Correlation between white blood cell count and mood-stabilising treatment response in two bipolar disorder trials.


Journal

Acta neuropsychiatrica
ISSN: 1601-5215
Titre abrégé: Acta Neuropsychiatr
Pays: England
ID NLM: 9612501

Informations de publication

Date de publication:
Aug 2019
Historique:
pubmed: 7 6 2019
medline: 10 1 2020
entrez: 7 6 2019
Statut: ppublish

Résumé

Immune system markers may predict affective disorder treatment response, but whether an overall immune system marker predicts bipolar disorder treatment effect is unclear. Bipolar CHOICE (N = 482) and LiTMUS (N = 283) were similar comparative effectiveness trials treating patients with bipolar disorder for 24 weeks with four different treatment arms (standard-dose lithium, quetiapine, moderate-dose lithium plus optimised personalised treatment (OPT) and OPT without lithium). We performed secondary mixed effects linear regression analyses adjusted for age, gender, smoking and body mass index to investigate relationships between pre-treatment white blood cell (WBC) levels and clinical global impression scale (CGI) response. Compared to participants with WBC counts of 4.5-10 × 109/l, participants with WBC < 4.5 or WBC ≥ 10 showed similar improvement within each specific treatment arm and in gender-stratified analyses. An overall immune system marker did not predict differential treatment response to four different treatment approaches for bipolar disorder all lasting 24 weeks.

Sections du résumé

BACKGROUND BACKGROUND
Immune system markers may predict affective disorder treatment response, but whether an overall immune system marker predicts bipolar disorder treatment effect is unclear.
METHODS METHODS
Bipolar CHOICE (N = 482) and LiTMUS (N = 283) were similar comparative effectiveness trials treating patients with bipolar disorder for 24 weeks with four different treatment arms (standard-dose lithium, quetiapine, moderate-dose lithium plus optimised personalised treatment (OPT) and OPT without lithium). We performed secondary mixed effects linear regression analyses adjusted for age, gender, smoking and body mass index to investigate relationships between pre-treatment white blood cell (WBC) levels and clinical global impression scale (CGI) response.
RESULTS RESULTS
Compared to participants with WBC counts of 4.5-10 × 109/l, participants with WBC < 4.5 or WBC ≥ 10 showed similar improvement within each specific treatment arm and in gender-stratified analyses.
CONCLUSIONS CONCLUSIONS
An overall immune system marker did not predict differential treatment response to four different treatment approaches for bipolar disorder all lasting 24 weeks.

Identifiants

pubmed: 31169098
pii: S092427081900019X
doi: 10.1017/neu.2019.19
doi:

Substances chimiques

Antimanic Agents 0
Quetiapine Fumarate 2S3PL1B6UJ
Lithium 9FN79X2M3F

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

230-234

Auteurs

Ole Köhler-Forsberg (O)

Department of Clinical Medicine,Aarhus University.

Louisa G Sylvia (LG)

Department of Psychiatry,Massachusetts General Hospital,Boston, MA,USA.

Charles L Bowden (CL)

Department of Psychiatry, University of Texas Health Science Center,San Antonio, TX,USA.

Joseph R Calabrese (JR)

Department of Psychiatry, Case Western Reserve University,Cleveland, OH,USA.

Michael E Thase (ME)

Department of Psychiatry, University of Pennsylvania,Philadelphia, PA,USA.

Richard C Shelton (RC)

Department of Psychiatry, University of Alabama at Birmingham,Birmingham, AL,USA.

Melvin McInnis (M)

Department of Psychiatry, University of Michigan,Ann Arbor, MI,USA.

Mauricio Tohen (M)

Department of Psychiatry, University of New Mexico Health Science Center,Albuquerque, NM,USA.

James H Kocsis (JH)

Department of Psychiatry, Weill Cornell Medical College,New York, NY,USA.

Terence A Ketter (TA)

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine,Stanford, CA,USA.

Edward S Friedman (ES)

Department of Psychiatry, University of Pittsburgh Medical Center,Pittsburgh, PA,USA.

Thilo Deckersbach (T)

Department of Psychiatry,Massachusetts General Hospital,Boston, MA,USA.

Michael J Ostacher (MJ)

Department of Psychiatry,Massachusetts General Hospital,Boston, MA,USA.

Dan V Iosifescu (DV)

Department of Psychiatry,Massachusetts General Hospital,Boston, MA,USA.

Susan McElroy (S)

Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine,Cincinnati, OH and Lindner Center of HOPE, Mason, OH,USA.

Andrew A Nierenberg (AA)

Department of Psychiatry,Massachusetts General Hospital,Boston, MA,USA.

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Classifications MeSH