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Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst

OBJECTIVE: The association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst was studied in this paper. METHODS: Eighty‐five patients diagnosed with intracranial arachnoid cysts by cerebral computed tomography scan were selected. Sixty‐three healthy...

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Autores principales: Li, Kai, Kong, De‐Sheng, Zhang, Jun, Wang, Xin‐Sheng, Ye, Xun, Zhao, Yuan‐Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908874/
https://www.ncbi.nlm.nih.gov/pubmed/31743616
http://dx.doi.org/10.1002/brb3.1480
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author Li, Kai
Kong, De‐Sheng
Zhang, Jun
Wang, Xin‐Sheng
Ye, Xun
Zhao, Yuan‐Li
author_facet Li, Kai
Kong, De‐Sheng
Zhang, Jun
Wang, Xin‐Sheng
Ye, Xun
Zhao, Yuan‐Li
author_sort Li, Kai
collection PubMed
description OBJECTIVE: The association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst was studied in this paper. METHODS: Eighty‐five patients diagnosed with intracranial arachnoid cysts by cerebral computed tomography scan were selected. Sixty‐three healthy volunteers for medical examination in hospitals served as controls. The cognition, depressive symptoms, and the likelihood of headache, dizziness, head trauma history, dementia, depression, and epilepsy were assessed. ELP4 genotypes and its allele frequency were determined by PCR, endonuclease restriction analysis, and gel electrophoresis. RESULTS: ELP4 rs986527 had three genotypes: TT, TC, and CC. The intracranial arachnoid cyst group showed no statistically significant difference in genotype frequencies compared with healthy controls. There was no significant correlation between ELP4 rs986527 polymorphism and location of intracranial arachnoid cyst. TC and C genotype frequencies were associated with a higher incidence of clinical symptoms than TT genotype frequencies, and C allele frequencies were associated with a significantly higher incidence of clinical symptoms compared with T allele frequencies. There was no significant difference in TNF‐α and IL‐1β levels between TT/TC/CC genotypes before treatment. After treatment, the levels of TNF‐α and IL‐1β were significantly decreased in different genotypes, and the decrease in CC was the greatest. The frequency of TT and TC genotypes was higher than that of CC genotypes. CONCLUSION: ELP4 rs986527 polymorphism affected the incidence of clinical symptoms and the levels of TNF‐α and IL‐1β in patients with intracranial arachnoid cysts.
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spelling pubmed-69088742019-12-20 Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst Li, Kai Kong, De‐Sheng Zhang, Jun Wang, Xin‐Sheng Ye, Xun Zhao, Yuan‐Li Brain Behav Original Research OBJECTIVE: The association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst was studied in this paper. METHODS: Eighty‐five patients diagnosed with intracranial arachnoid cysts by cerebral computed tomography scan were selected. Sixty‐three healthy volunteers for medical examination in hospitals served as controls. The cognition, depressive symptoms, and the likelihood of headache, dizziness, head trauma history, dementia, depression, and epilepsy were assessed. ELP4 genotypes and its allele frequency were determined by PCR, endonuclease restriction analysis, and gel electrophoresis. RESULTS: ELP4 rs986527 had three genotypes: TT, TC, and CC. The intracranial arachnoid cyst group showed no statistically significant difference in genotype frequencies compared with healthy controls. There was no significant correlation between ELP4 rs986527 polymorphism and location of intracranial arachnoid cyst. TC and C genotype frequencies were associated with a higher incidence of clinical symptoms than TT genotype frequencies, and C allele frequencies were associated with a significantly higher incidence of clinical symptoms compared with T allele frequencies. There was no significant difference in TNF‐α and IL‐1β levels between TT/TC/CC genotypes before treatment. After treatment, the levels of TNF‐α and IL‐1β were significantly decreased in different genotypes, and the decrease in CC was the greatest. The frequency of TT and TC genotypes was higher than that of CC genotypes. CONCLUSION: ELP4 rs986527 polymorphism affected the incidence of clinical symptoms and the levels of TNF‐α and IL‐1β in patients with intracranial arachnoid cysts. John Wiley and Sons Inc. 2019-11-19 /pmc/articles/PMC6908874/ /pubmed/31743616 http://dx.doi.org/10.1002/brb3.1480 Text en © 2019 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Li, Kai
Kong, De‐Sheng
Zhang, Jun
Wang, Xin‐Sheng
Ye, Xun
Zhao, Yuan‐Li
Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst
title Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst
title_full Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst
title_fullStr Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst
title_full_unstemmed Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst
title_short Association between ELP4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst
title_sort association between elp4 rs986527 polymorphism and the occurrence and development of intracranial arachnoid cyst
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908874/
https://www.ncbi.nlm.nih.gov/pubmed/31743616
http://dx.doi.org/10.1002/brb3.1480
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