TY - JOUR
T1 - Pathophysiology of Major Depression by Clinical Stages
AU - de Menezes Galvão, Ana Cecília
AU - Almeida, Raíssa Nobrega
AU - de Sousa, Geovan Menezes
AU - Leocadio-Miguel, Mario André
AU - Palhano-Fontes, Fernanda
AU - de Araujo, Dráulio Barros
AU - Lobão-Soares, Bruno
AU - Maia-de-Oliveira, João Paulo
AU - Nunes, Emerson Arcoverde
AU - Hallak, Jaime Eduardo Cecilio
AU - Schuch, Felipe Barreto
AU - Sarris, Jerome
AU - Galvão-Coelho, Nicole Leite
N1 - Funding information: This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brazil (CAPES) – Finance Code 001. This study was funded by the Brazilian National Council for Scientific and Technological Development (CNPq, Grant Nos. 466760/2014 and 479466/2013) and CAPES Foundation within the Brazilian Ministry of Education (Grant Nos. 1677/2012 and 1577/2013). NG-C and AM were supported by the CAPES Foundation from Brazilian Ministry of Education (Research Fellowship 88887.466701/2019-00 and 88882.344060/2019-01, respectively). JS was funded by an NHMRC Clinical Research Fellowship (APP1125000).
PY - 2021/8/5
Y1 - 2021/8/5
N2 - The comprehension of the pathophysiology of the major depressive disorder (MDD) is essential to the strengthening of precision psychiatry. In order to determine the relationship between the pathophysiology of the MDD and its clinical progression, analyzed by severity of the depressive symptoms and sleep quality, we conducted a study assessing different peripheral molecular biomarkers, including the levels of plasma C-reactive protein (CRP), serum mature brain-derived neurotrophic factor (mBDNF), serum cortisol (SC), and salivary cortisol awakening response (CAR), of patients with MDD (n = 58) and a control group of healthy volunteers (n = 62). Patients with the first episode of MDD (n = 30) had significantly higher levels of CAR and SC than controls (n = 32) and similar levels of mBDNF of controls. Patients with treatment-resistant depression (TRD, n = 28) presented significantly lower levels of SC and CAR, and higher levels of mBDNF and CRP than controls (n = 30). An increased severity of depressive symptoms and worse sleep quality were correlated with levels low of SC and CAR, and with high levels of mBDNF. These results point out a strong relationship between the stages clinical of MDD and changes in a range of relevant biological markers. This can assist in the development of precision psychiatry and future research on the biological tests for depression.
AB - The comprehension of the pathophysiology of the major depressive disorder (MDD) is essential to the strengthening of precision psychiatry. In order to determine the relationship between the pathophysiology of the MDD and its clinical progression, analyzed by severity of the depressive symptoms and sleep quality, we conducted a study assessing different peripheral molecular biomarkers, including the levels of plasma C-reactive protein (CRP), serum mature brain-derived neurotrophic factor (mBDNF), serum cortisol (SC), and salivary cortisol awakening response (CAR), of patients with MDD (n = 58) and a control group of healthy volunteers (n = 62). Patients with the first episode of MDD (n = 30) had significantly higher levels of CAR and SC than controls (n = 32) and similar levels of mBDNF of controls. Patients with treatment-resistant depression (TRD, n = 28) presented significantly lower levels of SC and CAR, and higher levels of mBDNF and CRP than controls (n = 30). An increased severity of depressive symptoms and worse sleep quality were correlated with levels low of SC and CAR, and with high levels of mBDNF. These results point out a strong relationship between the stages clinical of MDD and changes in a range of relevant biological markers. This can assist in the development of precision psychiatry and future research on the biological tests for depression.
KW - brain-derived neurotrophic factor
KW - C-reactive protein
KW - cortisol
KW - precision psychiatry
KW - sleep quality
UR - http://www.scopus.com/inward/record.url?scp=85113145310&partnerID=8YFLogxK
U2 - 10.3389/fpsyg.2021.641779
DO - 10.3389/fpsyg.2021.641779
M3 - Article
AN - SCOPUS:85113145310
SN - 1664-1078
VL - 12
JO - Frontiers in Psychology
JF - Frontiers in Psychology
M1 - 641779
ER -