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Serum FSTL-1 and AI-assessed muscle parameters in cancer-related malnutrition
Daniel de Luis1, David Primo1, Olatz Izaola1
1Center of Investigation of Endocrinology and Clinical Nutrition, Medicine School, Department of Endocrinology and Nutrition Hospital Clinico Universitario, University of Valladolid, Valladolid, Spain; Health Research Institute of Valladolid (IBioVALL), Valladolid, Spain.
Objectives:
Follistatin-like protein-1 (FSTL-1) is emerging as a myokine linking skeletal and muscle biology. We investigated the relationship between circulating FSTL-1 levels and muscle mass and quality, using an artificial intelligence (AI)-enhanced ultrasonographic evaluation of the rectus femoris in patients with cancer-related disease-related malnutrition.
Methods:
A total of 91 patients diagnosed with cancer and disease-related malnutrition were included in the study. Muscle mass assessment was performed through US evaluation of the rectus femoris, using an AI-based analytical ultrasound system. Complementary evaluations comprised BIA to determine skeletal muscle mass, appendicular skeletal muscle mass, and the appendicular skeletal muscle mass index, with determination of circulating FSTL-1 concentrations.
Results:
Thirty-seven women and 54 men, with a mean age of 69.5 ± 10.6 years were enrolled. Sarcopenia was identified in 41 individuals (45.9%). Patients with sarcopenia showed significantly reduced values: body weight (-4.1 ± 1.0 kg; P = 0.02), calf circumference (-2.5 ± 0.3 cm; P = 0.03), phase angle (-0.7 ± 0.2°; P = 0.01), and reactance (-6.3 ± 1.3 Ω; P = 0.03), skeletal muscle mass (-2.3 ± 0.3 kg; P = 0.03), appendicular skeletal muscle mass (-3.7 ± 0.1 kg; P = 0.02), and appendicular skeletal muscle mass index (-1.3 ± 0.3 kg/m²; P = 0.02), cross-sectional area (-0.4 ± 0.2 cm²; P = 0.04), and y-axis (-0.27 ± 0.1 cm; P = 0.03), and pennation angle (-1.1 ± 0.2°; P = 0.02). Circulating levels of FSTL-1 were markedly reduced in patients with sarcopenia. In the multivariate logistic regression model, lower FSTL-1 concentrations remained significantly associated with an increased likelihood of sarcopenia (OR = 1.63, 95% CI: 1.10-4.21; P = 0.03. FSTL-1 demonstrated a moderate discriminative capacity for identifying sarcopenia, with an area under the receiver operating characteristic curve of 0.69 (95% CI: 0.51-0.73; P = 0.03).
Conclusions:
Reduced circulating FSTL-1 levels were independently associated with sarcopenia in patients with cancer-related malnutrition. These results indicate that FSTL-1 may act as a biomarker of impaired muscle quality and mass, as reflected by AI-assisted ultrasound and bioimpedance parameters.
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