2014
DOI: 10.1186/s12881-014-0112-7
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Genetic polymorphisms at SIRT1 and FOXO1 are associated with carotid atherosclerosis in the SAPHIR cohort

Abstract: BackgroundSIRT1 and FOXO1 interact with each other in multiple pathways regulating aging, metabolism and resistance to oxidative stress and control different pathways involved in atherosclerotic process. It is not known, if genetic polymorphisms (SNPs) at the SIRT1 and FOXO1 have an influence on carotid atherosclerosis.MethodsIntima-media thickness (IMT) was measured on the common and internal carotid arteries. Morphological alterations of the carotid arteries and size of these alterations were included in the… Show more

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Cited by 50 publications
(40 citation statements)
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“…Therefore, further studies are needed to Although SIRT1 is expressed in all trophoblast layers of the placenta and is important for proper trophoblast differentiation and placental development [43], the relationship between LPS-associated placental inflammation and SIRT1 expression has not been studied previously. Recent studies showed that single nucleotide polymorphisms (SNPs) in the SIRT1 gene are associated with carotid atherosclerosis, major depressive disorder, age-related macular degeneration, and severe obesity [44][45][46][47]. However, it is not known whether SNPs in the SIRT1 gene have an influence on the NLRP3 inflammasome-mediated inflammatory diseases.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, further studies are needed to Although SIRT1 is expressed in all trophoblast layers of the placenta and is important for proper trophoblast differentiation and placental development [43], the relationship between LPS-associated placental inflammation and SIRT1 expression has not been studied previously. Recent studies showed that single nucleotide polymorphisms (SNPs) in the SIRT1 gene are associated with carotid atherosclerosis, major depressive disorder, age-related macular degeneration, and severe obesity [44][45][46][47]. However, it is not known whether SNPs in the SIRT1 gene have an influence on the NLRP3 inflammasome-mediated inflammatory diseases.…”
Section: Discussionmentioning
confidence: 99%
“…SIRT1 promotes the protein complex formation between LKB1 and HECT and the RLD domain containing E3 ubiquitin-protein ligase 2 (HERC2) which leads to LKB1 degradation [44]. In clinical studies, the genetic variations of SIRT1 have been reported to be correlated to intimal-medial thickening in human carotid arteries, suggesting that endothelial SIRT1 is important in regulating arterial remodelling [45].…”
Section: Improvement Of Endothelial Functionmentioning
confidence: 99%
“…Recently, Sirt1‐mediated autophagy was proved to be one of the mechanisms for metformin treatment of hepatic steatosis . Moreover, genetic polymorphisms at SIRT1 and FOXO1 have been proved to be associated with carotid atherosclerosis, highlighting the need for functional investigation of Sirt1 in atherosclerosis . Further studies using animal models are needed to elucidate a detailed mechanism by which Sirt1 dysfunction‐induced inflammation through dysregulation of autophagy in monocytes/macrophages causes insulin resistance and atherosclerosis.…”
Section: Sirt1 Recently Emerges As a Regulator In Immune Regulationmentioning
confidence: 99%