Hyppää sisältöön
    • Suomeksi
    • In English
Trepo
  • Suomeksi
  • In English
  • Kirjaudu
Näytä viite 
  •   Etusivu
  • Trepo
  • TUNICRIS-julkaisut
  • Näytä viite
  •   Etusivu
  • Trepo
  • TUNICRIS-julkaisut
  • Näytä viite
JavaScript is disabled for your browser. Some features of this site may not work without it.

The Effect of Metformin on Insulin Requirement, Glycaemic Control and Weight Gain in Type 1 Diabetes During Pregnancy: a Randomised, Placebo-Controlled Multicentre Study

Juuma, Elina; Tihtonen, Kati; Metso, Saara E.; Hannula, Päivi M.; Helminen, Mika; Tertti, Kristiina; Immonen, Heidi; Georgiadis, Leena; Väyrynen, Kirsi; Ahtiainen, Petteri; Nikkinen, Hilkka; Koivikko, Minna; Laivuori, Hannele; Uotila, Jukka (2025-09)

 
Avaa tiedosto
Diabetes_Metabolism_Res_-_2025_-_Juuma_-_The_Effect_of_Metformin_on_Insulin_Requirement_Glycaemic_Control_and_Weight_Gain.pdf (764.6Kt)
Lataukset: 



Juuma, Elina
Tihtonen, Kati
Metso, Saara E.
Hannula, Päivi M.
Helminen, Mika
Tertti, Kristiina
Immonen, Heidi
Georgiadis, Leena
Väyrynen, Kirsi
Ahtiainen, Petteri
Nikkinen, Hilkka
Koivikko, Minna
Laivuori, Hannele
Uotila, Jukka
09 / 2025

Diabetes/Metabolism Research and Reviews
e70085
doi:10.1002/dmrr.70085
Näytä kaikki kuvailutiedot
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202510079712

Kuvaus

Peer reviewed
Tiivistelmä
Aim: Our aim was to ascertain whether metformin can reduce insulin requirement without compromising glycaemic control during pregnancy in women with type 1 diabetes. Methods: A total of 126 pregnant women with type 1 diabetes were recruited for a randomised, double-blind, placebo-controlled multicentre study. The primary outcome was total insulin change, defined as the difference between baseline and third trimester maximum insulin dose (IU). Results: Fifty women in the placebo group and 51 women in the metformin group completed the study. A predetermined sample size of 200 participants was not achieved. There was no significant difference in the primary outcome, that is, in the change of total insulin requirement (33 vs. 27 IU, p = 0.193). However, the metformin group showed a significantly lower increase in the prandial insulin change, with 24 versus 14 IU (p = 0.014) and 0.3 versus 0.2 IU/kg (p = 0.048). In the exploratory subgroup analysis, metformin attenuated prandial insulin increase in women with high BMI (> 25 kg/m2) or high baseline insulin requirement (> 40 IU) (25 vs. 15 IU, p = 0.028, 30 vs. 14 IU, p = 0.007). Weight gain remained more often within target in the metformin group (20% vs. 40%, p = 0.029). A similar weight benefit was observed in subgroups (BMI> 25 kg/m2 8% vs. 32%, p = 0.005, insulin requirement> 40 IU 6% vs. 34%, p = 0.004). No differences were seen in glycaemic control or neonatal outcome between the groups. Conclusions: Metformin was not shown to affect total insulin change but reduced the prandial insulin change and improved weight gain control especially in insulin-resistant subgroups. These findings warrant further studies on metformin as an adjunctive medicine. Trial Registration: ClinicalTrials.gov: NCT03765359.
Kokoelmat
  • TUNICRIS-julkaisut [22206]
Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste
 

 

Selaa kokoelmaa

TekijätNimekkeetTiedekunta (2019 -)Tiedekunta (- 2018)Tutkinto-ohjelmat ja opintosuunnatAvainsanatJulkaisuajatKokoelmat

Omat tiedot

Kirjaudu sisäänRekisteröidy
Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste