Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients

Transforming growth factor beta (TGF-β) is a cytokine with important involvement in biological processes related to the pathogenesis of sickle cell disease (SCD), including endothelial and vascular dysfunction, inflammation, and hematopoietic homeostasis. This study is aimed at investigating associa...

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Main Authors: Rayra P. Santiago, Magda O. S. Carvalho, Camylla V. B. Figueiredo, Luciana M. Fiuza, Rodrigo M. Oliveira, Sètondji C. M. A. Yahouédéhou, Valma M. L. Nascimento, Isa M. Lyra, Théo Araujo-Santos, Nívea F. Luz, Milena M. Aleluia, Caroline C. Guarda, Valéria M. Borges, Marilda S. Goncalves
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2021/4651891
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author Rayra P. Santiago
Magda O. S. Carvalho
Camylla V. B. Figueiredo
Luciana M. Fiuza
Rodrigo M. Oliveira
Sètondji C. M. A. Yahouédéhou
Valma M. L. Nascimento
Isa M. Lyra
Théo Araujo-Santos
Nívea F. Luz
Milena M. Aleluia
Caroline C. Guarda
Valéria M. Borges
Marilda S. Goncalves
author_facet Rayra P. Santiago
Magda O. S. Carvalho
Camylla V. B. Figueiredo
Luciana M. Fiuza
Rodrigo M. Oliveira
Sètondji C. M. A. Yahouédéhou
Valma M. L. Nascimento
Isa M. Lyra
Théo Araujo-Santos
Nívea F. Luz
Milena M. Aleluia
Caroline C. Guarda
Valéria M. Borges
Marilda S. Goncalves
author_sort Rayra P. Santiago
collection DOAJ
description Transforming growth factor beta (TGF-β) is a cytokine with important involvement in biological processes related to the pathogenesis of sickle cell disease (SCD), including endothelial and vascular dysfunction, inflammation, and hematopoietic homeostasis. This study is aimed at investigating associations between levels of TGF-β1 and classical laboratory biomarkers and inflammatory mediators, as well as the tissue inhibitor of metalloproteases-1 (TIMP-1) and matrix metalloproteinase-9 (MMP-9), in pediatric patients (n=123) with SCD in steady state: 84 with sickle cell anemia (HbSS) and 39 with hemoglobin SC disease (HbSC). A healthy control (HC) group of 59 individuals was also included. Hematological and biochemical analyses were carried out using electronic methods. TGF-β1, TIMP-1, and MMP-9 plasma quantifications were performed by ELISA. TGF-β1 plasma levels were higher in HbSS individuals than in HbSC and HC. In individuals with HbSS, TGF-β1 levels were positively correlated with red blood cells, hemoglobin, hematocrit, platelets, and TIMP-1. In addition, HbSS individuals with TGF-β1 levels above the median (≥72.29 ng/mL) also presented increased monocyte counts and decreased albumin levels. In patients with HbSC, TGF-β1 levels were positively correlated with leukocytes, eosinophils, lymphocytes, monocytes, and platelets, as well as levels of TIMP-1, VLDL-C, triglycerides, heme, and AST. Additionally, HbSC individuals with TGF-β1 levels above the median (≥47.80 ng/mL) presented increased leukocyte and platelet counts, as well as increased levels of triglycerides, VLDL-C, MMP-9, and TIMP-1, and decreased HDL-C. Our findings suggest that TGF-β1 may play important roles in vascular remodeling, vasculopathy, angiogenesis, and inflammation in pediatric patients with SCD.
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spelling doaj-art-892c705b9cbd49e4a9629b06f20715bc2025-02-03T05:49:15ZengWileyMediators of Inflammation0962-93511466-18612021-01-01202110.1155/2021/46518914651891Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell PatientsRayra P. Santiago0Magda O. S. Carvalho1Camylla V. B. Figueiredo2Luciana M. Fiuza3Rodrigo M. Oliveira4Sètondji C. M. A. Yahouédéhou5Valma M. L. Nascimento6Isa M. Lyra7Théo Araujo-Santos8Nívea F. Luz9Milena M. Aleluia10Caroline C. Guarda11Valéria M. Borges12Marilda S. Goncalves13Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilHospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, 40110-060 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilFundação de Hematologia e Hemoterapia do Estado da Bahia, 40286-240 Salvador, BrazilHospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, 40110-060 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilDepartamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, 45.662-900 Ilhéus, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, 40.296-710 Salvador, BrazilTransforming growth factor beta (TGF-β) is a cytokine with important involvement in biological processes related to the pathogenesis of sickle cell disease (SCD), including endothelial and vascular dysfunction, inflammation, and hematopoietic homeostasis. This study is aimed at investigating associations between levels of TGF-β1 and classical laboratory biomarkers and inflammatory mediators, as well as the tissue inhibitor of metalloproteases-1 (TIMP-1) and matrix metalloproteinase-9 (MMP-9), in pediatric patients (n=123) with SCD in steady state: 84 with sickle cell anemia (HbSS) and 39 with hemoglobin SC disease (HbSC). A healthy control (HC) group of 59 individuals was also included. Hematological and biochemical analyses were carried out using electronic methods. TGF-β1, TIMP-1, and MMP-9 plasma quantifications were performed by ELISA. TGF-β1 plasma levels were higher in HbSS individuals than in HbSC and HC. In individuals with HbSS, TGF-β1 levels were positively correlated with red blood cells, hemoglobin, hematocrit, platelets, and TIMP-1. In addition, HbSS individuals with TGF-β1 levels above the median (≥72.29 ng/mL) also presented increased monocyte counts and decreased albumin levels. In patients with HbSC, TGF-β1 levels were positively correlated with leukocytes, eosinophils, lymphocytes, monocytes, and platelets, as well as levels of TIMP-1, VLDL-C, triglycerides, heme, and AST. Additionally, HbSC individuals with TGF-β1 levels above the median (≥47.80 ng/mL) presented increased leukocyte and platelet counts, as well as increased levels of triglycerides, VLDL-C, MMP-9, and TIMP-1, and decreased HDL-C. Our findings suggest that TGF-β1 may play important roles in vascular remodeling, vasculopathy, angiogenesis, and inflammation in pediatric patients with SCD.http://dx.doi.org/10.1155/2021/4651891
spellingShingle Rayra P. Santiago
Magda O. S. Carvalho
Camylla V. B. Figueiredo
Luciana M. Fiuza
Rodrigo M. Oliveira
Sètondji C. M. A. Yahouédéhou
Valma M. L. Nascimento
Isa M. Lyra
Théo Araujo-Santos
Nívea F. Luz
Milena M. Aleluia
Caroline C. Guarda
Valéria M. Borges
Marilda S. Goncalves
Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients
Mediators of Inflammation
title Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients
title_full Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients
title_fullStr Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients
title_full_unstemmed Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients
title_short Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients
title_sort associations between tgf β1 levels and markers of hemolysis inflammation and tissue remodeling in pediatric sickle cell patients
url http://dx.doi.org/10.1155/2021/4651891
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