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DOI 10.1002/bdra.23265

Медицинская библиотека · Birth defects research. Part A, Clinical and molecular teratology · 2014

Periconceptional parental conditions and perimembranous ventricular septal defects in the offspring.

Wijnands Kim P J, Zeilmaker Gerda A, Meijer Willemijn M, Helbing Willem A, Steegers-Theunissen Régine P M

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

The perimembranous ventricular septal (pVSD) defect is the most common congenital heart disease phenotype. Several parental factors are associated with pVSD risk in the offspring. To contribute to the future prevention of pVSDs, we investigated associations with nongenetic parental conditions.

METHODS

In a case-control study with standardized data collection at 17 months after birth, 115 parents of a child with pVSD and 484 parents of a healthy child completed questionnaires about periconceptional nongenetic conditions. Univariable and multivariable logistic regression analyses were used to estimate odds ratios (OR) with 95% confidence intervals (95% CI).

RESULTS

Complete data were available for 588 families (98%). Maternal risk conditions associated with pVSD offspring were a positive family history of congenital heart disease (OR, 2.61; 95%CI, 0.98-6.91), medication use (OR, 1.80; 95%CI, 1.13-2.85) and advanced age (OR, 1.07; 95%CI, 1.02-1.12). Exposure to phthalates (OR, 1.93; 95%CI, 1.05-3.54) was the only paternal risk condition associated with pVSD offspring.

CONCLUSION

Four periconceptional parental conditions contributed to pVSD risk in the offspring. Couples planning pregnancy should be counseled on these risk conditions which are partially modifiable to contribute to the future prevention of pVSDs.

Для цитирования: Wijnands Kim P J, Zeilmaker Gerda A, Meijer Willemijn M, Helbing Willem A, Steegers-Theunissen Régine P M. Periconceptional parental conditions and perimembranous ventricular septal defects in the offspring.. Birth defects research. Part A, Clinical and molecular teratology. 2014. DOI: 10.1002/bdra.23265.

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