NMR-based metabolomics in giant cell arteritis and polymyalgia rheumatica sequential sera differentiates active and inactive disease

Author:

Iliou Aikaterini1,Argyropoulou Ourania D2,Palamidas Dimitris-Anastasios23,Karagiannakou Marianna1,Benaki Dimitra1,Tsezou Konstantina-Ismini24,Vlachoyiannopoulos Panayiotis G23,Mikros Emmanuel145,Tzioufas Athanasios G236

Affiliation:

1. Department of Pharmaceutical Chemistry, School of Pharmacy, National and Kapodistrian University of Athens , Athens, Greece

2. Department of Pathophysiology, School of Medicine, National and Kapodistrian University of Athens , Athens, Greece

3. Research Institute for Systemic Autoimmune Rheumatic Diseases (RISARD) , Athens, Greece

4. Pharmagnose S.A. , Inofyta, Greece

5. Pharma - Informatics Unit, Athena Research and Innovation Center in Information Communication & Knowledge Technologies , Marousi, Greece

6. Center of Stratified Medicine in Autoimmune and Rheumatic Diseases, Biomedical Research Foundation Academy of Athens, Athens, Greece

Abstract

Abstract Objectives GCA is an inflammatory disease following a chronic, relapsing course. The metabolic alterations related to the intense inflammatory process during the active phase and the rapid impact of steroid treatment remain unknown. This study aims to investigate the serum metabolome in active and inactive disease states. Methods A total of 110 serum samples from 50 patients (33 GCA and 17 PMR) at three time points—0 (V1: active disease), 1 and 6 months (V2 and V3: remission)—of treatment with glucocorticoids (GCs) were subjected to NMR-based metabolomic analysis. Multi- and univariate statistical analyses were utilized to unveil metabolome alterations following treatment. Results Distinct metabolic profiles were identified between activity and remission, independent of disease type. N-acetylglycoproteins and cholines of bound phospholipids emerged as predictive markers of disease activity. Altered levels of 4 of the 21 small molecules were also observed, including increased levels of phenylalanine and decreased glutamine, alanine and creatinine in active disease. Metabolic fingerprinting discriminated GCA from PMR in remission. GCA and PMR patients exhibited characteristic lipid alterations as a response and/or adverse effect of GC treatment. Correlation analysis showed that several identified biomarkers were further associated with acute phase reactants, CRP and ESR. Conclusion The NMR profile of serum metabolome could identify and propose sensitive biomarkers of inflammation. Metabolome alterations, following GC treatment, could provide predictors for future steroid-induced side effects.

Funder

H2020 ITN consortium ArthritisHeal

Stavros Niarchos Foundation grant at the National and Kapodistrian University of Athens

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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