Effects of treating helminths during pregnancy and early childhood on risk of allergy‐related outcomes: Follow‐up of a randomized controlled trial

Background Helminth infections, common in low‐income countries, may protect against allergy‐related disease. Early exposure may be a key. In the Entebbe Mother and Baby Study, treating helminths during pregnancy resulted in increased eczema rates in early childhood. We followed the cohort to determi...

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Veröffentlicht in:Pediatric allergy and immunology 2017-12, Vol.28 (8), p.784-792
Hauptverfasser: Namara, Benigna, Nash, Stephen, Lule, Swaib A., Akurut, Hellen, Mpairwe, Harriet, Akello, Florence, Tumusiime, Josephine, Kizza, Moses, Kabagenyi, Joyce, Nkurunungi, Gyaviira, Muhangi, Lawrence, Webb, Emily L., Muwanga, Moses, Elliott, Alison M.
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container_end_page 792
container_issue 8
container_start_page 784
container_title Pediatric allergy and immunology
container_volume 28
creator Namara, Benigna
Nash, Stephen
Lule, Swaib A.
Akurut, Hellen
Mpairwe, Harriet
Akello, Florence
Tumusiime, Josephine
Kizza, Moses
Kabagenyi, Joyce
Nkurunungi, Gyaviira
Muhangi, Lawrence
Webb, Emily L.
Muwanga, Moses
Elliott, Alison M.
description Background Helminth infections, common in low‐income countries, may protect against allergy‐related disease. Early exposure may be a key. In the Entebbe Mother and Baby Study, treating helminths during pregnancy resulted in increased eczema rates in early childhood. We followed the cohort to determine whether this translated to increased asthma rates at school age. Methods This randomized, double‐blind, placebo‐controlled trial, conducted in Entebbe, Uganda, had three interventions. During pregnancy, women were randomized, simultaneously, to albendazole vs placebo and to praziquantel vs placebo. Their children were independently randomized to quarterly albendazole vs placebo from age 15 months to 5 years. We here report follow‐up to age 9 years. Primary outcomes at 9 years were recent reported wheeze, skin prick test positivity (SPT) to common allergens and allergen‐specific IgE positivity to dust mite or cockroach. Secondary outcomes were doctor‐diagnosed asthma and eczema rates between 5 and 9 years, recent eczema, rhinitis and urticaria at 9 years, and SPT and IgE responses to individual allergens. Results 2507 pregnant women were enrolled; 1215 children were seen at age nine, of whom 1188 are included in this analysis. Reported wheeze was rare at 9 years (3.7%) while SPT positivity (25.0%) and IgE positivity (44.1%) were common. There was no evidence of a treatment effect for any of the three interventions on any of the primary outcomes. Conclusions Prenatal and early‐life treatment of helminths, in the absence of change in other exposures, is unlikely to increase the risk of atopic diseases later in childhood in this tropical, low‐income setting.
doi_str_mv 10.1111/pai.12804
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Early exposure may be a key. In the Entebbe Mother and Baby Study, treating helminths during pregnancy resulted in increased eczema rates in early childhood. We followed the cohort to determine whether this translated to increased asthma rates at school age. Methods This randomized, double‐blind, placebo‐controlled trial, conducted in Entebbe, Uganda, had three interventions. During pregnancy, women were randomized, simultaneously, to albendazole vs placebo and to praziquantel vs placebo. Their children were independently randomized to quarterly albendazole vs placebo from age 15 months to 5 years. We here report follow‐up to age 9 years. Primary outcomes at 9 years were recent reported wheeze, skin prick test positivity (SPT) to common allergens and allergen‐specific IgE positivity to dust mite or cockroach. Secondary outcomes were doctor‐diagnosed asthma and eczema rates between 5 and 9 years, recent eczema, rhinitis and urticaria at 9 years, and SPT and IgE responses to individual allergens. Results 2507 pregnant women were enrolled; 1215 children were seen at age nine, of whom 1188 are included in this analysis. Reported wheeze was rare at 9 years (3.7%) while SPT positivity (25.0%) and IgE positivity (44.1%) were common. There was no evidence of a treatment effect for any of the three interventions on any of the primary outcomes. Conclusions Prenatal and early‐life treatment of helminths, in the absence of change in other exposures, is unlikely to increase the risk of atopic diseases later in childhood in this tropical, low‐income setting.</description><identifier>ISSN: 0905-6157</identifier><identifier>EISSN: 1399-3038</identifier><identifier>DOI: 10.1111/pai.12804</identifier><identifier>PMID: 28892575</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Age ; Albendazole ; Albendazole - therapeutic use ; Allergens ; Allergies ; Anthelmintics - therapeutic use ; Asthma ; Asthma - diagnosis ; Asthma - etiology ; Atopy ; Child ; Child, Preschool ; Childhood ; Children ; Double-Blind Method ; Eczema ; Exposure ; Female ; Follow-Up Studies ; Health risks ; helminth ; Helminthiasis - drug therapy ; Helminthiasis - immunology ; Humans ; IgE ; Immunoglobulin E ; Infant ; Low income groups ; Male ; Original ; Praziquantel ; Praziquantel - therapeutic use ; Pregnancy ; Pregnancy Complications, Parasitic - drug therapy ; Pregnancy Complications, Parasitic - immunology ; prenatal ; Prenatal Exposure Delayed Effects - etiology ; Randomization ; Rhinitis ; Risk Factors ; school age ; Skin diseases ; Skin tests ; Treatment Outcome ; Uganda ; Urticaria ; wheeze</subject><ispartof>Pediatric allergy and immunology, 2017-12, Vol.28 (8), p.784-792</ispartof><rights>2017 The Authors. Pediatric Allergy and Immunology Published by John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2017 John Wiley &amp; Sons A/S</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4434-153571cf394f3ded0f34fc64903552aff722d29a3ef189f09211715bf2678ed73</citedby><cites>FETCH-LOGICAL-c4434-153571cf394f3ded0f34fc64903552aff722d29a3ef189f09211715bf2678ed73</cites><orcidid>0000-0003-2086-1740 ; 0000-0002-6271-2033 ; 0000-0003-4062-9105</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpai.12804$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpai.12804$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28892575$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Namara, Benigna</creatorcontrib><creatorcontrib>Nash, Stephen</creatorcontrib><creatorcontrib>Lule, Swaib A.</creatorcontrib><creatorcontrib>Akurut, Hellen</creatorcontrib><creatorcontrib>Mpairwe, Harriet</creatorcontrib><creatorcontrib>Akello, Florence</creatorcontrib><creatorcontrib>Tumusiime, Josephine</creatorcontrib><creatorcontrib>Kizza, Moses</creatorcontrib><creatorcontrib>Kabagenyi, Joyce</creatorcontrib><creatorcontrib>Nkurunungi, Gyaviira</creatorcontrib><creatorcontrib>Muhangi, Lawrence</creatorcontrib><creatorcontrib>Webb, Emily L.</creatorcontrib><creatorcontrib>Muwanga, Moses</creatorcontrib><creatorcontrib>Elliott, Alison M.</creatorcontrib><title>Effects of treating helminths during pregnancy and early childhood on risk of allergy‐related outcomes: Follow‐up of a randomized controlled trial</title><title>Pediatric allergy and immunology</title><addtitle>Pediatr Allergy Immunol</addtitle><description>Background Helminth infections, common in low‐income countries, may protect against allergy‐related disease. Early exposure may be a key. In the Entebbe Mother and Baby Study, treating helminths during pregnancy resulted in increased eczema rates in early childhood. We followed the cohort to determine whether this translated to increased asthma rates at school age. Methods This randomized, double‐blind, placebo‐controlled trial, conducted in Entebbe, Uganda, had three interventions. During pregnancy, women were randomized, simultaneously, to albendazole vs placebo and to praziquantel vs placebo. Their children were independently randomized to quarterly albendazole vs placebo from age 15 months to 5 years. We here report follow‐up to age 9 years. Primary outcomes at 9 years were recent reported wheeze, skin prick test positivity (SPT) to common allergens and allergen‐specific IgE positivity to dust mite or cockroach. Secondary outcomes were doctor‐diagnosed asthma and eczema rates between 5 and 9 years, recent eczema, rhinitis and urticaria at 9 years, and SPT and IgE responses to individual allergens. Results 2507 pregnant women were enrolled; 1215 children were seen at age nine, of whom 1188 are included in this analysis. Reported wheeze was rare at 9 years (3.7%) while SPT positivity (25.0%) and IgE positivity (44.1%) were common. There was no evidence of a treatment effect for any of the three interventions on any of the primary outcomes. Conclusions Prenatal and early‐life treatment of helminths, in the absence of change in other exposures, is unlikely to increase the risk of atopic diseases later in childhood in this tropical, low‐income setting.</description><subject>Age</subject><subject>Albendazole</subject><subject>Albendazole - therapeutic use</subject><subject>Allergens</subject><subject>Allergies</subject><subject>Anthelmintics - therapeutic use</subject><subject>Asthma</subject><subject>Asthma - diagnosis</subject><subject>Asthma - etiology</subject><subject>Atopy</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Childhood</subject><subject>Children</subject><subject>Double-Blind Method</subject><subject>Eczema</subject><subject>Exposure</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Health risks</subject><subject>helminth</subject><subject>Helminthiasis - drug therapy</subject><subject>Helminthiasis - immunology</subject><subject>Humans</subject><subject>IgE</subject><subject>Immunoglobulin E</subject><subject>Infant</subject><subject>Low income groups</subject><subject>Male</subject><subject>Original</subject><subject>Praziquantel</subject><subject>Praziquantel - therapeutic use</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Parasitic - drug therapy</subject><subject>Pregnancy Complications, Parasitic - immunology</subject><subject>prenatal</subject><subject>Prenatal Exposure Delayed Effects - etiology</subject><subject>Randomization</subject><subject>Rhinitis</subject><subject>Risk Factors</subject><subject>school age</subject><subject>Skin diseases</subject><subject>Skin tests</subject><subject>Treatment Outcome</subject><subject>Uganda</subject><subject>Urticaria</subject><subject>wheeze</subject><issn>0905-6157</issn><issn>1399-3038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp1kcFuFSEUhonR2Gt14QsYEjd2MS0MMAwuTJqm1SZNdKFrQpnDHSozXGHGZlz1EVz5gD6J3N7aqIlsIPxfvpyTH6HnlBzSco42xh_SuiX8AVpRplTFCGsfohVRRFQNFXIPPcn5ihAqWUMfo726bVUtpFihH6fOgZ0yjg5PCczkxzXuIQx-nPqMuzltPzYJ1qMZ7YLN2GEwKSzY9j50fYwdjiNOPn_eKkwIkNbLz5vvCYKZoITzZOMA-TU-iyHE6xLNm1sUpyKLg_9WKBvHKZW8PKfkTXiKHjkTMjy7u_fRp7PTjyfvqov3b89Pji8qyznjFRVMSGodU9yxDjriGHe24YowIWrjnKzrrlaGgaOtckTVlEoqLl3dyBY6yfbRm513M18O0FkoY5igN8kPJi06Gq__Tkbf63X8qoVsBBesCF7dCVL8MkOe9OCzhRDMCHHOmirWUiVYIwr68h_0Ks5pLOsVSiouhOKkUAc7yqaYcwJ3Pwwletu2Lm3r27YL--LP6e_J3_UW4GgHXPsAy_9N-sPx-U75C5O1uPw</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Namara, Benigna</creator><creator>Nash, Stephen</creator><creator>Lule, Swaib A.</creator><creator>Akurut, Hellen</creator><creator>Mpairwe, Harriet</creator><creator>Akello, Florence</creator><creator>Tumusiime, Josephine</creator><creator>Kizza, Moses</creator><creator>Kabagenyi, Joyce</creator><creator>Nkurunungi, Gyaviira</creator><creator>Muhangi, Lawrence</creator><creator>Webb, Emily L.</creator><creator>Muwanga, Moses</creator><creator>Elliott, Alison M.</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2086-1740</orcidid><orcidid>https://orcid.org/0000-0002-6271-2033</orcidid><orcidid>https://orcid.org/0000-0003-4062-9105</orcidid></search><sort><creationdate>201712</creationdate><title>Effects of treating helminths during pregnancy and early childhood on risk of allergy‐related outcomes: Follow‐up of a randomized controlled trial</title><author>Namara, Benigna ; Nash, Stephen ; Lule, Swaib A. ; Akurut, Hellen ; Mpairwe, Harriet ; Akello, Florence ; Tumusiime, Josephine ; Kizza, Moses ; Kabagenyi, Joyce ; Nkurunungi, Gyaviira ; Muhangi, Lawrence ; Webb, Emily L. ; Muwanga, Moses ; Elliott, Alison M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4434-153571cf394f3ded0f34fc64903552aff722d29a3ef189f09211715bf2678ed73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Age</topic><topic>Albendazole</topic><topic>Albendazole - therapeutic use</topic><topic>Allergens</topic><topic>Allergies</topic><topic>Anthelmintics - therapeutic use</topic><topic>Asthma</topic><topic>Asthma - diagnosis</topic><topic>Asthma - etiology</topic><topic>Atopy</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Childhood</topic><topic>Children</topic><topic>Double-Blind Method</topic><topic>Eczema</topic><topic>Exposure</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Health risks</topic><topic>helminth</topic><topic>Helminthiasis - drug therapy</topic><topic>Helminthiasis - immunology</topic><topic>Humans</topic><topic>IgE</topic><topic>Immunoglobulin E</topic><topic>Infant</topic><topic>Low income groups</topic><topic>Male</topic><topic>Original</topic><topic>Praziquantel</topic><topic>Praziquantel - therapeutic use</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Parasitic - drug therapy</topic><topic>Pregnancy Complications, Parasitic - immunology</topic><topic>prenatal</topic><topic>Prenatal Exposure Delayed Effects - etiology</topic><topic>Randomization</topic><topic>Rhinitis</topic><topic>Risk Factors</topic><topic>school age</topic><topic>Skin diseases</topic><topic>Skin tests</topic><topic>Treatment Outcome</topic><topic>Uganda</topic><topic>Urticaria</topic><topic>wheeze</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Namara, Benigna</creatorcontrib><creatorcontrib>Nash, Stephen</creatorcontrib><creatorcontrib>Lule, Swaib A.</creatorcontrib><creatorcontrib>Akurut, Hellen</creatorcontrib><creatorcontrib>Mpairwe, Harriet</creatorcontrib><creatorcontrib>Akello, Florence</creatorcontrib><creatorcontrib>Tumusiime, Josephine</creatorcontrib><creatorcontrib>Kizza, Moses</creatorcontrib><creatorcontrib>Kabagenyi, Joyce</creatorcontrib><creatorcontrib>Nkurunungi, Gyaviira</creatorcontrib><creatorcontrib>Muhangi, Lawrence</creatorcontrib><creatorcontrib>Webb, Emily L.</creatorcontrib><creatorcontrib>Muwanga, Moses</creatorcontrib><creatorcontrib>Elliott, Alison M.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pediatric allergy and immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Namara, Benigna</au><au>Nash, Stephen</au><au>Lule, Swaib A.</au><au>Akurut, Hellen</au><au>Mpairwe, Harriet</au><au>Akello, Florence</au><au>Tumusiime, Josephine</au><au>Kizza, Moses</au><au>Kabagenyi, Joyce</au><au>Nkurunungi, Gyaviira</au><au>Muhangi, Lawrence</au><au>Webb, Emily L.</au><au>Muwanga, Moses</au><au>Elliott, Alison M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of treating helminths during pregnancy and early childhood on risk of allergy‐related outcomes: Follow‐up of a randomized controlled trial</atitle><jtitle>Pediatric allergy and immunology</jtitle><addtitle>Pediatr Allergy Immunol</addtitle><date>2017-12</date><risdate>2017</risdate><volume>28</volume><issue>8</issue><spage>784</spage><epage>792</epage><pages>784-792</pages><issn>0905-6157</issn><eissn>1399-3038</eissn><abstract>Background Helminth infections, common in low‐income countries, may protect against allergy‐related disease. Early exposure may be a key. In the Entebbe Mother and Baby Study, treating helminths during pregnancy resulted in increased eczema rates in early childhood. We followed the cohort to determine whether this translated to increased asthma rates at school age. Methods This randomized, double‐blind, placebo‐controlled trial, conducted in Entebbe, Uganda, had three interventions. During pregnancy, women were randomized, simultaneously, to albendazole vs placebo and to praziquantel vs placebo. Their children were independently randomized to quarterly albendazole vs placebo from age 15 months to 5 years. We here report follow‐up to age 9 years. Primary outcomes at 9 years were recent reported wheeze, skin prick test positivity (SPT) to common allergens and allergen‐specific IgE positivity to dust mite or cockroach. Secondary outcomes were doctor‐diagnosed asthma and eczema rates between 5 and 9 years, recent eczema, rhinitis and urticaria at 9 years, and SPT and IgE responses to individual allergens. Results 2507 pregnant women were enrolled; 1215 children were seen at age nine, of whom 1188 are included in this analysis. Reported wheeze was rare at 9 years (3.7%) while SPT positivity (25.0%) and IgE positivity (44.1%) were common. There was no evidence of a treatment effect for any of the three interventions on any of the primary outcomes. Conclusions Prenatal and early‐life treatment of helminths, in the absence of change in other exposures, is unlikely to increase the risk of atopic diseases later in childhood in this tropical, low‐income setting.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28892575</pmid><doi>10.1111/pai.12804</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2086-1740</orcidid><orcidid>https://orcid.org/0000-0002-6271-2033</orcidid><orcidid>https://orcid.org/0000-0003-4062-9105</orcidid><oa>free_for_read</oa></addata></record>
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subjects Age
Albendazole
Albendazole - therapeutic use
Allergens
Allergies
Anthelmintics - therapeutic use
Asthma
Asthma - diagnosis
Asthma - etiology
Atopy
Child
Child, Preschool
Childhood
Children
Double-Blind Method
Eczema
Exposure
Female
Follow-Up Studies
Health risks
helminth
Helminthiasis - drug therapy
Helminthiasis - immunology
Humans
IgE
Immunoglobulin E
Infant
Low income groups
Male
Original
Praziquantel
Praziquantel - therapeutic use
Pregnancy
Pregnancy Complications, Parasitic - drug therapy
Pregnancy Complications, Parasitic - immunology
prenatal
Prenatal Exposure Delayed Effects - etiology
Randomization
Rhinitis
Risk Factors
school age
Skin diseases
Skin tests
Treatment Outcome
Uganda
Urticaria
wheeze
title Effects of treating helminths during pregnancy and early childhood on risk of allergy‐related outcomes: Follow‐up of a randomized controlled trial
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