Literature DB >> 20881411

Haptoglobin gene polymorphisms in sickle cell disease patients with different βS-globin gene haplotypes.

A D Adekile1, M Z Haider.   

Abstract

OBJECTIVE: To investigate the prevalence of haptoglobin (Hp) gene alleles in Kuwaiti sickle cell disease (SCD) patients, who generally have a mild phenotype, and compare the pattern to Nigerian SCD patients whose SCD phenotype is more severe. SUBJECTS AND METHODS: Hp genotyping was carried out in a group of 82 and 54 SCD patients from Kuwait and Nigeria, respectively, and appropriate Hb AA controls. The Hp genotyping was done using a PCR technique followed by agarose gel electrophoresis.
RESULTS: The frequency of the Hp-2 allele was 73.8% among Kuwaiti SCD patients, while the Hp-1 allele predominated among Nigerian patients (60.7%). However, the differences were not significant (p > 0.05) when the allele distributions were compared between Kuwaiti SCD and their AA counterparts or between Nigerian SCD and their AA controls. There was no association of Hp-2 allele with frequent vaso-occlusive crisis among the Kuwaiti SCD patients.
CONCLUSION: The distribution of Hp alleles appears to follow ethnic and geographical trends. Their role in the pathophysiology of pain crisis is not clear.
Copyright © 2010 S. Karger AG, Basel.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20881411     DOI: 10.1159/000320302

Source DB:  PubMed          Journal:  Med Princ Pract        ISSN: 1011-7571            Impact factor:   1.927


  7 in total

1.  Haptoglobin genotype predicts severe acute vaso-occlusive pain episodes in children with sickle cell anemia.

Authors:  Shaina M Willen; Joel Brennan McNeil; Mark Rodeghier; Vern Eric Kerchberger; Ciara M Shaver; Julie A Bastarache; Martin H Steinberg; Michael R DeBaun; Lorraine B Ware
Journal:  Am J Hematol       Date:  2020-01-30       Impact factor: 13.265

2.  Prevalence and Determinants of Anemia and Iron Deficiency in Kuwait.

Authors:  Sameer Al Zenki; Husam Alomirah; Suad Al Hooti; Nawal Al Hamad; Robert T Jackson; Aravinda Rao; Nasser Al Jahmah; Ina'am Al Obaid; Jameela Al Ghanim; Mona Al Somaie; Sahar Zaghloul; Amani Al Othman
Journal:  Int J Environ Res Public Health       Date:  2015-07-31       Impact factor: 3.390

3.  Haptoglobin gene polymorphisms and interleukin-6 and -8 levels in patients with sickle cell anemia.

Authors:  Bruna Spinella Pierrot-Gallo; Perla Vicari; Sandra Satiko Matsuda; Samuel Ademola Adegoke; Grazielle Mecabo; Maria Stella Figueiredo
Journal:  Rev Bras Hematol Hemoter       Date:  2015-07-31

4.  Haptoglobin Gene Polymorphism in Patients with Sickle Cell Anemia: Findings from a Nigerian Cohort Study.

Authors:  Oladele Simeon Olatunya; Dulcineia Martins Albuquerque; Magnun Nueldo Nunes Santos; Tolorunju Segun Kayode; Adekunle Adekile; Fernando Ferreira Costa
Journal:  Appl Clin Genet       Date:  2020-05-08

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

Authors:  Christian Bernard Kengne Fotsing; Constant Anatole Pieme; Prosper Cabral Biapa Nya; Jean Paul Chedjou; Solange Dabou; Carine Nguemeni; Georges Teto; Wilfred Fon Mbacham; Donatien Gatsing
Journal:  Health Sci Rep       Date:  2022-01-21

6.  Haptoglobin: an emerging candidate for phenotypic modulation of sickle cell anemia?

Authors:  Magnun Nueldo Nunes Dos Santos
Journal:  Rev Bras Hematol Hemoter       Date:  2015-10-09

Review 7.  Influence of Haptoglobin Polymorphism on Stroke in Sickle Cell Disease Patients.

Authors:  Olivia Edwards; Alicia Burris; Josh Lua; Diana J Wilkie; Miriam O Ezenwa; Sylvain Doré
Journal:  Genes (Basel)       Date:  2022-01-14       Impact factor: 4.096

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.