Evidence map›Paper›PMID 36733554›Full record

ReviewCureus2023

An Overview of the History, Pathophysiology, and Pharmacological Interventions of Multiple Sclerosis.

Ibrahim M Dighriri, Ahood A Aldalbahi, Fatimah Albeladi, Asimah A Tahiri, Elaf M Kinani, Rand A Almohsen, Nouf H Alamoudi, Abeer A Alanazi, Sultan J Alkhamshi, Noha A Althomali and 2 more

Open access · diamondAbstract readReview
In one paragraph

Review in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 6 pooled it
15.8field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 6 syntheses or guidelines pooled it, 62 citations in OpenAlex.

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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

12 authors at 11 institutions in 1 country.

Ibrahim M DighririDepartment of Pharmacy, King Abdulaziz Specialist Hospital, Taif, SAU.
Ahood A AldalbahiDepartment of Medicine, PHC Al-Qassim Health Cluster, Buraidah, SAU.
Fatimah AlbeladiDepartment of Pharmacy, Maternity and Children Hospital, Dammam, SAU.
Asimah A TahiriDepartment of Pharmacy, Armed Forces Hospital, Jazan, SAU.
Elaf M KinaniDepartment of Pharmacy, Al Thaghr Hospital, Jeddah, SAU.
Rand A AlmohsenFaculty of Pharmacy, University of Shaqra, Al-Dawadmi, SAU.
Nouf H AlamoudiFaculty of Pharmacy, Umm Al Qura University, Mecca, SAU.
Abeer A AlanaziFaculty of Pharmacy, Northern Border University, Rafha, SAU.
Sultan J AlkhamshiFaculty of Pharmacy, Buraydah College, Al-Qassim, SAU.
Noha A AlthomaliDepartment of Pharmacy, Taif University, Taif, SAU.
Sultan N AlrubaieiDepartment of Pharmacy, King Abdulaziz Specialist Hospital, Taif, SAU.
Faisal K AltowairqiDepartment of Pharmacy, Community Pharmacy, Riyadh, SAU.
King Abdulaziz Hospital · SAAl Amal Hospital Jeddah · SAArmed Forces Hospital · SABuraydah Colleges · SAMaternity and Children's Hospital · SANorthern Border University · SAQassim University · SARiyadh Elm University · SAShaqra University · SATaif University · SAUmm al-Qura University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an immune-inflammatory disease that attacks and damages myelinated axons in the central nervous system (CNS) and causes nontraumatic neurological impairment in young people. Historically, Lidwina of Schiedam documented the first MS case. After that, Augustus d'Este wrote for years about how his MS symptoms worsened. Age, sex, genetics, environment, smoking, injuries, and infections, including herpes simplex and rabies, are risk factors for MS. According to epidemiology, the average age of onset is between 20 and 40 years. MS is more prevalent in women and is common in Europe and America. As diagnostic methods and criteria change, people with MS may be discovered at earlier and earlier stages of the disease. MS therapy has advanced dramatically due to breakthroughs in our knowledge of the disease's etiology and progression. Therefore, the efficacy and risk of treatment medications increased exponentially. Management goals include reducing lesion activity and avoiding secondary progression. Current treatment approaches focus on managing acute episodes, relieving symptoms, and reducing biological activity. Disease-modifying drugs such as fingolimod, interferon-beta, natalizumab, and dimethyl fumarate are the most widely used treatments for MS. For proof of the efficacy and safety of these medications, investigations in the real world are necessary.

Indexed as

cnsdisease-modifying therapiesmsmultiple sclerosispathogenesis

Identifiers

PMID36733554
PMCPMC9888604
OpenAlexW4313469508

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.