Evidence map›Paper›PMID 35322936›Full record

ArticleActa ophthalmologica2022

Heritability of retinal drusen in the Copenhagen Twin Cohort Eye Study.

Mohamed Belmouhand, Simon Paul Rothenbuehler, Jacob B Hjelmborg, Sami Dabbah, Jakob Bjerager, Birgit Agnes Sander, Christine Dalgård, Michael Larsen

Open access · hybridAbstract readTwin Study
In one paragraph

Article in Acta ophthalmologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 2 countries.

Mohamed BelmouhandDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID https://orcid.org/0000-0001-5855-4733
Simon Paul RothenbuehlerDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID https://orcid.org/0000-0002-5223-6483
Jacob B HjelmborgEpidemiology, Biostatistics and Biodemography, Department of Public Health, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0001-9630-9149
Sami DabbahDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID https://orcid.org/0000-0003-4061-9361
Jakob BjeragerDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID https://orcid.org/0000-0002-6620-6242
Birgit Agnes SanderDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.
Christine DalgårdThe Danish Twin Research Center, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0001-8184-3429
Michael LarsenDepartment of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Glostrup, Denmark.ORCID https://orcid.org/0000-0002-5172-5891
Glostrup Hospital · DKUniversity of Copenhagen · DKUniversity of Southern Denmark · DKOdense University Hospital · DK

Funding

Aase og Ejnar Danielsens Fond 18-10-0698Alfred-Vogt FoundationBeckett-Fonden 19-2-3490Einar Willumsen Foundation 500028H2020 European Research Council 780989Helsefonden 19-B-0063OPUS FoundationP. Carl Petersens Fond 19102Rigshospitalet E-23334-02VELUX Foundation 00028975
6 · The paper itself

Abstract

purposeTo study age- and sex-adjusted heritability of small hard drusen and early age-related macular degeneration (AMD) in a population-based twin cohort.

methodsThis was a single-centre, cross-sectional, classical twin study with ophthalmic examination including refraction, biometry, best-corrected visual acuity assessment, colour and autofluorescence fundus photography, and fundus optical coherence tomography. Grading and categorization of drusen was by diameter and location.

resultsThe study enrolled 176 same-sex pairs of twins of mean (SD) age 58.6 (9.9) years. The prevalence of the four phenotypes ≥20 small hard macular drusen (largest diameter < 63 μm), ≥20 small hard extramacular drusen, intermediate drusen (63-125 μm) anywhere, and large drusen (>125 μm) anywhere was 12.4%, 36.4%, 5.8%, and 8.4%, respectively, and the respective heritabilities, adjusted for age and sex, were 78.2% [73.5-82.9], 69.1% [62.3-75.9], 30.1% [4.1-56.1], and 65.6% [26.4-100]. Age trajectory analysis supported a gradual transition to larger numbers of small hard drusen with increasing age. The heritability of ≥20 small hard drusen was markedly lower than the 99% found in the 40% overlapping twin cohort that was seen 20 years earlier.

conclusionNumerous (≥20) small hard drusen and larger drusen that fit the definition of dry AMD were highly heritable. Small hard drusen counts increased with age. Decreasing heritability with increasing age suggests that the impact of behavioural and environmental factors on the development of small hard drusen increases with age.

Indexed as

Geographic AtrophyMacular DegenerationRetinal DrusenCross-Sectional StudiesHumansTomography, Optical CoherenceTwins, MonozygoticCopenhagen Twin Cohort Eye Studydrusenheritabilitysmall hard drusentwins

Identifiers

PMID35322936
PMCPMC9790204
OpenAlexW4221098626

What OpenQuestion holds

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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.