Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon

Information on the etiology of anemia is necessary to design effective anemia control programs. Our objective was to measure the prevalence of inherited hemoglobin disorders (IHD) in a representative sample of children in urban Cameroon, and examine the relationships between IHD and anemia. In a clu...

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Main Authors: Reina Engle-Stone, Thomas N. Williams, Martin Nankap, Alex Ndjebayi, Marie-Madeleine Gimou, Yannick Oyono, Ann Tarini, Kenneth H. Brown, Ralph Green
Format: Article
Language:English
Published: MDPI AG 2017-07-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/9/7/693
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spelling doaj-22b7a061f4064d4d863597bdb858cb0b2020-11-25T00:57:52ZengMDPI AGNutrients2072-66432017-07-019769310.3390/nu9070693nu9070693Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, CameroonReina Engle-Stone0Thomas N. Williams1Martin Nankap2Alex Ndjebayi3Marie-Madeleine Gimou4Yannick Oyono5Ann Tarini6Kenneth H. Brown7Ralph Green8Department of Nutrition, University of California, Davis, CA 95616, USAKEMRI/Wellcome Trust Research Programme, Kilifi, KenyaHelen Keller International, Cameroon, BP 14227 Yaoundé, CameroonHelen Keller International, Cameroon, BP 14227 Yaoundé, CameroonCentre Pasteur du Cameroun, BP 1274 Yaoundé, CameroonCentre Pasteur du Cameroun, BP 1274 Yaoundé, CameroonHelen Keller International, Cameroon, BP 14227 Yaoundé, CameroonDepartment of Nutrition, University of California, Davis, CA 95616, USADepartment of Medical Pathology and Laboratory Medicine, UC Davis Medical Center, Sacramento, CA 95817, USAInformation on the etiology of anemia is necessary to design effective anemia control programs. Our objective was to measure the prevalence of inherited hemoglobin disorders (IHD) in a representative sample of children in urban Cameroon, and examine the relationships between IHD and anemia. In a cluster survey of children 12–59 months of age (n = 291) in Yaoundé and Douala, we assessed hemoglobin (Hb), malaria infection, and plasma indicators of inflammation and micronutrient status. Hb S was detected by HPLC, and α+thalassemia (3.7 kb deletions) by PCR. Anemia (Hb < 110 g/L), inflammation, and malaria were present in 45%, 46%, and 8% of children. A total of 13.7% of children had HbAS, 1.6% had HbSS, and 30.6% and 3.1% had heterozygous and homozygous α+thalassemia. The prevalence of anemia was greater among HbAS compared to HbAA children (60.3 vs. 42.0%, p = 0.038), although mean Hb concentrations did not differ, p = 0.38). Hb and anemia prevalence did not differ among children with or without single gene deletion α+thalassemia. In multi-variable models, anemia was independently predicted by HbAS, HbSS, malaria, iron deficiency (ID; inflammation-adjusted ferritin <12 µg/L), higher C-reactive protein, lower plasma folate, and younger age. Elevated soluble transferrin receptor concentration (>8.3 mg/L) was associated with younger age, malaria, greater mean reticulocyte counts, inflammation, HbSS genotype, and ID. IHD are prevalent but contribute modestly to anemia among children in urban Cameroon.https://www.mdpi.com/2072-6643/9/7/693anemiahemoglobinopathyironchildrenthalassemiasickle cell
collection DOAJ
language English
format Article
sources DOAJ
author Reina Engle-Stone
Thomas N. Williams
Martin Nankap
Alex Ndjebayi
Marie-Madeleine Gimou
Yannick Oyono
Ann Tarini
Kenneth H. Brown
Ralph Green
spellingShingle Reina Engle-Stone
Thomas N. Williams
Martin Nankap
Alex Ndjebayi
Marie-Madeleine Gimou
Yannick Oyono
Ann Tarini
Kenneth H. Brown
Ralph Green
Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon
Nutrients
anemia
hemoglobinopathy
iron
children
thalassemia
sickle cell
author_facet Reina Engle-Stone
Thomas N. Williams
Martin Nankap
Alex Ndjebayi
Marie-Madeleine Gimou
Yannick Oyono
Ann Tarini
Kenneth H. Brown
Ralph Green
author_sort Reina Engle-Stone
title Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon
title_short Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon
title_full Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon
title_fullStr Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon
title_full_unstemmed Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon
title_sort prevalence of inherited hemoglobin disorders and relationships with anemia and micronutrient status among children in yaoundé and douala, cameroon
publisher MDPI AG
series Nutrients
issn 2072-6643
publishDate 2017-07-01
description Information on the etiology of anemia is necessary to design effective anemia control programs. Our objective was to measure the prevalence of inherited hemoglobin disorders (IHD) in a representative sample of children in urban Cameroon, and examine the relationships between IHD and anemia. In a cluster survey of children 12–59 months of age (n = 291) in Yaoundé and Douala, we assessed hemoglobin (Hb), malaria infection, and plasma indicators of inflammation and micronutrient status. Hb S was detected by HPLC, and α+thalassemia (3.7 kb deletions) by PCR. Anemia (Hb < 110 g/L), inflammation, and malaria were present in 45%, 46%, and 8% of children. A total of 13.7% of children had HbAS, 1.6% had HbSS, and 30.6% and 3.1% had heterozygous and homozygous α+thalassemia. The prevalence of anemia was greater among HbAS compared to HbAA children (60.3 vs. 42.0%, p = 0.038), although mean Hb concentrations did not differ, p = 0.38). Hb and anemia prevalence did not differ among children with or without single gene deletion α+thalassemia. In multi-variable models, anemia was independently predicted by HbAS, HbSS, malaria, iron deficiency (ID; inflammation-adjusted ferritin <12 µg/L), higher C-reactive protein, lower plasma folate, and younger age. Elevated soluble transferrin receptor concentration (>8.3 mg/L) was associated with younger age, malaria, greater mean reticulocyte counts, inflammation, HbSS genotype, and ID. IHD are prevalent but contribute modestly to anemia among children in urban Cameroon.
topic anemia
hemoglobinopathy
iron
children
thalassemia
sickle cell
url https://www.mdpi.com/2072-6643/9/7/693
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