We have located links that may give you full text access.
The relationship between pulse pressure and inflammation with left ventricular diastolic dysfunction in chronic kidney disease patients.
Internal Medicine Journal 2018 July 11
INTRODUCTION: Diastolic dysfunction (DD) is an important cause of cardiovascular disease (CVD) mortality in chronic kidney disease (CKD) patients. Non-traditional risk factors such as arterial stiffness and inflammation are implicated in the pathogenesis of DD in CKD patients.
AIM: To determine the association between inflammatory markers [interleukin(IL)-12, IL-18, highly sensitive C-reactive protein (hsCRP)] and non-invasive markers of arterial stiffness [24-hour pulse pressure (PP)] with DD in stage 3-4 CKD patients.
METHODS: We performed a sub-analysis of 78 non-diabetic stage 3-4 CKD subjects to determine the relationship between 24-hour PP, IL-12, IL-18 and hsCRP with DD.
RESULTS: DD was present in 38 subjects (49%). Subjects with DD were significantly older (61.0±1.9 vs 50.2±2.0years; p<0.001) and had higher 24-hour PP [48(95%CI 45, 52) vs 43(95%CI 41, 45)mmHg; p<0.005]. 24-hour PP was associated with DD (p=0.02) but this was no longer significant after adjustment for age (p=0.31). Serum IL-12, IL-18 and hsCRP levels were not significantly different between subjects with or without DD.
CONCLUSION: Asymptomatic subclinical DD was present in 50% of a cohort of stage 3-4 CKD patients but was not associated with IL-12, IL-18 or hsCRP. The association between 24-hour PP and DD was no longer apparent following adjustment for age but given the small sample size our findings will need to be explored in larger sized cohorts of individuals with moderate stage CKD. This article is protected by copyright. All rights reserved.
AIM: To determine the association between inflammatory markers [interleukin(IL)-12, IL-18, highly sensitive C-reactive protein (hsCRP)] and non-invasive markers of arterial stiffness [24-hour pulse pressure (PP)] with DD in stage 3-4 CKD patients.
METHODS: We performed a sub-analysis of 78 non-diabetic stage 3-4 CKD subjects to determine the relationship between 24-hour PP, IL-12, IL-18 and hsCRP with DD.
RESULTS: DD was present in 38 subjects (49%). Subjects with DD were significantly older (61.0±1.9 vs 50.2±2.0years; p<0.001) and had higher 24-hour PP [48(95%CI 45, 52) vs 43(95%CI 41, 45)mmHg; p<0.005]. 24-hour PP was associated with DD (p=0.02) but this was no longer significant after adjustment for age (p=0.31). Serum IL-12, IL-18 and hsCRP levels were not significantly different between subjects with or without DD.
CONCLUSION: Asymptomatic subclinical DD was present in 50% of a cohort of stage 3-4 CKD patients but was not associated with IL-12, IL-18 or hsCRP. The association between 24-hour PP and DD was no longer apparent following adjustment for age but given the small sample size our findings will need to be explored in larger sized cohorts of individuals with moderate stage CKD. This article is protected by copyright. All rights reserved.
Full text links
Related Resources
Trending Papers
Challenges in Septic Shock: From New Hemodynamics to Blood Purification Therapies.Journal of Personalized Medicine 2024 Februrary 4
Molecular Targets of Novel Therapeutics for Diabetic Kidney Disease: A New Era of Nephroprotection.International Journal of Molecular Sciences 2024 April 4
The 'Ten Commandments' for the 2023 European Society of Cardiology guidelines for the management of endocarditis.European Heart Journal 2024 April 18
A Guide to the Use of Vasopressors and Inotropes for Patients in Shock.Journal of Intensive Care Medicine 2024 April 14
Diagnosis and Management of Cardiac Sarcoidosis: A Scientific Statement From the American Heart Association.Circulation 2024 April 19
Essential thrombocythaemia: A contemporary approach with new drugs on the horizon.British Journal of Haematology 2024 April 9
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.
By using this service, you agree to our terms of use and privacy policy.
Your Privacy Choices
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app