Evidence map›Paper›PMID 35455059›Full record

ArticleLife (Basel, Switzerland)2022

Microvascular and Morphologic Changes of the Macula over Lifetime.

Mael Lever, Ying Chen, Moritz Glaser, Jan Darius Unterlauft, Claudia Lommatzsch, Nikolaos E Bechrakis, Michael R R Böhm

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Diabetic Retinopathy (DR) nomogram construction based on optical coherence tomography angiography parameters: a preliminary exploration of DR prediction.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2025
    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

7 authors.

Mael LeverDepartment of Ophthalmology, University Hospital Essen, 45147 Essen, Germany.ORCID 0000-0002-3244-6782
Ying ChenDepartment of Ophthalmology, University Hospital Essen, 45147 Essen, Germany.
Moritz GlaserAchim Wessing Institute for Imaging in Ophthalmology, University Hospital Essen, 45147 Essen, Germany.
Jan Darius UnterlauftDepartment of Ophthalmology, University Hospital of Ophthalmology, Inselspital, 3010 Bern, Switzerland.
Claudia LommatzschAchim Wessing Institute for Imaging in Ophthalmology, University Hospital Essen, 45147 Essen, Germany.
Nikolaos E BechrakisDepartment of Ophthalmology, University Hospital Essen, 45147 Essen, Germany.
Michael R R BöhmDepartment of Ophthalmology, University Hospital Essen, 45147 Essen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In ocular, neurologic, and cardiovascular diseases, macular segmentation data from spectral-domain optical coherence tomography (SD-OCT) provide morphologic, and OCT-angiography (OCTA) results give microvascular information about the macula. Age was shown to influence both methods' measurements. To further characterize this association, macular SD-OCT and OCTA changes were investigated in a population of juvenile, adult, and older individuals. Macular segment thickness and superficial (SCP) and deep plexus (DCP) vascular density (VD) of 157 healthy individuals aged 10-79 years were analyzed retrospectively. One-way analysis of variance (ANOVA) was used to compare age groups. The association between macular segmentation and OCTA parameters and between these and age was evaluated using linear regression. ANOVA and linear regression analysis showed a thickness decrease in the whole macular and in the ganglion cell and inner plexiform layers with age. While the foveal avascular zone area remained constant between age groups, VD of the SCP and DCP also decreased with age. In multiple linear regression, SCP and DCP VD were associated with inner macular segment thickness in an age-independent way. To conclude, the age-related microvascular and morphological changes in the macula described in this study can contribute to improving the understanding of macular aging processes and better interpreting OCT(A) results in healthy individuals and patients suffering from various retinal diseases.

Indexed as

agingblood flowcapillary densitymaculamacular segmentationoptical coherence tomography-angiographyvascular disease

Identifiers

PMID35455059
PMCPMC9024868

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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.