Evaluation of oxidative stress and coagulation factors in MS patients throughout both relapse and remission stages

Nima Naseri1, Mohammad Hossein Harirchian2, Iraj Khodadadi1

  • 1Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Abstract

Insights

Relapsing-remitting Multiple Sclerosis (RRMS) patients show elevated coagulation, inflammation, and oxidative stress markers during relapse compared to remission. These markers, including fibrinogen and ferritin, may aid in diagnosing MS.

Area of Science:

  • Neurology
  • Biochemistry
  • Immunology

Background:

  • Relapsing-remitting Multiple Sclerosis (RRMS) involves myelin damage driven by inflammation.
  • Coagulation factors, inflammation, and oxidative stress are implicated in MS pathogenesis.
  • Monitoring these factors during disease phases may reveal therapeutic and diagnostic targets.

Purpose of the Study:

  • To investigate differences in coagulation, inflammation, and oxidative stress markers between relapse and remission phases in RRMS patients.
  • To compare these markers in RRMS patients against healthy controls.
  • To explore the diagnostic potential of these markers in MS.

Main Methods:

  • Blood samples were collected from 24 RRMS patients during relapse and again in remission after 3 months.
  • 24 healthy individuals served as controls.
  • Measured markers included coagulation factors (d-dimer, fibrinogen), inflammatory markers (IL-6, ferritin, CRP, ESR), and oxidative stress markers (TOS, MDA, TAC).

Main Results:

  • Expanded Disability Status Scale (EDSS) scores were higher during relapse.
  • D-dimer, ferritin, CRP, ESR, MDA, and TOS were significantly elevated in relapse versus remission.
  • Fibrinogen, ferritin, IL-6, and TOS were significantly higher in RRMS patients compared to controls.

Conclusions:

  • Fibrinogen, TOS, ferritin, and IL-6 show potential diagnostic utility for distinguishing MS patients from controls.
  • Elevated coagulation, inflammatory, and oxidative stress markers during relapse highlight their role in disease activity.
  • Future studies could explore these markers in cerebrospinal fluid (CSF).