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Establishing a clinical phenotype for cachexia in end stage kidney disease - study protocol
Joanne Reid1, Helen R Noble2, Gary Adamson3
1School of Nursing and Midwifery, Queen's University Belfast Medical Biology Centre, 97 Lisburn Rd, Belfast, BT9 7BL, UK. j.reid@qub.ac.uk.
Muscle wasting, or cachexia, is common in end-stage kidney disease (ESKD). This study aims to define cachexia in ESKD patients to improve research and treatment for this high-risk population.
Area of Science:
- Nephrology
- Clinical Nutrition
- Chronic Disease Management
Background:
- Muscle wasting (cachexia) is prevalent in end-stage kidney disease (ESKD), affecting up to 75% of dialysis patients.
- ESKD is linked to inflammation and cachexia, characterized by anorexia, lean muscle loss, and altered energy expenditure.
- Existing cachexia definitions for other chronic diseases do not apply to ESKD, hindering research and treatment.
Purpose of the Study:
- To determine the clinical phenotype of cachexia specific to individuals with end-stage kidney disease.
- To establish a precise definition for cachexia in ESKD to standardize research and clinical interventions.
- To improve quality of life and reduce premature mortality associated with cachexia in ESKD patients.
Main Methods:
- A 12-month longitudinal study of adult ESKD patients undergoing hemodialysis in the UK.
- Bi-monthly collection of data on weight, lean muscle mass, muscle strength, fatigue, anorexia, and quality of life.
- Assessment of the degree to which patients exhibit known cachexia characteristics.
Main Results:
- Data collection on patient characteristics and cachexia indicators is ongoing.
- Analysis will identify the specific clinical phenotype of cachexia in the ESKD population.
Conclusions:
- A specific cachexia definition for ESKD is crucial for accurate incidence studies and treatment development.
- This research will provide essential data to inform clinical practice, policy, and education for ESKD patients with cachexia.
- Establishing a standardized definition will facilitate the testing of novel treatment modalities to improve patient outcomes.
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