A Prospective, Cross-Sectional, Case-Control, Molecular Study of Health Assessment and Risk in Ethnic Groups
试验速览
- 阶段
- 不适用
- 入组人数
- 120
- 试验地点
- 1
研究概览
简要总结
The purpose of this study is to directly compare the body composition, body fat distribution, and morphological and functional features of adipose tissue and skeletal muscle between South Asians and European Caucasians.
详细描述
Excess body fat, the hallmark of obesity is a major risk factor for the development of insulin resistance (decreased insulin sensitivity), type 2 diabetes, and cardiovascular disease. Previous studies have shown that South Asians (people who originate from the Indian subcontinent) appear particularly prone to develop diabetes and heart disease compared to white Caucasians of European origin. In Canada, in the Study of Health Assessment and Risk in Ethnic groups (SHARE), it was observed that in a random selection of South Asian and European individuals, South Asians had twice as much type 2 diabetes and cardiovascular disease and were significantly more insulin resistant than Europeans despite a similar body mass index (BMI) and waist circumference. It is possible that the increased propensity of South Asians to develop insulin resistance, type 2 diabetes, and cardiovascular disease is related to greater total body fat and/or increased visceral fat in addition to the possible biological differences in adipose tissue and skeletal muscle tissues. The primary objective of this study is therefore to determine differences among age, sex, and BMI-matched people of South Asian and European Caucasian descent in body composition (specifically total body fat, lean body mass) and fat distribution (where the fat is stored in the body). This study will therefore test the hypothesis that for a similar BMI, South Asians have more total body fat and less lean body mass than age and sex-matched European Caucasians. The secondary objectives of this study are to look at the differences in the two ethnic groups at a biological level, including: differences in visceral fat, adipose tissue morphology, imflammation and adipokine production, skeletal muscle fat content, fatty acid oxidation and mitochondrial activity.
研究设计
- 研究类型
- Observational
- 观察模型
- Defined Population
- 时间视角
- Other
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Written informed consent
- •Between 18-50 years of age
- •Fits into one of the following BMI-Strata:
- •Stratum 1: BMI 18.5 - 25 kg/m2
- •Stratum 2: BMI 25.1 -29.9 kg/m2
- •Stratum 3: BMI 30 -45 kg/m2
- •Ability and willingness to complete dietary and activity diaries and questionnaires
排除标准
- •Concurrent antidiabetic, antithypertensive, antiobesity or lipid-lowering medication
- •Use of systemic glucocorticosteroids (topical and inhaled corticosteroids are acceptable)
- •If the participant has any one or more of the following medical disorders:
- •Known Diabetes
- •Known renal impairment
- •Known uncontrolled endocrine disorder (e.g. hyperthyroidism, Cushing's syndrome, acromegaly, etc.)
- •Recent (less than three months) major surgery or hopitalization for severe illness
- •History of active malignancy, chronic inflammatory disorder, or chronic infections which would interfere with the protocol completion
- •Any other medical, social or geographic condition, which in the opinion of the investigator would not allow safe or reliable completion of the protocol
- •Anticoagulant therapy (e.g. Coumadin)
- •Orthopaedic contraindication to exercise test
- •Significant fluctuations in weight over past 3 months (e.g. >10%)
- •Extreme weight loss diets (e.g. Atkins, Bernstein)
- •History of drug or alcohol dependency within six months prior to signing the informed consent form
- •If the participant has any contraindications to MRI:
- •If the participant is clautrophobic or suffers from fear of closed spaces
- •If participant has had significant contact with metal (e.g. welding)
- •If participant has foreign body in their eye as confirmed by X-ray of the orbits
- •Body Mass Index > 45 kg/m2
- •Participant has had hip or joint replacement surgery 6-8 weeks prior to start of study
- •If participant has:
- •Cardiac pacemaker
- •Artificial cardiac valve
- •Aneurysm clip
- •Neurostimulator
- •Other implanted devices or metal objects in their body