The DALI vitamin D randomized controlled trial for gestational diabetes mellitus prevention: No major benefit shown besides vitamin D sufficiency

As vitamin D deficiency is associated with an increased risk of gestational diabetes mellitus (GDM), we aimed to test vitamin D supplementation as a strategy to reduce GDM risk (evaluated after fasting plasma glucose (FPG), insulin resistance and weight gain) in pregnant overweight/obese women. The...

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Veröffentlicht in:Clinical nutrition (Edinburgh, Scotland) Scotland), 2020-03, Vol.39 (3), p.976-984
Hauptverfasser: Corcoy, Rosa, Mendoza, Lilian C., Simmons, David, Desoye, Gernot, Adelantado, J.M., Chico, Ana, Devlieger, Roland, van Assche, Andre, Galjaard, Sander, Timmerman, Dirk, Lapolla, Annunziata, Dalfra, Maria G., Bertolotto, Alessandra, Harreiter, Jürgen, Wender-Ozegowska, Ewa, Zawiejska, Agnieszka, Kautzky-Willer, Alexandra, Dunne, Fidelma P., Damm, Peter, Mathiesen, Elisabeth R., Jensen, Dorte M., Andersen, Lise Lotte T., Tanvig, Mette, Hill, David J., Jelsma, Judith G., Snoek, Frank J., Köfeler, Harald, Trötzmüller, Martin, Lips, Paul, van Poppel, Mireille N.M.
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Zusammenfassung:As vitamin D deficiency is associated with an increased risk of gestational diabetes mellitus (GDM), we aimed to test vitamin D supplementation as a strategy to reduce GDM risk (evaluated after fasting plasma glucose (FPG), insulin resistance and weight gain) in pregnant overweight/obese women. The DALI vitamin D multicenter study enrolled women with prepregnancy body mass index (BMI) ≥ 29 kg/m2, ≤19 + 6 weeks of gestation and without GDM. Participants were randomized to receive 1600 IU/day vitamin D3 or placebo (each with or without lifestyle intervention) on top of (multi)vitamins supplements. Women were assessed for vitamin D status (sufficiency defined as serum 25-hydroxyvitamin D (25(OH)D) ≥ 50 nmol/l), FPG, insulin resistance and weight at baseline, 24–28 and 35–37 weeks. Linear or logistic regression analyses were performed to assess intervention effects. Average baseline serum 25(OH)D was ≥50 nmol/l across all study sites. In the vitamin D intervention arm (n = 79), 97% of participants achieved target serum vitamin 25(OH)D (≥50 nmol/l) at 24–28 weeks and 98% at 35–37 weeks vs 74% and 78% respectively in the placebo arm (n = 75, p 
ISSN:0261-5614
1532-1983
DOI:10.1016/j.clnu.2019.04.006