Evidence map›Paper›PMID 33241537›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2021

Superoxide dismutase (SOD), advanced oxidation protein products (AOPP), and disease-modifying treatment are related to better relapse recovery after corticosteroid treatment in multiple sclerosis.

Dragana Obradovic, Tamara Andjelic, Milica Ninkovic, Bratislav Dejanovic, Jelena Kotur-Stevuljevic

Abstract read
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In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
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  4. Is Obesity a Modifiable Risk Factor in Multiple Sclerosis? Mechanistic Insights into Neuroinflammation and Oxidative Damage.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  5. Article
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  10. Oxidative Stress Markers in Multiple Sclerosis.International journal of molecular sciences · 2024
    Review
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  15. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Dragana ObradovicNeurology Clinic, Military Medical Academy, Faculty of Medicine, University of Defense, Belgrade, Serbia. dena.obradovic@gmail.com.ORCID http://orcid.org/0000-0003-4073-0457
Tamara AndjelicInstitute of Medical Biochemistry, Military Medical Academy, Faculty of Medicine, University of Defense, Belgrade, Serbia.
Milica NinkovicInstitute for Medical Research, Military Medical Academy, Faculty of Medicine, University of Defense, Belgrade, Serbia.
Bratislav DejanovicInstitute of Medical Biochemistry, Military Medical Academy, Faculty of Medicine, University of Defense, Belgrade, Serbia.
Jelena Kotur-StevuljevicInstitute of Medical Biochemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia.
Military Medical Academy · RSUniversity of Belgrade · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim of our study was to analyze oxidative stress (OS) markers in multiple sclerosis (MS) patients during relapse and remission and to evaluate the effects of corticosteroid relapse treatment on oxidative status, and also to determine possible relationship between OS markers and relapse disability recovery after corticosteroid treatment.

methodsOur study included 118 MS patients, (59 relapse/59 remission) 70 females and 48 males, mean age 40.2 ± 9.4 years, and 88 matched healthy controls. Undergoing disease-modifying therapy (DMT) was present in 30.5% of relapse and 88% of remission MS patients. We analyzed in plasma/serum the following: pro-oxidative-antioxidative balance (PAB), nitrates and nitrites (NO

resultsBetter clinical recovery after relapse treatment was associated with increased baseline SOD, decreased AOPP, and ongoing DMT (all p < 0.05). There was no difference between OS markers in relapse and remission. MS patients had higher MDA, NO

conclusionIncreased baseline antioxidative activity of SOD and decreased baseline levels of pro-oxidant AOPP along with ongoing DMT were related to better clinical recovery after corticosteroid relapse treatment. Increase of pro-oxidants and antioxidant enzyme activity in relapse and remission confirms ongoing oxidative injury irrelevant of MS clinical presentation.

Indexed as

Advanced Oxidation Protein ProductsMultiple SclerosisAdrenal Cortex HormonesBiomarkersFemaleHumansMaleMalondialdehydeOxidative StressRecurrenceSuperoxide DismutaseAdrenal Cortex HormonesAdvanced Oxidation Protein ProductsBiomarkersMalondialdehydeSuperoxide DismutaseCorticosteroidsEDSSMultiple sclerosisOxidative stressRelapseSOD

Identifiers

PMID33241537
OpenAlexW3108235750

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.