Micromapping of thalassemia and hemoglobinopathies in diferent regions of northeast Thailand and Vientiane, Laos People's Democratic Republic
- PMID: 22122810
- DOI: 10.3109/03630269.2011.637149
Micromapping of thalassemia and hemoglobinopathies in diferent regions of northeast Thailand and Vientiane, Laos People's Democratic Republic
Abstract
In order to determine the prevalence of thalassemia and hemoglobinopathies in different regions of northeast (NE) Thailand and Vientiane, Laos People's Democratic Republic (PDR), a total of 1,809 blood samples were collected consecutively from individuals attending antenatal care services at 11 community hospitals in different regions of NE Thailand and three hospitals in Vientiane, Laos PDR, from May 2009 to April 2010. All individuals were investigated for thalassemia and hemoglobinopathies using standard methods. For individuals from NE Thailand, the carrier frequencies were 41.7% for Hb E [β26(B8)Glu→Lys, GAG>AAG], 5.8% for α(0)-thalassemia (α(0)-thal), and 0.9% for β-thal. The THAI deletion type of α(0)-thal was found in one individual from an ethnic minority. From a group of pregnant Laotian women, 30.1% were Hb E carriers. The prevalence of α(0)-thal of 8.6% for the Laotian women was similar to that found in the upper northeastern part of Thailand. The frequency of β-thal was 2.3 %. The proportion of carriers of α(+)-thal and Hb Constant Spring (Hb CS, α142, Term→Gln (TAA>CAA in α2)] ) from Thailand and Laos was significantly different. The frequency of Hb Paksé [α142, Term→Tyr (TAA>TAT in α2)] was relatively low for Thailand as well as for Laos. The results indicate that thalassemia and hemoglobinopathies are a significant health burden in the region and that a prevention and control program for severe thalassemia diseases should be established in Laos.
Similar articles
-
Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand.Hemoglobin. 2020 May;44(3):162-167. doi: 10.1080/03630269.2020.1780252. Epub 2020 Jun 26. Hemoglobin. 2020. PMID: 32586159
-
Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.Hemoglobin. 2009;33(6):507-14. doi: 10.3109/03630260903343780. Hemoglobin. 2009. PMID: 19958198
-
Detection of coinherited Hb H-Constant Spring/Paksé disease and Hb E by capillary electrophoresis and high performance liquid chromatography.Hemoglobin. 2013;37(2):176-82. doi: 10.3109/03630269.2012.752744. Epub 2012 Dec 13. Hemoglobin. 2013. PMID: 23234508
-
Current Status of Thalassemia in Lao People's Democratic Republic.Hemoglobin. 2022 Jan;46(1):58-61. doi: 10.1080/03630269.2022.2069034. Hemoglobin. 2022. PMID: 35950579 Review.
-
Changing patterns of thalassemia worldwide.Ann N Y Acad Sci. 2005;1054:18-24. doi: 10.1196/annals.1345.003. Ann N Y Acad Sci. 2005. PMID: 16339647 Review.
Cited by
-
Effects of Daily Zinc, Daily Multiple Micronutrient Powder, or Therapeutic Zinc Supplementation for Diarrhea Prevention on Physical Growth, Anemia, and Micronutrient Status in Rural Laotian Children: A Randomized Controlled Trial.J Pediatr. 2019 Apr;207:80-89.e2. doi: 10.1016/j.jpeds.2018.11.022. Epub 2018 Dec 21. J Pediatr. 2019. PMID: 30580974 Free PMC article. Clinical Trial.
-
Interaction of hemoglobin Grey Lynn (Vientiane) with a non-deletional α(+)-thalassemia in an adult Thai proband.Biochem Med (Zagreb). 2014 Feb 15;24(1):167-74. doi: 10.11613/BM.2014.019. eCollection 2014. Biochem Med (Zagreb). 2014. PMID: 24627726 Free PMC article.
-
Prevalence of Thalassemia among Newborns: A Re-visited after 20 Years of a Prevention and Control Program in Northeast Thailand.Mediterr J Hematol Infect Dis. 2018 Sep 1;10(1):e2018054. doi: 10.4084/MJHID.2018.054. eCollection 2018. Mediterr J Hematol Infect Dis. 2018. PMID: 30210747 Free PMC article.
-
Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis.Heliyon. 2023 Aug 12;9(8):e19116. doi: 10.1016/j.heliyon.2023.e19116. eCollection 2023 Aug. Heliyon. 2023. PMID: 37649848 Free PMC article.
-
Alpha-globin gene cluster haplotypes and D1S80, D17S5, and TPO VNTR polymorphisms among four ethnic populations from lower northeastern Thailand.Sci Rep. 2025 Mar 6;15(1):7851. doi: 10.1038/s41598-025-91071-3. Sci Rep. 2025. PMID: 40050353 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous