Evidence map›Paper›PMID 36548342›Full record

ArticlePloS one2022

Small hard drusen and associated factors in early seniority.

Mohamed Belmouhand, Simon P Rothenbuehler, Sami Dabbah, Jakob Bjerager, Birgit Sander, Jacob B Hjelmborg, Christine Dalgård, Rasmus Jensen, Michael Larsen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. 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
0.8field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Cuticular drusen in Asian neovascular age-related macular degeneration: Clinical features and polypoidal choroidal vasculopathy association.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Article
  2. Article
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

9 authors at 3 institutions in 2 countries.

Mohamed BelmouhandDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID 0000-0001-5855-4733
Simon P RothenbuehlerDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.
Sami DabbahDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID 0000-0003-4061-9361
Jakob BjeragerDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID 0000-0002-6620-6242
Birgit SanderDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.
Jacob B HjelmborgEpidemiology, Biostatistics and Biodemography, Department of Public Health, University of Southern Denmark, Odense, Denmark.
Christine DalgårdDanish Twin Research Center, University of Southern Denmark, Odense, Denmark.ORCID 0000-0001-8184-3429
Rasmus JensenEpidemiology, Biostatistics and Biodemography, Department of Public Health, University of Southern Denmark, Odense, Denmark.
Michael LarsenDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID 0000-0002-5172-5891
Glostrup Hospital · DKUniversity of Southern Denmark · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purpose of this study was to examine the ocular and systemic risk profile of the fundus phenotype ≥ 20 small hard (macular) drusen (< 63 μm in diameter).

methodsThis single-center, cross-sectional study of 176 same-sex twin pairs aged 30 to 80 (median 60) years was a component of a framework study of the transition from not having age-related macular degeneration to having early AMD. Drusen categories assessed using fundus photography and optical coherence tomography included small hard drusen (diameter < 63 μm), intermediate soft drusen (63-125 μm), and large soft drusen (> 125 μm), of which the soft drusen are compatible with a diagnosis of AMD.

resultsHaving ≥ 20 small hard drusen within or outside the macula was associated with increasing age, lower body mass index, shorter axial length, hyperopia, female sex, increasing high-density lipoprotein (HDL), high alcohol consumption, and with the presence of soft drusen.

conclusionsHaving ≥ 20 small hard drusen was associated with some AMD-related risk factors, but not with smoking, increasing body mass index, and higher blood pressure. Having ≥ 20 small hard drusen was also associated with soft drusen, in agreement with previous studies. These findings suggest that small hard drusen are not an early manifestation of AMD but the product of a distinct process of tissue alteration that promotes the development of AMD or some subtype thereof.

Indexed as

Macular DegenerationRetinal DrusenCross-Sectional StudiesFemaleHumansRetinaRisk FactorsTomography, Optical Coherence

Identifiers

PMID36548342
PMCPMC9778563
OpenAlexW4312090054

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.