Literature DB >> 30221402

Laboratory diagnosis for thalassemia intermedia: Are we there yet?

Saqib Ansari1,2, Nabil Rashid2, Anny Hanifa1, Saima Siddiqui1, Bushra Kaleem2, Arshi Naz2, Kousar Perveen2, Zeeshan Hussain1, Iqra Ansari2, Qammar Jabbar2, Tahir Khan2, Muhammad Nadeem2, Tahir Shamsi1,2.   

Abstract

BACKGROUND: Differentiation between thalassemia major and thalassemia intermedia at presentation is not uniformly characterized, for which an absolute criteria needs to be developed. This study investigated the primary and secondary genetic modifiers to develop a laboratory finding by forming different genetic mutational combinations seen among thalassemia intermedia patients and comparing them with thalassemia major.
METHODS: This cross-sectional study analyzed 315 thalassemia intermedia patients. One hundred and five thalassemia major patients were recruited on the basis of documented evidence of diagnosis and were receiving blood transfusion therapy regularly. Various mutational combinations were identified, and comparison was performed between thalassemia intermedia and major using statistical software STATA 11.1.
RESULTS: The mean age of the total population was 5.9 ± 5.32 years of which 165 (52%) were males. Of the two groups (thalassemia intermedia and thalassemia major), IVSI-5, IVSI-1, and Fr 8-9 were more prevalent among the thalassemia intermedia cohort. When comparison was performed between the thalassemia intermedia and thalassemia major patients, it showed significant results for the presence of Xmn-1 polymorphism.
CONCLUSION: The presence of IVSI-5 homozygous with Xmn-1, IVSI-5 heterozygous with Xmn-1, Cd 30 homozygous with or without Xmn-1 and IVSI-1 homozygous or heterozygous either with or without Xmn-1 prove to be strong indicators towards diagnosis of thalassemia intermedia.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  Xmn1 polymorphism; genetic modifiers; genetic mutational combinations; product transfusion; thalassemia

Mesh:

Year:  2018        PMID: 30221402      PMCID: PMC6430353          DOI: 10.1002/jcla.22647

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


  23 in total

Review 1.  β-thalassemia intermedia: a clinical perspective.

Authors:  Khaled M Musallam; Ali T Taher; Eliezer A Rachmilewitz
Journal:  Cold Spring Harb Perspect Med       Date:  2012-07       Impact factor: 6.915

Review 2.  Beta-thalassemia.

Authors:  Deborah Rund; Eliezer Rachmilewitz
Journal:  N Engl J Med       Date:  2005-09-15       Impact factor: 91.245

3.  Pathophysiology of beta thalassemia--a guide to molecular therapies.

Authors:  Swee Lay Thein
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2005

4.  New approaches to the transfusion management of thalassemia.

Authors:  R D Propper; L N Button; D G Nathan
Journal:  Blood       Date:  1980-01       Impact factor: 22.113

5.  Molecular characterization of beta-thalassemia in Pakistan.

Authors:  S N Khan; S Riazuddin
Journal:  Hemoglobin       Date:  1998-07       Impact factor: 0.849

Review 6.  Beta-thalassemia.

Authors:  Renzo Galanello; Raffaella Origa
Journal:  Orphanet J Rare Dis       Date:  2010-05-21       Impact factor: 4.123

7.  Beta-thalassemia intermedia from southern Iran: IVS-II-1 (G-->A) is the prevalent thalassemia intermedia allele.

Authors:  Mehran Karimi; Hooman Yarmohammadi; Shirin Farjadian; Sirus Zeinali; Zahra Moghaddam; Maria D Cappellini; Piero C Giordano
Journal:  Hemoglobin       Date:  2002-05       Impact factor: 0.849

8.  Thalassaemia intermedia: an update.

Authors:  Ali T Taher; Khaled M Musallam; Maria D Cappellini
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-08-29       Impact factor: 2.576

Review 9.  Beta-thalassemia.

Authors:  Antonio Cao; Renzo Galanello
Journal:  Genet Med       Date:  2010-02       Impact factor: 8.822

Review 10.  Transfusion-transmitted infections.

Authors:  Florian Bihl; Damiano Castelli; Francesco Marincola; Roger Y Dodd; Christian Brander
Journal:  J Transl Med       Date:  2007-06-06       Impact factor: 5.531

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  1 in total

1.  Laboratory diagnosis for thalassemia intermedia: Are we there yet?

Authors:  Saqib Ansari; Nabil Rashid; Anny Hanifa; Saima Siddiqui; Bushra Kaleem; Arshi Naz; Kousar Perveen; Zeeshan Hussain; Iqra Ansari; Qammar Jabbar; Tahir Khan; Muhammad Nadeem; Tahir Shamsi
Journal:  J Clin Lab Anal       Date:  2018-09-17       Impact factor: 2.352

  1 in total

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