Body Mass Index, waist circumference or sagittal abdominal diameter: Which parameter is better correlated with body fat changes in postmenopausal women after combined training protocol?
Autor: | Eddie Fernando Candido Murta, Kely R. C. Teixeira, Larissa S. Limirio, Luana T. Rossato, Cinthia D. Barbosa, Fernanda Maria Martins, Rosekeila Simões Nomelini, Fábio Lera Orsatti, Erick P. de Oliveira, Paula C. Nahas, Flávia M.S. de Branco |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Waist Endocrinology Diabetes and Metabolism 030209 endocrinology & metabolism Body Mass Index 03 medical and health sciences 0302 clinical medicine Weight loss Internal medicine medicine Humans Sagittal Abdominal Diameter 030109 nutrition & dietetics Nutrition and Dietetics Postmenopausal women business.industry Anthropometry Circumference Postmenopause Endocrinology Adipose Tissue Female Android fat distribution Waist Circumference medicine.symptom business Body mass index |
Zdroj: | Clinical Nutrition ESPEN. 38:192-195 |
ISSN: | 2405-4577 0320-0639 |
Popis: | We aimed to verify whether exercise-induced changes in body mass index (BMI), waist circumference (WC) and sagittal abdominal diameter (SAD) are correlated with changes in body fat (BF) in postmenopausal women.Seventeen postmenopausal women performed combined training three times a week, for 12 weeks. Correlations of delta (Δ) BMI, Δ WC, and Δ SAD with Δ total BF, Δ android and Δ gynoid fats were performed.Weight, BMI and android fat decreased over time. A tendency of reductions in gynoid fat was found (p = 0.070). Delta BMI was positively correlated with Δ total BF (r = 0.56; p 0.05), Δ android fat (r = 0.64; p 0.05), and Δ gynoid fat (r = 0.72; p 0.05). The Δ WC was only correlated with Δ gynoid fat (r = 0.55; p 0.05). The Δ SAD was not correlated with all the Δ body fat parameters evaluated.We conclude that changes in BMI were better associated with body fat changes induced by combined training when compared to WC and SAD in postmenopausal women. The patients were part of a 12-week training study (ClinicalTrials.gov Identifier: NCT03200639). |
Databáze: | OpenAIRE |
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