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Review
Copyright: ©Author(s) 2026.
World J Gastrointest Surg. Oct 27, 2026; 18(10): 124479
Published online Oct 27, 2026. doi: 10.4240/wjgs.124479
Table 1 Computed tomography-based body composition parameters
Parameter
Clinical meaning
Assessment method
Common diagnostic cut-off
Prognostic role
Strengths
Limitations
SMIMuscle quantity, normalized for body sizeCross-sectional skeletal muscle area at L3 (cm2), indexed to height2 (cm2/m2)Sarcopenia: < 52.4 cm2/m2 (men), < 38.5 cm2/m2 (women); BMI-adjusted cut-offs also usedOverall survival; predicts chemotherapy toxicity, postoperative complicationsWell-validated; single L3 slice correlates strongly with whole-body muscle mass; widely used across cancer/surgical literatureNo universal cut-off (varies by ethnicity, population, scanner protocol); requires dedicated software/manual segmentation; height2 normalization may under/overcorrect in obese or very short/tall patients
PMISurrogate for muscle mass using a single muscleCross-sectional area of bilateral psoas muscles at L3 or L4, indexed to height2 (cm2/m2)No consensus; commonly cited thresholds approximately < 5.0 cm2/m2 (men), < 3.4 cm2/m2 (women), varies widely by studyPostoperative complications, morbidityFast to measure (small, discrete structure); minimal manual tracing needed; feasible even on lower-quality/Limited-slice scansPoorly correlates with total skeletal muscle mass; high inter-study variability in cut-offs; psoas size affected by positioning and vertebral level chosen; less validated than SMI
SMDMuscle quality (myosteatosis/fatty infiltration)Mean CT attenuation (HU) of skeletal muscle at L3Myosteatosis: < 41 HU (BMI < 25) or < 33 HU (BMI ≥ 25)Overall survival, independent of muscle quantityCaptures muscle quality, not just size - adds prognostic information beyond SMI; low cost (same CT slice as SMI)Attenuation affected by CT protocol/reconstruction settings and contrast phase; BMI-stratified cut-offs complicate use; less intuitive for clinicians
VFAAdiposity, visceral fat burdenCross-sectional visceral adipose tissue area at L3 (or umbilicus level), cm2Visceral obesity: ≥ 100 cm2 (women), ≥ 130-163 cm2 (men), varies by study/ethnicityPostoperative and infectious complicationsStrong correlate of metabolic risk and surgical complication risk; reproducible measurementCut-offs not standardized across populations; requires accurate delineation from subcutaneous fat; single-slice VFA may not reflect total visceral fat volume
IMACPoor muscle quality (fat infiltration within/around muscle)Ratio of CT attenuation of intramuscular/paraspinal fat to that of paraspinal muscle (using psoas or paraspinal muscles)No universal threshold; typically defined by cohort-specific median or tertile splitMortalityComplements SMD; useful when psoas is the only reliably visualized muscle group; correlates with frailtyLacks standardized cut-off; formula/muscle group varies between studies, limiting comparability; less widely validated than SMI/SMD
Table 2 Integrated prognostic models and composite indices in gastric cancer body-composition assessment
Model/index
Main components
Clinical meaning
Prognostic value
Main limitation
GLIM criteriaPhenotypic criteria, including weight loss, low BMI, reduced muscle mass; etiologic criteria, including reduced intake, inflammation, or disease burdenStandardized assessment of malnutrition with body-composition relevanceIdentifies patients at higher risk of postoperative morbidity, poor recovery, and worse survivalRequires nutritional and clinical assessment; cut-offs and implementation may vary across populations
GNRISerum albumin and body weight relative to ideal body weightNutritional risk and systemic reserveAssociated with postoperative complications, treatment tolerance, and long-term survivalDoes not directly measure muscle mass or muscle quality
PNISerum albumin and lymphocyte countCombined nutritional and immune statusPredicts postoperative morbidity, recurrence risk, and overall survivalInfluenced by inflammation, infection, hydration status, and non-cancer-related conditions
CXISkeletal muscle index × serum albumin/neutrophil-to-lymphocyte ratioIntegrates muscle mass, nutrition, and systemic inflammationMay improve risk stratification beyond isolated CT-derived or laboratory markersRequires standardized CT assessment and laboratory timing
ALBI-related modelsSerum albumin and bilirubin, alone or combined with sarcopenia/body-composition variablesReflects hepatic and nutritional reserveMay help identify patients with impaired physiological reserve and poorer prognosisMore relevant when liver function has prognostic impact; should not be confused with liver-disease scores such as MELD or CTP
Radiomics modelsCT texture features from tumor and/or body-composition compartments combined with clinical variablesImaging-based prediction of recurrence and survivalCan improve individualized prediction beyond conventional staging aloneRequires software, technical standardization, and external validation
AI-based nomogramsMachine-learning or deep-learning features combined with clinicopathological, CT-derived, nutritional, and inflammatory variablesMultivariable personalized risk predictionMay predict postoperative complications, recurrence, and overall survival more accurately than single markersLimited by retrospective datasets, black-box interpretability, and generalizability across centers
Integrated body-composition scoresSMI, SMD/myosteatosis, visceral fat, sarcopenic obesity, functional tests, and inflammatory/nutritional markersMultidimensional assessment of host reserveCaptures the combined prognostic impact of muscle quantity, muscle quality, adiposity, and inflammationLack of universally accepted thresholds and standardized scoring systems


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