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Maternal risk factors for the VACTERL association: A EUROCAT case-control study.
van de Putte, Romy; van Rooij, Iris A L M; Haanappel, Cynthia P; Marcelis, Carlo L M; Brunner, Han G; Addor, Marie-Claude; Cavero-Carbonell, Clara; Dias, Carlos M; Draper, Elizabeth S; Etxebarriarteun, Larraitz; Gatt, Miriam; Khoshnood, Babak; Kinsner-Ovaskainen, Agnieszka; Klungsoyr, Kari; Kurinczuk, Jenny J; Latos-Bielenska, Anna; Luyt, Karen; O'Mahony, Mary T; Miller, Nicola; Mullaney, Carmel; Nelen, Vera; Neville, Amanda J; Perthus, Isabelle; Pierini, Anna; Randrianaivo, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Schaub, Bruno; Tucker, David; Wellesley, Diana; Wiesel, Awi; Zymak-Zakutnia, Natalya; Loane, Maria; Barisic, Ingeborg; de Walle, Hermien E K; Bergman, Jorieke E H; Roeleveld, Nel.
Afiliação
  • van de Putte R; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, The Netherlands.
  • van Rooij IALM; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, The Netherlands.
  • Haanappel CP; Paediatric Surgery, Radboudumc Amalia Children's Hospital, Nijmegen, The Netherlands.
  • Marcelis CLM; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, The Netherlands.
  • Brunner HG; Department of Human Genetics, Nijmegen, The Netherlands.
  • Addor MC; Department of Human Genetics, Nijmegen, The Netherlands.
  • Cavero-Carbonell C; Department of Clinical Genetics and School for Oncology & Developmental Biology (GROW), Maastricht University Medical Center, Maastricht, The Netherlands.
  • Dias CM; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.
  • Draper ES; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Etxebarriarteun L; Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
  • Gatt M; Department of Health Sciences, University of Leicester, Leicester, UK.
  • Khoshnood B; Department of Health, Public Health Service, Basque Government Basque Country, Vitoria-Gasteiz, Spain.
  • Kinsner-Ovaskainen A; Malta Congenital Anomalies Register, Directorate for Health Information and Research, Pietà, Malta.
  • Klungsoyr K; INSERM UMR 1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), Center of Research in Epidemiology and Statistics Sorbonne Paris Cité (CRESS), DHU Risks in Pregnancy, Paris Descartes University, Paris, France.
  • Kurinczuk JJ; European Commission, Joint Research Centre (JRC), Ispra, Italy.
  • Latos-Bielenska A; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Luyt K; Division for Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.
  • O'Mahony MT; National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Miller N; Department of Medical Genetics, University of Medical Sciences, Poznan, Poland.
  • Mullaney C; South West Congenital Anomaly Register (SWCAR), Bristol Medical School, University of Bristol, Bristol, UK.
  • Nelen V; Department of Public Health, Health Service Executive - South, Cork, Ireland.
  • Neville AJ; National Congenital Anomaly and Rare Disease Registration Service, Public Health England, Newcastle upon Tyne, UK.
  • Perthus I; Department of Public Health, Health Service Executive - South East, Kilkenny, Ireland.
  • Pierini A; Provinciaal Instituut voor Hygiene (PIH), Antwerp, Belgium.
  • Randrianaivo H; Registro IMER - IMER Registry (Emilia Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara, Azienda Ospedaliero-Universitaria di Ferrara, Ferrara, Italy.
  • Rankin J; Auvergne registry of congenital anomalies (CEMC-Auvergne), Department of clinical genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.
  • Rissmann A; Tuscany Registry of Congenital Defects (RTDC), Institute of Clinical Physiology - National Research Council / Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Rouget F; Register of congenital malformations of Reunion Island, CHU Réunion, St Pierre, France.
  • Schaub B; Institute of Health & Society, Newcastle University, Newcastle, UK.
  • Tucker D; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University, Magdeburg, Germany.
  • Wellesley D; Brittany Registry of congenital anomalies, CHU Rennes, University Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail), Rennes, France.
  • Wiesel A; French West Indies Registry, Registre des Malformations des Antilles (REMALAN), Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort-de-France, France.
  • Zymak-Zakutnia N; CARIS, Public Health Wales, Singleton Hospital, Swansea, UK.
  • Loane M; Wessex Clinical Genetics Department, Princess Anne Hospital, Southampton, UK.
  • Barisic I; Department of Pediatrics, Birth Registry Mainz Model, University Medical Center of Mainz, Mainz, Germany.
  • de Walle HEK; OMNI-Net Ukraine Birth Defects Program and Khmelnytsky City Children's Hospital, Khmelnytsky, Ukraine.
  • Bergman JEH; Centre for Maternal, Fetal and lnfant Research, lnstitute of Nursing and Health Research, Ulster University, Belfast, UK.
  • Roeleveld N; Centre of Excellence for Reproductive and Regenerative Medicine, Children's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.
Birth Defects Res ; 112(9): 688-698, 2020 05 15.
Article em En | MEDLINE | ID: mdl-32319733
BACKGROUND: The VACTERL association (VACTERL) is the nonrandom occurrence of at least three of these congenital anomalies: vertebral, anal, cardiac, tracheoesophageal, renal, and limb anomalies. Despite suggestions for involvement of several genes and nongenetic risk factors from small studies, the etiology of VACTERL remains largely unknown. OBJECTIVE: To identify maternal risk factors for VACTERL in offspring in a large European study. METHODS: A case-control study was performed using data from 28 EUROCAT registries over the period 1997-2015 with case and control ascertainment through hospital records, birth and death certificates, questionnaires, and/or postmortem examinations. Cases were diagnosed with VACTERL, while controls had a genetic syndrome and/or chromosomal abnormality. Data collected included type of birth defect and maternal characteristics, such as age, use of assisted reproductive techniques (ART), and chronic illnesses. Multivariable logistic regression analyses were performed to estimate confounder adjusted odds ratios (aOR) with 95% confidence intervals (95% CI). RESULTS: The study population consisted of 329 VACTERL cases and 49,724 controls with recognized syndromes or chromosomal abnormality. For couples who conceived through ART, we found an increased risk of VACTERL (aOR 2.3 [95% CI 1.3, 3.9]) in offspring. Pregestational diabetes (aOR 3.1 [95% CI 1.1, 8.6]) and chronic lower obstructive pulmonary diseases (aOR 3.9 [95% CI 2.2, 6.7]) also increased the risk of having a child with VACTERL. Twin pregnancies were not associated with VACTERL (aOR 0.6 [95% CI 0.3, 1.4]). CONCLUSION: We identified several maternal risk factors for VACTERL in offspring befitting a multifactorial etiology.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deformidades Congênitas dos Membros / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deformidades Congênitas dos Membros / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda