TY - JOUR
T1 - Birth defects after maternal exposure to corticosteroids
T2 - Prospective cohort study and meta-analysis of epidemiological studies
AU - Park-Wyllie, Laura
AU - Mazzotta, Paolo
AU - Pastuszak, Anne
AU - Moretti, Myla E.
AU - Beique, Lizanne
AU - Hunnisett, Laura
AU - Friesen, Mark H.
AU - Jacobson, Sheila
AU - Kasapinovic, S.
AU - Chang, Debra
AU - Diav-Citrin, Orna
AU - Chitayat, David
AU - Nulman, Irena
AU - Einarson, Thomas R.
AU - Koren, Gideon
PY - 2000
Y1 - 2000
N2 - Background: Corticosteroids are first-line drugs for the treatment of a variety of conditions in women of childbearing age. Information regarding human pregnancy outcome with corticosteroids is limited. Methods: We collected prospectively and followed up 184 women exposed to prednisone in pregnancy and 188 pregnant women who were counseled by Motherisk for nonteratogenic exposure. The primary outcome was the rate of major birth defects. A meta-analysis of all epidemiological studies was conducted. The Mantel-Haenszel summary odds ratio was calculated for the pooled studies with 95% confidence intervals. A cumulative summary odds ratio was also calculated by combining studies in chronological order. Chi-squared for homogeneity was determined to establish the comparability of the studies. Results: In our prospective study, there was no statistical difference in the rate of major anomalies between the corticosteroid-exposed and control groups. In the meta-analysis, the Mantel-Haenszel summary odds ratio for major malformations with all cohort studies was 1.45 [95% Cl 0.80, 2.60] and 3.03 [95% Cl 1.08, 8.54] when Heinonen et al. ('77) was removed. This suggests a marginally increased risk of major malformations after first-trimester exposure to corticosteroids. In addition, summary odds ratio for case-control studies examining oral clefts was significant (3.35 [95% Cl 1.97, 5.69]). Conclusions: Although prednisone does not represent a major teratogenic risk in humans at therapeutic doses, it does increase by an order of 3.4-fold the risk of oral cleft, which is consistent with the existing animal studies. (C) 2000 Wiley-Liss, Inc.
AB - Background: Corticosteroids are first-line drugs for the treatment of a variety of conditions in women of childbearing age. Information regarding human pregnancy outcome with corticosteroids is limited. Methods: We collected prospectively and followed up 184 women exposed to prednisone in pregnancy and 188 pregnant women who were counseled by Motherisk for nonteratogenic exposure. The primary outcome was the rate of major birth defects. A meta-analysis of all epidemiological studies was conducted. The Mantel-Haenszel summary odds ratio was calculated for the pooled studies with 95% confidence intervals. A cumulative summary odds ratio was also calculated by combining studies in chronological order. Chi-squared for homogeneity was determined to establish the comparability of the studies. Results: In our prospective study, there was no statistical difference in the rate of major anomalies between the corticosteroid-exposed and control groups. In the meta-analysis, the Mantel-Haenszel summary odds ratio for major malformations with all cohort studies was 1.45 [95% Cl 0.80, 2.60] and 3.03 [95% Cl 1.08, 8.54] when Heinonen et al. ('77) was removed. This suggests a marginally increased risk of major malformations after first-trimester exposure to corticosteroids. In addition, summary odds ratio for case-control studies examining oral clefts was significant (3.35 [95% Cl 1.97, 5.69]). Conclusions: Although prednisone does not represent a major teratogenic risk in humans at therapeutic doses, it does increase by an order of 3.4-fold the risk of oral cleft, which is consistent with the existing animal studies. (C) 2000 Wiley-Liss, Inc.
UR - http://www.scopus.com/inward/record.url?scp=0033662284&partnerID=8YFLogxK
U2 - 10.1002/1096-9926(200012)62:6<385::AID-TERA5>3.0.CO;2-Z
DO - 10.1002/1096-9926(200012)62:6<385::AID-TERA5>3.0.CO;2-Z
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C2 - 11091360
AN - SCOPUS:0033662284
SN - 0040-3709
VL - 62
SP - 385
EP - 392
JO - Teratology
JF - Teratology
IS - 6
ER -