2024/10/17 by Karen M. Ryan, Myles Corrigan, Therese M. Murphy +2 · 1 voice · 1 citation
Chemistry · Medicine · Neuroscience · Psychology · #Antidepressant #Biochemistry #Biomarker #Chemistry #Depression (economics) #Electroconvulsive therapy #Endocrinology #Glucocorticoid #Indoleamine 2,3-dioxygenase #Internal medicine #Kynurenine #Kynurenine pathway #Medicine #Oncology #Psychology #Stress Responses and Cortisol #Treatment of Major Depression #Tryptophan #Tryptophan and brain disorders
paper · pdf · doi:10.1017/neu.2024.34
openalex publication_date 2024/10/17 · openalex created_date 2025/10/10 · openalex updated_date 2026/08/05
Abstract Objective: This study aimed to investigate changes in mRNA expression of the kynurenine pathway (KP) enzymes tryptophan 2, 3-dioxygenase ( TDO ), indoleamine 2, 3-dioxygenase 1 and 2 ( IDO1 , IDO2 ), kynurenine aminotransferase 1 and 2 ( KAT1, KAT2 ), kynurenine monooxygenase ( KMO ) and kynureninase ( KYNU ) in medicated patients with depression ( n = 74) compared to age- and sex-matched healthy controls ( n = 55) and in patients with depression after electroconvulsive therapy (ECT). Associations with mood score (24-item Hamilton Depression Rating Scale, HAM-D24), plasma KP metabolites and selected glucocorticoid and inflammatory immune markers known to regulate KP enzyme expression were also explored. Methods: HAM-D24 was used to evaluate depression severity. Whole blood mRNA expression was assessed using quantitative real-time polymerase chain reaction. Results: KAT1, KYNU and IDO2 were significantly reduced in patient samples compared to control samples, though results did not survive statistical adjustment for covariates or multiple comparisons. ECT did not alter KP enzyme mRNA expression. Changes in IDO1 and KMO and change in HAM-D24 score post-ECT were negatively correlated in subgroups of patients with unipolar depression ( IDO1 only), psychotic depression and ECT responders and remitters. Further exploratory correlative analyses revealed altered association patterns between KP enzyme expression, KP metabolites, NR3C1 and IL-6 in depressed patients pre- and post-ECT. Conclusion: Further studies are warranted to determine if KP measures have sufficient sensitivity, specificity and predictive value to be integrated into stress and immune associated biomarker panels to aid patient stratification at diagnosis and in predicting treatment response to antidepressant therapy.