Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative Stress

Introduction: Crohn’s disease (CD) is characterized by chronic and relapsing inflammation of the gastro-intestinal tract. It is assumed that oxidative stress contributes to CD pathogenesis, but systemic biomarkers for oxidative stress in CD are not yet identified. A reduction in free thiol groups in...

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Main Authors: Arno R. Bourgonje, Julius Z. H. von Martels, Marian L. C. Bulthuis, Marco van Londen, Klaas Nico Faber, Gerard Dijkstra, Harry van Goor
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-04-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphys.2019.00499/full
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spelling doaj-460ed709f7214447bdd7d2fd30ec7bfc2020-11-24T20:46:35ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2019-04-011010.3389/fphys.2019.00499448482Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative StressArno R. Bourgonje0Julius Z. H. von Martels1Marian L. C. Bulthuis2Marco van Londen3Klaas Nico Faber4Gerard Dijkstra5Harry van Goor6Department of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, NetherlandsDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, NetherlandsDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, NetherlandsDepartment of Internal Medicine, Division of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, NetherlandsDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, NetherlandsDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, NetherlandsDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, NetherlandsIntroduction: Crohn’s disease (CD) is characterized by chronic and relapsing inflammation of the gastro-intestinal tract. It is assumed that oxidative stress contributes to CD pathogenesis, but systemic biomarkers for oxidative stress in CD are not yet identified. A reduction in free thiol groups in plasma proteins (“plasma free thiols”) reflects systemic oxidative stress since they are prime substrates for reactive oxygen species. Here, we determined the concentrations of plasma free thiols in CD patients and healthy controls and studied the putative correlation with disease parameters.Methods: Free thiols were quantified in plasma of patients with CD in clinical remission [according to the Harvey Bradshaw Index (HBI)] and healthy controls and adjusted for plasma albumin. Albumin-adjusted free thiol concentrations were analyzed for associations with clinical and biochemical disease markers.Results: Mean plasma free thiol concentrations were significantly lower in patients with CD (n = 51) compared to healthy controls (n = 27) (14.7 ± 2.4 vs. 17.9 ± 1.8 μmol/g albumin; P < 0.001). Patients with CD with above-average free thiols had significantly lower CRP levels (median 1.4 [interquartile range] [0.4; 2.6] vs. 3.6 [0.6; 7.0] mg/L; P < 0.05) and BMI (23.6 ± 4.8 vs. 27.1 ± 5.2 kg/m2; P < 0.05). Patients with CD having solely colonic disease demonstrated markedly reduced plasma free thiol concentrations compared to patients with ileocolonic involvement (13.2 ± 1.8 vs. 15.2 ± 2.2 μmol/g; P < 0.05). Finally, plasma free thiol concentrations negatively correlated with biomarkers of inflammation, including hsCRP, SAA, IL-17A (all P < 0.05), and VEGF.Conclusion: Plasma free thiols are reduced in patients with CD in clinical remission compared to healthy controls. Thus, subclinical CD disease activity is reflected by systemic oxidative stress and plasma free thiols may be a relevant therapeutic target and biomarker to monitor disease activity in CD.https://www.frontiersin.org/article/10.3389/fphys.2019.00499/fullCrohn’s diseasefree thiolsoxidative stressredox statusdisease activitybiomarker
collection DOAJ
language English
format Article
sources DOAJ
author Arno R. Bourgonje
Julius Z. H. von Martels
Marian L. C. Bulthuis
Marco van Londen
Klaas Nico Faber
Gerard Dijkstra
Harry van Goor
spellingShingle Arno R. Bourgonje
Julius Z. H. von Martels
Marian L. C. Bulthuis
Marco van Londen
Klaas Nico Faber
Gerard Dijkstra
Harry van Goor
Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative Stress
Frontiers in Physiology
Crohn’s disease
free thiols
oxidative stress
redox status
disease activity
biomarker
author_facet Arno R. Bourgonje
Julius Z. H. von Martels
Marian L. C. Bulthuis
Marco van Londen
Klaas Nico Faber
Gerard Dijkstra
Harry van Goor
author_sort Arno R. Bourgonje
title Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative Stress
title_short Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative Stress
title_full Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative Stress
title_fullStr Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative Stress
title_full_unstemmed Crohn’s Disease in Clinical Remission Is Marked by Systemic Oxidative Stress
title_sort crohn’s disease in clinical remission is marked by systemic oxidative stress
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2019-04-01
description Introduction: Crohn’s disease (CD) is characterized by chronic and relapsing inflammation of the gastro-intestinal tract. It is assumed that oxidative stress contributes to CD pathogenesis, but systemic biomarkers for oxidative stress in CD are not yet identified. A reduction in free thiol groups in plasma proteins (“plasma free thiols”) reflects systemic oxidative stress since they are prime substrates for reactive oxygen species. Here, we determined the concentrations of plasma free thiols in CD patients and healthy controls and studied the putative correlation with disease parameters.Methods: Free thiols were quantified in plasma of patients with CD in clinical remission [according to the Harvey Bradshaw Index (HBI)] and healthy controls and adjusted for plasma albumin. Albumin-adjusted free thiol concentrations were analyzed for associations with clinical and biochemical disease markers.Results: Mean plasma free thiol concentrations were significantly lower in patients with CD (n = 51) compared to healthy controls (n = 27) (14.7 ± 2.4 vs. 17.9 ± 1.8 μmol/g albumin; P < 0.001). Patients with CD with above-average free thiols had significantly lower CRP levels (median 1.4 [interquartile range] [0.4; 2.6] vs. 3.6 [0.6; 7.0] mg/L; P < 0.05) and BMI (23.6 ± 4.8 vs. 27.1 ± 5.2 kg/m2; P < 0.05). Patients with CD having solely colonic disease demonstrated markedly reduced plasma free thiol concentrations compared to patients with ileocolonic involvement (13.2 ± 1.8 vs. 15.2 ± 2.2 μmol/g; P < 0.05). Finally, plasma free thiol concentrations negatively correlated with biomarkers of inflammation, including hsCRP, SAA, IL-17A (all P < 0.05), and VEGF.Conclusion: Plasma free thiols are reduced in patients with CD in clinical remission compared to healthy controls. Thus, subclinical CD disease activity is reflected by systemic oxidative stress and plasma free thiols may be a relevant therapeutic target and biomarker to monitor disease activity in CD.
topic Crohn’s disease
free thiols
oxidative stress
redox status
disease activity
biomarker
url https://www.frontiersin.org/article/10.3389/fphys.2019.00499/full
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