Physical Activity Following Surgery-Induced Weight Loss
Physical Activity Following Surgery-Induced Weight Loss
批准号:
7878282
负责人:
Bret H Goodpaster
金额:
$6.0万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-03-01 至 2011-08-31
关键词:
AbdomenAddressAdipose tissueBariatricsBody CompositionBody Weight decreasedCaloric RestrictionCardiovascular DiseasesCeramidesCharacteristicsDataDevelopmentExerciseFatty AcidsFatty acid glycerol estersFunctional disorderHealthIndividualInsulinInsulin ResistanceIntervention TrialLife StyleLinkLipidsMeasuresMetabolicMetabolic syndromeMitochondriaMorbidity - disease rateMuscleNon-Insulin-Dependent Diabetes MellitusObesityOperative Surgical ProceduresOutcomePatientsPhysical activityPopulations at RiskPreventionRandomizedRegulationResearchRiskRisk FactorsRoleSkeletal MuscleStimulusTriglyceridesWeightWeight maintenance regimenabdominal fatabstractingbariatric surgerycardiovascular disorder riskeffective therapyexperiencefatty acid metabolismfatty acid oxidationimprovedinsulin sensitivitymoderate obesitymortalitynoveloxidationpreventsedentary
中文摘要
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英文摘要
ABSTRACT
Obesity and physical inactivity are both related to increased mortality and morbidity in
conjunction with increased risk for the development of type 2 diabetes, the metabolic
syndrome and cardiovascular disease. We propose to examine if physical activity will
provide an additive effect of reducing risk factors for CVD in an extremely at risk
population (very obese individuals) following bariatric weight loss surgery.
Preliminary data from each of our research groups has indicated that an inefficient use
of fatty acids and diminished oxidative capacity is strongly associated with the
pathophysiology of insulin resistance of obesity. Thus impaired fatty acid utilization and
insulin resistance are both characteristic of the metabolic inflexibility in obesity. The
prevailing paradigm is that ¿mitochondrial dysfunction¿ underpins metabolic inflexibility
and thus directly contributes to the pathophysiology of skeletal muscle insulin resistance.
While this hypothesis is attractive, it has not been experimentally proven. Although
weight loss itself can improve insulin resistance, it does little, if anything to improve
mitochondria function or to promote more efficient utilization of fatty acids in obesity.
Moreover, physical activity may promote positive effects on mitochondria function, fatty
acid metabolism and insulin resistance independent of weight loss.
We propose to employ a randomized controlled physical activity intervention trial in a
group of patients following their weight loss surgery. Our primary hypotheses are that
the combination of weight loss + physical activity will provide additive (and thus
independent) positive effects on: 1) weight loss and body composition; 2) metabolic risk
factors such as insulin action and other markers of the metabolic syndrome; and 3)
markers of mitochondria function and the capacity for efficient fat utilization by muscle.
These findings will be novel and relevant to treating obesity, as morbidly obese
individuals are likely genetically and environmentally predisposed towards a negative
metabolic status and a sedentary lifestyle; it is not evident if physical activity can provide
an additional positive stimulus to dramatic weight loss in these patients.
Investigating the role of increased physical activity following surgery-induced weight loss
is critical to our understanding of the most effective strategies to treat obesity and its
associated conditions. Information emanating from this study would thus help to
determine the most effective treatments to prevent weight regain and to improve
outcomes of these patients following surgery. PROJECT NARRATIVE
Obesity and physical inactivity are both related to increased mortality and morbidity in
conjunction with increased risk for the development of type 2 diabetes, the metabolic
syndrome and cardiovascular disease. We propose to examine if physical activity will
provide an additive effect of reducing risk factors for CVD in an extremely at risk
population (very obese individuals) following bariatric weight loss surgery.
Preliminary data from each of our research groups has indicated that an inefficient use
of fatty acids and diminished oxidative capacity is strongly associated with the
pathophysiology of insulin resistance of obesity. Thus impaired fatty acid utilization and
insulin resistance are both characteristic of the metabolic inflexibility in obesity. The
prevailing paradigm is that ¿mitochondrial dysfunction¿ underpins metabolic inflexibility
and thus directly contributes to the pathophysiology of skeletal muscle insulin resistance.
While this hypothesis is attractive, it has not been experimentally proven. Although
weight loss itself can improve insulin resistance, it does little, if anything to improve
mitochondria function or to promote more efficient utilization of fatty acids in obesity.
Moreover, physical activity may promote positive effects on mitochondria function, fatty
acid metabolism and insulin resistance independent of weight loss.
We propose to employ a randomized controlled physical activity intervention trial in a
group of patients following their weight loss surgery. Our primary hypotheses are that
the combination of weight loss + physical activity will provide additive (and thus
independent) positive effects on: 1) weight loss and body composition; 2) metabolic risk
factors such as insulin action and other markers of the metabolic syndrome; and 3)
markers of mitochondria function and the capacity for efficient fat utilization by muscle.
These findings will be novel and relevant to treating obesity, as morbidly obese
individuals are likely genetically and environmentally predisposed towards a negative
metabolic status and a sedentary lifestyle; it is not evident if physical activity can provide
an additional positive stimulus to dramatic weight loss in these patients.
Investigating the role of increased physical activity following surgery-induced weight loss
is critical to our understanding of the most effective strategies to treat obesity and its
associated conditions. Information emanating from this study would thus help to
determine the most effective treatments to prevent weight regain and to improve
outcomes of these patients following surgery.
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Physical Activity Following Surgery-Induced Weight Loss
-
批准号:7574455
-
项目类别:
-
资助金额:$57.0万
-
财政年份:2008
-
负责人:Bret H Goodpaster
-
依托单位:
Physical Activity Following Surgery-Induced Weight Loss
-
批准号:8018185
-
项目类别:
-
资助金额:$57.52万
-
财政年份:2008
-
负责人:Bret H Goodpaster
-
依托单位:
Physical Activity Following Surgery-Induced Weight Loss
-
批准号:8210988
-
项目类别:
-
资助金额:$57.51万
-
财政年份:2008
-
负责人:Bret H Goodpaster
-
依托单位:
SKELETAL MUSCLE LIPID INSULIN RESISTANCE: EFFECTS PHYSICAL ACTIVITY/WEIGHT LOSS
-
批准号:7201130
-
项目类别:
-
资助金额:$2.23万
-
财政年份:2005
-
负责人:Bret H Goodpaster
-
依托单位:
MUSCLE LIPID AND INSULIN RESISTANCE IN THE ELDERLY
-
批准号:7201129
-
项目类别:
-
资助金额:$1.03万
-
财政年份:2005
-
负责人:Bret H Goodpaster
-
依托单位:
EFFECTS EXERCISE TRAINING/DIETARY SUPP ON FAT METAB/BODY COMP IN OBESE WOMEN
-
批准号:7201114
-
项目类别:
-
资助金额:$2.96万
-
财政年份:2005
-
负责人:Bret H Goodpaster
-
依托单位:
MRI to Quantify Skeletal Muscle Lipid Content
-
批准号:6974674
-
项目类别:
-
资助金额:$0.05万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Aerobic vs. Resistance Exercise on Insulin Sensitivity
-
批准号:6974705
-
项目类别:
-
资助金额:$1.58万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle lipid and Insulin Resistance in Aging
-
批准号:8526303
-
项目类别:
-
资助金额:$61.54万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle Lipid and Insulin Resistance in Aging
-
批准号:7248606
-
项目类别:
-
资助金额:$30.78万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle Lipid and Insulin Resistance in Aging
-
批准号:7086147
-
项目类别:
-
资助金额:$31.7万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle lipid and Insulin Resistance in Aging
-
批准号:8732586
-
项目类别:
-
资助金额:$64.56万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle Lipid and Insulin Resistance in Aging
-
批准号:6931526
-
项目类别:
-
资助金额:$32.47万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle lipid and Insulin Resistance in Aging
-
批准号:8336930
-
项目类别:
-
资助金额:$55.7万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Changes in Physical Fitness/Body Comp/Energy Balance
-
批准号:6974717
-
项目类别:
-
资助金额:$0.05万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Resistance and Aerobic Training in Fat Metabolism
-
批准号:6974707
-
项目类别:
-
资助金额:$0.86万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle Lipid and Insulin Resistance in Aging
-
批准号:6821231
-
项目类别:
-
资助金额:$32.09万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Skeletal Muscle lipid and Insulin Resistance in Aging
-
批准号:8245288
-
项目类别:
-
资助金额:$50.09万
-
财政年份:2004
-
负责人:Bret H Goodpaster
-
依托单位:
Effects of Training on Fat Metabolism in Obese Women
-
批准号:7041318
-
项目类别:
-
资助金额:$0.25万
-
财政年份:2003
-
负责人:Bret H Goodpaster
-
依托单位:
Effects of Aerobic & Resistance Exercise on Insulin Sensitivity in Older M/F
-
批准号:7041317
-
项目类别:
-
资助金额:$0.27万
-
财政年份:2003
-
负责人:Bret H Goodpaster
-
依托单位:
海外基金