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Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese

INTRODUCTION: Adenosine 5’-monophosphate (AMP)-activated protein kinase (AMPK) can influence energy metabolism. Energy metabolism imbalance is closely associated with the occurrence of neuropathic pain (NeP). Rs10789038 and rs2796498 are genetic polymorphisms of PRKAA2, the gene encoding AMPK, which...

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Autores principales: Mei, Yang, Mu, Yang, Wang, Win, Tan, Bo-Tao, Chen, Yao-Hua, Li, Yu-Ping, Zhu, Dan, Li, Wei, Cui, Jian, Yu, Le-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595063/
https://www.ncbi.nlm.nih.gov/pubmed/36304487
http://dx.doi.org/10.2147/JPR.S385913
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author Mei, Yang
Mu, Yang
Wang, Win
Tan, Bo-Tao
Chen, Yao-Hua
Li, Yu-Ping
Zhu, Dan
Li, Wei
Cui, Jian
Yu, Le-Hua
author_facet Mei, Yang
Mu, Yang
Wang, Win
Tan, Bo-Tao
Chen, Yao-Hua
Li, Yu-Ping
Zhu, Dan
Li, Wei
Cui, Jian
Yu, Le-Hua
author_sort Mei, Yang
collection PubMed
description INTRODUCTION: Adenosine 5’-monophosphate (AMP)-activated protein kinase (AMPK) can influence energy metabolism. Energy metabolism imbalance is closely associated with the occurrence of neuropathic pain (NeP). Rs10789038 and rs2796498 are genetic polymorphisms of PRKAA2, the gene encoding AMPK, which is closely related to energy metabolism imbalance. This study aimed to explore the relationship between PRKAA2 and postherpetic neuralgia (PHN) in the southwestern Chinese Han population. METHODS: This study enrolled 132 PHN patients and 118 healthy subjects. The rs10789038 and rs2796498 PRKAA2 genotypes were identified in all participants. The association between these single nucleotide polymorphisms and PHN susceptibility was evaluated in the dominant and recessive models. Haplotype analysis of patients with PHN and healthy controls was performed. RESULTS: The PHN patients were older than the healthy subjects (P < 0.05); however, the other clinical characteristics between two groups were not significantly different (all P >0.05). Genotypes and allele frequencies differed significantly between PHN patients and healthy subjects in the rs10789038 polymorphism (P < 0.05), but not in rs2796498 (P > 0.05). In addition, the GG haplotype of rs10789038-rs2796498 correlated negatively with PHN occurrence in haplotype analysis (P < 0.05). CONCLUSION: PHN occurrence may be related to the PRKAA2 rs10789038 A>G genetic polymorphism in the southwestern Chinese Han population.
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spelling pubmed-95950632022-10-26 Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese Mei, Yang Mu, Yang Wang, Win Tan, Bo-Tao Chen, Yao-Hua Li, Yu-Ping Zhu, Dan Li, Wei Cui, Jian Yu, Le-Hua J Pain Res Original Research INTRODUCTION: Adenosine 5’-monophosphate (AMP)-activated protein kinase (AMPK) can influence energy metabolism. Energy metabolism imbalance is closely associated with the occurrence of neuropathic pain (NeP). Rs10789038 and rs2796498 are genetic polymorphisms of PRKAA2, the gene encoding AMPK, which is closely related to energy metabolism imbalance. This study aimed to explore the relationship between PRKAA2 and postherpetic neuralgia (PHN) in the southwestern Chinese Han population. METHODS: This study enrolled 132 PHN patients and 118 healthy subjects. The rs10789038 and rs2796498 PRKAA2 genotypes were identified in all participants. The association between these single nucleotide polymorphisms and PHN susceptibility was evaluated in the dominant and recessive models. Haplotype analysis of patients with PHN and healthy controls was performed. RESULTS: The PHN patients were older than the healthy subjects (P < 0.05); however, the other clinical characteristics between two groups were not significantly different (all P >0.05). Genotypes and allele frequencies differed significantly between PHN patients and healthy subjects in the rs10789038 polymorphism (P < 0.05), but not in rs2796498 (P > 0.05). In addition, the GG haplotype of rs10789038-rs2796498 correlated negatively with PHN occurrence in haplotype analysis (P < 0.05). CONCLUSION: PHN occurrence may be related to the PRKAA2 rs10789038 A>G genetic polymorphism in the southwestern Chinese Han population. Dove 2022-10-21 /pmc/articles/PMC9595063/ /pubmed/36304487 http://dx.doi.org/10.2147/JPR.S385913 Text en © 2022 Mei 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
Mei, Yang
Mu, Yang
Wang, Win
Tan, Bo-Tao
Chen, Yao-Hua
Li, Yu-Ping
Zhu, Dan
Li, Wei
Cui, Jian
Yu, Le-Hua
Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese
title Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese
title_full Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese
title_fullStr Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese
title_full_unstemmed Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese
title_short Effect of AMPK Subunit Alpha 2 Polymorphisms on Postherpetic Pain Susceptibility in Southwestern Han Chinese
title_sort effect of ampk subunit alpha 2 polymorphisms on postherpetic pain susceptibility in southwestern han chinese
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595063/
https://www.ncbi.nlm.nih.gov/pubmed/36304487
http://dx.doi.org/10.2147/JPR.S385913
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