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α+地中海贫血对疟疾传播严重地区的尼日利亚人群贫血的影响。

The contribution of alpha+-thalassaemia to anaemia in a Nigerian population exposed to intense malaria transmission.

作者信息

Mockenhaupt F P, Falusi A G, May J, Ademowo O G, Olumese P E, Meyer C G, Bienzle U

机构信息

Institute for Tropical Medicine and Medical Faculty Charité, Humboldt-University, Berlin, Germany.

出版信息

Trop Med Int Health. 1999 Apr;4(4):302-7. doi: 10.1046/j.1365-3156.1999.00386.x.

Abstract

The proportion to which alpha-thalassaemia contributes to anaemia in Africa is not well recognized. In an area of intense malaria transmission in South-West Nigeria, haematological parameters of alpha-thalassaemia were examined in 494 children and 119 adults. The -alpha3.7 type of alpha+-thalassaemia was observed at a gene frequency of 0.27. Nine and 36.5% of individuals were homozygous and heterozygous, respectively. P.falciparum-infection was present in 78% of children and in 39% of adults. The alpha-globin genotypes did not correlate with the prevalence of P. falciparum-infection. alpha+-thalassaemic individuals had significantly lower mean values of haemoglobin, mean corpuscular volume, and mean corpuscular haemoglobin than non-thalassaemic subjects. Anaemia was seen in 54. 7% of children with a normal alpha-globin genotype, in 69.9% of heterozygous (odds ratio: 1.99, 95% confidence interval: 1.32-3.00, P = 0.001), and in 88.4% of homozygous alpha+-thalassaemic children (odds ratio: 7.72, 95% confidence interval: 2.85-20.90, P = 0.0001). The findings show that alpha+-thalassaemia contributes essentially to mild anaemia, microcytosis, and hypochromia in Nigeria.

摘要

α地中海贫血在非洲导致贫血的比例尚未得到充分认识。在尼日利亚西南部疟疾传播猖獗的地区,对494名儿童和119名成年人的α地中海贫血血液学参数进行了检查。观察到α+地中海贫血的-α3.7型基因频率为0.27。分别有9%和36.5%的个体为纯合子和杂合子。78%的儿童和39%的成年人感染了恶性疟原虫。α珠蛋白基因型与恶性疟原虫感染率无关。α+地中海贫血个体的血红蛋白、平均红细胞体积和平均红细胞血红蛋白平均值显著低于非地中海贫血受试者。α珠蛋白基因型正常的儿童中54.7%出现贫血,杂合子儿童中69.9%出现贫血(优势比:1.99,95%置信区间:1.32 - 3.00,P = 0.001),α+地中海贫血纯合子儿童中88.4%出现贫血(优势比:7.72,95%置信区间:2.85 - 20.90,P = 0.0001)。研究结果表明,α+地中海贫血在尼日利亚主要导致轻度贫血、小红细胞症和低色素血症。

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