Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved]
Background: Aniridia is a disorder predominately caused by heterozygous loss-of-function mutations of the PAX6 gene, which is a transcriptional regulator necessary for normal eye and brain development. The ocular abnormalities of aniridia have been well characterized, but mounting evidence has impl...
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doaj-9c3e5357a6c1448b8dda58ceb7399b152020-11-25T03:35:34ZengF1000 Research LtdF1000Research2046-14022017-09-01610.12688/f1000research.11063.213553Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved]Madison K. Grant0Anastasia M. Bobilev1Jordan E. Pierce2Jon DeWitte3James D. Lauderdale4Department of Cellular Biology, University of Georgia, Athens, GA, 30602, USANeuroscience Division of the Biomedical and Health Sciences Institute, University of Georgia, Athens, GA, 30602, USADepartment of Psychology, University of Georgia, Athens, GA, 30602, USAAthens Radiology Associates, Athens, GA, 30604, USANeuroscience Division of the Biomedical and Health Sciences Institute, University of Georgia, Athens, GA, 30602, USABackground: Aniridia is a disorder predominately caused by heterozygous loss-of-function mutations of the PAX6 gene, which is a transcriptional regulator necessary for normal eye and brain development. The ocular abnormalities of aniridia have been well characterized, but mounting evidence has implicated brain-related phenotypes as a prominent feature of this disorder as well. Investigations using neuroimaging in aniridia patients have shown reductions in discrete brain structures and changes in global grey and white matter. However, limited sample sizes and substantive heterogeneity of structural phenotypes in the brain remain a challenge. Methods: Here, we examined brain structure in a new population sample in an effort to add to the collective understanding of anatomical abnormalities in aniridia. The current study used 3T magnetic resonance imaging to acquire high-resolution structural data in 12 persons with aniridia and 12 healthy demographically matched comparison subjects. Results: We examined five major structures: the anterior commissure, the posterior commissure, the pineal gland, the corpus callosum, and the optic chiasm. The most consistent reductions were found in the anterior commissure and the pineal gland; however, abnormalities in all of the other structures examined were present in at least one individual. Conclusions: Our results indicate that the anatomical abnormalities in aniridia are variable and largely individual-specific. These findings suggest that future studies investigate this heterogeneity further, and that normal population variation should be considered when evaluating structural abnormalities.https://f1000research.com/articles/6-255/v2Corneal & External DisordersNeuroimaging |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Madison K. Grant Anastasia M. Bobilev Jordan E. Pierce Jon DeWitte James D. Lauderdale |
spellingShingle |
Madison K. Grant Anastasia M. Bobilev Jordan E. Pierce Jon DeWitte James D. Lauderdale Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved] F1000Research Corneal & External Disorders Neuroimaging |
author_facet |
Madison K. Grant Anastasia M. Bobilev Jordan E. Pierce Jon DeWitte James D. Lauderdale |
author_sort |
Madison K. Grant |
title |
Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved] |
title_short |
Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved] |
title_full |
Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved] |
title_fullStr |
Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved] |
title_full_unstemmed |
Structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved] |
title_sort |
structural brain abnormalities in 12 persons with aniridia [version 2; referees: 2 approved] |
publisher |
F1000 Research Ltd |
series |
F1000Research |
issn |
2046-1402 |
publishDate |
2017-09-01 |
description |
Background: Aniridia is a disorder predominately caused by heterozygous loss-of-function mutations of the PAX6 gene, which is a transcriptional regulator necessary for normal eye and brain development. The ocular abnormalities of aniridia have been well characterized, but mounting evidence has implicated brain-related phenotypes as a prominent feature of this disorder as well. Investigations using neuroimaging in aniridia patients have shown reductions in discrete brain structures and changes in global grey and white matter. However, limited sample sizes and substantive heterogeneity of structural phenotypes in the brain remain a challenge. Methods: Here, we examined brain structure in a new population sample in an effort to add to the collective understanding of anatomical abnormalities in aniridia. The current study used 3T magnetic resonance imaging to acquire high-resolution structural data in 12 persons with aniridia and 12 healthy demographically matched comparison subjects. Results: We examined five major structures: the anterior commissure, the posterior commissure, the pineal gland, the corpus callosum, and the optic chiasm. The most consistent reductions were found in the anterior commissure and the pineal gland; however, abnormalities in all of the other structures examined were present in at least one individual. Conclusions: Our results indicate that the anatomical abnormalities in aniridia are variable and largely individual-specific. These findings suggest that future studies investigate this heterogeneity further, and that normal population variation should be considered when evaluating structural abnormalities. |
topic |
Corneal & External Disorders Neuroimaging |
url |
https://f1000research.com/articles/6-255/v2 |
work_keys_str_mv |
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