Prognostic Biomarkers of Sarcoidosis: A Comparative Study of Serum Chitotriosidase, ACE, Lysozyme, and KL-6.


Journal

Disease markers
ISSN: 1875-8630
Titre abrégé: Dis Markers
Pays: United States
ID NLM: 8604127

Informations de publication

Date de publication:
2019
Historique:
received: 26 11 2018
revised: 19 01 2019
accepted: 31 01 2019
entrez: 5 4 2019
pubmed: 5 4 2019
medline: 18 7 2019
Statut: epublish

Résumé

Sarcoidosis is a systemic granulomatous disease with unknown etiology. Many clinical presentations have been reported, and acute disease needs to be distinguished from subacute and chronic disease. The unpredictable clinical course of the disease prompted us to evaluate the clinical utility of biomarker serum detection in sarcoidosis follow-up. Serum concentrations of chitotriosidase, ACE, KL-6, and lysozyme were analyzed by different methods in a population of 74 sarcoidosis patients (46 on steroid therapy at sampling) regularly monitored at Siena Sarcoidosis Regional Referral Centre and in a group of controls with the aim of comparing their contribution to clinical management of sarcoidosis patients. KL-6 concentrations were significantly elevated in sarcoidosis patients with lung fibrosis and were significantly correlated with DLco and CPI score, while chitotriosidase was significantly higher in patients with extrapulmonary localizations. With a cut-off value of 303.5 IU/ml, KL-6 showed the best sensitivity (78%), while chitotriosidase reported the best specificity (85%) among the biomarkers. KL-6 is a reliable biomarker of fibrotic lung involvement in sarcoidosis patients. Among biomarkers, KL-6 showed the best sensitivity and serum chitotriosidase the best specificity, even in patients on chronic steroid therapy, and seemed to correlate with extrapulmonary localizations.

Identifiants

pubmed: 30944672
doi: 10.1155/2019/8565423
pmc: PMC6421736
doi:

Substances chimiques

Biomarkers 0
MUC1 protein, human 0
Mucin-1 0
Hexosaminidases EC 3.2.1.-
chitotriosidase EC 3.2.1.-
Muramidase EC 3.2.1.17
ACE protein, human EC 3.4.15.1
Peptidyl-Dipeptidase A EC 3.4.15.1

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8565423

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Auteurs

Laura Bergantini (L)

Department of Clinical Medicine and Immunological Sciences, Respiratory Disease and Lung Transplant Unit, Respiratory Diseases and Transplant Unit, Siena University, Siena, Italy.

Francesco Bianchi (F)

Department of Clinical Medicine and Immunological Sciences, Respiratory Disease and Lung Transplant Unit, Respiratory Diseases and Transplant Unit, Siena University, Siena, Italy.

Paolo Cameli (P)

Department of Clinical Medicine and Immunological Sciences, Respiratory Disease and Lung Transplant Unit, Respiratory Diseases and Transplant Unit, Siena University, Siena, Italy.

Maria Antonietta Mazzei (MA)

Department of Clinical Medicine and Immunological Sciences, Radiology Unit, Siena University, Siena, Italy.

Annalisa Fui (A)

Department of Clinical Medicine and Immunological Sciences, Respiratory Disease and Lung Transplant Unit, Respiratory Diseases and Transplant Unit, Siena University, Siena, Italy.

Piersante Sestini (P)

Department of Clinical Medicine and Immunological Sciences, Respiratory Disease and Lung Transplant Unit, Respiratory Diseases and Transplant Unit, Siena University, Siena, Italy.

Paola Rottoli (P)

Department of Clinical Medicine and Immunological Sciences, Respiratory Disease and Lung Transplant Unit, Respiratory Diseases and Transplant Unit, Siena University, Siena, Italy.

Elena Bargagli (E)

Department of Clinical Medicine and Immunological Sciences, Respiratory Disease and Lung Transplant Unit, Respiratory Diseases and Transplant Unit, Siena University, Siena, Italy.

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Classifications MeSH