Innovative screening test for the early detection of sickle cell anemia.


Journal

Talanta
ISSN: 1873-3573
Titre abrégé: Talanta
Pays: Netherlands
ID NLM: 2984816R

Informations de publication

Date de publication:
01 Nov 2020
Historique:
received: 10 02 2020
revised: 25 05 2020
accepted: 27 05 2020
entrez: 5 9 2020
pubmed: 6 9 2020
medline: 1 5 2021
Statut: ppublish

Résumé

In this study, the capability of thermogravimetry in conjuction with a multivariate statistical analysis, was investigated for the screening of Sickle Cell Anemia (SCA), a hereditary disorder of hemoglobin characterized by severe hemolytic anemia with different severe clinical manifestations. SCA results from a mutation in the sixth codon of the beta globin gene, which results in the substitution of glutamic acid for valine and leads to the production of an altered form of hemoglobin, hemoglobin S (HbS). People with this disorder have atypical hemoglobin molecules which tend to aggregate together and form filaments inside the red blood cells. These deformed red blood cells called half-moon or sickle, are rigid and unable to flow inside the small vessels, creating occlusions of the small circulation. Systematic screening for SCA is not a common practice, and diagnosis is usually made when a severe complication occurs. An early and rapid diagnosis is important for patients in order to prevent and treat the painful episodes that can occur when sickled red blood cells, which are stiff and inflexible, get stuck in small blood vessels. A novel test was developed using whole blood samples from patients with congenital defects and analyzed by the TG7 thermobalance (PerkinElmer) without any pretreatment. The resulting TG and DTG curves of blood samples were compared to those typical of healthy individuals and results demonstrated a different thermal behaviour of the anemic patients with respect to healthy individuals as result of the different amounts of water content and corpuscular fraction. The multivariate statistical analysis performed by chemometrics allowed a quick identification of differences between the two population and provided a model of prediction in patients with heterogeneous congenital hematological disorders. The predictive ability of the model was tested by processing patient affected by SCA and with a confirmed diagnosis obtained by the molecular analysis. The model provided for a sensitivity and an accuracy of a 100% and an error of prediction of about 0.1%.

Identifiants

pubmed: 32887134
pii: S0039-9140(20)30534-8
doi: 10.1016/j.talanta.2020.121243
pii:
doi:

Substances chimiques

Hemoglobin, Sickle 0
Hemoglobins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

121243

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Roberta Risoluti (R)

Department of Chemistry, Sapienza - University of Rome, Rome, Italy. Electronic address: roberta.risoluti@uniroma1.it.

Patrizia Caprari (P)

National Centre for the Control and Evaluation of Medicines, Istituto Superiore di Sanità, Rome, Italy.

Giuseppina Gullifa (G)

Department of Chemistry, Sapienza - University of Rome, Rome, Italy.

Sara Massimi (S)

National Centre for the Control and Evaluation of Medicines, Istituto Superiore di Sanità, Rome, Italy.

Francesco Sorrentino (F)

Thalassemia Unit, S. Eugenio Hospital, Rome, Italy.

Laura Maffei (L)

Thalassemia Unit, S. Eugenio Hospital, Rome, Italy.

Stefano Materazzi (S)

Department of Chemistry, Sapienza - University of Rome, Rome, Italy.

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Classifications MeSH