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Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis

Background and aim Sarcoidosis is a multisystem inflammatory disease of unknown aetiology. This study aimed to evaluate the relationship between systemic inflammatory parameters, the systemic immune-inflammation index (SII) and the lymphocyte-to-monocyte ratio (LMR), and disease stage, clinical find...

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Autores principales: Sahin Ozdemirel, Tugce, Akıncı Özyürek, Berna, Tatci, Ebru, Ertan, Ozlem, Akkurt, Esma Sevil, Senturk, Aysegul, Ozmen, Ozlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120846/
https://www.ncbi.nlm.nih.gov/pubmed/37090303
http://dx.doi.org/10.7759/cureus.36521
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author Sahin Ozdemirel, Tugce
Akıncı Özyürek, Berna
Tatci, Ebru
Ertan, Ozlem
Akkurt, Esma Sevil
Senturk, Aysegul
Ozmen, Ozlem
author_facet Sahin Ozdemirel, Tugce
Akıncı Özyürek, Berna
Tatci, Ebru
Ertan, Ozlem
Akkurt, Esma Sevil
Senturk, Aysegul
Ozmen, Ozlem
author_sort Sahin Ozdemirel, Tugce
collection PubMed
description Background and aim Sarcoidosis is a multisystem inflammatory disease of unknown aetiology. This study aimed to evaluate the relationship between systemic inflammatory parameters, the systemic immune-inflammation index (SII) and the lymphocyte-to-monocyte ratio (LMR), and disease stage, clinical findings, and 18F-fluoro-2-deoxy-D-glucose (18F-FDG) tomography/computed tomography (PET/CT) uptake. Materials and methods Our study included 73 patients. The general characteristics, radiological features, spirometric tests, PET/CT findings, and laboratory parameters of the patients were recorded. Results Relapse and parenchymal fibrosis were not associated with metabolic parameters, such as LMR and SII. Serum angiotensin-converting enzyme (ACE) levels were lower in the relapsed group than in the non-relapse group. However, the patients’ PET/CT images indicated that 18F-FDG parenchym maximum standard uptake value (SUV max), lymph node SUV max, lymph node short axis dimension, SII, and LMR were similar between all patients, relapsed or not. Conclusion Although found to be significant in other inflammatory diseases, we found that SII and LMR alone did not indicate disease prognosis in sarcoidosis due to the small number of patients and the lack of homogeneity between the groups in our study. The usefulness of these markers for clinical use should be investigated by studies that include those with extrapulmonary sarcoidosis, and that calculate these markers at the time of disease diagnosis and during the post-treatment period.
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spelling pubmed-101208462023-04-22 Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis Sahin Ozdemirel, Tugce Akıncı Özyürek, Berna Tatci, Ebru Ertan, Ozlem Akkurt, Esma Sevil Senturk, Aysegul Ozmen, Ozlem Cureus Pulmonology Background and aim Sarcoidosis is a multisystem inflammatory disease of unknown aetiology. This study aimed to evaluate the relationship between systemic inflammatory parameters, the systemic immune-inflammation index (SII) and the lymphocyte-to-monocyte ratio (LMR), and disease stage, clinical findings, and 18F-fluoro-2-deoxy-D-glucose (18F-FDG) tomography/computed tomography (PET/CT) uptake. Materials and methods Our study included 73 patients. The general characteristics, radiological features, spirometric tests, PET/CT findings, and laboratory parameters of the patients were recorded. Results Relapse and parenchymal fibrosis were not associated with metabolic parameters, such as LMR and SII. Serum angiotensin-converting enzyme (ACE) levels were lower in the relapsed group than in the non-relapse group. However, the patients’ PET/CT images indicated that 18F-FDG parenchym maximum standard uptake value (SUV max), lymph node SUV max, lymph node short axis dimension, SII, and LMR were similar between all patients, relapsed or not. Conclusion Although found to be significant in other inflammatory diseases, we found that SII and LMR alone did not indicate disease prognosis in sarcoidosis due to the small number of patients and the lack of homogeneity between the groups in our study. The usefulness of these markers for clinical use should be investigated by studies that include those with extrapulmonary sarcoidosis, and that calculate these markers at the time of disease diagnosis and during the post-treatment period. Cureus 2023-03-22 /pmc/articles/PMC10120846/ /pubmed/37090303 http://dx.doi.org/10.7759/cureus.36521 Text en Copyright © 2023, Sahin Ozdemirel et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pulmonology
Sahin Ozdemirel, Tugce
Akıncı Özyürek, Berna
Tatci, Ebru
Ertan, Ozlem
Akkurt, Esma Sevil
Senturk, Aysegul
Ozmen, Ozlem
Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis
title Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis
title_full Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis
title_fullStr Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis
title_full_unstemmed Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis
title_short Relationships Between Systemic Inflammatory Markers and 18F-FDG PET/CT Imaging and Clinical Findings in Pulmonary Sarcoidosis
title_sort relationships between systemic inflammatory markers and 18f-fdg pet/ct imaging and clinical findings in pulmonary sarcoidosis
topic Pulmonology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120846/
https://www.ncbi.nlm.nih.gov/pubmed/37090303
http://dx.doi.org/10.7759/cureus.36521
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