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Neurodevelopment in normocephalic children with and without prenatal Zika virus exposure
ObjectiveZika virus (ZIKV) targets neural stem cells in the developing brain. However, the majority of ZIKV-exposed children are born without apparent neurological manifestations. It remains unclear if these children were protected from ZIKV neurotropism or if they harbour subtle pathology that is d...
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Published in: | Archives of disease in childhood 2022-03, Vol.107 (3), p.244-250 |
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creator | Blackmon, Karen Evans, Roberta Fernandes, Michelle Landon, Barbara Noel, Trevor Macpherson, Calum Cudjoe, Nikita Burgen, Kemi S Punch, Bianca Krystosik, Amy Grossi-Soyster, Elysse N LaBeaud, Angelle Desiree Waechter, Randall |
description | ObjectiveZika virus (ZIKV) targets neural stem cells in the developing brain. However, the majority of ZIKV-exposed children are born without apparent neurological manifestations. It remains unclear if these children were protected from ZIKV neurotropism or if they harbour subtle pathology that is disruptive to brain development. We assess this by comparing neurodevelopmental outcomes in normocephalic ZIKV-exposed children relative to a parallel control group of unexposed controls.DesignCohort study.SettingPublic health centres in Grenada, West Indies.Patients384 mother–child pairs were enrolled during a period of active ZIKV transmission (April 2016–March 2017) and prospectively followed up to 30 months. Child exposure status was based on laboratory assessment of prenatal and postnatal maternal serum.Main outcome measuresThe INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) package and Cardiff Vision Tests, administered and scored by research staff masked to child’s exposure status.ResultsA total of 131 normocephalic ZIKV exposed (n=68) and unexposed (n=63) children were assessed between 22 and 30 months of age. Approximately half of these children completed vision testing. There were no group differences in sociodemographics. Deficits in visual acuity (31%) and contrast sensitivity (23%) were apparent in the ZIKV-exposed infants in the absence of cognitive, motor, language or behavioural delays.ConclusionsOverall neurodevelopment is likely to be unaffected in ZIKV-exposed children with normal head circumference at birth and normal head growth in the first 2 years of life. However, the visual system may be selectively vulnerable, which indicates the need for vision testing by 3 years of age. |
doi_str_mv | 10.1136/archdischild-2020-321031 |
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However, the majority of ZIKV-exposed children are born without apparent neurological manifestations. It remains unclear if these children were protected from ZIKV neurotropism or if they harbour subtle pathology that is disruptive to brain development. We assess this by comparing neurodevelopmental outcomes in normocephalic ZIKV-exposed children relative to a parallel control group of unexposed controls.DesignCohort study.SettingPublic health centres in Grenada, West Indies.Patients384 mother–child pairs were enrolled during a period of active ZIKV transmission (April 2016–March 2017) and prospectively followed up to 30 months. Child exposure status was based on laboratory assessment of prenatal and postnatal maternal serum.Main outcome measuresThe INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) package and Cardiff Vision Tests, administered and scored by research staff masked to child’s exposure status.ResultsA total of 131 normocephalic ZIKV exposed (n=68) and unexposed (n=63) children were assessed between 22 and 30 months of age. Approximately half of these children completed vision testing. There were no group differences in sociodemographics. Deficits in visual acuity (31%) and contrast sensitivity (23%) were apparent in the ZIKV-exposed infants in the absence of cognitive, motor, language or behavioural delays.ConclusionsOverall neurodevelopment is likely to be unaffected in ZIKV-exposed children with normal head circumference at birth and normal head growth in the first 2 years of life. However, the visual system may be selectively vulnerable, which indicates the need for vision testing by 3 years of age.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2020-321031</identifier><identifier>PMID: 34479857</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><subject>Acuity ; Adult ; Age ; Brain - growth & development ; Child Development ; Child, Preschool ; Children ; Children & youth ; Cognitive ability ; Cohort Studies ; Control Groups ; Cross Cultural Studies ; Dengue fever ; Developmental Delays ; Education ; Family income ; Female ; Females ; Food security ; Global Child Health ; Households ; Humans ; Infant ; Infants ; Infections ; Infectious Disease Transmission, Vertical ; Interviews ; Laboratories ; Male ; Measurement Techniques ; Medical imaging ; Microcephaly ; Microcephaly - epidemiology ; Mothers ; neonatology ; Neural stem cells ; Neurodevelopment ; neurology ; ophthalmology ; Parent educational background ; Pediatrics ; Pregnancy ; Pregnancy Complications, Infectious - virology ; Prenatal experience ; Prenatal Exposure Delayed Effects - virology ; Prospective Studies ; psychology ; Public health ; Questionnaires ; Reference Groups ; Skill Development ; Sociodemographics ; Stem cells ; Toddlers ; Vector-borne diseases ; virology ; Viruses ; Vision ; Visual Acuity ; Visual system ; West Indies ; Young Children ; Zika Virus ; Zika Virus Infection - transmission</subject><ispartof>Archives of disease in childhood, 2022-03, Vol.107 (3), p.244-250</ispartof><rights>Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . 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Published by BMJ. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b537t-5b3d4aac1c2da6794f280bbd6d38d2374ead9b68c960fb68541c61b985c309da3</citedby><cites>FETCH-LOGICAL-b537t-5b3d4aac1c2da6794f280bbd6d38d2374ead9b68c960fb68541c61b985c309da3</cites><orcidid>0000-0002-2665-7807</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2629558493/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2629558493?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,780,784,885,21378,21394,27924,27925,33611,33612,33877,33878,43733,43880,74221,74397</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34479857$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blackmon, Karen</creatorcontrib><creatorcontrib>Evans, Roberta</creatorcontrib><creatorcontrib>Fernandes, Michelle</creatorcontrib><creatorcontrib>Landon, Barbara</creatorcontrib><creatorcontrib>Noel, Trevor</creatorcontrib><creatorcontrib>Macpherson, Calum</creatorcontrib><creatorcontrib>Cudjoe, Nikita</creatorcontrib><creatorcontrib>Burgen, Kemi S</creatorcontrib><creatorcontrib>Punch, Bianca</creatorcontrib><creatorcontrib>Krystosik, Amy</creatorcontrib><creatorcontrib>Grossi-Soyster, Elysse N</creatorcontrib><creatorcontrib>LaBeaud, Angelle Desiree</creatorcontrib><creatorcontrib>Waechter, Randall</creatorcontrib><title>Neurodevelopment in normocephalic children with and without prenatal Zika virus exposure</title><title>Archives of disease in childhood</title><addtitle>Arch Dis Child</addtitle><addtitle>Arch Dis Child</addtitle><description>ObjectiveZika virus (ZIKV) targets neural stem cells in the developing brain. However, the majority of ZIKV-exposed children are born without apparent neurological manifestations. It remains unclear if these children were protected from ZIKV neurotropism or if they harbour subtle pathology that is disruptive to brain development. We assess this by comparing neurodevelopmental outcomes in normocephalic ZIKV-exposed children relative to a parallel control group of unexposed controls.DesignCohort study.SettingPublic health centres in Grenada, West Indies.Patients384 mother–child pairs were enrolled during a period of active ZIKV transmission (April 2016–March 2017) and prospectively followed up to 30 months. Child exposure status was based on laboratory assessment of prenatal and postnatal maternal serum.Main outcome measuresThe INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) package and Cardiff Vision Tests, administered and scored by research staff masked to child’s exposure status.ResultsA total of 131 normocephalic ZIKV exposed (n=68) and unexposed (n=63) children were assessed between 22 and 30 months of age. Approximately half of these children completed vision testing. There were no group differences in sociodemographics. Deficits in visual acuity (31%) and contrast sensitivity (23%) were apparent in the ZIKV-exposed infants in the absence of cognitive, motor, language or behavioural delays.ConclusionsOverall neurodevelopment is likely to be unaffected in ZIKV-exposed children with normal head circumference at birth and normal head growth in the first 2 years of life. However, the visual system may be selectively vulnerable, which indicates the need for vision testing by 3 years of age.</description><subject>Acuity</subject><subject>Adult</subject><subject>Age</subject><subject>Brain - growth & development</subject><subject>Child Development</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Children & youth</subject><subject>Cognitive ability</subject><subject>Cohort Studies</subject><subject>Control Groups</subject><subject>Cross Cultural Studies</subject><subject>Dengue fever</subject><subject>Developmental Delays</subject><subject>Education</subject><subject>Family income</subject><subject>Female</subject><subject>Females</subject><subject>Food security</subject><subject>Global Child Health</subject><subject>Households</subject><subject>Humans</subject><subject>Infant</subject><subject>Infants</subject><subject>Infections</subject><subject>Infectious Disease Transmission, Vertical</subject><subject>Interviews</subject><subject>Laboratories</subject><subject>Male</subject><subject>Measurement Techniques</subject><subject>Medical imaging</subject><subject>Microcephaly</subject><subject>Microcephaly - epidemiology</subject><subject>Mothers</subject><subject>neonatology</subject><subject>Neural stem cells</subject><subject>Neurodevelopment</subject><subject>neurology</subject><subject>ophthalmology</subject><subject>Parent educational background</subject><subject>Pediatrics</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Infectious - virology</subject><subject>Prenatal experience</subject><subject>Prenatal Exposure Delayed Effects - virology</subject><subject>Prospective Studies</subject><subject>psychology</subject><subject>Public health</subject><subject>Questionnaires</subject><subject>Reference Groups</subject><subject>Skill Development</subject><subject>Sociodemographics</subject><subject>Stem cells</subject><subject>Toddlers</subject><subject>Vector-borne diseases</subject><subject>virology</subject><subject>Viruses</subject><subject>Vision</subject><subject>Visual Acuity</subject><subject>Visual system</subject><subject>West Indies</subject><subject>Young Children</subject><subject>Zika Virus</subject><subject>Zika Virus Infection - 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growth & development</topic><topic>Child Development</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Children & youth</topic><topic>Cognitive ability</topic><topic>Cohort Studies</topic><topic>Control Groups</topic><topic>Cross Cultural Studies</topic><topic>Dengue fever</topic><topic>Developmental Delays</topic><topic>Education</topic><topic>Family income</topic><topic>Female</topic><topic>Females</topic><topic>Food security</topic><topic>Global Child Health</topic><topic>Households</topic><topic>Humans</topic><topic>Infant</topic><topic>Infants</topic><topic>Infections</topic><topic>Infectious Disease Transmission, Vertical</topic><topic>Interviews</topic><topic>Laboratories</topic><topic>Male</topic><topic>Measurement Techniques</topic><topic>Medical imaging</topic><topic>Microcephaly</topic><topic>Microcephaly - epidemiology</topic><topic>Mothers</topic><topic>neonatology</topic><topic>Neural stem cells</topic><topic>Neurodevelopment</topic><topic>neurology</topic><topic>ophthalmology</topic><topic>Parent educational background</topic><topic>Pediatrics</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Infectious - virology</topic><topic>Prenatal experience</topic><topic>Prenatal Exposure Delayed Effects - virology</topic><topic>Prospective Studies</topic><topic>psychology</topic><topic>Public health</topic><topic>Questionnaires</topic><topic>Reference Groups</topic><topic>Skill Development</topic><topic>Sociodemographics</topic><topic>Stem cells</topic><topic>Toddlers</topic><topic>Vector-borne diseases</topic><topic>virology</topic><topic>Viruses</topic><topic>Vision</topic><topic>Visual Acuity</topic><topic>Visual system</topic><topic>West Indies</topic><topic>Young Children</topic><topic>Zika Virus</topic><topic>Zika Virus Infection - transmission</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blackmon, Karen</creatorcontrib><creatorcontrib>Evans, Roberta</creatorcontrib><creatorcontrib>Fernandes, Michelle</creatorcontrib><creatorcontrib>Landon, Barbara</creatorcontrib><creatorcontrib>Noel, Trevor</creatorcontrib><creatorcontrib>Macpherson, Calum</creatorcontrib><creatorcontrib>Cudjoe, Nikita</creatorcontrib><creatorcontrib>Burgen, Kemi S</creatorcontrib><creatorcontrib>Punch, Bianca</creatorcontrib><creatorcontrib>Krystosik, Amy</creatorcontrib><creatorcontrib>Grossi-Soyster, Elysse N</creatorcontrib><creatorcontrib>LaBeaud, Angelle Desiree</creatorcontrib><creatorcontrib>Waechter, Randall</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals: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>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Social Science Premium Collection</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Education</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Archives of disease in childhood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blackmon, Karen</au><au>Evans, Roberta</au><au>Fernandes, Michelle</au><au>Landon, Barbara</au><au>Noel, Trevor</au><au>Macpherson, Calum</au><au>Cudjoe, Nikita</au><au>Burgen, Kemi S</au><au>Punch, Bianca</au><au>Krystosik, Amy</au><au>Grossi-Soyster, Elysse N</au><au>LaBeaud, Angelle Desiree</au><au>Waechter, Randall</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurodevelopment in normocephalic children with and without prenatal Zika virus exposure</atitle><jtitle>Archives of disease in childhood</jtitle><stitle>Arch Dis Child</stitle><addtitle>Arch Dis Child</addtitle><date>2022-03-01</date><risdate>2022</risdate><volume>107</volume><issue>3</issue><spage>244</spage><epage>250</epage><pages>244-250</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><abstract>ObjectiveZika virus (ZIKV) targets neural stem cells in the developing brain. However, the majority of ZIKV-exposed children are born without apparent neurological manifestations. It remains unclear if these children were protected from ZIKV neurotropism or if they harbour subtle pathology that is disruptive to brain development. We assess this by comparing neurodevelopmental outcomes in normocephalic ZIKV-exposed children relative to a parallel control group of unexposed controls.DesignCohort study.SettingPublic health centres in Grenada, West Indies.Patients384 mother–child pairs were enrolled during a period of active ZIKV transmission (April 2016–March 2017) and prospectively followed up to 30 months. Child exposure status was based on laboratory assessment of prenatal and postnatal maternal serum.Main outcome measuresThe INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) package and Cardiff Vision Tests, administered and scored by research staff masked to child’s exposure status.ResultsA total of 131 normocephalic ZIKV exposed (n=68) and unexposed (n=63) children were assessed between 22 and 30 months of age. Approximately half of these children completed vision testing. There were no group differences in sociodemographics. Deficits in visual acuity (31%) and contrast sensitivity (23%) were apparent in the ZIKV-exposed infants in the absence of cognitive, motor, language or behavioural delays.ConclusionsOverall neurodevelopment is likely to be unaffected in ZIKV-exposed children with normal head circumference at birth and normal head growth in the first 2 years of life. However, the visual system may be selectively vulnerable, which indicates the need for vision testing by 3 years of age.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</pub><pmid>34479857</pmid><doi>10.1136/archdischild-2020-321031</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-2665-7807</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acuity Adult Age Brain - growth & development Child Development Child, Preschool Children Children & youth Cognitive ability Cohort Studies Control Groups Cross Cultural Studies Dengue fever Developmental Delays Education Family income Female Females Food security Global Child Health Households Humans Infant Infants Infections Infectious Disease Transmission, Vertical Interviews Laboratories Male Measurement Techniques Medical imaging Microcephaly Microcephaly - epidemiology Mothers neonatology Neural stem cells Neurodevelopment neurology ophthalmology Parent educational background Pediatrics Pregnancy Pregnancy Complications, Infectious - virology Prenatal experience Prenatal Exposure Delayed Effects - virology Prospective Studies psychology Public health Questionnaires Reference Groups Skill Development Sociodemographics Stem cells Toddlers Vector-borne diseases virology Viruses Vision Visual Acuity Visual system West Indies Young Children Zika Virus Zika Virus Infection - transmission |
title | Neurodevelopment in normocephalic children with and without prenatal Zika virus exposure |
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