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Blood Markers Help Predict MS Disease Progression

Meeting Coverage > > ECTRIMS– Patients with high NfL at illness beginning might take advantage of high-efficacy treatments

by Judy George, Deputy Managing Editor, MedPage Today September 19, 2024

Blood biomarkers at illness beginning might assist anticipate relapse-associated intensifying and development independent of regression activity (PIRA) in several sclerosis (MS), an observational research study recommended.

Serum levels of neurofilament light (NfL), a marker of axonal injury, forecasted both relapse-associated worsening and PIRA, reported Enric Monreal, MD, PhD, of the Hospital Universitario Ramón y Cajal in Madrid, who provided the findings at the yearly European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) conference in Copenhagen.

Serum levels of glial fibrillary acidic protein (GFAP), an intermediate filament of astrocytes, associated with PIRA in clients who had low NfL levels, Monreal stated.

NfL has actually gotten traction as an MS biomarker in the last few years. In March, an agreement panel of professionals for the Consortium of Multiple Sclerosis Centers provided assistance on NfL as a cerebrospinal fluid and blood biomarker in MS management. GFAP might be more highly related to illness development than NfL, according to earlier research study

In this research study, Monreal and co-authors evaluated blood samples that were gathered within 12 months of illness beginning from 725 MS clients throughout 13 health centers in Spain and Italy. A lot of individuals (70.2%) were ladies, and the mean standard age was 34.2.

“The time from very first regression to analysis was a bit more than 3 months,” Monreal mentioned. “Nearly a 3rd of clients were treated with monoclonal antibodies and the mean follow-up time was more than 6 years.” Monoclonal antibodies were thought about high-efficacy disease-modifying treatments (DMTs).

The scientists utilized a single-molecule selection to evaluate the prognostic worth of serum NfL and GFAP levels. Multivariable Cox regression analysis revealed:

  • Greater serum NfL z-rating levels were connected with a 45% greater threat of relapse-associated worsening (HR 1.45, 95% CI 1.19-1.76, P< 0.001) and a 43% greater danger of PIRA (HR 1.43, 95% 1.13-1.81, P=0.003)
  • Greater serum GFAP worths were related to an increased danger of PIRA (HR 1.86, 95% CI 1.01-3.45, P=0.047), however just in clients with low levels of serum NfL

“We saw that neurofilament levels were impacting the capability of GFAP to anticipate the danger of PIRA,” Monreal stated.

The scientists even more organized clients into 3 classifications: those with low levels of serum NfL and GFAP (31.3% of individuals), those with high levels of NfL (55.3% of individuals), and those with low levels of NfL and high levels of GFAP (13.4% of individuals).

Compared to the low NfL-GFAP group, clients in the high NfL group revealed a greater danger of relapse-associated worsening and PIRA if they were not dealt with or utilizing injectable or oral treatments.

All individuals had a comparable threat of relapse-associated getting worse or PIRA if treated with high-efficacy DMTs.

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