Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial Osteomyelitis

ObjectivesChronic recurrent multifocal osteomyelitis (CRMO), the most severe form of chronic nonbacterial osteomyelitis (CNO), is an autoinflammatory bone disorder. In the absence of diagnostic criteria or biomarkers, CNO/CRMO remains a diagnosis of exclusion. The aim of this study was to identify b...

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Main Authors: Sigrun Ruth Hofmann, Fanny Böttger, Ursula Range, Christian Lück, Henner Morbach, Hermann Joseph Girschick, Meinolf Suttorp, Christian Michael Hedrich
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-12-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fped.2017.00256/full
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spelling doaj-26792101e86d407a9c23a2ada82d6fa12020-11-25T00:01:18ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602017-12-01510.3389/fped.2017.00256312174Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial OsteomyelitisSigrun Ruth Hofmann0Fanny Böttger1Ursula Range2Christian Lück3Henner Morbach4Hermann Joseph Girschick5Meinolf Suttorp6Christian Michael Hedrich7Christian Michael Hedrich8Christian Michael Hedrich9Department of Pediatrics, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, GermanyDepartment of Pediatrics, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, GermanyInstitute for Medical Informatics and Biometry, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, GermanyInstitute for Medical Microbiology, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, GermanyUniversity Children’s Hospital Würzburg, University of Würzburg, Würzburg, GermanyChildren’s Hospital, Vivantes Klinikum im Friedrichshain, Berlin, GermanyDepartment of Pediatrics, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, GermanyDepartment of Pediatrics, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, GermanyDepartment of Women’s and Children’s Health, Institute of Translational Medicine, University of Liverpool, Liverpool, United KingdomDepartment of Paediatric Rheumatology, Alder Hey Children’s NHS Foundation Trust Hospital, Liverpool, United KingdomObjectivesChronic recurrent multifocal osteomyelitis (CRMO), the most severe form of chronic nonbacterial osteomyelitis (CNO), is an autoinflammatory bone disorder. In the absence of diagnostic criteria or biomarkers, CNO/CRMO remains a diagnosis of exclusion. The aim of this study was to identify biomarkers for diagnosing multifocal disease (CRMO).Study designSera from 71 pediatric CRMO patients, 11 patients with osteoarticular infections, 62 patients with juvenile idiopathic arthritis (JIA), 7 patients with para-infectious or reactive arthritis, and 43 patients with acute leukemia or lymphoma, as well as 59 healthy individuals were collected. Multiplex analysis of 18 inflammation- and/or bone remodeling-associated serum proteins was performed. Statistical analysis included univariate ANOVA, discriminant analysis, univariate receiver operating characteristic (ROC) analysis, and logistic regression analyses.ResultsFor 14 of 18 blood serum proteins, significant differences were determined between CRMO patients, at least one alternative diagnosis, or healthy controls. Multi-component discriminant analysis delivered five biomarkers (IL-6, CCL11/eotaxin, CCL5/RANTES, collagen Iα, sIL-2R) for the diagnosis of CRMO. ROC analysis allowed further reduction to a core set of 2 biomarkers (CCL11/eotaxin, IL-6) that are sufficient to discern between CRMO, healthy controls, and alternative diagnoses.ConclusionSerum biomarkers CCL11/eotaxin and IL-6 differentiate between patients with CRMO, healthy controls, and alternative diagnoses (leukemia and lymphoma, osteoarticular infections, para-infectious arthritis, and JIA). Easily accessible biomarkers may aid in diagnosing CRMO. Further studies testing biomarkers in larger unrelated cohorts are warranted.http://journal.frontiersin.org/article/10.3389/fped.2017.00256/fullchronic nonbacterial osteomyelitischronic recurrent multifocal osteomyelitisinflammationbiomarkerautoinflammationdiagnosis
collection DOAJ
language English
format Article
sources DOAJ
author Sigrun Ruth Hofmann
Fanny Böttger
Ursula Range
Christian Lück
Henner Morbach
Hermann Joseph Girschick
Meinolf Suttorp
Christian Michael Hedrich
Christian Michael Hedrich
Christian Michael Hedrich
spellingShingle Sigrun Ruth Hofmann
Fanny Böttger
Ursula Range
Christian Lück
Henner Morbach
Hermann Joseph Girschick
Meinolf Suttorp
Christian Michael Hedrich
Christian Michael Hedrich
Christian Michael Hedrich
Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial Osteomyelitis
Frontiers in Pediatrics
chronic nonbacterial osteomyelitis
chronic recurrent multifocal osteomyelitis
inflammation
biomarker
autoinflammation
diagnosis
author_facet Sigrun Ruth Hofmann
Fanny Böttger
Ursula Range
Christian Lück
Henner Morbach
Hermann Joseph Girschick
Meinolf Suttorp
Christian Michael Hedrich
Christian Michael Hedrich
Christian Michael Hedrich
author_sort Sigrun Ruth Hofmann
title Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial Osteomyelitis
title_short Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial Osteomyelitis
title_full Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial Osteomyelitis
title_fullStr Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial Osteomyelitis
title_full_unstemmed Serum Interleukin-6 and CCL11/Eotaxin May Be Suitable Biomarkers for the Diagnosis of Chronic Nonbacterial Osteomyelitis
title_sort serum interleukin-6 and ccl11/eotaxin may be suitable biomarkers for the diagnosis of chronic nonbacterial osteomyelitis
publisher Frontiers Media S.A.
series Frontiers in Pediatrics
issn 2296-2360
publishDate 2017-12-01
description ObjectivesChronic recurrent multifocal osteomyelitis (CRMO), the most severe form of chronic nonbacterial osteomyelitis (CNO), is an autoinflammatory bone disorder. In the absence of diagnostic criteria or biomarkers, CNO/CRMO remains a diagnosis of exclusion. The aim of this study was to identify biomarkers for diagnosing multifocal disease (CRMO).Study designSera from 71 pediatric CRMO patients, 11 patients with osteoarticular infections, 62 patients with juvenile idiopathic arthritis (JIA), 7 patients with para-infectious or reactive arthritis, and 43 patients with acute leukemia or lymphoma, as well as 59 healthy individuals were collected. Multiplex analysis of 18 inflammation- and/or bone remodeling-associated serum proteins was performed. Statistical analysis included univariate ANOVA, discriminant analysis, univariate receiver operating characteristic (ROC) analysis, and logistic regression analyses.ResultsFor 14 of 18 blood serum proteins, significant differences were determined between CRMO patients, at least one alternative diagnosis, or healthy controls. Multi-component discriminant analysis delivered five biomarkers (IL-6, CCL11/eotaxin, CCL5/RANTES, collagen Iα, sIL-2R) for the diagnosis of CRMO. ROC analysis allowed further reduction to a core set of 2 biomarkers (CCL11/eotaxin, IL-6) that are sufficient to discern between CRMO, healthy controls, and alternative diagnoses.ConclusionSerum biomarkers CCL11/eotaxin and IL-6 differentiate between patients with CRMO, healthy controls, and alternative diagnoses (leukemia and lymphoma, osteoarticular infections, para-infectious arthritis, and JIA). Easily accessible biomarkers may aid in diagnosing CRMO. Further studies testing biomarkers in larger unrelated cohorts are warranted.
topic chronic nonbacterial osteomyelitis
chronic recurrent multifocal osteomyelitis
inflammation
biomarker
autoinflammation
diagnosis
url http://journal.frontiersin.org/article/10.3389/fped.2017.00256/full
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