TY - JOUR
T1 - Increased pre-procedural urinary microalbumin is associated with a risk for renal functional deterioration after coronary computed tomography angiography
AU - Isobe, Satoshi
AU - Yuba, Miyuki
AU - Mori, Hiroaki
AU - Suzuki, Susumu
AU - Sato, Kimihide
AU - Ishii, Hideki
AU - Murohara, Toyoaki
N1 - Publisher Copyright:
© 2016 Elsevier Ireland Ltd
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Background Urinary microalbumin is a marker for preclinical nephropathy. A percentage change in cystatin C (%CyC) of ≥ 10% for 24 h after tests with contrast media is reportedly an independent predictor for developing contrast-induced nephropathy. We investigated the relationship between the presence of urinary microalbumin and changes in CyC after coronary computed tomography angiography (CCTA). Methods Three hundred and thirty-three patients with known or suspected coronary artery disease who scheduled for CCTA using a 70 mL of Iopamidol were enrolled. Serum creatinine and CyC levels were measured at baseline and 24 h post-procedure. The %CyC, absolute changes in estimated glomerular filtration rate (ΔeGFR), and oral fluid volume from pre- to post-procedure were calculated. The patients were dichotomized into 2 groups as follows: group A comprised 83 patients showing a %CyC of ≥ 10%; and group B comprised 250 patients showing a %CyC of < 10%. Results The ΔeGFR, fasting plasma glucose levels, HbA1c, and pre-procedural urinary microalbumin levels were significantly greater in group A than in group B. Oral fluid intake volume was significantly less in group A than in group B. The urinary microalbumin significantly correlated with %CyC (r = 0.504, P < 0.0001). Multivariate logistic regression analysis revealed that pre-procedural urinary microalbumin and oral fluid volume were independent predictors for %CyC ≥ 10%. The optimal cut-off value of a pre-procedural urinary microalbumin level was 58 mg/g·creatinine for predicting a %CyC ≥ 10% using receiver-operating-characteristic analysis. Conclusions Renal functional changes should be carefully paid attention to after CCTA, particularly in patients exhibiting increased pre-procedural urinary microablumin levels.
AB - Background Urinary microalbumin is a marker for preclinical nephropathy. A percentage change in cystatin C (%CyC) of ≥ 10% for 24 h after tests with contrast media is reportedly an independent predictor for developing contrast-induced nephropathy. We investigated the relationship between the presence of urinary microalbumin and changes in CyC after coronary computed tomography angiography (CCTA). Methods Three hundred and thirty-three patients with known or suspected coronary artery disease who scheduled for CCTA using a 70 mL of Iopamidol were enrolled. Serum creatinine and CyC levels were measured at baseline and 24 h post-procedure. The %CyC, absolute changes in estimated glomerular filtration rate (ΔeGFR), and oral fluid volume from pre- to post-procedure were calculated. The patients were dichotomized into 2 groups as follows: group A comprised 83 patients showing a %CyC of ≥ 10%; and group B comprised 250 patients showing a %CyC of < 10%. Results The ΔeGFR, fasting plasma glucose levels, HbA1c, and pre-procedural urinary microalbumin levels were significantly greater in group A than in group B. Oral fluid intake volume was significantly less in group A than in group B. The urinary microalbumin significantly correlated with %CyC (r = 0.504, P < 0.0001). Multivariate logistic regression analysis revealed that pre-procedural urinary microalbumin and oral fluid volume were independent predictors for %CyC ≥ 10%. The optimal cut-off value of a pre-procedural urinary microalbumin level was 58 mg/g·creatinine for predicting a %CyC ≥ 10% using receiver-operating-characteristic analysis. Conclusions Renal functional changes should be carefully paid attention to after CCTA, particularly in patients exhibiting increased pre-procedural urinary microablumin levels.
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U2 - 10.1016/j.ijcard.2016.12.049
DO - 10.1016/j.ijcard.2016.12.049
M3 - Article
C2 - 28057367
AN - SCOPUS:85008469149
SN - 0167-5273
VL - 230
SP - 599
EP - 603
JO - International Journal of Cardiology
JF - International Journal of Cardiology
ER -