Neuroimmunometabolic alterations and severity of depressive symptoms in people with HIV: An exploratory diffusion-weighted MRS study

Depression is associated with inflammation in the periphery and the central nervous system. People with HIV are at greater risk for depression, which may in part be driven by sustained neuroinflammation, although individuals with severe depression are often excluded from studies of HIV-related co-mo...

Full description

Saved in:
Bibliographic Details
Published inBrain and neuroscience advances Vol. 9; p. 23982128251335792
Main Authors Mudra Rakshasa-Loots, Arish, Diteko, Goabaone, Dowell, Nicholas G., Ronen, Itamar, Vera, Jaime H.
Format Journal Article
LanguageEnglish
Published United States SAGE Publications 01.01.2025
Subjects
Online AccessGet full text
ISSN2398-2128
2398-2128
DOI10.1177/23982128251335792

Cover

Loading…
Abstract Depression is associated with inflammation in the periphery and the central nervous system. People with HIV are at greater risk for depression, which may in part be driven by sustained neuroinflammation, although individuals with severe depression are often excluded from studies of HIV-related co-morbidities. In this exploratory study, we aimed to explore the neuroimaging signatures of severe and persistent depression among people with HIV. We enrolled N = 20 adults with HIV in Brighton, UK, of whom n = 11 had a Patient Health Questionnaire-9 (PHQ-9) score ⩾15 and a history of receiving antidepressant medication. We used diffusion-weighted magnetic resonance spectroscopy (DW-MRS), an emerging neuroimaging technique sensitive to neuroinflammation, to assess neurometabolite diffusion in the anterior cingulate cortex. Participants also underwent standard magnetic resonance spectroscopy (MRS) to assess neurometabolite concentrations in the anterior cingulate cortex, and dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to assess blood–brain barrier permeability in the whole brain and the thalamus. We observed a significant positive correlation between intracellular diffusion of creatine and depressive symptom severity (ρ = 0.46, p = 0.047). Increased creatine diffusion has previously been reported in conditions characterised by hypermetabolism and neuroinflammation, suggesting that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic alterations. Metabolite concentrations and blood–brain barrier permeability largely did not correlate with depressive symptom severity in this sample. In summary, we explored neuroimaging signatures of severe depression in people with HIV, including by applying diffusion-weighted magnetic resonance spectroscopy in this population. We report early evidence that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic dysfunction, evidenced by increased diffusion of creatine, likely reflecting hypermetabolism and neuroinflammation. Future research may aim to replicate these findings in larger and more diverse samples and compare the diffusion of neurometabolites between people with and without HIV living with severe depression.
AbstractList Depression is associated with inflammation in the periphery and the central nervous system. People with HIV are at greater risk for depression, which may in part be driven by sustained neuroinflammation, although individuals with severe depression are often excluded from studies of HIV-related co-morbidities. In this exploratory study, we aimed to explore the neuroimaging signatures of severe and persistent depression among people with HIV. We enrolled N = 20 adults with HIV in Brighton, UK, of whom n = 11 had a Patient Health Questionnaire-9 (PHQ-9) score ⩾15 and a history of receiving antidepressant medication. We used diffusion-weighted magnetic resonance spectroscopy (DW-MRS), an emerging neuroimaging technique sensitive to neuroinflammation, to assess neurometabolite diffusion in the anterior cingulate cortex. Participants also underwent standard magnetic resonance spectroscopy (MRS) to assess neurometabolite concentrations in the anterior cingulate cortex, and dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to assess blood-brain barrier permeability in the whole brain and the thalamus. We observed a significant positive correlation between intracellular diffusion of creatine and depressive symptom severity (ρ = 0.46, p = 0.047). Increased creatine diffusion has previously been reported in conditions characterised by hypermetabolism and neuroinflammation, suggesting that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic alterations. Metabolite concentrations and blood-brain barrier permeability largely did not correlate with depressive symptom severity in this sample. In summary, we explored neuroimaging signatures of severe depression in people with HIV, including by applying diffusion-weighted magnetic resonance spectroscopy in this population. We report early evidence that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic dysfunction, evidenced by increased diffusion of creatine, likely reflecting hypermetabolism and neuroinflammation. Future research may aim to replicate these findings in larger and more diverse samples and compare the diffusion of neurometabolites between people with and without HIV living with severe depression.Depression is associated with inflammation in the periphery and the central nervous system. People with HIV are at greater risk for depression, which may in part be driven by sustained neuroinflammation, although individuals with severe depression are often excluded from studies of HIV-related co-morbidities. In this exploratory study, we aimed to explore the neuroimaging signatures of severe and persistent depression among people with HIV. We enrolled N = 20 adults with HIV in Brighton, UK, of whom n = 11 had a Patient Health Questionnaire-9 (PHQ-9) score ⩾15 and a history of receiving antidepressant medication. We used diffusion-weighted magnetic resonance spectroscopy (DW-MRS), an emerging neuroimaging technique sensitive to neuroinflammation, to assess neurometabolite diffusion in the anterior cingulate cortex. Participants also underwent standard magnetic resonance spectroscopy (MRS) to assess neurometabolite concentrations in the anterior cingulate cortex, and dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to assess blood-brain barrier permeability in the whole brain and the thalamus. We observed a significant positive correlation between intracellular diffusion of creatine and depressive symptom severity (ρ = 0.46, p = 0.047). Increased creatine diffusion has previously been reported in conditions characterised by hypermetabolism and neuroinflammation, suggesting that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic alterations. Metabolite concentrations and blood-brain barrier permeability largely did not correlate with depressive symptom severity in this sample. In summary, we explored neuroimaging signatures of severe depression in people with HIV, including by applying diffusion-weighted magnetic resonance spectroscopy in this population. We report early evidence that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic dysfunction, evidenced by increased diffusion of creatine, likely reflecting hypermetabolism and neuroinflammation. Future research may aim to replicate these findings in larger and more diverse samples and compare the diffusion of neurometabolites between people with and without HIV living with severe depression.
Depression is associated with inflammation in the periphery and the central nervous system. People with HIV are at greater risk for depression, which may in part be driven by sustained neuroinflammation, although individuals with severe depression are often excluded from studies of HIV-related co-morbidities. In this exploratory study, we aimed to explore the neuroimaging signatures of severe and persistent depression among people with HIV. We enrolled N = 20 adults with HIV in Brighton, UK, of whom n = 11 had a Patient Health Questionnaire-9 (PHQ-9) score ⩾15 and a history of receiving antidepressant medication. We used diffusion-weighted magnetic resonance spectroscopy (DW-MRS), an emerging neuroimaging technique sensitive to neuroinflammation, to assess neurometabolite diffusion in the anterior cingulate cortex. Participants also underwent standard magnetic resonance spectroscopy (MRS) to assess neurometabolite concentrations in the anterior cingulate cortex, and dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to assess blood-brain barrier permeability in the whole brain and the thalamus. We observed a significant positive correlation between intracellular diffusion of creatine and depressive symptom severity (ρ = 0.46, p = 0.047). Increased creatine diffusion has previously been reported in conditions characterised by hypermetabolism and neuroinflammation, suggesting that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic alterations. Metabolite concentrations and blood-brain barrier permeability largely did not correlate with depressive symptom severity in this sample. In summary, we explored neuroimaging signatures of severe depression in people with HIV, including by applying diffusion-weighted magnetic resonance spectroscopy in this population. We report early evidence that worse depressive symptom severity in people with HIV may be correlated with neuroimmunometabolic dysfunction, evidenced by increased diffusion of creatine, likely reflecting hypermetabolism and neuroinflammation. Future research may aim to replicate these findings in larger and more diverse samples and compare the diffusion of neurometabolites between people with and without HIV living with severe depression.
Author Dowell, Nicholas G.
Diteko, Goabaone
Ronen, Itamar
Vera, Jaime H.
Mudra Rakshasa-Loots, Arish
AuthorAffiliation 2 Edinburgh Neuroscience, School of Biomedical Sciences, The University of Edinburgh, Edinburgh, UK
1 Department of Global Health and Infection, Brighton and Sussex Medical School, University of Sussex, Brighton, UK
4 Clinical Imaging Sciences Centre (CISC), Brighton and Sussex Medical School, University of Sussex, Brighton, UK
3 University Hospitals Sussex NHS Foundation Trust, Brighton, UK
AuthorAffiliation_xml – name: 4 Clinical Imaging Sciences Centre (CISC), Brighton and Sussex Medical School, University of Sussex, Brighton, UK
– name: 1 Department of Global Health and Infection, Brighton and Sussex Medical School, University of Sussex, Brighton, UK
– name: 3 University Hospitals Sussex NHS Foundation Trust, Brighton, UK
– name: 2 Edinburgh Neuroscience, School of Biomedical Sciences, The University of Edinburgh, Edinburgh, UK
Author_xml – sequence: 1
  givenname: Arish
  orcidid: 0000-0003-1860-3865
  surname: Mudra Rakshasa-Loots
  fullname: Mudra Rakshasa-Loots, Arish
  organization: Department of Global Health and Infection, Brighton and Sussex Medical School, University of Sussex, Brighton, UK, Edinburgh Neuroscience, School of Biomedical Sciences, The University of Edinburgh, Edinburgh, UK
– sequence: 2
  givenname: Goabaone
  surname: Diteko
  fullname: Diteko, Goabaone
  organization: University Hospitals Sussex NHS Foundation Trust, Brighton, UK
– sequence: 3
  givenname: Nicholas G.
  surname: Dowell
  fullname: Dowell, Nicholas G.
  organization: Clinical Imaging Sciences Centre (CISC), Brighton and Sussex Medical School, University of Sussex, Brighton, UK
– sequence: 4
  givenname: Itamar
  surname: Ronen
  fullname: Ronen, Itamar
  organization: Clinical Imaging Sciences Centre (CISC), Brighton and Sussex Medical School, University of Sussex, Brighton, UK
– sequence: 5
  givenname: Jaime H.
  surname: Vera
  fullname: Vera, Jaime H.
  organization: Department of Global Health and Infection, Brighton and Sussex Medical School, University of Sussex, Brighton, UK
BackLink https://www.ncbi.nlm.nih.gov/pubmed/40308263$$D View this record in MEDLINE/PubMed
BookMark eNplkc1u1TAQhS1UREvpA7BBXrIJeOzcxGaDqqrQSgUk_raWE497jRI72M4t2fPg5KqlKmI1ozNH35HmPCUHIQYk5DmwVwBt-5oLJTlwyTcgxKZV_BE52mvVXjx4sB-Sk5x_MMZA8pZz9YQc1kwwyRtxRH5_xDlFP45ziCMW08XB99QMBZMpPoZMTbA04w6TLwuNjlqcEubsd0jzMk4ljpn6QCeM04D0xpctvbj8_oaeBoq_piGunJgWar1zc16J1Q36621BSz98_kJzme3yjDx2Zsh4cjePybd351_PLqqrT-8vz06vqh5UyyvubFdLIxW6jeWNqutGSNugkh0a4xwqEHULtjGs7aB3DaCAFlzXdKvKuTgmb2-509yNaHsMJZlBT8mPJi06Gq__vQS_1ddxp4GzGhrJVsLLO0KKP2fMRY8-9zgMJmCcsxag5JrJlFitLx6G3af8_f1qgFtDn2LOCd29BZjeV6z_q1j8AWYPm-c
Cites_doi 10.1016/j.bbi.2021.10.005
10.1093/brain/aww031
10.1002/nbm.4206
10.1046/j.1525-1497.2001.016009606.x
10.1038/nrn3475
10.3389/fimmu.2017.01321
10.3389/fimmu.2019.01965
10.1016/S2215-0366(21)00395-3
10.1212/WNL.0000000000002485
10.1007/s40336-015-0142-y
10.3389/fpubh.2020.00180
10.1111/bpa.12197
10.1148/radiol.220430
10.1007/s11481-013-9460-x
10.1016/j.bbi.2024.08.034
10.1038/s41386-020-00948-6
10.1186/1742-2094-8-94
10.1007/s10571-021-01153-9
10.1177/1745691617693393
10.1186/s12889-016-3638-0
10.1038/s41380-018-0259-2
10.1038/tp.2016.239
10.3389/fncel.2015.00212
10.1002/wps.21120
10.1310/hct1304-222
10.1016/j.ejrad.2008.02.033
10.1016/j.pscychresns.2013.03.004
10.1016/j.jad.2022.12.020
10.1002/mrm.1910300604
10.1002/nbm.3914
10.1007/s00127-022-02241-x
10.1002/mrm.25094
10.1007/s11126-019-09707-3
10.1177/1352458517698249
10.1177/2515245919847202
10.1016/j.nbd.2020.105080
10.1016/j.biopsych.2017.08.005
10.1371/journal.pone.0092842
10.1038/mp.2016.73
10.1016/j.pscychresns.2023.111761
10.1016/j.nicl.2021.102926
10.5334/pme.1324
10.3389/fnins.2023.1134867
10.1016/j.euroneuro.2015.06.007
10.1016/j.brainres.2011.05.015
10.1097/QAD.0000000000002300
10.1002/mrm.22821
10.1002/mrm.24542
10.1016/j.bbih.2022.100528
10.1002/jmri.24478
ContentType Journal Article
Copyright The Author(s) 2025.
The Author(s) 2025 2025 SAGE Publications Ltd and British Neuroscience Association, unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses
Copyright_xml – notice: The Author(s) 2025.
– notice: The Author(s) 2025 2025 SAGE Publications Ltd and British Neuroscience Association, unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses
DBID AAYXX
CITATION
NPM
7X8
5PM
DOI 10.1177/23982128251335792
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
PubMed

CrossRef
Database_xml – sequence: 1
  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
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
EISSN 2398-2128
ExternalDocumentID PMC12041680
40308263
10_1177_23982128251335792
Genre Journal Article
GrantInformation_xml – fundername: ;
  grantid: 218493/Z/19/Z
– fundername: ;
  grantid: Pilot Project Funding
GroupedDBID 0R~
54M
7RV
7X7
88E
8FI
8FJ
AASGM
AAYXX
ABAWP
ABNCE
ABQXT
ABUWG
ACARO
ACDXX
ACGFS
ACHEB
ACROE
ADBBV
ADEBD
ADOGD
ADZYD
AEWDL
AFCOW
AFKRA
AFKRG
AFRWT
AJUZI
ALMA_UNASSIGNED_HOLDINGS
ARTOV
AUTPY
AYAKG
AZQEC
BDDNI
BENPR
BPHCQ
BVXVI
CCPQU
CITATION
DC.
DWQXO
EBS
EJD
EMOBN
FYUFA
GNUQQ
GROUPED_DOAJ
H13
HMCUK
J8X
K.F
M1P
M2M
M~E
NAPCQ
O9-
OK1
PHGZM
PHGZT
PIMPY
PQQKQ
PSQYO
PSYQQ
ROL
RPM
SAUOL
SCDPB
SCNPE
SFC
UKHRP
NPM
PJZUB
PPXIY
7X8
5PM
ID FETCH-LOGICAL-c1972-2fdb48a89ef5d26944638d6e98beaaffe913471d6a07b1cf61e3171fb6b71d223
ISSN 2398-2128
IngestDate Thu Aug 21 18:26:31 EDT 2025
Fri Jul 11 18:23:22 EDT 2025
Mon Jul 21 06:08:18 EDT 2025
Tue Jul 01 04:53:06 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords magnetic resonance spectroscopy
Immunopsychiatry
major depressive disorder
neuroinflammation
neuroimaging
Language English
License The Author(s) 2025.
This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c1972-2fdb48a89ef5d26944638d6e98beaaffe913471d6a07b1cf61e3171fb6b71d223
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0003-1860-3865
OpenAccessLink http://dx.doi.org/10.1177/23982128251335792
PMID 40308263
PQID 3198317093
PQPubID 23479
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_12041680
proquest_miscellaneous_3198317093
pubmed_primary_40308263
crossref_primary_10_1177_23982128251335792
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2025 Jan-Dec
PublicationDateYYYYMMDD 2025-01-01
PublicationDate_xml – month: 01
  year: 2025
  text: 2025 Jan-Dec
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Sage UK: London, England
PublicationTitle Brain and neuroscience advances
PublicationTitleAlternate Brain Neurosci Adv
PublicationYear 2025
Publisher SAGE Publications
Publisher_xml – name: SAGE Publications
References e_1_3_3_52_1
e_1_3_3_50_1
e_1_3_3_18_1
e_1_3_3_39_1
e_1_3_3_14_1
e_1_3_3_16_1
e_1_3_3_35_1
e_1_3_3_10_1
e_1_3_3_33_1
e_1_3_3_12_1
e_1_3_3_31_1
e_1_3_3_40_1
e_1_3_3_7_1
e_1_3_3_9_1
e_1_3_3_29_1
e_1_3_3_25_1
e_1_3_3_48_1
e_1_3_3_27_1
e_1_3_3_46_1
e_1_3_3_3_1
e_1_3_3_21_1
e_1_3_3_44_1
e_1_3_3_5_1
e_1_3_3_23_1
e_1_3_3_42_1
e_1_3_3_30_1
e_1_3_3_51_1
e_1_3_3_17_1
e_1_3_3_19_1
e_1_3_3_13_1
e_1_3_3_38_1
e_1_3_3_15_1
e_1_3_3_36_1
e_1_3_3_34_1
e_1_3_3_11_1
e_1_3_3_53_1
e_1_3_3_41_1
e_1_3_3_6_1
Negeri ZF (e_1_3_3_32_1) 2021; 375
e_1_3_3_8_1
e_1_3_3_28_1
Ronen I (e_1_3_3_37_1) 2007; 4
e_1_3_3_24_1
e_1_3_3_49_1
e_1_3_3_26_1
e_1_3_3_47_1
e_1_3_3_2_1
e_1_3_3_20_1
e_1_3_3_45_1
e_1_3_3_4_1
e_1_3_3_22_1
e_1_3_3_43_1
References_xml – ident: e_1_3_3_14_1
  doi: 10.1016/j.bbi.2021.10.005
– ident: e_1_3_3_18_1
  doi: 10.1093/brain/aww031
– volume: 375
  year: 2021
  ident: e_1_3_3_32_1
  article-title: Accuracy of the Patient Health Questionnaire-9 for screening to detect major depression: Updated systematic review and individual participant data meta-analysis
  publication-title: BMJ
– ident: e_1_3_3_25_1
  doi: 10.1002/nbm.4206
– ident: e_1_3_3_27_1
  doi: 10.1046/j.1525-1497.2001.016009606.x
– ident: e_1_3_3_9_1
  doi: 10.1038/nrn3475
– ident: e_1_3_3_45_1
  doi: 10.3389/fimmu.2017.01321
– ident: e_1_3_3_4_1
  doi: 10.3389/fimmu.2019.01965
– ident: e_1_3_3_23_1
  doi: 10.1016/S2215-0366(21)00395-3
– ident: e_1_3_3_48_1
  doi: 10.1212/WNL.0000000000002485
– ident: e_1_3_3_35_1
  doi: 10.1007/s40336-015-0142-y
– ident: e_1_3_3_42_1
  doi: 10.3389/fpubh.2020.00180
– ident: e_1_3_3_53_1
  doi: 10.1111/bpa.12197
– ident: e_1_3_3_24_1
  doi: 10.1148/radiol.220430
– ident: e_1_3_3_12_1
  doi: 10.1007/s11481-013-9460-x
– ident: e_1_3_3_5_1
  doi: 10.1016/j.bbi.2024.08.034
– ident: e_1_3_3_33_1
  doi: 10.1038/s41386-020-00948-6
– ident: e_1_3_3_41_1
  doi: 10.1186/1742-2094-8-94
– ident: e_1_3_3_49_1
  doi: 10.1007/s10571-021-01153-9
– ident: e_1_3_3_51_1
  doi: 10.1177/1745691617693393
– ident: e_1_3_3_20_1
  doi: 10.1186/s12889-016-3638-0
– ident: e_1_3_3_30_1
  doi: 10.1038/s41380-018-0259-2
– ident: e_1_3_3_38_1
  doi: 10.1038/tp.2016.239
– ident: e_1_3_3_3_1
  doi: 10.3389/fncel.2015.00212
– ident: e_1_3_3_29_1
  doi: 10.1002/wps.21120
– ident: e_1_3_3_47_1
  doi: 10.1310/hct1304-222
– ident: e_1_3_3_28_1
  doi: 10.1016/j.ejrad.2008.02.033
– volume: 4
  start-page: 733
  year: 2007
  ident: e_1_3_3_37_1
  article-title: Diffusion-weighted magnetic resonance spectroscopy
  publication-title: EMagRes
– ident: e_1_3_3_13_1
  doi: 10.1016/j.pscychresns.2013.03.004
– ident: e_1_3_3_50_1
  doi: 10.1016/j.jad.2022.12.020
– ident: e_1_3_3_34_1
  doi: 10.1002/mrm.1910300604
– ident: e_1_3_3_22_1
  doi: 10.1002/nbm.3914
– ident: e_1_3_3_52_1
  doi: 10.1007/s00127-022-02241-x
– ident: e_1_3_3_31_1
  doi: 10.1002/mrm.25094
– ident: e_1_3_3_10_1
  doi: 10.1007/s11126-019-09707-3
– ident: e_1_3_3_6_1
  doi: 10.1177/1352458517698249
– ident: e_1_3_3_21_1
  doi: 10.1177/2515245919847202
– ident: e_1_3_3_46_1
  doi: 10.1016/j.nbd.2020.105080
– ident: e_1_3_3_26_1
  doi: 10.1016/j.biopsych.2017.08.005
– ident: e_1_3_3_15_1
  doi: 10.1371/journal.pone.0092842
– ident: e_1_3_3_19_1
  doi: 10.1038/mp.2016.73
– ident: e_1_3_3_40_1
  doi: 10.1016/j.pscychresns.2023.111761
– ident: e_1_3_3_2_1
  doi: 10.1016/j.nicl.2021.102926
– ident: e_1_3_3_7_1
  doi: 10.5334/pme.1324
– ident: e_1_3_3_39_1
  doi: 10.3389/fnins.2023.1134867
– ident: e_1_3_3_43_1
  doi: 10.1016/j.euroneuro.2015.06.007
– ident: e_1_3_3_44_1
  doi: 10.1016/j.brainres.2011.05.015
– ident: e_1_3_3_11_1
  doi: 10.1097/QAD.0000000000002300
– ident: e_1_3_3_36_1
  doi: 10.1002/mrm.22821
– ident: e_1_3_3_8_1
  doi: 10.1002/mrm.24542
– ident: e_1_3_3_17_1
  doi: 10.1016/j.bbih.2022.100528
– ident: e_1_3_3_16_1
  doi: 10.1002/jmri.24478
SSID ssj0001827229
Score 2.2794192
Snippet Depression is associated with inflammation in the periphery and the central nervous system. People with HIV are at greater risk for depression, which may in...
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage 23982128251335792
SubjectTerms Research Paper
Title Neuroimmunometabolic alterations and severity of depressive symptoms in people with HIV: An exploratory diffusion-weighted MRS study
URI https://www.ncbi.nlm.nih.gov/pubmed/40308263
https://www.proquest.com/docview/3198317093
https://pubmed.ncbi.nlm.nih.gov/PMC12041680
Volume 9
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLa67oUXBIxLuVRGQjxQZUq8XBzeCox1iE2obKhv1XHiaNHUZGpS0Hjm1_ArObZz61okhipFlZNabs9X-_icz98h5JXvhwJC4Vl-EkSWGyWJBeDalpQMAg5h7Ep1UPjk1J-cu59m3qzX-91hLa1KsR_93Hqu5H-sim1oV3VK9haWbTrFBnyP9sUrWhiv_2RjrayRqhMe-UKWaE6lWK3z3xXBTUfFJX6vinhR816_y1Fxvbgq80WHRm5ispPjb1WwUGp6nsnCqzoqKxVYs37oWCq6qSfTrx1x2kYjCVJDb-4IZcqaaVC05o2XMJrCZXEBBVif87w0VZFVvfvGt0Zv-FJHco9yEJC3BIAPecPlTvXmvBgd7bepo8xMpcclLGDZDWswrxPW0LOf0iW0cF01k7Pc0lZN3-H2hUCnotUH1PNMVbHxAlN1b110-8Zi2FAUnUoHfaOLHbLLcEvC-mT33eHpl2kb0eMMm0NdzbAaZ5VGVwpfG_2sO0Ibu5ubJN2O13N2j9yttit0bLB3n_Rk9oDsjTNExeKavqaaQKwzM3vk1zY40g4cKeKC1nCkeUJbONIajjTNqIEjVXCkCMe3dJzRDhjpJhgpgpFqMD4k5x8Pz95PrKrIhxWpincWS2LhcuChTLxYHat2cUWIfRlyIQGSRCpqSODEPtiBcKLEdyS6vE4ifIGt6Nw-Iv0MgfWEUCZ4wAWAI2LXdTm-Al9l9ZljR3HEYEDe1L_4_Mpoucz_auYBeVnbZI4zrkqjQSbzVTHHRYvjEOzwYEAeGxs13bla_snHO3zNes0DSs19_U6WXmhVd4fZuDni9tPbjPIZudP-eZ6TfrlcyRfoJZdiSHaCWTCsQDrUsaY_HNjDFQ
linkProvider ProQuest
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=Neuroimmunometabolic+alterations+and+severity+of+depressive+symptoms+in+people+with+HIV%3A+An+exploratory+diffusion-weighted+MRS+study&rft.jtitle=Brain+and+neuroscience+advances&rft.au=Mudra+Rakshasa-Loots%2C+Arish&rft.au=Diteko%2C+Goabaone&rft.au=Dowell%2C+Nicholas+G.&rft.au=Ronen%2C+Itamar&rft.date=2025-01-01&rft.issn=2398-2128&rft.eissn=2398-2128&rft.volume=9&rft_id=info:doi/10.1177%2F23982128251335792&rft.externalDBID=n%2Fa&rft.externalDocID=10_1177_23982128251335792
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2398-2128&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2398-2128&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2398-2128&client=summon