Prediagnostic Neurofilament Light Chain Levels in Amyotrophic Lateral Sclerosis.

Neurology

From the Departments of Nutrition (K.B., E.J.O., S.M., A.A.) and Epidemiology (A.A.), Harvard T.H. Chan School of Public Health, Boston, MA; School of Public Health, College of Medicine (E.J.O.), University College Cork, Ireland; Epidemiology Program (L.N.K., L.L.M.), University of Hawaii Cancer Center, Honolulu; Department of Physical Medicine and Rehabilitation, Spaulding Rehabilitation Hospital and Healey Center for ALS (S.P.), and Department of Neurology (M.A.S.), Massachusetts General Hospital, Boston; Harvard Medical School (S.P., M.A.S.), Boston, MA; Clinical Trial Unit, Department of Clinical Research (P.B.), and Neurologic Clinic and Policlinic, MS Center and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), Departments of Biomedicine and Clinical Research (J.K.), University Hospital Basel, University of Basel, Switzerland; and Channing Division of Network Medicine (A.A.), Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Published: October 2021

AI Article Synopsis

  • The study aimed to determine if plasma neurofilament light chain (NfL) levels are higher before an ALS diagnosis and if these levels link to metabolic changes.
  • Researchers examined plasma samples from 84 ALS patients collected before diagnosis and found that higher NfL levels correlated with an increased risk of ALS when samples were taken within 5 years of diagnosis.
  • The findings suggest that elevated plasma NfL may serve as an early biomarker for ALS, although metabolic alterations linked to NfL levels were not conclusively supported after adjusting for multiple comparisons.

Article Abstract

Background And Objectives: To assess whether plasma neurofilament light chain (NfL) levels are elevated before amyotrophic lateral sclerosis (ALS) diagnosis and to evaluate whether prediagnostic NfL levels are associated with metabolic alterations.

Methods: We conducted a matched case-control study nested in 3 large prospective US cohorts (the Nurses' Health Study, the Health Professionals Follow-up Study, and the Multiethnic Cohort Study) and identified 84 individuals who developed ALS during follow-up and had available plasma samples prior to disease diagnosis. For each ALS case, we randomly selected controls from those who were alive at the time of the case diagnosis and matched on birth year, sex, race/ethnicity, fasting status, cohort, and time of blood draw. We measured NfL in the plasma samples and used conditional logistic regression to estimate rate ratios (RRs) and 95% confidence intervals (CIs) for ALS, adjusting for body mass index, smoking, physical activity, and urate levels.

Results: Higher NfL levels were associated with a higher ALS risk in plasma samples collected within 5 years of the ALS diagnosis (RR per 1 SD increase 2.68, 95% CI 1.18-6.08), but not in samples collected further away from the diagnosis (RR per 1 SD increase 1.16, 95% CI 0.78-1.73). A total of 21 metabolites were correlated with prediagnostic NfL levels in ALS cases ( < 0.05), but none of these remained significant after multiple comparison adjustments.

Discussion: Plasma NfL levels were elevated in prediagnostic ALS cases, indicating that NfL may be a useful biomarker already in the earliest stages of the disease.

Classification Of Evidence: This study provides Class II evidence that plasma NfL levels are elevated in prediagnostic ALS.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575132PMC
http://dx.doi.org/10.1212/WNL.0000000000012632DOI Listing

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