Metformin for overweight women at midlife: a double-blind, randomized, controlled trial

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Abstract

Aim This study was undertaken to determine whether metformin would ameliorate insulin resistance, reduce weight and waist circumference and improve lipids in obese, but not morbidly obese, euglycemic women. Methods Obese women (body mass index (BMI) = 30 and <40 kg/m2 and/or waist circumference > 88 cm), aged 35?65 were randomized (1:1) to metformin 850 mg or identical placebo, twice daily for 26 weeks. The primary outcome was the change in insulin resistance determined by the homeostasis model of assessment (HOMA-IR). Secondary outcomes included fasting insulin, glucose, weight, waist circumference and BMI. Results Of the 125 women screened, 117 enrolled and 100 women, mean age 53 years, were included in the primary intention-to-treat analysis. Metformin resulted in statistically significant between-group difference in the change in HOMA-IR (change in median - 0.04 vs. placebo + 0.1, p = 0.018) and BMI (mean change - 1.00 kg/m2; 95 confidence interval (CI) 1.37 to - 0.62 vs. placebo mean change 0.00; 95 CI - 0.29 to 0.28, p <0.001). Statistically significant reductions in HbA1c (p = 0.008) and fasting insulin (p = 0.03) and a borderline decrease in high density lipoprotein cholesterol (p = 0.07) were also observed for metformin, compared with placebo. No effects were seen for waist circumference, fasting glucose or other lipids. Conclusion Treatment of euglycemic, obese, middle-aged women with metformin 1700 mg per day reduced insulin resistance and weight compared with placebo. Further studies are needed to determine whether the use of metformin will prevent the progression of insulin resistance to type 2 diabetes mellitus in obese women.
Original languageEnglish
Pages (from-to)270 - 277
Number of pages8
JournalClimacteric
Volume18
Issue number2
DOIs
Publication statusPublished - 2015

Cite this

@article{336ff61b9895468bb36dc31bd063781b,
title = "Metformin for overweight women at midlife: a double-blind, randomized, controlled trial",
abstract = "Aim This study was undertaken to determine whether metformin would ameliorate insulin resistance, reduce weight and waist circumference and improve lipids in obese, but not morbidly obese, euglycemic women. Methods Obese women (body mass index (BMI) = 30 and <40 kg/m2 and/or waist circumference > 88 cm), aged 35?65 were randomized (1:1) to metformin 850 mg or identical placebo, twice daily for 26 weeks. The primary outcome was the change in insulin resistance determined by the homeostasis model of assessment (HOMA-IR). Secondary outcomes included fasting insulin, glucose, weight, waist circumference and BMI. Results Of the 125 women screened, 117 enrolled and 100 women, mean age 53 years, were included in the primary intention-to-treat analysis. Metformin resulted in statistically significant between-group difference in the change in HOMA-IR (change in median - 0.04 vs. placebo + 0.1, p = 0.018) and BMI (mean change - 1.00 kg/m2; 95 confidence interval (CI) 1.37 to - 0.62 vs. placebo mean change 0.00; 95 CI - 0.29 to 0.28, p <0.001). Statistically significant reductions in HbA1c (p = 0.008) and fasting insulin (p = 0.03) and a borderline decrease in high density lipoprotein cholesterol (p = 0.07) were also observed for metformin, compared with placebo. No effects were seen for waist circumference, fasting glucose or other lipids. Conclusion Treatment of euglycemic, obese, middle-aged women with metformin 1700 mg per day reduced insulin resistance and weight compared with placebo. Further studies are needed to determine whether the use of metformin will prevent the progression of insulin resistance to type 2 diabetes mellitus in obese women.",
author = "Roisin Worsley and Jane, {Fiona Margaret} and Robinson, {Penelope Jane} and Bell, {Robin Jean} and Davis, {Susan Ruth}",
year = "2015",
doi = "10.3109/13697137.2014.954997",
language = "English",
volume = "18",
pages = "270 -- 277",
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publisher = "Taylor & Francis",
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Metformin for overweight women at midlife: a double-blind, randomized, controlled trial. / Worsley, Roisin; Jane, Fiona Margaret; Robinson, Penelope Jane; Bell, Robin Jean; Davis, Susan Ruth.

In: Climacteric, Vol. 18, No. 2, 2015, p. 270 - 277.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - Metformin for overweight women at midlife: a double-blind, randomized, controlled trial

AU - Worsley, Roisin

AU - Jane, Fiona Margaret

AU - Robinson, Penelope Jane

AU - Bell, Robin Jean

AU - Davis, Susan Ruth

PY - 2015

Y1 - 2015

N2 - Aim This study was undertaken to determine whether metformin would ameliorate insulin resistance, reduce weight and waist circumference and improve lipids in obese, but not morbidly obese, euglycemic women. Methods Obese women (body mass index (BMI) = 30 and <40 kg/m2 and/or waist circumference > 88 cm), aged 35?65 were randomized (1:1) to metformin 850 mg or identical placebo, twice daily for 26 weeks. The primary outcome was the change in insulin resistance determined by the homeostasis model of assessment (HOMA-IR). Secondary outcomes included fasting insulin, glucose, weight, waist circumference and BMI. Results Of the 125 women screened, 117 enrolled and 100 women, mean age 53 years, were included in the primary intention-to-treat analysis. Metformin resulted in statistically significant between-group difference in the change in HOMA-IR (change in median - 0.04 vs. placebo + 0.1, p = 0.018) and BMI (mean change - 1.00 kg/m2; 95 confidence interval (CI) 1.37 to - 0.62 vs. placebo mean change 0.00; 95 CI - 0.29 to 0.28, p <0.001). Statistically significant reductions in HbA1c (p = 0.008) and fasting insulin (p = 0.03) and a borderline decrease in high density lipoprotein cholesterol (p = 0.07) were also observed for metformin, compared with placebo. No effects were seen for waist circumference, fasting glucose or other lipids. Conclusion Treatment of euglycemic, obese, middle-aged women with metformin 1700 mg per day reduced insulin resistance and weight compared with placebo. Further studies are needed to determine whether the use of metformin will prevent the progression of insulin resistance to type 2 diabetes mellitus in obese women.

AB - Aim This study was undertaken to determine whether metformin would ameliorate insulin resistance, reduce weight and waist circumference and improve lipids in obese, but not morbidly obese, euglycemic women. Methods Obese women (body mass index (BMI) = 30 and <40 kg/m2 and/or waist circumference > 88 cm), aged 35?65 were randomized (1:1) to metformin 850 mg or identical placebo, twice daily for 26 weeks. The primary outcome was the change in insulin resistance determined by the homeostasis model of assessment (HOMA-IR). Secondary outcomes included fasting insulin, glucose, weight, waist circumference and BMI. Results Of the 125 women screened, 117 enrolled and 100 women, mean age 53 years, were included in the primary intention-to-treat analysis. Metformin resulted in statistically significant between-group difference in the change in HOMA-IR (change in median - 0.04 vs. placebo + 0.1, p = 0.018) and BMI (mean change - 1.00 kg/m2; 95 confidence interval (CI) 1.37 to - 0.62 vs. placebo mean change 0.00; 95 CI - 0.29 to 0.28, p <0.001). Statistically significant reductions in HbA1c (p = 0.008) and fasting insulin (p = 0.03) and a borderline decrease in high density lipoprotein cholesterol (p = 0.07) were also observed for metformin, compared with placebo. No effects were seen for waist circumference, fasting glucose or other lipids. Conclusion Treatment of euglycemic, obese, middle-aged women with metformin 1700 mg per day reduced insulin resistance and weight compared with placebo. Further studies are needed to determine whether the use of metformin will prevent the progression of insulin resistance to type 2 diabetes mellitus in obese women.

UR - http://informahealthcare.com/doi/abs/10.3109/13697137.2014.954997

U2 - 10.3109/13697137.2014.954997

DO - 10.3109/13697137.2014.954997

M3 - Article

VL - 18

SP - 270

EP - 277

JO - Climacteric

JF - Climacteric

SN - 1369-7137

IS - 2

ER -