Evidence map›Paper›PMID 27684406›Full record

ArticleHuman brain mapping2017

Altered whole-brain connectivity in albinism.

Thomas Welton, Sarim Ather, Frank A Proudlock, Irene Gottlob, Robert A Dineen

Open access · greenAbstract read
In one paragraph

Article in Human brain mapping, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Clinical spectrum of blunted foveal contour.Therapeutic advances in ophthalmology
    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 at 2 institutions in 1 country.

Thomas WeltonRadiological Sciences, Division of Clinical Neuroscience, University of Nottingham, Room W/B 1441, Queen's Medical Centre, Derby Road, Nottingham, NG7 2UH, United Kingdom.
Sarim AtherRadiological Sciences, Division of Clinical Neuroscience, University of Nottingham, Room W/B 1441, Queen's Medical Centre, Derby Road, Nottingham, NG7 2UH, United Kingdom.
Frank A ProudlockLeicester Royal Infirmary, Ulverscroft Eye Unit, Ophthalmology, University of Leicester, Knighton Street Offices, Leicester, LE2 7LX, United Kingdom.
Irene GottlobLeicester Royal Infirmary, Ulverscroft Eye Unit, Ophthalmology, University of Leicester, Knighton Street Offices, Leicester, LE2 7LX, United Kingdom.
Robert A DineenRadiological Sciences, Division of Clinical Neuroscience, University of Nottingham, Room W/B 1441, Queen's Medical Centre, Derby Road, Nottingham, NG7 2UH, United Kingdom.ORCID 0000-0002-9523-2546
University of Nottingham · GBUniversity of Leicester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Albinism is a group of congenital disorders of the melanin synthesis pathway. Multiple ocular, white matter and cortical abnormalities occur in albinism, including a greater decussation of nerve fibres at the optic chiasm, foveal hypoplasia and nystagmus. Despite this, visual perception is largely preserved. It was proposed that this may be attributable to reorganisation among cerebral networks, including an increased interhemispheric connectivity of the primary visual areas. A graph-theoretic model was applied to explore brain connectivity networks derived from resting-state functional and diffusion-tensor magnetic resonance imaging data in 23 people with albinism and 20 controls. They tested for group differences in connectivity between primary visual areas and in summary network organisation descriptors. Main findings were supplemented with analyses of control regions, brain volumes and white matter microstructure. Significant functional interhemispheric hyperconnectivity of the primary visual areas in the albinism group were found (P = 0.012). Tests of interhemispheric connectivity based on the diffusion-tensor data showed no significant group difference (P = 0.713). Second, it was found that a range of functional whole-brain network metrics were abnormal in people with albinism, including the clustering coefficient (P = 0.005), although this may have been driven partly by overall differences in connectivity, rather than reorganisation. Based on the results, it was suggested that changes occur in albinism at the whole-brain level, and not just within the visual processing pathways. It was proposed that their findings may reflect compensatory adaptations to increased chiasmic decussation, foveal hypoplasia and nystagmus. Hum Brain Mapp 38:740-752, 2017. © 2016 Wiley Periodicals, Inc.

Indexed as

Brain MappingAdolescentAdultAlbinismBrainDiffusion Magnetic Resonance ImagingFemaleHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleMiddle AgedNerve Fibers, MyelinatedNeural PathwaysOxygenSeverity of Illness IndexOxygenAlbinismbrain connectivitybrain networksdiffusion tensor imagingfunctional magnetic resonance imagingneuronal plasticityvision disordersvisual cortex

Identifiers

PMID27684406
PMCPMC6866891
OpenAlexW2528117929

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.