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The ektacytometric elongation Index (EI) of erythrocytes, validation of a prognostic, rheological biomarker for patients with sickle cell disease.
Franck, Paul; Buijs, Petra; Meenhuis, Annemarie; Dane, Martijn; Postma, Cobie; Spaans, Anja; Gijsbertha, Niegel; Kuypers, Frans A; Hudig, Cisca; Kerkhoffs, Jean Louis.
Afiliação
  • Franck P; Laboratory of Clinical Chemistry and Hematology, LabWest / Haga Teaching Hospital, The Hague, The Netherlands.
  • Buijs P; Department of Hematology, Haga Teaching Hospital, The Hague, The Netherlands.
  • Meenhuis A; Laboratory of Clinical Chemistry and Hematology, Tergooi Medical Centre, Hilversum, The Netherlands.
  • Dane M; Laboratory of Clinical Chemistry and Hematology, LabWest / Haga Teaching Hospital, The Hague, The Netherlands.
  • Postma C; Laboratory of Clinical Chemistry and Hematology, LabWest / Haga Teaching Hospital, The Hague, The Netherlands.
  • Spaans A; Laboratory of Clinical Chemistry and Hematology, LabWest / Haga Teaching Hospital, The Hague, The Netherlands.
  • Gijsbertha N; Sanquin Diagnostics, Amsterdam, The Netherlands.
  • Kuypers FA; Division of Hematology, Department of Pediatrics, University of California, San Francisco, USA.
  • Hudig C; Laboratory of Clinical Chemistry and Hematology, LabWest / Haga Teaching Hospital, The Hague, The Netherlands.
  • Kerkhoffs JL; Department of Hematology, Haga Teaching Hospital, The Hague, The Netherlands.
Eur J Haematol ; 108(5): 413-422, 2022 May.
Article em En | MEDLINE | ID: mdl-35088912
ABSTRACT

OBJECTIVES:

Validation of the measurement of erythrocyte deformability as a useful prognostic, rheological biomarker for patients with sickle cell disease (SCD).

METHODS:

The degree of reduced deformability was based on the value of the maximum elongation index (EImax ) of the deformability curve of an osmotic gradient ektacytometer. The performance of this technique was analytically and clinically validated by analysing 200 normal subjects and 100 patients with well-documented thalassemia's and Hb variants in relation to their clinical condition.

RESULTS:

In this study, we show that EImax is a reproducible parameter with a small inter-individual coefficient of (Biological) variation (CV)=1.6% and a small intra-individual CV=3.5%. We demonstrate that loss of deformability correlates with the clinical condition and the various mutations underlying sickle cell disease and thalassemia. For SCD patients, a strongly reduced EImax with a cut-off =0.360 is a signal for future vaso-occlusive (VOC) events requiring hospitalisation with a specificity=85%, sensitivity=80%, PPV=81% and NPV=84% based on a ROC curve (AUC=0.89).

CONCLUSION:

This study validated the clinical utility of EImax as a prognostic marker for future clinical problems in individual high-risk SCD patients. In addition, EImax may help to achieve an adequate personal transfusion policy for an optimal blood flow in anaemic patients with SCD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deformação Eritrocítica / Anemia Falciforme Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Eur J Haematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deformação Eritrocítica / Anemia Falciforme Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Eur J Haematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda