ObjectiveIn patients with type 2 diabetes and diabetic kidney disease (DKD), explore the relationship between estimated glomerular filtration rate decline (eGFR-d) and simultaneously assessed vascular risk markers including office, ambulatory or central blood pressure, pulse pressure, carotid-femoral pulse wave velocity (PWV), carotid intima-media thickness (IMT) and renal resistive indexes (RRI). Research design and methodsAt baseline, vascular risk markers were measured in addition to the routine clinical workup. The eGFR-d was based on 2000-2019 creatinine values. Parameters were compared by eGFR-d quartiles. Regression models of eGFR-d and vascular markers were assessed. ResultsIn total, 135 patients were included. Mean age was 63.8 & PLUSMN; 10.8y, baseline eGFR 60.2 & PLUSMN; 26.4 ml/min/1.73 m(2) and urine albumin-creatinine ratio (ACR) 49 & PLUSMN; 108 mg/mmol. Mean eGFR-d was based on 43 & PLUSMN; 39 creatinine values within a time span of 7.0 & PLUSMN; 1.9y. The average yearly eGFR decline was -1.8 & PLUSMN; 3.0 ml/min/1.73 m(2) ranging from -5.8 & PLUSMN; 2.3 in the first quartile to +1.4 & PLUSMN; 1.7 in the fourth quartile. Mean 24 h systolic (SBP) and diastolic (DBP) blood pressure were 126 & PLUSMN; 17 and 74 & PLUSMN; 9 mmHg. Mean PWV was 11.8 & PLUSMN; 2.8 m/s, RRI 0.76 & PLUSMN; 0.07 and IMT 0.77 & PLUSMN; 0.21 mm. SBP and pulse pressure correlated with eGFR-d but not DBP. 24 h SBP stood out as a stronger predictor of eGFR-d than office or central SBP. PWV and RRI correlated with eGFR decline in univariate, but not multivariate regression models including 24 SBP and ACR. ConclusionsIn this study, eGFR decline was highly variable in patients with type 2 diabetes and DKD. Twenty-four hour SBP provided an added value to the routine measurement of ACR in predicting eGFR decline, whereas PWV and RRI did not.
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Peking Univ, Hosp 1, Div Renal, Beijing 100871, Peoples R ChinaUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Chen, Yuqing
Lipkowitz, Michael S.
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Mt Sinai Sch Med, Div Renal, New York, NY USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Lipkowitz, Michael S.
Salem, Rany M.
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机构:Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Salem, Rany M.
Fung, Maple M.
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机构:Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Fung, Maple M.
Bhatnagar, Vibha
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Univ Calif San Diego, Dept Family & Prevent Med, La Jolla, CA 92093 USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Bhatnagar, Vibha
Mahata, Manjula
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机构:Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Mahata, Manjula
Nievergelt, Caroline M.
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Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Nievergelt, Caroline M.
Rao, Fangwen
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机构:Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Rao, Fangwen
Mahata, Sushil K.
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VA San Diego Healthcare Syst, San Diego, CA USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Mahata, Sushil K.
Schork, Nicholas J.
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Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Schork, Nicholas J.
Hicks, Pamela J.
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Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Hicks, Pamela J.
Bowden, Donald W.
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Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Bowden, Donald W.
Freedman, Barry I.
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Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Freedman, Barry I.
Brophy, Victoria H.
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Roche Mol Syst, Dept Human Genet, Alameda, CA USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Brophy, Victoria H.
O'Connor, Daniel T.
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Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
VA San Diego Healthcare Syst, San Diego, CA USAUniv Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA