Literature DB >> 15645468

Beta-thalassaemia carrier detection by ELISA: a simple screening strategy for developing countries.

M Shyla Ravindran1, Zareen M Patel, M Ikram Khatkhatay, S P Dandekar.   

Abstract

The frequency of beta-thalassaemia in India ranges from 3.5% to 15% in the general population and of the 100,000 children born with thalassaemia major in the world, 10,000 are in India alone. Affected children do not die immediately, but treatment by regular transfusion is costly and leads to iron overload and death. Therefore, health services in lower-economic countries can sustain patients only if the numbers can be limited. Detecting carrier couples by simple blood test can prevent thalassaemia and at-risk couples can be identified and informed of their genetic risk before having children. A prevention programme including population screening, counselling, and prenatal diagnosis will markedly reduce the birth prevalence of affected individuals. Hemoglobin A2 (HbA2) measurement in human hemolysates has great significance, since its level can indicate beta-thalassaemia carrier status in otherwise healthy individuals. We have developed a rapid, simple, and inexpensive enzyme linked immunosorbent assay (ELISA) for the quantitation of HbA2, which can be used in carrier screening programmes in developing countries like India. In a limited trial for beta-thalassaemia carrier screening, the results obtained with ELISAs were compared with those obtained with the microcolumn chromatography method (r = 0.89). Copyright 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15645468      PMCID: PMC6807968          DOI: 10.1002/jcla.20050

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   2.352


  6 in total

Review 1.  Carrier screening and prenatal diagnosis of beta-thalassemia.

Authors:  M Maheshwari; S Arora; M Kabra; P S Menon
Journal:  Indian Pediatr       Date:  1999-11       Impact factor: 1.411

2.  Enzyme-linked immunosorbent assay, Elisa. 3. Quantitation of specific antibodies by enzyme-labeled anti-immunoglobulin in antigen-coated tubes.

Authors:  E Engvall; P Perlmann
Journal:  J Immunol       Date:  1972-07       Impact factor: 5.422

3.  Studies on the heterogeneity of hemoglobin. IX. The use of Tris(hydroxymethyl)aminomethanehcl buffers in the anion-exchange chromatography of hemoglobins.

Authors:  T H Huisman; A M Dozy
Journal:  J Chromatogr       Date:  1965-07

4.  Identification and quantitation of sickle cell hemoglobin with an enzyme-linked immunosorbent assay (ELISA).

Authors:  H E Grenett; F A Garver
Journal:  J Lab Clin Med       Date:  1980-10

5.  Inherited haemoglobin disorders: an increasing global health problem.

Authors:  D J Weatherall; J B Clegg
Journal:  Bull World Health Organ       Date:  2001-10-24       Impact factor: 9.408

6.  Development and validation of an ELISA for hemoglobin-A2: a novel method for beta-thalassemia screening in developing countries.

Authors:  Shyla R Menon; M Ikram Khatkhatay; Sucheta P Dandekar; Zarine M Patel
Journal:  J Immunoassay Immunochem       Date:  2004
  6 in total
  1 in total

Review 1.  Past, present & future scenario of thalassaemic care & control in India.

Authors:  Ishwar C Verma; Renu Saxena; Sudha Kohli
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

  1 in total

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