Pulmonary cachexia, observed in individuals with chronic obstructive pulmonary disease (COPD) is a multifactorial syndrome characterized by disruptions in energy metabolism, increased protein degradation, and an impaired capacity to preserve muscle mass. These metabolic disturbances not only exacerbate the underlying respiratory condition but also significantly contribute to elevated mortality rates among affected individuals. Current therapeutic strategies for managing cachexia primarily emphasize pharmacological treatments, nutritional interventions, and multimodal approaches. Among the nutritional interventions, various supplements have shown potential in mitigating the catabolic processes associated with cachexia. Notably, supplementation with n-3 polyunsaturated fatty acids (n-3 PUFAs) and vitamin D has emerged as a promising intervention, likely due to their involvement in key pathological mechanisms underlying the disease. While previous studies have investigated the combined effects of these supplements through oral nutritional supplementation, this study aims to evaluate and compare the clinical effectiveness of n-3 PUFAs and vitamin D as distinct therapeutic interventions for managing pulmonary cachexia.
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Change in Body Mass Index (BMI)
Timeframe: Baseline and Week 6
Fat-Free Mass Index (FFMI)
Timeframe: Baseline and week 6
Fat Mass Index (FMI)
Timeframe: Baseline and week 6
Handgrip Strength (HGS)
Timeframe: Baseline and week 6
Mid-Arm Muscle Circumference (MAMC)
Timeframe: Baseline and week 6
Simplified Nutritional Appetite Questionnaire (SNAQ) - Anorexia
Timeframe: Baseline and week 6
Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F)
Timeframe: Baseline and week 6
Edmonton Symptom Assessment System (ESAS) - Symptom Burden
Timeframe: Baseline and week 6