Agouti-related Peptide (AgRP) and the GH/IGF-1 Axis in Children
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 156
- 主要终点
- Protocol 1: Correlation of Plasma AgRP levels with IGF-1 levels
研究概览
简要总结
Recent data support the existence of a GH-Agouti-related peptide (AgRP) axis. The neuropeptide AgRP promotes food intake and has important effects on energy homeostasis. Recent evidence suggest that GH stimulates AgRP and AgRP may mediate some of GH's important nutritional and metabolic effects. main goals of this project are to characterize, for the first time, plasma levels of AgRP in children and to determine how these relate to GH and IGF-1 levels, age, body composition, clinical and other endocrine parameters. To accomplish this, we will conduct two studies, one being a cross-sectional study that will measure AgRP levels in 140 healthy children ages 5-17 and the second being a prospective study that will measure the change in plasma AgRP levels in response to GH treatment in 16 children who receive this as part of their clinical care for GH deficiency or short stature.
详细描述
Protocol 1 This will be a cross-sectional study in 140 healthy children. Participation will include one visit that will take place between 8-9 am and after a fast from midnight the night before.
Procedures at the visit will include:
- Review of medical history
- Anthropometrics measurements: Weight, height, waist and hip circumferences.
- Collection of information from medical record including growth records and physical examination findings including features relevant to pubertal stage in all children and onset of menses in females.
- Assessment of pubertal status and Tanner stage based on physical examination.
- Collection of information on diet, activity level and sleep.
- Blood Sampling: venous blood will be sampled from a peripheral vein for measurement of AgRP, GH, IGF-1, leptin, SOb-R, triglycerides, insulin, glucose, testosterone(males), estradiol(females), DHEAS and cortisol levels. Insulin and glucose levels will be used to assess insulin resistance by HOMA & QUICKI.
Protocol 2 This will be a prospective study in 16 children who will be studied before and at 4 time points (1 week, 2 weeks, 1 month and 2 months) after starting GH treatment as part of their clinical care. This protocol will study subjects Groups 2 and 3. Growth hormone will not be prescribed as part of this study. Children will be treated clinically with GH as prescribed by their Pediatric Endocrinologist for FDA approved indications and according to standard guidelines for dosing for treatment of GH deficiency in children.
Each visit that will take place between 8-9 am and after a fast from midnight the night before.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 5 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Ambulatory male and female children aged 5-17 years
- •Normal weight at birth
- •Height between the 3rd and 99th percentiles of the mean as per the CDC growth percentiles.
排除标准
- •Genetic defects, chronic illnesses.
- •Current prescription medication use
- •Use of glucocorticoids, thyroid hormone or medications that may affect the GH-IGF-1 axis within 6 months of study entry.
- •Children with GH deficiency:
- •Inclusion Criteria:
- •Ambulatory male and female children aged 5-9 years who are prepubertal
- •Normal weight at birth
- •Growth failure
- •Peak GH response to 2 GH stimulation tests < 10 ng/ml
- •Normal renal and liver function
- •Exclusion criteria:
- •Multiple pituitary hormone deficiencies,
- •GH deficiency or poor growth associated with any acute or chronic medical condition such as renal disease or Turner's syndrome.
- •History of diabetes or malignancy
- •Use of glucocorticoids or medications known to affect the GH-IGF-1 axis within 6 months of study entry.
- •Children with idiopathic Short Stature:
- •Inclusion Criteria:
- •Ambulatory male and female children aged 5-9 years who are prepubertal
- •Normal weight at birth
- •Height >2.25 SD below mean for age
- •Peak GH response to 2 stimulation tests >10 ng/ml or normal IGF-1 and IGFBP-3 levels
- •No prior supplemental growth hormone exposure
- •Normal renal and liver function
- •Exclusion criteria:
- •Poor growth associated with any acute or chronic medical condition such as renal disease or Turner's syndrome.
- •History of diabetes or malignancy
- •Use of glucocorticoids or medications known to affect the GH-IGF-1 axis within 6 months of study entry.
结局指标
主要结局
Protocol 1: Correlation of Plasma AgRP levels with IGF-1 levels
时间窗: Baseline (cross-sectional at single time point, no intervention)
Plasma AgRP levels correlation with IGF-1 levels Protocol 1: Correlation of Plasma AgRP levels with IGF-1 levels
Protocol 2: Change in plasma AgRP levels with GH therapy
时间窗: baseline to 2 months
Change in plasma AgRP levels from pre-GH therapy to post-GH therapy
次要结局
- Protocol 1: Correlation of plasma AgRP levels with age(Baseline (cross-sectional testing at one time point, no intervention))
- Protocol 1: Correlation of plasma AgRP with percent body fat (determined from skinfold thickness)(Baseline (cross-sectional testing at one time point, no intervention))
- Protocol 2: Change in AgRP levels correlation with change in IGF-1 levels(Baseline to 2 months)
- Protocol 2: Change in AgRP level correlation with pre-treatment leptin levels(Baseline to 2 months)
- Protocol 1: Correlation of plasma AgRP levels with leptin levels(Baseline (cross-sectional testing at one time point, no intervention))
研究者
Pamela U. Freda
Professor of Medicine at CUIMC
Columbia University