Metformin in gestational diabetes: the offspring follow-up (MiG TOFU): body composition and metabolic outcomes at 7–9 years of age
ObjectiveTo compare body composition and metabolic outcomes at 7–9 years in offspring of women with gestational diabetes (GDM) randomized to metformin (±insulin) or insulin treatment during pregnancy.Research design and methodsChildren were assessed at 7 years in Adelaide (n=109/181) and 9 years in...
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Published in | BMJ open diabetes research & care Vol. 6; no. 1; p. e000456 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BMJ Publishing Group LTD
01.04.2018
BMJ Publishing Group |
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Abstract | ObjectiveTo compare body composition and metabolic outcomes at 7–9 years in offspring of women with gestational diabetes (GDM) randomized to metformin (±insulin) or insulin treatment during pregnancy.Research design and methodsChildren were assessed at 7 years in Adelaide (n=109/181) and 9 years in Auckland (n=99/396) by anthropometry, bioimpedance analysis (BIA), dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI) (n=92/99) and fasting bloods (n=82/99).ResultsIn the Adelaide subgroup, mothers were similar at enrollment. Women randomized to metformin versus insulin had higher treatment glycemia (p=0.002) and more infants with birth weight >90th percentile (20.7% vs 5.9%; p=0.029). At 7 years, there were no differences in offspring measures. In Auckland, at enrollment, women randomized to metformin had a higher body mass index (BMI) (p=0.08) but gained less weight during treatment (p=0.07). Offspring birth measures were similar. At 9 years, metformin offspring were larger by measures of weight, arm and waist circumferences, waist:height (p<0.05); BMI, triceps skinfold (p=0.05); DXA fat mass and lean mass (p=0.07); MRI abdominal fat volume (p=0.051). Body fat percent was similar between treatment groups by DXA and BIA. Abdominal fat percentages (visceral adipose tissue, subcutaneous adipose tissue and liver) were similar by MRI. Fasting glucose, triglyceride, insulin, insulin resistance, glycosylated hemoglobin (HbA1c), cholesterol, liver transaminases, leptin and adiponectin were similar.ConclusionsMetformin or insulin for GDM was associated with similar offspring total and abdominal body fat percent and metabolic measures at 7–9 years. Metformin-exposed children were larger at 9 years. Metformin may interact with fetal environmental factors to influence offspring outcomes. |
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AbstractList | Objective
To compare body composition and metabolic outcomes at 7–9 years in offspring of women with gestational diabetes (GDM) randomized to metformin (±insulin) or insulin treatment during pregnancy.
Research design and methods
Children were assessed at 7 years in Adelaide (n=109/181) and 9 years in Auckland (n=99/396) by anthropometry, bioimpedance analysis (BIA), dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI) (n=92/99) and fasting bloods (n=82/99).
Results
In the Adelaide subgroup, mothers were similar at enrollment. Women randomized to metformin versus insulin had higher treatment glycemia (p=0.002) and more infants with birth weight >90th percentile (20.7% vs 5.9%; p=0.029). At 7 years, there were no differences in offspring measures. In Auckland, at enrollment, women randomized to metformin had a higher body mass index (BMI) (p=0.08) but gained less weight during treatment (p=0.07). Offspring birth measures were similar. At 9 years, metformin offspring were larger by measures of weight, arm and waist circumferences, waist:height (p<0.05); BMI, triceps skinfold (p=0.05); DXA fat mass and lean mass (p=0.07); MRI abdominal fat volume (p=0.051). Body fat percent was similar between treatment groups by DXA and BIA. Abdominal fat percentages (visceral adipose tissue, subcutaneous adipose tissue and liver) were similar by MRI. Fasting glucose, triglyceride, insulin, insulin resistance, glycosylated hemoglobin (HbA1c), cholesterol, liver transaminases, leptin and adiponectin were similar.
Conclusions
Metformin or insulin for GDM was associated with similar offspring total and abdominal body fat percent and metabolic measures at 7–9 years. Metformin-exposed children were larger at 9 years. Metformin may interact with fetal environmental factors to influence offspring outcomes. ObjectiveTo compare body composition and metabolic outcomes at 7–9 years in offspring of women with gestational diabetes (GDM) randomized to metformin (±insulin) or insulin treatment during pregnancy.Research design and methodsChildren were assessed at 7 years in Adelaide (n=109/181) and 9 years in Auckland (n=99/396) by anthropometry, bioimpedance analysis (BIA), dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI) (n=92/99) and fasting bloods (n=82/99).ResultsIn the Adelaide subgroup, mothers were similar at enrollment. Women randomized to metformin versus insulin had higher treatment glycemia (p=0.002) and more infants with birth weight >90th percentile (20.7% vs 5.9%; p=0.029). At 7 years, there were no differences in offspring measures. In Auckland, at enrollment, women randomized to metformin had a higher body mass index (BMI) (p=0.08) but gained less weight during treatment (p=0.07). Offspring birth measures were similar. At 9 years, metformin offspring were larger by measures of weight, arm and waist circumferences, waist:height (p<0.05); BMI, triceps skinfold (p=0.05); DXA fat mass and lean mass (p=0.07); MRI abdominal fat volume (p=0.051). Body fat percent was similar between treatment groups by DXA and BIA. Abdominal fat percentages (visceral adipose tissue, subcutaneous adipose tissue and liver) were similar by MRI. Fasting glucose, triglyceride, insulin, insulin resistance, glycosylated hemoglobin (HbA1c), cholesterol, liver transaminases, leptin and adiponectin were similar.ConclusionsMetformin or insulin for GDM was associated with similar offspring total and abdominal body fat percent and metabolic measures at 7–9 years. Metformin-exposed children were larger at 9 years. Metformin may interact with fetal environmental factors to influence offspring outcomes. To compare body composition and metabolic outcomes at 7-9 years in offspring of women with gestational diabetes (GDM) randomized to metformin (±insulin) or insulin treatment during pregnancy. Children were assessed at 7 years in Adelaide (n=109/181) and 9 years in Auckland (n=99/396) by anthropometry, bioimpedance analysis (BIA), dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI) (n=92/99) and fasting bloods (n=82/99). In the Adelaide subgroup, mothers were similar at enrollment. Women randomized to metformin versus insulin had higher treatment glycemia (p=0.002) and more infants with birth weight >90th percentile (20.7% vs 5.9%; p=0.029). At 7 years, there were no differences in offspring measures. In Auckland, at enrollment, women randomized to metformin had a higher body mass index (BMI) (p=0.08) but gained less weight during treatment (p=0.07). Offspring birth measures were similar. At 9 years, metformin offspring were larger by measures of weight, arm and waist circumferences, waist:height (p<0.05); BMI, triceps skinfold (p=0.05); DXA fat mass and lean mass (p=0.07); MRI abdominal fat volume (p=0.051). Body fat percent was similar between treatment groups by DXA and BIA. Abdominal fat percentages (visceral adipose tissue, subcutaneous adipose tissue and liver) were similar by MRI. Fasting glucose, triglyceride, insulin, insulin resistance, glycosylated hemoglobin (HbA1c), cholesterol, liver transaminases, leptin and adiponectin were similar. Metformin or insulin for GDM was associated with similar offspring total and abdominal body fat percent and metabolic measures at 7-9 years. Metformin-exposed children were larger at 9 years. Metformin may interact with fetal environmental factors to influence offspring outcomes. |
Author | Rowan, Janet A Rush, Elaine C Obolonkin, Victor Hague, William M Coat, Suzette Lu, Jun Plank, Lindsay D |
AuthorAffiliation | 5 Department of Obstetrics , Women’s and Children’s Hospital , Adelaide , South Australia 3 Department of Surgery , University of Auckland , Auckland , New Zealand 2 Faculty of Health and Environmental Sciences , Auckland University of Technology , Auckland , New Zealand 4 Robinson Research Institute, University of Adelaide , Adelaide , South Australia , Australia 1 Department of Obstetrics , National Women’s Health at Auckland City Hospital , Auckland , New Zealand |
AuthorAffiliation_xml | – name: 2 Faculty of Health and Environmental Sciences , Auckland University of Technology , Auckland , New Zealand – name: 3 Department of Surgery , University of Auckland , Auckland , New Zealand – name: 5 Department of Obstetrics , Women’s and Children’s Hospital , Adelaide , South Australia – name: 1 Department of Obstetrics , National Women’s Health at Auckland City Hospital , Auckland , New Zealand – name: 4 Robinson Research Institute, University of Adelaide , Adelaide , South Australia , Australia |
Author_xml | – sequence: 1 givenname: Janet A orcidid: 0000-0001-8406-3452 surname: Rowan fullname: Rowan, Janet A email: janetrowan1@gmail.com organization: Department of Obstetrics, National Women’s Health at Auckland City Hospital, Auckland, New Zealand – sequence: 2 givenname: Elaine C surname: Rush fullname: Rush, Elaine C email: janetrowan1@gmail.com organization: Faculty of Health and Environmental Sciences, Auckland University of Technology, Auckland, New Zealand – sequence: 3 givenname: Lindsay D surname: Plank fullname: Plank, Lindsay D email: janetrowan1@gmail.com organization: Department of Surgery, University of Auckland, Auckland, New Zealand – sequence: 4 givenname: Jun surname: Lu fullname: Lu, Jun email: janetrowan1@gmail.com organization: Faculty of Health and Environmental Sciences, Auckland University of Technology, Auckland, New Zealand – sequence: 5 givenname: Victor surname: Obolonkin fullname: Obolonkin, Victor email: janetrowan1@gmail.com organization: Faculty of Health and Environmental Sciences, Auckland University of Technology, Auckland, New Zealand – sequence: 6 givenname: Suzette surname: Coat fullname: Coat, Suzette email: janetrowan1@gmail.com organization: Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia – sequence: 7 givenname: William M orcidid: 0000-0002-5355-2955 surname: Hague fullname: Hague, William M email: janetrowan1@gmail.com organization: Department of Obstetrics, Women’s and Children’s Hospital, Adelaide, South Australia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29682291$$D View this record in MEDLINE/PubMed |
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Snippet | ObjectiveTo compare body composition and metabolic outcomes at 7–9 years in offspring of women with gestational diabetes (GDM) randomized to metformin... To compare body composition and metabolic outcomes at 7-9 years in offspring of women with gestational diabetes (GDM) randomized to metformin (±insulin) or... Objective To compare body composition and metabolic outcomes at 7–9 years in offspring of women with gestational diabetes (GDM) randomized to metformin... |
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SubjectTerms | Abdomen Age Antidiabetics Birth weight Blood pressure Body composition Body fat Clinical Care/Education/Nutrition Diabetes Gender Gestational diabetes Insulin Metabolism Mothers Obesity Pediatrics Pregnancy Software Soy products |
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Title | Metformin in gestational diabetes: the offspring follow-up (MiG TOFU): body composition and metabolic outcomes at 7–9 years of age |
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