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Reduced Levels of Circulating Endothelial Cells and Endothelial Progenitor Cells in Patients with Heart Failure with Reduced Ejection Fraction.
Lopes, José; Teixeira, Manuel; Cavalcante, Suiane; Gouveia, Marisol; Duarte, Ana; Ferreira, Miriam; Simões, Maria I; Conceição, Maria; Ribeiro, Ilda P; Gonçalves, Ana C; Schmidt, Cristine; de Jesus, Bruno Bernardes; Almeida, Ramiro; Viamonte, Sofia; Santos, Mário; Ribeiro, Fernando.
  • Lopes J; Institute of Biomedicine-iBiMED, Department of Medical Sciences, University of Aveiro, Aveiro, Portugal.
  • Teixeira M; Institute of Biomedicine-iBiMED, Department of Medical Sciences, University of Aveiro, Aveiro, Portugal.
  • Cavalcante S; Research Centre in Physical Activity, Health and Leisure, CIAFEL, Faculty of Sport, University of Porto, Porto, Portugal.
  • Gouveia M; Institute of Biomedicine-iBiMED, Department of Medical Sciences, University of Aveiro, Aveiro, Portugal.
  • Duarte A; Unidade Cuidados na Comunidade Cubo Mágico da Saúde, ACES Baixo Vouga, Oliveira do Bairro, Portugal.
  • Ferreira M; Unidade Cuidados na Comunidade Cubo Mágico da Saúde, ACES Baixo Vouga, Oliveira do Bairro, Portugal.
  • Simões MI; Unidade Cuidados na Comunidade Cubo Mágico da Saúde, ACES Baixo Vouga, Oliveira do Bairro, Portugal.
  • Conceição M; Unidade Cuidados na Comunidade Cubo Mágico da Saúde, ACES Baixo Vouga, Oliveira do Bairro, Portugal.
  • Ribeiro IP; Cytogenetics and Genomics Laboratory, Institute of Cellular and Molecular Biology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal; Institute for Clinical and Biomedical Research and Center of Investigation on Environment Genetics and Oncobiology, Faculty of Medicine, University of Coi
  • Gonçalves AC; Institute for Clinical and Biomedical Research and Center of Investigation on Environment Genetics and Oncobiology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal; Laboratory of Oncobiology and Hematology and University Clinic of Hematology, Faculty of Medicine (FMUC), University of C
  • Schmidt C; Research Centre in Physical Activity, Health and Leisure, CIAFEL, Faculty of Sport, University of Porto, Porto, Portugal; Cardiovascular Research Unit, Department of Surgery and Physiology, Faculty of Medicine University of Porto, Porto, Portugal.
  • de Jesus BB; Institute of Biomedicine-iBiMED, Department of Medical Sciences, University of Aveiro, Aveiro, Portugal.
  • Almeida R; Institute of Biomedicine-iBiMED, Department of Medical Sciences, University of Aveiro, Aveiro, Portugal.
  • Viamonte S; North Rehabilitation Center-Dr. Ferreira Alves, Centro Hospital Vila Nova de Gaia-Espinho, Vila Nova de Gaia, Portugal.
  • Santos M; Department of Cardiology, Hospital Center of Porto & UMIB, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal.
  • Ribeiro F; Institute of Biomedicine-iBiMED, School of Health Sciences, University of Aveiro, Aveiro, Portugal. Electronic address: fernando.ribeiro@ua.pt.
Arch Med Res ; 53(3): 289-295, 2022 04.
Article en En | MEDLINE | ID: mdl-35183379
ABSTRACT

BACKGROUND:

Endothelial dysfunction has been suggested as a potential mechanism contributing to the development and progression of heart failure (HF). Levels of circulating endothelial cells (CECs), endothelial progenitor cells (EPCs), and hematopoietic stem and progenitor cells (HSPCs) have been recognized as useful markers of vascular damage and endothelial repair in response to tissue injury.

AIMS:

To evaluate the circulating levels of EPCs, CECs, and HSPCs among patients with HF with reduced ejection fraction (HFrEF).

METHODS:

In 82 individuals (42 patients with HFrEF and 42 age-matched subjects without established cardiovascular disease), peripheral blood was drawn and levels of EPCs, CECs, and HSPCs were quantified by flow cytometry.

RESULTS:

Patients with HFrEF showed lower levels of circulating EPCs (5.28 × 10-3 ± 6.83 × 10-4% vs. 7.76 × 10-3 ± 4.91 × 10-4%, p ≤0.001) and CECs (5.11 × 10-3 ± 7.87 × 10-4% vs. 6.51 × 10-3 ± 5.21 × 10-4%, p = 0.005) when compared to the age-matched group. Circulating levels of HSPCs were not significantly different between groups (p = 0.590). Additionally, the number of EPCs and CECs was significantly higher in HFrEF patients with overweight/obesity (n = 24) compared to patients with normal weight (n = 17).

CONCLUSION:

Circulating levels of EPCs and CECs were significantly decreased in patients with HFrEF in comparison to age-matched subjects without established cardiovascular disease, suggesting that the levels of CECs and EPCs may be potential biomarkers of the cellular response to vascular injury in patients with HFrEF.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Células Progenitoras Endoteliales / Insuficiencia Cardíaca Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Células Progenitoras Endoteliales / Insuficiencia Cardíaca Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article