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numbers recruited to show adequate association but not primary outcome
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| Name | Class |
|---|---|
| Medical Research Council | OTHER_GOV |
| Royal Brompton & Harefield NHS Foundation Trust | OTHER |
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Pulmonary arterial hypertension (PAH) is a disease that causes raised blood pressure in blood vessels that pick up oxygen from the lungs. It has a life expectancy similar to some cancers. There is treatment available but there is no cure. We now know that PAH is associated with weakness in the muscles in the legs, which contributes to the symptoms patients' experience. Researchers believe that certain proteins found in high levels in the blood of patients with other chronic diseases can affect muscle function and growth. One of these proteins is called growth differentiating factor (GDF) 8, high levels of which are associated with muscle weakness in chronic obstructive pulmonary disease(COPD) and heart failure (HF). Interestingly there are drugs available which block the actions of GDF-8 on muscle cells which has been shown in animals to result in increased muscle size. A related protein called GDF-15 is found in elevated levels in patients PAH, and is linked to prognosis. Our preliminary data suggests that GDF-15 can also directly influence muscle size in a number of situations. We aim to investigate the role of GDF-15 and related molecules in the development of muscle weakness in patients with PAH. We will do this by measuring certain markers of muscle weakness and taking blood and muscle samples in patients and controls. We will then compare the levels of GDF-15 in these tissues in those with and without muscle wasting. We hope this work will lead to a greater understanding of the role of GDF-15 in the development of muscle weakness in patients with PAH. GDF-15 levels may be important in allowing us to define which patients have muscle weakness. In the future we aim to perform a clinical trial of drugs which block the actions of GDF-15.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PH with wasting | This group of patients with idiopathic pulmonary arterial hypertension exhibit quadriceps wasting | ||
| PH no wasting | This groups of patients with idiopathic pulmonary arterial hypertension exhibit no evidence of muscle wasting | ||
| Controls | This group of volunteers does not have pulmonary arterial hypertension and would not be expected to have muscle wasting |
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| Measure | Description | Time Frame |
|---|---|---|
| Plasma growth and differentiation factor 15 levels in participants with and without muscle wasting | Muscle wasting will be defined by quadriceps cross sectional area measured by ultrasound | 30 months |
| Measure | Description | Time Frame |
|---|---|---|
| Correlation of plasma Growth and differentiation factor 15 levels with muscle strength | Muscle strength will be measured by quadriceps maximal volitional capacity percent predicted | 30 months |
| Change in fibre type in muscle biopsy |
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Inclusion Criteria:
Exclusion Criteria:
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Clinics at Royal Brompton and Hammersmith hospital
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| Name | Affiliation | Role |
|---|---|---|
| Stephen J Wort, MBBS | Imperial College / Royal Brompton Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Royal Brompton Hospital | London | SW36NP | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 30554141 | Derived | Garfield BE, Crosby A, Shao D, Yang P, Read C, Sawiak S, Moore S, Parfitt L, Harries C, Rice M, Paul R, Ormiston ML, Morrell NW, Polkey MI, Wort SJ, Kemp PR. Growth/differentiation factor 15 causes TGFbeta-activated kinase 1-dependent muscle atrophy in pulmonary arterial hypertension. Thorax. 2019 Feb;74(2):164-176. doi: 10.1136/thoraxjnl-2017-211440. Epub 2018 Dec 15. |
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| ID | Term |
|---|---|
| D018908 | Muscle Weakness |
| D000081029 | Pulmonary Arterial Hypertension |
| D003966 | Camurati-Engelmann Syndrome |
| ID | Term |
|---|---|
| D009135 | Muscular Diseases |
| D009140 | Musculoskeletal Diseases |
| D020879 | Neuromuscular Manifestations |
| D009461 | Neurologic Manifestations |
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Muscle biopsy and blood specimens will be retained by Imperial College and are subject to thier restrictions ad regulations
| 30 months |
| GDF-15 levels in biopsy specimens | 30 months |
| Correlation of plasma Growth and differentiation factor 15 levels with brain natriuretic protein levels | 30 months |
| Correlation of plasma Growth and differentiation factor 15 levels with fat free mass index | Fat free mass index will be measured by bioelectrical impedence | 30 months |
| Correlation of plasma Growth and differentiation factor 15 levels with quality of life | Quality of life will be measured by St. George's respiratory questionnaire | 30 months |
| Correlation of plasma Growth and differentiation factor 15 levels with exercise tolerance | Exercise tolerance will be measured by six minute walk test | 30 months |
| Correlation of plasma Growth and differentiation factor levels 15 with physical activity levels | Physical activity will be measured by Sensewear armband | 30 months |
| Correlation of plasma Growth and differentiation factor levels 15 with echocardiographic measures of severity of pulmonary hypertension | 30 months |
| Correlation of GDF-15 levels in biopsy specimens with muscle wasting and weakness | Wasting will be measured by quadriceps cross sectional area and weakness will be defined by quadriceps maximal volitional capacity | 30 months |
| Determine the contribution of atrophy and autophagy to muscle wasting in PAH | Muscle biopsy specimens will be evaluated using microscopy and real time polymerase chain reaction | 30 months |
| Determine the contribution of SMAD and non-SMAD signalling pathways to the development of muscle weakness and wasting in PAH | Phosphorylation of SMAD and non-SMAD signalling will be determined by western blot | 30 months |
| D009422 | Nervous System Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D012816 | Signs and Symptoms |
| D006976 | Hypertension, Pulmonary |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D010009 | Osteochondrodysplasias |
| D001848 | Bone Diseases, Developmental |
| D001847 | Bone Diseases |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |