
Cachexia as a common characteristic in multiple chronic disease
Author(s) -
Scherbakov Nadja,
Doehner Wolfram
Publication year - 2018
Publication title -
journal of cachexia, sarcopenia and muscle
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.803
H-Index - 66
eISSN - 2190-6009
pISSN - 2190-5991
DOI - 10.1002/jcsm.12388
Subject(s) - cachexia , wasting , medicine , cancer , lean body mass , anorexia , disease , adipose tissue , wasting syndrome , gastroenterology , body weight
Cachexia, or body wasting, is a serious complication and frequently occurs at advanced stage of the variety of chronic diseases, including cancer, multiple inflammatory organ-specific disease, and cardiovascular disease. Cachexia affects the life quality and survival of the patients. The prevalence of cachexia depends on the underlying disease and widely ranges between 15 and 90%. Patients with cancer are most commonly affected by cachexia that often occurs as a latestage complication. In cancer, the prevalence of cachexia may vary between 50 and 90% depending on the type of cancer, where a clinical course of gastrointestinal or lung cancers is most frequently associated with the development of cachexia. The multifactorial pathogenesis of cachexia, including anorexia, inflammatory activation, and impaired metabolic turnover of both structural and energy metabolism, lead to a decrease of adipose and lean tissue mass and low muscle strength. The discussion is ongoing whether cachexia in various chronic diseases should be viewed as a common final metabolic pathway regardless of the underlying disease or if it is disease specific, and distinct pathophysiological mechanisms exist in different diseases. A recent retrospective clinical study described different phenotypes of cachexia in patients with advanced pancreatic ductal adenocarcinoma (PDAC) undergoing chemotherapy. The assessment of longitudinal changes of body composition by computed tomography (CT) revealed three phenotypes of body wasting in these patients: patients who lost skeletal muscle and fat tissue, patients who only lost fat tissue, and patients without wasting who had a significantly improved survival. Several other studies investigated patients with different types of gastrointestinal cancer and reported either a loss of muscle tissue or a loss of both skeletal muscle and adipose tissue mass. In addition, loss of cardiac muscle tissue in cancer cachexia (CC) has been shown in clinical and experimental studies. It is known that cachexia is characterized by body wasting that involves all compartments of body tissue (i.e. muscle, adipose, and bone tissues). From all of these compartments, the loss of muscle tissue is considered the key pathophysiological mechanism to explain reduced physical capacity, increased frailty, susceptibility to disease progression, increased hospitalization rate, and, consequently, increased mortality. A major hurdle for the research on loss of muscle tissue, or sarcopenia, is a lack of the reference standard for determination of skeletal muscle mass. A number of clinical diagnostic methods are available ranging from easy applicable, such as bioelectrical impedance analysis (BIA), to highly complex, challenging, and costly techniques, such as magnetic resonance imaging (MRI) or CT. The setting of the research question and specific study design define the appropriate method to be used for the given context. Importantly, apart from the assessment of muscle bulk, functional and metabolic characteristics of the skeletal muscle tissue might have a role in the determination of functional capacity and symptomatic severity of muscle wasting and hence may have an impact on clinical outcome. As previously mentioned, cachexia is usually reported as a complication of chronic diseases, including chronic obstructive pulmonary disease (COPD), rheumatoid arthritis, chronic hepatitis and cirrhosis, diabetes mellitus, chronic kidney disease (CKD), and chronic heart failure (CHF). A hypothesis has been proposed that independent of the individual chronic disease, the wasting process follows a common final metabolic pattern. This metabolic pattern ED ITOR IAL