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Maternal age and the prevalence of congenital heart defects in Europe, 1995-2015: A register-based study.
Mamasoula, Chrysovalanto; Bigirumurame, Theophile; Chadwick, Thomas; Addor, Marie-Claude; Cavero-Carbonell, Clara; Dias, Carlos M; Echevarría-González-de-Garibay, Luis-Javier; Gatt, Miriam; Khoshnood, Babak; Klungsoyr, Kari; Randall, Kay; Stoianova, Sylvia; Haeusler, Martin; Nelen, Vera; Neville, Amanda J; Perthus, Isabelle; Pierini, Anna; Bertaut-Nativel, Bénédicte; Rissmann, Anke; Rouget, Florence; Schaub, Bruno; Tucker, David; Wellesley, Diana; Zymak-Zakutnia, Natalya; Barisic, Ingeborg; de Walle, Hermien E K; Lanzoni, Monica; Sayers, Gerardine; Mullaney, Carmel; Pennington, Lindsay; Rankin, Judith.
Afiliación
  • Mamasoula C; Population Health Sciences Institute, Newcastle University, Newcastle, UK.
  • Bigirumurame T; Population Health Sciences Institute, Newcastle University, Newcastle, UK.
  • Chadwick T; Population Health Sciences Institute, Newcastle University, Newcastle, UK.
  • Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Dias CM; Population Health Sciences Institute, Newcastle University, Newcastle, UK.
  • Echevarría-González-de-Garibay LJ; Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
  • Gatt M; Ministry of Health of the Basque Government. Directorate for Healthcare Planning, Organisation and Evaluation, Registries and Health Information Unit, Vitoria-Gasteiz, Spain.
  • Khoshnood B; Malta Congenital Anomalies Register, Directorate for Health Information and Research, Pietà, Malta.
  • Klungsoyr K; Université de Paris, INSERM U1153, CRESS, Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), Paris, France.
  • Randall K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Stoianova S; Division for Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.
  • Haeusler M; National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Nelen V; South West Congenital Anomaly Register, Bristol Medical School, University of Bristol, Bristol, UK.
  • Neville AJ; Styrian Malformation Registry, Med. University of Graz, Graz, Austria.
  • Perthus I; Provinciaal Instituut voor Hygiene (PIH), Antwerp, Belgium.
  • Pierini A; Registro IMER - IMER Registry (Emilia Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy.
  • Bertaut-Nativel B; 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, Saint-Denis, France.
  • Schaub B; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University, Magdeburg, Germany.
  • Tucker D; Brittany Registry of Congenital Anomalies, CHU Rennes, University Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail), Rennes, France.
  • Wellesley D; 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.
  • Barisic I; Wessex Clinical Genetics Department, Princess Anne Hospital, Southampton, UK.
  • de Walle HEK; OMNI-Net Ukraine Birth Defects Program and Khmelnytsky City Children's Hospital, Khmelnytsky, Ukraine.
  • Lanzoni M; Centre of Excellence for Reproductive and Regenerative Medicine, Children's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.
  • Sayers G; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, Netherlands.
  • Mullaney C; European Commission, Joint Research Centre (JRC), Ispra, Italy.
  • Pennington L; Health Service Executive, Dr Steeven's Hospital, Dublin, Ireland.
  • Rankin J; Department of Public Health, Service Executive (HSE) South East Area, Limerick, Ireland.
Birth Defects Res ; 115(6): 583-594, 2023 04 01.
Article en En | MEDLINE | ID: mdl-36734416
ABSTRACT

BACKGROUND:

Evidence on the direction and strength of association between maternal age and the prevalence of congenital heart defects (CHD) in different age group categories is conflicting. Some studies have illustrated different trends with an increase in prevalence in younger and older age groups while other studies have reported a linear relationship. Given the increase in maternal age over recent years, it is important to study the CHD prevalence by maternal age.

OBJECTIVES:

To examine the association between maternal age and the prevalence of CHD in Europe between 1995 and 2015 using population-based data from 24 registries belonging to the European Surveillance of Congenital Anomalies (EUROCAT) network.

METHODS:

Associations over time of all nonsyndromic CHD according to maternal age category and for three CHD severity groupings (severity group I very severe; severity group II severe; severity group III less severe) were examined using Bayesian multilevel Poisson regression modeling. Further subgroup analyses were undertaken within four maternal age-bands ≤24, 25-29, 30-34 and 35-44 years. Descriptive summaries are also presented.

RESULTS:

There were 51,608 nonsyndromic CHD cases in Europe over the 20-year study period. Total prevalence for all CHD combined was increased for younger mothers (≤24 years) and for mothers 35-44 years of age when compared with mothers aged 25-29 years (reference group) (IRR 1.05, 95% CI 1.02, 1.07). The total prevalence was increased for severity group I (very severe) only for younger mothers compared to those aged 25-29 years (IRR 1.14, 95% CI 1.04, 1.23). We found an increased prevalence of the following CHD subtypes double outlet right ventricle (IRR1.33, 95% CI 1.09, 1.60), hypoplastic left heart syndrome (IRR 1.18, 95% CI 1.05, 1.32), hypoplastic right heart syndrome (IRR 1.41, 95% CI 1.05, 1.84), atrioventricular septal defect (IRR 1.15, 95% CI 1.01, 1.32), coarctation of aorta (IRR 1.15, 95% CI 1.03, 1.28) and atrial septal defect (IRR 1.08, 95% CI 1.02, 1.13). For older mothers (35-44 years) compared to the reference category, we observed an increased risk in the prevalence for severity group II (IRR 1.09, 95% CI 1.03, 1.14), severity group III (IRR 1.05, 95% CI 1.01, 1.08) and an increased prevalence of the CHD subtypes Pulmonary valve stenosis (IRR 1.22, 95% CI 1.09, 1.34), ASD (IRR 1.07, 95% CI 1.02, 1.13), CoA (IRR 1.18, 95% CI 1.06, 1.32) and Tetralogy of Fallot (IRR 1.14, 95% CI 1.01, 1.28). Finally, for all age categories compared to the reference category, different associations of ASD and an increased prevalence of CoA was also observed.

CONCLUSIONS:

Based on data for cases of CHD from 24 European population-based registries, evidence of a positive association between maternal age and the total prevalence of CHD for younger (≤24 years old) and older (35-44 years old) mothers was observed. The results suggest that young maternal age (≤24 years old) is a factor associated with severe CHD phenotypes while a positive association between advanced maternal age (35-44 years old) and mild CHD phenotypes was observed.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Edad Materna / Cardiopatías Congénitas Tipo de estudio: Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans País/Región como asunto: Europa Idioma: En Revista: Birth Defects Res Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Edad Materna / Cardiopatías Congénitas Tipo de estudio: Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans País/Región como asunto: Europa Idioma: En Revista: Birth Defects Res Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido