Evidence map›Paper›PMID 41552666›Full record

ArticleMultiple sclerosis journal - experimental, translational and clinical

Comorbidities in newly diagnosed multiple sclerosis patients: A population-based register study in Finland.

Henrik Ahvenjärvi, Johanna Krüger, Matias Viitala, Elina Jokinen, Henri Autio, Anne M Portaankorva, Merja Soilu-Hänninen, Mervi Ryytty

Abstract read
In one paragraph

Article in Multiple sclerosis journal - experimental, translational and clinical. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Henrik AhvenjärviResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland.ORCID https://orcid.org/0000-0003-3641-3504
Johanna KrügerResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland; Medical Research Center, Oulu University Hospital, OYS, Oulu, Finland; Neurocenter, Neurology, Oulu University Hospital, OYS, Oulu, Finland.ORCID https://orcid.org/0000-0003-4346-1133
Matias ViitalaStellarQ Ltd, Turku, Finland.ORCID https://orcid.org/0000-0003-2854-2410
Elina JokinenNovartis Finland Ltd, Espoo, Finland.
Henri AutioNovartis Finland Ltd, Espoo, Finland.
Anne M PortaankorvaResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland; Medical Research Center, Oulu University Hospital, OYS, Oulu, Finland; Clinical Neurosciences, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Merja Soilu-HänninenClinical Neurosciences, University of Turku, Turku, Finland; Neurocenter, Turku University Hospital, TYKS, Turku, Finland.ORCID https://orcid.org/0000-0001-6930-0229
Mervi RyyttyResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland; Medical Research Center, Oulu University Hospital, OYS, Oulu, Finland; Neurocenter, Neurology, Oulu University Hospital, OYS, Oulu, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Comorbidities are common among people with multiple sclerosis (pwMS) and have been suggested to affect the usage of disease-modifying treatments (DMTs). Objectives: We investigated the prevalence and types of comorbidities in newly diagnosed pwMS, as well as the associations between comorbidities and the choice and persistence of the initial DMT. Methods: This retrospective register study used data from the Finnish MS register (85% of national coverage). The inclusion criteria were a diagnosis of relapsing-remitting MS between 2010 and 2022, the first DMT started between 2016 and 2022, and an age of at least 18 years. The exclusion criteria were a diagnosis of secondary progressive MS and initiation of azathioprine or mitoxantrone. Results: The inclusion criteria were met by 1630 pwMS. At least one comorbidity was present in 50.9% of the pwMS. Respiratory comorbidities were associated with the choice of medium-efficacy DMT over high-efficacy DMT (OR = 0.58, CI = 0.36-0.91). Multicomorbidity was associated with lower persistence on all DMTs. Additionally, lower persistence on medium-efficacy DMTs was associated with autoimmune and psychiatric comorbidities and the injectable administration route. Conclusions: Comorbidities are prevalent among newly diagnosed pwMS. Clinicians should consider comorbidities carefully, as they are associated with DMT persistence.

Indexed as

comorbidityCOVID-19disease-modifying treatmentMS registerMultiple sclerosis

Identifiers

PMID41552666
PMCPMC12804660

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Registered trials

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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.