Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study

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...

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Main Authors: Grace Ndeezi, MBChB PhD, Charles Kiyaga, MSc MPhil, Arielle G Hernandez, BA, Deogratias Munube, MBChB, Thad A Howard, MS, Isaac Ssewanyana, MSc, Jesca Nsungwa, MBChB PhD, Sarah Kiguli, MBChB, Christopher M Ndugwa, MBChB, Dr. Russell E Ware, MD PhD, Jane R Aceng, MBChB MPH
Format: Article
Language:English
Published: Elsevier 2016-03-01
Series:The Lancet Global Health
Online Access:http://www.sciencedirect.com/science/article/pii/S2214109X15002880
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spelling doaj-a2fd245eac9a488a9a816aa064f2be9f2020-11-25T02:39:19ZengElsevierThe Lancet Global Health2214-109X2016-03-0143e195e20010.1016/S2214-109X(15)00288-0Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional studyGrace Ndeezi, MBChB PhD0Charles Kiyaga, MSc MPhil1Arielle G Hernandez, BA2Deogratias Munube, MBChB3Thad A Howard, MS4Isaac Ssewanyana, MSc5Jesca Nsungwa, MBChB PhD6Sarah Kiguli, MBChB7Christopher M Ndugwa, MBChB8Dr. Russell E Ware, MD PhD9Jane R Aceng, MBChB MPH10Department of Paediatrics and Child Health, Makerere University College of Health Sciences, Kampala, UgandaCentral Public Health Laboratories, Kampala, UgandaDivision of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USAMulago Hospital, Kampala, UgandaDivision of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USACentral Public Health Laboratories, Kampala, UgandaMinistry of Health for the Republic of Uganda, Kampala, UgandaDepartment of Paediatrics and Child Health, Makerere University College of Health Sciences, Kampala, UgandaDepartment of Paediatrics and Child Health, Makerere University College of Health Sciences, Kampala, UgandaDivision of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USAMinistry of Health for the Republic of Uganda, Kampala, UgandaBackground: 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.http://www.sciencedirect.com/science/article/pii/S2214109X15002880
collection DOAJ
language English
format Article
sources DOAJ
author Grace Ndeezi, MBChB PhD
Charles Kiyaga, MSc MPhil
Arielle G Hernandez, BA
Deogratias Munube, MBChB
Thad A Howard, MS
Isaac Ssewanyana, MSc
Jesca Nsungwa, MBChB PhD
Sarah Kiguli, MBChB
Christopher M Ndugwa, MBChB
Dr. Russell E Ware, MD PhD
Jane R Aceng, MBChB MPH
spellingShingle Grace Ndeezi, MBChB PhD
Charles Kiyaga, MSc MPhil
Arielle G Hernandez, BA
Deogratias Munube, MBChB
Thad A Howard, MS
Isaac Ssewanyana, MSc
Jesca Nsungwa, MBChB PhD
Sarah Kiguli, MBChB
Christopher M Ndugwa, MBChB
Dr. Russell E Ware, MD PhD
Jane R Aceng, MBChB MPH
Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study
The Lancet Global Health
author_facet Grace Ndeezi, MBChB PhD
Charles Kiyaga, MSc MPhil
Arielle G Hernandez, BA
Deogratias Munube, MBChB
Thad A Howard, MS
Isaac Ssewanyana, MSc
Jesca Nsungwa, MBChB PhD
Sarah Kiguli, MBChB
Christopher M Ndugwa, MBChB
Dr. Russell E Ware, MD PhD
Jane R Aceng, MBChB MPH
author_sort Grace Ndeezi, MBChB PhD
title Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study
title_short Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study
title_full Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study
title_fullStr Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study
title_full_unstemmed Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study
title_sort burden of sickle cell trait and disease in the uganda sickle surveillance study (us3): a cross-sectional study
publisher Elsevier
series The Lancet Global Health
issn 2214-109X
publishDate 2016-03-01
description 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.
url http://www.sciencedirect.com/science/article/pii/S2214109X15002880
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