Literature DB >> 21239386

TLR-4+ peripheral blood monocytes and cardiovascular events in patients with chronic kidney disease--a prospective follow-up study.

Johan M Lorenzen1, Sascha David, Alena Richter, Kirsten de Groot, Jan T Kielstein, Hermann Haller, Thomas Thum, Danilo Fliser.   

Abstract

BACKGROUND: Atherosclerosis is an inflammatory process mediated by circulating immune cells, including monocytes. There is accumulating evidence for the involvement of Toll-like receptor 4 (TLR-4) as a mediator of atherogenesis.
METHODS: We evaluated the association between CD14+/TLR-4+ monocytes in peripheral blood (flow cytometry) and future cardiovascular events (CVE), e.g. myocardial infarction, percutaneous transluminal coronary angioplasty (including stenting), aortocoronary bypass, stroke and angiographically verified stenosis of peripheral arteries and cardiovascular (CV) death, in 191 patients with chronic kidney disease Stage V receiving hemodialysis therapy.
RESULTS: At baseline, CD14+/TLR-4+ monocytes correlated significantly with age (r = 0.2; P = 0.007), high-sensitivity C-reactive protein (r = 0.2; P = 0.008) and mean arterial pressure (r = -0.2; P = 0.02), but not with gender (P = 0.5), smoking (P = 0.6) and the presence of diabetes (P = 0.5). During a median follow-up period of 36 [1-54] months, 79 (41%) patients experienced a CVE. A total of 55 patients died during the follow-up period, 25 of those due to a confirmed CV cause. Log-rank test did not reveal statistical significance for TLR-4+ monocytes concerning incident CVE (P = 0.3), CV death (P = 0.85) and overall death (P = 0.8). In a multiple Cox-regression analysis, we identified age (P = 0.003) and smoking (P = 0.001) as the only independent variables associated with incident CVE.
CONCLUSIONS: Unexpectedly, we could not detect an association between CD14+/TLR-4+ monocytes and incident CVE as well as CV death in stable hemodialysis patients. Further studies have to clarify the potential role of this cell population for CV outcome in this population.

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Year:  2011        PMID: 21239386     DOI: 10.1093/ndt/gfq758

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  6 in total

1.  Decreased number of CD14+TLR4+ monocytes and their impaired cytokine responses to lipopolysaccharide in patients with chronic kidney disease.

Authors:  Zhi Liu; Yan-Hong Kan; Yu-Dan Wei; Xiu-Jiang Li; Fan Yang; Yue Hou; Yu-Jun Du
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2015-04-16

Review 2.  Cell death, dysglycemia and myocardial infarction.

Authors:  Xiao-Fang Tian; Ming-Xia Cui; Shi-Wei Yang; Yu-Jie Zhou; DA-Yi Hu
Journal:  Biomed Rep       Date:  2013-02-25

Review 3.  Monocytes in Uremia.

Authors:  Matthias Girndt; Bogusz Trojanowicz; Christof Ulrich
Journal:  Toxins (Basel)       Date:  2020-05-21       Impact factor: 4.546

4.  End-stage renal disease is different from chronic kidney disease in upregulating ROS-modulated proinflammatory secretome in PBMCs - A novel multiple-hit model for disease progression.

Authors:  Ruijing Zhang; Jason Saredy; Ying Shao; Tian Yao; Lu Liu; Fatma Saaoud; William Y Yang; Yu Sun; Candice Johnson; Charles Drummer; Hangfei Fu; Yifan Lu; Keman Xu; Ming Liu; Jirong Wang; Elizabeth Cutler; Daohai Yu; Xiaohua Jiang; Yafeng Li; Rongshan Li; Lihua Wang; Eric T Choi; Hong Wang; Xiaofeng Yang
Journal:  Redox Biol       Date:  2020-02-20       Impact factor: 11.799

5.  Basic inflammatory indices and chosen neutrophil receptors expression in chronic haemodialysed patients.

Authors:  Zbigniew Baj; Zbigniew Zbróg; Adam Szuflet; Sylwia Mańka; Piotr Bartnicki; Ewa Majewska
Journal:  Cent Eur J Immunol       Date:  2018-06-30       Impact factor: 2.085

Review 6.  Human Monocyte Subsets and Phenotypes in Major Chronic Inflammatory Diseases.

Authors:  Theodore S Kapellos; Lorenzo Bonaguro; Ioanna Gemünd; Nico Reusch; Adem Saglam; Emily R Hinkley; Joachim L Schultze
Journal:  Front Immunol       Date:  2019-08-30       Impact factor: 7.561

  6 in total

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