TY - JOUR
T1 - Pregnancy outcome following use of large doses of vitamin B6 in the first trimester
AU - Shrim, A.
AU - Boskovic, R.
AU - Maltepe, C.
AU - Navios, Y.
AU - Garcia-Bournissen, F.
AU - Koren, G.
N1 - Funding Information:
Supported in part by the Research Leadership for better Pharmacotherapy during pregnancy and lactation (Hospital for Sick Children) and the Ivey Chair in Molecular Toxicology, Department of Medicine, University of Western Ontario. As was supported by a grant from the Hospital for Sick Children’s Research Training Centre. The Motherisk NVP this is supported in part by Duchesnay Inc, Laval, Canada.
PY - 2006/11/1
Y1 - 2006/11/1
N2 - Vitamin B6 is often prescribed for the treatment of nausea and vomiting of pregnancy (NVP), at much higher doses than initially recommended. Large doses of vitamin B6 have been associated with cases of neuropathy. We set out to assess whether higher than standard doses of vitamin B6 during the first trimester of pregnancy were associated with a risk of maternal adverse events, major malformations, miscarriages or low birth weight. This was a prospective comparative observational study. The study group included women who were exposed to >50 mg/day of vitamin B6 during the first trimester; the control group included pregnant women with a non-teratogen exposure. A total of 192 pregnancies were followed-up. The mean dose of B6 used in the study group was 132.3 mg/day (median 110 mg/day, range 50 - 510 mg/day), for a mean period of 9 ± 4.2 weeks. In this group (n = 96), there were 91 live births, one major malformation and the mean birth weight was 3,542 ± 512 g. There were no statistical differences in the study endpoints between the vitamin B6 and the control groups. Within the limits of our sample size, higher than standard doses of vitamin B6 do not appear to be associated with an increased risk for major malformations.
AB - Vitamin B6 is often prescribed for the treatment of nausea and vomiting of pregnancy (NVP), at much higher doses than initially recommended. Large doses of vitamin B6 have been associated with cases of neuropathy. We set out to assess whether higher than standard doses of vitamin B6 during the first trimester of pregnancy were associated with a risk of maternal adverse events, major malformations, miscarriages or low birth weight. This was a prospective comparative observational study. The study group included women who were exposed to >50 mg/day of vitamin B6 during the first trimester; the control group included pregnant women with a non-teratogen exposure. A total of 192 pregnancies were followed-up. The mean dose of B6 used in the study group was 132.3 mg/day (median 110 mg/day, range 50 - 510 mg/day), for a mean period of 9 ± 4.2 weeks. In this group (n = 96), there were 91 live births, one major malformation and the mean birth weight was 3,542 ± 512 g. There were no statistical differences in the study endpoints between the vitamin B6 and the control groups. Within the limits of our sample size, higher than standard doses of vitamin B6 do not appear to be associated with an increased risk for major malformations.
UR - http://www.scopus.com/inward/record.url?scp=33845337675&partnerID=8YFLogxK
U2 - 10.1080/01443610600955826
DO - 10.1080/01443610600955826
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C2 - 17130022
AN - SCOPUS:33845337675
SN - 0144-3615
VL - 26
SP - 749
EP - 751
JO - Journal of Obstetrics and Gynaecology
JF - Journal of Obstetrics and Gynaecology
IS - 8
ER -