA); assessment of cognitive functions was performed using the Color Trail Test (CTT), The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and the Stroop Color-Word Test (SCWT).We found that compared with HCs, MDD patients had cognitive impairments and showed different α-diversity and β-diversity of gut microbiota composition. LDA effect size (LEfSe) analysis found MDD have higher Deinococcaceae and lower Bacteroidaceae, Turicibacteraceae, Clostridiaceae and Barnesiellaceae at family level. Deinococcus and Odoribacter was higher in the MDD group, however, Bacteroides, Alistipes, Turicibacter, Clostridium, Roseburia, and Enterobacter were lower at genus level. Furthermore, In MDD patients, the Bacteroidaceae and Bacteroides were both positively correlated with hsCRP, CCT1, CCT2. Alistipes was positively correlated with IL-6, Word time, Color time, Word-Color time, Color-Word time and negatively correlated with Delayed Memory, Total score and Standardized score. Turicibacteraceae and Turicibacter were both negatively correlated with IL-1β and IL-6.RESULTSWe found that compared with HCs, MDD patients had cognitive impairments and showed different α-diversity and β-diversity of gut microbiota composition. LDA effect size (LEfSe) analysis found MDD have higher Deinococcaceae and lower Bacteroidaceae, Turicibacteraceae, Clostridiaceae and Barnesiellaceae at family level. Deinococcus and Odoribacter was higher in the MDD group, however, Bacteroides, Alistipes, Turicibacter, Clostridium, Roseburia, and Enterobacter were lower at genus level. Furthermore, In MDD patients, the Bacteroidaceae and Bacteroides were both positively correlated with hsCRP, CCT1, CCT2. Alistipes was positively correlated with IL-6, Word time, Color time, Word-Color time, Color-Word time and negatively correlated with Delayed Memory, Total score and Standardized score. Turicibacteraceae and Turicibacter were both negatively correlated with IL-1β and IL-6.The present findings confirm that the gut microbiota in MDD patients have altered gut microbes that are closely associated with inflammatory factors and cognitive function in MDD patients.CONCLUSIONThe present findings confirm that the gut microbiota in MDD patients have altered gut microbes that are closely associated with inflammatory factors and cognitive function in MDD patients.
The microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive disorder (MDD). However, studies on the microbiota-inflammatory-cognitive function axis in MDD are lacking. The aim of the present study was to analyze the gut microbiota composition and explore the correlation between gut microbiota and inflammatory factors, cognitive function in MDD patients. Study participants included 66 first-episode, drug naïve MDD patients as well as 43 healthy subjects (HCs). The composition of fecal microbiota was evaluated using16S rRNA sequencing and bioinformatics analysis. The cytokines such as hs-CRP, IL-1β, IL-6, IL-10, and TNF-α in peripheral blood were detected enzyme linked immunosorbent assay (ELISA); assessment of cognitive functions was performed using the Color Trail Test (CTT), The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and the Stroop Color-Word Test (SCWT). We found that compared with HCs, MDD patients had cognitive impairments and showed different α-diversity and β-diversity of gut microbiota composition. LDA effect size (LEfSe) analysis found MDD have higher and lower and at family level. and was higher in the MDD group, however, , and were lower at genus level. Furthermore, In MDD patients, the and were both positively correlated with hsCRP, CCT1, CCT2. was positively correlated with IL-6, Word time, Color time, Word-Color time, Color-Word time and negatively correlated with Delayed Memory, Total score and Standardized score. and were both negatively correlated with IL-1β and IL-6. The present findings confirm that the gut microbiota in MDD patients have altered gut microbes that are closely associated with inflammatory factors and cognitive function in MDD patients.
Abstract Objective: The microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive disorder (MDD). However, studies on the microbiota-Inflammatory-cognitive function axis in MDD are lacking. The aim of the present study was to analyze the gut microbiota composition and explore the correlation between gut microbiota and inflammatory factors, cognitive function in MDD patients. Method: Study participants included 66 first-episode, drug naïve MDD patients as well as 43 healthy subjects (HCs). The composition of fecal microbiota was evaluated using16S rRNA sequencing and bioinformatics analysis. The cytokines such as hs-CRP, IL-1β, IL-6, IL-10 and TNF-α in peripheral blood were detected via enzyme linked immunosorbent assay (ELISA); Assessment of cognitive functions was performed using the Color Trail Test (CTT), The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and the Stroop Color-Word Test (SCWT). Results: We found that compared with HCs, MDD patients had cognitive impairments and showed different α-diversity and β-diversity of gut microbiota composition. LDA Effect Size (LEfSe) analysis found MDD have higher the Deinococcaceae and lower Bacteroidaceae, Turicibacteraceae, Clostridiaceae and Barnesiellaceae at family level. the Deinococcus and Odoribacter was higher in the MDD group, however, the Bacteroides, Alistipes, Turicibacter, Clostridium, Roseburia and Enterobacter were lower at genus level. Furthermore, In MDD patients, the Bacteroidaceae and Bacteroides were both positively correlated with hsCRP, CCT1, CCT2. The Alistipes was positively correlated with IL-6 ,Word time, Color time, Word-Color time, Color-Word time and negatively correlated with Delayed Memory, Total score and Standardized score. The Turicibacteraceae and Turicibacter were both negatively correlated with IL-1βand IL-6. Conclusion: The present findings confirm that the gut microbiota in MDD patients is altered. Altered gut microbiota is closely associated with inflammatory factors and cognitive function in MDD patients.
Author Liu, Penghong
Sun, Ning
Gao, Mingxue
Liu, Zhifen
Li, Gaizhi
Zhang, Kerang
Yang, Chunxia
Tu, Hongwei
Lei, Lei
Zhang, Aixia
Wu, Peiyi
Zhang, Yanyan
AuthorAffiliation 1 First Hospital of Shanxi Medical University , Taiyuan , China
2 Department of Psychiatry, First Hospital of Shanxi Medical University , Taiyuan , China
AuthorAffiliation_xml – name: 1 First Hospital of Shanxi Medical University , Taiyuan , China
– name: 2 Department of Psychiatry, First Hospital of Shanxi Medical University , Taiyuan , China
Author_xml – sequence: 1
  givenname: Penghong
  surname: Liu
  fullname: Liu, Penghong
– sequence: 2
  givenname: Mingxue
  surname: Gao
  fullname: Gao, Mingxue
– sequence: 3
  givenname: Zhifen
  surname: Liu
  fullname: Liu, Zhifen
– sequence: 4
  givenname: Yanyan
  surname: Zhang
  fullname: Zhang, Yanyan
– sequence: 5
  givenname: Hongwei
  surname: Tu
  fullname: Tu, Hongwei
– sequence: 6
  givenname: Lei
  surname: Lei
  fullname: Lei, Lei
– sequence: 7
  givenname: Peiyi
  surname: Wu
  fullname: Wu, Peiyi
– sequence: 8
  givenname: Aixia
  surname: Zhang
  fullname: Zhang, Aixia
– sequence: 9
  givenname: Chunxia
  surname: Yang
  fullname: Yang, Chunxia
– sequence: 10
  givenname: Gaizhi
  surname: Li
  fullname: Li, Gaizhi
– sequence: 11
  givenname: Ning
  surname: Sun
  fullname: Sun, Ning
– sequence: 12
  givenname: Kerang
  surname: Zhang
  fullname: Zhang, Kerang
BackLink https://www.ncbi.nlm.nih.gov/pubmed/35153660$$D View this record in MEDLINE/PubMed
BookMark eNp1kk1v1DAQhiNURD_gB3BBlrhwIIvtOI5zQUK73bLSFjiAxM3yVxYviZ3aTqX-DP4xTrdFbSVOM7KfeTUz75wWR847UxSvEVxUFWs_dM66uMAQowWDsKHkWXGCKMUlqaufRw_y4-I0xj2EFDOCXxTHVY3qilJ4Uvy5mBK4tCp4af1gwNIPo482We_A1rrfRoPkwcZ1vRgGkXy4AWuhcoxAOJ3xncvwtQHryam5KgLrwNqGmMrz0UavzXuwCtOu_CJm7FLsfQArMwYT4_ywykzQJoBvIlnjUnxZPO9EH82ru3hW_Fiff19-LrdfLzbLT9tS1XWbypY0dYWMUFopjbBopUGGCdLISjW6w1jOeSekpAjnsamkAkOlsWokg5k6KzYHXe3Fno_BDiLccC8sv33wYcdFSFb1hksNmTCSkrpjeZ2EESgVxa1slFDQ0Kz18aA1TnIwWuU5gugfiT7-cfYX3_lrzliFmqrOAu_uBIK_mkxMfLBRmb4Xzvgpcpydow1rKcno2yfo3k_B5VXNVEVaUlOUqTcPO_rXyr3zGWgOQLY-xmA6rmwSs4O5QdtzBPl8Y_z2xvh8Y_xwY7kSPam8F_9_zV8539lQ
CitedBy_id crossref_primary_10_1016_j_neubiorev_2024_105722
crossref_primary_10_3390_ani15040601
crossref_primary_10_3390_biomedicines12122654
crossref_primary_10_1038_s41398_023_02670_5
crossref_primary_10_1111_1753_0407_13542
crossref_primary_10_1017_neu_2023_21
crossref_primary_10_1016_j_jad_2023_08_129
crossref_primary_10_1186_s12940_024_01078_y
crossref_primary_10_3390_biomedicines11102658
crossref_primary_10_1016_j_heliyon_2025_e42045
crossref_primary_10_3389_fncel_2022_1046692
crossref_primary_10_3389_fmicb_2022_955115
crossref_primary_10_1038_s41398_024_03122_4
crossref_primary_10_3389_fmicb_2024_1483626
crossref_primary_10_1016_j_ejphar_2024_176939
crossref_primary_10_3389_fnut_2023_1303405
crossref_primary_10_3390_nu16162659
crossref_primary_10_3390_laws13040046
crossref_primary_10_1016_j_neuroscience_2023_05_002
crossref_primary_10_24075_brsmu_2023_018
crossref_primary_10_1016_j_ajp_2024_104210
crossref_primary_10_3390_ijms241411551
crossref_primary_10_1186_s13041_023_01020_2
crossref_primary_10_3390_cells12091240
crossref_primary_10_1007_s12602_024_10326_z
crossref_primary_10_3390_antiox11112098
crossref_primary_10_1038_s41398_024_03211_4
crossref_primary_10_1186_s13041_024_01146_x
crossref_primary_10_3390_ph16040565
crossref_primary_10_1186_s12888_024_05778_0
crossref_primary_10_3389_fnins_2024_1453325
crossref_primary_10_3390_biology13010018
crossref_primary_10_3390_ijms25189776
crossref_primary_10_1039_D4FO00886C
crossref_primary_10_1159_000542696
crossref_primary_10_1186_s12888_024_05547_z
crossref_primary_10_3389_fmicb_2023_1283276
crossref_primary_10_3390_cells13050423
crossref_primary_10_1038_s42003_024_06409_w
Cites_doi 10.1016/j.jinorgbio.2019.110886
10.1016/j.chom.2016.03.007
10.1016/j.neurobiolaging.2016.08.019
10.1136/jnnp.23.1.56
10.3389/fgene.2019.00098
10.1016/j.immuni.2015.09.007
10.1016/j.jad.2020.01.102
10.1038/s41587-019-0252-6
10.1076/jcen.23.5.695.1249
10.1016/j.biopsych.2018.12.020
10.1016/j.euroneuro.2015.06.007
10.1038/nrgastro.2009.35
10.1128/CMR.00053-08
10.1037/a0028727
10.3389/fpsyt.2018.00044
10.1016/j.biopsych.2017.08.014
10.1038/nature12721
10.1038/s41598-017-13601-y
10.3389/fnins.2019.01361
10.1017/S1092852918001207
10.3390/nu13062099
10.3390/nu10111765
10.1038/s41380-020-0729-1
10.1017/S0033291713002535
10.1016/j.bbi.2015.03.016
10.1093/nar/gks1219
10.3389/fpsyt.2021.645045
10.1111/nmo.12378
10.1186/s12916-016-0560-3
10.1136/gut.2009.202515
10.1371/journal.pone.0197267
10.2147/NDT.S188340
10.1016/j.jalz.2019.07.002
10.1177/0300060520925930
10.1016/j.bbi.2016.12.010
10.1192/bjp.178.3.200
10.1038/s41398-021-01531-3
10.1017/S0033291719003027
10.31887/DCNS.2010.12.3/areichenberg
10.1038/nmeth.3869
10.3389/fmicb.2016.01544
10.1016/j.pnpbp.2017.04.021
10.1016/j.clinthera.2015.04.002
10.1076/jcen.20.3.310.823
10.1016/j.bbi.2015.04.004
10.1037/neu0000319
10.1016/j.jalz.2016.02.010
10.1016/j.bbi.2020.03.026
10.1037/h0054651
10.1038/s41398-021-01689-w
10.1016/j.pnpbp.2020.109955
10.1016/j.jpsychires.2016.07.019
10.1128/mSystems.00046-17
10.1017/S003329170800411X
10.1016/j.pnpbp.2020.110076
10.1186/gb-2011-12-6-r60
10.1016/j.eswa.2019.05.028
10.1053/j.gastro.2010.01.053
10.1038/mp.2016.44
ContentType Journal Article
Copyright Copyright © 2022 Liu, Gao, Liu, Zhang, Tu, Lei, Wu, Zhang, Yang, Li, Sun and Zhang.
2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright © 2022 Liu, Gao, Liu, Zhang, Tu, Lei, Wu, Zhang, Yang, Li, Sun and Zhang. 2022 Liu, Gao, Liu, Zhang, Tu, Lei, Wu, Zhang, Yang, Li, Sun and Zhang
Copyright_xml – notice: Copyright © 2022 Liu, Gao, Liu, Zhang, Tu, Lei, Wu, Zhang, Yang, Li, Sun and Zhang.
– notice: 2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Copyright © 2022 Liu, Gao, Liu, Zhang, Tu, Lei, Wu, Zhang, Yang, Li, Sun and Zhang. 2022 Liu, Gao, Liu, Zhang, Tu, Lei, Wu, Zhang, Yang, Li, Sun and Zhang
DBID AAYXX
CITATION
NPM
3V.
7XB
88I
8FE
8FH
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
GNUQQ
HCIFZ
LK8
M2P
M7P
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
Q9U
7X8
5PM
DOA
DOI 10.3389/fnins.2021.800764
DatabaseName CrossRef
PubMed
ProQuest Central (Corporate)
ProQuest Central (purchase pre-March 2016)
Science Database (Alumni Edition)
ProQuest SciTech Collection
ProQuest Natural Science Collection
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
ProQuest Central Student
SciTech Premium Collection
Biological Sciences
Science Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic
ProQuest Publicly Available Content
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Open Access Full Text
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest Natural Science Collection
ProQuest Central China
ProQuest Central
ProQuest One Applied & Life Sciences
Natural Science Collection
ProQuest Central Korea
Biological Science Collection
ProQuest Central (New)
ProQuest Science Journals (Alumni Edition)
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest Science Journals
ProQuest One Academic Eastern Edition
Biological Science Database
ProQuest SciTech Collection
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
PubMed
Publicly Available Content Database
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
EISSN 1662-453X
ExternalDocumentID oai_doaj_org_article_bd08aeb645f84534840bc629b7cac0e6
PMC8831735
35153660
10_3389_fnins_2021_800764
Genre Journal Article
GrantInformation_xml – fundername: ;
  grantid: 82001802; 81601192
GroupedDBID ---
29H
2WC
53G
5GY
5VS
8FE
8FH
9T4
AAFWJ
AAYXX
ABUWG
ACGFO
ACGFS
ACXDI
ADRAZ
AEGXH
AENEX
AFKRA
AFPKN
AIAGR
ALMA_UNASSIGNED_HOLDINGS
AZQEC
BBNVY
BENPR
BHPHI
BPHCQ
CITATION
CS3
DIK
DU5
E3Z
EBS
EJD
EMOBN
F5P
FRP
GROUPED_DOAJ
GX1
HCIFZ
HYE
KQ8
LK8
M2P
M48
M7P
O5R
O5S
OK1
OVT
P2P
PGMZT
PIMPY
PQQKQ
PROAC
RNS
RPM
W2D
88I
C1A
CCPQU
DWQXO
GNUQQ
NPM
PHGZM
PHGZT
PQGLB
3V.
7XB
8FK
PKEHL
PQEST
PQUKI
PRINS
Q9U
7X8
5PM
ID FETCH-LOGICAL-c559t-947531eacdccd12a9be1e8a47b3c7df22ba47bfabb6122846b6a20cd2c7b807b3
IEDL.DBID M48
ISSN 1662-453X
1662-4548
IngestDate Wed Aug 27 01:22:09 EDT 2025
Thu Aug 21 17:42:22 EDT 2025
Fri Jul 11 16:24:51 EDT 2025
Mon Jun 30 09:51:57 EDT 2025
Mon Jul 21 05:45:46 EDT 2025
Thu Apr 24 23:08:49 EDT 2025
Tue Jul 01 01:39:32 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords cognitive function
diversity
gut microbiome
major depressive disorder
inflammatory factors
Language English
License Copyright © 2022 Liu, Gao, Liu, Zhang, Tu, Lei, Wu, Zhang, Yang, Li, Sun 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.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c559t-947531eacdccd12a9be1e8a47b3c7df22ba47bfabb6122846b6a20cd2c7b807b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
This article was submitted to Gut-Brain Axis, a section of the journal Frontiers in Neuroscience
Edited by: Shaohua Hu, Zhejiang University, China
Reviewed by: Dominik Strzelecki, Medical University of Lodz, Poland; Manli Huang, Zhejiang University, China
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fnins.2021.800764
PMID 35153660
PQID 2623494561
PQPubID 4424402
ParticipantIDs doaj_primary_oai_doaj_org_article_bd08aeb645f84534840bc629b7cac0e6
pubmedcentral_primary_oai_pubmedcentral_nih_gov_8831735
proquest_miscellaneous_2628678964
proquest_journals_2623494561
pubmed_primary_35153660
crossref_citationtrail_10_3389_fnins_2021_800764
crossref_primary_10_3389_fnins_2021_800764
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-01-28
PublicationDateYYYYMMDD 2022-01-28
PublicationDate_xml – month: 01
  year: 2022
  text: 2022-01-28
  day: 28
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
– name: Lausanne
PublicationTitle Frontiers in neuroscience
PublicationTitleAlternate Front Neurosci
PublicationYear 2022
Publisher Frontiers Research Foundation
Frontiers Media S.A
Publisher_xml – name: Frontiers Research Foundation
– name: Frontiers Media S.A
References Chen (B12) 2021; 13
Cicchetti (B13) 2001; 23
Lukiw (B33) 2016; 7
Desbonnet (B14) 2015; 48
Misiak (B34) 2018; 80
Alexandrov (B3) 2020; 203
Giau (B18) 2018; 10
Cattaneo (B11) 2017; 49
Liu (B31) 2020; 88
Stroop (B53) 1935; 18
Pan (B37) 2019; 24
Petra (B38) 2015; 37
Li (B29) 2019; 15
Hazan (B21) 2020; 48
Hamilton (B20) 1960; 23
Speiser (B51) 2019; 134
Tyburski (B54) 2020; 102
Callahan (B9) 2016; 13
Lamers (B28) 2019; 85
Naseribafrouei (B36) 2014; 26
Austin (B4) 2001; 178
Vogt (B55) 2017; 7
Ahern (B1) 2016; 31
Liu (B32) 2021; 11
Furusawa (B16) 2013; 504
Reppermund (B42) 2009; 39
Strawbridge (B52) 2015; 25
Yuan (B57) 2021; 11
Liśkiewicz (B30) 2021; 106
Gareau (B17) 2011; 60
Segata (B47) 2011; 12
Lai (B27) 2021; 51
Randolph (B40) 1998; 20
Reichenberg (B41) 2010; 12
Calsolaro (B10) 2016; 12
Bortolato (B6) 2016; 14
Snyder (B49) 2013; 139
Soret (B50) 2010; 138
Yong (B58) 2019; 13
Zheng (B60) 2016; 21
Sears (B46) 2009; 22
Sheehan (B48) 1998; 59
Zou (B61) 2018; 13
Jiang (B25) 2015; 48
Kelly (B26) 2016; 82
Huang (B23) 2019; 10
Dickerson (B15) 2017; 62
Bolyen (B5) 2019; 37
Huang (B24) 2018; 14
Breit (B7) 2018; 9
Hennezel (B22) 2017; 2
Yang (B56) 2020; 25
Quast (B39) 2013; 41
Sanada (B45) 2020; 266
Haghikia (B19) 2015; 43
Ahern (B2) 2017; 31
Rhee (B43) 2009; 6
Zhang (B59) 2021; 12
Rock (B44) 2014; 44
Moschen (B35) 2016; 19
Bruce-Keller (B8) 2018; 83
References_xml – volume: 203
  year: 2020
  ident: B3
  article-title: Aluminum-induced generation of lipopolysaccharide (LPS) from the human gastrointestinal (GI)-tract microbiome-resident Bacteroides fragilis.
  publication-title: J. Inorg. Biochem.
  doi: 10.1016/j.jinorgbio.2019.110886
– volume: 19
  start-page: 455
  year: 2016
  ident: B35
  article-title: Lipocalin 2 protects from inflammation and tumorigenesis associated with gut microbiota alterations.
  publication-title: Cell Host Microbe
  doi: 10.1016/j.chom.2016.03.007
– volume: 49
  start-page: 60
  year: 2017
  ident: B11
  article-title: Association of brain amyloidosis with pro-inflammatory gut bacterial taxa and peripheral inflammation markers in cognitively impaired elderly.
  publication-title: Neurobiol. Aging
  doi: 10.1016/j.neurobiolaging.2016.08.019
– volume: 23
  start-page: 56
  year: 1960
  ident: B20
  article-title: A rating scale for depression.
  publication-title: J. Neurol. Neurosurg. Psychiatry
  doi: 10.1136/jnnp.23.1.56
– volume: 10
  year: 2019
  ident: B23
  article-title: Current understanding of gut microbiota in mood disorders: an update of human studies.
  publication-title: Front. Genet.
  doi: 10.3389/fgene.2019.00098
– volume: 43
  start-page: 817
  year: 2015
  ident: B19
  article-title: Dietary fatty acids directly impact central nervous system autoimmunity via the small intestine.
  publication-title: Immunity
  doi: 10.1016/j.immuni.2015.09.007
– volume: 266
  start-page: 1
  year: 2020
  ident: B45
  article-title: Gut microbiota and major depressive disorder: a systematic review and meta-analysis.
  publication-title: J. Affect. Disord.
  doi: 10.1016/j.jad.2020.01.102
– volume: 37
  year: 2019
  ident: B5
  article-title: Author correction: reproducible, interactive, scalable and extensible microbiome data science using QIIME 2.
  publication-title: Nat. Biotechnol.
  doi: 10.1038/s41587-019-0252-6
– volume: 23
  start-page: 695
  year: 2001
  ident: B13
  article-title: The precision of reliability and validity estimates re-visited: distinguishing between clinical and statistical significance of sample size requirements.
  publication-title: J. Clin. Exp. Neuropsychol.
  doi: 10.1076/jcen.23.5.695.1249
– volume: 85
  start-page: 829
  year: 2019
  ident: B28
  article-title: Longitudinal association between depression and inflammatory markers: results from the netherlands study of depression and anxiety.
  publication-title: Biol. Psychiatry
  doi: 10.1016/j.biopsych.2018.12.020
– volume: 25
  start-page: 1532
  year: 2015
  ident: B52
  article-title: Inflammation and clinical response to treatment in depression: a meta-analysis.
  publication-title: Eur. Neuropsychopharmacol.
  doi: 10.1016/j.euroneuro.2015.06.007
– volume: 6
  start-page: 306
  year: 2009
  ident: B43
  article-title: Principles and clinical implications of the brain-gut-enteric microbiota axis.
  publication-title: Nat. Rev. Gastroenterol. Hepatol.
  doi: 10.1038/nrgastro.2009.35
– volume: 22
  start-page: 349
  year: 2009
  ident: B46
  article-title: Enterotoxigenic Bacteroides fragilis: a rogue among symbiotes.
  publication-title: Clin. Microbiol. Rev.
  doi: 10.1128/CMR.00053-08
– volume: 139
  start-page: 81
  year: 2013
  ident: B49
  article-title: Major depressive disorder is associated with broad impairments on neuropsychological measures of executive function: a meta-analysis and review.
  publication-title: Psychol. Bull.
  doi: 10.1037/a0028727
– volume: 9
  year: 2018
  ident: B7
  article-title: Vagus nerve as modulator of the brain-gut axis in psychiatric and inflammatory disorders.
  publication-title: Front. Psychiatry
  doi: 10.3389/fpsyt.2018.00044
– volume: 83
  start-page: 214
  year: 2018
  ident: B8
  article-title: Harnessing gut microbes for mental health: getting from here to there.
  publication-title: Biol. Psychiatry
  doi: 10.1016/j.biopsych.2017.08.014
– volume: 504
  start-page: 446
  year: 2013
  ident: B16
  article-title: Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells.
  publication-title: Nature
  doi: 10.1038/nature12721
– volume: 7
  year: 2017
  ident: B55
  article-title: Gut microbiome alterations in Alzheimer’s disease.
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-017-13601-y
– volume: 13
  year: 2019
  ident: B58
  article-title: Antidepressive mechanisms of probiotics and their therapeutic potential.
  publication-title: Front. Neurosci.
  doi: 10.3389/fnins.2019.01361
– volume: 24
  start-page: 22
  year: 2019
  ident: B37
  article-title: Cognitive impairment in major depressive disorder.
  publication-title: CNS Spectr.
  doi: 10.1017/S1092852918001207
– volume: 13
  year: 2021
  ident: B12
  article-title: Regulation of neurotransmitters by the gut microbiota and effects on cognition in neurological disorders.
  publication-title: Nutrients
  doi: 10.3390/nu13062099
– volume: 10
  year: 2018
  ident: B18
  article-title: Gut microbiota and their neuroinflammatory implications in Alzheimer’s disease.
  publication-title: Nutrients
  doi: 10.3390/nu10111765
– volume: 25
  start-page: 2759
  year: 2020
  ident: B56
  article-title: Updated review of research on the gut microbiota and their relation to depression in animals and human beings.
  publication-title: Mol. Psychiatry
  doi: 10.1038/s41380-020-0729-1
– volume: 44
  start-page: 2029
  year: 2014
  ident: B44
  article-title: Cognitive impairment in depression: a systematic review and meta-analysis.
  publication-title: Psychol. Med.
  doi: 10.1017/S0033291713002535
– volume: 59
  start-page: 22-33;quiz 34
  year: 1998
  ident: B48
  article-title: The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10.
  publication-title: J. Clin. Psychiatry
– volume: 48
  start-page: 186
  year: 2015
  ident: B25
  article-title: Altered fecal microbiota composition in patients with major depressive disorder.
  publication-title: Brain Behav. Immun.
  doi: 10.1016/j.bbi.2015.03.016
– volume: 41
  start-page: D590
  year: 2013
  ident: B39
  article-title: The SILVA ribosomal RNA gene database project: improved data processing and web-based tools.
  publication-title: Nucleic Acids Res.
  doi: 10.1093/nar/gks1219
– volume: 12
  year: 2021
  ident: B59
  article-title: Gut microbiome composition associated with major depressive disorder and sleep quality.
  publication-title: Front. Psychiatry
  doi: 10.3389/fpsyt.2021.645045
– volume: 26
  start-page: 1155
  year: 2014
  ident: B36
  article-title: Correlation between the human fecal microbiota and depression.
  publication-title: Neurogastroenterol. Motility
  doi: 10.1111/nmo.12378
– volume: 14
  year: 2016
  ident: B6
  article-title: Cognitive remission: a novel objective for the treatment of major depression.
  publication-title: BMC Med.
  doi: 10.1186/s12916-016-0560-3
– volume: 60
  start-page: 307
  year: 2011
  ident: B17
  article-title: Bacterial infection causes stress-induced memory dysfunction in mice.
  publication-title: Gut
  doi: 10.1136/gut.2009.202515
– volume: 13
  year: 2018
  ident: B61
  article-title: Changes in the serum levels of inflammatory cytokines in antidepressant drug-naïve patients with major depression.
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0197267
– volume: 14
  start-page: 3329
  year: 2018
  ident: B24
  article-title: Possible association of Firmicutes in the gut microbiota of patients with major depressive disorder.
  publication-title: Neuropsychiatric Dis. Treatment
  doi: 10.2147/NDT.S188340
– volume: 15
  start-page: 1357
  year: 2019
  ident: B29
  article-title: Mild cognitive impairment has similar alterations as Alzheimer’s disease in gut microbiota.
  publication-title: Alzheimer’s Dement.
  doi: 10.1016/j.jalz.2019.07.002
– volume: 48
  year: 2020
  ident: B21
  article-title: Rapid improvement in Alzheimer’s disease symptoms following fecal microbiota transplantation: a case report.
  publication-title: J. Int. Med. Res.
  doi: 10.1177/0300060520925930
– volume: 62
  start-page: 46
  year: 2017
  ident: B15
  article-title: The microbiome, immunity, and schizophrenia and bipolar disorder.
  publication-title: Brain Behav. Immun.
  doi: 10.1016/j.bbi.2016.12.010
– volume: 178
  start-page: 200
  year: 2001
  ident: B4
  article-title: Cognitive deficits in depression: possible implications for functional neuropathology.
  publication-title: Br. J. Psychiatry
  doi: 10.1192/bjp.178.3.200
– volume: 11
  year: 2021
  ident: B57
  article-title: Gut microbial biomarkers for the treatment response in first-episode, drug-naïve schizophrenia: a 24-week follow-up study
  publication-title: Transl. Psychiatry
  doi: 10.1038/s41398-021-01531-3
– volume: 51
  start-page: 90
  year: 2021
  ident: B27
  article-title: Shotgun metagenomics reveals both taxonomic and tryptophan pathway differences of gut microbiota in major depressive disorder patients.
  publication-title: Psychol. Med.
  doi: 10.1017/S0033291719003027
– volume: 12
  start-page: 383
  year: 2010
  ident: B41
  article-title: The assessment of neuropsychological functioning in schizophrenia.
  publication-title: Dial. Clin. Neurosci.
  doi: 10.31887/DCNS.2010.12.3/areichenberg
– volume: 13
  start-page: 581
  year: 2016
  ident: B9
  article-title: DADA2: high-resolution sample inference from Illumina amplicon data.
  publication-title: Nat. Methods
  doi: 10.1038/nmeth.3869
– volume: 7
  year: 2016
  ident: B33
  article-title: Bacteroides fragilis lipopolysaccharide and inflammatory signaling in Alzheimer’s disease.
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2016.01544
– volume: 80
  start-page: 177
  year: 2018
  ident: B34
  article-title: Cytokine alterations and cognitive impairment in major depressive disorder: from putative mechanisms to novel treatment targets.
  publication-title: Prog. Neuro-Psychopharmacol. Biol. Psychiatry
  doi: 10.1016/j.pnpbp.2017.04.021
– volume: 37
  start-page: 984
  year: 2015
  ident: B38
  article-title: Gut-Microbiota-Brain axis and its effect on neuropsychiatric disorders with suspected immune dysregulation.
  publication-title: Clin. Ther.
  doi: 10.1016/j.clinthera.2015.04.002
– volume: 20
  start-page: 310
  year: 1998
  ident: B40
  article-title: The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS): preliminary clinical validity.
  publication-title: J. Clin. Exp. Neuropsychol.
  doi: 10.1076/jcen.20.3.310.823
– volume: 48
  start-page: 165
  year: 2015
  ident: B14
  article-title: Gut microbiota depletion from early adolescence in mice: implications for brain and behaviour.
  publication-title: Brain Behav. Immun.
  doi: 10.1016/j.bbi.2015.04.004
– volume: 31
  start-page: 52
  year: 2016
  ident: B1
  article-title: Cognitive functioning in the first-episode of major depressive disorder: a systematic review and meta-analysis.
  publication-title: Neuropsychology
  doi: 10.1037/neu0000319
– volume: 12
  start-page: 719
  year: 2016
  ident: B10
  article-title: Neuroinflammation in Alzheimer’s disease: current evidence and future directions.
  publication-title: Alzheimer’s Dement.
  doi: 10.1016/j.jalz.2016.02.010
– volume: 88
  start-page: 308
  year: 2020
  ident: B31
  article-title: Reductions in anti-inflammatory gut bacteria are associated with depression in a sample of young adults.
  publication-title: Brain Behav. Immun.
  doi: 10.1016/j.bbi.2020.03.026
– volume: 18
  start-page: 643
  year: 1935
  ident: B53
  article-title: Studies of interference in serial verbal reactions
  publication-title: J. Exp. Psychol.
  doi: 10.1037/h0054651
– volume: 11
  year: 2021
  ident: B32
  article-title: Proteomics analysis of the gut-brain axis in a gut microbiota-dysbiosis model of depression.
  publication-title: Translational Psychiatry
  doi: 10.1038/s41398-021-01689-w
– volume: 102
  year: 2020
  ident: B54
  article-title: The relationship between cingulum bundle integrity and different aspects of executive functions in chronic schizophrenia.
  publication-title: Prog. Neuro-psychopharmacol. Biol. Psychiatry
  doi: 10.1016/j.pnpbp.2020.109955
– volume: 82
  start-page: 109
  year: 2016
  ident: B26
  article-title: Transferring the blues: depression-associated gut microbiota induces neurobehavioural changes in the rat.
  publication-title: J. Psychiatr. Res.
  doi: 10.1016/j.jpsychires.2016.07.019
– volume: 2
  year: 2017
  ident: B22
  article-title: Total lipopolysaccharide from the human gut microbiome silences toll-like receptor signaling.
  publication-title: mSystems
  doi: 10.1128/mSystems.00046-17
– volume: 39
  start-page: 603
  year: 2009
  ident: B42
  article-title: Cognitive impairment in unipolar depression is persistent and non-specific: further evidence for the final common pathway disorder hypothesis.
  publication-title: Psychol. Med.
  doi: 10.1017/S003329170800411X
– volume: 31
  start-page: 52
  year: 2017
  ident: B2
  article-title: Cognitive functioning in the first-episode of major depressive disorder: a systematic review and meta-analysis.
  publication-title: Neuropsychology
  doi: 10.1037/neu0000319
– volume: 106
  year: 2021
  ident: B30
  article-title: Analysis of gut microbiota and intestinal integrity markers of inpatients with major depressive disorder.
  publication-title: Prog. Neuro-psychopharmacol. Biol. Psychiatry
  doi: 10.1016/j.pnpbp.2020.110076
– volume: 12
  year: 2011
  ident: B47
  article-title: Metagenomic biomarker discovery and explanation.
  publication-title: Genome Biol.
  doi: 10.1186/gb-2011-12-6-r60
– volume: 134
  start-page: 93
  year: 2019
  ident: B51
  article-title: A comparison of random forest variable selection methods for classification prediction modeling.
  publication-title: Expert Systems Appl.
  doi: 10.1016/j.eswa.2019.05.028
– volume: 138
  start-page: 1772
  year: 2010
  ident: B50
  article-title: Short-chain fatty acids regulate the enteric neurons and control gastrointestinal motility in rats.
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2010.01.053
– volume: 21
  start-page: 786
  year: 2016
  ident: B60
  article-title: Gut microbiome remodeling induces depressive-like behaviors through a pathway mediated by the host’s metabolism.
  publication-title: Mol. Psychiatry
  doi: 10.1038/mp.2016.44
SSID ssj0062842
Score 2.4987648
Snippet The microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major depressive...
Abstract Objective: The microbiota-gut-brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in...
ObjectiveThe microbiota–gut–brain axis, especially the inflammatory pathway, may play a critical role in the pathogenesis of cognitive impairment in major...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 800764
SubjectTerms Alistipes
Alzheimer's disease
Bacteroidaceae
Bacteroides
Bioinformatics
Brain research
Cognitive ability
cognitive function
Color
Cytokines
Dementia
diversity
Enzyme-linked immunosorbent assay
Fecal microflora
Feces
gut microbiome
IL-1β
Inflammation
inflammatory factors
Interleukin 10
Interleukin 6
Intestinal microflora
major depressive disorder
Memory
Mental depression
Mental disorders
Microbiomes
Microbiota
Nervous system
Neuroscience
Patients
Peripheral blood
rRNA
Tumor necrosis factor-α
SummonAdditionalLinks – databaseName: DOAJ Open Access Full Text
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Nb9QwELVQT1wQUD4CBRkJcUCYJo7t2MdCGwrSVhyo1Fvkr0Aq1qm22QM_g3_M2M6uugjBhVvkTBTHM7bfi8fPCL3UNQcYKnrSaO0J07UlRjFGqqqpjdROexX3Oy_OxOk5-3TBL24c9RVzwrI8cG64Q-NKqb0RjPeS8ZoBITFWUGUaq23pk9g2zHkbMpXHYAGDLs1rmEDB1GEfhhC1uWn1Vsa1J7YzCyWx_j8hzN8TJW_MPO1ddGeGjPgoV_UeuuXDfbR_FIAuL3_gVzglcaa_4_vo54f1hBdDVldaehy7-5yWhSPt9A5PI_4YegiEZVpgx20-cQfr4MB8TibCLcx3KSTxEHA7AEYkJ1fD9ej8G3y8Wn8lZzqaLfTluMLHczotFGzUPPHnLNh6_QCdtydf3p-S-dQFYoFdTEQxYDAVjMfOWldRrYyvvNSsMbVtXE-pide9NgbAEbSzMELT0jpqGyNLsHqI9sIY_GOEVRSPabiXtOEA_LTmwJ8MF0YaIGZOFqjceKGzsyR5PBnjewfUJDquS47rouO67LgCvd4-cpX1OP5m_C66dmsYpbRTAQRYNwdY968AK9DBJjC6uX_DSwA1MhXBZ4FebG9Dz4zLLTr4cZ1sJEABFevxKMfRtiY1wMhaiLJAzU6E7VR1904YviX1bykB8tX8yf_4tqfoNo3bOcqKUHmA9qbV2j8DkDWZ56k__QJYoCm2
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: ProQuest Central
  dbid: BENPR
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lj9MwELage-GCgOURWJCREAeE2cRxHOeEdtmWBanVCrHS3iK_sgRRp7TpgZ_BP2bsOBVFaG9VMlWtznjmG8_4G4ReybwAGMobUkppCZO5JqpijGRZmSshjbSVv-88X_DzS_b5qriKB26b2FY5-sTgqE2n_Rn5MYU4zSof7t-vfhI_NcpXV-MIjdvoAFywEBN0cDpdXHwZfTEH5xvqndzfDQJwPtQ1IS2rjhvXOs_XTbN3wtej2F5kCgT-_0Od_zZP_hWNZvfQ3Qgj8cmg9_volnUP0OGJgxR6-Qu_xqGxM5yYH6LfH7c9nrcD49LSYu8CYqsW9qmoNbjv8CfXgHEsQ9Edz4YpPFg6A-KxwQjPIAYGM8Wtw7MWcCOZrtpNZ-xbfLbeXpOF9GJz-b1b47PYYgsPRoZPfDGQuG4eosvZ9OuHcxInMRANGUdPKgZZTQY-2mhtMiorZTMrJCtVrkvTUKr850YqBYAJ_nOuuKSpNlSXSqQg9QhNXOfsE4QrTyhTFlbQsgAwKGUBOZUquBIKkjUjEpSOWqh1pCn30zJ-1JCueMXVQXG1V1w9KC5Bb3ZfWQ0cHTcJn3rV7gQ9vXZ40K2v67hba2VSIa3irGgEK3IGWbDSnFaq1FKnlifoaDSMOu55-JGdhSbo5e417FZfgpHOdtsgIwAeVH4djwc72q0kB2iZc54mqNyzsL2l7r9x7bfACC4EwMC8eHrzsp6hO9Rf3kgzQsURmvTrrX0OkKpXL-K--QOmAiQI
  priority: 102
  providerName: ProQuest
Title Gut Microbiome Composition Linked to Inflammatory Factors and Cognitive Functions in First-Episode, Drug-Naive Major Depressive Disorder Patients
URI https://www.ncbi.nlm.nih.gov/pubmed/35153660
https://www.proquest.com/docview/2623494561
https://www.proquest.com/docview/2628678964
https://pubmed.ncbi.nlm.nih.gov/PMC8831735
https://doaj.org/article/bd08aeb645f84534840bc629b7cac0e6
Volume 15
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3fb9MwELbG9sILAsaPwKiMhHhAZCSO4zgPCG2s3UBqNSEq9S2yHWcErc5IW4n9GfzH3DlpRVGFeKmi5NJYubPv-3LnO0JeqSQFGCqqMFPKhlwlJtQ552EcZ4mWqlQ2x_3O44m4mPLPs3S2R9btrfoXuNhJ7bCf1LS9Pv754_YDTPj3yDjB376rXO2w8jaLjyVGlvgdcgCOKcOGBmO-CSoIWIl98FPgRiFA6l2Qc_dfbLkpX81_FwT9O5PyD9c0uk_u9ZiSnnRG8IDsWfeQHJ444NPzW_qa-ixP__n8kPw6Xy3puO7KL80txfWgz9uiyEttSZcN_eQqsJS5j8DTUdeShypXgnifbURH4BC9zdLa0VENIDIc3tSLprRv6Vm7ugonCsXG6nvT0rM-3xZOrMt90suuouviEZmOhl8_XoR9W4bQAP1YhjkHihPDgl0aU8ZM5drGViqe6cRkZcWYxuNKaQ3oCd650EKxyJTMZFpGIPWY7LvG2aeE5lhdJkutZFkKyFCpFAiWToWWGphbKQMSrbVQmL5mObbOuC6Au6DiCq-4AhVXdIoLyJvNLTddwY5_CZ-iajeCWGvbn2jaq6KfuoUuI6msFjytJE8TDpRYG8FynRllIisCcrQ2jGJtvwUDWMlzRKcBebm5DFMX4zHK2WblZSRghRzH8aSzo81IEsCZiRBRQLItC9sa6vYVV3_z5cGlBEyYpM_-47nPyV2G2zmiOGTyiOwv25V9ASBrqQfk4HQ4ufwy8B8p4Pd8Fg_8dPoNXSosHw
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEF6V9AAXBJRHoMAiAQfEtvZ6vV4fEGpJQkKbqEKt1JvZl4sRsUMeQv0Z_BF-I7NrOyII9dabZU_ilWZ25vs8szMIvZRRDDCU5ySR0hImI01UyhgJwyRSQhppU3feeTzhwzP26Tw-30K_27Mwrqyy9YneUZtKu2_k-xTiNEtduH8_-0Hc1CiXXW1HaNRmcWQvfwJlW7wb9UC_rygd9E8_DEkzVYBoQM9LkjJA6CH4G6O1CalMlQ2tkCxRkU5MTqly17lUCoI_OG-uuKSBNlQnSgQgBf97A22ziAe0g7YP-5OTz63v5yDv86vcnUUCMlDnUYEGpvt5WZSuPzgN94TLf7GNSOgHBvwP5f5brPlX9BvcQbcb2IoPaju7i7ZseQ_tHJRA2aeX-DX2haT-C_0O-vVxtcTjou7wNLXYuZymNAw76msNXlZ4VOZgjFOf5MeDeuoPlqUB8aagCQ8g5vptgYsSDwrAqaQ_KxaVsW9xb766IBPpxMbyWzXHvaakF260HUXxSd00dnEfnV2Ljh6gTlmV9hHCqWtgk8RW0CQG8CllDBxOxVwJBeTQiC4KWi1kummL7qZzfM-AHjnFZV5xmVNcViuui96sfzKre4JcJXzoVLsWdO28_Y1qfpE13iFTJhDSKs7iXLA4YsC6leY0VYmWOrC8i3Zbw8gaHwMvWe-ILnqxfgzewaV8ZGmrlZcRAEdSt46HtR2tVxIBlI04D7oo2bCwjaVuPimLr74DuRAAO6P48dXLeo5uDk_Hx9nxaHL0BN2i7uBIEBIqdlFnOV_ZpwDnlupZs4cw-nLd2_YPUAdivw
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3NbtNAEF6VVEJcEFB-AgUWCTggtrHX9np9QKglMQ0lUYSo1JvZXa-LEbFD4gj1MXgdno4Z_0QEod56s-xJvNLMznyfZ3aGkOfKCwCGioyFSlnmK88wHfk-c93Q01KlykZ43nkyFcen_oez4GyH_O7OwmBZZecTa0edlga_kQ84xGk_wnA_yNqyiNkwfrv4wXCCFGZau3EajYmc2IufQN9Wb8ZD0PULzuPR53fHrJ0wwAwg6YpFPqB1F3xPakzqchVp61qp_FB7JkwzzjVeZ0prAALgyIUWijsm5SbU0gEp-N9rZDdEVtQju0ej6exTFwcEyNe5VoHnkoAYNDlVoITRICvyAnuFc_dAYi7M34qK9fCA_yHefws3_4qE8S1ys4Ww9LCxudtkxxZ3yN5hAfR9fkFf0rqotP5av0d-vV9XdJI33Z7mlqL7acvEKNJgm9KqpOMiA8Oc1wl_GjcTgKgqUhBvi5toDPG33iI0L2icA2Zlo0W-KlP7mg6X63M2VSg2Ud_KJR225b1wo-suSmdNA9nVXXJ6JTq6R3pFWdgHhEbYzCYMrORhAEBUqQD4nA6ElhqIYir7xOm0kJi2RTpO6vieAFVCxSW14hJUXNIork9ebX6yaPqDXCZ8hKrdCGJr7_pGuTxPWk-R6NSRymrhB5n0A88HBq6N4JEOjTKOFX2y3xlG0vobeMlmd_TJs81j8BSY_lGFLde1jARoEuE67jd2tFmJB7DWE8Lpk3DLwraWuv2kyL_W3cilBAjqBQ8vX9ZTch22a_JxPD15RG5wPEPiuIzLfdKrlmv7GJBdpZ-0W4iSL1e9a_8AmM9m9A
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Gut+Microbiome+Composition+Linked+to+Inflammatory+Factors+and+Cognitive+Functions+in+First-Episode%2C+Drug-Naive+Major+Depressive+Disorder+Patients&rft.jtitle=Frontiers+in+neuroscience&rft.au=Liu%2C+Penghong&rft.au=Gao%2C+Mingxue&rft.au=Liu%2C+Zhifen&rft.au=Zhang%2C+Yanyan&rft.date=2022-01-28&rft.issn=1662-4548&rft.volume=15&rft.spage=800764&rft_id=info:doi/10.3389%2Ffnins.2021.800764&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1662-453X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1662-453X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1662-453X&client=summon