Prospective Observational Study of Metabolic Myopathy in Cushing's Syndrome or Pheochromocytoma Patients Undergoing Adrenalectomy
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 1
- 试验地点
- 1
- 主要终点
- Change in bio-impedance indices of body composition
研究概览
简要总结
Endocrine diseases including Cushing's syndrome and phaeochromocytoma/paraganglioma (PPGL) but not Conn's syndrome are associated with muscle wasting and weakness. The study's aim is to identify epigenetic determinants of muscle homeostasis in these conditions following medical treatment and adrenalectomy. This is an observational pilot study that will recruit 66 patients from 3 diagnostic groups: Cushing's syndrome (16), PPGL (20) and Conn's syndrome (30). Indices of muscle bulk and strength will be assessed at diagnosis and at outpatient follow-up 6-9 weeks after adrenalectomy. At these times blood and urine will be collected and a muscle biopsy taken from the operation site at the time of surgery. Pathway analysis in these samples will identify potentially novel signalling pathways contributing to muscle wasting via prolonged exposure to high levels of corticosteroid and catecholamines. This will highlight commonalities and differences in pathogenesis of muscle wasting from a variety of different causes. Finally, it will inform identification of novel therapies for muscle atrophy.
详细描述
Muscle wasting and weakness is important because it accounts for a large proportion of the disability associated with disease and normal aging. The annual economic cost in the USA alone has been estimated at $1.8 billion.
The investigators have studied muscle wasting associated with chronic and acute illness, finding a marked dissociation between wasting and disease severity. This indicated that epigenetic and genetic factors may contribute to individual susceptibility to wasting. To analyse factors controlling muscle mass, the investigators have developed a novel clinical model of muscle loss. Hence, in patients undergoing aortic surgery, a large insult is imposed on patients with a background of a disease that leads to muscle wasting (reduced cardiac function). As the timing of the insult is known, the investigators can follow muscle wasting longitudinally. Our recent work using this model has characterised novel muscle signalling pathways that mediate muscle breakdown. Specifically, the investigators found that 50% of patients undergoing cardiac surgery lose significant muscle mass (>10% in the "wasters" group) in the 7 days after uncomplicated surgery, which correlated with loss of strength 7-9 Expression of microRNAs (miRNAs) from imprinted loci (C19MC miRNAs and miR-675) in muscle biopsy samples was strongly associated with subsequent muscle wasting and weakness. Furthermore, expression of these miRNA in myoblasts and animal models confirms their effects on muscle and suggests modes of action through transforming growth factor signalling pathways, ribosome assembly and mitochondrial function. Finally, metabolomic analysis of plasma samples from these patients suggested that exposure to higher levels of active intrinsic corticosteroid, a known cause of sarcopenia, was correlated with muscle loss. Acute muscle wasting (ICU acquired weakness) is associated with high levels of corticosteroids, owing to a defect in deactivation, and shock which is countered with high doses of catecholamines. The investigators will measure miR expression, and longitudinal muscle bulk and strength in patients undergoing adrenalectomy at SBH.
Group 1: Cushing's syndrome caused by very elevated levels of corticosteroids, associated with severe wasting.
Group 2: Phaeochromocytoma and paraganglioma (PPGL) caused by very elevated levels of catecholamines, associated with moderate wasting.
Group 3: Conn's syndrome caused by elevated mineralocorticoid, not associated with muscle wasting (Control group) All patients will be assessed at diagnosis, after medical treatment and after completed reversal of the defect after surgery. Various measures of focal and global strength and function will be recorded alongside measures of muscle bulk. A muscle biopsy from the wound site will be taken at surgery.
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
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Above the age of 18
- •Receiving both medical management and adrenalectomy for treatment of Cushing's syndrome or phaeochromocytoma at St Bartholomew's Hospital (SBH)
排除标准
- •Previous Stroke
- •Neuromuscular disease
- •Disseminated Malignancy
- •Underlying neuromuscular disease
- •Paediatrics
- •Non-consenting adults
结局指标
主要结局
Change in bio-impedance indices of body composition
时间窗: Day 0/ at presentation to 6-9 week follow up.
Indices of body composition will be measured by electrical impedance.
Change in Short Physical Performance Battery (SPPB)
时间窗: Day 0/ at presentation to 6-9 week follow up.
SPPB is a measure of patients' functional status: scores range from 0 (worst performance) to 12 (best performance).
Change in Hand Held Dynamometry strength (grip strength)
时间窗: Day 0/ at presentation to 6-9 week follow up.
Hand-held dynamometry will be assessed in both hands (the maximum of 3 attempts)
Change in rectus femoris pixel intensity
时间窗: Day 0/ at presentation to 6-9 week follow up.
Pixel intensity is a measure of muscle quality measured by B mode ultrasound
Change in Knee straightening dynamometry
时间窗: Day 0/ at presentation to 6-9 week follow up.
The test will be conducted using a Lafayette Manual Muscle Tester. Joint knee moment (torque) and strength will be measured.
Change in Lying and Standing Vital Capacity (FVC - forced vital capacity) ratio
时间窗: Day 0/ at presentation to 6-9 week follow up.
Lying and standing vital capacity will be measured using a hand held spirometer
Change in cross sectional area of the Rectus Femoris (RFcsa)
时间窗: Day 0/ at presentation to 6-9 week follow up.
RFcsa will be calculated using B-mode ultrasound (US) at pre-determined time points
次要结局
- Changes in plasma markers of muscle homeostasis by enzyme-linked immunosorbent assay (ELISA)(Day 0/ at presentation & 6-9 week follow up.)
- Changes in steroid metabolism by mass spectroscopy in blood and urine(Day 0/ at presentation to 6-9 week follow up.)
- Assay in abdominal muscle of markers of muscle atrophy by western blot(Intra-operatively during adrenalectomy)
- Unbiased RNA sequencing and targetted qPCR for micro RNAs(Intra-operatively during adrenalectomy)
- Changes in biomarkers of myolysis in urine(Day 0/ at presentation to 6-9 week follow up.)
- Changes in the metabolome(Day 0/ at presentation to 6-9 week follow up.)
- Changes in circulating micro-RNAs(Day 0/ at presentation to 6-9 week follow up.)
