The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Association Between Maternal Chronic Conditions and Congenital Heart Defects: A Population-Based Cohort Study
Open accessAbstract
Background—: This study quantifies the association between maternal medical conditions/illnesses and congenital heart defects (CHDs) among infants. Methods and Results—: We carried out a population-based study of all mother-infant pairs (n=2 278 838) in Canada (excluding Quebec) from 2002 to 2010 using data from the Canadian Institute for Health Information. CHDs among infants were classified phenotypically through a hierarchical grouping of International Statistical Classification of Diseases and Related Health Problems, 10th Revision, Canada codes. Maternal conditions such as multifetal pregnancy, diabetes mellitus, hypertension, and congenital heart disease were defined by use of diagnosis codes. The association between maternal conditions and CHDs and its subtypes was modeled using logistic regression with adjustment for maternal age, parity, residence, and other factors. There were 26 488 infants diagnosed with CHDs at birth or at rehospitalization in infancy; the overall CHD prevalence was 116.2 per 10 000 live births, of which the severe CHD rate was 22.3 per 10 000. Risk factors for CHD included maternal age ≥40 years (adjusted odds ratio [aOR], 1.48; 95% confidence interval [CI], 1.39–1.58), multifetal pregnancy (aOR, 4.53; 95% CI, 4.28–4.80), diabetes mellitus (type 1: aOR, 4.65; 95% CI, 4.13–5.24; type 2: aOR, 4.12; 95% CI, 3.69–4.60), hypertension (aOR, 1.81; 95% CI, 1.61–2.03), thyroid disorders (aOR, 1.45; 95% CI, 1.26–1.67), congenital heart disease (aOR, 9.92; 95% CI, 8.36–11.8), systemic connective tissue disorders (aOR, 3.01; 95% CI, 2.23–4.06), and epilepsy and mood disorders (aOR, 1.41; 95% CI, 1.16–1.72). Specific CHD subtypes were associated with different maternal risk factors. Conclusions—: Several chronic maternal medical conditions, including diabetes mellitus, hypertension, connective tissue disorders, and congenital heart disease, confer an increased risk of CHD in the offspring.
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Cites
The incidence of congenital heart disease.
Hoffman, J. I. E., & Kaplan, S. (2002) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(02)01886-7 · Cited by 6,099
Canadian Institute for Health Information.
Lalonde, A. (1994) · PubMed · Cited by 4,738
Congenital Heart Disease in the General Population: Changing Prevalence and Age Distribution
Marelli, A. J., Mackie, A. S., Ionescu-Ittu, R., Rahme, E., & Pilote, L. (2007) · Circulation · doi:10.1161/circulationaha.106.627224 · Cited by 1,747
Use and misuse of population attributable fractions
Rockhill, B., Newman, B., & Weinberg, C. (1998) · American Journal of Public Health · doi:10.2105/ajph.88.1.15 · Cited by 1,683
Task Force 1: the changing profile of congenital heart disease in adult life
Warnes, C. A., Liberthson, R., Danielson, G. K., Dore, A., Harris, L., Hoffman, J. I. E., Somerville, J., Williams, R. G., & Webb, G. D. (2001) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(01)01272-4 · Cited by 1,441
Prevalence of Congenital Heart Defects in Metropolitan Atlanta, 1998–2005
Reller, M. D., Strickland, M. J., Riehle-Colarusso, T., Mahle, W. T., & Correa, A. (2008) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2008.05.059 · Cited by 1,232
Congenital Heart Defects in Europe: Prevalence and Perinatal Mortality, 2000 to 2005
Dolk, H., Loane, M., Garne, E., & a European Surveillance of Congenital Anomalies (EUROCAT) Working Group (2011) · Circulation · doi:10.1161/circulationaha.110.958405 · Cited by 944
Jenkins, K. J., Correa, A., Feinstein, J. A., Botto, L., Britt, A. E., Daniels, S. R., Elixson, M., Warnes, C. A., & Webb, C. L. (2007) · Circulation · doi:10.1161/circulationaha.106.183216 · Cited by 818
The changing epidemiology of congenital heart disease
van der Bom, T., Zomer, A. C., Zwinderman, A. H., Meijboom, F. J., Bouma, B. J., & Mulder, B. J. M. (2011) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2010.166 · Cited by 734
Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies
Botto, L. D., Lin, A. E., Riehle‐Colarusso, T., Malik, S., & Correa, A. (2007) · Birth Defects Research Part A: Clinical and Molecular Teratology · doi:10.1002/bdra.20403 · Cited by 469
Cited by
Birth prevalence of congenital heart defects in Norway 1994-2009—A nationwide study
Leirgul, E., Fomina, T., Brodwall, K., Greve, G., Holmstrøm, H., Vollset, S. E., Tell, G. S., & Øyen, N. (2014) · American Heart Journal · doi:10.1016/j.ahj.2014.07.030 · Cited by 164
N-Acetylcysteine prevents congenital heart defects induced by pregestational diabetes
Moazzen, H., Lu, X., Ma, N. L., Velenosi, T. J., Urquhart, B. L., Wisse, L. J., Gittenberger-de Groot, A. C., & Feng, Q. (2014) · Cardiovascular Diabetology · doi:10.1186/1475-2840-13-46 · Cited by 111
Hedermann, G., Hedley, P. L., Thagaard, I. N., Krebs, L., Ekelund, C. K., Sørensen, T. I. A., & Christiansen, M. (2021) · PLOS ONE · doi:10.1371/journal.pone.0252343 · Cited by 48
Saiyin, T., Engineer, A., Greco, E. R., Kim, M. Y., Lu, X., Jones, D. L., & Feng, Q. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14439 · Cited by 47
Gaillard, R., & Jaddoe, V. W. V. (2023) · Nature Reviews Cardiology · doi:10.1038/s41569-023-00869-z · Cited by 34
Metadata
- Authors
- Liu, S., Joseph, K. S., Lisonkova, S., Rouleau, J., Van den Hof, M., Sauve, R., & Kramer, M. S.
- Venue
- Circulation
- Published
- 2013-08-06
- Volume
- 128
- Issue
- 6
- Pages
- 583-589
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- OpenAlex
- W1979195459
- Cited by
- 272
- References
- 36
- FWCI
- 10.16
- Type
- journal article
- Language
- en
- Open access
- bronze
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