Life‐course of atopy and allergy‐related disease events in tropical sub‐Saharan Africa: A birth cohort study
Background In high‐income countries, allergy‐related diseases (ARDs) follow a typical sequence, the ‘Atopic March’. Little is known about the life‐course of ARDs in the markedly different, low‐income, tropical environment. We describe ARDs in a tropical, African birth cohort. Methods Ugandan childre...
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Published in | Pediatric allergy and immunology Vol. 28; no. 4; pp. 377 - 383 |
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Main Authors | , , , , , , , , , , , , , |
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01.06.2017
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Abstract | Background
In high‐income countries, allergy‐related diseases (ARDs) follow a typical sequence, the ‘Atopic March’. Little is known about the life‐course of ARDs in the markedly different, low‐income, tropical environment. We describe ARDs in a tropical, African birth cohort.
Methods
Ugandan children were followed from birth to 9 years. ISAAC questionnaires were completed at intervals; doctor‐diagnosed ARDs were recorded throughout follow‐up. Skin prick tests (SPTs) were performed at 3 and 9 years. Atopy was defined as ≥1 positive SPT.
Results
Of the 2345 live‐born children, 1214 (52%) were seen at 9 years. Wheeze and eczema were common in infancy, but by 9 years, only 4% reported recent wheeze, 5% eczema and 5% rhinitis. Between 3 and 9 years, atopy prevalence increased from 19% to 25%. Atopy at 3 or 9 years was associated with reported ARD events at 9 years, for example OR = 5.2 (95% CI 2.9–10.7) for atopy and recent wheeze at 9 years. Reported or doctor‐diagnosed ARD events in early childhood were associated with the same events in later childhood, for example OR = 4.4 (2.3–8.4) for the association between reported wheeze before 3 years with reported recent wheeze at 9 years, but progression from early eczema to later rhinitis or asthma was not observed.
Conclusion
Allergen sensitization started early in childhood and increased with age. Eczema and wheeze were common in infancy and declined with age. Atopy was strongly associated with ARD among the few affected children. The typical Atopic March did not occur. Environmental exposures during childhood may dissociate atopy and ARD. |
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AbstractList | Background
In high‐income countries, allergy‐related diseases (ARDs) follow a typical sequence, the ‘Atopic March’. Little is known about the life‐course of ARDs in the markedly different, low‐income, tropical environment. We describe ARDs in a tropical, African birth cohort.
Methods
Ugandan children were followed from birth to 9 years. ISAAC questionnaires were completed at intervals; doctor‐diagnosed ARDs were recorded throughout follow‐up. Skin prick tests (SPTs) were performed at 3 and 9 years. Atopy was defined as ≥1 positive SPT.
Results
Of the 2345 live‐born children, 1214 (52%) were seen at 9 years. Wheeze and eczema were common in infancy, but by 9 years, only 4% reported recent wheeze, 5% eczema and 5% rhinitis. Between 3 and 9 years, atopy prevalence increased from 19% to 25%. Atopy at 3 or 9 years was associated with reported ARD events at 9 years, for example OR = 5.2 (95% CI 2.9–10.7) for atopy and recent wheeze at 9 years. Reported or doctor‐diagnosed ARD events in early childhood were associated with the same events in later childhood, for example OR = 4.4 (2.3–8.4) for the association between reported wheeze before 3 years with reported recent wheeze at 9 years, but progression from early eczema to later rhinitis or asthma was not observed.
Conclusion
Allergen sensitization started early in childhood and increased with age. Eczema and wheeze were common in infancy and declined with age. Atopy was strongly associated with ARD among the few affected children. The typical Atopic March did not occur. Environmental exposures during childhood may dissociate atopy and ARD. BACKGROUNDIn high-income countries, allergy-related diseases (ARDs) follow a typical sequence, the 'Atopic March'. Little is known about the life-course of ARDs in the markedly different, low-income, tropical environment. We describe ARDs in a tropical, African birth cohort.METHODSUgandan children were followed from birth to 9 years. ISAAC questionnaires were completed at intervals; doctor-diagnosed ARDs were recorded throughout follow-up. Skin prick tests (SPTs) were performed at 3 and 9 years. Atopy was defined as ≥1 positive SPT.RESULTSOf the 2345 live-born children, 1214 (52%) were seen at 9 years. Wheeze and eczema were common in infancy, but by 9 years, only 4% reported recent wheeze, 5% eczema and 5% rhinitis. Between 3 and 9 years, atopy prevalence increased from 19% to 25%. Atopy at 3 or 9 years was associated with reported ARD events at 9 years, for example OR = 5.2 (95% CI 2.9-10.7) for atopy and recent wheeze at 9 years. Reported or doctor-diagnosed ARD events in early childhood were associated with the same events in later childhood, for example OR = 4.4 (2.3-8.4) for the association between reported wheeze before 3 years with reported recent wheeze at 9 years, but progression from early eczema to later rhinitis or asthma was not observed.CONCLUSIONAllergen sensitization started early in childhood and increased with age. Eczema and wheeze were common in infancy and declined with age. Atopy was strongly associated with ARD among the few affected children. The typical Atopic March did not occur. Environmental exposures during childhood may dissociate atopy and ARD. In high-income countries, allergy-related diseases (ARDs) follow a typical sequence, the 'Atopic March'. Little is known about the life-course of ARDs in the markedly different, low-income, tropical environment. We describe ARDs in a tropical, African birth cohort. Ugandan children were followed from birth to 9 years. ISAAC questionnaires were completed at intervals; doctor-diagnosed ARDs were recorded throughout follow-up. Skin prick tests (SPTs) were performed at 3 and 9 years. Atopy was defined as ≥1 positive SPT. Of the 2345 live-born children, 1214 (52%) were seen at 9 years. Wheeze and eczema were common in infancy, but by 9 years, only 4% reported recent wheeze, 5% eczema and 5% rhinitis. Between 3 and 9 years, atopy prevalence increased from 19% to 25%. Atopy at 3 or 9 years was associated with reported ARD events at 9 years, for example OR = 5.2 (95% CI 2.9-10.7) for atopy and recent wheeze at 9 years. Reported or doctor-diagnosed ARD events in early childhood were associated with the same events in later childhood, for example OR = 4.4 (2.3-8.4) for the association between reported wheeze before 3 years with reported recent wheeze at 9 years, but progression from early eczema to later rhinitis or asthma was not observed. Allergen sensitization started early in childhood and increased with age. Eczema and wheeze were common in infancy and declined with age. Atopy was strongly associated with ARD among the few affected children. The typical Atopic March did not occur. Environmental exposures during childhood may dissociate atopy and ARD. Background In high-income countries, allergy-related diseases (ARDs) follow a typical sequence, the 'Atopic March'. Little is known about the life-course of ARDs in the markedly different, low-income, tropical environment. We describe ARDs in a tropical, African birth cohort. Methods Ugandan children were followed from birth to 9 years. ISAAC questionnaires were completed at intervals; doctor-diagnosed ARDs were recorded throughout follow-up. Skin prick tests (SPTs) were performed at 3 and 9 years. Atopy was defined as ≥1 positive SPT. Results Of the 2345 live-born children, 1214 (52%) were seen at 9 years. Wheeze and eczema were common in infancy, but by 9 years, only 4% reported recent wheeze, 5% eczema and 5% rhinitis. Between 3 and 9 years, atopy prevalence increased from 19% to 25%. Atopy at 3 or 9 years was associated with reported ARD events at 9 years, for example OR = 5.2 (95% CI 2.9-10.7) for atopy and recent wheeze at 9 years. Reported or doctor-diagnosed ARD events in early childhood were associated with the same events in later childhood, for example OR = 4.4 (2.3-8.4) for the association between reported wheeze before 3 years with reported recent wheeze at 9 years, but progression from early eczema to later rhinitis or asthma was not observed. Conclusion Allergen sensitization started early in childhood and increased with age. Eczema and wheeze were common in infancy and declined with age. Atopy was strongly associated with ARD among the few affected children. The typical Atopic March did not occur. Environmental exposures during childhood may dissociate atopy and ARD. Abstract Background In high‐income countries, allergy‐related diseases ( ARD s) follow a typical sequence, the ‘Atopic March’. Little is known about the life‐course of ARD s in the markedly different, low‐income, tropical environment. We describe ARD s in a tropical, African birth cohort. Methods Ugandan children were followed from birth to 9 years. ISAAC questionnaires were completed at intervals; doctor‐diagnosed ARD s were recorded throughout follow‐up. Skin prick tests ( SPT s) were performed at 3 and 9 years. Atopy was defined as ≥1 positive SPT . Results Of the 2345 live‐born children, 1214 (52%) were seen at 9 years. Wheeze and eczema were common in infancy, but by 9 years, only 4% reported recent wheeze, 5% eczema and 5% rhinitis. Between 3 and 9 years, atopy prevalence increased from 19% to 25%. Atopy at 3 or 9 years was associated with reported ARD events at 9 years, for example OR = 5.2 (95% CI 2.9–10.7) for atopy and recent wheeze at 9 years. Reported or doctor‐diagnosed ARD events in early childhood were associated with the same events in later childhood, for example OR = 4.4 (2.3–8.4) for the association between reported wheeze before 3 years with reported recent wheeze at 9 years, but progression from early eczema to later rhinitis or asthma was not observed. Conclusion Allergen sensitization started early in childhood and increased with age. Eczema and wheeze were common in infancy and declined with age. Atopy was strongly associated with ARD among the few affected children. The typical Atopic March did not occur. Environmental exposures during childhood may dissociate atopy and ARD . |
Author | Kabagenyi, Joyce Mpairwe, Harriet Webb, Emily L. Elliott, Alison M. Muwanga, Moses Muhangi, Lawrence Nampijja, Margaret Namara, Benigna Lule, Swaib A. Nash, Stephen Nkurunungi, Gyaviira Kizito, Dennison Akello, Florence Kahwa, Joseph |
AuthorAffiliation | 2 MRC/UVRI Uganda Research Unit Entebbe Uganda 1 London School of Hygiene and Tropical Medicine London UK 3 Entebbe Hospital Entebbe Uganda |
AuthorAffiliation_xml | – name: 3 Entebbe Hospital Entebbe Uganda – name: 2 MRC/UVRI Uganda Research Unit Entebbe Uganda – name: 1 London School of Hygiene and Tropical Medicine London UK |
Author_xml | – sequence: 1 givenname: Swaib A. orcidid: 0000-0002-6271-2033 surname: Lule fullname: Lule, Swaib A. email: swaiblule@yahoo.com organization: MRC/UVRI Uganda Research Unit – sequence: 2 givenname: Harriet surname: Mpairwe fullname: Mpairwe, Harriet organization: MRC/UVRI Uganda Research Unit – sequence: 3 givenname: Margaret surname: Nampijja fullname: Nampijja, Margaret organization: MRC/UVRI Uganda Research Unit – sequence: 4 givenname: Florence surname: Akello fullname: Akello, Florence organization: MRC/UVRI Uganda Research Unit – sequence: 5 givenname: Joyce surname: Kabagenyi fullname: Kabagenyi, Joyce organization: MRC/UVRI Uganda Research Unit – sequence: 6 givenname: Benigna surname: Namara fullname: Namara, Benigna organization: MRC/UVRI Uganda Research Unit – sequence: 7 givenname: Gyaviira orcidid: 0000-0003-4062-9105 surname: Nkurunungi fullname: Nkurunungi, Gyaviira organization: MRC/UVRI Uganda Research Unit – sequence: 8 givenname: Dennison surname: Kizito fullname: Kizito, Dennison organization: MRC/UVRI Uganda Research Unit – sequence: 9 givenname: Joseph surname: Kahwa fullname: Kahwa, Joseph organization: MRC/UVRI Uganda Research Unit – sequence: 10 givenname: Lawrence surname: Muhangi fullname: Muhangi, Lawrence organization: MRC/UVRI Uganda Research Unit – sequence: 11 givenname: Stephen orcidid: 0000-0003-2086-1740 surname: Nash fullname: Nash, Stephen organization: London School of Hygiene and Tropical Medicine – sequence: 12 givenname: Moses surname: Muwanga fullname: Muwanga, Moses organization: Entebbe Hospital – sequence: 13 givenname: Emily L. surname: Webb fullname: Webb, Emily L. organization: London School of Hygiene and Tropical Medicine – sequence: 14 givenname: Alison M. surname: Elliott fullname: Elliott, Alison M. organization: MRC/UVRI Uganda Research Unit |
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Copyright | 2017 The Authors Published by John Wiley & Sons Ltd. 2017 The Authors Pediatric Allergy and Immunology Published by John Wiley & Sons Ltd. Copyright © 2017 John Wiley & Sons A/S |
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Keywords | birth cohort wheeze Africa urticaria atopy eczema Uganda rhinitis conjunctivitis |
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In high‐income countries, allergy‐related diseases (ARDs) follow a typical sequence, the ‘Atopic March’. Little is known about the life‐course of... In high-income countries, allergy-related diseases (ARDs) follow a typical sequence, the 'Atopic March'. Little is known about the life-course of ARDs in the... Abstract Background In high‐income countries, allergy‐related diseases ( ARD s) follow a typical sequence, the ‘Atopic March’. Little is known about the... Background In high-income countries, allergy-related diseases (ARDs) follow a typical sequence, the 'Atopic March'. Little is known about the life-course of... BACKGROUNDIn high-income countries, allergy-related diseases (ARDs) follow a typical sequence, the 'Atopic March'. Little is known about the life-course of... |
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SubjectTerms | Africa Africa South of the Sahara - epidemiology Allergens Allergens - immunology Allergies Asthma Atopy birth cohort Child Child, Preschool Children Cohort analysis Cohort Studies Comorbidity conjunctivitis Developing Countries Eczema Epidemiology Female Follow-Up Studies Humans Hypersensitivity, Immediate - epidemiology Male Original Pediatrics Poverty Prevalence Respiratory Sounds Rhinitis Skin diseases Skin Tests Surveys and Questionnaires Tropical environment Uganda Uganda - epidemiology urticaria wheeze |
Title | Life‐course of atopy and allergy‐related disease events in tropical sub‐Saharan Africa: A birth cohort study |
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