Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD

Background Although renal impairment has been described in COPD, there is opportunity to evaluate further to determine nature and consider optimal management. Increased aortic stiffness, as seen in COPD, leads to reduced buffering of pulsatile flow. We hypothesised that urinary albumin creatinine r...

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Main Authors: John, Michelle, Hussain, Samia, Prayle, Andrew, Simms, Rebecca, Cockroft, John R., Bolton, Charlotte E.
Format: Article
Published: BioMed Central 2013
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Online Access:https://eprints.nottingham.ac.uk/3140/
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author John, Michelle
Hussain, Samia
Prayle, Andrew
Simms, Rebecca
Cockroft, John R.
Bolton, Charlotte E.
author_facet John, Michelle
Hussain, Samia
Prayle, Andrew
Simms, Rebecca
Cockroft, John R.
Bolton, Charlotte E.
author_sort John, Michelle
building Nottingham Research Data Repository
collection Online Access
description Background Although renal impairment has been described in COPD, there is opportunity to evaluate further to determine nature and consider optimal management. Increased aortic stiffness, as seen in COPD, leads to reduced buffering of pulsatile flow. We hypothesised that urinary albumin creatinine ratio (UACR) would reflect glomerular damage related to aortic stiffness. Methods Patients with COPD and controls underwent spirometry, blood pressure, arterial stiffness - aortic pulse wave velocity (PWV) and provided a spot urine sample for UACR, with other renal biomarkers measured. Results The UACR was increased in patients (n = 52): 0.80 mg/mmol compared to controls (n = 34): 0.46 mg/mmol, p < 0.05. Aortic PWV was related to log10 UACR in all subjects (r = 0.426, p < 0.001) and COPD patients alone. Aortic PWV was a significant variable for UACR with oxygen saturations, after accounting for potential confounders. Eight subjects (7 patients) reached a defined clinical microalbuminuria threshold, with aortic PWV greater in these patients compared to those patients without, although albuminuria is a continuum. Proximal tubular damage biomarkers, unlike the glomerular marker, were not different between patients and controls. Conclusions There is glomerular damage in patients with COPD evidenced by increased UACR, related to increased aortic stiffness. Besides the macrovascular prognostic implications of increased aortic stiffness, the microvascular state in COPD management should be considered.
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spelling nottingham-31402024-08-15T15:33:17Z https://eprints.nottingham.ac.uk/3140/ Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD John, Michelle Hussain, Samia Prayle, Andrew Simms, Rebecca Cockroft, John R. Bolton, Charlotte E. Background Although renal impairment has been described in COPD, there is opportunity to evaluate further to determine nature and consider optimal management. Increased aortic stiffness, as seen in COPD, leads to reduced buffering of pulsatile flow. We hypothesised that urinary albumin creatinine ratio (UACR) would reflect glomerular damage related to aortic stiffness. Methods Patients with COPD and controls underwent spirometry, blood pressure, arterial stiffness - aortic pulse wave velocity (PWV) and provided a spot urine sample for UACR, with other renal biomarkers measured. Results The UACR was increased in patients (n = 52): 0.80 mg/mmol compared to controls (n = 34): 0.46 mg/mmol, p < 0.05. Aortic PWV was related to log10 UACR in all subjects (r = 0.426, p < 0.001) and COPD patients alone. Aortic PWV was a significant variable for UACR with oxygen saturations, after accounting for potential confounders. Eight subjects (7 patients) reached a defined clinical microalbuminuria threshold, with aortic PWV greater in these patients compared to those patients without, although albuminuria is a continuum. Proximal tubular damage biomarkers, unlike the glomerular marker, were not different between patients and controls. Conclusions There is glomerular damage in patients with COPD evidenced by increased UACR, related to increased aortic stiffness. Besides the macrovascular prognostic implications of increased aortic stiffness, the microvascular state in COPD management should be considered. BioMed Central 2013-03 Article PeerReviewed John, Michelle, Hussain, Samia, Prayle, Andrew, Simms, Rebecca, Cockroft, John R. and Bolton, Charlotte E. (2013) Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD. Respiratory Research, 14 (31). pp. 1-7. ISSN 1465-9921 Arterial Stiffness Biomarkers Haemodynamics Kidney Renal Microvascular http://respiratory-research.com/content/14/1/31/abstract# doi:10.1186/1465-9921-14-31 doi:10.1186/1465-9921-14-31
spellingShingle Arterial Stiffness
Biomarkers
Haemodynamics
Kidney
Renal
Microvascular
John, Michelle
Hussain, Samia
Prayle, Andrew
Simms, Rebecca
Cockroft, John R.
Bolton, Charlotte E.
Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD
title Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD
title_full Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD
title_fullStr Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD
title_full_unstemmed Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD
title_short Target renal damage: the microvascular associations of increased aortic stiffness in patients with COPD
title_sort target renal damage: the microvascular associations of increased aortic stiffness in patients with copd
topic Arterial Stiffness
Biomarkers
Haemodynamics
Kidney
Renal
Microvascular
url https://eprints.nottingham.ac.uk/3140/
https://eprints.nottingham.ac.uk/3140/
https://eprints.nottingham.ac.uk/3140/