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. 2022 Sep;269(9):5085-5092.
doi: 10.1007/s00415-022-11165-0. Epub 2022 May 16.

Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1)

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Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1)

Tommaso F Nicoletti et al. J Neurol. 2022 Sep.

Abstract

Background: Cognitive and behavioural symptoms due to involvement of the central nervous system (CNS) are among the main clinical manifestations of Myotonic Dystrophy type 1 (DM1). Such symptoms affect patients' quality of life and disease awareness, impacting on disease prognosis by reducing compliance to medical treatments. Therefore, CNS is a key therapeutic target in DM1. Deeper knowledge of DM1 pathogenesis is prompting development of potential disease-modifying therapies: as DM1 is a rare, multisystem and slowly progressive disease, there is need of sensitive, tissue-specific prognostic and monitoring biomarkers in view of forthcoming clinical trials. Circulating Neurofilament light chain (NfL) levels have been recognized as a sensitive prognostic and monitoring biomarker of neuroaxonal damage in various CNS disorders.

Methods: We performed a cross-sectional study in a cohort of 40 adult DM1 patients, testing if serum NfL might be a potential biomarker of CNS involvement also in DM1. Moreover, we collected cognitive data, brain MRI, and other DM1-related diagnostic findings for correlation studies.

Results: Mean serum NfL levels resulted significantly higher in DM1 (25.32 ± 28.12 pg/ml) vs 22 age-matched healthy controls (6.235 ± 0.4809 pg/ml). Their levels positively correlated with age, and with one cognitive test (Rey's Auditory Verbal learning task). No correlations were found either with other cognitive data, or diagnostic parameters in the DM1 cohort.

Conclusions: Our findings support serum NfL as a potential biomarker of CNS damage in DM1, which deserves further evaluation on larger cross-sectional and longitudinal studies to test its ability in assessing brain disease severity and/or progression.

Keywords: Biomarkers; Central nervous system; Cognition; Myotonic dystrophy; Neurofilament protein.

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
Histogram showing mean levels of Neurofilament Light chain (NfL) [pg/ml] in DM1 patients (n = 40) vs controls (CTR, n = 22). Asterisks (**) indicate significant difference (p = 0.0024) by Mann–Whitney U test
Fig. 2
Fig. 2
Panel displaying in A scatter plot with linear regression showing correlation between Neurofilament Light chain (NfL) levels [pg/ml] and patients’ age at examination (n = 40), and B corresponding scatter plot of controls (n = 22)

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