Catherine E. Simpson, Anjira S. Ambade, Robert Harlan, Aurelie Roux, Susan Aja, David Graham, Ami A. Shah, Laura K. Hummers, Anna R. Humnes, Jane A. Leopold, Evelyn M. Horn, Erika S. Berman-Rosenzweig, Gabrielle Grunig, Michaela A. Aldred, John Barnard, Suzy A. A. Comhair, W. H. Wilson Tang, Megan Griffiths, Franz Rischard, Robert P. Frantz, Serpil C. Erzurum, Gerald J. Beck, Nicholas S. Hill, Stephen C. Mathai, Paul M. Hassoun, Rachel L. Damico
Johns Hopkins University. Johns Hopkins All Children’s Hospital. Vanderbilt University, Nashville. Brigham and Women’s Hospital. Cornell University. Columbia University. New York University. Indiana University School of Medicine. Cleveland Clinic. University of Texas Southwestern Medical Center. University of Arizona. Mayo Clinic. Tufts Medical Center.
United States
American Journal of Physiology Lung Cellular and Molecular Physiology
Am J Physiol Lung Cell Mol Physiol 2023;
DOI: 10.1152/ajplung.00177.2023
Abstract
Background: Understanding metabolic evolution underlying pulmonary arterial hypertension (PAH) development may clarify pathobiology and reveal disease-specific biomarkers. Systemic sclerosis (SSc) patients are regularly surveilled for PAH, presenting an opportunity to examine metabolic change as disease develops in an at-risk cohort.
Methods: We performed mass spectrometry-based metabolomics on longitudinal serum samples collected prior to and near SSc-PAH diagnosis, compared to time-matched SSc subjects without PAH, in a SSc surveillance cohort. We validated metabolic differences in a second cohort and determined metabolite-phenotype relationships. In parallel, we performed serial metabolomic and hemodynamic assessments as disease developed in a preclinical model. For differentially expressed metabolites, we investigated corresponding gene expression in human and rodent PAH lungs.
Results: Kynurenine and its ratio to tryptophan (kyn/trp) increased over the surveillance period in SSc patients who developed PAH. Higher kyn/trp measured two years prior to diagnostic right heart catheterization increased the odds of SSc-PAH diagnosis (OR 1.57, 95% CI 1.05-2.36, p = 0.028). The slope of kyn/trp rise during SSc surveillance predicted PAH development and mortality. In both clinical and experimental PAH, higher kynurenine pathway metabolites correlated with adverse pulmonary vascular and RV measurements. In human and rodent PAH lungs, expression of TDO2, which catalyzes tryptophan conversion to kynurenine, was significantly upregulated and tightly correlated with pulmonary hypertensive features.
Conclusions: Upregulated kynurenine pathway metabolism occurs early in PAH, localizes to the lung, and may be modulated by TDO2. Kynurenine pathway metabolites may be candidate PAH biomarkers.
Category
Class I. Pulmonary Hypertension Associated with Connective Tissue Disease
Potential Biomarkers Associated with Pulmonary Vascular Disease
Acquired Patient Factors Associated with Pulmonary Vascular Disease
Animal Models of Pulmonary Vascular Disease and Therapy
Age Focus: Adult Pulmonary Vascular Disease
Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication
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