Expression of PON1, PON2, PON3 and MPO Genes in Patients with Depressive Disorders.
Katarzyna M Bliźniewska-KowalskaPiotr GałeckiKuan-Pin SuAngelos HalarisJanusz Zbigniew SzemrajMałgorzata GałeckaPublished in: Journal of clinical medicine (2022)
Background: Taking into account the role of oxidative stress in neurodegeneration, we sought to evaluate the expression of genes for select enzymes with antioxidant properties (paraoxonases PON1, PON2 and PON3 and myeloperoxidase MPO) at the mRNA and protein levels in patients with depressive disorders. We further sought to determine the impact of oxidative stress in the etiopathogenesis of this group of mood disorders. Methods: A total of 290 subjects (190 depressed patients, 100 healthy controls) took part in the study. Sociodemographic and clinical data were collected. The severity of depressive symptoms was assessed using the Hamilton Depression Rating Scale (HDRS). Venous blood was collected. RT-PCR was used to assess gene expression at the mRNA level, while enzyme-linked immunosorbent assay (ELISA) was used to assess gene expression at the protein level. Results: The expression of the PON2 and PON3 genes at the protein level was significantly higher in depressive patients than in healthy controls. mRNA expression of the PON1, PON2 and PON3 genes was slightly higher in patients with depressive disorders than in the control group, however, this relationship was not statistically significant. On the other hand, the expression of the MPO gene at both mRNA and protein levels was significantly lower in patients with depressive disorder than in the control group. Conclusions: Our results are not in agreement with many studies on enzymes involved in maintaining oxidative balance. Our findings may not support the utility of paraoxonases (PON) or myeloperoxidase (MPO) as promising biomarker candidates of depression pending larger and well controlled studies.
Keyphrases
- binding protein
- gene expression
- oxidative stress
- depressive symptoms
- poor prognosis
- bipolar disorder
- end stage renal disease
- genome wide
- ejection fraction
- newly diagnosed
- chronic kidney disease
- genome wide identification
- sleep quality
- protein protein
- stress induced
- amino acid
- dna damage
- peritoneal dialysis
- patient reported outcomes
- ischemia reperfusion injury
- long non coding rna
- machine learning
- physical activity
- transcription factor
- big data
- signaling pathway
- heat shock protein