Effects of 2wk fructose & HFCS consumption on lipid dysregulation & insulin resis
Effects of 2wk fructose & HFCS consumption on lipid dysregulation & insulin resis
批准号:
7920510
负责人:
PETER J HAVEL
金额:
$3.15万
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:
2008-03-15 至 2013-02-28
关键词:
AdultAge-YearsAnimalsBlindedBloodCarbohydratesCardiovascular DiseasesCenter for Translational Science ActivitiesCholesterolClinicalClinical ResearchCollectionComplexConsumptionDataDepositionDevelopmentDiabetes MellitusDietDoseEpidemicFood SupplyFructoseFundingGlucoseGlucose IntoleranceHepaticHome environmentHormonesHourHumanIncidenceInflammationInsulinInsulin ResistanceIntakeInterventionIntervention StudiesInvestigationLaboratoriesLeadLipidsLipoproteinsLiverMagnetic Resonance ImagingMeasurementMeasuresMediatingMetabolicMetabolic syndromeMetabolismObesityOverweightParticipantPersonsPhasePopulationProceduresPublic HealthSweetening AgentsTestingTimeTriglyceridesWeightWomandesigndrinkingglucose disposalglucose toleranceheart disease riskindexinginsulin sensitivitymenoral glucose toleranceprospectiveresponsesugarsweetened beverage
中文摘要
描述(由申请人提供):我们正在进行一项正在进行的研究,比较在老年(40岁以上)、超重/肥胖(BMI: 25-35 kg/m2)成年人中,以25%的能量消耗10周果糖或葡萄糖对脂质参数和胰岛素抵抗和炎症指标的影响。本研究目前的结果提供证据表明,摄入果糖会在2周内促进致动脉粥样硬化的脂质谱和葡萄糖耐受不良/胰岛素抵抗的发展,而摄入葡萄糖则不会。因此,高果糖饮食可能会导致代谢综合征和心血管疾病的发生。我们建议通过追求以下具体目标来扩大我们的研究:1:确定在年轻、正常体重和超重/肥胖成年人(18-40岁)中产生脂质失调和胰岛素抵抗所需的膳食果糖量。我们建议进行一项剂量反应研究,在该研究中,受试者自行选择,随意饮食2周,补充10%,17.5%或25%的能量需求作为果糖加糖饮料。2:比较在正常体重和超重/肥胖成年人(18-40岁)中,两周自行选择的随意饮食中含有10%、17.5%或25%的能量需求的高果糖玉米糖浆(HFCS)甜饮料的影响与果糖引起的影响。我们有初步的数据表明,尽管含果糖的饮料比纯果糖少45%,但以25%的能量需求消耗含hfcs的饮料,餐后甘油三酯的增加程度与消耗25%的能量的纯果糖相同。因此,我们假设HFCS与单独的果糖相比会促进动脉粥样硬化性脂质谱的发展。3:验证果糖和高果糖玉米糖浆会导致异位肝甘油三酯积累和胰岛素抵抗增加的假设。我们提出果糖消耗导致的胰岛素抵抗的诱导是通过果糖诱导的脂质失调和肝脏异位脂质沉积增加的机制介导的,而不是通过肝脏果糖代谢更直接的作用机制。该研究被设计为一项前瞻性、盲法饮食干预研究,包括3天的复杂碳水化合物饮食基线期和2周的饮食干预期,在此期间,参与者在用餐时饮用含果糖或含氢氟烃类化合物的饮料(提供10%、17.5%或25%的能量)。在干预期间,受试者住在家中,并提供含果糖或hfcs的饮料,与自行选择的随意(通常)饮食一起饮用。在加州大学戴维斯分校临床与转化科学中心临床研究中心,在基线期间和干预第1周和第2周结束时,进行4小时口服葡萄糖耐量和氘化葡萄糖处理试验,通过MRI测量肝脏甘油三酯积累,以及24小时采血。项目简介:我们实验室最近的研究结果表明,连续两周每餐饮用含果糖的饮料(含热量需求的25%)会导致40岁以上超重和肥胖男性和女性血液中胆固醇和甘油三酯水平升高,胰岛素抵抗增加。这些变化与患心脏病和糖尿病的风险增加有关,而且由于1977年至2001年间,含果糖的含糖饮料的消费量增加了一倍多,因此这些发现具有重要的公共卫生意义。建议的研究需要确定饮用含果糖和高果糖玉米糖浆的饮料对年轻、正常体重和超重成年人的影响,并确定产生这些不良影响所需的果糖摄入量,以便确定糖的安全摄入量。
英文摘要
DESCRIPTION (provided by applicant): We are conducting an ongoing study comparing the effects of 10 weeks of fructose or glucose consumption at 25 percent of energy requirements on lipid parameters and indices of insulin resistance and inflammation in older (+40 years), overweight/obese (BMI: 25-35 kg/m2) adults. Current results from this study provide evidence that consumption of fructose promotes the development of an atherogenic lipid profile and glucose intolerance/insulin resistance within 2 weeks, while glucose consumption does not. Thus, it is likely that diets high in fructose could contribute to the development of metabolic syndrome and cardiovascular disease. We propose to expand our investigation by pursuing the following Specific Aims: 1: Determine the amount of dietary fructose required to produce lipid dysregulation and insulin resistance in younger, normal weight and overweight/obese adults (18-40 years). We propose to conduct a dose-response study in which subjects consume self-selected, ad libitum diets for 2 weeks supplemented with 10, 17.5 or 25 percent of energy requirements as fructose-sweetened beverages. 2: Compare the effects of consuming two weeks self-selected ad libitum diets containing 10, 17.5 or 25 percent of energy requirements as high fructose corn syrup (HFCS)-sweetened beverages to the effects induced by fructose in normal weight and overweight/obese adults (18-40 years). We have preliminary data demonstrating that consumption of HFCS-sweetened beverages at 25 percent of energy requirements, despite containing 45 percent less fructose than pure fructose, increases postprandial triglycerides to the same degree as consuming 25 percent energy as pure fructose. Therefore, we hypothesize that HFCS will promote the development of an atherogenic lipid profile comparably to fructose alone. 3: Test the hypothesis that fructose and HFCS will cause comparable increases in ectopic hepatic triglyceride accumulation and insulin resistance. We propose that induction of insulin resistance resulting from fructose consumption is mediated through a mechanism that involves fructose-induced lipid dysregulation and increased ectopic lipid deposition in the liver, rather than a mechanism involving more direct effects of hepatic fructose metabolism. The study is designed as a prospective, blinded diet intervention study, with a 3-day baseline period on a complex carbohydrate diet and a 2-week diet intervention phase, during which the participants consume either fructose- or HFCS-sweetened beverages (providing 10 percent, 17.5 percent or 25 percent of energy) with meal. During the intervention, the subjects reside at home and are provided with fructose- or HFCS-sweetened beverages that are consumed along with a self-selected ad libitum (usual) diet. Procedures, which include 4-hour oral glucose tolerance and deuterated glucose disposal tests, measurement of hepatic triglyceride accumulation by MRI, and 24-hour blood collections are performed during the baseline period and at the end of Intervention Weeks 1 and 2 at the UC Davis Clinical & Translational Science Center Clinical Research Center. Project Narrative: Recent results from our laboratory indicate that drinking beverages sweetened with fructose at 25 percent of caloric requirements at each meal for 2 weeks causes increased cholesterol and triglyceride levels in the blood and increased insulin resistance in overweight and obese men and women over 40 years old. These changes are associated with an increased risk for heart disease and diabetes, and since consumption of sugar-sweetened beverages containing fructose has more than doubled between 1977 and 2001, these findings have important public health implications. The proposed studies are needed to determine the effects of drinking beverages sweetened with fructose and high fructose corn syrup in younger, normal weight and overweight adults, and to determine the amount of fructose intake that is required to produce these undesirable effects so that safe levels of sugar consumption can be established.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Adverse metabolic effects of dietary sugar _ Ad libitum vs energy-balanced diets
-
批准号:9067515
-
项目类别:
-
资助金额:$83.3万
-
财政年份:2014
-
负责人:PETER J HAVEL
-
依托单位:
Adverse Metabolic Effects of Dietary Sugar _ Ad Libitum vs Energy-Balanced Diets
-
批准号:9102557
-
项目类别:
-
资助金额:$6.58万
-
财政年份:2014
-
负责人:PETER J HAVEL
-
依托单位:
Adverse metabolic effects of dietary sugar _ Ad libitum vs energy-balanced diets
-
批准号:8916824
-
项目类别:
-
资助金额:$73.51万
-
财政年份:2014
-
负责人:PETER J HAVEL
-
依托单位:
Adverse metabolic effects of dietary sugar: Ad libitum vs energy-balanced diets
-
批准号:9283193
-
项目类别:
-
资助金额:$3.05万
-
财政年份:2014
-
负责人:PETER J HAVEL
-
依托单位:
Adverse metabolic effects of dietary sugar _ Ad libitum vs energy-balanced diets
-
批准号:8613141
-
项目类别:
-
资助金额:$74.34万
-
财政年份:2014
-
负责人:PETER J HAVEL
-
依托单位:
MAINTENANCE AND MONITORING OF RHESUS MONKEYS WITH TYPE-2 DIABETES
-
批准号:8357303
-
项目类别:
-
资助金额:$7.56万
-
财政年份:2011
-
负责人:PETER J HAVEL
-
依托单位:
Fatty acid sources of fructose and HFCS-induced postprandial hypertriglyceridemia
-
批准号:8487437
-
项目类别:
-
资助金额:$36.02万
-
财政年份:2011
-
负责人:PETER J HAVEL
-
依托单位:
EFF OF FISH OIL AND ALPHA-LIPOIC ACID ON THE PROGR OF INSULIN RESIST
-
批准号:8357277
-
项目类别:
-
资助金额:$7.56万
-
财政年份:2011
-
负责人:PETER J HAVEL
-
依托单位:
Fatty acid sources of fructose and HFCS-induced postprandial hypertriglyceridemia
-
批准号:8680329
-
项目类别:
-
资助金额:$35.56万
-
财政年份:2011
-
负责人:PETER J HAVEL
-
依托单位:
Fatty acid sources of fructose and HFCS-induced postprandial hypertriglyceridemia
-
批准号:8215574
-
项目类别:
-
资助金额:$37.99万
-
财政年份:2011
-
负责人:PETER J HAVEL
-
依托单位:
Fatty acid sources of fructose and HFCS-induced postprandial hypertriglyceridemia
-
批准号:8321550
-
项目类别:
-
资助金额:$37.86万
-
财政年份:2011
-
负责人:PETER J HAVEL
-
依托单位:
EFFECTS OF FISH OIL AND ALPHA-LIPOIC ACID ON THE PROGR OF INSUL RESIST
-
批准号:8172550
-
项目类别:
-
资助金额:$11.41万
-
财政年份:2010
-
负责人:PETER J HAVEL
-
依托单位:
MAINTENANCE AND MONITORING OF RHESUS MONKEYS WITH TYPE-2 DIABETES
-
批准号:8172580
-
项目类别:
-
资助金额:$11.41万
-
财政年份:2010
-
负责人:PETER J HAVEL
-
依托单位:
EFFECT OF CHROMIUM ON PROGRESSION OF INSULIN RESISTANCE
-
批准号:7959019
-
项目类别:
-
资助金额:$10.67万
-
财政年份:2009
-
负责人:PETER J HAVEL
-
依托单位:
EFFECTS OF FISH OIL AND ALPHA-LIPOIC ACID ON THE PROGR OF INSUL RESIST
-
批准号:7959044
-
项目类别:
-
资助金额:$10.67万
-
财政年份:2009
-
负责人:PETER J HAVEL
-
依托单位:
MAINTENANCE AND MONITORING OF RHESUS MONKEYS WITH TYPE-2 DIABETES
-
批准号:7959082
-
项目类别:
-
资助金额:$10.67万
-
财政年份:2009
-
负责人:PETER J HAVEL
-
依托单位:
Effects of 2wk fructose & HFCS consumption on lipid dysregulation & insulin resis
-
批准号:7582425
-
项目类别:
-
资助金额:$38.0万
-
财政年份:2008
-
负责人:PETER J HAVEL
-
依托单位:
EFFECTS OF FISH OIL AND ALPHA-LIPOIC ACID ON THE PROGR OF INSUL RESIST
-
批准号:7715638
-
项目类别:
-
资助金额:$8.13万
-
财政年份:2008
-
负责人:PETER J HAVEL
-
依托单位:
Effects of 2wk fructose & HFCS consumption on lipid dysregulation & insulin resis
-
批准号:7787050
-
项目类别:
-
资助金额:$41.0万
-
财政年份:2008
-
负责人:PETER J HAVEL
-
依托单位:
Effects of 2wk fructose & HFCS consumption on lipid dysregulation & insulin resis
-
批准号:8036082
-
项目类别:
-
资助金额:$38.0万
-
财政年份:2008
-
负责人:PETER J HAVEL
-
依托单位:
海外基金