Literature DB >> 12353305

Molecular analysis of beta-thalassemia in South Vietnam.

Saovaros Svasti1, Tran Minh Hieu, Thongperm Munkongdee, Pranee Winichagoon, Tran Van Be, Tran Van Binh, Suthat Fucharoen.   

Abstract

In Vietnam, the carrier rate for beta-thalassemia varies from 1.5% to 25% depending on the ethnic groups of the population. The molecular basis of beta-thalassemia in South Vietnam was studied in 50 unrelated beta-thalassemia patients. Of these, 31 had beta-thalassemia/Hb E, 18 were homozygous for beta-thalassemia, and 1 carried the beta-thalassemia trait. The majority of the patients were Kinh, four were Chinese, and two were Kinh-Chinese. All had severe anemia and received blood transfusions regularly, every 1-3 months. Hepatosplenomegaly was found in all patients, and splenectomy had been done in six patients. Normal alpha-globin genotype (alpha alpha/alpha alpha) was found in all subjects. Reverse dot-blot hybridization using oligonucleotide probes specific for Southeast Asian mutations can detect beta-thalassemia in 60 chromosomes in addition to 31 chromosomes with beta(E) mutation. Excluding the beta(E) gene, six previously reported Thai and Chinese beta-thalassemia mutations were found, including codons 41/42 (-TCTT) 35.3%, codon 17 (A-->T) 25.0%, -28 (A-->G) 7.3%, codons 71/72 (+A) 7.3%, IVS-II nt 654 (C-->T) 7.3%, and IVS-I nt 1 (G-->T) 6.0%. The Vietnamese frameshift mutation at codon 95 (+A) was detected by ARMS in seven chromosomes (10.3%). DNA polymorphism of the beta-globin gene cluster carrying the codon 95 mutation was - + - - - - - + for (G)gamma/XmnI, epsilon/HincII, (G)gamma/HindIII, (A)gamma/HindIII, psi beta/HincII, 3' psi beta/HincII, beta/AvaII, and 3'beta/BamHI, respectively. The remaining mutation detected by the gap PCR was a large deletion known as the Chinese (G)gamma((A)gamma delta beta)(0)-thalassemia. The two most common mutations were the frameshift at codons 41/42 (-TCTT) and the nonsense mutation in codon 17 (A-->T). Thus beta-thalassemia mutations in South Vietnam is similar to the previous report from the North, although at different frequencies. This result will help to establish a center for prenatal diagnosis and for prevention and control of thalassemia in Vietnam. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12353305     DOI: 10.1002/ajh.10193

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  7 in total

1.  Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia.

Authors:  Sarifah Hanafi; Rosline Hassan; Rosnah Bahar; Wan Zaidah Abdullah; Muhammad Farid Johan; Noor Diana Rashid; Nurul Fatihah Azman; Ariffin Nasir; Syahzuwan Hassan; Rahimah Ahmad; Azizah Othman; Mohd Ismail Ibrahim; Surianti Sukeri; Sarina Sulong; Surini Yusoff; Nor Sarwany Mohamad; Adil Hussein; Rozita Hassan; Narazah Yusoff; Badrul Hisyam Yahaya; Endom Ismail; Nik Khairuddin Nik Yussof; Sinari Salleh; Bin Alwi Zilfalil
Journal:  Am J Blood Res       Date:  2014-09-05

2.  Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction.

Authors:  Syahzuwan Hassan; Rahimah Ahmad; Zubaidah Zakaria; Zefarina Zulkafli; Wan Zaidah Abdullah
Journal:  Malays J Med Sci       Date:  2013-01

3.  Multicausal etiology of anemia among women of reproductive age in Vietnam.

Authors:  P H Nguyen; I Gonzalez-Casanova; H Nguyen; H Pham; T V Truong; S Nguyen; R Martorell; U Ramakrishnan
Journal:  Eur J Clin Nutr       Date:  2014-09-10       Impact factor: 4.016

4.  Genetic heterogeneity of the β-globin gene in various geographic populations of Yunnan in southwestern China.

Authors:  Jie Zhang; Jing He; Xiao-Hong Zeng; Shi-Jun Ge; Yu Huang; Jie Su; Xue-Mei Ding; Ji-Qing Yang; Yong-Jiu Cao; Hong Chen; Ying-Hong Zhang; Bao-Sheng Zhu
Journal:  PLoS One       Date:  2015-04-07       Impact factor: 3.240

5.  A Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese Heterozygote.

Authors:  Monica Pirastru; Paolo Mereu; Chau Quynh Nguyen; Nhan Viet Nguyen; Thang Duy Nguyen; Laura Manca
Journal:  Biomed Res Int       Date:  2017-04-19       Impact factor: 3.411

6.  Increased Prevalence of Thalassemia in Young People in Korea: Impact of Increasing Immigration.

Authors:  Hyun Ji Lee; Kyung Hwa Shin; Hyung Hoi Kim; Eu Jeen Yang; Kyung Hee Park; Min Ju Kim; Jeong Ran Kwon; Young Sil Choi; Jun Nyun Kim; Myung Geun Shin; Yong Gon Cho; Sun Jun Kim; Kyeong Hee Kim; Seri Jeong; Seom Gim Kong; Yu Jin Jung; Nayoung Lee; Man Jin Kim; Moon Woo Seong
Journal:  Ann Lab Med       Date:  2019-03       Impact factor: 3.464

7.  A free weekly iron-folic acid supplementation and regular deworming program is associated with improved hemoglobin and iron status indicators in Vietnamese women.

Authors:  Gerard J Casey; Tran Q Phuc; Lachlan Macgregor; Antonio Montresor; Seema Mihrshahi; Tran D Thach; Nong T Tien; Beverley-Ann Biggs
Journal:  BMC Public Health       Date:  2009-07-24       Impact factor: 3.295

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.