Lower serum zinc in major depression is a sensitive marker of treatment resistance and of the immune/inflammatory response in that illness
- PMID: 9276075
- DOI: 10.1016/S0006-3223(96)00365-4
Lower serum zinc in major depression is a sensitive marker of treatment resistance and of the immune/inflammatory response in that illness
Abstract
The aims of the present study were to examine i) serum zinc (Zn) and copper (Cu) in treatment resistant depression (TRD); ii) the effects of subchronic antidepressant therapy on these trace elements; and iii) the relationships between serum Zn and Cu and immune/inflammatory markers. Serum Zn was significantly lower in TRD than in normal controls. There was a significant inverse correlation between baseline serum Zn and staging of depression based on severity of prior treatment resistance. There were no significant effects of antidepressive treatment on serum Zn, whereas serum Cu was significantly reduced. There were highly significant correlations between serum Zn and the CD4+/CD8+ T-cell ratio (negative), and total serum protein, serum albumin, and transferrin (all positive). The results suggest that lower serum Zn is a marker of TRD and of the immune/inflammatory response in depression. It is suggested that treatment resistance may bear a relationship with the immune/inflammatory alterations in major depression.
Similar articles
-
Is serum copper a "trait marker" of unipolar depression? A preliminary clinical study.Pol J Pharmacol. 1999 Nov-Dec;51(6):535-8. Pol J Pharmacol. 1999. PMID: 10817533 Clinical Trial.
-
Lower plasma Coenzyme Q10 in depression: a marker for treatment resistance and chronic fatigue in depression and a risk factor to cardiovascular disorder in that illness.Neuro Endocrinol Lett. 2009;30(4):462-9. Neuro Endocrinol Lett. 2009. PMID: 20010493
-
Levels of selenium, zinc, copper, and antioxidant enzyme activity in patients with leukemia.Biol Trace Elem Res. 2006 Winter;114(1-3):41-53. doi: 10.1385/BTER:114:1:41. Biol Trace Elem Res. 2006. PMID: 17205986
-
Mechanisms contributing to antidepressant zinc actions.Pol J Pharmacol. 2002 Nov-Dec;54(6):587-92. Pol J Pharmacol. 2002. PMID: 12866713 Review.
-
Drug disease interactions: role of inflammatory mediators in depression and variability in antidepressant drug response.J Pharm Pharm Sci. 2006;9(3):292-306. J Pharm Pharm Sci. 2006. PMID: 17207413 Review.
Cited by
-
The interleukin-6/interleukin-23/T helper 17-axis as a driver of neuro-immune toxicity in the major neurocognitive psychosis or deficit schizophrenia: A precision nomothetic psychiatry analysis.PLoS One. 2022 Oct 18;17(10):e0275839. doi: 10.1371/journal.pone.0275839. eCollection 2022. PLoS One. 2022. PMID: 36256663 Free PMC article.
-
Sex differences in depression: An immunological perspective.Brain Res Bull. 2023 May;196:34-45. doi: 10.1016/j.brainresbull.2023.02.016. Epub 2023 Feb 28. Brain Res Bull. 2023. PMID: 36863664 Free PMC article. Review.
-
Role of immune-inflammatory and oxidative and nitrosative stress pathways in the etiology of depression: therapeutic implications.CNS Drugs. 2014 Jan;28(1):1-10. doi: 10.1007/s40263-013-0119-1. CNS Drugs. 2014. PMID: 24150993 Review.
-
Increased Root Canal Endotoxin Levels are Associated with Chronic Apical Periodontitis, Increased Oxidative and Nitrosative Stress, Major Depression, Severity of Depression, and a Lowered Quality of Life.Mol Neurobiol. 2018 Apr;55(4):2814-2827. doi: 10.1007/s12035-017-0545-z. Epub 2017 Apr 28. Mol Neurobiol. 2018. PMID: 28455694
-
Serum and urinary essential trace elements in association with major depressive disorders: a case-control study.Front Psychiatry. 2023 Dec 1;14:1297411. doi: 10.3389/fpsyt.2023.1297411. eCollection 2023. Front Psychiatry. 2023. PMID: 38106999 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials