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ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery

BACKGROUND: Several studies have shown that ATP-binding cassette transporter A7 (ABCA7) gene variation is associated with cognitive impairment. This study was aimed to investigate the relationship between ABCA7 rs3764650 polymorphism and perioperative neurocognitive disorder (pNCD). METHODS: A total...

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Autores principales: Yu, Lu, Ji, Haiyan, Zhou, Minmin, Guo, Yaxin, Liu, Junfeng, Lei, Daoyun, Han, Chao, Ma, Tieliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977477/
https://www.ncbi.nlm.nih.gov/pubmed/35387413
http://dx.doi.org/10.2147/PGPM.S352810
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author Yu, Lu
Ji, Haiyan
Zhou, Minmin
Guo, Yaxin
Liu, Junfeng
Lei, Daoyun
Han, Chao
Ma, Tieliang
author_facet Yu, Lu
Ji, Haiyan
Zhou, Minmin
Guo, Yaxin
Liu, Junfeng
Lei, Daoyun
Han, Chao
Ma, Tieliang
author_sort Yu, Lu
collection PubMed
description BACKGROUND: Several studies have shown that ATP-binding cassette transporter A7 (ABCA7) gene variation is associated with cognitive impairment. This study was aimed to investigate the relationship between ABCA7 rs3764650 polymorphism and perioperative neurocognitive disorder (pNCD). METHODS: A total of 132 elderly patients aged 65 and over who underwent elective non-cardiac surgery were enrolled in the study, while 28 healthy volunteers matching age and sex were recruited as the control group. A battery of neuropsychological tests was conducted 1 day before, 7 days, and 3 months after surgeries. Delayed neurocognitive recovery (dNCR) and postoperative mild or major neurocognitive disorder (POCD) were determined using the Z value method. The venous blood sample of the surgical patients was taken before the operation. Genotyping of rs3764650 was performed using polymerase chain reaction amplification and restriction fragment length polymorphism analysis. RESULTS: The incidences of dNCR and POCD were 29.7% and 16.8% at 7 days and 3 months after surgery, respectively. The G allele frequency and GG frequency of dNCR patients were significantly higher than that of non-dNCR patients (43.3% vs 28.2%, P=0.035; 23.3% vs 4.2%, P=0.013, respectively) at 7 days following surgery. No significant differences in ABCA7 alleles between POCD and non-POCD patients were observed 3 months postoperatively. CONCLUSION: ABCA7 rs3764650 gene polymorphism is associated with dNCR and GG genotype might be a predisposing factor for postoperative cognitive impairment in Chinese Han elderly populations.
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spelling pubmed-89774772022-04-05 ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery Yu, Lu Ji, Haiyan Zhou, Minmin Guo, Yaxin Liu, Junfeng Lei, Daoyun Han, Chao Ma, Tieliang Pharmgenomics Pers Med Original Research BACKGROUND: Several studies have shown that ATP-binding cassette transporter A7 (ABCA7) gene variation is associated with cognitive impairment. This study was aimed to investigate the relationship between ABCA7 rs3764650 polymorphism and perioperative neurocognitive disorder (pNCD). METHODS: A total of 132 elderly patients aged 65 and over who underwent elective non-cardiac surgery were enrolled in the study, while 28 healthy volunteers matching age and sex were recruited as the control group. A battery of neuropsychological tests was conducted 1 day before, 7 days, and 3 months after surgeries. Delayed neurocognitive recovery (dNCR) and postoperative mild or major neurocognitive disorder (POCD) were determined using the Z value method. The venous blood sample of the surgical patients was taken before the operation. Genotyping of rs3764650 was performed using polymerase chain reaction amplification and restriction fragment length polymorphism analysis. RESULTS: The incidences of dNCR and POCD were 29.7% and 16.8% at 7 days and 3 months after surgery, respectively. The G allele frequency and GG frequency of dNCR patients were significantly higher than that of non-dNCR patients (43.3% vs 28.2%, P=0.035; 23.3% vs 4.2%, P=0.013, respectively) at 7 days following surgery. No significant differences in ABCA7 alleles between POCD and non-POCD patients were observed 3 months postoperatively. CONCLUSION: ABCA7 rs3764650 gene polymorphism is associated with dNCR and GG genotype might be a predisposing factor for postoperative cognitive impairment in Chinese Han elderly populations. Dove 2022-03-30 /pmc/articles/PMC8977477/ /pubmed/35387413 http://dx.doi.org/10.2147/PGPM.S352810 Text en © 2022 Yu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Yu, Lu
Ji, Haiyan
Zhou, Minmin
Guo, Yaxin
Liu, Junfeng
Lei, Daoyun
Han, Chao
Ma, Tieliang
ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery
title ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery
title_full ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery
title_fullStr ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery
title_full_unstemmed ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery
title_short ABCA7 rs3764650 Polymorphism is Associated with Delayed Neurocognitive Recovery
title_sort abca7 rs3764650 polymorphism is associated with delayed neurocognitive recovery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977477/
https://www.ncbi.nlm.nih.gov/pubmed/35387413
http://dx.doi.org/10.2147/PGPM.S352810
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