Association between cytokine levels, verbal memory and hippocampus volume in psychotic disorders and healthy controls

Objective We investigated whether elevated plasma levels of immune markers were associated with verbal memory and hippocampal subfield volumes in patients with severe mental illnesses and in healthy controls. Method In total, 230 patients with a broad DSM‐IV schizophrenia spectrum illness or bipolar...

Full description

Saved in:
Bibliographic Details
Published inActa psychiatrica Scandinavica Vol. 133; no. 1; pp. 53 - 62
Main Authors Hoseth, E. Z., Westlye, L. T., Hope, S., Dieset, I., Aukrust, P., Melle, I., Haukvik, U. K., Agartz, I., Ueland, T., Andreassen, O. A.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.01.2016
Munksgaard Forlag
Subjects
Online AccessGet full text
ISSN0001-690X
1600-0447
1600-0447
DOI10.1111/acps.12467

Cover

More Information
Summary:Objective We investigated whether elevated plasma levels of immune markers were associated with verbal memory and hippocampal subfield volumes in patients with severe mental illnesses and in healthy controls. Method In total, 230 patients with a broad DSM‐IV schizophrenia spectrum illness or bipolar disorder and 236 healthy controls were recruited. Memory was assessed using the Wechsler Memory Scale‐Third Edition (WMS‐III) Logical Memory immediate and delayed recall, and the California Verbal Learning Test summed recall over learning list (CVLT learning) and delayed free recall. We measured plasma levels of soluble tumor necrosis factor receptor 1 (sTNF‐R1), interleukin‐1 receptor antagonist, interleukin‐6, von Willebrand factor, osteoprotegerin, high‐sensitivity C‐reactive protein and sCD40 ligand. Hippocampal subfield estimates were obtained using FreeSurfer. Results We found a moderate negative association between sTNF‐R1 and performance on verbal memory learning and recall tests as measured by the WMS‐III Logical Memory after controlling for age, sex and diagnosis. We observed no interaction effect of diagnosis and sTNF‐R1 on memory scores. We also found a nominally significant positive association between CVLT learning and hippocampal volumes. Conclusion The findings suggest a role for immune involvement in memory independent of severe mental disorders and may support the ‘bigger is better’ hypothesis of hippocampal subfield volumes.
Bibliography:ark:/67375/WNG-8Z96SWMR-2
istex:C2C83208FB4D640BCA5A8553A6548E89221AB45B
Table S1. Demographic and clinical characteristics of participants in the MRI subgroup (N = 224). Table S2. Immune and verbal memory characteristics for the Main group (N = 462). Table S3. Immune, verbal memory and hippocampal volume characteristics for the MRI subgroup (N = 224). Table S4. Linear regression models investigating the associations between verbal memory and cytokines in whole sample (N = 462) after controlling for age, sex and diagnosis. Table S5. Linear regression analyses of associations between verbal memory and hippocampal volumes in subsample (N = 224) after controlling for age, sex, estimated total intracranial volume and diagnosis (patient or control). Table S6. Linear regression analyses investigating associations between hippocampal subvolumes and cytokines in MRI subgroup (N = 224) after controlling for age, sex, estimated total intracranial volume and diagnosis (patient or control). Table S7. Spearman's rank correlation between cytokines and time of blood sampling for the control group (N = 174)
ArticleID:ACPS12467
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
NFR/204966
ISSN:0001-690X
1600-0447
1600-0447
DOI:10.1111/acps.12467