Background Multivitamin supplementation in pregnant women mayreduce the risks of cardiovascular defects, oral clefts, andurinary tract defects in their infants. We evaluated whetherthe folic acid component of multivitamins is responsible forthe reduction in risk by examining the associations betweenmaternal use of folic acid antagonists and these congenitalmalformations.
Methods We assessed exposure to folic acid antagonists thatact as dihydrofolate reductase inhibitors and to certain antiepilepticdrugs in 3870 infants with cardiovascular defects, 1962 infantswith oral clefts, and 1100 infants with urinary tract defectsand also in 8387 control infants with malformations the riskof which is not reduced after vitamin supplementation. Motherswere interviewed within six months after delivery about theirmedication use during pregnancy.
Results The relative risks of cardiovascular defects and oralclefts in infants whose mothers were exposed to dihydrofolatereductase inhibitors during the second or third month afterthe last menstrual period, as compared with infants whose mothershad no such exposure, were 3.4 (95 percent confidence interval,1.8 to 6.4) and 2.6 (95 percent confidence interval, 1.1 to6.1), respectively. The relative risks of cardiovascular defects,oral clefts, and urinary tract defects after maternal exposureto antiepileptic drugs were 2.2 (95 percent confidence interval,1.4 to 3.5), 2.5 (95 percent confidence interval, 1.5 to 4.2),and 2.5 (95 percent confidence interval, 1.2 to 5.0), respectively.Use of multivitamin supplements containing folic acid diminishedthe adverse effects of dihydrofolate reductase inhibitors, butnot that of antiepileptic drugs.
Conclusions Folic acid antagonists, which include such commondrugs as trimethoprim, triamterene, carbamazepine, phenytoin,phenobarbital, and primidone, may increase the risk not onlyof neural-tube defects, but also of cardiovascular defects,oral clefts, and urinary tract defects. The folic acid componentof multivitamins may reduce the risks of these defects.
Source Information
From the Slone Epidemiology Unit, Boston University School of Public Health, Brookline, Mass. (S.H.-D., M.M.W., A.A.M.); and the Department of Epidemiology, Harvard School of Public Health, Boston (S.H.-D., A.M.W.).
Address reprint requests to Dr. Hernández-Díaz at the Slone Epidemiology Unit, Boston University School of Public Health, 1371 Beacon St., Brookline, MA 02446, or at shernan{at}bu.edu.
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