The diagnostic value of urinary N-Terminal fragment of titin for skeletal muscle damage in idiopathic inflammatory myopathy

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Abstract

Objectives: N-Terminal fragment of titin (N-Titin) is a marker of sarcomere damage in striated muscles; however, its value in patients with IIM (idiopathic inflammatory myopathy) is unclear. This study aimed to investigate the diagnostic value of N-Titin for skeletal muscle damage in patients with IIM. Methods: Urine samples from 62 patients with IIM, 59 patients with other CTD diseases, and 29 healthy controls were collected to detect N-Titin by ELISA assays. Clinical features and laboratory data were all included in logistic regression analysis to obtain the independent predictive factor for skeletal muscle damage. Results: Urinary N-Titin level of the IIM group [168.3 (19.0, 1279.0) pmol/mg cr] was significantly higher than that in CTD controls [2.80 (1.53, 3.60)] and healthy controls [1.83 (1.09, 2.95)] (P < 0.001). IIM patients with skeletal muscle injury had a significantly higher level of urinary N-Titin [1001.0, (181.8, 1977.0)] than those without [9.3, (5.8, 23.9)] (P < 0.001). The N-Titin level was strongly correlated with CK (r = 0.907, P < 0.001) and muscle disease activity assessment scores by Spearman correlation analysis. After adjusting for the anti-MDA5 antibody and cardiac troponin T, N-Titin was shown to independently predict skeletal muscle damage in patients with IIM (odds ratio = 1.035, 95% CI: 1.002, 1.069, P = 0.039). The cut-off value of urinary N-Titin to diagnose skeletal muscle damage was 89.9 pmol/mg Cr, with a sensitivity of 87.8% and a specificity of 100% (AUC = 0.971, 95% CI: 0.938, 1.000, P < 0.001). Conclusion: Urinary N-Titin is a non-invasive and independent predictive factor for determining skeletal muscle damage in patients with IIM.

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Sun, J., Ye, S., Yin, G., & Xie, Q. (2023). The diagnostic value of urinary N-Terminal fragment of titin for skeletal muscle damage in idiopathic inflammatory myopathy. Rheumatology (United Kingdom), 62(11), 3742–3748. https://doi.org/10.1093/rheumatology/kead109

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