PREVALENCE OF THALASSEMIA AMONG NEWBORNS: A RE-VISITED AFTER 20 YEARS OF A PREVENTION AND CONTROL PROGRAM IN NORTHEAST THAILAND.

• Main Author: Goonnapa Fucharoen
• Format: Article
• Language: English
• Published: PAGEPress Publications 2018-09-01
• Series: Mediterranean Journal of Hematology and Infectious Diseases
• Subjects: Thalassemic syndrome, Newborn screening, Prevention and control program
• Online Access: https://www.mjhid.org/index.php/mjhid/article/view/3454

Background: To provide accurate prevalence information of thalassemia in northeast Thailand after 20 years implementation of a prevention and control program, thalassemia screening was carried out in newborns.   Methods: Study was done on 350 cord blood specimens collected consecutively at Maternal and Child Hospital, Regional Health Promotion Center 7, Khon Kaen, Thailand. All kinds of a- and β-thalassemias were identified using combined hemoglobin (Hb) and DNA analyses.  Results: Among 350 newborns examined, subjects with thalassemia genes were identified in 184 (52.6%) cases with as many as 22 different genotypes. The most prevalent one was Hb E (39.1%). The incidence of 3.1% a0-thalassemia, 25.9% a+-thalassemia, 5.4% Hb Constant Spring and 1.4% of Hb Paksé were encountered. Heterozygous β-thalassemia was found in 2 cases (0.6%). Hb capillary electrophoresis could demonstrate Hb E in all cases with Hb E and detected different levels of Hb Bart’s for different a-thalassemia genotypes but not in all cases with a-thalassemia. No newborn with severe thalassemia diseases was encountered. Conclusion: This study reveals that a-thalassemia, β-thalassemia and Hb E carriers as well as complex thalassemia syndromes are still prevalence and indicates a need for continuing a prevention and control program in the region.