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 |
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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 |
format | Article |
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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><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 & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & 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 & Medical Complete (Alumni)</collection><collection>Nursing & 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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