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Clinical phenotyping in sarcoidosis management

Sarcoidosis is a heterogeneous granulomatous disease. Biological markers and clinical features could allow specific phenotypes to be associated with different prognosis, severity and treatment responses. This retrospective multicentre study aims to analyse the clinical and immunological features of...

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Autores principales: Rana, Giuseppe Domenico, d’Alessandro, Miriana, Rizzi, Luigi, Bergantini, Laura, Cameli, Paolo, Vozza, Alfredo, Sestini, Piersante, Suppressa, Patrizia, Bargagli, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288209/
https://www.ncbi.nlm.nih.gov/pubmed/34316252
http://dx.doi.org/10.36141/svdld.v38i2.10423
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author Rana, Giuseppe Domenico
d’Alessandro, Miriana
Rizzi, Luigi
Bergantini, Laura
Cameli, Paolo
Vozza, Alfredo
Sestini, Piersante
Suppressa, Patrizia
Bargagli, Elena
author_facet Rana, Giuseppe Domenico
d’Alessandro, Miriana
Rizzi, Luigi
Bergantini, Laura
Cameli, Paolo
Vozza, Alfredo
Sestini, Piersante
Suppressa, Patrizia
Bargagli, Elena
author_sort Rana, Giuseppe Domenico
collection PubMed
description Sarcoidosis is a heterogeneous granulomatous disease. Biological markers and clinical features could allow specific phenotypes to be associated with different prognosis, severity and treatment responses. This retrospective multicentre study aims to analyse the clinical and immunological features of sarcoidosis and to identify a routine non-invasive biomarker useful in clinical practice. MATERIALS AND METHODS: 129 Caucasian patients with sarcoidosis (median age IQR, 56 (47-62)) were enrolled retrospectively in the study. Medical history, routine laboratory findings, lung function results and radiological features from the last examination of October 2019 – February 2020 were gathered from the patients’ clinical records. RESULTS: Regardless their clinical status at disease onset, at the last clinical examination we didn’t observe any differences in terms of therapeutic management between symptomatic and asymptomatic patients. Stratifying sarcoidosis population according to therapeutic management, the N/L ratio was higher in the treated group than in the non-treated group (p=0.0034). Receiver operating curve (ROC) analysis distinguished these two groups according to N/L ratio with an area under the curve (AUC) of 65.3% and a best cut-off value of 2.21. Peripheral N/L ratio was significantly higher in radiological stages 2-4 than in stages 0-1 (p=0.0090) distinguishing these two groups with an AUC of 64% and a best cut-off value of 2.13. DISCUSSION: In our multicentric cohort study similar periodic follow-up can be suggested for symptomatic and asymptomatic sarcoidosis patients at onset. In the heterogeneous context of this disease, N/L ratio proved to be a useful and simple routine laboratory biomarker related to disease activity and need for treatment.
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spelling pubmed-82882092021-07-26 Clinical phenotyping in sarcoidosis management Rana, Giuseppe Domenico d’Alessandro, Miriana Rizzi, Luigi Bergantini, Laura Cameli, Paolo Vozza, Alfredo Sestini, Piersante Suppressa, Patrizia Bargagli, Elena Sarcoidosis Vasc Diffuse Lung Dis Original Article: Clinical Research Sarcoidosis is a heterogeneous granulomatous disease. Biological markers and clinical features could allow specific phenotypes to be associated with different prognosis, severity and treatment responses. This retrospective multicentre study aims to analyse the clinical and immunological features of sarcoidosis and to identify a routine non-invasive biomarker useful in clinical practice. MATERIALS AND METHODS: 129 Caucasian patients with sarcoidosis (median age IQR, 56 (47-62)) were enrolled retrospectively in the study. Medical history, routine laboratory findings, lung function results and radiological features from the last examination of October 2019 – February 2020 were gathered from the patients’ clinical records. RESULTS: Regardless their clinical status at disease onset, at the last clinical examination we didn’t observe any differences in terms of therapeutic management between symptomatic and asymptomatic patients. Stratifying sarcoidosis population according to therapeutic management, the N/L ratio was higher in the treated group than in the non-treated group (p=0.0034). Receiver operating curve (ROC) analysis distinguished these two groups according to N/L ratio with an area under the curve (AUC) of 65.3% and a best cut-off value of 2.21. Peripheral N/L ratio was significantly higher in radiological stages 2-4 than in stages 0-1 (p=0.0090) distinguishing these two groups with an AUC of 64% and a best cut-off value of 2.13. DISCUSSION: In our multicentric cohort study similar periodic follow-up can be suggested for symptomatic and asymptomatic sarcoidosis patients at onset. In the heterogeneous context of this disease, N/L ratio proved to be a useful and simple routine laboratory biomarker related to disease activity and need for treatment. Mattioli 1885 2021 2021-06-28 /pmc/articles/PMC8288209/ /pubmed/34316252 http://dx.doi.org/10.36141/svdld.v38i2.10423 Text en Copyright: © 2021 SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Original Article: Clinical Research
Rana, Giuseppe Domenico
d’Alessandro, Miriana
Rizzi, Luigi
Bergantini, Laura
Cameli, Paolo
Vozza, Alfredo
Sestini, Piersante
Suppressa, Patrizia
Bargagli, Elena
Clinical phenotyping in sarcoidosis management
title Clinical phenotyping in sarcoidosis management
title_full Clinical phenotyping in sarcoidosis management
title_fullStr Clinical phenotyping in sarcoidosis management
title_full_unstemmed Clinical phenotyping in sarcoidosis management
title_short Clinical phenotyping in sarcoidosis management
title_sort clinical phenotyping in sarcoidosis management
topic Original Article: Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288209/
https://www.ncbi.nlm.nih.gov/pubmed/34316252
http://dx.doi.org/10.36141/svdld.v38i2.10423
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