Evidence map›Paper›PMID 27231702›Full record

ArticleAnnals of clinical and translational neurology2016

PAX6, brain structure and function in human adults: advanced MRI in aniridia.

Mahinda Yogarajah, Mar Matarin, Christian Vollmar, Pamela J Thompson, John S Duncan, Mark Symms, Anthony T Moore, Joan Liu, Maria Thom, Veronica van Heyningen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Review
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  16. Article
  17. Review
  18. Epistasis between Pax6Gene therapy · 2018
    Article
  19. Article
  20. 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

11 authors at 3 institutions in 1 country.

Mahinda YogarajahDepartment of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom; Present address: St George's University Hospitals NHS Foundation Trust London United Kingdom.
Mar MatarinDepartment of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom.
Christian VollmarDepartment of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom.
Pamela J ThompsonDepartment of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom.
John S DuncanDepartment of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom.
Mark SymmsDepartment of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom.
Anthony T MooreUCL Institute of Ophthalmology and Moorfields Eye Hospital London United Kingdom; Present address: Department of Ophthalmology University of California San Francisco California.
Joan LiuDivision of Neuropathology UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London United Kingdom.
Maria ThomDivision of Neuropathology UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London United Kingdom.
Veronica van HeyningenMRC Human Genetics UnitI GMM University of Edinburgh Crewe Road Edinburgh EH4 2XU United Kingdom; Present address: UCL Institute of Ophthalmology London United Kingdom.ORCID 0000-0003-0359-0141
Sanjay M SisodiyaDepartment of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom; Epilepsy Society Chalfont-St-Peter Bucks SL9 0RJ United Kingdom.
National Hospital for Neurology and Neurosurgery · GBInstitute of Genetics and Cancer · GBMoorfields Eye Hospital NHS Foundation Trust · GB

Funding

Medical Research Council MC_PC_U127527199Medical Research Council MC_U127527199Medical Research Council MR/J01270X/1
6 · The paper itself

Abstract

objectivePAX6 is a pleiotropic transcription factor essential for the development of several tissues including the eyes, central nervous system, and some endocrine glands. Recently it has also been shown to be important for the maintenance and functioning of corneal and pancreatic tissues in adults. We hypothesized that PAX6 is important for the maintenance of brain integrity in humans, and that adult heterozygotes may have abnormalities of cortical patterning analogous to those found in mouse models.

methodsWe used advanced magnetic resonance imaging techniques, including surface-based morphometry and region-of-interest analysis in adult humans heterozygously mutated for PAX6 mutations (n = 19 subjects and n = 21 controls). Using immunohistochemistry, we also studied PAX6 expression in the adult brain tissue of healthy subjects (n = 4) and patients with epilepsy (n = 42), some of whom had focal injuries due to intracranial electrode track placement (n = 17).

resultsThere were significant reductions in frontoparietal cortical area after correcting for age and intracranial volume. A greater decline in thickness of the frontoparietal cortex with age, in subjects with PAX6 mutations compared to controls, correlated with age-corrected, accelerated decline in working memory. These results also demonstrate genotypic effects: those subjects with the most severe genotypes have the most widespread differences compared with controls. We also demonstrated significant increases in PAX6-expressing cells in response to acute injury in the adult human brain.

interpretationThese findings suggest a role for PAX6 in the maintenance and consequent functioning of the adult brain, homologous to that found in other tissues. This has significant implications for the understanding and treatment of neurodegenerative diseases.

Identifiers

PMID27231702
PMCPMC4863745
OpenAlexW2337288008

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.