• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

血清对氧磷酶活性水平低是代谢综合征的特征之一,并且可能影响与代谢综合征相关的冠状动脉疾病风险。

Low levels of serum paraoxonase activities are characteristic of metabolic syndrome and may influence the metabolic-syndrome-related risk of coronary artery disease.

作者信息

Martinelli Nicola, Micaglio Roberta, Consoli Letizia, Guarini Patrizia, Grison Elisa, Pizzolo Francesca, Friso Simonetta, Trabetti Elisabetta, Pignatti Pier Franco, Corrocher Roberto, Olivieri Oliviero, Girelli Domenico

机构信息

Department of Medicine, University of Verona, Policlinico G.B. Rossi, Italy.

出版信息

Exp Diabetes Res. 2012;2012:231502. doi: 10.1155/2012/231502. Epub 2011 Sep 22.

DOI:10.1155/2012/231502
PMID:21960992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3179885/
Abstract

Low concentrations of plasma high-density lipoprotein (HDLs) are characteristic in metabolic syndrome (MS). The antioxidant ability of HDLs is, at least in part, attributable to pleiotropic serum paraoxonase (PON1). Different PON1 activities have been assessed in 293 subjects with (n = 88) or without MS (n = 205) and with (n = 195) or without (n = 98) angiographically proven coronary artery disease (CAD). MS subjects had low PON1 activities, with a progressively decreasing trend by increasing the number of MS abnormalities. The activity versus 7-O-diethyl phosphoryl,3-cyano,4-methyl,7-hydroxycoumarin (DEPCyMC), which is considered a surrogate marker of PON1 concentration, showed the most significant association with MS, independently of both HDL and apolipoprotein A-I levels. Subjects with MS and low DEPCyMCase activity had the highest CAD risk (OR 4.34 with 95% CI 1.44-13.10), while no significant increase of risk was found among those with MS but high DEPCyMCase activity (OR 1.45 with 95% CI 0.47-4.46). Our results suggest that low PON1 concentrations are typical in MS and may modulate the MS-related risk of CAD.

摘要

血浆高密度脂蛋白(HDL)浓度低是代谢综合征(MS)的特征。HDL的抗氧化能力至少部分归因于多效性血清对氧磷酶(PON1)。对293名有(n = 88)或无MS(n = 205)以及有(n = 195)或无(n = 98)血管造影证实的冠状动脉疾病(CAD)的受试者评估了不同的PON1活性。MS受试者的PON1活性较低,随着MS异常数量的增加呈逐渐下降趋势。与7-O-二乙基磷酰基、3-氰基、4-甲基、7-羟基香豆素(DEPCyMC)的活性,DEPCyMC被认为是PON1浓度的替代标志物,显示出与MS最显著的关联,独立于HDL和载脂蛋白A-I水平。MS且DEPCyMCase活性低的受试者CAD风险最高(OR 4.34,95%CI 1.44 - 13.10),而MS但DEPCyMCase活性高的受试者中未发现风险显著增加(OR 1.45,95%CI 0.47 - 4.46)。我们的结果表明,低PON1浓度是MS的典型特征,可能调节与MS相关的CAD风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b4/3179885/374e9544eed9/EDR2012-231502.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b4/3179885/0d551293e53d/EDR2012-231502.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b4/3179885/8cc4f031a227/EDR2012-231502.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b4/3179885/374e9544eed9/EDR2012-231502.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b4/3179885/0d551293e53d/EDR2012-231502.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b4/3179885/8cc4f031a227/EDR2012-231502.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b4/3179885/374e9544eed9/EDR2012-231502.003.jpg

相似文献

1
Low levels of serum paraoxonase activities are characteristic of metabolic syndrome and may influence the metabolic-syndrome-related risk of coronary artery disease.血清对氧磷酶活性水平低是代谢综合征的特征之一,并且可能影响与代谢综合征相关的冠状动脉疾病风险。
Exp Diabetes Res. 2012;2012:231502. doi: 10.1155/2012/231502. Epub 2011 Sep 22.
2
Novel serum paraoxonase activity assays are associated with coronary artery disease.新型血清对氧磷酶活性检测与冠状动脉疾病相关。
Clin Chem Lab Med. 2009;47(4):432-40. doi: 10.1515/CCLM.2009.108.
3
Serum myeloperoxidase/paraoxonase 1 ratio as potential indicator of dysfunctional high-density lipoprotein and risk stratification in coronary artery disease.血清髓过氧化物酶/对氧磷酶1比值作为冠状动脉疾病中功能失调的高密度脂蛋白和风险分层的潜在指标。
Atherosclerosis. 2014 Jun;234(2):288-94. doi: 10.1016/j.atherosclerosis.2014.03.009. Epub 2014 Mar 19.
4
Lactonase activity and status of paraoxonase 1 in Chinese women with polycystic ovarian syndrome.多囊卵巢综合征中国女性的内酯酶活性和对氧磷酶 1 状况。
Eur J Endocrinol. 2015 Apr;172(4):391-402. doi: 10.1530/EJE-14-0863. Epub 2015 Jan 9.
5
Lactonase Activity, Status, and Genetic Variations of Paraoxonase 1 in Women with Gestational Diabetes Mellitus.妊娠糖尿病妇女的内酯酶活性、状态和对氧磷酶 1 的遗传变异。
J Diabetes Res. 2020 Feb 3;2020:3483427. doi: 10.1155/2020/3483427. eCollection 2020.
6
Improved risk assessment of coronary artery disease by substituting paraoxonase 1 activity for HDL-C: Novel cardiometabolic biomarkers based on HDL functionality.通过替代载脂蛋白 1 活性来评估冠心病风险:基于高密度脂蛋白功能的新型代谢相关心血管生物标志物。
Nutr Metab Cardiovasc Dis. 2021 Apr 9;31(4):1166-1176. doi: 10.1016/j.numecd.2020.12.026. Epub 2021 Jan 1.
7
Low paraoxonase 1 arylesterase activity and high von Willebrand factor levels are associated with severe coronary atherosclerosis in patients with non-diabetic stable coronary artery disease.低对氧磷酶1芳基酯酶活性和高血管性血友病因子水平与非糖尿病稳定型冠心病患者的严重冠状动脉粥样硬化相关。
Med Sci Monit. 2014 Nov 25;20:2421-9. doi: 10.12659/MSM.890911.
8
Association of elevated apoA-I glycation and reduced HDL-associated paraoxonase1, 3 activity, and their interaction with angiographic severity of coronary artery disease in patients with type 2 diabetes mellitus.2型糖尿病患者中载脂蛋白A-I糖基化升高与高密度脂蛋白相关对氧磷酶1、3活性降低的关联及其与冠状动脉疾病血管造影严重程度的相互作用。
Cardiovasc Diabetol. 2015 May 13;14:52. doi: 10.1186/s12933-015-0221-4.
9
Serum paraoxonase 1 activity in women with metabolic syndrome.代谢综合征女性血清对氧磷酶 1 活性。
Kardiol Pol. 2010 Nov;68(11):1219-24.
10
Paraoxonase responses to exercise and niacin therapy in men with metabolic syndrome.代谢综合征男性对运动和烟酸疗法的对氧磷酶反应。
Redox Rep. 2015 Jan;20(1):42-8. doi: 10.1179/1351000214Y.0000000103. Epub 2014 Sep 2.

引用本文的文献

1
A Multi-Omics Analysis of PON1 Lactonase Activity in Relation to Human Health and Disease.多组学分析 PON1 内酯酶活性与人类健康和疾病的关系。
OMICS. 2021 Jan;25(1):38-51. doi: 10.1089/omi.2020.0160. Epub 2020 Dec 11.
2
Cross-sectional correlates of paraoxonase 1 and soluble intercellular adhesion molecule-1 in metabolic syndrome patients with and without diabetes.伴有和不伴有糖尿病的代谢综合征患者中对氧磷酶1和可溶性细胞间黏附分子-1的横断面相关性
Ther Adv Endocrinol Metab. 2018 Jul 18;9(10):303-310. doi: 10.1177/2042018818787396. eCollection 2018 Oct.
3
Paraoxonase activity in metabolic syndrome in children and adolescents.

本文引用的文献

1
PON-dering differences in HDL function in coronary artery disease.思考在冠心病中 HDL 功能的差异。
J Clin Invest. 2011 Jul;121(7):2545-8. doi: 10.1172/JCI57671. Epub 2011 Jun 23.
2
Mechanisms underlying adverse effects of HDL on eNOS-activating pathways in patients with coronary artery disease.冠心病患者中 HDL 对 eNOS 激活途径产生不良影响的机制。
J Clin Invest. 2011 Jul;121(7):2693-708. doi: 10.1172/JCI42946. Epub 2011 Jun 23.
3
The role of oxidative stress in the metabolic syndrome.氧化应激在代谢综合征中的作用。
儿童和青少年代谢综合征中的对氧磷酶活性
Caspian J Intern Med. 2018 Spring;9(2):116-120. doi: 10.22088/cjim.9.2.116.
4
Systematic Review of Metabolic Syndrome Biomarkers: A Panel for Early Detection, Management, and Risk Stratification in the West Virginian Population.代谢综合征生物标志物的系统评价:西弗吉尼亚州人群早期检测、管理及风险分层的指标体系
Int J Med Sci. 2016 Jan 1;13(1):25-38. doi: 10.7150/ijms.13800. eCollection 2016.
5
Q192R Paraoxonase (PON)1 Polymorphism, Insulin Sensitivity, and Endothelial Function in Essential Hypertensive Men.原发性高血压男性中Q192R对氧磷酶(PON)1多态性、胰岛素敏感性和内皮功能的影响
Clin Med Insights Cardiol. 2014 Jul 14;8:57-62. doi: 10.4137/CMC.S15493. eCollection 2014.
6
Paraoxonase (PON)1 Q192R functional genotypes and PON1 Q192R genotype by smoking interactions are risk factors for the metabolic syndrome, but not overweight or obesity.对氧磷酶(PON)1 Q192R功能基因型以及吸烟相互作用导致的PON1 Q192R基因型是代谢综合征的危险因素,但不是超重或肥胖的危险因素。
Redox Rep. 2014 Nov;19(6):232-41. doi: 10.1179/1351000214Y.0000000093. Epub 2014 Jul 18.
7
Soluble Lectin-Like Oxidized LDL Receptor 1 as a Possible Mediator of Endothelial Dysfunction in Patients With Metabolic Syndrome.可溶性凝集素样氧化型低密度脂蛋白受体1作为代谢综合征患者内皮功能障碍的潜在介质
J Clin Lab Anal. 2015 May;29(3):184-90. doi: 10.1002/jcla.21748. Epub 2014 May 5.
8
Paraoxonase-1 status in patients with hereditary hemochromatosis.原发性血色病患者的对氧磷酶-1 状况。
J Lipid Res. 2013 May;54(5):1484-92. doi: 10.1194/jlr.P028977. Epub 2013 Mar 6.
9
Association between paraoxonase gene and stroke in the Han Chinese population.载脂蛋白基因与汉族人群中风的相关性研究。
BMC Med Genet. 2013 Jan 28;14:16. doi: 10.1186/1471-2350-14-16.
Rev Cardiovasc Med. 2011;12(1):21-9. doi: 10.3909/ricm0555.
4
Paraoxonase-1 is a major determinant of clopidogrel efficacy.对氧磷酶 1 是氯吡格雷疗效的主要决定因素。
Nat Med. 2011 Jan;17(1):110-6. doi: 10.1038/nm.2281. Epub 2010 Dec 19.
5
Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile.载脂蛋白 LDLR 基因多态性可能通过调节凝血因子 VIII 活性,并独立于血脂谱,与冠心病相关。
Blood. 2010 Dec 16;116(25):5688-97. doi: 10.1182/blood-2010-03-277079. Epub 2010 Sep 1.
6
Implications of torcetrapib failure for the future of HDL therapy: is HDL-cholesterol the right target?托彻普失败对高密度脂蛋白治疗未来的启示:高密度脂蛋白胆固醇是正确的靶点吗?
Expert Rev Cardiovasc Ther. 2010 Mar;8(3):345-58. doi: 10.1586/erc.10.6.
7
Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity.代谢综合征的协调:国际糖尿病联盟流行病学与预防特别工作组、美国国立心肺血液研究所、美国心脏协会、世界心脏联盟、国际动脉粥样硬化学会以及国际肥胖研究协会的联合中期声明
Circulation. 2009 Oct 20;120(16):1640-5. doi: 10.1161/CIRCULATIONAHA.109.192644. Epub 2009 Oct 5.
8
The roles of PON1 and PON2 in cardiovascular disease and innate immunity.对氧磷酶1和对氧磷酶2在心血管疾病及天然免疫中的作用。
Curr Opin Lipidol. 2009 Aug;20(4):288-92. doi: 10.1097/MOL.0b013e32832ca1ee.
9
Novel serum paraoxonase activity assays are associated with coronary artery disease.新型血清对氧磷酶活性检测与冠状动脉疾病相关。
Clin Chem Lab Med. 2009;47(4):432-40. doi: 10.1515/CCLM.2009.108.
10
The paraoxonases: role in human diseases and methodological difficulties in measurement.对氧磷酶:在人类疾病中的作用及测量方法上的困难
Crit Rev Clin Lab Sci. 2009;46(2):83-106. doi: 10.1080/10408360802610878.