Literature DB >> 25842370

Severity of Brazilian sickle cell disease patients: severity scores and feasibility of the Bayesian network model use.

Edis Belini Junior1, Danilo Grünig Humberto Silva2, Lidiane de Souza Torres2, Jéssika Viviani Okumura2, Clarisse Lopes de Castro Lobo3, Claudia Regina Bonini-Domingos2.   

Abstract

The integration of the several clinical and laboratory dimensions and the influence of each parameter on the sickle cell disease (SCD)-related mortality is useful for predicting the phenotype of an individual. This study evaluated the feasibility of the SCD severity calculator use to measure disease severity in Brazilian patients. The study group was composed of 500 SCD patients (440 HbSS and 60 HbSC) diagnosed by molecular biology. We observed a decrease in severity scores in 72 SCD patients assessed before and after the hydroxyurea (HU) use. Furthermore, the HU influenced the increase of mean corpuscular volume (MCV) and HbF concentration, and the decrease of leukocytes and total bilirubin. We found 180 (36.0%) patients with intermediate phenotype, 170 (34.0%) mild phenotype and 150 (30.0%) with severe phenotype. Patients with ages >40 years had higher mean score (0.778±0.177) than patients between 18 and 40 years (0.562±0.152) and patients between 5 and 17 years (0.322±0.145). We observe that there is a tendency of individuals with leg ulcers, avascular necrosis and cardiac complications with increasing age. Correlation analysis showed relations between severity scores with leukocytes, reticulocytes, bilirubin, lactate dehydrogenase, HbS, hemoglobin and hematocrit (p<0.05). Several comparisons involving age groups, SCD genotype and phenotypic classification had satisfactory results and this classification will be used for future studies involving genetic polymorphisms, response to treatment with HU and oxidative stress markers in SCD.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hemoglobin S; Hydroxyurea; Sickle cell anemia

Mesh:

Substances:

Year:  2015        PMID: 25842370     DOI: 10.1016/j.bcmd.2015.01.011

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  9 in total

1.  Association between renal function parameters, clinical severity score and mortality risk among adult Sudanese sickle anemia patients.

Authors:  Mohamed Ao Suliman; Alnazeer Ma Hassan; Lamis A Kaddam
Journal:  Am J Blood Res       Date:  2020-12-15

2.  Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients.

Authors:  Gabriela Queila de Carvalho-Siqueira; Galina Ananina; Bruno Batista de Souza; Murilo Guimarães Borges; Mirta Tomie Ito; Sueli Matilde da Silva-Costa; Igor de Farias Domingos; Diego Arruda Falcão; Iscia Lopes-Cendes; Marcos André Cavalcanti Bezerra; Aderson da Silva Araújo; Antônio Roberto Lucena-Araújo; Marilda de Souza Gonçalves; Sara Teresinha Olalla Saad; Fernando Ferreira Costa; Mônica Barbosa de Melo
Journal:  Exp Biol Med (Maywood)       Date:  2019-05-12

3.  Development of a New Adult Sickle Cell Disease Center Within an Academic Cancer Center: Impact on Hospital Utilization Patterns and Care Quality.

Authors:  Biree Andemariam; Sasia Jones
Journal:  J Racial Ethn Health Disparities       Date:  2015-07-21

4.  Prevalence and Predictive Factors for Leg Ulcers in Sickle Cell Disease Patients in Saudi Arabia: A Cross-Sectional Observational Study.

Authors:  Feroze Kaliyadan; Ahmed Z Alkhars; Alreem A Albaqshi; Hajar M AlHajri; Norah K Albaqshi; Rawan M Aldihnayn; Zainab Y Almarzooq
Journal:  Cureus       Date:  2020-10-31

5.  Sickle cell disease in the era of precision medicine: looking to the future.

Authors:  Martin H Steinberg; Sara Kumar; George J Murphy; Kim Vanuytsel
Journal:  Expert Rev Precis Med Drug Dev       Date:  2019-11-07

6.  Economic burden of sickle cell disease in Brazil.

Authors:  Ana Cristina Silva-Pinto; Fernando F Costa; Sandra Fatima Menosi Gualandro; Patricia Belintani Blum Fonseca; Carmela Maggiuzzu Grindler; Homero C R Souza Filho; Carolina Tosin Bueno; Rodolfo D Cançado
Journal:  PLoS One       Date:  2022-06-16       Impact factor: 3.752

Review 7.  Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.

Authors:  Alawi Habara; Martin H Steinberg
Journal:  Exp Biol Med (Maywood)       Date:  2016-03-01

8.  Biomarker signatures of sickle cell disease severity.

Authors:  Mengtian Du; Sarah Van Ness; Victor Gordeuk; Sayed M Nouraie; Sergei Nekhai; Mark Gladwin; Martin H Steinberg; Paola Sebastiani
Journal:  Blood Cells Mol Dis       Date:  2018-05-16       Impact factor: 3.039

9.  Sickle Cell Anemia Patients Display an Intricate Cellular and Serum Biomarker Network Highlighted by TCD4+CD69+ Lymphocytes, IL-17/MIP-1β, IL-12/VEGF, and IL-10/IP-10 Axis.

Authors:  Nadja Pinto Garcia; Alexander Leonardo S Júnior; Geyse Adriana S Soares; Thainá Cristina C Costa; Alicia Patrine C Dos Santos; Allyson Guimarães Costa; Andréa Monteiro Tarragô; Rejane Nina Martins; Flávia do Carmo Leão Pontes; Emerson Garcia de Almeida; Erich Vinícius de Paula; Olindo Assis Martins-Filho; Adriana Malheiro
Journal:  J Immunol Res       Date:  2020-01-08       Impact factor: 4.818

  9 in total

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