Autoimmune Encephalitis in Postpartum Psychosis

Objective:Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have highlighted the possibility that a subset of patients with first-onset severe psychiatric episodes might suffer from undiagnosed autoimmu...

Full description

Saved in:
Bibliographic Details
Published inAmerican Journal of Psychiatry Vol. 172; no. 9; pp. 901 - 908
Main Authors Bergink, Veerle, Armangue, Thaís, Titulaer, Maarten J, Markx, Sander, Dalmau, Josep, Kushner, Steven A
Format Journal Article
LanguageEnglish
Published United States American Psychiatric Association 01.09.2015
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Objective:Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have highlighted the possibility that a subset of patients with first-onset severe psychiatric episodes might suffer from undiagnosed autoimmune encephalitis. Therefore, the authors performed a three-step immunohistochemistry-based screening for CNS autoantibodies in a large cohort of patients with postpartum psychosis and matched postpartum comparison subjects.Method:Ninety-six consecutive patients with postpartum psychosis and 64 healthy postpartum women were included. Screening for antibodies in patient serum was performed using immunohistochemistry. Samples showing any staining were further examined by immunocytochemistry using live hippocampal neurons and cell-based assays to test for anti-N-methyl-d-aspartate (NMDA) receptor antibodies. Cell-based assays for all other known CNS antigens were performed in those samples with immunocytochemistry labeling but negative for NMDA receptor antibodies.Results:Four patients (4%) with neuropil labeling suggestive for extracellular antigen reactivity were identified. Serum samples from all four patients showed clear extracellular labeling of live hippocampal neurons. Two women had the specific staining pattern characteristic for anti-NMDA receptor antibody positivity, which was confirmed by cell-based assays. Neither patient with anti-NMDA receptor antibody positivity had evidence of an ovarian teratoma. The other two patients tested negative by cell-based assays for all known CNS antigens. None of the matched postpartum comparison subjects had confirmed neuronal surface antibodies. The two patients with anti-NMDA receptor antibodies both showed extrapyramidal symptoms following initiation of treatment with low-dose haloperidol.Conclusions:In patients with acute psychosis during the postpartum period, systematic screening for anti-NMDA receptor autoantibodies should be considered. The acute onset of severe atypical psychiatric symptoms in young female patients should raise the index of suspicion for anti-NMDA receptor encephalitis, particularly in the setting of neurological symptoms, including extrapyramidal side effects of antipsychotic treatment.
AbstractList Objective:Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have highlighted the possibility that a subset of patients with first-onset severe psychiatric episodes might suffer from undiagnosed autoimmune encephalitis. Therefore, the authors performed a three-step immunohistochemistry-based screening for CNS autoantibodies in a large cohort of patients with postpartum psychosis and matched postpartum comparison subjects.Method:Ninety-six consecutive patients with postpartum psychosis and 64 healthy postpartum women were included. Screening for antibodies in patient serum was performed using immunohistochemistry. Samples showing any staining were further examined by immunocytochemistry using live hippocampal neurons and cell-based assays to test for anti-N-methyl-d-aspartate (NMDA) receptor antibodies. Cell-based assays for all other known CNS antigens were performed in those samples with immunocytochemistry labeling but negative for NMDA receptor antibodies.Results:Four patients (4%) with neuropil labeling suggestive for extracellular antigen reactivity were identified. Serum samples from all four patients showed clear extracellular labeling of live hippocampal neurons. Two women had the specific staining pattern characteristic for anti-NMDA receptor antibody positivity, which was confirmed by cell-based assays. Neither patient with anti-NMDA receptor antibody positivity had evidence of an ovarian teratoma. The other two patients tested negative by cell-based assays for all known CNS antigens. None of the matched postpartum comparison subjects had confirmed neuronal surface antibodies. The two patients with anti-NMDA receptor antibodies both showed extrapyramidal symptoms following initiation of treatment with low-dose haloperidol.Conclusions:In patients with acute psychosis during the postpartum period, systematic screening for anti-NMDA receptor autoantibodies should be considered. The acute onset of severe atypical psychiatric symptoms in young female patients should raise the index of suspicion for anti-NMDA receptor encephalitis, particularly in the setting of neurological symptoms, including extrapyramidal side effects of antipsychotic treatment.
Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have highlighted the possibility that a subset of patients with first-onset severe psychiatric episodes might suffer from undiagnosed autoimmune encephalitis. Therefore, the authors performed a three-step immunohistochemistry-based screening for CNS autoantibodies in a large cohort of patients with postpartum psychosis and matched postpartum comparison subjects. Ninety-six consecutive patients with postpartum psychosis and 64 healthy postpartum women were included. Screening for antibodies in patient serum was performed using immunohistochemistry. Samples showing any staining were further examined by immunocytochemistry using live hippocampal neurons and cell-based assays to test for anti-N-methyl-d-aspartate (NMDA) receptor antibodies. Cell-based assays for all other known CNS antigens were performed in those samples with immunocytochemistry labeling but negative for NMDA receptor antibodies. Four patients (4%) with neuropil labeling suggestive for extracellular antigen reactivity were identified. Serum samples from all four patients showed clear extracellular labeling of live hippocampal neurons. Two women had the specific staining pattern characteristic for anti-NMDA receptor antibody positivity, which was confirmed by cell-based assays. Neither patient with anti-NMDA receptor antibody positivity had evidence of an ovarian teratoma. The other two patients tested negative by cell-based assays for all known CNS antigens. None of the matched postpartum comparison subjects had confirmed neuronal surface antibodies. The two patients with anti-NMDA receptor antibodies both showed extrapyramidal symptoms following initiation of treatment with low-dose haloperidol. In patients with acute psychosis during the postpartum period, systematic screening for anti-NMDA receptor autoantibodies should be considered. The acute onset of severe atypical psychiatric symptoms in young female patients should raise the index of suspicion for anti-NMDA receptor encephalitis, particularly in the setting of neurological symptoms, including extrapyramidal side effects of antipsychotic treatment.
Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have highlighted the possibility that a subset of patients with first-onset severe psychiatric episodes might suffer from undiagnosed autoimmune encephalitis. Therefore, the authors performed a three-step immunohistochemistry-based screening for CNS autoantibodies in a large cohort of patients with postpartum psychosis and matched postpartum comparison subjects. Ninety-six consecutive patients with postpartum psychosis and 64 healthy postpartum women were included. Screening for antibodies in patient serum was performed using immunohistochemistry. Samples showing any staining were further examined by immunocytochemistry using live hippocampal neurons and cell-based assays to test for anti-N-methyl-d-aspartate (NMDA) receptor antibodies. Cell-based assays for all other known CNS antigens were performed in those samples with immunocytochemistry labeling but negative for NMDA receptor antibodies. Four patients (4%) with neuropil labeling suggestive for extracellular antigen reactivity were identified. Serum samples from all four patients showed clear extracellular labeling of live hippocampal neurons. Two women had the specific staining pattern characteristic for anti-NMDA receptor antibody positivity, which was confirmed by cell-based assays. Neither patient with anti-NMDA receptor antibody positivity had evidence of an ovarian teratoma. The other two patients tested negative by cell-based assays for all known CNS antigens. None of the matched postpartum comparison subjects had confirmed neuronal surface antibodies. The two patients with anti-NMDA receptor antibodies both showed extrapyramidal symptoms following initiation of treatment with low-dose haloperidol. In patients with acute psychosis during the postpartum period, systematic screening for anti-NMDA receptor autoantibodies should be considered. The acute onset of severe atypical psychiatric symptoms in young female patients should raise the index of suspicion for anti-NMDA receptor encephalitis, particularly in the setting of neurological symptoms, including extrapyramidal side effects of antipsychotic treatment.
Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have highlighted the possibility that a subset of patients with first-onset severe psychiatric episodes might suffer from undiagnosed autoimmune encephalitis. Therefore, the authors performed a three-step immunohistochemistry-based screening for CNS autoantibodies in a large cohort of patients with postpartum psychosis and matched postpartum comparison subjects.OBJECTIVESignificant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have highlighted the possibility that a subset of patients with first-onset severe psychiatric episodes might suffer from undiagnosed autoimmune encephalitis. Therefore, the authors performed a three-step immunohistochemistry-based screening for CNS autoantibodies in a large cohort of patients with postpartum psychosis and matched postpartum comparison subjects.Ninety-six consecutive patients with postpartum psychosis and 64 healthy postpartum women were included. Screening for antibodies in patient serum was performed using immunohistochemistry. Samples showing any staining were further examined by immunocytochemistry using live hippocampal neurons and cell-based assays to test for anti-N-methyl-d-aspartate (NMDA) receptor antibodies. Cell-based assays for all other known CNS antigens were performed in those samples with immunocytochemistry labeling but negative for NMDA receptor antibodies.METHODNinety-six consecutive patients with postpartum psychosis and 64 healthy postpartum women were included. Screening for antibodies in patient serum was performed using immunohistochemistry. Samples showing any staining were further examined by immunocytochemistry using live hippocampal neurons and cell-based assays to test for anti-N-methyl-d-aspartate (NMDA) receptor antibodies. Cell-based assays for all other known CNS antigens were performed in those samples with immunocytochemistry labeling but negative for NMDA receptor antibodies.Four patients (4%) with neuropil labeling suggestive for extracellular antigen reactivity were identified. Serum samples from all four patients showed clear extracellular labeling of live hippocampal neurons. Two women had the specific staining pattern characteristic for anti-NMDA receptor antibody positivity, which was confirmed by cell-based assays. Neither patient with anti-NMDA receptor antibody positivity had evidence of an ovarian teratoma. The other two patients tested negative by cell-based assays for all known CNS antigens. None of the matched postpartum comparison subjects had confirmed neuronal surface antibodies. The two patients with anti-NMDA receptor antibodies both showed extrapyramidal symptoms following initiation of treatment with low-dose haloperidol.RESULTSFour patients (4%) with neuropil labeling suggestive for extracellular antigen reactivity were identified. Serum samples from all four patients showed clear extracellular labeling of live hippocampal neurons. Two women had the specific staining pattern characteristic for anti-NMDA receptor antibody positivity, which was confirmed by cell-based assays. Neither patient with anti-NMDA receptor antibody positivity had evidence of an ovarian teratoma. The other two patients tested negative by cell-based assays for all known CNS antigens. None of the matched postpartum comparison subjects had confirmed neuronal surface antibodies. The two patients with anti-NMDA receptor antibodies both showed extrapyramidal symptoms following initiation of treatment with low-dose haloperidol.In patients with acute psychosis during the postpartum period, systematic screening for anti-NMDA receptor autoantibodies should be considered. The acute onset of severe atypical psychiatric symptoms in young female patients should raise the index of suspicion for anti-NMDA receptor encephalitis, particularly in the setting of neurological symptoms, including extrapyramidal side effects of antipsychotic treatment.CONCLUSIONSIn patients with acute psychosis during the postpartum period, systematic screening for anti-NMDA receptor autoantibodies should be considered. The acute onset of severe atypical psychiatric symptoms in young female patients should raise the index of suspicion for anti-NMDA receptor encephalitis, particularly in the setting of neurological symptoms, including extrapyramidal side effects of antipsychotic treatment.
Author Kushner, Steven A
Bergink, Veerle
Dalmau, Josep
Titulaer, Maarten J
Armangue, Thaís
Markx, Sander
Author_xml – sequence: 1
  givenname: Veerle
  surname: Bergink
  fullname: Bergink, Veerle
– sequence: 2
  givenname: Thaís
  surname: Armangue
  fullname: Armangue, Thaís
– sequence: 3
  givenname: Maarten J
  surname: Titulaer
  fullname: Titulaer, Maarten J
– sequence: 4
  givenname: Sander
  surname: Markx
  fullname: Markx, Sander
– sequence: 5
  givenname: Josep
  surname: Dalmau
  fullname: Dalmau, Josep
– sequence: 6
  givenname: Steven A
  surname: Kushner
  fullname: Kushner, Steven A
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26183699$$D View this record in MEDLINE/PubMed
BookMark eNqFkVFr2zAUhcXoWNN0fyEE9tIXp7qSbMtQCiVkXaGwPmzQNyHb142CLXmWXMi_n9I02dqH7UmI-53DufeckRPrLBIyA7oAyLNL3fdmoTf9glFIFyCAAufsA5lAytMkZ0yekAmllCVFyh9PyZn3m_ilPGefyCnLQPKsKCbk8mYMznTdaHG-shX2a92aYPzc2PmD86HXQxi7-YPfVmvnjT8nHxvdevz8-k7Jz6-rH8tvyf3327vlzX2ihcxCEv1LgZohkwIzBJY20AioJOZUIstKzJGlUhdlzaHWDeTAi1rXtKhlWUrKp-R679uPZYd1hTYMulX9YDo9bJXTRr2dWLNWT-5ZCZmKlEM0uHg1GNyvEX1QnfEVtq226EavIAYpKEgpI_rlHbpx42DjepECISAukUVq9neiY5TDLSOQ7YFqcN4P2BwRoGpXmtqVpmJpaleaOpQWhVfvhJUJOhi328y0_5fzvfxl_if6v1W_Ae-jsE4
CODEN AJPSAO
CitedBy_id crossref_primary_10_3390_antib5020009
crossref_primary_10_5498_wjp_v7_i2_77
crossref_primary_10_1038_tp_2016_212
crossref_primary_10_3389_fgwh_2021_758748
crossref_primary_10_34883_PI_2021_12_2_012
crossref_primary_10_1001_jamapsychiatry_2019_3679
crossref_primary_10_1016_j_psym_2020_03_009
crossref_primary_10_1007_s15005_016_1780_y
crossref_primary_10_1007_s00415_019_09590_9
crossref_primary_10_1016_j_yfrne_2021_100975
crossref_primary_10_1016_j_npbr_2015_12_007
crossref_primary_10_1093_ejendo_lvad092
crossref_primary_10_1530_JME_17_0219
crossref_primary_10_1017_S0033291716002038
crossref_primary_10_3389_fimmu_2022_970448
crossref_primary_10_5692_clinicalneurol_cn_001314
crossref_primary_10_1038_s41398_020_01083_y
crossref_primary_10_1016_j_psiq_2018_11_005
crossref_primary_10_1111_bdi_12523
crossref_primary_10_1192_bjb_2021_35
crossref_primary_10_1016_j_autrev_2022_103145
crossref_primary_10_1007_s40278_016_14967_2
crossref_primary_10_1159_000515930
crossref_primary_10_1016_j_psyneuen_2021_105218
crossref_primary_10_1017_S0033291715001385
crossref_primary_10_1080_13854046_2015_1132772
crossref_primary_10_1371_journal_pone_0281133
crossref_primary_10_1016_S1474_4422_19_30244_3
crossref_primary_10_1159_000493740
crossref_primary_10_47795_LLEP2170
crossref_primary_10_1111_imm_12795
crossref_primary_10_1016_j_psychres_2017_10_043
crossref_primary_10_1016_j_jneuroim_2017_06_002
crossref_primary_10_1007_s00213_015_4156_y
crossref_primary_10_1176_appi_focus_23021033
crossref_primary_10_1016_S2215_0366_19_30001_X
crossref_primary_10_1038_s41398_021_01701_3
crossref_primary_10_1016_j_pmip_2018_02_001
crossref_primary_10_3389_fpsyt_2024_1425623
crossref_primary_10_1016_j_molmed_2018_09_002
crossref_primary_10_1176_appi_ajp_2015_15070877
crossref_primary_10_1016_j_jad_2017_12_069
crossref_primary_10_1017_cjn_2019_305
crossref_primary_10_1038_nrdp_2018_22
crossref_primary_10_1016_j_praneu_2021_07_001
crossref_primary_10_1016_j_schres_2019_11_023
crossref_primary_10_3389_fpsyt_2017_00013
crossref_primary_10_1176_appi_ajp_2015_15010124
crossref_primary_10_1016_j_neuarg_2017_05_004
crossref_primary_10_1016_j_schres_2020_12_038
crossref_primary_10_1177_1756286420949808
crossref_primary_10_1016_j_bbi_2016_03_011
crossref_primary_10_1192_bjo_2018_8
crossref_primary_10_1007_s00737_021_01175_8
crossref_primary_10_1016_j_euroneuro_2015_09_017
crossref_primary_10_1136_gutjnl_2018_317610
crossref_primary_10_1177_02698811231181573
crossref_primary_10_1002_vrc2_702
crossref_primary_10_1007_s11920_015_0658_x
crossref_primary_10_3389_fneur_2022_1048502
crossref_primary_10_1002_wps_20780
crossref_primary_10_2169_internalmedicine_56_7442
crossref_primary_10_1007_s00737_018_0816_3
crossref_primary_10_1152_physrev_00010_2016
crossref_primary_10_1016_j_autrev_2019_102348
crossref_primary_10_1093_schbul_sby021
crossref_primary_10_1176_appi_ajp_2016_16040454
crossref_primary_10_1016_S2215_0366_20_30432_6
crossref_primary_10_1007_s10654_021_00818_5
crossref_primary_10_1136_jnnp_2016_315251
Cites_doi 10.1038/nrendo.2010.46
10.1016/S1474-4422(13)70072-3
10.1212/WNL.0000000000001425
10.1001/2013.jamapsychiatry.86
10.1016/0361-9230(91)90003-3
10.1176/appi.ajp.2008.08121899
10.1001/jamaneurol.2013.3216
10.1002/ana.24189
10.1016/j.psyneuen.2013.03.019
10.1212/01.wnl.0000327606.50322.f0
10.1212/WNL.0000000000000126
10.1136/jnnp-2014-308736
10.1016/S1474-4422(08)70224-2
10.1016/S1474-4422(13)70282-5
10.1016/j.psym.2011.01.043
10.1017/S003329171300295X
10.1192/bjp.bp.110.082990
10.1038/nrneurol.2012.99
10.1001/jamapsychiatry.2014.469
10.1002/ana.23756
10.1016/S1474-4422(13)70299-0
10.1176/appi.ajp.2014.13121652
10.1016/j.autrev.2007.04.002
10.4088/JCP.10m06648
10.1016/j.biopsych.2013.07.018
10.1016/j.biopsych.2012.11.006
10.1001/jama.296.21.2582
10.1002/ana.21589
10.1016/0165-0327(94)90034-5
10.1038/mp.2013.110
10.1093/brain/aws256
10.1176/appi.ajp.2012.11071047
10.5144/0256-4947.2012.421
10.1177/1352458513507816
10.1016/S1474-4422(12)70310-1
10.1007/s00415-010-5788-9
10.1002/jlb.63.3.281
10.1007/s00737-009-0117-y
10.1016/S1474-4422(10)70253-2
10.1038/nm.3411
ContentType Journal Article
Copyright Copyright © 2015 by the American Psychiatric Association
Copyright American Psychiatric Publishing, Inc. Sep 1, 2015
Copyright_xml – notice: Copyright © 2015 by the American Psychiatric Association
– notice: Copyright American Psychiatric Publishing, Inc. Sep 1, 2015
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
K9.
NAPCQ
7X8
5PM
DOI 10.1176/appi.ajp.2015.14101332
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Premium
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Premium
MEDLINE - Academic
DatabaseTitleList
MEDLINE
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
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
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1535-7228
EndPage 908
ExternalDocumentID PMC4854531
3814451851
26183699
10_1176_appi_ajp_2015_14101332
10.1176/appi.ajp.2015.14101332
Genre Research Support, Non-U.S. Gov't
Journal Article
Case Reports
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NINDS NIH HHS
  grantid: R01 NS077851
– fundername: NINDS NIH HHS
  grantid: R01NS077851
– fundername: NIMH NIH HHS
  grantid: R01MH094741
– fundername: NIMH NIH HHS
  grantid: R01 MH094741
GroupedDBID 1QT
BAJDF
G0H
RAY
RYA
---
--Z
-DZ
-~X
.55
1HT
23M
2WC
4.4
53G
5GY
5RE
6J9
7K8
85S
8R4
8R5
AAIKC
AAJMC
AAMNW
AAWTL
AAWTO
AAYXX
ABIVO
ABPPZ
ABZEH
ACBMB
ACGFO
ACGOD
ACHQT
ACNCT
ADBBV
ADCOW
ADMHG
AENEX
AFAZI
AFOSN
AGHSJ
AGNAY
AHMBA
ALMA_UNASSIGNED_HOLDINGS
ASUFR
BAWUL
CITATION
CS3
DIK
E3Z
EBS
EJD
EX3
F5P
F8P
FJW
H13
HF~
HZ~
L7B
MVM
N9A
NHB
OK1
P2P
PQQKQ
Q.-
Q2X
RXW
S10
SJN
TAE
TEORI
TR2
TWZ
UHB
UKR
ULE
UPT
VVN
WH7
WOQ
WOW
X6Y
X7M
XJT
XSW
XZL
YFH
YOC
YSK
YWH
YZZ
ZCA
ZHY
ZRR
ZY1
CGR
CUY
CVF
ECM
EIF
NPM
K9.
NAPCQ
7X8
5PM
ADXHL
ID FETCH-LOGICAL-a486t-618b4ea2e284e6e125f1f41c8e708e26be7e258a9bd31daf17139dad09d8bb803
ISSN 0002-953X
1535-7228
IngestDate Thu Aug 21 13:37:40 EDT 2025
Fri Jul 11 16:39:15 EDT 2025
Mon Jun 30 02:40:02 EDT 2025
Tue Jul 15 03:06:26 EDT 2025
Tue Jul 01 04:09:06 EDT 2025
Thu Apr 24 22:56:18 EDT 2025
Sun Apr 21 10:10:12 EDT 2019
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 9
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-a486t-618b4ea2e284e6e125f1f41c8e708e26be7e258a9bd31daf17139dad09d8bb803
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
ObjectType-Case Study-2
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/4854531
PMID 26183699
PQID 1714412846
PQPubID 40661
PageCount 8
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4854531
proquest_miscellaneous_1708901888
proquest_journals_1714412846
pubmed_primary_26183699
crossref_primary_10_1176_appi_ajp_2015_14101332
crossref_citationtrail_10_1176_appi_ajp_2015_14101332
appi_journals_10_1176_appi_ajp_2015_14101332
ProviderPackageCode RAY
RYA
1QT
BAJDF
G0H
CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2015-09-01
PublicationDateYYYYMMDD 2015-09-01
PublicationDate_xml – month: 09
  year: 2015
  text: 2015-09-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Washington
PublicationTitle American Journal of Psychiatry
PublicationTitleAlternate Am J Psychiatry
PublicationYear 2015
Publisher American Psychiatric Association
Publisher_xml – name: American Psychiatric Association
References B20
B42
B21
B22
B23
Koksal A (B27)
B24
B25
B26
B28
B29
B30
B31
B10
B32
B11
B12
B34
B13
B35
B14
B36
B15
B37
B16
B38
B17
B39
B18
B19
Kayser MS (B33)
B1
B2
B3
B4
B5
B6
B7
B8
B9
B40
B41
23225603 - Ann Neurol. 2013 Jan;73(1):120-8
25267686 - Neurol Sci. 2015 Jul;36(7):1257-8
17854751 - Autoimmun Rev. 2007 Sep;6(8):572-6
23988024 - Biol Psychiatry. 2014 Feb 15;75(4):284-91
23344076 - JAMA Psychiatry. 2013 Mar;70(3):271-8
20127455 - Arch Womens Ment Health. 2010 Feb;13(1):45-7
17148723 - JAMA. 2006 Dec 6;296(21):2582-9
20972895 - J Neurol. 2011 Apr;258(4):686-8
25458857 - Schizophr Res. 2016 Sep;176(1):36-40
23602157 - Lancet Neurol. 2013 May;12(5):425-6
22705616 - Ann Saudi Med. 2012 Jul-Aug;32(4):421-3
25724228 - Neurology. 2015 Mar 31;84(13):1379-81
23270599 - Biol Psychiatry. 2013 May 15;73(10):1000-7
20421883 - Nat Rev Endocrinol. 2010 Jun;6(6):311-8
21903022 - J Clin Psychiatry. 2011 Nov;72(11):1531-7
25246644 - J Neurol Neurosurg Psychiatry. 2015 Jul;86(7):708-13
23999527 - Mol Psychiatry. 2014 Oct;19(10):1143-9
21163445 - Lancet Neurol. 2011 Jan;10(1):63-74
18852446 - Neurology. 2008 Oct 14;71(16):1291-2
18851928 - Lancet Neurol. 2008 Dec;7(12):1091-8
2049599 - Brain Res Bull. 1991 Mar;26(3):333-8
24330811 - Psychol Med. 2014 Sep;44(12):2475-87
24871043 - JAMA Psychiatry. 2014 Jul 1;71(7):838-9
23290630 - Lancet Neurol. 2013 Feb;12(2):157-65
23877059 - JAMA Neurol. 2013 Sep 1;70(9):1133-9
23608136 - Psychoneuroendocrinology. 2013 Oct;38(10):1929-52
24443452 - Neurology. 2014 Feb 18;82(7):556-63
23065479 - Brain. 2012 Nov;135(Pt 11):3453-68
24853231 - Ann Neurol. 2014 Jul;76(1):82-94
8201128 - J Affect Disord. 1994 Feb;30(2):77-87
22407083 - Am J Psychiatry. 2012 Jun;169(6):609-15
24360484 - Lancet Neurol. 2014 Feb;13(2):167-77
25640930 - Am J Psychiatry. 2015 Feb 1;172(2):115-23
19339365 - Am J Psychiatry. 2009 Apr;166(4):405-8
24462240 - Lancet Neurol. 2014 Mar;13(3):276-86
26324300 - Am J Psychiatry. 2015 Sep 1;172(9):824-6
9500514 - J Leukoc Biol. 1998 Mar;63(3):281-7
24107309 - Mult Scler. 2014 May;20(6):739-46
22710628 - Nat Rev Neurol. 2012 Jul;8(7):380-90
24317118 - Nat Med. 2014 Jan;20(1):69-74
21343331 - Br J Psychiatry. 2011 Apr;198(4):264-8
22054628 - Psychosomatics. 2011 Nov-Dec;52(6):568-70
19338055 - Ann Neurol. 2009 Apr;65(4):424-34
References_xml – ident: B38
  doi: 10.1038/nrendo.2010.46
– ident: B40
  doi: 10.1016/S1474-4422(13)70072-3
– ident: B42
  doi: 10.1212/WNL.0000000000001425
– ident: B27
  publication-title: Neurol Sci
– ident: B31
  doi: 10.1001/2013.jamapsychiatry.86
– ident: B20
  doi: 10.1016/0361-9230(91)90003-3
– ident: B2
  doi: 10.1176/appi.ajp.2008.08121899
– ident: B29
  doi: 10.1001/jamaneurol.2013.3216
– ident: B36
  doi: 10.1002/ana.24189
– ident: B8
  doi: 10.1016/j.psyneuen.2013.03.019
– ident: B19
  doi: 10.1212/01.wnl.0000327606.50322.f0
– ident: B41
  doi: 10.1212/WNL.0000000000000126
– ident: B34
  doi: 10.1136/jnnp-2014-308736
– ident: B13
  doi: 10.1016/S1474-4422(08)70224-2
– ident: B14
  doi: 10.1016/S1474-4422(13)70282-5
– ident: B25
  doi: 10.1016/j.psym.2011.01.043
– ident: B30
  doi: 10.1017/S003329171300295X
– ident: B9
  doi: 10.1192/bjp.bp.110.082990
– ident: B10
  doi: 10.1038/nrneurol.2012.99
– ident: B35
  doi: 10.1001/jamapsychiatry.2014.469
– ident: B17
  doi: 10.1002/ana.23756
– ident: B16
  doi: 10.1016/S1474-4422(13)70299-0
– ident: B21
  doi: 10.1176/appi.ajp.2014.13121652
– ident: B7
  doi: 10.1016/j.autrev.2007.04.002
– ident: B4
  doi: 10.4088/JCP.10m06648
– ident: B12
  doi: 10.1016/j.biopsych.2013.07.018
– ident: B6
  doi: 10.1016/j.biopsych.2012.11.006
– ident: B1
  doi: 10.1001/jama.296.21.2582
– ident: B15
  doi: 10.1002/ana.21589
– ident: B33
  publication-title: Schizophr Res
– ident: B5
  doi: 10.1016/0165-0327(94)90034-5
– ident: B32
  doi: 10.1038/mp.2013.110
– ident: B18
  doi: 10.1093/brain/aws256
– ident: B22
  doi: 10.1176/appi.ajp.2012.11071047
– ident: B26
  doi: 10.5144/0256-4947.2012.421
– ident: B39
  doi: 10.1177/1352458513507816
– ident: B24
  doi: 10.1016/S1474-4422(12)70310-1
– ident: B28
  doi: 10.1007/s00415-010-5788-9
– ident: B37
  doi: 10.1002/jlb.63.3.281
– ident: B3
  doi: 10.1007/s00737-009-0117-y
– ident: B11
  doi: 10.1016/S1474-4422(10)70253-2
– ident: B23
  doi: 10.1038/nm.3411
– reference: 24360484 - Lancet Neurol. 2014 Feb;13(2):167-77
– reference: 23602157 - Lancet Neurol. 2013 May;12(5):425-6
– reference: 17854751 - Autoimmun Rev. 2007 Sep;6(8):572-6
– reference: 23988024 - Biol Psychiatry. 2014 Feb 15;75(4):284-91
– reference: 24317118 - Nat Med. 2014 Jan;20(1):69-74
– reference: 24330811 - Psychol Med. 2014 Sep;44(12):2475-87
– reference: 19338055 - Ann Neurol. 2009 Apr;65(4):424-34
– reference: 22407083 - Am J Psychiatry. 2012 Jun;169(6):609-15
– reference: 21163445 - Lancet Neurol. 2011 Jan;10(1):63-74
– reference: 23225603 - Ann Neurol. 2013 Jan;73(1):120-8
– reference: 20127455 - Arch Womens Ment Health. 2010 Feb;13(1):45-7
– reference: 23344076 - JAMA Psychiatry. 2013 Mar;70(3):271-8
– reference: 17148723 - JAMA. 2006 Dec 6;296(21):2582-9
– reference: 21343331 - Br J Psychiatry. 2011 Apr;198(4):264-8
– reference: 22710628 - Nat Rev Neurol. 2012 Jul;8(7):380-90
– reference: 23999527 - Mol Psychiatry. 2014 Oct;19(10):1143-9
– reference: 24871043 - JAMA Psychiatry. 2014 Jul 1;71(7):838-9
– reference: 25458857 - Schizophr Res. 2016 Sep;176(1):36-40
– reference: 22054628 - Psychosomatics. 2011 Nov-Dec;52(6):568-70
– reference: 25640930 - Am J Psychiatry. 2015 Feb 1;172(2):115-23
– reference: 8201128 - J Affect Disord. 1994 Feb;30(2):77-87
– reference: 20972895 - J Neurol. 2011 Apr;258(4):686-8
– reference: 18852446 - Neurology. 2008 Oct 14;71(16):1291-2
– reference: 23608136 - Psychoneuroendocrinology. 2013 Oct;38(10):1929-52
– reference: 24853231 - Ann Neurol. 2014 Jul;76(1):82-94
– reference: 25724228 - Neurology. 2015 Mar 31;84(13):1379-81
– reference: 25267686 - Neurol Sci. 2015 Jul;36(7):1257-8
– reference: 9500514 - J Leukoc Biol. 1998 Mar;63(3):281-7
– reference: 26324300 - Am J Psychiatry. 2015 Sep 1;172(9):824-6
– reference: 23270599 - Biol Psychiatry. 2013 May 15;73(10):1000-7
– reference: 24107309 - Mult Scler. 2014 May;20(6):739-46
– reference: 24462240 - Lancet Neurol. 2014 Mar;13(3):276-86
– reference: 22705616 - Ann Saudi Med. 2012 Jul-Aug;32(4):421-3
– reference: 25246644 - J Neurol Neurosurg Psychiatry. 2015 Jul;86(7):708-13
– reference: 24443452 - Neurology. 2014 Feb 18;82(7):556-63
– reference: 23290630 - Lancet Neurol. 2013 Feb;12(2):157-65
– reference: 21903022 - J Clin Psychiatry. 2011 Nov;72(11):1531-7
– reference: 18851928 - Lancet Neurol. 2008 Dec;7(12):1091-8
– reference: 23065479 - Brain. 2012 Nov;135(Pt 11):3453-68
– reference: 20421883 - Nat Rev Endocrinol. 2010 Jun;6(6):311-8
– reference: 19339365 - Am J Psychiatry. 2009 Apr;166(4):405-8
– reference: 2049599 - Brain Res Bull. 1991 Mar;26(3):333-8
– reference: 23877059 - JAMA Neurol. 2013 Sep 1;70(9):1133-9
SSID ssj0000372
Score 2.4577644
Snippet Objective:Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies...
Significant immunological alterations have been observed in women with first-onset affective psychosis during the postpartum period. Recent studies have...
SourceID pubmedcentral
proquest
pubmed
crossref
appi
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 901
SubjectTerms Adult
Animals
Autoantibodies - immunology
Brain
Case-Control Studies
Encephalitis
Encephalitis - diagnosis
Encephalitis - etiology
Female
Hashimoto Disease - diagnosis
Hashimoto Disease - etiology
Hippocampus - immunology
Humans
Immunohistochemistry
Postpartum depression
Postpartum Period
Psychosis
Psychotic Disorders - diagnosis
Psychotic Disorders - etiology
Psychotic Disorders - immunology
Puerperal Disorders - diagnosis
Puerperal Disorders - immunology
Rats - immunology
Receptors, N-Methyl-D-Aspartate - immunology
Women
Young Adult
Title Autoimmune Encephalitis in Postpartum Psychosis
URI http://dx.doi.org/10.1176/appi.ajp.2015.14101332
https://www.ncbi.nlm.nih.gov/pubmed/26183699
https://www.proquest.com/docview/1714412846
https://www.proquest.com/docview/1708901888
https://pubmed.ncbi.nlm.nih.gov/PMC4854531
Volume 172
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnR3LjtMw0CqLhLgg3mRZUJC4QbaNk_hxXMGiBVTEoSvtLXIahwZVadUmEtrP4IuZcRLHZSuV5RI1duykM-N52PMg5K2KOUMxG8gsV0HM5kkgJ1IFiZKiiCOaU4UnutNv7OIy_nKVXI1Gvx2vpabOTufXe-NK_ger0AZ4xSjZW2DWTgoN8BvwC1fAMFz_CcdnTb0qMcBDvzvH6MMFKtWl8XDFIrxrGIJ-7obHbcutq4jakxpHI_2-4_ncRu9sfoCxapxhtd4sXfrAjc42Ze9CmeP2j1Y9n5V1s1QtMUwVeo1Ww_ETRgf9ajejMbDG3XYIE-tXVTue_j2fbmuK3KCogefKxFT9BYnTs1ksotuFhfd8mFOH4KTDVWX3Yt3dif28n5ukx2uMAfyJqUjD5BS9WMEKp4O0sz6Ih4bcIXcpmB7GTP_8dZDuEae9SYX_qos6h5nG--cBWY8du3rPDWPmb59cR8mZPSQPOlrwz1pSe0RGunpM7k07_4snZDxQnO9SnF9W_kBxvqW4p-Ty0_nsw0XQldwIVCxYHbBQZLFWVIPWopkG7bcIizicC80nQlOWaa5pIhSs7CjMVRFysCBylU9kLrJMTKJn5KhaVfoF8Tkqo6Af8UwVICgKlWOphlzCDeiIeeGR9wiXtFtP29SYo5ylphXAmCIY0x6MHkl6-KXzLn09VlFZHhw3tuPWbQKXgyNOevQ4H8dx5wGgwjzyxnYDK8bzNVXpVYPPTASQqhDCI89bbNpXUoBsxKT0CN_Bs30A07zv9lTlwqR7jwVYOVF4fDt4vST3h2V7Qo7qTaNfgf5cZ68NQf8B18jCIg
linkProvider Flying Publisher
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=Autoimmune+Encephalitis+in+Postpartum+Psychosis&rft.jtitle=American+Journal+of+Psychiatry&rft.au=Bergink%2C+Veerle&rft.au=Armangue%2C+Tha%C3%ADs&rft.au=Titulaer%2C+Maarten+J&rft.au=Markx%2C+Sander&rft.date=2015-09-01&rft.pub=American+Psychiatric+Association&rft.issn=0002-953X&rft.eissn=1535-7228&rft.volume=172&rft.issue=9&rft.spage=901&rft.epage=908&rft_id=info:doi/10.1176%2Fappi.ajp.2015.14101332&rft.externalDocID=10.1176%2Fappi.ajp.2015.14101332
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0002-953X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0002-953X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0002-953X&client=summon