4.6 Article

The Kynurenine Pathway in Healthy Subjects and Subjects with Obesity, Depression and Chronic Obstructive Pulmonary Disease

Journal

PHARMACEUTICALS
Volume 16, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/ph16030351

Keywords

kynurenine pathway; obesity; depression; chronic obstructive pulmonary disease; inflammation

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This study compared the metabolism of the kynurenine pathway (KP) in healthy individuals and individuals with obesity, depression, and chronic obstructive pulmonary disease (COPD). The results showed that the KP was upregulated in the disease groups, and there were significant differences in the metabolites produced. In the obesity group, body mass index (BMI), smoking, diabetes, and C-reactive protein were important predictors of the differences. However, these factors were not related to the differences in the depression and COPD groups.
Background: Changes in tryptophan metabolism through the kynurenine pathway (KP) are observed in several disorders and coupled with pathophysiological deviations. Methods: This study retrospectively compared the KP in serum in healthy subjects (108) with subjects with obesity (141), depression (49), and chronic obstructive pulmonary disease (COPD) (22) participating in four clinical studies and explored predictors of the changes in the KP metabolites. Results: Compared with the healthy group, the KP was upregulated in the disease groups with high kynurenine, quinolinic acid (QA), kynurenine/tryptophan-ratio and QA/xanthurenic acid-ratio and low kynurenic acid/QA-ratio. Tryptophan and xanthurenic acid were upregulated in the depressed group compared with the groups with obesity and COPD. The covariates BMI, smoking, diabetes, and C-reactive protein explained the significant differences between the healthy group and the group with obesity but not between the healthy group and the groups with depression and COPD, indicating that different pathophysiological conditions result in the same changes in the KP. Conclusions: The KP was significantly upregulated in the disease groups compared with the healthy group, and there were significant differences between the disease groups. Different pathophysiological abnormalities seemed to result in the same deviations in the KP.

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