Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population
ß-thalassemia is one of the most common inherited blood disorders in the world and a major deterrent to the public health of Bangladesh. The management of thalassemia patients requires lifelong frequent blood transfusion and the available treatment options are unsatisfactory. A national policy on thalassemia prevention is mandatory in Bangladesh. However, precise and up-to-date information on the frequency of ß-thalassemia carriers are missing due to lack of accurate diagnostic approaches, limited access to information and absence of national screening program. This study aims to determine the nationwide carrier frequency of hemoglobin E (HbE) and β- thalassemia and mutation spectrum among the carriers using molecular, hematological and biochemical methods.
The study enrolled a total of 1877 individuals (60.1% male and 39.9% female) aged between 18 and 35 years. Total sample size and its division-wise breakdown were calculated in proportion to national and division-wise population. Venous blood was collected and subjected to CBC analysis and Hb-electrophoresis for each participant. Serum ferritin was measured to detect coexistence of iron deficiency anemia with thalassemia carrier. DNA-based High Resolution Melting (HRM) curve analysis was performed for confirmation of carrier status by mutation detection.
Of 11.89% (95% CI, 10.43–13.35) carriers of β-globin gene mutations, 8.68% (95% CI, 7.41–9.95) had HbE trait (ETT) and 2.24% (95% CI, 1.57–2.91) had beta-thalassemia trait (BTT). Among eight divisions, Rangpur had the highest carrier frequency of 27.1% (ETT-25%, BTT-2.1%), whereas Khulna had the lowest frequency of 4.2% (ETT-4.2% only). Moreover, α- thalassemia, HbD trait, HbE disease, hereditary persistence of HbF were detected in 0.11, 0.16, 0.43 and 0.16% participants, respectively. HRM could identify two individuals with reported pathogenic mutations in both alleles who were erroneously interpreted as carriers by hematological indices. Finally, a total of nine different mutations including a novel mutation (c.151A > G) were detected in the β-globin gene.
Since carrier frequency for both HbE and β-thalassemia is alarmingly high in Bangladesh, a nationwide awareness and prevention program should be made mandatory to halt the current deteriorating situations. Mutation-based confirmation is highly recommended for the inconclusive cases with conventional carrier screening methods to avoid any faulty detection of thalassemia carriers.
Keywordsß-thalassemia Carrier frequency HRM curve analysis Detection accuracy Novel mutation National policy
Bone Marrow Transplantation
Complete Blood Count
Ethylenediamine tetra acetic acid
Hemoglobin beta subunit gene
Hereditary Persistence of Fetal Hemoglobin
High Resolution Melting
Iron Deficiency Anemia
Krueppel-like factor 1
Mean Corpuscular Hemoglobin
Mean Corpuscular Volume
Non Transfusion Dependent Thalassemia
Polymerase Chain Reaction
World Health Organization
β-thalassemia, characterized by reduced or absent β-globin chain synthesis, is one of the most common inherited blood disorders in the world and hence a major deterrent to public health. Although widespread, the major at-risk populations are mainly from Mediterranean, Middle East and Southeast Asian countries including Bangladesh [1, 2]. WHO reported that approximately 1.5% of global population are carriers of β-thalassemia and 68,000 children are born each year with various thalassemia syndromes . However, precise and up-to-date data on the frequency of β-thalassemia carriers and patients are missing due to lack of accurate diagnostic approach, limited access to information and absence of national screening program in many of the thalassemia-inflicted countries.
Although thalassemia carriers are usually healthy, the patients with β-thalassemia major and HbE/β-thalassemia require lifelong blood transfusion and iron chelation therapy for survival . Cardiac failure due to iron overload and transfusion-related infections have remained the leading causes of deaths of patients with thalassemia [5, 6]. Still, there is no cure for thalassemia except allogeneic bone marrow transplantation (BMT). Also, BMT therapy is too expensive to afford for majority of the world population and the outcome is often unsatisfactory. Due to lack of regular treatment and optimal health care facilities, most thalassemia patients die before adulthood in developing countries . However, many at-risk populations in Cyprus, Greece, Sardinia, Iran etc. have successfully reduced the births of β-thalassemia children by adopting and implementing various preventive measures including nationwide awareness, carrier screening and prenatal diagnosis combined with genetic counseling [8, 9, 10, 11].
Although Bangladesh has gained tremendous success in fulfilling Millennium Development Goal-4 by reducing under-5 mortality, there has been an increasingly rapid transition in the burden of disease from primarily communicable to non-communicable diseases. Thalassemia is the single most inherited monogenic blood disorder in Bangladesh and it causes not only substantial morbidity and deaths but also inflicts emotional and financial burden on the family and society . An estimation using limited prevalence data has shown that roughly 33/10,000 newborns are being born each year with thalassemia in Bangladesh . However, thalassemia patient-care and support facilities are barely available in most public and private hospitals. Moreover, health awareness on thalassemia remains highly inadequate among mass population. So, in addition to adoption of proper patient management strategy, prevention by premarital screening and/or prenatal diagnosis should be a useful approach for reducing the risk of thalassemia [7, 8, 9, 11]. However, considering socio-religious and financial issues as well as health risk associated with prenatal diagnosis and abortion of the affected fetus, pre-marital screening followed by genetic counseling is arguably the best approach to prevent thalassemia in Bangladesh. In order to weigh the future situation and implement an appropriate policy to tackle thalassemia, precise and up-to-date information on current carrier status is required. The last thalassemia carrier screening was conducted in 2005 on 735 school-going children in Bangladesh . Moreover, the hematological and biochemical methods which are commonly used for screening purposes have limitations as these often end up in false positive and false negative results [14, 15]. In this regard, supplemental molecular methods have been in wide use for their accuracy in carrier screening and predicting severity of the thalassemia patients including their treatment, prognosis and overall management [4, 11]. Recently, the Government of Bangladesh has launched a National Thalassemia Prevention Program. As a part of that strategy, this study was conducted using funds from Non Communicable Disease Control (NCDC) Program, Director General of Health Services, MOHFW, Government of Bangladesh and Rotary Club of Dhaka North. In addition to conventional methods, the study applied DNA-based approaches to determine the accurate status of carriers and also incidence of the at-risk cases with both mutant alleles of HBB gene, which might be responsible for transition from asymptomatic to symptomatic non-transfusion dependent thalassemia in future. Accordingly, the study was conducted on a total of 1877 marriageable-aged participants. Also, a methodical approach was used to accurately determine the division-wise distribution of thalassemia carriers across Bangladesh.
This cross-sectional study enrolled a total of 1877 participants (aged between18–35 years) from March 2018 to February 2019 from 10 different (4 universities, 4 medical colleges, and 2 business organization) institutions of Dhaka city with the intent to conduct awareness campaign and screen young unmarried adults. In addition, these institutes are attended by the students and employees from all 8 administrative divisions across Bangladesh. Upon obtaining written informed consent, approximately 5.0 mL of venous blood was collected from each participant via standard venipuncture in EDTA tube. The study was ethically approved by Bangladesh Medical Research Council (BMRC). After completion of the thalassemia screening tests, each participant received the report through email. Those who were found to be carriers of mutations in β- globin gene, were further given an opportunity to receive additional information and counseling.
Sample size calculation
Where, α = the probability of type I error
β = the probability of type II error (power of the test)
p1 = 10.2% previously estimated prevalence 
p2 = 15% expected prevalence
Considering 95% confidence interval (CI), power 80% and a design effect of 2.5, the estimated sample size was 1875. To eliminate bias and for proper representation of each administrative division, samples were collected proportionately to the population size of that division by quota sampling method.
Analysis of hematological parameters
About 2.0 ml of collected whole blood were used for CBC (Complete Blood Count) analysis to determine RBC indices including hematocrit, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC) and Red cell distribution width (RDW) using automated Hematology analyzer (Sysmex kx-21, Sysmex Corporation, Kobe, Japan).
Hemoglobin electrophoresis was performed on Sebia CAPILLARYS-2 Flex Piercing (Sebia, Lisses, France) using Capillarys Hemoglobin (E) kit to measure HbA, HbA2, HbF and other abnormal Hb variants following manufacturer’s instructions.
Serum ferritin assay
Serum ferritin was assayed on miniVIDAS® Immunoassay Analyzer (bioMérieux, USA) using VIDAS® FERRITIN kit (bioMérieux SA, Marcy, France) following manufacturer’s instructions.
Real-time PCR-based high resolution melting (HRM) curve analysis
Genomic DNA was extracted from whole blood using QIAGEN flexigene® DNA kit (Qiagen, Hilden, Germany) according to manufacturer’s guidelines. Real-time PCR and HRM curve analysis using Precision Melt Analysis™ Software (BioRad) were performed on Bio-Rad CFX96 Real-Time System. This HRM method was previously developed for mutation screening in the β-globin gene of Bangladeshi and regional population of thalassemic endemic countries [2, 17, 18]. This high throughput approach enables to screen mutation(s) in unknown specimens in the presence of reference samples without nucleotide sequencing as well as to screen a large number of samples in a quick and cost-effective manner.
Sanger DNA sequencing
In this study, once the mutation positive specimens with a new HRM patterns other than the references were identified, nucleotide sequencing was carried out for those samples to identify the mutation. Sanger DNA sequencing using ABI PRISM-310 software version 3.1.0 (Applied Biosystems) was performed following the polymerase chain reactions (PCR) targeting the mutational hot-spot region of HBB gene for Bangladesh (exon1, intron 1 and a portion of exon 2 of beta-globin gene) and the PCR products purification using the MinElute® PCR purification kit (Qiagen) following the manufacturer’s instructions. Then the retrieved sequence results were compared with the reference sequences (NC_000011.10) for confirmation of the mutation.
The comparison of sensitivity and specificity between traditional methods and molecular approach were performed using https://www.openepi.com/DiagnosticTest/DiagnosticTest.htm with 95% CI. The CI for an observed proportion was calculated using Stata software (version 14.2). With the known genotype frequency, the number of expected newborns with thalassemia was calculated by Hardy-Weinberg equation .
Participants’ information regarding gender, parental consanguinity, residence and their knowledge on thalassemia
No. of Participants, n (%)
Knowledge regarding thalassemia
Prior knowledge about thalassemia
Knowledge about how thalassemia is acquired
Presence of patients or carriers in the participants family
Screening for thalassemia carriers based on MCV, MCH and hemoglobin electrophoresis
Hemoglobin electrophoresis information of the study participants categorized based on MCV and MCH parameters
No. of participants, n (%) Total, N = 1877
Hb electrophoresis results
BTT suspects, n (%) (HbA2 > 3.5%)
ETT Suspects, n (%) (HbE = 25–30%)
HbE disease, n (%) (HbE > 90%HbA = 0%)
Others Hb Variants, n (%)
Total participants with abnormal Hb-electrophoresis, n (%)
Normal Hb electrophoresis results, n (%)
(MCV ≥ 80 fL and MCH ≥ 27 pg)
(MCV < 80 fL and MCH < 27 pg)
(MCV < 80 fL and MCH ≥ 27 pg)
(MCV ≥ 80 fL and MCH < 27 pg)
Second to MCV and MCH, hemoglobin electrophoresis using Sebia capillary electrophoresis was performed for all the samples as it is the gold standard for thalassemia carrier detections. HbA2 level of > 3.5% was used as a cutoff for screening of β-thalassemia carriers [21, 22]. Since Sebia capillary electrophoresis was able to separate HbA2 distinctly from HbE and other Hb variants like HbD, HbC, HbS and Hb Barts or HbH, the presence of HbE fraction or other hemoglobin variants could indicate the carriers of respective hemoglobin gene mutation.
Table 2 summarizes the results of hematological and electrophoresis analysis of the study participants. About 35% (215/612) of Group B participants had abnormal Hb electrophoresis results compare to 0.9% (9/995), 0% (0/13) and 1.6% (4/257) participants of Group A, C and D, respectively, with abnormal Hb electrophoresis results.
However, in Group-A having apparently normal RBC indices, there were 3 participants with BTT, 2 with ETT and 4 with other Hb variants. In addition, there were two BTT and two ETT carriers among Group-D participants. Finally, all the suspected cases based on MCV, MCH and Hb electrophoresis were subjected to DNA analysis for β-globin gene mutation.
Second-tier tests using high resolution melt curve analysis and sanger DNA sequencing for detection of β-globin gene mutations
Molecular analysis of the selected participants for confirmation of the carrier status
Mutation Absent, n
Number of participants having mutation in β-globin gene, n
HbA2 < 2.2% Hb < 10 g/dl
Hb A2: 3.3–3.5% (borderline suspected)
HbA2 > 3.5%
HbE > 90% HbA = 0%
For Group 1 samples, serum ferritin was measured to confirm IDA and HRM was then performed to detect any coexistence of β-globin gene mutation with IDA. Absence of β-globin gene mutation confirmed that there was no carrier in this group and thus none of the β-thalassemia traits was overlooked because of low level of HbA2.
Identification of a single β-globin gene mutation in 41 out of 46 participants of group-3 could confirm their carrier status. However, of the rest five samples, three having 3.7% HbA2, one with 4% and one having 3.6% HbA2 turned out to be normal in HRM curve analysis and the HRM results were further confirmed by Sanger sequencing. All of these five participants had lower MCH values than the cutoff value (< 27 pg) and three of them showed MCV within normal range i.e. higher than the cutoff value (> 80 fL). Table S1 (Additional file 1: Table S1) shows the hematological features of these 5 participants having HbA2 > 3.5% without mutation in HBB gene.
Hemoglobin indices of the two participants containing compound heterozygous mutation
Comparison of sensitivity and specificity among the conventional hematological-analysis based approaches for thalassemia carrier detection
Mean sensitivity, % (95% CI)
Mean specificity, % (95% CI)
Positive predictive value, % (95% CI)
Negative predictive value,% (95% CI)
Diagnostic accuracy, % (95% CI)
True +ve (n)
False + ve (n)
True –ve (n)
MCV + MCH only
MCV+ MCH and Hb Electrophoresis
Mutation spectrum in the HBB gene of the study participants with thalassemia traits
Mutation spectrum of β-globin gene in the β-thalassemia and HbE carriers in Bangladeshi population
Number of samples, n (%; 95% CI)
c.79G > A (HbE)
163 (73.42; 67.62–79.22)
c.92 + 5G > C
32 (14.41; 9.8–19.02)
c.79G > A + c.79G > A
8 (3.61; 1.16–6.06)
c.92 + 130G > C
01 (0.45; 0.43–1.33)
c.151A > G a
01 (0.45; 0.43–1.33)
03 (1.35; 0.16–2.86)
02 (0.90; 0.34–2.14)
c.47G > A
03 (1.35; 0.16–2.86)
c.79G > A + c.92 + 5G > C
02 (0.90; 0.34–2.14)
Frequency of thalassemia carriers and other hemoglobinopathies among Bangladeshi population
Distribution of thalassemia carriers and other Hb variants among the study participants
Types of thalassemia carriers and other Hb variants
Number of participants, n
Frequency %, (95% CI)
HbE Trait (ETT)
β-thalassemia trait (BTT)
Suspected NTD HbE/β-thalassemia
Total carriers of mutations in one or both alleles of globin genes
Contribution of consanguinity to increase thalassemia carrier frequency in the country
There were 81 (4.32%; 95% CI, 3.4–5.24) participants of consanguineous parents. The carrier frequency among the participants with history of consanguinity was 23.5% (19/81), whereas it was almost half (11.4%, 204/1796) among the children of non-consanguineous parents. The highest consanguinity was observed in Rangpur division (8/140; 5.7%), which also had the highest carrier frequency among the eight administrative divisions of Bangladesh. The findings suggest that consanguinity contributes significantly to the increased rate of thalassemia in Bangladesh.
Distribution of β-thalassemia and HbE carriers across eight divisions of Bangladesh
This is the first thalassemia carrier screening study conducted among young individuals of marriageable-age in Bangladesh. The study aimed to determine (1) nationwide carrier frequencies of β-thalassemia and HbE traits more precisely using molecular approach as supplementation to hematological and electrophoretic indices for rectification of the false positive or false negative cases (2) distribution of division-wise carrier frequencies, and (3) the mutation spectrum in the HBB gene of the carriers.
Carrier frequency of ETT plus BTT was 10.92% (95% CI, 9.51–12.33), where ETT had the highest frequency (8.68%; 95% CI, 7.41–9.95) followed by BTT (2.24%; 95% CI, 1.57–2.91). A previous study conducted in 2005 by Khan et al. reported an average frequency of 10.2% in Bangladeshi population with 6.1% ETT and 4.1% BTT . This difference in frequencies between these two studies can be explained by the fact that previous studies used only conventional hematological approaches which often give false positive and false negative results [14, 15], whereas the present study applied molecular approach to avoid faulty detection of any carriers. Moreover, this study was conducted on a larger number of participants and the number of total participants as well as division-wise enrollment was enumerated statistically in proportion to the population size of each division for a precise apprehension of distribution of carrier frequency. Other studies conducted in neighboring India and Sri Lanka reported the comparable BTT frequencies of 2.68–4.05% and 2·2%, respectively, where the ETT frequencies were 3.4 and 0.5%, respectively [24, 25, 26]. However, our study showing an alarmingly high ETT frequency (8.68%) is supported by the previous study in Bangladesh . Among eight administrative divisions, the highest carrier frequency was detected in Rangpur Division, where the HbE carrier frequency was 25%. Previous study showed the highest thalassemia carrier frequency in Rajshahi Division because the newly created administrative region of Rangpur was the part of Rajshahi Division during that study.
The first line of screening for identification of thalassemia carriers is a complete blood count followed by a measurement of HbA2 and HbF proportions. Since screening by hematological indices may result in misdetection of carriers due to factors like co-inheritance of α-thalassemia, mutations in β- and δ-globin genes, mutations in KLF1 gene and iron deficiency anemia [15, 27, 28], this study applied a comparatively cheaper and easy-to-perform DNA-based HRM curve analysis method to confirm and characterize mutations in the β-globin gene. This method supplements the conventional hematological and electrophoretic parameter based approaches for identification of the thalassemia carriers and patients . For example, although the parameters MCV ≥ 80 fL and MCH ≥ 27 pg are usually considered as a negative indicator for HbE trait, our study using electrophoresis had identified two HbE carriers with MCV ≥ 80 fL and MCH ≥ 27 pg and a case having MCV > 80 fL and MCH < 27 pg as HbE carrier, indicating the shortcomings of hematological indices in screening of HbE carriers. Similarly, five participants with HbA2 > 3.5%, which is a widely used indicator of beta thalassemia trait, turned out to be normal by HRM curve analysis and Sanger sequencing, thereby further demonstrating shortfalls of Hb electrophoresis in detection of thalassemia carriers. The higher HbA2 might be caused by mutations in the KLF1 gene leading to borderline high HbA2 and thus may result in false positive findings in Hb electrophoresis . Moreover, a number of studies reported frequent detections of high HbA2 levels in healthy individuals without any mutation in the HBB gene [29, 30]. On the other hand, specimens with HbA2 level in the borderline range (3.3–3.5%) with low MCV and/or low MCH must be subjected to DNA-based analysis to determine the carrier status of the participants. Notably, borderline HbA2 level might result from coinheritance of β-globin gene mutations with iron deficiency anemia and α thalassemia traits that usually lower the level of HbA2 to normal or borderline range in the β-thalassemia carriers . In this study, all the specimens with abnormal hematological indices were tested using high resolution melt (HRM) curve analysis to confirm the presence of mutation in β-globin gene and if the molecular tests were not performed, about 5 in every 1000 carriers of the β-thalassemia and HbE variants would have been missed and around 1.8% cases could have been interpreted erroneously. Therefore, although the combination of MCV, MCH and Hb electrophoresis resulted in high sensitivity and specificity, the DNA-based approaches like HRM curve analysis and Sanger sequencing had been proved to be very useful to avoid false positive and false negative results by detecting mutations in the β-globin gene, and thereby confirming the true thalassemia carrier status of the participants. In a previous study, we described the advantages and cost-effective nature of this approach over other DNA-based screening methods like Denaturing High Performance Liquid Chromatography (DHPLC), Single Strand Conformational Polymorphism (SSCP) and Denaturing Gradient Gel Electrophoresis (DGGE), Amplification Refractory Mutation System (ARMS) PCR, Sanger nucleotide sequencing etc. . Notably, this real time PCR-based high throughput HRM curve analysis is easy to perform and time-saving as there is no need of post PCR amplification processes like PCR product purification, gel electrophoresis etc. All these advantages offered by the HRM-based techniques make it an ideal candidate for molecular screening of thalassemia in countries of thalassemia belt and resource limitation.
More importantly, this study identified two clinically asymptomatic individuals with pathogenic mutations in both alleles of HBB gene using HRM method, who were detected as carriers by Hb electrophoresis. Although the association between genotype and phenotype is established for both α- and β-thalassemia, differentiation into various phenotypes of thalassemia is mostly based on clinical signs and symptoms. However, the same mutations i.e. c.79 G > A + c.92 + 5G > C have been reported as pathogenic in patients with mild to severe form of HbE-beta thalassemia [32, 33]. Hence, although currently these two individuals who seem to be carriers without any clinical manifestations, they might be at risk of developing non-transfusion dependent thalassemia (NTDT) in future. In our ongoing study on the role of various genetic modifiers on clinical heterogeneity of thalassemia patients in Bangladesh, the age of first transfusion of NTDT patients ranged from 13 to 60 years (unpublished data). It should also be mentioned that patients with hemoglobin E/β-thalassemia show different phenotypic variability at different stages of development . Since numerous factors have been identified to be associated with disease severity of the NTDT patients, identification of NTDT patients is vital for prognosis because increased intestinal iron absorption in such patients increases the risk of thrombotic disease, pulmonary hypertension, sudden cardiac arrest, and liver damages etc. [34, 35, 36]. Thus the significance of diagnosis of NTDT is crucial because a timely treatment intervention will curtail the progression of disease severity and thus prevent an untimely death. All these aspects emphasize on the requirement of molecular-based carrier screening which is the ultimate confirmation of a carrier status. Furthermore, the study identified 9 different mutations including a novel mutation (c.151A > G) in the beta-globin gene of the carriers. Further studies are needed to know the pathogenesis of this novel mutation.
With the current ETT plus BTT carrier frequency of 10.92%, 9176 babies are born with thalassemia each year (according to Hardy-Weinberg equation), thereby further worsening the situations of thalassemia patients [13, 19]. Moreover, the study found that the thalassemia carrier frequency was almost double among the children with history of consanguineous marriage, a common socio-culture of this region and thus consanguinity contributes to increased burden of thalassemia. Even though majority of the participants were university/college going students, 62% of them did not know the disease etiology and about 32% did not have any knowledge about the disease prior to enrolment suggesting that the knowledge regarding thalassemia is quite insufficient among the mass population.
At present, the yearly medical cost required for thalassemia patient ranges from $1632 to $3960 in Bangladesh and there is neither a national insurance facility nor a subsidized or free treatment system from the government , suggesting a severe health, economic and emotional burden to the nation and thus adoption of a national thalassemia prevention strategy is a demand of time. Several thalassemia endemic countries have set up comprehensive national prevention programs, which include public awareness and education; carrier screening using molecular diagnostics, genetic counseling and prenatal diagnosis [37, 38]. Effectiveness of such prevention program in Sardinia is evidenced by a reduction in the birth rate with thalassemia major from 1:250 live births to 1:4000 and such success is also achieved by other countries including Cyprus, Iran, and Turkey [10, 38, 39]. Although carrier screening and counseling are being performed on a voluntary basis in some countries, countries like UAE, Saudi Arabia, Jordan, Cyprus, Iran and Turkey are performing compulsory premarital screening for thalassemia to discourage marriage between two carriers . These strategies may help guide health policy makers of Bangladesh to adopt an appropriate thalassemia prevention strategy considering the available resources, religious values and social culture.
In summary, as prevention of thalassemia is far cheaper and better than treatment and currently no affordable cure is available, an immediate and concerted action on thalassemia prevention should be made mandatory in Bangladesh. A massive awareness program targeting general population and an intensive educational program for health personnel including physicians, nurses, health and family planning workers should be carried out nationwide promptly. Also, appropriate screening methods combining hematological, electrophoretic and molecular approaches associated with genetic counseling should be required in existing hospitals and health facilities. The information of this study will be helpful in several ways, such as measuring nationwide carrier frequency with accuracy and grasp the gravity of the situation, identifying the at-risk population and thus prioritizing them, and necessities and benefits of molecular-based carrier screening. Moreover, this study demonstrated the feasibility and usefulness of cost-effective HRM approach in resource limited settings which can be followed in other countries of thalassemia-belt for detection of HBB gene mutations and confirmation of the carrier status.
This study highlights that adoption of a molecular screening method for detection of mutations in the HBB gene could overcome the shortcomings of the conventional methods, in particular, for prenatal and newborn screening and for confirmation of the inconclusive cases by the traditional approaches. With the current carrier frequency, HbE/β-thalassemia will be posing a tremendous threat to the public health of Bangladesh if necessary measures like awareness program for mass population and medical personnel and; establishment of carrier screening facilities aligned with genetic counselling in health centers and hospitals across the country, are not implemented immediately. Lastly, the HRM-based cost-effective molecular methods can be initiated in other thalassemia-prone countries and help in fighting these non-curable and life-threatening disorders.
We are thankful to Centre for Medical Biotechnology (CMBT), Management Information System (MIS), DGHS, MoHFW, Government of Bangladesh; Dr. Tahmina Shirin, Chief Scientific Officer of Institute of Epidemiology Disease Control and Research (IEDCR); Nirod Chandra Shaha, Statistician, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b). We especially thank Saad Hasan Hasib for preparation of the Map. For technical support we are grateful to Dr. Rosy Sultana, Md. Sazzadul Islam, Polash Chandra Karmakar, Mst. Noorjahan Begum, MA Mahmud-Un-Nabi, Kazi Sarjana Safain, Sadia Tasnim Tuba, Khalid Arafath Abboy, Maliha Islam, Jumanah Amatullah, Md. Jonayed Sharker, Md. Shahriar Alam, Shekh Rezwan Hossain, Samia Afroz and Shabnam Syeed.
FAN, GSB, MTI and MH conducted the laboratory work, data analysis and manuscript draft writing. NS, SKS, KI, WAH, MR and SKQ assisted in clinical information collection, interpretation and to improve the manuscript. KM, FQ, SSQ, HUS designed the study plan and supervised the overall project. All authors read and approved the final manuscript.
This study was funded by Non Communicable Disease Control (NCDC) Program, Director General of Health Services (DGHS), Ministry of Health and Family Welfare (MOHFW), Government of Bangladesh and Rotary Club of Dhaka North.
Ethics approval and consent to participate
This study was approved by the National Ethics Research Committee (NERC) of Bangladesh Medical Research Council (BMRC). Registration no # 102 03 04 2018.
Consent for publication
All the participants described in this article provided written informed consent for participation in the study and for publication of the results. All the authors have read and approved the paper for publication.
The authors declare that they have no competing interests.
- 2.Islam MT, Sarkar SK, Sultana N, Begum MN, Bhuyan GS, Talukder S, Muraduzzaman A, Alauddin M, Islam MS, Biswas PP. High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genet. 2018;19(1):1.CrossRefGoogle Scholar
- 9.Voskaridou E, Ladis V, Kattamis A, Hassapopoulou E, Economou M, Kourakli A, Maragkos K, Kontogianni K, Lafioniatis S, Vrettou E. A national registry of haemoglobinopathies in Greece: deducted demographics, trends in mortality and affected births. Ann Hematol. 2012;91(9):1451–8.CrossRefGoogle Scholar
- 13.Khan W, Banu B, Amin S, Selimuzzaman M, Rahman M, Hossain B, Sarwardi G, Sadiya S, Iqbal A, Rahman Y. Prevalence of beta thalassemia trait and Hb E trait in Bangladeshi school children and health burden of thalassemia in our population. DS (Child) HJ. 2005;21(1):1–7.Google Scholar
- 16.Population Monograph Of Bangladesh. In. Edited by (Bbs) BBOS, vol. 06. Bangladesh: Statistics And Informatics Division (Sid), Ministry of Planning; 2015: 15. http://18.104.22.168:8008/WebTestApplication/userfiles/Image/PopMonographs/Volume-6_PDIM.pdf
- 18.George E, Teh L, Rosli R, Lai M, Tan J. Beta Thalassaemia mutations in Malays: a simplified cost-effective strategy to identify the mutations. Malaysian J Med Health Sci. 2012;8(1):1–8.Google Scholar
- 20.Viprakasit V, Origa R, Fucharoen S. Genetic basis, pathophysiology and diagnosis. In: Guidelines for the Management of Transfusion Dependent Thalassaemia (TDT). 3rd ed. Cyprus: Thalassaemia International Federation, TIF publishers; 2014.Google Scholar
- 32.George E. HbE β-thalassaemia in Malaysia: revisited. J Hematol Thromb Dis. 2013;1(101):2.Google Scholar
- 36.Taher A, Vichinsky E, Musallam K, Cappellini M-D, Viprakasit V. Guidelines for the management of non transfusion dependent thalassaemia (NTDT). Nicosia: Thalassaemia International Federation; 2013.Google Scholar
- 39.Cao A, Cristina Rosatelli M, Galanello R. Control of β-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experience. In: Ciba Foundation Symposium 197-Variation in the Human Genome: Variation in the Human Genome: Ciba Foundation Symposium 197: 2007. USA: Wiley Online Library; 2007. p. 137–55.CrossRefGoogle Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.