Maternal solubility test and high performance liquid chromatography of newborns in combination as a better neonatal screening protocol for sickle cell disease

  • Dr. Sharja Phuljhele Professor, Department of Paediatrics, Pt. J. N. M. Medical Raipur, Chhattisgarh, India
  • Dr. K. Ramnani Assistant Professor, Department of Pediatrics, Pt. J. N. M. Medical Raipur, Chhattisgarh, India
  • Dr. S. Hiwale Associate Professor, Department of Biochemistry, Pt. J. N. M. Medical Raipur, Chhattisgarh, India
  • Dr. Priyanka Pruthviraj Ramteke Postgraduate fellow, Department of Pediatrics, Pt. J. N. M. Medical Raipur, Chhattisgarh, India
Keywords: High Performance Liquid Chromatography, Sickle Cell Disease, Solubility Test

Abstract

Introduction: The incidence and prevalence of sickle cell disease in India is high and they are major health problem in India. Neonatal detection and prophylactic management can reduce morbidity and mortality in childhood. A study is therefore planned for analyzing maternal solubility test and HPLC of newborn as effective screening protocol.

Material and Method: The infants born of solubility positive mothers were taken for hemoglobin analysis using Biorad Hemoglobin variant by high performance liquid chromatography (HPLC) at birth and the test was repeated at six months of age. Data were analyzed using appropriate statistical method.

Results: A total of 100 mothers were positive on solubility test, their infants underwent Hb analysis by high performance liquid chromatography. 74 infants shows normal hemoglobin variants while 19 were heterozygous for Hbs (sickle cell trait) and 7 babies were homozygous for HbS at birth. On follow up at 6 month of age cases were reanalyzed by HPLC , 12 cases were lost in follow up, 7 cases who were heterozygous for sickle cell turned out to be homozygous for sickle cell, and of those with normal reports 7 cases were homozygous.

Conclusion: Maternal solubility test and HPLC of newborn at birth is good screening protocol for sickle cell anemia

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References

1. James V.Neel. The inheritance of sickle cell anemia. Science1949; Volume 110: 64.

2. Ingram VM. A specific chemical difference between the globin of normal human and sickle cell anemia. Hb Nature 1956; 178: 792-794.

3. Dr. James B.Herrick. Peculiar elongated and sickled shaped RBC in peripheral smear of American Negros. Arch Int Med 1910; 6:57:517-521.

4. Lehman and Cutbush. Sickle cell trait in southern India. M Brit Med.J. 1952 Feb; 1: 404.

5. Bernardette Modell, Matthew Darlison. Global epidemiology of hemoglobin disorders and derived service indicators. Bull World Health Organ June 2008 Vol.86n.6Geneva .

6. Elisa Ballardini, Anna Tarocco, Maria Marsella, Roberto Bernerdoni, Gianni Carandina, Claudia Melandri, et al. Univeral neonatal screening for sickle cell disease in Ferrara, Italy. Blood Tranfus. 2013 Apr; 11(2): 245-249.

7. Agrawal MB. The burden of hemoglobinopathies in India- time to wake up. J Assoc Physicians India2005; 53: 1017-1078.

8. Pradip K. Patra ,Virander S. Chauhan et al. screening for sickle cell gene in Chhattisgarh state, India; an approach to major publichealth problem . j. community Genet 2011 Sept; 2(3): 147-151.doi 10. 1007/s 12687-011-0050-4.

9. Sapna Thakur, Ravindra Sharma and Sharda Nandan Raw. Incidence of Thalassemia and Sickle Cell Disease in Chhattisgarh, Central India: Using Hardy-Weinberg Equations. J Mol Genet Med 2015; 9(1): 1-5.

10. Dipty L. Jain, Vijaya Sarathi, Dipty Upadhye, Rohini Gulhane, Anita H. Nadkarni, Kanjaksha Ghosh, and Roshan B. Colah. Newborn Screening Shows High Incidence of Sickle Cell Anemia in Central India. Hemoglobin 2012; 36(4) : 316-322.

11. J.Watson . A study of sickling of young erythrocytes in sickle cell anemia . Blood 1948; 3: 465-469.

12. Sumanta Panigrahi, Pradeep Kumar Patra, Prafulla Kumar Khodiar. Neonatal Screening of Sickle Cell Anemia: A Preliminary Report. Indian J Pediatr June 2012 ; 79(6): 747-750.

13. Nancy Robitaille,Edgard E Delvin, Heather A Hume. Newborn screening for sickle cell disease : A 1983-2003 Quebec experience. Journal of pediatric child health 2006 Apr; 11(4): 223- 227.

14. N Adjaye, B J Bain, P Steer et al (1983-1986) . Prediction and diagnosis of sickling disorder in neonates at London. Archives of disease in childhood 1989; 64: 39-43.

15. Renee V.Gardner, Alan Keitt. University of Florida sickle cell screening program for neonates : design and results. J National Med Asso. 1988 mar; 80(3): 2753.

16. Pradeep K. Patra, Tripathi sumit, Khodiar Prafulla, Sablania Pravin ,Keshari JR, Dalla A.R., Epidemiology of sickle cell disease in Chattisgarh. Indian Journal of Public Health Reaserch and Development 2010; 1(2): 64-68.
Maternal solubility test and high performance liquid chromatography of newborns in combination as a better neonatal screening protocol for sickle cell disease
CITATION
DOI: 10.17511/ijmrr.2016.i06.23
Published: 2016-06-30
How to Cite
1.
Phuljhele S, Ramnani K, Hiwale S, Pruthviraj Ramteke P. Maternal solubility test and high performance liquid chromatography of newborns in combination as a better neonatal screening protocol for sickle cell disease. Int J Med Res Rev [Internet]. 2016Jun.30 [cited 2024Nov.8];4(6):999-1004. Available from: https://ijmrr.medresearch.in/index.php/ijmrr/article/view/594
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Original Article