Role of Cardiometabolic Risk Factors in Childhood Bone Development (Healthy Heart 'N' Bones Study)
试验速览
- 阶段
- 不适用
- 入组人数
- 400
- 试验地点
- 1
- 主要终点
- Bone mineral mass
研究概览
简要总结
The proposed research brings together complementary expertise to systematically elucidate the longitudinal effects of (1) total and regional body fat and (2) the metabolic impairment that accompanies obesity on bone development during growth. The contribution of this research will be significant because it will provide a solid foundation for understanding the influence of fat (total and regional distribution) on overall bone strength, and whether insulin resistance, beta-cell dysfunction, abnormal lipids, and inflammation could be underpinning factors in the fat-bone strength relationship via effects on bone modeling activity. This knowledge will provide critical information needed to maximize potential therapeutic interventions to counter the linked risks of obesity and osteoporosis, both major public health concerns.
详细描述
The overall goal of this study is to clarify the relationship of adiposity with bone development during adolescence, and to explicate the mechanisms that regulate the effect of excess adiposity on bone. In this effort, we will conduct a 2-year longitudinal study in 400 children and adolescents aged 9-15 years. Using the peak adolescent growth period as a model for probing determinants of bone health may allow for a clearer picture of the processes that regulate bone development, as these processes are highly active at this growth stage. Unlike other studies with surrogates for adiposity, we plan to measure total and central adiposity directly, using dual energy X-ray absorptiometry (DXA) and magnetic resonance imaging. Both bone quantity and bone quality, the two principal determinants of bone strength, will be assessed by peripheral quantitative computed tomography (pQCT) at weight-bearing (tibia) and non-weight-bearing (radius) skeletal sites. Peripheral QCT provides 3-dimensional bone measurements that are not confounded by changes in bone size, a significant confounder of most past studies, which have relied on 2-dimensional bone imaging techniques. To identify mechanistic factors, which may explain the effect of adiposity on bone development, we will measure arterial stiffness, endothelial function, and fasting levels of glucose, insulin, lipids, and C-reactive protein (CRP) to assess how vascular dysfunction, insulin resistance, abnormal lipids, and inflammation are related to bone modeling activity, as measured by serum markers of bone formation and resorption. All measurements will be assessed at baseline and after 1 and 2 years of follow-up.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 9 Years 至 15 Years(Child)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Otherwise healthy children and adolescents between 9 and 15 years old
- •Subject and parent/guardian understands the study protocol and agrees to comply with it
- •Informed Consent Form signed by the parent/guardian and assent signed by the subject
排除标准
- •Subjects with (a history of) metabolic or gastrointestinal diseases including hepatic disorders
- •Subjects presenting chronic degenerative and/or inflammatory diseases
- •Subjects receiving systemic treatment or topical treatment likely to interfere with evaluation of the study parameters (salicylates, antibiotics)
- •Subjects receiving corticosteroid treatment
- •Subjects using oral anticoagulants
- •Subjects who have participated in a clinical study more recently than one month before the current study
结局指标
主要结局
Bone mineral mass
时间窗: Change from baseline bone mineral mass at 2 years
Measurement of bone quantity assessed by peripheral quantitative computed tomography
Bone strength-strain index
时间窗: Change from baseline bone strength-strain index at 2 years
Measurement of bone quality assessed by peripheral quantitative computed tomography
次要结局
- Serum N-terminal propeptide of type 1 procollagen (P1NP)(Change from baseline P1NP at 2 years)
- Serum C-terminal telopeptide of type 1 collagen (CTX)(Change from baseline CTX at 2 years)
研究者
Norman Pollock
Associate Professor, Department of Medicine
Augusta University
