乌干达镰状细胞监测研究(US3)中的镰状细胞特征和疾病负担:一项横断面研究。
Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study.
机构信息
Department of Paediatrics and Child Health, Makerere University College of Health Sciences, Kampala, Uganda.
Central Public Health Laboratories, Kampala, Uganda.
出版信息
Lancet Glob Health. 2016 Mar;4(3):e195-200. doi: 10.1016/S2214-109X(15)00288-0. Epub 2016 Jan 29.
BACKGROUND
Sickle cell disease contributes substantially to mortality in children younger than 5 years in sub-Saharan Africa. In Uganda, 20,000 babies per year are thought to be born with sickle cell disease, but accurate data are not available. We did the cross-sectional Uganda Sickle Surveillance Study to assess the burden of disease.
METHODS
The primary objective of the study was to calculate prevalence of sickle cell trait and disease. We obtained punch samples from dried blood spots routinely collected from HIV-exposed infants in ten regions and 112 districts across Uganda for the national Early Infant Diagnosis programme. Haemoglobin electrophoresis by isoelectric focusing was done on all samples to identify those from babies with sickle trait or disease.
FINDINGS
Between February, 2014, and March, 2015, 99,243 dried blood spots were analysed and results were available for 97,631. The overall number of children with sickle cell trait was 12,979 (13·3%) and with disease was 716 (0·7%). Sickle cell numbers ranged from 631 (4·6%) for trait and 23 (0·2%) for disease of 13,649 in the South Western region to 1306 (19·8%) for trait and 96 (1·5%) for disease of 6581 in the East Central region. Sickle cell trait was seen in all districts. The lowest prevalence was less than 3·0% in two districts. Eight districts had prevalence greater than 20·0%, with the highest being 23·9%. Sickle cell disease was less common in children older than 12 months or who were HIV positive, which is consistent with comorbidity and early mortality.
INTERPRETATION
Prevalence of sickle cell trait and disease were high in Uganda, with notable variation between regions and districts. The data will help to inform national strategies for sickle cell disease, including neonatal screening.
FUNDING
Cincinnati Children's Research Foundation.
背景
在撒哈拉以南非洲,镰状细胞病导致 5 岁以下儿童的死亡率居高不下。在乌干达,每年约有 2 万名婴儿出生时患有镰状细胞病,但没有准确的数据。我们进行了乌干达镰状细胞监测研究,以评估疾病负担。
方法
该研究的主要目的是计算镰状细胞特征和疾病的患病率。我们从十个地区和乌干达 112 个区的艾滋病毒暴露婴儿常规收集的干血斑中获得了样本,用于国家早期婴儿诊断计划。我们对所有样本进行等电聚焦血红蛋白电泳,以确定那些来自镰状细胞特征或疾病的婴儿。
结果
在 2014 年 2 月至 2015 年 3 月期间,我们分析了 99243 个干血斑,其中 97631 个有结果。镰状细胞特征的儿童总数为 12979 人(13.3%),镰状细胞疾病为 716 人(0.7%)。镰状细胞数量从西南部地区的 13649 人中有 631 人(4.6%)的特征和 23 人(0.2%)的疾病,到中东部地区的 6581 人中有 1306 人(19.8%)的特征和 96 人(1.5%)的疾病不等。镰状细胞特征在所有地区都有出现。两个地区的最低患病率低于 3.0%。八个地区的患病率超过 20.0%,其中最高的是 23.9%。镰状细胞疾病在 12 个月以上或艾滋病毒阳性的儿童中较为少见,这与合并症和早期死亡率一致。
解释
镰状细胞特征和疾病在乌干达的患病率很高,地区和地区之间存在显著差异。这些数据将有助于为镰状细胞病的国家战略提供信息,包括新生儿筛查。
资助
辛辛那提儿童研究基金会。