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A Cluster of Hypoplastic Left Heart Malformation in Baltimore, Maryland

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Abstract

Congenital cardiovascular malformations (CCVMs) of the left side of the heart show familial recurrence of various forms of obstructive malformations, including hypoplastic left heart (HLH), interrupted aortic arch, coarctation of the aorta, and aortic stenosis. In a previous population-based study in the Baltimore–Washington region, these malformations were associated with parental reports of occupational or leisure solvent exposure, overt diabetes, and family history of CCVM in first-degree relatives. Spatial analysis in this well-characterized study population may augment self-reported data by revealing additional associations with potential environmental risk factors. We used spatial analysis to identify clusters of HLH as a group. The study population included all live-born cases of hypoplastic left heart syndrome diagnosed in the first year of life between 1981 and 1989 and a random sample of unaffected infant controls matched by year and hospital of birth. The nested case–control cohort in this spatial analysis included 77 HLH cases and 1894 controls in Maryland and the District of Columbia. Nonparametric and regression analyses included personal variables from the interview data set as well as spatial variables. A region of Baltimore was identified that contained HLH at twice the expected frequency based on the distribution of population younger than 5 years of age. The region included 30 of 77 geocoded cases of HLH in the cohort and is significant by spatial scanning at p = 0.056. Within this region, male cases of HLH were disproportionately present compared to females. This cluster is in a region of Baltimore with industrial release of solvents, dioxin, and polychlorinated biphenyls in air. Outside the cluster, HLH is associated with family history of CCVM in a first-degree relative, maternal exposure to miscellaneous solvents, paternal anesthesia, maternal art painting, aspirin ingestion, and maternal diabetes. Inside the cluster, father’s painting and exposure to sympathomimetic drugs were associated risk factors. Spatial analysis of HLH cases delineated an urban region with increased prevalence of this left heart malformation. Within this region, excess male cases of HLH occurred, and industrial release to air of solvents, dioxin, and polychlorinated biphenyl compounds was documented. We propose that both genetic and environmental factors contribute to the phenotype of HLH.

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References

  1. Arfsten DP, Silbergeld EK, Loffredo CA (2004) Fetal ADH2*3 maternal ethanol consumption and fetal growth. Int J Toxicol 23:47–52

    Article  CAS  PubMed  Google Scholar 

  2. Arnold GL, Kirby RS, Langendoerfer S, Wilkins-Haug L (1994) Toluene embryopathy: clinical delineation and developmental follow-up. Pediatrics 93:216–220

    CAS  PubMed  Google Scholar 

  3. Boughman JA (1991) Variation of familial risks of congenital cardiovascular malformation (CCVM): higher risk in left flow defect families. Am J Hum Genet Suppl 49:465

    Google Scholar 

  4. Boughman JA, Berg KA, Astemborski JA, et al. (1987) Familial risks of congenital heart defects assessed in a population based epidemiologic study. Am J Med Genet 26:839–849

    Article  CAS  PubMed  Google Scholar 

  5. Brender J, Suarez L, Hendricks K, Baetz RA, Larsen R (2002) Parental occupation and neural tube defect-affected pregnancies among Mexican Americans. J Occup Environ Med 44:650–656

    Article  PubMed  Google Scholar 

  6. Brenner JI (2004) Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta and d transposition of the great arteries. Am J Med Genet 124A:224–230

    Google Scholar 

  7. Brenner JI, Berg KA, Schneider DS, Clark EB, Boughman JA (1989) Cardiac malformations in relatives of infants with hypoplastic left heart syndrome. Am J Dis Child 143:1492–1494

    CAS  PubMed  Google Scholar 

  8. Caldas M, Dhillon R (2000) Coarctation of the aorta in dizygotic twins. Cardiol Young 10:46–48

    Article  CAS  PubMed  Google Scholar 

  9. Cronk CE, Pelech AN, Malloy ME, McCarver DG (2004) Excess birth prevalence of hypoplastic left heart syndrome in eastern Wisconsin for birth cohorts 1997–1999. Birth Defects Res A Clin Mol Teratol 70:114–120

    Article  CAS  PubMed  Google Scholar 

  10. Dasgupta C, Martinez AM, Zuppan CW, et al. (2001) Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE). Mutat Res 479:173–186

    Article  CAS  PubMed  Google Scholar 

  11. Elliott DA, Kirk EP, Yeoh T, et al. (2003) Cardiac homeobox gene NKX2–5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. J Am Coll Cardiol 41:2072–2076

    Article  CAS  PubMed  Google Scholar 

  12. Ferencz C (1987) Familial risks of congenital heart defect assessed in a population-based epidemiologic study. Am J Hum Genet 26:839–849

    Article  Google Scholar 

  13. Ferencz C, Rubin JD, McCarter RJ, et al. (1985) Congenital heart disease: prevalence at live birth. The Baltimore–Washington Infant Study. Am J Epidemiol 121:31–36

    Article  CAS  PubMed  Google Scholar 

  14. Genetic relationships among left sided heart defects (1997) In: Ferencz C, Loffredo CA, Correa-Villasenor A, Wilson PD (eds) Genetic and Environmental Risk Factors of Cardiac Defects, Perspectives in Pediatric Cardiology Vol. 5, Futura, Armonk, NY, pp 168–171

  15. Gilliam DM, Kotch LE (1990) Alcohol related birth defects in long and short sleep mice. Alcohol 7:483–487

    Article  CAS  PubMed  Google Scholar 

  16. Grobman W, Pergament E (1996) Isolated hypoplastic left heart syndrome in three siblings. Obstet Gynecol 88:673–675

    Article  CAS  PubMed  Google Scholar 

  17. Grossfeld P (1999) The genetics of hypoplastic left heart syndrome. Cardiol Young 9:627–632

    Article  CAS  PubMed  Google Scholar 

  18. Hodach RJ, Hodach AE, Fallon JF (1975) The role of beta-adrenergic activity in the production of cardiac and aortic arch anomalies in chick embryos. Teratology 12:33–45

    Article  CAS  PubMed  Google Scholar 

  19. Johnson PD, Goldberg SJ, Mays MZ, Dawson BV (2003) Threshold of trichloroethylene contamination in maternal drinking waters affecting fetal heart development in the rat. Environ Health Perspect 111:289–292

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Junker R, Kotthoff S, Vielhaber H, et al. (2001) Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease. Cardiovasc Res 51:251–254

    Article  CAS  PubMed  Google Scholar 

  21. Khattak S, K-Moghtader G, McMartin K, et al. (1999) Pregnancy outcome following gestational exposure to organic solvents: a prospective controlled study. J Am Med Assoc 281:1106–1109

    Article  CAS  Google Scholar 

  22. Kuhlmann RS, Kolesari GL, Kalbfleisch JH (1983) Reduction of catecholamine-induced cardiovascular malformations in the chick embryo with metoprolol. Teratology 28:9–14

    Article  CAS  PubMed  Google Scholar 

  23. Kulldorff M (1997) A spatial scan statistic. Commun Stat Theory Methods 26:1481–1496

    Article  Google Scholar 

  24. Kulldorff M, Nagarwalla N (1995) Spatial disease clusters: detection and inference. Stat Med 14:799–810

    Article  CAS  PubMed  Google Scholar 

  25. Laumon B, Martin JL, Collet P, et al. (1996) Exposure to organic solvents during pregnancy and oral clefts: a case control study. Reprod Toxicol 10:15–19

    Article  CAS  PubMed  Google Scholar 

  26. Loffredo CA (2000) Epidemiology of cardiovascular malformations: prevalence and risk factors. Am J Med Genet 97:319–325

    Article  CAS  PubMed  Google Scholar 

  27. Loffredo CA, Chokkalingam A, Silll Am, et al. (1989) Familial aortic valve disease: evidence for a genetic influences? Eur Heart J 10:676–677

    Article  Google Scholar 

  28. Loffredo CA, Ferencz C, Wilson PD, Lurie IW (2000) Interrupted aortic arch: an epidemiologic study. Teratology 61:368

    Article  CAS  PubMed  Google Scholar 

  29. Nakada T, Yonesaka S (1996) Interruption of aortic arch type A in two siblings. Acta Paediatr Jpn 38:63–65

    Article  CAS  PubMed  Google Scholar 

  30. Narotsky MG, Weller EA, Chinchilli VM, Kavlock RJ (1995) Nonadditive developmental toxicity in mixtures of trichloroethylene, di [2ethylhexyl] phthalate, and heptachlor in a 5 × 5 × 5 design. Fundam Appl Toxicol 27:203–216

    Article  CAS  PubMed  Google Scholar 

  31. Pearson MA, Hoyme HE, Seaver LH, Rimsza ME (1994) Toluene embryopathy delineation of the phenotype and comparison with fetal alcohol syndrome. Pediatrics 93:211–215

    CAS  PubMed  Google Scholar 

  32. Phillips HM, Renforth GL, Spalluto C, et al. (2002) Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis. Genomics 79:475–478

    Article  CAS  PubMed  Google Scholar 

  33. Stoll C, Alembik Y, Dott B (1999) Familial coarctation of the aorta in three generations. Ann Genet 42:174–176

    CAS  PubMed  Google Scholar 

  34. Whittemore R, Wells JA, Castellsague X (1994) A second-generation study of 427 probands with congenital heart defects and their 837 children. J Am Coll Cardiol 23:1459–1467

    Article  CAS  PubMed  Google Scholar 

  35. Wilkins-Haug L (1997) Teratogen update: toluene. Teratology 55:145–151

    Article  CAS  PubMed  Google Scholar 

Download references

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Kuehl, K., Loffredo, C. A Cluster of Hypoplastic Left Heart Malformation in Baltimore, Maryland. Pediatr Cardiol 27, 25–31 (2006). https://doi.org/10.1007/s00246-005-0859-x

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