PMID- 34967503 OWN - NLM STAT- MEDLINE DCOM- 20220314 LR - 20220531 IS - 2162-3279 (Electronic) VI - 12 IP - 1 DP - 2022 Jan TI - Serum concentration of zinc is elevated in clinically stable bipolar disorder patients. PG - e2472 LID - 10.1002/brb3.2472 [doi] LID - e2472 AB - BACKGROUND: Bipolar disorder (BD) is a chronic psychiatric disorder characterized by recurrent mood episodes interspersed with euthymic periods. A growing number of studies have indicated that zinc plays an important role in coordinating immune responses, as well as being involved in synaptic transmission. In the current study, we set out to measure serum levels of zinc in a meticulously phenotyped cohort of 121 euthymic BD subjects and 30 matched controls. METHODS: Serum levels of zinc were measured by photometry. To assess the interplay between zinc levels and immune activation in BD, we measured serum levels of high-sensitive C-reactive protein (hsCRP) levels by immunoturbidimetric assay, and serum levels of monocyte chemoattractant protein-1 (MCP-1), chitinase 3-like protein 1 (YKL-40), and soluble cluster of differentiation 14 (sCD14) by electrochemiluminescence enzyme-linked immunosorbent assays. The baseline clinical diagnostic instrument for BD was the Affective Disorder Evaluation, and executive functioning was assessed by using the Delis-Kaplan Executive Function System. RESULTS: Controlling for potential confounding factors, BD patients displayed increased serum levels of zinc unrelated to hsCRP, MCP-1, YKL-40, and sCD14 levels. Serum levels of zinc did not associate with executive functioning or measurements of disease severity. DISCUSSION: This study suggests that the zinc homeostasis is disturbed in BD and that this dyshomeostasis is not related to ongoing mood symptoms or immune activation. Of note, serum levels were increased and hence do not support continuous zinc supplementation in BD. CI - (c) 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC. FAU - Jonsson, Bo H AU - Jonsson BH AUID- ORCID: 0000-0002-6942-1482 AD - Department of Clinical Neuroscience, Centre for Psychiatry Research, Stockholm & Stockholm Health Care Services, Stockholm County Council, Karolinska Institutet, Stockholm, Sweden. FAU - Orhan, Funda AU - Orhan F AD - Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden. FAU - Bruno, Sanna AU - Bruno S AD - Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden. FAU - Oliveira, Ana Osorio AU - Oliveira AO AD - Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden. FAU - Sparding, Timea AU - Sparding T AD - Section of Psychiatry and Neurochemistry, The Sahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden. FAU - Landen, Mikael AU - Landen M AD - Section of Psychiatry and Neurochemistry, The Sahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden. AD - Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden. FAU - Sellgren, Carl M AU - Sellgren CM AD - Department of Clinical Neuroscience, Centre for Psychiatry Research, Stockholm & Stockholm Health Care Services, Stockholm County Council, Karolinska Institutet, Stockholm, Sweden. AD - Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20211230 PL - United States TA - Brain Behav JT - Brain and behavior JID - 101570837 RN - 9007-41-4 (C-Reactive Protein) RN - J41CSQ7QDS (Zinc) SB - IM MH - Affect MH - *Bipolar Disorder/metabolism MH - C-Reactive Protein MH - Executive Function MH - Humans MH - *Zinc/blood/metabolism PMC - PMC8785612 OTO - NOTNLM OT - C-reactive protein OT - bipolar patients OT - cognition OT - serum OT - zinc COIS- Carl M. Sellgren is a scientific adviser for Outermost Therapeutics (of no relevance to this work). The authors have no financial conflicts of interest. EDAT- 2021/12/31 06:00 MHDA- 2022/03/15 06:00 PMCR- 2021/12/30 CRDT- 2021/12/30 08:47 PHST- 2021/11/06 00:00 [revised] PHST- 2021/07/04 00:00 [received] PHST- 2021/12/01 00:00 [accepted] PHST- 2021/12/31 06:00 [pubmed] PHST- 2022/03/15 06:00 [medline] PHST- 2021/12/30 08:47 [entrez] PHST- 2021/12/30 00:00 [pmc-release] AID - BRB32472 [pii] AID - 10.1002/brb3.2472 [doi] PST - ppublish SO - Brain Behav. 2022 Jan;12(1):e2472. doi: 10.1002/brb3.2472. Epub 2021 Dec 30.