Key result
Urinary levels of titin N-terminal fragment were significantly higher in patients with ALS compared to healthy controls (27.2 vs 5.8 pmol/mg/dL; p<0.001).
Why the study?
The study aimed to investigate the validity of urinary N-terminal titin fragment as a biomarker for amyotrophic lateral sclerosis.
Is the ratio of urinary N-terminal titin fragment to urinary creatinine a valid biomarker for disease severity and prognosis in patients with amyotrophic lateral sclerosis?
Case-Control (n=113)
Is the ratio of urinary N-terminal titin fragment to urinary creatinine a valid biomarker for disease severity and prognosis in patients with amyotrophic lateral sclerosis?
Absolute Event Rate: 27.2% vs 5.8%
p-value: p=<0.001
Urinary N-terminal titin fragment normalized to creatinine is a promising non-invasive biomarker for assessing muscle damage, monitoring disease severity, and predicting prognosis in patients with ALS.
Urinary titin/Cr may support ALS monitoring and prognosis with NfL; leaves open clinical adoption pending prospective validation.
Objective We aimed to investigate the validity of urinary N-terminal titin fragment as a biomarker for amyotrophic lateral sclerosis (ALS). Methods We consecutively enrolled patients with ALS (n=70) and healthy controls (HC) (n=43). We assessed the urinary titin N-terminal fragment, urinary neurotrophin receptor p75 extracellular domain, serum neurofilament light chain (NfL), motor functional measurements and prognosis. We used urinary creatinine (Cr) levels to normalise the urinary levels of titin fragment. Results Compared with HC, patients with ALS had significantly increased urinary levels of titin N-terminal fragment normalised with Cr (titin/Cr) (ALS, 27.2 pmol/mg/dL; HC, 5.8 pmol/mg/dL; p<0.001), which were correlated with the scores of the Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (r=−0.422, p<0.001). A Cox proportional hazards model demonstrated that the high urinary level of titin/Cr was a survival predictor in patients with ALS. Multivariate analysis of prognostic factors showed that the urinary titin/Cr and serum NfL were independent factors for poor prognosis. Conclusions Our findings indicate that urinary N-terminal titin fragment is a non-invasive measure of muscle damage in ALS, which could be applied in disease monitoring and prediction of disease progression, in combination with serum NfL.
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Yamada et al. (2021) conducted a case-control in amyotrophic lateral sclerosis (ALS) (n=113). Urinary N-terminal titin fragment vs. Healthy controls was evaluated on Urinary levels of titin N-terminal fragment normalised with Cr (titin/Cr) (p=<0.001). Urinary levels of titin N-terminal fragment were significantly higher in patients with ALS compared to healthy controls (27.2 vs 5.8 pmol/mg/dL; p<0.001).
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