Risk factors for heart disease associated with abnormal sidedness

被引:47
作者
Kuehl, KS
Loffredo, C
机构
[1] George Washington Univ, Sch Med, Childrens Natl Med Ctr, Washington, DC 20010 USA
[2] Georgetown Univ, Sch Med, Washington, DC 20057 USA
关键词
D O I
10.1002/tera.10099
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The purpose of this study is to obtain information on potential familial and environmental risk factors for liveborn cases of heart disease associated with abnormal visceral and vascular sidedness, heterotaxy heart disease, so that hypotheses about this congenital cardiovascular malformation (CCVM) and its risk factors can be generated. We describe the characteristics of infants with heterotaxy heart malformations and case-control comparisons of interview data obtained on parental socio-demographic characteristics, occupational and household environmental exposures. Methods: Cases and controls are drawn from the Baltimore Washington Infant Study (BWIS) a population based case control study of CCVM diagnosed in the region from 1981-89. Results: Maternal diabetes (OR = 5.5, 95% CI = 1.6-19.1) and family history of malformations (OR = 5.1, 95% CI = 2.0-12.9) are strongly associated with cardiac disorders of sidedness. Cocaine use by mothers during the first trimester is associated with heterotaxy heart disease with odds of 3.7 (95% CI = 1.310.7). Cases of isolated dextrocardia shared risk factors with other heterotaxy malformations. The odds of a twin proband having heterotaxy heart disease is 4.8 (95% CI = 1.9-11.8) compared to singleton births. Twin probands are predominantly monozygotic twins in contrast to twin probands in other congenital cardiovascular malformations. Conclusions: Our findings are consistent with a role for multiple genetic factors in the development of left-right axis formation and with variable cardiac phenotypes according to gene expression and possible gene-environment interactions. Association with monozygotic twinning and with parental cocaine use may point to additional mechanistic clues for future research. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:242 / 248
页数:7
相关论文
共 39 条
[1]   Fetal effects of cocaine: an updated meta-analysis [J].
Addis, A ;
Moretti, ME ;
Syed, FA ;
Einarson, TR ;
Koren, G .
REPRODUCTIVE TOXICOLOGY, 2001, 15 (04) :341-369
[2]   Defective lateralisation in children with congenitally malformed hearts [J].
Anderson, RH ;
Webb, S ;
Brown, NA .
CARDIOLOGY IN THE YOUNG, 1998, 8 (04) :512-531
[3]   CONGENITAL DEXTROCARDIA - CLINICAL, ANGIOCARDIOGRAPHIC, AND AUTOPSY STUDIES ON 50 PATIENTS [J].
ARCILLA, RA ;
GASUL, BM .
JOURNAL OF PEDIATRICS, 1961, 58 (01) :39-+
[4]   CONGENITAL DEXTROCARDIA - CLINICAL, ANGIOCARDIOGRAPHIC, AND AUTOPSY STUDIES ON 50 PATIENTS [J].
ARCILLA, RA ;
GASUL, BM .
JOURNAL OF PEDIATRICS, 1961, 58 (02) :251-+
[5]   FISH studies in 45 patients with Rubinstein-Taybi syndrome:: deletions associated with polysplenia, hypoplastic left heart and death in infancy [J].
Bartsch, O ;
Wagner, A ;
Hinkel, GK ;
Krebs, P ;
Stumm, M ;
Schmalenberger, B ;
Böhm, S ;
Balci, S ;
Majewski, F .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1999, 7 (07) :748-756
[6]   The search for congenital malformations in newborns with fetal cocaine exposure [J].
Behnke, M ;
Eyler, FD ;
Garvan, CW ;
Wobie, K .
PEDIATRICS, 2001, 107 (05) :E74
[7]   TERATOGENICITY OF COCAINE IN HUMANS [J].
BINGOL, N ;
FUCHS, M ;
DIAZ, V ;
STONE, RK ;
GROMISCH, DS .
JOURNAL OF PEDIATRICS, 1987, 110 (01) :93-96
[8]   Left-right axis malformations in man and mouse [J].
Casey, B ;
Hackett, BP .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2000, 10 (03) :257-261
[9]   MAPPING A GENE FOR FAMILIAL SITUS ABNORMALITIES TO HUMAN-CHROMOSOME XQ24-Q27.1 [J].
CASEY, B ;
DEVOTO, M ;
JONES, KL ;
BALLABIO, A .
NATURE GENETICS, 1993, 5 (04) :403-407
[10]   Two rights make a wrong: human left-right malformations [J].
Casey, B .
HUMAN MOLECULAR GENETICS, 1998, 7 (10) :1565-1571