Literature DB >> 18577791

Iron deficiency anaemia in sickle cell disorders in India.

D Mohanty1, M B Mukherjee, R B Colah, M Wadia, K Ghosh, G P Chottray, D Jain, Y Italia, K Ashokan, R Kaul, D K Shukla, V Muthuswamy.   

Abstract

BACKGROUND &
OBJECTIVE: Iron deficiency anaemia (IDA) is uncommon in individuals with sickle cell disease (SCD) because of availability of an adequate iron source potentially from increased red cell turnover and from blood transfusions. Also, iron deficiency anaemia can often go unnoticed because the sickle cell disease patients are already anaemic. Iron deficiency in sickle cell patients may result in lowering the intracellular haemoglobin concentration and this may ameliorate sickling. The present study was undertaken to determine the prevalence of iron deficiency anaemia and the response of iron supplementation in sickle cell disorders in tribal population of the four States viz. Maharashtra, Gujarat, Orissa and Tamil Nadu.
METHODS: A total of 8434 individuals (7105 AA, 1267 AS and 62 SS) were tested for zinc protoporphyrin/haem (ZPP/H) ratio and haemoglobin levels. Twenty two sickle cell anaemia (SS), 47 sickle cell trait (AS) and 150 normal control (AA) individuals who were iron deficient, were given iron therapy for a period of 12 wk and the laboratory investigations were repeated at the 13th wk.
RESULTS: Sixty seven per cent of subjects with sickle cell anaemia and 26 per cent with sickle cell trait had elevated ZPP/H ratios (>80 micromol/mol) as against 22.8 per cent of normal individuals. The elevated ZPP/H ratios is an indicator of microcytic anaemia of iron deficiency. Following iron therapy, an improvement in the Hb levels and ZPP/H ratios was observed in both sickle cell disorders and normal individual cases. INTERPRETATION &
CONCLUSION: This study suggests that iron deficiency anaemia is an important problem in Indian sickle cell anaemia patients and iron supplementation should be given only in proven cases of iron deficiency anaemia.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18577791

Source DB:  PubMed          Journal:  Indian J Med Res        ISSN: 0971-5916            Impact factor:   2.375


  21 in total

1.  Hematological, Biochemical Properties, and Clinical Correlates of Hemoglobin S Variant Disorder: A New Insight Into Sickle Cell Trait.

Authors:  Safaa A A Khaled; Heba A Ahmed; Mahmoud I Elbadry; Eman NasrEldin; Sahar M Hassany; Shimaa A Ahmed
Journal:  J Hematol       Date:  2022-06-27

2.  Variability of Iron Load in Patients of Sickle Cell Anaemia (HbSS): A study from Eastern India.

Authors:  Pranati Mohanty; Rabindra Kumar Jena; Sudha Sethy
Journal:  J Clin Diagn Res       Date:  2017-03-01

3.  Hematological profile of sickle cell disease from South Gujarat, India.

Authors:  Sanjeev Shyam Rao; Jagdish Prasad Goyal; S V Raghunath; Vijay B Shah
Journal:  Hematol Rep       Date:  2012-05-22

4.  The Role of Nutrition in Sickle Cell Disease.

Authors:  H I Hyacinth; B E Gee; J M Hibbert
Journal:  Nutr Metab Insights       Date:  2010-01-01

5.  Explaining anthropometric variations in sickle cell disease requires a multidimensional approach.

Authors:  Malay B Mukherjee; Kanjaksha Ghosh
Journal:  Indian J Hum Genet       Date:  2012-01

6.  Sickle cell disease in tribal populations in India.

Authors:  Roshan B Colah; Malay B Mukherjee; Snehal Martin; Kanjaksha Ghosh
Journal:  Indian J Med Res       Date:  2015-05       Impact factor: 2.375

7.  Iron Deficiency Anaemia among Pre-School Children with Sickle Cell Anaemia: Still a Rare Diagnosis?

Authors:  Samuel Olufemi Akodu; Omolara Adeolu Kehinde; Ijeoma Nnenna Diaku-Akinwumi; Olisamedua Fidelis Njokanma
Journal:  Mediterr J Hematol Infect Dis       Date:  2013-11-07       Impact factor: 2.576

8.  GDP versus ESHAP Regimen in Relapsed and/or Refractory Hodgkin lymphoma: A Comparison Study.

Authors:  Mani Ramzi; Aliraza Rezvani; Mehdi Dehghani
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2015-01-01

9.  Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State.

Authors:  Samuel Olufemi Akodu; Olisamedua Fidelis Njokanma; Omolara AdeoluKehinde
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2015-01-01

10.  Serum iron status of under-five children with sickle cell anaemia in lagos, Nigeria.

Authors:  S O Akodu; I N Diaku-Akinwumi; O A Kehinde; O F Njokanma
Journal:  Anemia       Date:  2013-10-31
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.