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巴布亚新几内亚的α地中海贫血

Alpha thalassaemia in Papua New Guinea.

作者信息

Oppenheimer S J, Higgs D R, Weatherall D J, Barker J, Spark R A

出版信息

Lancet. 1984 Feb 25;1(8374):424-6. doi: 10.1016/s0140-6736(84)91754-9.

Abstract

Haemoglobin Bart's was detected in cord blood samples from 81% of 217 infants born in Madang on the north coast of Papua New Guinea. Analysis of the alpha globin genes of 30 infants and adults from the same region showed that all but 3 were heterozygous or homozygous for the deletion form of alpha + thalassaemia. None of 18 cord blood samples from infants born in Goroka in the Eastern Highlands Province had haemoglobin Bart's, and in each case the alpha globin genes were normal. Preliminary geographical and linguistic analyses of both groups suggest that the prevalence of alpha thalassaemia may be related to altitude rather than to linguistic grouping and hence that resistance to malaria may be at least one reason why alpha thalassaemia is so common in some populations.

摘要

在巴布亚新几内亚北海岸马当出生的217名婴儿中,81%的脐带血样本检测到了巴特氏血红蛋白。对来自同一地区的30名婴儿和成人的α珠蛋白基因进行分析后发现,除3人外,其余均为α+地中海贫血缺失型的杂合子或纯合子。东高地省戈罗卡出生的婴儿的18份脐带血样本中均未检测到巴特氏血红蛋白,且每份样本的α珠蛋白基因均正常。对两组人群进行的初步地理和语言分析表明,α地中海贫血的患病率可能与海拔高度有关,而非与语言群体有关,因此对疟疾的抵抗力可能至少是α地中海贫血在某些人群中如此常见的一个原因。

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