Evidence map›Paper›PMID 38386047›Full record

ArticleJournal of neurology2024

Increased incidence of motor neuron disease in Sweden: a population-based study during 2002-2021.

Sofia Imrell, Fang Fang, Caroline Ingre, Stefan Sennfält

Abstract read
In one paragraph

Article in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

4 authors.

Sofia ImrellDepartment of Neurology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden. sofia.imrell@regionorebrolan.se.ORCID http://orcid.org/0009-0009-3855-5937
Fang FangUnit of Integrative Epidemiology, Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden.
Caroline IngreDepartment of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
Stefan SennfältDepartment of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.

Funding

Vetenskapsrådet Swedish Research Grant DNR 2019-01088
6 · The paper itself

Abstract

backgroundMotor neuron diseases (MND), with amyotrophic lateral sclerosis constituting most cases, are rare conditions of unknown etiology. There have been reports of an increase in incidence during the latter half of the twentieth century in various Western countries, including Sweden. This study provides updated data on the incidence of MND in Sweden during the last 20 years.

methodsData was obtained from the Swedish National Patient Register on individuals diagnosed with MND from 2002 to 2021 and analysed in relation to group level data for the entire Swedish population. Incidence rates were calculated and presented in relation to year, age, sex, and region.

resultsIn the early 2000s, there was a crude incidence rate of 3.5-3.7 per 100,000 person-years, which then increased to 4.0-4.6 from 2008 onward. Age standardization to the starting year (2002) partially mitigated this increase. The incidence rate was greater among men compared to women and was highest within the age range of 70 to 84 years. There were indications of a higher incidence rate in the northernmost parts of the country, although the difference was not statistically significant.

conclusionsThe incidence rate of MND in Sweden now seems to have surpassed 4 cases per 100,000 person-years. This is higher when compared to both other European countries and previous Swedish studies. It remains to be determined if this increase reflects an actual increasing incidence of MND in Sweden or is due to other factors such as better registry coverage.

Indexed as

Motor Neuron DiseaseRegistriesAdolescentAdultAgedAged, 80 and overFemaleHumansIncidenceMaleMiddle AgedSwedenYoung AdultAmyotrophic lateral sclerosisEpidemiologyIncidenceMotor neuron disease

Identifiers

PMID38386047
PMCPMC11055737

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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.