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Circulating haematopoietic stem cells and long-term outcomes of COVID-19.
Bonora, Benedetta Maria; Marassi, Marella; Fogar, Paola; Zuin, Jenny; Cappellari, Roberta; Marinello, Serena; Ferrari, Anna; Cattelan, Annamaria; Avogaro, Angelo; Basso, Daniela; Fadini, Gian Paolo.
Afiliación
  • Bonora BM; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Marassi M; Veneto Institute of Molecular Medicine, Padua, Italy.
  • Fogar P; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Zuin J; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Cappellari R; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Marinello S; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Ferrari A; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Cattelan A; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Avogaro A; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Basso D; Department of Medicine, University Hospital of Padova, Padua, Italy.
  • Fadini GP; Department of Medicine, University Hospital of Padova, Padua, Italy.
Eur J Clin Invest ; 54(4): e14150, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38088242
ABSTRACT
BACKGROUND AND

AIMS:

An acute depletion of circulating haematopoietic stem/progenitor cells (HSPCs) occurs during COVID-19, especially among patients with a poorer disease course. We herein examined whether HSPCs levels at hospital admission for COVID-19 predict 1-year mortality and the long-COVID syndrome. MATERIALS AND

METHODS:

Patients hospitalized for COVID-19 in an infectious disease ward were consecutively enrolled. Circulating HSPC levels were assessed by flow cytometry as cells expressing CD34 and/or CD133. Follow-up was performed for 12 months after hospitalization through the review of electronic medical records and demographic local registers.

RESULTS:

The study included 100 patients, 36 of whom reported symptoms of long-COVID and 20 died during follow-up. The reduction of 1-SD of HSPCs was associated with a 3- to 5-fold increase in the risk of 1-year mortality. Age, admission hyperglycaemia, C-reactive protein peak, liver enzymes, the need of high-flow oxygen and/or invasive ventilation were predictors of mortality at univariate analysis. Among pre-existing comorbidities, coronary heart disease and chronic kidney disease, but not diabetes, were associated with 1-year mortality. In multivariate analyses, HSPCs remained significantly associated with 1-year mortality independently of confounders. The development of pneumonia an in-hospital treatment with glucocorticoids and convalescent plasma were associated with long-COVID symptoms at follow-up. HSPCs, diabetes and other comorbidities were not predictors of long-COVID.

CONCLUSIONS:

In a cohort of patients hospitalized for COVID-19, lower HSPC levels at the time of admission were independent predictors of 1-year mortality. However, COVID-19 severity, but not HSPC level, was significantly associated with the development of long-COVID symptoms.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Diabetes Mellitus / COVID-19 Límite: Humans Idioma: En Revista: Eur J Clin Invest Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Asunto principal: Diabetes Mellitus / COVID-19 Límite: Humans Idioma: En Revista: Eur J Clin Invest Año: 2024 Tipo del documento: Article País de afiliación: Italia