Evidence map›Paper›PMID 42538750›Full record

ArticleEuropean journal of neurology2026

Nationwide Epidemiology of Motor Neuron Diseases in Latvia (2020-2024): Incidence, Prevalence, and Clinical Characteristics.

Vladimirs Krutovs, Arta Grosmane, Renāte-Ruta Kažmere, Marija Roddate, Gundega Ķauķe, Diāna-Patrīcija Grosa, Signe Šetlere, Mikus Dīriks, Guntis Karelis, Viktorija Ķēniņa

Abstract read
In one paragraph

Article in European journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Vladimirs KrutovsDepartment of Neurology, Pauls Stradiņš Clinical University Hospital, Riga, Latvia.ORCID https://orcid.org/0009-0000-3596-9661
Arta GrosmaneDepartment of Neurology, Pauls Stradiņš Clinical University Hospital, Riga, Latvia.
Renāte-Ruta KažmereFaculty of Residency, Rīga Stradiņš University, Riga, Latvia.
Marija RoddateDepartment of Neurology, Pauls Stradiņš Clinical University Hospital, Riga, Latvia.
Gundega ĶauķeDepartment of Neurology, Pauls Stradiņš Clinical University Hospital, Riga, Latvia.
Diāna-Patrīcija GrosaDepartment of Neurology and Neurosurgery, Riga East University Hospital, Riga, Latvia.
Signe ŠetlereDepartment of Neurology and Neurosurgery, Children's Clinical University Hospital, Riga, Latvia.
Mikus DīriksDepartment of Neurology and Neurosurgery, Children's Clinical University Hospital, Riga, Latvia.
Guntis KarelisDepartment of Neurology and Neurosurgery, Riga East University Hospital, Riga, Latvia.
Viktorija ĶēniņaDepartment of Neurology, Pauls Stradiņš Clinical University Hospital, Riga, Latvia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMotor neuron diseases (MNDs), including amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), and spinal and bulbar muscular atrophy (SBMA), are rare, progressive neurodegenerative conditions. Although well-studied in Western Europe, no nationwide epidemiological data have been published from Latvia. This study aimed to assess the incidence, prevalence, and clinical characteristics of MNDs in the Latvian population.

methodsA retrospective, hospital-based analysis was performed using records from Pauls Stradiņš Clinical University Hospital, Riga East University Hospital, and the Children's Clinical University Hospital between January 2020 and December 2024. Patients were identified through relevant ICD-10 codes. Incidence and prevalence rates were calculated per 100,000 population and age-standardized to the 2013 European Standard Population.

resultsA total of 181 prevalent MND cases were identified: 131 with ALS or related phenotypes, 10 with adult-onset SMA, 33 with pediatric SMA, and 7 with SBMA. The age-standardized incidence of ALS was 1.22 per 100,000 person-years, and the prevalence was 4.69 per 100,000. Limb weakness or paresis was the most common initial symptom (48.1%). The mean diagnostic delay was 13.4 months for ALS, 43.8 months for PLS, 206.8 months for SBMA and 17.3 months for pediatric SMA. The prevalence of pediatric SMA was 9.91 per 100,000, with type II being the most frequent subtype. All SMA and SBMA cases were genetically confirmed.

conclusionThis first nationwide study of MNDs in Latvia highlights diagnostic delays and possible under-recognition of adult SMA and SBMA. Genetic testing, a national registry, and equitable therapy access should be prioritized.

Indexed as

Motor Neuron DiseaseAdolescentAdultAgedAged, 80 and overAmyotrophic Lateral SclerosisChildFemaleHumansIncidenceLatviaMaleMiddle AgedMuscular Atrophy, SpinalPrevalenceRetrospective Studiesamyotrophic lateral sclerosisepidemiologymotor neuron diseasespinal muscular atrophyX‐linked Bulbo‐spinal atrophy

Identifiers

PMID42538750
PMCPMC13428171

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