Caloric restriction alters the metabolic response to a mixed-meal: results from a randomized, controlled trial.
dc.contributor.author | Huffman, Kim M | |
dc.contributor.author | Redman, Leanne M | |
dc.contributor.author | Landerman, Lawrence R | |
dc.contributor.author | Pieper, Carl F | |
dc.contributor.author | Stevens, Robert D | |
dc.contributor.author | Muehlbauer, Michael J | |
dc.contributor.author | Wenner, Brett R | |
dc.contributor.author | Bain, James R | |
dc.contributor.author | Kraus, Virginia B | |
dc.contributor.author | Newgard, Christopher B | |
dc.contributor.author | Ravussin, Eric | |
dc.contributor.author | Kraus, William E | |
dc.contributor.editor | Tomé, Daniel | |
dc.coverage.spatial | United States | |
dc.date.accessioned | 2015-11-10T22:38:43Z | |
dc.date.issued | 2012 | |
dc.description.abstract | OBJECTIVES: To determine if caloric restriction (CR) would cause changes in plasma metabolic intermediates in response to a mixed meal, suggestive of changes in the capacity to adapt fuel oxidation to fuel availability or metabolic flexibility, and to determine how any such changes relate to insulin sensitivity (S(I)). METHODS: Forty-six volunteers were randomized to a weight maintenance diet (Control), 25% CR, or 12.5% CR plus 12.5% energy deficit from structured aerobic exercise (CR+EX), or a liquid calorie diet (890 kcal/d until 15% reduction in body weight)for six months. Fasting and postprandial plasma samples were obtained at baseline, three, and six months. A targeted mass spectrometry-based platform was used to measure concentrations of individual free fatty acids (FFA), amino acids (AA), and acylcarnitines (AC). S(I) was measured with an intravenous glucose tolerance test. RESULTS: Over three and six months, there were significantly larger differences in fasting-to-postprandial (FPP) concentrations of medium and long chain AC (byproducts of FA oxidation) in the CR relative to Control and a tendency for the same in CR+EX (CR-3 month P = 0.02; CR-6 month P = 0.002; CR+EX-3 month P = 0.09; CR+EX-6 month P = 0.08). After three months of CR, there was a trend towards a larger difference in FPP FFA concentrations (P = 0.07; CR-3 month P = 0.08). Time-varying differences in FPP concentrations of AC and AA were independently related to time-varying S(I) (P<0.05 for both). CONCLUSIONS: Based on changes in intermediates of FA oxidation following a food challenge, CR imparted improvements in metabolic flexibility that correlated with improvements in S(I). TRIAL REGISTRATION: ClinicalTrials.gov NCT00099151. | |
dc.identifier | ||
dc.identifier | PONE-D-11-13098 | |
dc.identifier.eissn | 1932-6203 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Public Library of Science (PLoS) | |
dc.relation.ispartof | PLoS One | |
dc.relation.isversionof | 10.1371/journal.pone.0028190 | |
dc.subject | Adult | |
dc.subject | Amino Acids | |
dc.subject | Caloric Restriction | |
dc.subject | Carnitine | |
dc.subject | Energy Intake | |
dc.subject | Exercise | |
dc.subject | Fasting | |
dc.subject | Fatty Acids, Nonesterified | |
dc.subject | Female | |
dc.subject | Glucose Tolerance Test | |
dc.subject | Humans | |
dc.subject | Insulin Resistance | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Overweight | |
dc.subject | Postprandial Period | |
dc.subject | Principal Component Analysis | |
dc.title | Caloric restriction alters the metabolic response to a mixed-meal: results from a randomized, controlled trial. | |
dc.type | Journal article | |
duke.contributor.orcid | Pieper, Carl F|0000-0003-4809-1725 | |
duke.contributor.orcid | Bain, James R|0000-0002-8917-9187 | |
duke.contributor.orcid | Kraus, Virginia B|0000-0001-8173-8258 | |
duke.contributor.orcid | Kraus, William E|0000-0003-1930-9684 | |
pubs.author-url | ||
pubs.begin-page | e28190 | |
pubs.issue | 4 | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Biochemistry | |
pubs.organisational-group | Biomedical Engineering | |
pubs.organisational-group | Biostatistics & Bioinformatics | |
pubs.organisational-group | Center for the Study of Aging and Human Development | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Duke Molecular Physiology Institute | |
pubs.organisational-group | Global Health Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, Cardiology | |
pubs.organisational-group | Medicine, Endocrinology, Metabolism, and Nutrition | |
pubs.organisational-group | Medicine, Geriatrics | |
pubs.organisational-group | Medicine, Rheumatology and Immunology | |
pubs.organisational-group | Orthopaedics | |
pubs.organisational-group | Pathology | |
pubs.organisational-group | Pharmacology & Cancer Biology | |
pubs.organisational-group | Pratt School of Engineering | |
pubs.organisational-group | Sarah Stedman Nutrition & Metabolism Center | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | School of Nursing | |
pubs.organisational-group | School of Nursing - Secondary Group | |
pubs.organisational-group | University Institutes and Centers | |
pubs.publication-status | Published | |
pubs.volume | 7 |
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