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Association between normal or mildly reduced kidney function, cardiovascular risk and biomarkers for atherosclerosis: results from the ENCORE trial.

Publication ,  Journal Article
Tyson, CC; Smith, PJ; Sherwood, A; Mabe, S; Hinderliter, AL; Blumenthal, JA
Published in: Clin Kidney J
October 2017

BACKGROUND: Moderate-to-severe kidney dysfunction is associated with atherosclerotic cardiovascular disease (ASCVD). Gradations of normal or mildly reduced kidney function may also associate with ASCVD risk. METHODS: We conducted a secondary analysis using baseline data from the Exercise and Nutritional Interventions for Cardiovascular Health (ENCORE) trial. Participants were sedentary, overweight and obese adults with unmedicated pre-hypertension or Stage I hypertension and an estimated glomerular filtration rate (eGFR) ≥60 mL/min/1.73 m2. The Pooled Cohorts Equations were used to estimate a 10-year risk for first ASCVD event. Carotid artery intima-media thickness (IMT) and brachial artery flow-mediated dilation (FMD) were measured to assess subclinical atherosclerosis and vascular endothelial function, respectively. Using linear regression, we examined the association between eGFR and ASCVD risk, IMT and FMD. RESULTS: Participants (N = 139) were predominantly women (65%), white (60%), with a mean age of 52.0 ± 9.6 years and mean eGFR of 89.1 ± 15.0 mL/min/1.73 m2. Lower eGFR of 15 mL/min/1.73 m2 was associated with higher ASCVD risk [b = -2.7% (95% confidence interval: -3.7, -1.8%), P < 0.001], higher IMT [b = 0.05 mm (0.03, 0.08 mm), P < 0.001] and lower FMD [b = -0.87% (-1.64, -0.11%), P = 0.026]. Compared with eGFR ≥90 mL/min/1.73 m2, those with eGFR 60-89 mL/min/1.73 m2 had higher mean ASCVD risk (7.6% versus 2.7%; P < 0.001), greater mean IMT (0.74 mm versus 0.66 mm; P < 0.001) and lower mean FMD (2.0% versus 3.7%; P = 0.026). After controlling for CVD risk factors, the association between eGFR and IMT remained significant (P < 0.001), and eGFR and FMD trended toward significance (P = 0.08). CONCLUSIONS: Among overweight and obese adults with unmedicated high blood pressure and eGFR ≥60 mL/min/1.73 m2, lower eGFR is associated with a greater 10-year risk for first ASCVD event, higher IMT and relatively impaired FMD.

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Published In

Clin Kidney J

DOI

ISSN

2048-8505

Publication Date

October 2017

Volume

10

Issue

5

Start / End Page

666 / 671

Location

England

Related Subject Headings

  • 3202 Clinical sciences
 

Citation

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Chicago
ICMJE
MLA
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Tyson, C. C., Smith, P. J., Sherwood, A., Mabe, S., Hinderliter, A. L., & Blumenthal, J. A. (2017). Association between normal or mildly reduced kidney function, cardiovascular risk and biomarkers for atherosclerosis: results from the ENCORE trial. Clin Kidney J, 10(5), 666–671. https://doi.org/10.1093/ckj/sfx025
Tyson, Crystal C., Patrick J. Smith, Andrew Sherwood, Stephanie Mabe, Alan L. Hinderliter, and James A. Blumenthal. “Association between normal or mildly reduced kidney function, cardiovascular risk and biomarkers for atherosclerosis: results from the ENCORE trial.Clin Kidney J 10, no. 5 (October 2017): 666–71. https://doi.org/10.1093/ckj/sfx025.
Tyson CC, Smith PJ, Sherwood A, Mabe S, Hinderliter AL, Blumenthal JA. Association between normal or mildly reduced kidney function, cardiovascular risk and biomarkers for atherosclerosis: results from the ENCORE trial. Clin Kidney J. 2017 Oct;10(5):666–71.
Tyson, Crystal C., et al. “Association between normal or mildly reduced kidney function, cardiovascular risk and biomarkers for atherosclerosis: results from the ENCORE trial.Clin Kidney J, vol. 10, no. 5, Oct. 2017, pp. 666–71. Pubmed, doi:10.1093/ckj/sfx025.
Tyson CC, Smith PJ, Sherwood A, Mabe S, Hinderliter AL, Blumenthal JA. Association between normal or mildly reduced kidney function, cardiovascular risk and biomarkers for atherosclerosis: results from the ENCORE trial. Clin Kidney J. 2017 Oct;10(5):666–671.

Published In

Clin Kidney J

DOI

ISSN

2048-8505

Publication Date

October 2017

Volume

10

Issue

5

Start / End Page

666 / 671

Location

England

Related Subject Headings

  • 3202 Clinical sciences