Association and birth prevalence of microcephaly attributable to Zika virus infection among infants in Paraíba, Brazil, in 2015–16: a case-control study
In 2015, the number of infants born with microcephaly increased in Paraíba, Brazil, after a suspected Zika virus outbreak. We did a retrospective case-control investigation to assess the association of microcephaly and Zika virus. We enrolled cases reported to the national database for microcephaly...
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creator | Krow-Lucal, Elisabeth R de Andrade, Marcia Regina Cananéa, Juliana Nunes Abath Moore, Cynthia A Leite, Priscila Leal Biggerstaff, Brad J Cabral, Cibelle Mendes Itoh, Megumi Percio, Jadher Wada, Marcelo Y Powers, Ann M Barbosa, Aristides Abath, Roberta Batista Staples, J Erin Coelho, Giovanini Evelim Araújo, Emerson Medeiros, Eva Lídia Arcoverde Brant, Jonas Cerroni, Matheus de Barros Moreira Beltrão, Henrique Fantinato, Francieli Fontana Sutile Tardetti Lise, Michael Laurence Zini Ohara, Patrícia Miyuki Resende, Elionardo Saad, Eduardo de St. Maurice, Annabelle Dieke, Ada Harrist, Alexia Kwit, Natalie Marlow, Mariel Soke, Gnakub de Arruda Pessoa, Roseanne da Silva, Renata Candido Diniz, Rogéria Chelly de Araújo Ariette, Micheline César Lira, Clarice França Matos, Sandra Wanderley, Taciana Mendonça Maia Silva, Vanessa Oliveira Costa da Silva, Hélio Soares Carmo, Eduardo Hage Carvalho, Myrian Lentini, Nena Miranda, Raquel Boland, Erin Burns, Paul Fischer, Marc Ledermann, Jeremy Coronado, Fatima Dicent-Taillepierre, Julio Flannery, Brendan Macedo de Oliveira, Alexandre Arena, José Fernando |
description | In 2015, the number of infants born with microcephaly increased in Paraíba, Brazil, after a suspected Zika virus outbreak. We did a retrospective case-control investigation to assess the association of microcephaly and Zika virus.
We enrolled cases reported to the national database for microcephaly and born between Aug 1, 2015, and Feb 1, 2016, on the basis of their birth head circumference and total body length. We identified controls from the national birth registry and matched them to cases by location, aiming to enrol a minimum of two controls per case. Mothers of both cases and controls were asked about demographics, exposures, and illnesses and infants were measured at a follow-up visit 1–7 months after birth. We took blood samples from mothers and infants and classified those containing Zika virus IgM and neutralising antibodies as evidence of recent infection. We calculated prevalence of microcephaly and odds ratios (ORs) using a conditional logistic regression model with maximum penalised conditional likelihood, and combined these ORs with exposure probability estimates to determine the attributable risk.
We enrolled 164 of 706 infants with complete information reported with microcephaly at birth, of whom we classified 91 (55%) as having microcephaly on the basis of their birth measurements, 36 (22%) as small, 21 (13%) as disproportionate, and 16 (10%) as not having microcephaly. 43 (26%) of the 164 infants had microcephaly at follow-up for an estimated prevalence of 5·9 per 1000 livebirths. We enrolled 114 control infants matched to the 43 infants classified as having microcephaly at follow-up. Infants with microcephaly at follow-up were more likely than control infants to be younger (OR 0·5, 95% CI 0·4–0·7), have recent Zika virus infection (21·9, 7·0–109·3), or a mother with Zika-like symptoms in the first trimester (6·2, 2·8–15·4). Once Zika virus infection and infant age were controlled for, we found no significant association between microcephaly and maternal demographics, medications, toxins, or other infections. Based on the presence of Zika virus antibodies in infants, we concluded that 35–87% of microcephaly occurring during the time of our investigation in northeast Brazil was attributable to Zika virus. We estimate 2–5 infants per 1000 livebirths in Paraíba had microcephaly attributable to Zika virus.
Time of exposure to Zika virus and evidence of infection in the infants were the only risk factors associated with microcephaly. This in |
doi_str_mv | 10.1016/S2352-4642(18)30020-8 |
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We enrolled cases reported to the national database for microcephaly and born between Aug 1, 2015, and Feb 1, 2016, on the basis of their birth head circumference and total body length. We identified controls from the national birth registry and matched them to cases by location, aiming to enrol a minimum of two controls per case. Mothers of both cases and controls were asked about demographics, exposures, and illnesses and infants were measured at a follow-up visit 1–7 months after birth. We took blood samples from mothers and infants and classified those containing Zika virus IgM and neutralising antibodies as evidence of recent infection. We calculated prevalence of microcephaly and odds ratios (ORs) using a conditional logistic regression model with maximum penalised conditional likelihood, and combined these ORs with exposure probability estimates to determine the attributable risk.
We enrolled 164 of 706 infants with complete information reported with microcephaly at birth, of whom we classified 91 (55%) as having microcephaly on the basis of their birth measurements, 36 (22%) as small, 21 (13%) as disproportionate, and 16 (10%) as not having microcephaly. 43 (26%) of the 164 infants had microcephaly at follow-up for an estimated prevalence of 5·9 per 1000 livebirths. We enrolled 114 control infants matched to the 43 infants classified as having microcephaly at follow-up. Infants with microcephaly at follow-up were more likely than control infants to be younger (OR 0·5, 95% CI 0·4–0·7), have recent Zika virus infection (21·9, 7·0–109·3), or a mother with Zika-like symptoms in the first trimester (6·2, 2·8–15·4). Once Zika virus infection and infant age were controlled for, we found no significant association between microcephaly and maternal demographics, medications, toxins, or other infections. Based on the presence of Zika virus antibodies in infants, we concluded that 35–87% of microcephaly occurring during the time of our investigation in northeast Brazil was attributable to Zika virus. We estimate 2–5 infants per 1000 livebirths in Paraíba had microcephaly attributable to Zika virus.
Time of exposure to Zika virus and evidence of infection in the infants were the only risk factors associated with microcephaly. This investigation has improved understanding of the outbreak of microcephaly in northeast Brazil and highlights the need to obtain multiple measurements after birth to establish if an infant has microcephaly and the need for further research to optimise testing criteria for congenital Zika virus infection.
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We enrolled cases reported to the national database for microcephaly and born between Aug 1, 2015, and Feb 1, 2016, on the basis of their birth head circumference and total body length. We identified controls from the national birth registry and matched them to cases by location, aiming to enrol a minimum of two controls per case. Mothers of both cases and controls were asked about demographics, exposures, and illnesses and infants were measured at a follow-up visit 1–7 months after birth. We took blood samples from mothers and infants and classified those containing Zika virus IgM and neutralising antibodies as evidence of recent infection. We calculated prevalence of microcephaly and odds ratios (ORs) using a conditional logistic regression model with maximum penalised conditional likelihood, and combined these ORs with exposure probability estimates to determine the attributable risk.
We enrolled 164 of 706 infants with complete information reported with microcephaly at birth, of whom we classified 91 (55%) as having microcephaly on the basis of their birth measurements, 36 (22%) as small, 21 (13%) as disproportionate, and 16 (10%) as not having microcephaly. 43 (26%) of the 164 infants had microcephaly at follow-up for an estimated prevalence of 5·9 per 1000 livebirths. We enrolled 114 control infants matched to the 43 infants classified as having microcephaly at follow-up. Infants with microcephaly at follow-up were more likely than control infants to be younger (OR 0·5, 95% CI 0·4–0·7), have recent Zika virus infection (21·9, 7·0–109·3), or a mother with Zika-like symptoms in the first trimester (6·2, 2·8–15·4). Once Zika virus infection and infant age were controlled for, we found no significant association between microcephaly and maternal demographics, medications, toxins, or other infections. Based on the presence of Zika virus antibodies in infants, we concluded that 35–87% of microcephaly occurring during the time of our investigation in northeast Brazil was attributable to Zika virus. We estimate 2–5 infants per 1000 livebirths in Paraíba had microcephaly attributable to Zika virus.
Time of exposure to Zika virus and evidence of infection in the infants were the only risk factors associated with microcephaly. This investigation has improved understanding of the outbreak of microcephaly in northeast Brazil and highlights the need to obtain multiple measurements after birth to establish if an infant has microcephaly and the need for further research to optimise testing criteria for congenital Zika virus infection.
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Costa</creatorcontrib><creatorcontrib>da Silva, Hélio Soares</creatorcontrib><creatorcontrib>Carmo, Eduardo Hage</creatorcontrib><creatorcontrib>Carvalho, Myrian</creatorcontrib><creatorcontrib>Lentini, Nena</creatorcontrib><creatorcontrib>Miranda, Raquel</creatorcontrib><creatorcontrib>Boland, Erin</creatorcontrib><creatorcontrib>Burns, Paul</creatorcontrib><creatorcontrib>Fischer, Marc</creatorcontrib><creatorcontrib>Ledermann, Jeremy</creatorcontrib><creatorcontrib>Coronado, Fatima</creatorcontrib><creatorcontrib>Dicent-Taillepierre, Julio</creatorcontrib><creatorcontrib>Flannery, Brendan</creatorcontrib><creatorcontrib>Macedo de Oliveira, Alexandre</creatorcontrib><creatorcontrib>Arena, José Fernando</creatorcontrib><creatorcontrib>Paraíba Microcephaly Work Group</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The lancet child & adolescent health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krow-Lucal, Elisabeth R</au><au>de Andrade, Marcia Regina</au><au>Cananéa, Juliana Nunes Abath</au><au>Moore, Cynthia A</au><au>Leite, Priscila Leal</au><au>Biggerstaff, Brad J</au><au>Cabral, Cibelle Mendes</au><au>Itoh, Megumi</au><au>Percio, Jadher</au><au>Wada, Marcelo Y</au><au>Powers, Ann M</au><au>Barbosa, Aristides</au><au>Abath, Roberta Batista</au><au>Staples, J Erin</au><au>Coelho, Giovanini Evelim</au><au>Araújo, Emerson</au><au>Medeiros, Eva Lídia Arcoverde</au><au>Brant, Jonas</au><au>Cerroni, Matheus</au><au>de Barros Moreira Beltrão, Henrique</au><au>Fantinato, Francieli Fontana Sutile Tardetti</au><au>Lise, Michael Laurence Zini</au><au>Ohara, Patrícia Miyuki</au><au>Resende, Elionardo</au><au>Saad, Eduardo</au><au>de St. Maurice, Annabelle</au><au>Dieke, Ada</au><au>Harrist, Alexia</au><au>Kwit, Natalie</au><au>Marlow, Mariel</au><au>Soke, Gnakub</au><au>de Arruda Pessoa, Roseanne</au><au>da Silva, Renata Candido</au><au>Diniz, Rogéria Chelly</au><au>de Araújo Ariette, Micheline César</au><au>Lira, Clarice França</au><au>Matos, Sandra</au><au>Wanderley, Taciana Mendonça Maia</au><au>Silva, Vanessa Oliveira Costa</au><au>da Silva, Hélio Soares</au><au>Carmo, Eduardo Hage</au><au>Carvalho, Myrian</au><au>Lentini, Nena</au><au>Miranda, Raquel</au><au>Boland, Erin</au><au>Burns, Paul</au><au>Fischer, Marc</au><au>Ledermann, Jeremy</au><au>Coronado, Fatima</au><au>Dicent-Taillepierre, Julio</au><au>Flannery, Brendan</au><au>Macedo de Oliveira, Alexandre</au><au>Arena, José Fernando</au><aucorp>Paraíba Microcephaly Work Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association and birth prevalence of microcephaly attributable to Zika virus infection among infants in Paraíba, Brazil, in 2015–16: a case-control study</atitle><jtitle>The lancet child & adolescent health</jtitle><addtitle>Lancet Child Adolesc Health</addtitle><date>2018-03</date><risdate>2018</risdate><volume>2</volume><issue>3</issue><spage>205</spage><epage>213</epage><pages>205-213</pages><issn>2352-4642</issn><eissn>2352-4650</eissn><abstract>In 2015, the number of infants born with microcephaly increased in Paraíba, Brazil, after a suspected Zika virus outbreak. We did a retrospective case-control investigation to assess the association of microcephaly and Zika virus.
We enrolled cases reported to the national database for microcephaly and born between Aug 1, 2015, and Feb 1, 2016, on the basis of their birth head circumference and total body length. We identified controls from the national birth registry and matched them to cases by location, aiming to enrol a minimum of two controls per case. Mothers of both cases and controls were asked about demographics, exposures, and illnesses and infants were measured at a follow-up visit 1–7 months after birth. We took blood samples from mothers and infants and classified those containing Zika virus IgM and neutralising antibodies as evidence of recent infection. We calculated prevalence of microcephaly and odds ratios (ORs) using a conditional logistic regression model with maximum penalised conditional likelihood, and combined these ORs with exposure probability estimates to determine the attributable risk.
We enrolled 164 of 706 infants with complete information reported with microcephaly at birth, of whom we classified 91 (55%) as having microcephaly on the basis of their birth measurements, 36 (22%) as small, 21 (13%) as disproportionate, and 16 (10%) as not having microcephaly. 43 (26%) of the 164 infants had microcephaly at follow-up for an estimated prevalence of 5·9 per 1000 livebirths. We enrolled 114 control infants matched to the 43 infants classified as having microcephaly at follow-up. Infants with microcephaly at follow-up were more likely than control infants to be younger (OR 0·5, 95% CI 0·4–0·7), have recent Zika virus infection (21·9, 7·0–109·3), or a mother with Zika-like symptoms in the first trimester (6·2, 2·8–15·4). Once Zika virus infection and infant age were controlled for, we found no significant association between microcephaly and maternal demographics, medications, toxins, or other infections. Based on the presence of Zika virus antibodies in infants, we concluded that 35–87% of microcephaly occurring during the time of our investigation in northeast Brazil was attributable to Zika virus. We estimate 2–5 infants per 1000 livebirths in Paraíba had microcephaly attributable to Zika virus.
Time of exposure to Zika virus and evidence of infection in the infants were the only risk factors associated with microcephaly. This investigation has improved understanding of the outbreak of microcephaly in northeast Brazil and highlights the need to obtain multiple measurements after birth to establish if an infant has microcephaly and the need for further research to optimise testing criteria for congenital Zika virus infection.
Centers for Disease Control and Prevention.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30169255</pmid><doi>10.1016/S2352-4642(18)30020-8</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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issn | 2352-4642 2352-4650 |
language | eng |
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title | Association and birth prevalence of microcephaly attributable to Zika virus infection among infants in Paraíba, Brazil, in 2015–16: a case-control study |
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