Literature DB >> 26907084

The Relationship Between Plasma Whole Blood Viscosity and Cardiovascular Events in Patients With Chronic Kidney Disease.

Turgay Celik1, Mahmut Ilker Yilmaz2, Sevket Balta1, Cengiz Ozturk1, Hilmi Umut Unal2, Mustafa Aparci3, Murat Karaman2, Mustafa Demir1, A Osman Yildirim1, Mutlu Saglam4, Selim Kilic5, Tayfun Eyileten2, İbrahim Aydin6, Atila Iyisoy1.   

Abstract

BACKGROUND: Plasma levels of estimated whole blood viscosity (eWBV) have been increased by endothelial inflammation. Because there were no consistent data for assessing the eWBV levels for prediction of cardiovascular event (CVE) in patients with chronic kidney disease (CKD). We aimed to investigate the relationship between plasma eWBV levels and CVEs in patients with CKD.
MATERIALS AND METHODS: We conducted a prospective, cross-sectional, long-term follow-up study, assessing the relationship between plasma eWBV levels and CVE (either fatal or nonfatal) in patients with newly diagnosed CKD. We also evaluated estimated glomerular filtration rate (eGFR), pentraxin 3 (PTX3), high-sensitivity C-reactive protein (hsCRP), and flow-mediated dilatation (FMD).
RESULTS: Study patients were divided into 2 groups: patients with CVE and patients without CVE. The eWBV levels were higher in patients with CVE. Additionally, PTX3 and hsCRP were higher, and FMD and eGFR were lower in patients with CVE compared to those without CVE. According to the Cox regression analysis, WBV, plasma asymmetric dimethylarginine levels, FMD, hsCRP, eGFR, systolic blood pressure, calcium, and history of diabetes were independent predictors of CVEs in patients with CKD. Kaplan Meier survival curves were generated to establish the impact of the WBV on the cumulative survival of the cohort. Patients with eWBV values higher than 5.2 centipoise (cP) had lower survival rates when compared to patients with eWBV values lower than 5.2 cP (log rank = 4.49 df = 1 P = .034).
CONCLUSION: In conclusion, plasma eWBV levels may increase the presence of lower eGFR and affect CVE in patients with CKD independent of classical and unconventional risk factors.

Entities:  

Keywords:  adverse cardiac events; blood viscosity; chronic kidney disease; inflammation

Mesh:

Year:  2016        PMID: 26907084     DOI: 10.1177/1076029616634888

Source DB:  PubMed          Journal:  Clin Appl Thromb Hemost        ISSN: 1076-0296            Impact factor:   2.389


  4 in total

1.  Increased Whole Blood Viscosity Is Associated with the Presence of Digital Ulcers in Systemic Sclerosis: Results from a Cross-Sectional Pilot Study.

Authors:  Peter Korsten; Timothy B Niewold; Michael Zeisberg; Tammy O Utset; Daniel Cho; Lawrence S Zachary; Nadera J Sweiss; Suncica Volkov
Journal:  Autoimmune Dis       Date:  2017-11-29

Review 2.  The Rheology of the Carotid Sinus: A Path Toward Bioinspired Intervention.

Authors:  Andrew Iskander; Coskun Bilgi; Rotem Naftalovich; Ilker Hacihaliloglu; Tolga Berkman; Daniel Naftalovich; Niema Pahlevan
Journal:  Front Bioeng Biotechnol       Date:  2021-06-10

3.  Whole Blood Viscosity and Cardiovascular Diseases: A Forgotten Old Player of the Game.

Authors:  Turgay Celik; Sevket Balta; Cengiz Ozturk; Atila Iyisoy
Journal:  Med Princ Pract       Date:  2016-05-19       Impact factor: 1.927

4.  Study on Association of Pentraxin 3 and Diabetic Nephropathy in a Rat Model.

Authors:  Xuehai Chen; Jiao Luo; Minmin Wu; Zhuo Pan; Yue Xie; Hongwei Wang; Bicheng Chen; Hong Zhu
Journal:  J Diabetes Res       Date:  2018-03-13       Impact factor: 4.011

  4 in total

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