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Maternal and perinatal characteristics, congenital malformations and the risk of wilms tumor: the ESTELLE study.
Bauer, Hélène; Rios, Paula; Schleiermacher, Gudrun; Valteau-Couanet, Dominique; Bertozzi, Anne-Isabelle; Thebaud, Estelle; Gandemer, Virginie; Pellier, Isabelle; Verschuur, Arnauld; Spiegel, Alexandra; Notz-Carrere, Anne; Bergeron, Christophe; Orsi, Laurent; Lacour, Brigitte; Clavel, Jacqueline.
Afiliación
  • Bauer H; CRESS, UMR1153, INSERM, Université de Paris, Villejuif, France.
  • Rios P; CRESS, UMR1153, INSERM, Université de Paris, Villejuif, France. paula.rios@inserm.fr.
  • Schleiermacher G; Institut Curie, Paris, France.
  • Valteau-Couanet D; Children and Adolescent Cancerology Department, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
  • Bertozzi AI; CHU Toulouse, Hôpital Purpan, Toulouse, France.
  • Thebaud E; CHU de Nantes, Hôtel Dieu, Nantes, France.
  • Gandemer V; CHU de Rennes, Hôpital Sud, Rennes, France.
  • Pellier I; CHU D'Angers, Angers, France.
  • Verschuur A; AP-HM, Hôpital La Timone, Marseille, France.
  • Spiegel A; CHU de Strasbourg, Hôpital Hautepierre, Strasbourg, France.
  • Notz-Carrere A; CHU de Bordeaux, Hôpital Pellegrin, Bordeaux, France.
  • Bergeron C; Centre Léon Bérard, IHOPe, Lyon, France.
  • Orsi L; CRESS, UMR1153, INSERM, Université de Paris, Villejuif, France.
  • Lacour B; CRESS, UMR1153, INSERM, Université de Paris, Villejuif, France.
  • Clavel J; National Registry of Childhood Cancers, APHP, CHU Paul Brousse, Villejuif, France.
Cancer Causes Control ; 31(5): 491-501, 2020 May.
Article en En | MEDLINE | ID: mdl-32144681
ABSTRACT

PURPOSE:

Wilms tumor (WT), or nephroblastoma, is an embryonic tumor that constitutes the most common renal tumor in children. Little is known about the etiology of WT. The aim of this study was to investigate whether maternal or perinatal characteristics were associated with the risk of WT.

METHODS:

The ESTELLE study is a national-based case-control study that included 117 cases of WT and 1,100 controls younger than 11 years old. The cases were children diagnosed in France in 2010-2011 and the controls were frequency matched with cases by age and gender. The mothers of case and control children responded to a telephone questionnaire addressing sociodemographic and perinatal characteristics, childhood environment, and lifestyle. Unconditional logistic regression models adjusted on potential cofounders were used to estimate the odds ratios (OR) and their confidence intervals (95% CI).

RESULTS:

High birth weight and the presence of congenital malformation were associated with WT (OR 1.9 [95% CI 1.0-3.7] and OR 2.5 [95% CI 1.1-5.8], respectively). No association with breastfeeding or folic acid supplementation was observed.

CONCLUSIONS:

Although potential recall bias cannot be excluded, our findings reinforce the hypothesis that high birth weight and the presence of congenital malformation may be associated with an increased risk of WT. Further investigations are needed to further elucidate the possible role of maternal characteristics in the etiology of WT.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Tumor de Wilms / Neoplasias Renales Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Cancer Causes Control Asunto de la revista: EPIDEMIOLOGIA / NEOPLASIAS Año: 2020 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Asunto principal: Tumor de Wilms / Neoplasias Renales Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Cancer Causes Control Asunto de la revista: EPIDEMIOLOGIA / NEOPLASIAS Año: 2020 Tipo del documento: Article País de afiliación: Francia