Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Fellendorf, FT; Gostner, JM; Lenger, M; Platzer, M; Birner, A; Maget, A; Queissner, R; Tmava-Berisha, A; Pater, CA; Ratzenhofer, M; Wagner-Skacel, J; Bengesser, SA; Dalkner, N; Fuchs, D; Reininghaus, EZ.
Tryptophan Metabolism in Bipolar Disorder in a Longitudinal Setting.
Antioxidants (Basel). 2021; 10(11): Doi: 10.3390/antiox10111795 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Fellendorf Frederike
Lenger Melanie
Co-Autor*innen der Med Uni Graz
Bengesser Susanne
Birner Armin
Dalkner Nina
Maget Alexander
Platzer Martina
Queissner Robert
Reininghaus Eva
Tmava-Berisha Adelina
Wagner-Skacel Jolana
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Immune-mediated inflammatory processes and oxidative stress are involved in the aetiopathogenesis of bipolar disorder (BD) and weight-associated comorbidities. Tryptophan breakdown via indoleamine 2,3-dioxygenase-1 (IDO-1) along the kynurenine axis concomitant with a pro-inflammatory state was found to be more active in BD, and associated with overweight/obesity. This study aimed to investigate tryptophan metabolism in BD compared to controls (C), stratified by weight classes, in a longitudinal setting, dependent on the incidence of BD episodes. Peripheral tryptophan, kynurenine, and neopterin were assessed in the serum of 226 BD individuals and 142 C. Three samples in a longitudinal assessment were used for 75 BD individuals. Results showed a higher kynurenine/tryptophan in both BD compared to C and overweight compared to normal weight persons. Levels remained stable over time. In the longitudinal course, no differences were found between individuals who were constantly euthymic or not, or who had an illness episode or had none. Findings indicate that tryptophan, kynurenine, and IDO-1 activity may play a role in pathophysiology in BD but are not necessarily associated with clinical manifestations. Accelerated tryptophan breakdown along the kynurenine axis may be facilitated by being overweight. This may increase the risk of accumulation of neurotoxic metabolites, impacting BD symptomatology, cognition, and somatic comorbidities.

Find related publications in this database (Keywords)
bipolar disorder
psychoneuroimmunology
kynurenine to tryptophan ratio
tryptophan metabolism
IDO-1
© Med Uni Graz Impressum