The Lancet Diabetes & Endocrinology: Published on
February, 2023
Metformin is increasingly being
used during pregnancy, with potentially adverse long-term effects on children.
This study aimed to examine
adiposity in children of women with type 2 diabetes from the Metformin in Women
with Type 2 Diabetes in Pregnancy (MiTy) trial, with and without in-utero
exposure to metformin, up to 24 months of age.
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This randomised controlled trial study
assessed the adiposity in children of women with type 2 diabetes up to 24
months of age who were exposed to metformin in utero from the MiTy trial. At 24
months, there was no difference in BMI with metformin or placebo exposure in
utero.
BMI was higher in the metformin
group between 6 and 24 months. There was no difference in the sum of skin folds
or BMI trajectory between the two groups.
Conclusion:
Anthropometric data were similar in children exposed to metformin or
placebo in utero. Metformin may be a safe option for patients with type 2
diabetes during pregnancy without any long-term health concerns in their
children.
Background: Metformin
is increasingly being used during pregnancy, with potentially adverse long-term
effects on children. Authors aimed to examine adiposity in children of women with
type 2 diabetes from the Metformin in Women with Type 2 Diabetes in Pregnancy
(MiTy) trial, with and without in-utero exposure to metformin, up to 24 months
of age.
Methods: MiTy Kids
is a follow-up study that included infants of women who participated in the
MiTy randomised controlled trial, receiving either oral 1000 mg metformin twice
daily or placebo. Caregivers and researchers remained masked to the type of
medication (metformin or placebo) mothers received during their pregnancy.
Anthropometric measurements, including weight, height, and skinfold
thicknesses, were taken at 3, 6, 12, 18, and 24 months. At 24 months, linear
regression was used to compare the BMI Z score and sum of skinfolds in the
metformin versus placebo groups, adjusted for confounders. Fractional
polynomials were used to assess growth trajectories.
Findings: Of the 465
eligible children, 283 (61%) were included from 19 centres in Canada and
Australia. At 24 months, there was no difference between groups in mean BMI Z
score (0·84 [SD 1·52] with metformin vs 0·91 [1·38] with placebo; mean difference
0·07) or mean sum of skinfolds (23·0 mm [5·2] vs 23·8 mm [5·4]; mean difference
0·8 mm [-0·7 to 2·3]). Metformin was not a predictor of BMI Z score at 24
months of age (mean difference -0·01). There was no overall difference in BMI
trajectory but, in males, trajectories were significantly different by
treatment; BMI in the metformin group was higher between 6 and 24 months.
Children of women with type 2 diabetes were approximately 1 SD heavier than the
WHO reference population.
Interpretation: Anthropometrics
were similar in children exposed and those not exposed to metformin in utero;
hence, overall, data are reassuring with regard to the use of metformin during
pregnancy in women with type 2 diabetes and the long-term health of their
children.
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