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首页> 外文期刊>BMC research notes >The association between malaria parasitaemia, erythrocyte polymorphisms, malnutrition and anaemia in children less than 10 years in Senegal: a case control study
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The association between malaria parasitaemia, erythrocyte polymorphisms, malnutrition and anaemia in children less than 10 years in Senegal: a case control study

机译:塞内加尔10岁以下儿童疟疾寄生虫血症,红细胞多态性,营养不良和贫血之间的关系:病例对照研究

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Background Malaria and anaemia ( Haemoglobin Methods Study participants were randomly selected from a list of children who participated in a survey in December 2010. Children aged from 1 to 10 years with haemoglobin level below 11 g/dl represented cases (anaemic children). Control participants were eligible if of same age group and their haemoglobin level was >= 11 g/dl. For each participant, a physical examination was done and anthropometric data collected prior to a biological assessment which included: malaria parasitaemia infection, intestinal worm carriage, G6PD deficiency, sickle cell disorders, and alpha-talassaemia. Results Three hundred and fifty two children 5 years (aOR=0.03, 95%CI[0.01-0.08]). Stratified by age group, anaemia was significantly associated with stunting in children less than 5 years (aOR=3.1 95%CI[1.4 – 6.8]), with, sickle cell disorders (aOR=3.5 95%CI [1.4 – 9.0]), alpha-thalassemia (or=2.4 95%CI[1.1–5.3]) and stunting (aOR=3.6 95%CI [1.6–8.2]) for children above 5 years. No association was found between G6PD deficiency, intestinal worm carriage and children’s gender. Conclusion Malaria parasitaemia, stunting and haemoglobin genetic disorders represented the major causes of anaemia among study participants. Anaemia control in this area could be achieved by developing integrated interventions targeting both malaria and malnutrition.
机译:背景疟疾和贫血(血红蛋白方法)研究参与者是从2010年12月参加调查的儿童列表中随机选择的。1至10岁的儿童血红蛋白水平低于11 g / dl的病例为贫血儿童(厌食症儿童)。如果年龄相同且血红蛋白水平> = 11 g / dl,则对每位参与者进行身体检查,并在进行生物学评估之前收集人体测量数据,包括:疟疾寄生虫血症感染,肠道蠕虫携带,G6PD缺乏结果302名5岁儿童(aOR = 0.03,95%CI [0.01-0.08])按年龄层分层,贫血与5岁以下儿童的发育迟缓显着相关年(aOR = 3.1 95%CI [1.4 – 6.8]),镰状细胞疾病(aOR = 3.5 95%CI [1.4 – 9.0]),地中海贫血(或= 2.4 95%CI [1.1–5.3])和儿童发育迟缓(aOR = 3.6 95%CI [1.6–8.2]) 5年以上。没有发现G6PD缺乏症,肠道蠕虫携带与儿童性别之间存在关联。结论疟疾寄生虫血症,发育迟缓和血红蛋白遗传疾病是研究参与者贫血的主要原因。通过制定针对疟疾和营养不良的综合干预措施,可以控制该地区的贫血。

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