Evidence map›Paper›PMID 34115275›Full record

ArticleMetabolic brain disease2021

Evaluation of matrix metalloproteinase-9 plasma levels in untreated new Relapsing-remitting multiple sclerosis patients and their first-degree family.

Mahsa Samangooei, Mojtaba Farjam, Zahra Niknam, Masoud Etemadifar, Mohammad Hasan Meshkibaf, Saam Noroozi

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Article in Metabolic brain disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Review
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

6 authors at 3 institutions in 1 country.

Mahsa SamangooeiDepartment of Clinical Biochemistry, School of Medicine, University of Medical Sciences, Fasa, Iran.
Mojtaba FarjamDepartment of Clinical Biochemistry, School of Medicine, University of Medical Sciences, Fasa, Iran.
Zahra NiknamIran Neurological Associations, Tehran, Iran.
Masoud EtemadifarDepartment of Neurosurgery, Isfahan University of Medical Sciences, Isfahan, Iran.
Mohammad Hasan MeshkibafDepartment of Clinical Biochemistry, School of Medicine, University of Medical Sciences, Fasa, Iran.
Saam NorooziDepartment of Clinical Biochemistry, School of Medicine, University of Medical Sciences, Fasa, Iran. saam.noroozi@gmail.com.ORCID 0000-0003-2890-6747
Fasa University of Medical Sciences · IRIranian Orthopedic Association · IRIsfahan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matrix metalloproteinase, especially Matrix metalloproteinase-9 (MMP-9) has vital roles in the disruption of blood barrier, neuroinflammation and pathogenesis of multiple sclerosis (MS) patients. The goal of this study is to estimate the plasma levels of MMP-9 in the first-degree family of MS patients. 35 untreated patients with definite RRMS (Relapsing-Remitting Multiple sclerosis) according to the McDonald criteria, 24 healthy controls (HC) and 26 high-risk families of untreated RRMS patients were enrolled in the study. Plasma levels of MMP-9 were analyzed by ELISA (enzyme-linked immunosorbent assay). Although the plasma protein levels of MMP-9 were elevated significantly in the untreated RRMS group (P < 0.05, P = 0.0203) as compared to the control group, but the family of MS patients was not significance (P = 0.208). The mean plasma MMP-9 concentration for HC, untreated RRMS and high-risk group was 322.268 pg/ml, 611.926 pg/ml and 518.939 pg/ml respectively. MMP-9 was used to understand the role of this biomarker in the pathogenesis of MS in the high-risk group. It found that plasma levels of MMP-9 in the new cases of MS were increased considerably. Confirming the importance of MMP-9 as a predictive marker in the high-risk group will be needed more researches.

Indexed as

Multiple SclerosisMultiple Sclerosis, Chronic ProgressiveMultiple Sclerosis, Relapsing-RemittingBiomarkersHumansMatrix Metalloproteinase 9BiomarkersMatrix Metalloproteinase 9MMP9 protein, humanFirst-degree familyMatrix metalloproteinaseRelapsing–remittingUntreated multiple sclerosisVitamin D

Identifiers

PMID34115275
OpenAlexW3170409441

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.