Literature DB >> 20132300

Evaluation of the genetic basis of phenotypic heterogeneity in north Indian patients with thalassemia major.

Nidhi Sharma1, Reena Das, Jasbir Kaur, Jasmina Ahluwalia, Amita Trehan, Deepak Bansal, Inusha Panigrahi, Ram Kumar Marwaha.   

Abstract

OBJECTIVES: To assess the molecular basis of phenotypic heterogeneity in north Indian patients with thalassemia major (TM).
METHODS: To determine the clinical severity, 130 patients of TM were studied for the age of first presentation and frequency of blood transfusion. The type of beta mutations, Xmn-1(G)gamma polymorphism and G6PD Mediterranean mutation was characterized. Analysis of the phenotypic presentation and the genotype was performed.
RESULTS: Majority (83.8%) presented before 1 year of age (mean 8.8 months). The caste distribution showed 41.6% were Aroras and 32.3% were migrants from Pakistan. IVS1-5(G-->C) was commonest (32.7%) and the common five Indian mutations comprised of 88.4% of alleles. The mean age of presentation with IVS1-5(G-->C), Fr 8/9, (+G) 619-bp del and IVS1-1(G-->T) homozygosity was 4.3, 6, 3.4 and 9.1 months respectively. Xmn-1(G)gamma status showed -/- in 66.9%, +/- in 26.1% and +/+ in 6.9% patients. Xmn-1(G)gamma-/- presented before 1 year of age. The mean age of presentation with +/+ was 18.3 months. Six hemizygous boys and one heterozygous girl with G6PD Mediterranean were found (prevalence 5.3%). Eight patients could be reclassified as thalassemia intermedia on follow up.
CONCLUSIONS: This study showed that majority of TM in north India present before 1 year of age and homozygous 619-bp deletion presents the earliest. The presence of Xmn-1(G)gamma polymorphism delays the presentation, is associated with the IVS 1-1 (G-->T) and shows variable improvement with hydroxyurea therapy. Based on the results of genotyping, reevaluation of patients can improve the outcome in a few patients.

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Year:  2010        PMID: 20132300     DOI: 10.1111/j.1600-0609.2010.01422.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  5 in total

1.  Impact of HFE-2 and HAMP Gene Variations on Iron Overload in Pediatric Patients with Non-Transfusion Dependent Thalassemia: A Pilot Study.

Authors:  Niteesh Bharadwaj; Srinivasan Peyam; Prateek Bhatia; Anmol Bhatia; Reena Das; Minu Singh; Deepak Bansal; Amita Trehan; Richa Jain
Journal:  Indian J Hematol Blood Transfus       Date:  2021-05-07       Impact factor: 0.900

Review 2.  Identification and key management of non-transfusion-dependent thalassaemia patients: not a rare but potentially under-recognised condition.

Authors:  Vip Viprakasit; Paul Tyan; Sarayuth Rodmai; Ali T Taher
Journal:  Orphanet J Rare Dis       Date:  2014-09-30       Impact factor: 4.123

3.  Prevalence of Xmnl Gγ polymorphism in Egyptian patients with β-thalassemia major.

Authors:  Azza A G Tantawy; Nevine G Andrawes; Amany Ismaeil; Solaf A Kamel; Wessam Emam
Journal:  Ann Saudi Med       Date:  2012 Sep-Oct       Impact factor: 1.526

Review 4.  Genomics of rare genetic diseases-experiences from India.

Authors:  Sridhar Sivasubbu; Vinod Scaria
Journal:  Hum Genomics       Date:  2019-09-25       Impact factor: 4.639

5.  The Effect of Xmn -1 Polymorphism and Coinheritance of Alpha Mutations on Age at First Blood Transfusion in Iranian Patients with Homozygote IVSI-5 Mutation.

Authors:  Mozhgan Hashemieh; Zahra Al Sadat Saadatmandi; Azita Azarkeivan; Hossein Najmabadi
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2022-01-01
  5 in total

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