Cargando…

Calprotectin as new potential clinical marker for multiple myeloma

Increased levels of inflammatory cytokines in multiple myeloma (MM) patients and the role of inflammation in disease pathogenesis, have recently been considered. The aim of this study was to quantitatively evaluation of fecal calprotectin (CP) as a non-invasive biomarker for the evaluation of inflam...

Descripción completa

Detalles Bibliográficos
Autores principales: Khosravi, Parisa, Abroun, Saeid, Kaviani, Saeid, Masoudifar, Saman, Farahani, Homayoun Sarough
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019635/
https://www.ncbi.nlm.nih.gov/pubmed/36928900
http://dx.doi.org/10.1371/journal.pone.0282841
_version_ 1784908065610399744
author Khosravi, Parisa
Abroun, Saeid
Kaviani, Saeid
Masoudifar, Saman
Farahani, Homayoun Sarough
author_facet Khosravi, Parisa
Abroun, Saeid
Kaviani, Saeid
Masoudifar, Saman
Farahani, Homayoun Sarough
author_sort Khosravi, Parisa
collection PubMed
description Increased levels of inflammatory cytokines in multiple myeloma (MM) patients and the role of inflammation in disease pathogenesis, have recently been considered. The aim of this study was to quantitatively evaluation of fecal calprotectin (CP) as a non-invasive biomarker for the evaluation of inflammation in patients with multiple myeloma. This study is a hospital-based case control study. MM patients referred to patients referred to medical centers of Tehran province, Iran, were identified and classified into two groups of new MM patients (n = 40) and patients undergoing treatment (n = 28). Healthy individuals were included in the study as healthy control (n = 25). Morning stool samples were collected and CP was extracted immediately. After collecting the samples, CP was measured according to ELISA method and was determined in μg/g of feces. Values ​​above 50 μg/g of feces are positive and indicate inflammation. The results revealed that there is a significant difference between groups in terms if CP mean (p = 0.001). The mean of CP among new cases, under treatment and control groups were 301.3 (SD: 141.0), 165.1 (SD: 153.9) and 36.9 (SD: 13.5), respectively. Then the groups were compared in pairs, the results showed that the new case group was significantly different from the under-treatment group (p = 0.001), and also the control group showed a significant difference with the new case group (p = 0.001) and the under-treatment group (p = 0.001) that the amount of CP in the control group was significantly lower than the other two groups. In addition, the results of the study showed a significant correlation between age and plasma cells with CP value, so that with increasing age and plasma cells, CP value also showed a significant increase. The results indicate that quantitative evaluation of CP as a non-invasive laboratory biomarker has a high potential as a clinical marker in patients with multiple myeloma and inflammation should considered as a hallmark of cancer. Further diagnostic studies are recommended.
format Online
Article
Text
id pubmed-10019635
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-100196352023-03-17 Calprotectin as new potential clinical marker for multiple myeloma Khosravi, Parisa Abroun, Saeid Kaviani, Saeid Masoudifar, Saman Farahani, Homayoun Sarough PLoS One Research Article Increased levels of inflammatory cytokines in multiple myeloma (MM) patients and the role of inflammation in disease pathogenesis, have recently been considered. The aim of this study was to quantitatively evaluation of fecal calprotectin (CP) as a non-invasive biomarker for the evaluation of inflammation in patients with multiple myeloma. This study is a hospital-based case control study. MM patients referred to patients referred to medical centers of Tehran province, Iran, were identified and classified into two groups of new MM patients (n = 40) and patients undergoing treatment (n = 28). Healthy individuals were included in the study as healthy control (n = 25). Morning stool samples were collected and CP was extracted immediately. After collecting the samples, CP was measured according to ELISA method and was determined in μg/g of feces. Values ​​above 50 μg/g of feces are positive and indicate inflammation. The results revealed that there is a significant difference between groups in terms if CP mean (p = 0.001). The mean of CP among new cases, under treatment and control groups were 301.3 (SD: 141.0), 165.1 (SD: 153.9) and 36.9 (SD: 13.5), respectively. Then the groups were compared in pairs, the results showed that the new case group was significantly different from the under-treatment group (p = 0.001), and also the control group showed a significant difference with the new case group (p = 0.001) and the under-treatment group (p = 0.001) that the amount of CP in the control group was significantly lower than the other two groups. In addition, the results of the study showed a significant correlation between age and plasma cells with CP value, so that with increasing age and plasma cells, CP value also showed a significant increase. The results indicate that quantitative evaluation of CP as a non-invasive laboratory biomarker has a high potential as a clinical marker in patients with multiple myeloma and inflammation should considered as a hallmark of cancer. Further diagnostic studies are recommended. Public Library of Science 2023-03-16 /pmc/articles/PMC10019635/ /pubmed/36928900 http://dx.doi.org/10.1371/journal.pone.0282841 Text en © 2023 Khosravi et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Khosravi, Parisa
Abroun, Saeid
Kaviani, Saeid
Masoudifar, Saman
Farahani, Homayoun Sarough
Calprotectin as new potential clinical marker for multiple myeloma
title Calprotectin as new potential clinical marker for multiple myeloma
title_full Calprotectin as new potential clinical marker for multiple myeloma
title_fullStr Calprotectin as new potential clinical marker for multiple myeloma
title_full_unstemmed Calprotectin as new potential clinical marker for multiple myeloma
title_short Calprotectin as new potential clinical marker for multiple myeloma
title_sort calprotectin as new potential clinical marker for multiple myeloma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019635/
https://www.ncbi.nlm.nih.gov/pubmed/36928900
http://dx.doi.org/10.1371/journal.pone.0282841
work_keys_str_mv AT khosraviparisa calprotectinasnewpotentialclinicalmarkerformultiplemyeloma
AT abrounsaeid calprotectinasnewpotentialclinicalmarkerformultiplemyeloma
AT kavianisaeid calprotectinasnewpotentialclinicalmarkerformultiplemyeloma
AT masoudifarsaman calprotectinasnewpotentialclinicalmarkerformultiplemyeloma
AT farahanihomayounsarough calprotectinasnewpotentialclinicalmarkerformultiplemyeloma