Literature DB >> 23105478

Pro-oxidant and anti-oxidant status in patients of sickle cell anaemia.

Jyoti Titus1, Suresh Chari, Madhur Gupta, Nitin Parekh.   

Abstract

The role of oxidant damage to red cells in sickle cell anaemia has been of interest in recent years. Although, available reports suggest that sickle cell erythrocytes are susceptible to endogenous free radical mediated oxidant damage there remains discrepancy in the status of antioxidant enzymes and antioxidant vitamins in these patients. In view of this, 107 cases of sickle cell anaemia (36 'SS' and 71 'AS' pattern-as confirmed by haemoglobin electrophoresis) were subjected to analysis of malondialdehyde, ascorbic acid, superoxide dismutase and albumin. The results were compared with 54 age and sex matched healthy controls. The results indicate a marked increase in lipid peroxidation and superoxide dismutase levels in both 'SS' and 'AS' types of sickle cell anaemia as compared to controls. Although no difference was observed in the levels of albumin in these groups the levels of ascorbic acid were significantly depleted in sickle cell anaemia patients. The results are indicative of enhanced lipid peroxidation along with imbalance in the pro-oxidant and antioxidant status in patients of sickle cell anaemia.

Entities:  

Keywords:  Pro-oxidant; antioxidant enzymes; antioxidant vitamins; sickle cell anaemia

Year:  2004        PMID: 23105478      PMCID: PMC3454190          DOI: 10.1007/BF02894279

Source DB:  PubMed          Journal:  Indian J Clin Biochem        ISSN: 0970-1915


  20 in total

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Review 2.  The sickle erythrocyte in double jeopardy: autoxidation and iron decompartmentalization.

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Journal:  Biochem J       Date:  1986-07-01       Impact factor: 3.857

9.  Blood pressure, hematologic and erythrocyte fragility changes in children suffering from sickle cell anemia following ascorbic acid supplementation.

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Journal:  J Trop Pediatr       Date:  2002-12       Impact factor: 1.165

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  11 in total

1.  A review of clinical profile in sickle cell traits.

Authors:  Nitin John
Journal:  Oman Med J       Date:  2010-01

2.  Increased oxidative stress alters nucleosides metabolite levels in sickle cell anemia.

Authors:  Lívia Gelain Castilhos; Juliana Sorraila de Oliveira; Stephen Adeniyi Adefegha; Luana Pereira Magni; Pedro Henrique Doleski; Fatima Husein Abdalla; Cínthia Melazzo de Andrade; Daniela Bitencourt Rosa Leal
Journal:  Redox Rep       Date:  2017-02-16       Impact factor: 4.412

3.  Association of Inflammatory Biomarker C-Reactive Protein, Lipid Peroxidation and Antioxidant Capacity Marker with HbF Level in Sickle Cell Disease Patients from Chattisgarh.

Authors:  Sanjana Bhagat; Pradeep Kumar Patra; Amar Singh Thakur
Journal:  Indian J Clin Biochem       Date:  2012-06-14

4.  Evaluation of Serum Zinc and Antioxidant Vitamins in Adolescent Homozygous Sickle Cell Patients in Wardha, District of Central India.

Authors:  Rina Raibhan Wasnik; Nilkanth Ramji Akarte
Journal:  J Clin Diagn Res       Date:  2017-08-01

5.  Gum Arabic as novel anti-oxidant agent in sickle cell anemia, phase II trial.

Authors:  Lamis Kaddam; Imad Fadl-Elmula; Omer Ali Eisawi; Haydar Awad Abdelrazig; Mohammed Abdelraman Salih; Florian Lang; Amal M Saeed
Journal:  BMC Hematol       Date:  2017-03-16

6.  Assessment of some indicators of oxidative stress in nigerian sickle cell anemic patients.

Authors:  C P Okorie; Theresa Nwagha; Fidelis Ejezie
Journal:  Ann Afr Med       Date:  2018 Jan-Mar

7.  The effect of xanthine oxidase and hypoxanthine on the permeability of red cells from patients with sickle cell anemia.

Authors:  Halima W M Al Balushi; David C Rees; John N Brewin; Anke Hannemann; John S Gibson
Journal:  Physiol Rep       Date:  2018-03

8.  Acacia Senegal (Gum Arabic) Supplementation Modulate Lipid Profile and Ameliorated Dyslipidemia among Sickle Cell Anemia Patients.

Authors:  Lamis Kaddam; Imad Fadl-Elmula; Omer Ali Eisawi; Haydar Awad Abdelrazig; Amal M Saeed
Journal:  J Lipids       Date:  2019-06-18

9.  Correlation of low levels of nitrite and high levels of fetal hemoglobin in patients with sickle cell disease at baseline.

Authors:  Darcielle Bruna Dias Elias; Lilianne Brito da Silva Rocha; Maritza Barbosa Cavalcante; Alano Martins Pedrosa; Izabel Cristina Bandeira Justino; Romélia Pinheiro Gonçalves
Journal:  Rev Bras Hematol Hemoter       Date:  2012

10.  Oxidative profile of sickle cell patients in a Cameroonian urban hospital.

Authors:  Vicky Jocelyne Ama Moor; Constant Anatole Pieme; Bernard Chetcha Chemegne; Helene Manonji; Borgia Legrand Njinkio Nono; Corine Tchoula Mamiafo; Bruno Moukette Moukette; Francine Tankeu Nzufo; Asonganyi Tazoacha
Journal:  BMC Clin Pathol       Date:  2016-09-21
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