4.7 Article

Weight stability masks changes in body composition in colorectal cancer: a retrospective cohort study

期刊

AMERICAN JOURNAL OF CLINICAL NUTRITION
卷 113, 期 6, 页码 1482-1489

出版社

OXFORD UNIV PRESS
DOI: 10.1093/ajcn/nqaa440

关键词

cachexia; colorectal neoplasms; obesity; sarcopenia; metabolism; myosteatosis

资金

  1. National Cancer Institute of the NIH [R00-CA218603, K01-CA226155, R01-CA175011, R25-CA203650]
  2. National Institute of General Medical Sciences of the NIH [U54-GM104940]
  3. Douglas Gray Woodruff Chair Fund
  4. Guo Shu Shi Fund, Anonymous Family Fund for Innovations in Colorectal Cancer, Project P Fund
  5. George Stone Family Foundation

向作者/读者索取更多资源

The study suggests that body weight stability may mask clinically meaningful skeletal muscle depletion, while skeletal muscle depletion may independently predict a higher risk of death apart from changes in body weight. Men are more likely to maintain weight stability compared to women, and among weight-stable men, the incidence of sarcopenia and myosteatosis is lower.
Background: There is an emerging viewpoint that change in body weight is not sufficiently sensitive to promptly identify clinically meaningful change in body composition, such as skeletal muscle depletion. Objectives: We aimed to determine whether body weight stability is associated with skeletal muscle depletion and whether skeletal muscle depletion is prognostic of death independently of change in body weight. Methods: This retrospective cohort included 1921 patients with stage I-III colorectal cancer. Computed tomography (CT)-based skeletal muscle characteristics and body weight were measured at diagnosis and after a mean 15.0-mo follow-up. Body weight stability was defined as weight change less than +/- 5% during follow-up. Sarcopenia and myosteatosis were defined using established thresholds for patients with cancer. Multivariable-adjusted logistic and flexible parametric proportional hazards survival models were used to quantify statistical associations. Results: At follow-up, 1026 (53.3%) patients were weight stable. Among patients with weight stability, incident sarcopenia and myosteatosis occurred in 8.5% (95% CI: 6.3%, 10.6%) and 13.5% (95% CI: 11.1%, 15.9%), respectively. Men were more likely to be weight stable than were women (56.7% compared with 49.9%; P = 0.04). Weight-stable men were less likely to develop incident sarcopenia (5.4% compared with 15.4%; P = 0.003) and myosteatosis (9.3% compared with 20.8%; P = 0.001) than weight-stable women. Among all patients, the development of incident sarcopenia (HR: 1.40; 95% CI: 1.02, 1.91) and of myosteatosis (HR: 1.41; 95% CI: 1.05, 1.90) were associated with a higher risk of death, independently of change in body weight. Patient sex did not modify the relation between skeletal muscle depletion and death. Conclusions: Body weight stability masks clinically meaningful skeletal muscle depletion. Body composition quantified using clinically acquired CT images may provide a vital sign to identify patients at increased risk of death. These data may inform the design of future cachexia trials.

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