• 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

银屑病患者心血管疾病的新标志物:单核细胞表型、ADAMTS7和mTOR活性的初步研究

New Markers for Cardiovascular Disease in Psoriatic Patients: Preliminary Study on Monocyte Phenotype, ADAMTS7, and mTOR Activity.

作者信息

Loyola Khanty, Karsulovic Claudio, Cabrera Raúl, Perez Claudio, Hojman Lía

机构信息

Dermatology Section, Surgery Department, Facultad de Medicina Clínica Alemana de Santiago, Universidad del Desarrollo, Santiago P.O. Box 7630000, Chile.

Rheumatology Section, Internal Medicine Department, Facultad de Medicina Clínica Alemana de Santiago, Universidad del Desarrollo, Santiago P.O. Box 7630000, Chile.

出版信息

Metabolites. 2023 Jan 11;13(1):116. doi: 10.3390/metabo13010116.

DOI:10.3390/metabo13010116
PMID:36677041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9864195/
Abstract

Psoriasis is a skin disease with occasional involvement of non-cutaneous territories. Beyond the usual, cardiovascular events are more frequent in these patients and correlate only partially with disease activity, suggesting the presence of other unknown factors. We selected ten psoriatic patients without treatment in the last year and matched them for age and gender with eleven healthy subjects. Ficoll-extracted mononuclear cells were analyzed with flow cytometry for monocyte surface phenotype markers, intracellular NFκB/inflammasome-dependent interleukins, and chemotaxis receptor CXCR3. Using ELISA, patient serum was evaluated for ADAMTS7 and CXCL10. Inflammatory M1 monocytes showed higher levels of IL-1β and IL-6 in psoriatic patients. M2 monocytes also showed higher levels of intracellular inflammatory cytokines. Nevertheless, IL-6 values were higher compared to other monocytes and IL-1β. The mTORC activation markers ADAMTS7 and S6Rp were higher in psoriatic patients than in healthy controls. In psoriatic patients, serum levels of ADAMTS7 were elevated, and M2 monocytes showed a distinct inflammatory response with higher relative levels of NFκB-dependent IL-6 and less activity of the CXCR3-CXCL10 chemotactic pathway. These data suggest pathways with potential markers for prediction and early detection of cardiovascular risk in psoriatic patients.

摘要

银屑病是一种偶尔累及非皮肤区域的皮肤病。除了常见情况外,这些患者心血管事件更为频繁,且仅部分与疾病活动相关,提示存在其他未知因素。我们选择了去年未接受治疗的10例银屑病患者,并根据年龄和性别将他们与11名健康受试者进行匹配。采用流式细胞术分析Ficoll分离的单核细胞的单核细胞表面表型标志物、细胞内NFκB/炎性小体依赖性白细胞介素和趋化因子受体CXCR3。使用酶联免疫吸附测定法(ELISA)评估患者血清中的ADAMTS7和CXCL10水平。炎症性M1单核细胞在银屑病患者中显示出较高水平的IL-1β和IL-6。M2单核细胞也显示出较高水平的细胞内炎性细胞因子。然而,与其他单核细胞相比,IL-6值更高,且IL-1β也是如此。银屑病患者中mTORC激活标志物ADAMTS7和S6Rp高于健康对照。在银屑病患者中,ADAMTS7血清水平升高,M2单核细胞表现出独特的炎症反应,NFκB依赖性IL-6相对水平较高,而CXCR3-CXCL10趋化途径活性较低。这些数据提示了银屑病患者心血管风险预测和早期检测的潜在标志物途径。

相似文献

1
New Markers for Cardiovascular Disease in Psoriatic Patients: Preliminary Study on Monocyte Phenotype, ADAMTS7, and mTOR Activity.银屑病患者心血管疾病的新标志物:单核细胞表型、ADAMTS7和mTOR活性的初步研究
Metabolites. 2023 Jan 11;13(1):116. doi: 10.3390/metabo13010116.
2
Non-Canonical WNT/Wnt5a Pathway Activity in Circulating Monocytes of Untreated Psoriatic Patients: An Exploratory Study of Its Association with Inflammatory Cytokines and Cardiovascular Risk Marker-ADAMTS7.未经治疗的银屑病患者循环单核细胞中的非经典WNT/Wnt5a信号通路活性:关于其与炎性细胞因子及心血管风险标志物ADAMTS7关联的探索性研究
Biomedicines. 2023 Feb 16;11(2):577. doi: 10.3390/biomedicines11020577.
3
In vitro Phenotype Induction of Circulating Monocytes: CD16 and CD163 Analysis.循环单核细胞的体外表型诱导:CD16和CD163分析
J Inflamm Res. 2021 Jan 26;14:191-198. doi: 10.2147/JIR.S292513. eCollection 2021.
4
Abnormal inflammatory traits and downregulated caveolin-1 expression in monocytes of psoriasis patients may be associated with psoriatic inflammation and atherosclerosis.银屑病患者单核细胞中异常的炎症特征和下调的窖蛋白-1 表达可能与银屑病炎症和动脉粥样硬化有关。
J Dermatol Sci. 2022 Aug;107(2):65-74. doi: 10.1016/j.jdermsci.2022.07.003. Epub 2022 Jul 5.
5
Interleukin-29 induces epithelial production of CXCR3A ligands and T-cell infiltration.白细胞介素-29诱导CXCR3A配体的上皮细胞产生及T细胞浸润。
J Mol Med (Berl). 2016 Apr;94(4):391-400. doi: 10.1007/s00109-015-1367-y. Epub 2015 Nov 26.
6
x cytokine production in psoriatic disease: Towards specific signatures in cutaneous psoriasis and peripheral psoriatic arthritis.银屑病发病过程中细胞因子的产生:皮肤银屑病和外周型银屑病关节炎的特异性特征。
Front Immunol. 2022 Nov 8;13:993363. doi: 10.3389/fimmu.2022.993363. eCollection 2022.
7
Increased microorganisms DNA levels in peripheral blood monocytes from psoriatic patients using PCR with universal ribosomal RNA primers.
J Dermatol. 2002 Sep;29(9):547-55. doi: 10.1111/j.1346-8138.2002.tb00179.x.
8
Peripheral blood monocytes in psoriatic patients overproduce cytokines.
J Dermatol Sci. 1998 Jul;17(3):223-32. doi: 10.1016/s0923-1811(98)00019-x.
9
Long pentraxin 3: a marker of inflammation in untreated psoriatic patients.长五聚体蛋白3:未经治疗的银屑病患者炎症的标志物。
Int J Mol Med. 2006 Sep;18(3):415-23.
10
Monocyte and neutrophil chemotaxis in psoriasis. Relation to the clinical status and the type of psoriasis.银屑病中单核细胞和中性粒细胞的趋化作用。与临床状态及银屑病类型的关系。
J Am Acad Dermatol. 1986 Dec;15(6):1191-9. doi: 10.1016/s0190-9622(86)70289-2.

引用本文的文献

1
mTORC1 and mTORC2 Levels in Patients with Psoriasis.银屑病患者体内的mTORC1和mTORC2水平
Dermatol Pract Concept. 2024 Oct 30;14(4):e2024266. doi: 10.5826/dpc.1404a266.
2
Pivotal Role of mTOR in Non-Skin Manifestations of Psoriasis.mTOR 在银屑病非皮肤表现中的关键作用。
Int J Mol Sci. 2024 Jun 20;25(12):6778. doi: 10.3390/ijms25126778.
3
Cardiovascular Considerations and Implications for Treatment in Psoriasis: An Updated Review.心血管问题的考虑因素及对银屑病治疗的影响:最新综述。

本文引用的文献

1
Human endothelial cell-derived exosomal microRNA-99a/b drives a sustained inflammatory response during sepsis by inhibiting mTOR expression.人内皮细胞衍生的外泌体 microRNA-99a/b 通过抑制 mTOR 表达在脓毒症期间驱动持续的炎症反应。
Front Cell Infect Microbiol. 2022 Aug 18;12:854126. doi: 10.3389/fcimb.2022.854126. eCollection 2022.
2
Psoriasis and Cardiovascular Diseases: An Immune-Mediated Cross Talk?银屑病与心血管疾病:一种免疫介导的串扰?
Front Immunol. 2022 May 24;13:868277. doi: 10.3389/fimmu.2022.868277. eCollection 2022.
3
Targeting the CCL2-CCR2 axis for atheroprotection.
Vasc Health Risk Manag. 2024 May 10;20:215-229. doi: 10.2147/VHRM.S464471. eCollection 2024.
4
Non-Canonical WNT/Wnt5a Pathway Activity in Circulating Monocytes of Untreated Psoriatic Patients: An Exploratory Study of Its Association with Inflammatory Cytokines and Cardiovascular Risk Marker-ADAMTS7.未经治疗的银屑病患者循环单核细胞中的非经典WNT/Wnt5a信号通路活性:关于其与炎性细胞因子及心血管风险标志物ADAMTS7关联的探索性研究
Biomedicines. 2023 Feb 16;11(2):577. doi: 10.3390/biomedicines11020577.
靶向 CCL2-CCR2 轴进行动脉粥样保护。
Eur Heart J. 2022 May 14;43(19):1799-1808. doi: 10.1093/eurheartj/ehac094.
4
Genome-wide pleiotropy analysis of coronary artery disease and pneumonia identifies shared immune pathways.全基因组多效性分析冠心病和肺炎,确定共同的免疫途径。
Sci Adv. 2022 Apr 22;8(16):eabl4602. doi: 10.1126/sciadv.abl4602.
5
Association of Cardiac Biomarkers With Cardiovascular Outcomes in Patients With Psoriatic Arthritis and Psoriasis: A Longitudinal Cohort Study.银屑病关节炎和银屑病患者中心血管生物标志物与心血管结局的关系:一项纵向队列研究。
Arthritis Rheumatol. 2022 Jul;74(7):1184-1192. doi: 10.1002/art.42079. Epub 2022 May 16.
6
Cardiovascular Disease-Associated Skin Conditions.心血管疾病相关皮肤状况。
Vasc Health Risk Manag. 2022 Feb 16;18:43-53. doi: 10.2147/VHRM.S343319. eCollection 2022.
7
Modulating mTOR Signaling as a Promising Therapeutic Strategy for Atherosclerosis.调节 mTOR 信号作为动脉粥样硬化有前途的治疗策略。
Int J Mol Sci. 2022 Jan 21;23(3):1153. doi: 10.3390/ijms23031153.
8
Vitamin D Inhibits IL-6 Pro-Atherothrombotic Effects in Human Endothelial Cells: A Potential Mechanism for Protection against COVID-19 Infection?维生素D抑制人内皮细胞中白细胞介素-6的促动脉粥样硬化血栓形成作用:这是预防新冠病毒感染的潜在机制吗?
J Cardiovasc Dev Dis. 2022 Jan 13;9(1):27. doi: 10.3390/jcdd9010027.
9
Soluble biomarkers for diagnosis, monitoring, and therapeutic response assessment in psoriasis.用于银屑病的诊断、监测和治疗反应评估的可溶性生物标志物。
J Dermatolog Treat. 2022 Jun;33(4):1967-1974. doi: 10.1080/09546634.2021.1966357. Epub 2021 Dec 22.
10
Coronary Disease Association With ADAMTS7 Is Due to Protease Activity.冠心病与 ADAMTS7 相关是由于其蛋白酶活性。
Circ Res. 2021 Aug 6;129(4):458-470. doi: 10.1161/CIRCRESAHA.121.319163. Epub 2021 Jun 28.