医学
肌萎缩
恶病质
结直肠癌
内科学
骨骼肌
背景(考古学)
浪费的
癌症
外科
胃肠病学
肿瘤科
古生物学
生物
作者
Kostan W. Reisinger,Joep P. M. Derikx,Jeroen L.A. van Vugt,M.F. von Meyenfeldt,Karel W. E. Hulsewé,Steven W.M. Olde Damink,Jan H.M.B. Stoot,Martijn Poeze
标识
DOI:10.1016/j.clnu.2015.07.005
摘要
Background & aims Sarcopenia in gastrointestinal cancer has been associated with poor clinical outcome after surgery. The effect of low muscle mass on the inflammatory response to surgery has not been investigated, however skeletal muscle wasting in the context of cachexia is associated with a hyperinflammatory state at baseline. Knowledge on this matter can provide new insight into the detrimental effects of sarcopenia on postoperative recovery, possibly leading to novel therapeutic strategies. The aim of this study was to evaluate whether low muscle mass is associated with increased inflammation after resection of colorectal malignancies. Methods Eighty-seven consecutive patients undergoing elective resection of a primary colorectal tumor were enrolled. Muscle mass was assessed on routine preoperative computed tomography (CT) scans using image analysis by Osirix® by measuring skeletal muscle at the third lumbar vertebra (L3) level. The effect of muscle mass on pre- and postoperative plasma concentrations of C-reactive protein (CRP), calprotectin and interleukin-6 (IL-6) was analyzed. Clinical outcome was assessed by HARM (HospitAl stay, Readmission, and Mortality) scores. Results Skeletal muscle mass was not predictive of plasma concentrations of CRP and IL-6. However, low skeletal muscle mass was significantly predictive of high plasma concentrations of calprotectin on postoperative days (POD) 2 through 5, reaching highest significance on POD4 (regression beta, −6.06; 95% confidence interval, −10.45 to −1.68; p = 0.007). Conclusions Low muscle mass in patients undergoing surgery for colorectal cancer was associated with an increased postoperative inflammatory response. This may be at least part of the explanation for the high incidence of postoperative complications in sarcopenic patients.
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