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Spatial trends in congenital malformations and stream water chemistry in Southern Brazil.
Ibañez, Humberto C; Melanda, Viviane S; Gerber, Viviane K Q; Licht, Otavio A B; Ibañez, Marilea V C; Aguiar Júnior, Terêncio R; Mello, Rosiane G; Komechen, Heloisa; Andrade, Diancarlos P; Picharski, Gledson L; Figueiredo, Damasio P G; Pianovski, Mara A D; Figueiredo, Mirna M O; Custódio, Gislaine; Parise, Ivy Z S; Castilho, Laura M; Paraizo, Mariana M; Edinger, Chloe; Fiori, Carmem M C M; Pedrini, Hélio; Kiesel Filho, Nilton; Fabro, Ana Luiza M R; Fachin, Rayssa D; Ogradowski, Karin R P; Parise, Guilherme A; Saldiva, Paulo H N; Legal, Edith F; Rosati, Roberto; Rodriguez-Galindo, Carlos; Ribeiro, Raul C; Zambetti, Gerard P; Lalli, Enzo; Figueiredo, Bonald C.
Affiliation
  • Ibañez HC; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Melanda VS; Departamento de Vigilância Epidemiológica, Secretaria do Estado da Saúde do Paraná, Curitiba, PR, Brazil.
  • Gerber VKQ; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Licht OAB; Instituto de Terras Cartografia e Geologia, Curitiba, PR, Brazil.
  • Ibañez MVC; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil.
  • Aguiar Júnior TR; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Mello RG; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Komechen H; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Andrade DP; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Picharski GL; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Figueiredo DPG; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Pianovski MAD; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil; Erasto Gaertner Hospital, Curitiba, PR, Brazil.
  • Figueiredo MMO; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Custódio G; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Parise IZS; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Castilho LM; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil.
  • Paraizo MM; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Edinger C; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil.
  • Fiori CMCM; União Oeste Paranaense de Estudos e Combate ao Câncer - UOPECCAN, Cascavel, PR, Brazil; Universidade Estadual do Oeste do Paraná, Cascavel, PR, Brazil.
  • Pedrini H; Instituto de Computação, Universidade de Campinas (UNICAMP), Campinas, SP, Brazil.
  • Kiesel Filho N; Hospital Pequeno Príncipe, Curitiba, PR, Brazil.
  • Fabro ALMR; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Hospital Pequeno Príncipe, Curitiba, PR, Brazil.
  • Fachin RD; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil.
  • Ogradowski KRP; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Parise GA; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Saldiva PHN; Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
  • Legal EF; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Rosati R; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil.
  • Rodriguez-Galindo C; Department of Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Ribeiro RC; Faculdades Pequeno Principe, Curitiba, PR, Brazil; Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Zambetti GP; Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Lalli E; Institut de Pharmacologie Moléculaire et Cellulaire CNRS, 660 route des Lucioles, Sophia Antipolis, Valbonne, France.
  • Figueiredo BC; Pelé Pequeno Príncipe Research Institute, Curitiba, PR, Brazil; Faculdades Pequeno Principe, Curitiba, PR, Brazil; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Universidade Federal do Paraná, Curitiba, PR, Brazil; Departamento de Saúde Coletiva, Universidade Federal do P
Sci Total Environ ; 650(Pt 1): 1278-1291, 2019 Feb 10.
Article in En | MEDLINE | ID: mdl-30308815
ABSTRACT
The incidence of variable congenital malformation (CM) among 399 municipalities in the state of Paraná, southern Brazil, suggests the etiological role of environmental factors. This study examined a) environmental concentrations of chlorine anions (Cl-) associated with organochlorines (OCs) and b) associations between these chemicals and agricultural output with CMs using a geographical information system. In one of the three years during the sampling period (2008, 2009 or 2010) Cl-, dichlorodiphenyltrichloroethane (p,p'-DDT), dichlorodiphenyldichloroethylene (p,p'-DDE), dichlorodiphenyldichloroethane (p,p'-DDD), and endosulfan levels were measured in 465 (465/736, 63%) catchment basins. Agricultural outputs for crops during 2006-2010 were also evaluated (t/km2). Further, CM kernel density for the 399 municipalities in Paraná during 2007-2014 was investigated. Cl- levels increased significantly in one of the three years (2008, 2009 or 2010) in western catchment basins, compared to 1996 (p < 0.0001). The municipalities were divided according to the obtained Cl- levels, where sub-region C2 (central-southern) < 1.8 mg/L ≤ sub-regions C1 (northern-western) and C3 (eastern-southern). We identified 8756 cases of CMs among 1,221,287 newborns (NB) in all sub-regions. C1 had higher DDT-DDE-DDD (p,p'-DDT + p,p'-DDE + p,p'-DDD) concentrations, agricultural output, and CM kernel density. C2 and C3 had minor agricultural outputs (per square kilometer) and CM densities. A 2.96 mg/L increase in Cl- between sub-regions C1 and C2 was co-localized with a 45% increase in CM density (spatial relative risk = 1.45, CI 95% 1.36-1.55). C1 had the highest log likelihood ratios (p = 0.001) identified via SaTScan clustering analyses. Organochlorines and other toxic chlorinated chemicals may contribute to CMs in humans, and these chemicals are ultimately transformed and release Cl- in rivers. Higher Cl- levels were correlated significantly with higher agricultural productivity, DDT-DDE-DDD levels, and CMs in some parts of the northern and western sub-regions (C1).
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Country/Region as subject: America do sul / Brasil Language: En Journal: Sci Total Environ Year: 2019 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Country/Region as subject: America do sul / Brasil Language: En Journal: Sci Total Environ Year: 2019 Document type: Article Affiliation country: Brazil