CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease
Author:
Affiliation:
1. Universidade Federal de Juiz de Fora - Campus Governador Valadares, Brasil
2. Fundação Hemominas, Brasil
3. Faculdade de Ciências Médicas de Minas Gerais, Brasil
Publisher
FapUNIFESP (SciELO)
Link
http://www.scielo.br/scielo.php?script=sci_pdf&pid=S0100-879X2024000100601&tlng=en
Reference38 articles.
1. Mortality attributed to sickle cell disease in children and adolescents in Brazil, 2000-2019;do Nascimento MI;Rev Saude Publica,2022
2. Sickle cell disease;Kato GJ;Nat Rev,2018
3. Higher values of triglycerides:HDL-cholesterol ratio hallmark disease severity in children and adolescents with sickle cell anemia;Teixeira RS;Braz J Med Biol Res,2019
4. Altered HDL particle in sickle cell disease: Decreased cholesterol content is associated with hemolysis, whereas decreased Apolipoprotein A1 is linked to inflammation;Yalcinkaya A;Lipids Health Dis,2019
5. Associations between endothelial dysfunction and clinical and laboratory parameters in children and adolescents with sickle cell anemia;Teixeira RS;PLoS One,2017
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1. Plasma monomeric ApoA1 and high‐density lipoprotein bound ApoA1 are markedly decreased and associated with low levels of lipophilic antioxidants in sickle cell disease: A potential new pathway for therapy;European Journal of Haematology;2024-08-20
2. Association of thalassemia, hemoglobinopathies, and vitamin D levels with lipid profile in adults: Community-based research in southern Thai population;Heliyon;2024-05
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