4.4 Article

Depression and anxiety disorders in patients with multiple sclerosis: association with neurodegeneration and neurofilaments

Journal

Publisher

ASSOC BRAS DIVULG CIENTIFICA
DOI: 10.1590/1414-431X202010428

Keywords

Neurofilaments; Depression; Anxiety; Multiple sclerosis

Funding

  1. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [2014/26431-0, 2016/17404-5]
  2. Fundacao de Apoio a Pesquisa do Distrito Federal [03/16-10597.56.41622.09042016]

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NF-L levels are elevated in patients with MS and psychiatric disorders, but the relationship between depression and anxiety in RRMS-Fingo patients and NF-L levels is not statistically significant. MS events such as anxiety and depression may contribute to the onset of clinical relapses, subclinical cases, and neurodegeneration.
There is increasing evidence that neurofilament light chain (NF-L) can be considered as a biomarker for neuro-axonal damage. This polypeptide can be released into the cerebrospinal fluid (CSF) and the blood, where it can be quantified. The concentration of NF-L is elevated in patients with multiple sclerosis (MS) and psychiatric disorders. We aimed to investigate the NF-L levels in the CSF from treated MS patients and the relationship with depression or anxiety. The study involved three groups: control group (individuals without inflammation), the relapse-remitting multiple sclerosis (RRMS)-untreated group, and the RRMS-Fingo group (RRMS patients who were treated with fingolimod). MS disability was assessed by the Expanded Disability Status Scale, and depression and anxiety were evaluated by a neuropsychologist, using the Hospital Anxiety and Depression Scale, the Beck Depression Inventory-II, and the Beck Anxiety Inventory. Individual CSF samples were collected to measure NF-L levels. The results of the statistical analysis on levels of NF-L in the CSF of control subjects, RRMS-untreated patients, and RRMS-Fingo patients were significant. The relationship between depression and anxiety in RRMS-Fingo patients and NF-L levels was not statistically significant. In conclusion, MS events such as anxiety and depression appear to contribute to the onset of clinical relapses, subclinical cases, and neurodegeneration.

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