Evolution of inflammatory dysregulation and oxidative stress in patients with first episode of mania

Introduction Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative processes in bipolar disorder. Thus, the study of these pathways in first episodes of mania (FEM) can increase knowledge about this issue. Aim To...

Full description

Saved in:
Bibliographic Details
Published inEuropean psychiatry Vol. 33; no. S1; p. S331
Main Authors García, S, López Peña, P, Zorrilla, I, García-Alocen, A, Martínez-Cengotitabengoa, M, Bermúdez-Ampudia, C, Mac-Dowell, K.S, Rodríguez, S, Leza, J.C, González-Pinto, A
Format Journal Article
LanguageEnglish
Published Elsevier Masson SAS 01.03.2016
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Introduction Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative processes in bipolar disorder. Thus, the study of these pathways in first episodes of mania (FEM) can increase knowledge about this issue. Aim To compare plasma concentrations of pro-inflammatory (MCP-1, PGE2, TNFα) and oxidative parameters (TAS, NO2 and TBARS) between controls and FEM patients and to analyze the evolution of these parameters in patients from baseline to 6 months assessment time. Methods This study included 44 FEM patients and 79 healthy controls, aged 18 to 40. Blood samples were available for controls at baseline and for patients at baseline and 6 months after. TAS and TBARS were measured using non-EIA assay kits, N02 was measured with Griess method and PGE2, MCP-1 and TNFα with ELISA kits. Results At baseline, TAS was significantly lower in patients than in controls and TBARS, MCP-1 and TNFα were significantly higher in patients. Among patients, TAS and MCP1 were lower at 6 months than at the illness onset and PGE2 and NO2 were significantly higher than at baseline. Conclusion Patients presented an increased oxidative damage and also a higher activation of pro-inflammatory pathways than healthy controls at baseline. After 6 months their level of oxidative stress continue increased. Pro-inflammatory parameters decreased overtime (MCP-1 and TNF α) but PGE2, increased surprisingly. This can be due to the fact that antipsychotics are not able to completely reverse baseline inflammation.
AbstractList Introduction Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative processes in bipolar disorder. Thus, the study of these pathways in first episodes of mania (FEM) can increase knowledge about this issue. Aim To compare plasma concentrations of pro-inflammatory (MCP-1, PGE2, TNFα) and oxidative parameters (TAS, NO2 and TBARS) between controls and FEM patients and to analyze the evolution of these parameters in patients from baseline to 6 months assessment time. Methods This study included 44 FEM patients and 79 healthy controls, aged 18 to 40. Blood samples were available for controls at baseline and for patients at baseline and 6 months after. TAS and TBARS were measured using non-EIA assay kits, N02 was measured with Griess method and PGE2, MCP-1 and TNFα with ELISA kits. Results At baseline, TAS was significantly lower in patients than in controls and TBARS, MCP-1 and TNFα were significantly higher in patients. Among patients, TAS and MCP1 were lower at 6 months than at the illness onset and PGE2 and NO2 were significantly higher than at baseline. Conclusion Patients presented an increased oxidative damage and also a higher activation of pro-inflammatory pathways than healthy controls at baseline. After 6 months their level of oxidative stress continue increased. Pro-inflammatory parameters decreased overtime (MCP-1 and TNF α) but PGE2, increased surprisingly. This can be due to the fact that antipsychotics are not able to completely reverse baseline inflammation.
Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative processes in bipolar disorder. Thus, the study of these pathways in first episodes of mania (FEM) can increase knowledge about this issue. To compare plasma concentrations of pro-inflammatory (MCP-1, PGE2, TNFα) and oxidative parameters (TAS, NO2 and TBARS) between controls and FEM patients and to analyze the evolution of these parameters in patients from baseline to 6 months assessment time. This study included 44 FEM patients and 79 healthy controls, aged 18 to 40. Blood samples were available for controls at baseline and for patients at baseline and 6 months after. TAS and TBARS were measured using non-EIA assay kits, N02 was measured with Griess method and PGE2, MCP-1 and TNFα with ELISA kits. At baseline, TAS was significantly lower in patients than in controls and TBARS, MCP-1 and TNFα were significantly higher in patients. Among patients, TAS and MCP1 were lower at 6 months than at the illness onset and PGE2 and NO2 were significantly higher than at baseline. Patients presented an increased oxidative damage and also a higher activation of pro-inflammatory pathways than healthy controls at baseline. After 6 months their level of oxidative stress continue increased. Pro-inflammatory parameters decreased overtime (MCP-1 and TNF α) but PGE2, increased surprisingly. This can be due to the fact that antipsychotics are not able to completely reverse baseline inflammation.
Introduction Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative processes in bipolar disorder. Thus, the study of these pathways in first episodes of mania (FEM) can increase knowledge about this issue. Aim To compare plasma concentrations of pro-inflammatory (MCP-1, PGE2, TNFα) and oxidative parameters (TAS, NO 2 and TBARS) between controls and FEM patients and to analyze the evolution of these parameters in patients from baseline to 6 months assessment time. Methods This study included 44 FEM patients and 79 healthy controls, aged 18 to 40. Blood samples were available for controls at baseline and for patients at baseline and 6 months after. TAS and TBARS were measured using non-EIA assay kits, N0 2 was measured with Griess method and PGE2, MCP-1 and TNFα with ELISA kits. Results At baseline, TAS was significantly lower in patients than in controls and TBARS, MCP-1 and TNFα were significantly higher in patients. Among patients, TAS and MCP1 were lower at 6 months than at the illness onset and PGE2 and NO 2 were significantly higher than at baseline. Conclusion Patients presented an increased oxidative damage and also a higher activation of pro-inflammatory pathways than healthy controls at baseline. After 6 months their level of oxidative stress continue increased. Pro-inflammatory parameters decreased overtime (MCP-1 and TNF α) but PGE2, increased surprisingly. This can be due to the fact that antipsychotics are not able to completely reverse baseline inflammation. Disclosure of interest The authors have not supplied their declaration of competing interest.
Author Martínez-Cengotitabengoa, M
Bermúdez-Ampudia, C
García-Alocen, A
Mac-Dowell, K.S
López Peña, P
Rodríguez, S
Leza, J.C
García, S
Zorrilla, I
González-Pinto, A
Author_xml – sequence: 1
  fullname: García, S
– sequence: 2
  fullname: López Peña, P
– sequence: 3
  fullname: Zorrilla, I
– sequence: 4
  fullname: García-Alocen, A
– sequence: 5
  fullname: Martínez-Cengotitabengoa, M
– sequence: 6
  fullname: Bermúdez-Ampudia, C
– sequence: 7
  fullname: Mac-Dowell, K.S
– sequence: 8
  fullname: Rodríguez, S
– sequence: 9
  fullname: Leza, J.C
– sequence: 10
  fullname: González-Pinto, A
BookMark eNqFUctu2zAQJIoUiJP2EwLwB6RyKZOSLgmCIC8gQA9JzwRFLls6MmmQshP9fak4p156WuxjBjOzZ-QkxICEXACrgYH8salxn3Z5rnnpagY1gOBfyAratqsa0YkTsmI9X1d903Sn5CznDWPQMiZXxN4e4riffAw0OuqDG_V2q6eYZmrnnPD3ftQfWx0sje_elu6ANE8Jcy73dFcGGKZM3_z0hzqf8kRx53O0uDBudfD6G_nq9Jjx-2c9J7_ubl9uHqqnn_ePN9dPlQHR8sr0xuq-d2vu1mg4N9ihGCSHobFy6NygW9kbkNxI5kwPVph-YNoIIVptJTTnRBx5TYq5iHdql_xWp1kBU0tUaqOOUaklKsVALVEV3NURh0XcwWNS2RRTBq1PaCZlo_8vw-U_DGb0wRs9vuKMeRP3KRTnClTmiqnn5R3LN0Cygi_S_wIbL46p
ContentType Journal Article
Copyright 2016
Copyright_xml – notice: 2016
DBID AAYXX
CITATION
DOI 10.1016/j.eurpsy.2016.01.1152
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList

CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1778-3585
EndPage S331
ExternalDocumentID 10_1016_j_eurpsy_2016_01_1152
S0924933816011561
1_s2_0_S0924933816011561
GroupedDBID ---
--K
--M
.1-
.FO
.~1
09C
09E
0R~
0SF
1B1
1P~
1~.
1~5
29G
4.4
457
4G.
53G
5GY
5VS
7-5
71M
8FI
8FJ
8P~
AABNK
AACTN
AAEDT
AAEDW
AAFWJ
AAIKJ
AAKOC
AALRI
AANRG
AAOAW
AAQXK
AASVR
AAXUO
ABBQC
ABBZL
ABFNM
ABIVO
ABJNI
ABMZM
ABUWG
ABVZP
ABXAU
ABXDB
ACDAQ
ACGFS
ACHQT
ACIUM
ACQPF
ACZWT
ADAZD
ADBBV
ADDNB
ADEZE
ADKIL
ADMUD
ADOVH
ADVJH
ADVLN
AEBAK
AEKER
AENCP
AENEX
AEVXI
AEYHU
AFCTW
AFKRA
AFRHN
AFTJW
AGABE
AGHFR
AGJUD
AGUBO
AGYEJ
AHIPN
AHRGI
AITUG
AJOXV
AJPFC
AJRQY
AJUYK
AKRWK
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMFUW
AMRAJ
ANZVX
AQJOH
ASPBG
AVWKF
AZFZN
AZQEC
BENPR
BLXMC
BLZWO
CCPQU
CCQAD
CCUQV
CFBFF
CGQII
CJCSC
CS3
CTKSN
DOHLZ
DU5
DWQXO
EBS
EGQIC
EJD
EO8
EO9
EP2
EP3
F5P
FDB
FEDTE
FGOYB
FIRID
FNPLU
FYUFA
G-Q
GBLVA
GNUQQ
GROUPED_DOAJ
HVGLF
HZ~
IHE
IKXGN
IOO
IPYYG
J1W
LN9
M2M
M41
MO0
N9A
NCXOZ
NZEOI
O-L
O9-
OAUVE
OH0
OK1
OU-
OZT
P-8
P-9
P2P
PC.
PIMPY
PSYQQ
Q38
R2-
RCA
RIG
ROL
RPM
RPZ
SCC
SDF
SDG
SDP
SES
SEW
SSZ
T5K
UHS
UKHRP
UV1
WFFJZ
Z5R
~G-
AFPKN
LW7
AAYXX
CITATION
ID FETCH-LOGICAL-c1572-c9cda99f42f4ec22ce8e5b621b3d6b8fba769c162c60fc91d5c9b0ac5557ad613
IEDL.DBID .~1
ISSN 0924-9338
IngestDate Thu Sep 26 16:14:38 EDT 2024
Sun Jul 07 06:46:17 EDT 2024
Tue Oct 15 23:01:35 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue S1
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c1572-c9cda99f42f4ec22ce8e5b621b3d6b8fba769c162c60fc91d5c9b0ac5557ad613
ParticipantIDs crossref_primary_10_1016_j_eurpsy_2016_01_1152
elsevier_sciencedirect_doi_10_1016_j_eurpsy_2016_01_1152
elsevier_clinicalkeyesjournals_1_s2_0_S0924933816011561
PublicationCentury 2000
PublicationDate March 2016
PublicationDateYYYYMMDD 2016-03-01
PublicationDate_xml – month: 03
  year: 2016
  text: March 2016
PublicationDecade 2010
PublicationTitle European psychiatry
PublicationYear 2016
Publisher Elsevier Masson SAS
Publisher_xml – name: Elsevier Masson SAS
SSID ssj0017006
Score 2.159511
Snippet Introduction Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative...
Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative processes in...
Introduction Recent studies have focused on the imbalance in inflammatory and antioxidant pathways as possible causes of the underlying neurodegenerative...
SourceID crossref
elsevier
SourceType Aggregation Database
Publisher
StartPage S331
SubjectTerms Internal Medicine
Psychiatry
Title Evolution of inflammatory dysregulation and oxidative stress in patients with first episode of mania
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0924933816011561
https://dx.doi.org/10.1016/j.eurpsy.2016.01.1152
Volume 33
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV07T8MwELaqDogF8RTlUXlgTZu4sROPqGqFkMoClbpZfqJUoq1IQXTht3NOnAICMTAmsp3o7nwP391nhK5cwkgmiYlozgZRyi2PJJM0ihXnxoEDLZ0_0J_csZtpejujsxYaNr0wvqwy6P5ap1faOrzpB2r2V0XRv4996DDwiS_v1lQhUArmD2S6974t8_Dwc1W-EgZHfvRnF09_7rEVV-XGF3gxD94Jy5Df7dMXmzPeR3vBWcTX9f8coJZdHKKdSUiHHyEzeg2Sg5cOg6wAe5-qtDk2G1j7MdzNheXC4OVbYSqUb1z3h8B4HFBVS-yPY7ErwBXEdlWUS2P9ih4bQx6j6Xj0MLyJwrUJkU5oRiLNtZGcu5S41GpCtM0tVYwkamCYyp2SGeMaeKRZ7DRPDNVcxVJTSjNpwLyfoPZiubCnCFPj5CBXzpicp7HMJNXGgAaAkJrmmco7qNcQS6xqdAzRlI3NRU1d4akr4kR46nZQ1pBUNK2foKxsGXZOKRJREhGLH9ztoHw785uACND9f3_07P9Tz9Guf6yLzi5Qe_38Yi_BC1mrbiVm3SqG_wCoTd4r
link.rule.ids 315,783,787,867,4509,27936,27937,45597
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LT8MwDI4QSMAF8RTjmQPXsjZr0uaIpk3jMS5sErcoT9RJbBMFBBd-O3Gb8hCIA9c2cSvbsZ3Y_oLQiUsYySQxEc1ZJ0q55ZFkkkax4tw4H0BLBwf6w2s2GKcXt_R2AXWbXhgoqwy2v7bplbUOT9qBm-15UbRvYtg6dCDxBWENbIGWUoiPvVKfvn3UeQD-XJWw9KMjGP7ZxtOeALjivHyFCi8G6J2eDvndQX1xOv11tBaiRXxW_9AGWrDTTbQ8DPnwLWR6z0F18MxhryxevvdV3hybV0_7LlzOheXU4NlLYSqYb1w3iPjxOMCqlhjOY7ErfCyI7bwoZ8YCRQDHkNto3O-NuoMo3JsQ6YRmJNJcG8m5S4lLrSZE29xSxUiiOoap3CmZMa69kDSLneaJoZqrWGpKaSaN9-87aHE6m9pdhKlxspMrZ0zO01hmkmpjvAnwe2qaZypvodOGWWJew2OIpm5sImruCuCuiBMB3G2hrGGpaHo_vbWyZVg6pUhESUQsfoi3hfKPmd80RHjj__dH9_4_9RitDEbDK3F1fn25j1bhVV2BdoAWHx-e7KEPSR7VUaVy77Fi4F0
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=Evolution+of+inflammatory+dysregulation+and+oxidative+stress+in+patients+with+first+episode+of+mania&rft.jtitle=European+psychiatry&rft.au=Garc%C3%ADa%2C+S&rft.au=L%C3%B3pez+Pe%C3%B1a%2C+P&rft.au=Zorrilla%2C+I&rft.au=Garc%C3%ADa-Alocen%2C+A&rft.date=2016-03-01&rft.issn=0924-9338&rft.volume=33&rft.spage=S331&rft.epage=S331&rft_id=info:doi/10.1016%2Fj.eurpsy.2016.01.1152&rft.externalDBID=ECK1-s2.0-S0924933816011561&rft.externalDocID=1_s2_0_S0924933816011561
thumbnail_m http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F09249338%2FS0924933816X00041%2Fcov150h.gif