| Literature DB >> 27800156 |
Kimberly L Mei1, John A Batsis2, Jeannine B Mills3, Stefan D Holubar4.
Abstract
Sarcopenia, or loss of skeletal muscle mass and quality, has been studied as part of aging and adverse health outcomes in elderly patients but has only recently been evaluated as a separate condition in cancer patients and important indicator of adverse outcomes. Currently, its definition and method of assessment are still being debated. Sarcopenia within an increasingly obese population has led to a subgroup with sarcopenic obesity, at even higher risk of adverse outcomes. Yet, sarcopenia often goes undiagnosed in these patients, hidden beneath higher body mass index. Identifying sarcopenic and sarcopenic obese subpopulations would allow for more effective treatment plans and potential avoidance of suboptimal outcomes, as well as the chance to intervene and combat these modifiable risk factors. This review will examine available literature on the definition and methods of evaluating sarcopenia and sarcopenic obesity, summarize the effectiveness of sarcopenia and sarcopenic obesity as predictors of outcomes after gastrointestinal cancer surgery, including colorectal cancer resection, liver resection, and pancreatic resection, and outline strategies to minimize the impact of sarcopenia. It is clear that untreated sarcopenia and sarcopenic obesity can be associated with suboptimal post-operative outcomes, especially infections and disease-free or overall survival.Entities:
Keywords: Body composition; Colorectal cancer; Hepatectomy; Malnutrition; Obesity; Oncologic; Pancreatic cancer; Sarcopenia; Surgery; Surgical oncology
Year: 2016 PMID: 27800156 PMCID: PMC5080704 DOI: 10.1186/s13741-016-0052-1
Source DB: PubMed Journal: Perioper Med (Lond) ISSN: 2047-0525
Definitions and cutoffs for sarcopenia and sarcopenic obesity assessment
| Sarcopenia definition | Study | Functional component of definition | Body composition analysis method | Muscle mass definition | Pros | Cons | Obesity definition | Pros | Cons |
|---|---|---|---|---|---|---|---|---|---|
| ASM index >2 SDs below sex-specific means of Rosetta study reference data (Gallagher et al. | Baumgartner (Baumgartner et al. | – | DXA | ASM/m2 (Heymsfield et al. | – | No functional component | % body fat | Measures have been experimentally validated in comparison with BMI (Gallagher et al. | – |
| Low gait speed or low handgrip strength with low muscle mass | Cruz-Jentoft (Cruz-Jentoft et al. | Gait speed ≤0.8 m/s or >0.8 m/s with handgrip strength below sex-specific cutoffs | – | – | Contains functional component, capturing more of sarcopenia due to poor muscle quality/fat infiltration | – | – | – | – |
| Low gait speed or inability to rise from chair with low handgrip strength and body mass-adjusted ASM below sex-specific cutoffs | Studenski (Studenski et al. | Gait speed ≤0.8 m/s or inability to rise from a chair with handgrip strength below sex-specific cutoffs (men <26 kg, women <16 kg) | DXA | ASM/BMI | Contains functional component, capturing more of sarcopenia due to poor muscle quality/fat infiltration | – | BMI | Most common and widely available measure, easy to evaluate | Inaccurate, fluctuates with changes in both muscle and fat |
| L3mi below sex-specific cutoffs associated with mortality in cohort obtained through optimum stratification | Prado (Prado et al. | – | Secondary analysis of CT images (Mitsiopoulos et al. | L3mi | – | No functional component | BMI | – | – |
| Dello (Dello et al. | |||||||||
| Voron (Voron et al. | |||||||||
| Levolger (Levolger et al. | |||||||||
| van Vledder (van Vledder et al. | Intra-abdominal fat (Yoshizumi et al. | Significantly associated with disease-free survival in men undergoing resection of colorectal liver metastases (van Vledder et al. | – | ||||||
| Harimoto (Harimoto et al. | – | – | – | ||||||
| Lodewick (Lodewick et al. | % body fat | – | – | ||||||
| L3mi in the lowest sex-specific quartile | Miyamoto (Miyamoto et al. | – | Secondary analysis of CT images | L3mi | – | No functional component | – | – | – |
| No specific cutoffs established (lower density reflects more frailty) | Sabel (Sabel et al. | – | Secondary analysis of CT images | PD | A measure of muscle quality or fat infiltration | No functional component | VF, SFD, TBF, or BMI | VF: risk factor for developing colorectal cancer and significantly associated with increased tumor recurrence in colorectal cancer patients (Moon et al. | – |
| TPA/m2 equal to or below cutoff obtained through optimum stratification | Peng (Peng et al. | – | Secondary analysis of CT images | TPA/m2 | – | No functional component | BMI | – | – |
| TPA/m2 in the lowest sex-specific quartile | Peng (Peng et al. | – | Secondary analysis of CT images | TPA/m2 | – | No functional component | BMI | – | – |
| Amini (Amini et al. | |||||||||
| Joglekar (Joglekar et al. | |||||||||
| TPV/m2 in the lowest sex-specific quartile | Amini (Amini et al. | – | Secondary analysis of CT image | TPV/m2 | Volumetric measure rather than cross-sectional assessment and which may be more accurate at assessing a larger sample of muscle mass | No functional component | BMI | – | – |
| HUAC in the lowest sex-specific quartile | Joglekar (Joglekar et al. | – | Secondary analysis of CT image | HUAC | A measure of muscle quality or fat infiltration | No functional component | BMI | – | – |
To determine ASM, the sum of lean soft-tissue masses for the arms and legs is computed from CT scans and adjusted by height. To determine L3mi, two consecutive CT images are taken from the L3 to the iliac crest, and cross-sectional areas of the sum of all the muscles in these regions are computed and adjusted by body surface area. To determine PD, CT scans of the left and right psoas muscles at the level of the fourth lumbar vertebrae are used. To determine TPA, measure the cross-sectional area of the right and left psoas muscles from CT images at the level of L3 where both vertebral spinae are clearly visible. To determine TPV, take three manual measurements at the level of L3 on the first slice where both iliac crests were visible to assess a total of 55 cm total psoas length and normalize for height. To determine HUAC, compute (right Hounsfield unit calculation + left Hounsfield unit calculation)/2, where the right Hounsfield unit calculation = (right Hounsfield unit*right psoas area)/(total psoas area) and left Hounsfield unit calculation = (left Hounsfield unit*left psoas area)/(total psoas area) from evaluation of both the right and left psoas at the L3 level
ASM appendicular skeletal muscle, SD standard deviation, L3mi L3 skeletal muscle index, or total skeletal muscle cross-sectional area at the level of the third lumbar vertebrae normalized for stature, Intra-abdominal fat total cross-sectional area of visceral adipose tissue, TPA total psoas muscle area, measured at the level of the L3, TPV total psoas volume, measured at the level of the L3, HUAC Hounsfield unit average calculation, measure of radiation attenuation or muscle density and fatty infiltration, measured at the level of the L3, PD psoas density or muscle attenuation (average radiodensity), measured at the cross-sectional areas of the left and right psoas muscles at the level of the L4, VF visceral fat, visceral anterior-to-posterior distance, or the average distance between the anterior aspect of the vertebra and the linea alba, SFD subcutaneous fat distance, or the average distance between the linea alba and the anterior skin along T-12 to L4, TBF total body fat or total AP distance, the sum of the SFD and VF
Fig. 1Comparison of sarcopenic and non-sarcopenic computed tomography images at the third lumbar vertebral level. A comparison of two cirrhotic patients with identical BMI (32 kg/m2). Red color indicates skeletal muscle: rectus abdominis, oblique and lateral abdominal muscles, psoas, and paraspinal muscles. The patient on the left is sarcopenic with L3mi of 49.82 cm2/m2; the patient on the right is not sarcopenic with L3mi of 70.8 cm2/m2. In their study of 112 cirrhotic patients, Montano-Loza et al. used abdominal CT images taken at the third lumbar vertebrae and cutoffs provided by Baumgartner et al. in 1998
Association between sarcopenia or sarcopenic obesity (SO) and oncological surgery outcomes
| Study | Cancer type | Association with short-term oncological outcomes? | Association with long-term oncological outcomes? | ||
|---|---|---|---|---|---|
| Sarcopenia | SO | Sarcopenia | SO | ||
| Prado (Prado et al. | Respiratory or GI tract | – | Unclear, but associated with poorer functional status than in non-sarcopenic obese | Yes, independently predicted median survival | Yes, independently predicted survival |
| Lieffers (Lieffers et al. | Colorectal (stages II–IV) | Yes, independently predicted post-operative infection risk, longer inpatient rehabilitation, associated with higher risk of obstruction, longer index hospitalization length of stay, longer mean length of stay overall | – | – | – |
| Sabel (Sabel et al. | Colon | Yes, independently predicted surgical complications and infectious complications, associated with infectious post-operative complications | Unclear, but SFD is the best predictor of post-operative wound infections, and associated with infectious complications | No, not an independent predictor of disease-free or overall survival | Unclear, but TBF independently predicted disease-free survival |
| Miyamoto (Miyamoto et al. | Colorectal (stages I–III) | – | – | Yes, independently associated with disease recurrence rate, overall mortality, cancer-specific mortality, recurrence-free survival, overall survival, cancer-specific survival | – |
| van Vledder (van Vledder et al. | Colorectal liver metastases | – | – | Yes, independently predicted disease-free survival and overall survival | – |
| Dello (Dello et al. | Colorectal liver metastases | Yes, independently predicted disproportionally small total functional liver volume | Unclear, but fat-free body mass and body surface area independently predicted disproportionally small total function liver volume | – | – |
| Peng (Peng et al. | Colorectal liver metastases | Yes, independently predicted major post-operative complications, associated with risk of post-operative complications, overall morbidity risk, longer hospital stays, extended ICU stays | Yes, associated with major post-operative complications, longer hospital stays, extended ICU stays | No, not associated with recurrence-free survival, overall survival or risk of recurrence | No, not associated with overall survival or recurrence-free survival |
| Lodewick (Lodewick et al. | Colorectal liver metastases | No, not significantly associated with risk of major post-operative complications, presence of liver surgery-specific composite endpointa (LSSCEP) items | No, not significantly associated with risk of major post-operative complications, occurrence of one or more of the LSSCEP items | No, not significantly associated with initial hospital length of stay, readmission rates, median disease-free survival, or overall survival | Yes, not predictive of initial hospital length of stay, disease-free survival, or overall survival, but significantly associated with readmission rates |
| Harimoto (Harimoto et al. | Liver | Yes, independent predictor of liver dysfunction | – | Yes, independent predictor of overall and recurrence-free survival | – |
| Voron (Voron et al. | Liver | No, not associated with severe post-operative complication rate, post-operative mortality or morbidity rates | – | Yes, independently associated with overall and disease-free survival | – |
| Levolger (Levolger et al. | Liver | Yes, associated with major post-operative complication (Clavien-Dindo grade ≥IIIa) and treatment-related mortality (within 90 days post-treatment) | – | Yes, associated with overall survival, but not associated with disease-free survival | Yes, associated with shorter median survival |
| Peng (Peng et al. | Pancreatic | No, not associated with overall morbidity, major post-operative complications, length of hospital stays, length of ICU stays, or hazard of 90-day death | – | Yes, independent predictor of 3-year mortality | – |
| Amini (Amini et al. | Pancreatic | Yes, TPA-sarcopenia not associated with morbidity, but TPV-sarcopenia associated with post-operative complications, major complications, and length of hospital stay. TPV-sarcopenia also independently associated with post-operative complications | Yes, TPV-SO associated with post-operative complications | Yes, TPV-sarcopenia associated with risk of death, and independently associated with risk of death | – |
| Joglekar (Joglekar et al. | Pancreatic | Yes, HUAC independently predicted length of stay, ICU stay, major grade III post-operative complications, incidence of any complications. TPA independently predicted length of stay | – | No, HUAC did not predict post-operative overall survival | – |
aThe liver surgery-specific composite endpoint (LSSCEP) is composed of ascites, post-resectional liver failure, bile leakage, intra-abdominal hemorrhage, intra-abdominal abscess, and mortality and was used to assess liver surgery-specific morbidity
Fig. 2Example segmented L3 computed tomography image for skeletal muscle assessment of patient undergoing hepatic resection. L3mi computed tomogram shows highlighted areas of subcutaneous (green) and intra-abdominal fat (yellow) and skeletal muscle mass (red). van Vledder et al. found a variety of body compositions within their population of 196 patients who underwent hepatic resection for colorectal liver metastases