F1000Res. 2014 Oct 21;3:248. doi: 10.12688/f1000research.4709.1. eCollection 2014.
Metabolomics in psoriatic disease: pilot study reveals metabolite differences in psoriasis and psoriatic arthritis.
F1000Research
April W Armstrong, Julie Wu, Mary Ann Johnson, Dmitry Grapov, Baktazh Azizi, Jaskaran Dhillon, Oliver Fiehn
Affiliations
Affiliations
- Department of Dermatology, University of Colorado Denver, Aurora, CO, 12801, USA.
- Department of Dermatology, University of California Davis, Sacramento, CA, 95816, USA.
- NIH West Coast Metabolomics Center, University of California Davis, Davis, CA, 95616, USA.
PMID: 25580230
PMCID: PMC4288418 DOI: 10.12688/f1000research.4709.1
Abstract
IMPORTANCE: While "omics" studies have advanced our understanding of inflammatory skin diseases, metabolomics is mostly an unexplored field in dermatology.
OBJECTIVE: We sought to elucidate the pathogenesis of psoriatic diseases by determining the differences in metabolomic profiles among psoriasis patients with or without psoriatic arthritis and healthy controls.
DESIGN: We employed a global metabolomics approach to compare circulating metabolites from patients with psoriasis, psoriasis and psoriatic arthritis, and healthy controls.
SETTING: Study participants were recruited from the general community and from the Psoriasis Clinic at the University of California Davis in United States.
PARTICIPANTS: We examined metabolomic profiles using blood serum samples from 30 patients age and gender matched into three groups: 10 patients with psoriasis, 10 patients with psoriasis and psoriatic arthritis and 10 control participants. Main outcome(s) and measures(s): Metabolite levels were measured calculating the mean peak intensities from gas chromatography time-of-flight mass spectrometry.
RESULTS: Multivariate analyses of metabolomics profiles revealed altered serum metabolites among the study population. Compared to control patients, psoriasis patients had a higher level of alpha ketoglutaric acid (Pso: 288 ± 88;
CONTROL: 209 ± 69; p=0.03), a lower level of asparagine (Pso: 5460 ± 980;
CONTROL: 7260 ± 2100; p=0.02), and a lower level of glutamine (Pso: 86000 ± 20000;
CONTROL: 111000 ± 27000; p=0.02). Compared to control patients, patients with psoriasis and psoriatic arthritis had increased levels of glucuronic acid (Pso + PsA: 638 ± 250;
CONTROL: 347 ± 61; p=0.001). Compared to patients with psoriasis alone, patients with both psoriasis and psoriatic arthritis had a decreased level of alpha ketoglutaric acid (Pso + PsA: 186 ± 80; Pso: 288 ± 88; p=0.02) and an increased level of lignoceric acid (Pso + PsA: 442 ± 280; Pso: 214 ± 64; p=0.02).
CONCLUSIONS AND RELEVANCE: The metabolite differences help elucidate the pathogenesis of psoriasis and psoriatic arthritis and they may provide insights for therapeutic development.
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