TY - JOUR
T1 - MicroRNAs and pro-inflammatory cytokines as candidate biomarkers for recent-onset psychosis
AU - Shafiee-Kandjani, Ali Reza
AU - Nezhadettehad, Negin
AU - Farhang, Sara
AU - Bruggeman, Richard
AU - Shanebandi, Dariush
AU - Hassanzadeh, Mohammadbagher
AU - Azizi, Hosein
N1 - Funding Information:
This work was elicited from the psychiatry residency dissertation of Dr. Negin Nejadettehad with the Reg. No. 59139 from the department of psychiatry, Tabriz University of Medical Sciences, Tabriz, Iran. We sincerely thank all the people and their family for their support and participation and all the medical staff involved in collecting blood samples.
Funding Information:
The present study was financially supported, reviewed and supervised by Tabriz University of Medical Sciences to number 65618/D/5.
Publisher Copyright:
© 2023, BioMed Central Ltd., part of Springer Nature.
PY - 2023
Y1 - 2023
N2 - Background: Recent studies on the schizophrenia spectrum and other psychotic disorders showed that alternation of immune system components, particularly microRNAs (miRNAs) and pro-inflammatory compounds, plays a significant role in developing the illness. The study aimed to evaluate serum expression of the miRNA-26a, miRNA-106a, and miRNA-125b as genetic factors and serum levels of IL-6, IL-1β, and TNF-α as pro-inflammatory factors in an IranianAzeri population. Methods: Forty patients with recent-onset non-affective psychosis and 40 healthy people as a control group were involved. Expression levels of miRNAs and serum levels of the cytokines were measured using RT-qPCR and ELISA, respectively. T-test, receiver operating characteristics (ROC), and spearman correlation coefficient were carried out data analysis. Results: Findings showed higher levels of IL-6, IL-1β, TNF-α, miR-26a, and miR-106a in the plasma of the patients’ group compared with the control. miRNA-26a showed a statistically significant higher level (p <.003) compared to the control group, with AUC = 0.84 (95% CI: 0.77 to 0.93, P <.001) and cut-off point = 0.17 in comparison to other miRNAs as mentioned above; in this regard, it might be a suggestive biomarker for schizophrenia in the early stage of the illness. Moreover, miRNAs’ expression level was not substantially associated with the level of any measured cytokines above. Conclusions: miR-26a might be a suggestive biomarker for schizophrenia in the early stage of the illness. Given that the relationship between other miRNAs and cytokines is not yet well understood; accordingly, there are encouragement and support for continued research in this fascinating field.
AB - Background: Recent studies on the schizophrenia spectrum and other psychotic disorders showed that alternation of immune system components, particularly microRNAs (miRNAs) and pro-inflammatory compounds, plays a significant role in developing the illness. The study aimed to evaluate serum expression of the miRNA-26a, miRNA-106a, and miRNA-125b as genetic factors and serum levels of IL-6, IL-1β, and TNF-α as pro-inflammatory factors in an IranianAzeri population. Methods: Forty patients with recent-onset non-affective psychosis and 40 healthy people as a control group were involved. Expression levels of miRNAs and serum levels of the cytokines were measured using RT-qPCR and ELISA, respectively. T-test, receiver operating characteristics (ROC), and spearman correlation coefficient were carried out data analysis. Results: Findings showed higher levels of IL-6, IL-1β, TNF-α, miR-26a, and miR-106a in the plasma of the patients’ group compared with the control. miRNA-26a showed a statistically significant higher level (p <.003) compared to the control group, with AUC = 0.84 (95% CI: 0.77 to 0.93, P <.001) and cut-off point = 0.17 in comparison to other miRNAs as mentioned above; in this regard, it might be a suggestive biomarker for schizophrenia in the early stage of the illness. Moreover, miRNAs’ expression level was not substantially associated with the level of any measured cytokines above. Conclusions: miR-26a might be a suggestive biomarker for schizophrenia in the early stage of the illness. Given that the relationship between other miRNAs and cytokines is not yet well understood; accordingly, there are encouragement and support for continued research in this fascinating field.
KW - Interleukin-1beta: Interleukin-6
KW - miRNAs
KW - Psychoneuroimmunology
KW - Schizophrenia
KW - Tumor necrosis factor-alpha
U2 - 10.1186/s12888-023-05136-6
DO - 10.1186/s12888-023-05136-6
M3 - Article
C2 - 37644489
AN - SCOPUS:85168937162
SN - 1471-244X
VL - 23
JO - BMC Psychiatry
JF - BMC Psychiatry
M1 - 631
ER -