The 'Hot spot' of Hb E [β26(B8)Glu→Lys] in southeast Asia:: β-globin anomalies in the Lao Theung population of southern Laos

被引:18
作者
Flatz, G
Sanguansermsri, T
Sengchanh, S
Horst, D
Horst, J
机构
[1] Hannover Med Sch, Hannover, Germany
[2] Chiang Mai Univ, Dept Pediat, Fac Med, Chiangmai, Thailand
[3] Univ Munster, Inst Humangenet, D-4400 Munster, Germany
关键词
Hb E; beta-thalassemia (thal); Laos; austroasiatics; population study;
D O I
10.1081/HEM-120040334
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hb E [beta26(B8)Glu-->Lys], is the most common abnormal hemoglobin (Hb) in Southeast Asian populations. The hitherto highest frequencies of the Hb E gene (HBB*E) in large population samples, similar to0.3, were observed in the southern part of northeastern Thailand. The finding of even higher frequencies in a small, isolated Austroasiatic group in Northeast Thailand prompted us to examine samples of three Austroasiatic populations in southern Laos (official designation: Lao Theung), an area inhabited by numerous ethnic groups belonging to the Mon-Khmer branch. Blood samples were collected from a total of 603 adult subjects. The HBB*E frequencies were 0.426 in the So of Khammuan Province, 0.433 in the Alak/Ngeh of Sekong Province and 0.253 in the Oy of Attapeu Province. The HBB*E frequencies in the So and Alak/Ngeh are the highest observed in Southeast Asia in representative population samples. None of the common Southeast Asian beta-thalassemia (thal) mutations were found. The results are discussed with respect to natural selection by malaria, selection time, effects of beta-thal and the ethnic history of the population of Southeast Asia.
引用
收藏
页码:197 / 204
页数:8
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