Title
Higher values of triglycerides:HDL-cholesterol ratio hallmark disease severity in children and adolescents with sickle cell anemia
Date Issued
2019
Access level
open access
Resource Type
journal article
Author(s)
Teixeira R.S.
Terse-Ramos R.
Ferreira T.A.
Machado V.R.
Rissatto-Lago M.R.
Silveira-Mattos P.S.
Boa-Sorte N.
Ladeia A.M.T.
Andrade B.B.
Instituto Gonçalo Moniz
Publisher(s)
Associacao Brasileira de Divulgacao Cientifica
Abstract
Dyslipidemia has been described in sickle cell anemia (SCA) but its association with increased disease severity is unknown. Here, we examined 55 children and adolescents with SCA as well as 41 healthy controls to test the association between the lipid profiles in peripheral blood and markers of hemolysis, inflammation, endothelial function, and SCA-related clinical outcomes. SCA patients exhibited lower levels of total cholesterol (Po0.001), low-density lipoprotein cholesterol (LDL-c) (Po0.001), and high-density lipoprotein cholesterol (HDL-c) (Po0.001), while displaying higher triglyceride (TG) levels and TG/ HDL-c ratio values (Po0.001). TG/HDL-c values were positively correlated with lactate dehydrogenase (P=0.047), leukocyte count (P=0.006), and blood flow velocity in the right (P=0.02) and left (P=0.05) cerebral artery, while being negatively correlated with hemoglobin levels (Po0.04). Acute chest syndrome (ACS) and vaso-occlusive events (VOE) were more frequent in SCA patients exhibiting higher TG/HDL-c values (odds ratio: 3.77, P=0.027). Multivariate logistic regression analysis confirmed independent associations between elevated TG/HDL-c values and SCA. Thus, children and adolescents with SCA exhibited a lipid profile associated with hemolysis and inflammatory parameters, with increased risk of ACS and VOE. TG/HDL-c is a potential biomarker of severity of disease.
Volume
52
Issue
10
Language
English
OCDE Knowledge area
EndocrinologĂ­a, Metabolismo (incluyendo diabetes, hormonas) PediatrĂ­a
Scopus EID
2-s2.0-85073413383
PubMed ID
Source
Brazilian Journal of Medical and Biological Research
ISSN of the container
1414431X
Sponsor(s)
The authors thank the Hematology and Hemotherapy Foundation of Bahia (HEMOBA) for the critical assistance in patient recruitment and evaluation. This work was supported by the Fundac??o de Amparo ? Pesquisa do Estado da Bahia (FAPESB) under the number 020/201 ? Research Program: Shared Health Management ? (PPSUS) of Bahia award number: EFP00006943. This study was also financed in part by Coordenac??o de Aperfeic?oamento de Pessoal de N?vel Superior (CAPES) (Finance Code 001). The work of B.B.A. was supported by a grant from NIH (U01AI115940). B.B.A. is a senior scientist of the Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico (CNPq), Brazil (Bolsa de Produtividade). M.B.A. and P.S.S.M. were supported by PhD fellowships from the Fundac??o de Amparo ? Pesquisa do Estado da Bahia (FAPESB).
Sources of information: Directorio de ProducciĂłn CientĂ­fica Scopus