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Hematological profile of sickle cell disease in central India

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Abstract

Hematological profile of homozygous sickle cell disease patients attending RHDMC from Central India is presented. Central India has a huge population of sickle cell disease patients. Though predicted SS in the region is 22–44 %, 81 homozygous of sickle cell patients reported during study period of Jan 2003–Dec 2005. The clinical course of these patients is characterized in most of the cases by relatively long period without any symptoms punctuated by acute clinical events. Hematological profile of these 81 patients with age ranging from 6 month to 64 years is presented. There are 44 males and 37 females with an average age of 14.55yrs in males and 18.13 yrs females. Males out number females in pediatric age group where as females with SCD are attending hospital more in reproductive age group. Very few patients are reported after the age of 30 yrs. Average hemoglobin in males is 7.11 ± 2.13 gms/dl and in females 6.75 ± 1.85 gms/dl with parallel low RBC count.Hemoglobin rise is seen after 14 years of age in males and females. Age related rise in MCV is more noted in females after the age of 5 as compared to males. No age or sex related difference was seen in MCHC values. Hb A2 levels for males is 2.13 ± 0.95% and for females 2.04 ± 0.91 %.Hb F in males is 19.58 + 5.86% and in females is 20.99 + 4.9%. There is no age and sex related difference in Hb F levels. Moderate to severe anemia with high Hb F dominate Central Indian sickle cell disease patient’s hematological profile. The hematological profile in Central India is similar to the profile in other parts of India and Saudi Arabia but different from Jamaica and Africa.

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Abbreviations

ANC:

Ante natal clinic

F:

female

Hb:

Hemoglobin

HbA2 :

Hemoglobin A2

Hb Ep:

Hemoglobin electrophoresis

HbF:

Fetal hemoglobin

HbS:

Sickle hemoglobin

HPLC:

High performance liquid chromatography

IGGMC:

Indira Gandhi Government Medical College

M:

male

MCHC:

Mean corpuscular hemoglobin concentration

MCV:

Mean corpuscular volume

OPD:

Out patient department

RBC:

Red blood cell

RHDMC:

Regional hemoglobinopathy detection and management centre

SCD:

Sickle cell disease

References

  1. Mohanty D and Pathare AV (1998) Sickle cell Anemia — the Indian scenario. Indian J. Hematol Blood Transfus 16(1–1): 1–2

    Google Scholar 

  2. Solanki BR, Shukla RN (1958) Sickle cell trait in Central India Lancet 1:297

    Google Scholar 

  3. Kar BC, Satapathy RK, Kulozik M, Sirr S, Serjeant BE, Serjeant GR. (1986) Sickle cell disease in Orissa state, India. Lancet ii, 1198–1201

    Article  Google Scholar 

  4. Roy B, Dey B, Balgir RS, Dash BP, Chakraborty M, Bhattacharya SK, Banerjee S, Roy M, Majumder PP. (1996) Identification of sickle cell homozygotes using haematological parameters. J Indian Anthrop Soc 31:191–199

    Google Scholar 

  5. Kaur M, Das GP, Verma IC. (1997) Sickle cell trait and disease among tribal communities in Orissa, Madhya Pradesh and Kerala. Indian J Med Res 105:111–116

    PubMed  CAS  Google Scholar 

  6. Hayes RJ, Beckford M, Grandison Y, Mason K, Serjeant BE, Serjeant GR. (1985) The haematology of steady state homozygous sickle cell disease: frequency distributions, variation with age and sex, longitudinal observations. 59:369–382

    CAS  Google Scholar 

  7. Wong YW, Elliott-Mills D, Powars D. (1996) Renal failure in sickle cell anaemia. Haematol Oncol Clinics of N Am 10: 1321–1331

    Article  CAS  Google Scholar 

  8. Lundh B, Gadner FH. (1970) The haematologic response to androgens in sickle cell anaemia. Scandanavian J Hematol 7:389–397

    CAS  Google Scholar 

  9. Sklar AH, Campbell H, Ccaruana RJ, Ligjtfoot BO, Gaier JG, Milner P. (1990) A population study of renal function in sickle cell anaemia. Internatl J Artific Organs 13: 231–236

    CAS  Google Scholar 

  10. De Ceulaer K, Higgs DR, Weatherall DJ, Hayes RJ, Serjeant BE, Serjeant GR. (1983) A — thalassaemia reduces the haemolytic rate in homozygous sickle cell disease. N Engl J Med 309:189–190

    Article  PubMed  Google Scholar 

  11. Serjeant GR, Serjeant BE (1983) sickle cell disease. 3rd ed. Jamaica: Oxford university press year: 430–431

    Google Scholar 

  12. Rucknagel DL, Hanash SH, Sing CF, Winter WP, Whitten CF, Prasad AS. (1979) Age and sex effect on haemoglobin F in sickle cell anemia In Stamatouannopoulos G, and Nienhuis AW. cellular and molecular regulation of haemoglobin switching; Grune and Stratton, New York pp 107–118

    Google Scholar 

  13. Serjeant GR, (1975) Fetal haemoglobin in homozygous sickle cell disease. Clinics in Haematol 4:109–122

    CAS  Google Scholar 

  14. Mason KP, Grandison Y, Hayes RJ, Serjeant BE, Serjeant GR, Vaidya S, Wood WG. (1982) Postnatal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parental HbF levels. British J Haematol 52:455–463

    Article  CAS  Google Scholar 

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Correspondence to A. V. Shrikhande.

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Shrikhande, A.V., Dani, A.A., Tijare, J.R. et al. Hematological profile of sickle cell disease in central India. Indian J Hematol Blood Transfus 23, 92–98 (2007). https://doi.org/10.1007/s12288-008-0005-z

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