Santana Marli Stela, de Lacerda Marcus Vinícius Guimarães, Barbosa Maria das Graças Vale, Alecrim Wilson Duarte, Alecrim Maria das Graças Costa
University of the State of Amazonas, Manaus, Amazonas, Brazil.
PLoS One. 2009;4(4):e5259. doi: 10.1371/journal.pone.0005259. Epub 2009 Apr 16.
There is a paucity of information regarding glucose-6-phosphate dehydrogenase (G6PD) deficiency in endemic areas for malaria in Latin America.
METHODOLOGY/PRINCIPAL FINDINGS: This study determined the prevalence of the G6PD deficiency in 200 male non-consanguineous individuals residing in the Ismail Aziz Community, on the outskirts of Manaus (Brazilian Amazon). Six individuals (3%) were deficient using the qualitative Brewer's test. Gel electrophoresis showed that five of these patients were G6PD A(-). The deficiency was not associated with the ethnic origin (P = 0.571). In a multivariate logistic regression analysis, G6PD deficiency protected against three or more episodes of malaria (P = 0.049), independently of the age, and was associated with a history of jaundice (P = 0.020) and need of blood transfusion (P = 0.045) during previous treatment for malarial infection, independently of the age and the previous malarial exposure.
CONCLUSIONS/SIGNIFICANCE: The frequency of G6PD deficiency was similar to other studies performed in Brazil and the finding of a predominant G6PD A(-) variant will help the clinical management of patients with drug-induced haemolysis. The history of jaundice and blood transfusion during previous malarial infection may trigger the screening of patients for G6PD deficiency. The apparent protection against multiple malarial infections in an area primarily endemic for Plasmodium vivax needs further investigation.
在拉丁美洲疟疾流行地区,关于葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症的信息匮乏。
方法/主要发现:本研究确定了居住在玛瑙斯(巴西亚马逊地区)郊区伊斯梅尔·阿齐兹社区的200名非近亲男性个体中G6PD缺乏症的患病率。采用定性布鲁尔试验,有6人(3%)缺乏该酶。凝胶电泳显示,其中5名患者为G6PD A(-)型。该缺乏症与种族起源无关(P = 0.571)。在多因素逻辑回归分析中,G6PD缺乏症可预防三次或更多次疟疾发作(P = 0.049),与年龄无关,且与疟疾感染既往治疗期间的黄疸病史(P = 0.020)和输血需求(P = 0.045)有关,与年龄和既往疟疾暴露无关。
结论/意义:G6PD缺乏症的发生率与在巴西进行的其他研究相似,且主要G6PD A(-)变异型的发现将有助于药物性溶血患者的临床管理。既往疟疾感染期间的黄疸和输血史可能促使对患者进行G6PD缺乏症筛查。在一个主要流行间日疟原虫的地区,G6PD缺乏症对多次疟疾感染的明显保护作用需要进一步研究。