Evidence map›Paper›PMID 39329444›Full record

ArticleActa ophthalmologica2025

The incidence of visual impairment due to retinitis pigmentosa has declined in Finland over the last 40 years.

Paula Mosallaei, Petri Purola, Laura Tolkkinen, Mika Gissler, Hannu Uusitalo

Abstract readMulticenter Study
In one paragraph

Article in Acta ophthalmologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Frontiers in pharmacology · 2025
    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

5 authors.

Paula MosallaeiDepartment of Ophthalmology, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID https://orcid.org/0009-0004-1085-4154
Petri PurolaDepartment of Ophthalmology, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID https://orcid.org/0000-0001-5308-8622
Laura TolkkinenFinnish Register of Visual Impairment, Finnish Federation of the Visually Impaired, Helsinki, Finland.
Mika GisslerDepartment of Knowledge Brokers, Finnish Institute for Health and Welfare, Helsinki, Finland.
Hannu UusitaloDepartment of Ophthalmology, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

Funding

Lars Erik Lundbergs Stiftelse srStiftelsen Leo, Mary och Mary-Ann Hackman sr
6 · The paper itself

Abstract

purposeTo study the changes in incidence, age at onset and severity of visual impairment (VI) due to retinitis pigmentosa (RP) in the Years 1980-2019, and the incidence and age at diagnosis of hereditary retinal dystrophy (HRD) diagnoses coded by ICD10 H35.5 in the Years 1998-2019 in Finland.

methodsA total of 1606 persons with VI due to RP registered by the Finnish Register of Visual Impairment and total of 4291 HRD diagnoses registered by the Care Register of the Finnish Institute for Health and Welfare were included. VI was classified according to the Finnish national definitions derived from the WHO definitions. The significance of the changes in incidence and age at onset were tested with statistical tests (Kruskal-Wallis, Mann-Whitney U and Cochran-Armitage). Two-tailed p-value below 0.05 was considered significant.

resultsThe incidence of VI due to RP has decreased from 0.96/100 000 in the 1980s to 0.55/100 000 in the 2010s (p 0.004). The age at onset of VI has increased from 41.6 to 50.3 years. The severity of VI has not changed. The incidence of HRD diagnoses has decreased from 3.66/100 000 in the 2000s to 2.86/100 000 in the 2010s (p 0.024). The age at diagnosis has risen in male patients from 42.1 to 44.5 years (p 0.024).

conclusionThe VI caused by RP in Finland has decreased. It develops at an older age than in the past. We hypothesize that this trend may be attributed to informed decisions by visually impaired persons to refrain from having offspring to prevent the transmission of hereditary mutations. The severity of VI due to RP has remained relatively unchanged. The incidence of HRD diagnoses has decreased, and the diagnosis occurs at an older age among men.

Indexed as

RegistriesRetinitis PigmentosaVisual AcuityAdolescentAdultAgedAge DistributionAge of OnsetChildFemaleFinlandFollow-Up StudiesHumansIncidenceMaleMiddle Agedage at onsetincidenceinherited retinal dystrophyretinitis pigmentosavisual impairment

Identifiers

PMID39329444
PMCPMC11704851

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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.