Relation between haptoglobin polymorphism and oxidative stress status, lipid profile, and cardiovascular risk in sickle cell anemia patients-Reference-Cited by-同舟云学术

Relation between haptoglobin polymorphism and oxidative stress status, lipid profile, and cardiovascular risk in sickle cell anemia patients

Published:2022-01 Issue:1 Volume:5 Page:
ISSN:2398-8835
Container-title:Health Science Reports
language:en
Short-container-title:Health Science Reports

Author:

Kengne Fotsing Christian Bernard¹²^ORCID,Pieme Constant Anatole³,Biapa Nya Prosper Cabral²^ORCID,Chedjou Jean Paul⁴,Dabou Solange¹,Nguemeni Carine⁵,Teto Georges⁶,Mbacham Wilfred Fon⁴,Gatsing Donatien¹

Affiliation:

1. Research Unit of Microbiology and Antimicrobial Substances, Department of Biochemistry, Faculty of Science University of Dschang Dschang Cameroon

2. Research Unit of Biochemistry of Medicinal Plants, Food Science and Nutrition, Department of Biochemistry, Faculty of Science University of Dschang Dschang Cameroon

3. Laboratory of Biochemistry, Department of Biochemistry and Physiological Science, Faculty of Medicine and Biomedical Science University of Yaounde I Yaounde Cameroon

4. Laboratory for Public Health Research Biotechnology, Department of Biochemistry University of Yaounde I Yaounde Cameroon

5. Department of Neurology University Hospital of Würzburg Würzburg Germany

6. Centre International de Recherche Chantal Biya Yaounde Cameroon

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hsr2.465

Reference57 articles.

1. Haptoglobin Genotype Is a Determinant of Hemoglobin Adducts and Vitamin E Content in HDL

2. Haptoglobin Gene Polymorphisms in Sickle Cell Disease Patients with Different β^S-Globin Gene Haplotypes

3. Lipid levels in sickle-cell disease associated with haemolytic severity, vascular dysfunction and pulmonary hypertension

4. Hemolysis and free hemoglobin revisited: exploring hemoglobin and hemin scavengers as a novel class of therapeutic proteins

5. Endothelial dysfunction inhibits the ability of haptoglobin to prevent hemoglobin-induced hypertension

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1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18

2. Influence of Haptoglobin and Hemoglobin Phenotypic Polymorphisms on Sickle Cell Disease Morbidity;Advances in Biological Chemistry;2023

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