Concurrent evolution of cancer cachexia and heart failure: bilateral effects exist

被引:66
作者
Kazemi-Bajestani, Seyyed M. R. [1 ]
Becher, Harald [2 ]
Fassbender, Konrad [1 ]
Chu, Quincy [3 ]
Baracos, Vickie E. [1 ]
机构
[1] Univ Alberta, Dept Oncol, Div Palliat Care Med, Edmonton, AB, Canada
[2] Univ Alberta, Dept Med, Div Cardiol, Alberta Cardiovasc & Stroke Res Ctr, Edmonton, AB, Canada
[3] Univ Alberta, Cross Canc Inst, Dept Oncol, Div Med Oncol, Edmonton, AB, Canada
关键词
Cancer cachexia; Cardiac atrophy; Cardiac cachexia; NF-KAPPA-B; SKELETAL-MUSCLE UBIQUITIN; OXIDATIVE STRESS; BODY-COMPOSITION; SYSTEMIC INFLAMMATION; CLINICAL-IMPLICATIONS; INSULIN-RESISTANCE; SOLID TUMORS; CARDIOTOXICITY; THERAPY;
D O I
10.1007/s13539-014-0137-y
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Cancer cachexia is defined as a multifactorial syndrome of involuntary weight loss characterized by an ongoing loss of skeletal muscle mass and progressive functional impairment. It is postulated that cardiac dysfunction/atrophy parallels skeletal muscle atrophy in cancer cachexia. Cardiotoxic chemotherapy may additionally result in cardiac dysfunction and heart failure in some cancer patients. Heart failure thus may be a consequence of either ongoing cachexia or chemotherapy-induced cardiotoxicity; at the same time, heart failure can result in cachexia, especially muscle wasting. Therefore, the subsequent heart failure and cardiac cachexia can exacerbate the existing cancer-induced cachexia. We discuss these bilateral effects between cancer cachexia and heart failure in cancer patients. Since cachectic patients are more susceptible to chemotherapy-induced toxicity overall, this may also include increased cardiotoxicity of antineoplastic agents. Patients with cachexia could thus be doubly unfortunate, with cachexia-related cardiac dysfunction/heart failure and increased susceptibility to cardiotoxicity during treatment. Cardiovascular risk factors as well as pre-existing heart failure seem to exacerbate cardiac susceptibility against cachexia and increase the rate of cardiac cachexia. Hence, chemotherapy-induced cardiotoxicity, cardiovascular risk factors, and pre-existing heart failure may accelerate the vicious cycle of cachexia-heart failure. The impact of cancer cachexia on cardiac dysfunction/heart failure in cancer patients has not been thoroughly studied. A combination of serial echocardiography for detection of cachexia-induced cardiac remodeling and computed tomography image analysis for detection of skeletal muscle wasting would appear a practical and non-invasive approach to develop an understanding of cardiac structural/functional alterations that are directly related to cachexia.
引用
收藏
页码:95 / 104
页数:10
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