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Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population
Objective: Metabolic syndrome (MetS) is a cluster of health problems that places individuals at higher risk of developing cardiovascular disease, diabetes and stroke. The prevalence of MetS is increasing worldwide. It is also well accepted that genetic and environmental factors play significant role...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803488/ https://www.ncbi.nlm.nih.gov/pubmed/33232281 http://dx.doi.org/10.18632/aging.104203 |
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author | Wang, Qiao Ren, Decheng Bi, Yan Yuan, Ruixue Li, Dong Wang, Jianying Wang, Ruirui Zhang, Lei He, Guang Liu, Baocheng |
author_facet | Wang, Qiao Ren, Decheng Bi, Yan Yuan, Ruixue Li, Dong Wang, Jianying Wang, Ruirui Zhang, Lei He, Guang Liu, Baocheng |
author_sort | Wang, Qiao |
collection | PubMed |
description | Objective: Metabolic syndrome (MetS) is a cluster of health problems that places individuals at higher risk of developing cardiovascular disease, diabetes and stroke. The prevalence of MetS is increasing worldwide. It is also well accepted that genetic and environmental factors play significant roles in the occurrence/development of MetS, but studies exploring genetic factors are still lacking. Here, we aimed to investigate the association of ADIPOQ gene variants with MetS in an elderly Chinese Han population. Results: We found that the allelic frequencies of rs6773957 and rs3774261 were significantly different between MetS and the control (p = 0.031; p = 0.049). Furthermore, a reduction in luciferase activity was observed when HEK293T cells were transfected with rs6773957 mutant fragments compared with wild type. Conclusion: Our results suggest that rs6773957 and rs3774261 of ADIPOQ were associated with MetS in the elderly Chinese Han population. The functional assays performed indicate that the rs6773957 variant might be pathogenic and may provide evidence for mechanistic studies of MetS in the future. Methods: Four single nucleotide polymorphisms (SNPs) were selected and genotyped (rs6773957, rs182052, rs3774261 and rs17366568) in 1337 subjects, including 569 healthy controls and 768 MetS cases. The clinical characteristics of all the subjects were obtained and analyzed. Additionally, a functional study of rs6773957 in regulating the expression of ADIPOQ was performed in this study. |
format | Online Article Text |
id | pubmed-7803488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-78034882021-01-15 Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population Wang, Qiao Ren, Decheng Bi, Yan Yuan, Ruixue Li, Dong Wang, Jianying Wang, Ruirui Zhang, Lei He, Guang Liu, Baocheng Aging (Albany NY) Research Paper Objective: Metabolic syndrome (MetS) is a cluster of health problems that places individuals at higher risk of developing cardiovascular disease, diabetes and stroke. The prevalence of MetS is increasing worldwide. It is also well accepted that genetic and environmental factors play significant roles in the occurrence/development of MetS, but studies exploring genetic factors are still lacking. Here, we aimed to investigate the association of ADIPOQ gene variants with MetS in an elderly Chinese Han population. Results: We found that the allelic frequencies of rs6773957 and rs3774261 were significantly different between MetS and the control (p = 0.031; p = 0.049). Furthermore, a reduction in luciferase activity was observed when HEK293T cells were transfected with rs6773957 mutant fragments compared with wild type. Conclusion: Our results suggest that rs6773957 and rs3774261 of ADIPOQ were associated with MetS in the elderly Chinese Han population. The functional assays performed indicate that the rs6773957 variant might be pathogenic and may provide evidence for mechanistic studies of MetS in the future. Methods: Four single nucleotide polymorphisms (SNPs) were selected and genotyped (rs6773957, rs182052, rs3774261 and rs17366568) in 1337 subjects, including 569 healthy controls and 768 MetS cases. The clinical characteristics of all the subjects were obtained and analyzed. Additionally, a functional study of rs6773957 in regulating the expression of ADIPOQ was performed in this study. Impact Journals 2020-11-20 /pmc/articles/PMC7803488/ /pubmed/33232281 http://dx.doi.org/10.18632/aging.104203 Text en Copyright: © 2020 Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wang, Qiao Ren, Decheng Bi, Yan Yuan, Ruixue Li, Dong Wang, Jianying Wang, Ruirui Zhang, Lei He, Guang Liu, Baocheng Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population |
title | Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population |
title_full | Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population |
title_fullStr | Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population |
title_full_unstemmed | Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population |
title_short | Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population |
title_sort | association and functional study between adipoq and metabolic syndrome in elderly chinese han population |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803488/ https://www.ncbi.nlm.nih.gov/pubmed/33232281 http://dx.doi.org/10.18632/aging.104203 |
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