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Detrimental effects of hypercortisolism on brain structure and related risk factors

Brain structural abnormalities are often observed on magnetic resonance imaging (MRI) scans of Cushing's syndrome patients, but the pathogenesis is not fully understood. To understand the relationship between brain structural abnormalities and potential risk factors in active Cushing's dis...

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Autores principales: Chen, Yaxi, Zhang, Junhuai, Tan, Huiwen, Li, Jiaqi, Yu, Yerong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391644/
https://www.ncbi.nlm.nih.gov/pubmed/32728036
http://dx.doi.org/10.1038/s41598-020-68166-0
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author Chen, Yaxi
Zhang, Junhuai
Tan, Huiwen
Li, Jiaqi
Yu, Yerong
author_facet Chen, Yaxi
Zhang, Junhuai
Tan, Huiwen
Li, Jiaqi
Yu, Yerong
author_sort Chen, Yaxi
collection PubMed
description Brain structural abnormalities are often observed on magnetic resonance imaging (MRI) scans of Cushing's syndrome patients, but the pathogenesis is not fully understood. To understand the relationship between brain structural abnormalities and potential risk factors in active Cushing's disease (CD) patients, a total of 101 treatment-naïve CD patients and 95 sex-, age- and education matched controls with non-functioning adenomas (NFA) underwent clinical evaluation and MRI investigation, and the relative risk factors were analyzed. 14 patients in sustained remission after transsphenoidal surgery were followed. Compared with the NFA subjects, the patients with CD had more cortical (P < 0.01) and subcortical atrophy (P < 0.01) and a higher prevalence of white matter hyperintensity (WMH) (P < 0.01). WMH severity in CD patients positively correlated with age (r = 0.532, P = 0.000), disease course (r = 0.257, P = 0.009), postprandial glucose (r = 0.278, P = 0.005), frequency of left ventricular hypertrophy (r = 0.398, P = 0.001) and hypothyroidism (r = 0.246, P = 0.014). The markers of cortical and subcortical atrophy (sylvian fissure ratio, bifrontal ratio, bicaudate ratio and third ventricle width) were positively associated with the progression of WMH in the CD patients. In the follow-up of 14 patients with CD, brain atrophy and WMH was partially reversible after correction of hypercortisolism. In conclusions, brain atrophy and WMH were more likely to appear in CD patients and were possibly partially reversible following correction of hypercortisolism.
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spelling pubmed-73916442020-07-31 Detrimental effects of hypercortisolism on brain structure and related risk factors Chen, Yaxi Zhang, Junhuai Tan, Huiwen Li, Jiaqi Yu, Yerong Sci Rep Article Brain structural abnormalities are often observed on magnetic resonance imaging (MRI) scans of Cushing's syndrome patients, but the pathogenesis is not fully understood. To understand the relationship between brain structural abnormalities and potential risk factors in active Cushing's disease (CD) patients, a total of 101 treatment-naïve CD patients and 95 sex-, age- and education matched controls with non-functioning adenomas (NFA) underwent clinical evaluation and MRI investigation, and the relative risk factors were analyzed. 14 patients in sustained remission after transsphenoidal surgery were followed. Compared with the NFA subjects, the patients with CD had more cortical (P < 0.01) and subcortical atrophy (P < 0.01) and a higher prevalence of white matter hyperintensity (WMH) (P < 0.01). WMH severity in CD patients positively correlated with age (r = 0.532, P = 0.000), disease course (r = 0.257, P = 0.009), postprandial glucose (r = 0.278, P = 0.005), frequency of left ventricular hypertrophy (r = 0.398, P = 0.001) and hypothyroidism (r = 0.246, P = 0.014). The markers of cortical and subcortical atrophy (sylvian fissure ratio, bifrontal ratio, bicaudate ratio and third ventricle width) were positively associated with the progression of WMH in the CD patients. In the follow-up of 14 patients with CD, brain atrophy and WMH was partially reversible after correction of hypercortisolism. In conclusions, brain atrophy and WMH were more likely to appear in CD patients and were possibly partially reversible following correction of hypercortisolism. Nature Publishing Group UK 2020-07-29 /pmc/articles/PMC7391644/ /pubmed/32728036 http://dx.doi.org/10.1038/s41598-020-68166-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chen, Yaxi
Zhang, Junhuai
Tan, Huiwen
Li, Jiaqi
Yu, Yerong
Detrimental effects of hypercortisolism on brain structure and related risk factors
title Detrimental effects of hypercortisolism on brain structure and related risk factors
title_full Detrimental effects of hypercortisolism on brain structure and related risk factors
title_fullStr Detrimental effects of hypercortisolism on brain structure and related risk factors
title_full_unstemmed Detrimental effects of hypercortisolism on brain structure and related risk factors
title_short Detrimental effects of hypercortisolism on brain structure and related risk factors
title_sort detrimental effects of hypercortisolism on brain structure and related risk factors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391644/
https://www.ncbi.nlm.nih.gov/pubmed/32728036
http://dx.doi.org/10.1038/s41598-020-68166-0
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