TY - JOUR
T1 - Clinical outcome of renal artery stenting for hypertension and chronic kidney disease up to 12 months in the J-RAS study
T2 - Prospective, single-arm, multicenter clinical study
AU - J-RAS Study Investigators
AU - Fujihara, Masahiko
AU - Yokoi, Yoshiaki
AU - Abe, Takaaki
AU - Soga, Yoshimitsu
AU - Yamashita, Takehiro
AU - Miyashita, Yusuke
AU - Nakamura, Masato
AU - Yokoi, Hiroyoshi
AU - Ito, Sadayoshi
N1 - Publisher Copyright:
© 2015, Japanese Circulation Society. All rights reserved.
PY - 2015/1/16
Y1 - 2015/1/16
N2 - Background: Atherosclerotic renal artery stenosis (ARAS) causes renovascular hypertension (HTN) and impairs renal function, leading to chronic kidney disease (CKD). The J-RAS study was a prospective, multicenter study to assess the clinical outcome of renal artery stenting for up to 1 year in Japanese patients with ARAS. Methods and Results: One hundred and forty-nine patients were enrolled between November 2010 and January 2013. The patients were classified into an HTN (n=121) group and a CKD (n=108) group in the primary analysis. The primary efficacy endpoints were change in blood pressure for the HTN group and change in estimated glomerular filtration rate (eGFR) for the CKD group at 1 months. The primary safety endpoint was freedom from major cardiovascular or renal events at 12 months. In the HTN group, the mean systolic blood pressure (SBP) significantly decreased from 161.6±21 mmHg at baseline to 137.0±21 mmHg (P<0.0001). In the CKD group, there was no significant difference in eGFR from 40.7±10 ml · min−1 · 1.73 m−2 at baseline to 40.8±13 ml · min−1 · 1.73 m−2 (P=0.32). The primary safety endpoint was 89.4% at 12 months. Conclusions: In the J-RAS trial, significant SBP reduction was seen in the HTN group, and stabilization of renal function in the CKD group. Renal artery stenting for ARAS is safe and effective in Japanese patients.
AB - Background: Atherosclerotic renal artery stenosis (ARAS) causes renovascular hypertension (HTN) and impairs renal function, leading to chronic kidney disease (CKD). The J-RAS study was a prospective, multicenter study to assess the clinical outcome of renal artery stenting for up to 1 year in Japanese patients with ARAS. Methods and Results: One hundred and forty-nine patients were enrolled between November 2010 and January 2013. The patients were classified into an HTN (n=121) group and a CKD (n=108) group in the primary analysis. The primary efficacy endpoints were change in blood pressure for the HTN group and change in estimated glomerular filtration rate (eGFR) for the CKD group at 1 months. The primary safety endpoint was freedom from major cardiovascular or renal events at 12 months. In the HTN group, the mean systolic blood pressure (SBP) significantly decreased from 161.6±21 mmHg at baseline to 137.0±21 mmHg (P<0.0001). In the CKD group, there was no significant difference in eGFR from 40.7±10 ml · min−1 · 1.73 m−2 at baseline to 40.8±13 ml · min−1 · 1.73 m−2 (P=0.32). The primary safety endpoint was 89.4% at 12 months. Conclusions: In the J-RAS trial, significant SBP reduction was seen in the HTN group, and stabilization of renal function in the CKD group. Renal artery stenting for ARAS is safe and effective in Japanese patients.
KW - Atherosclerotic renal artery stenosis
KW - Chronic kidney disease
KW - Hypertension
KW - Renal artery stenting
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U2 - 10.1253/circj.CJ-14-0908
DO - 10.1253/circj.CJ-14-0908
M3 - Article
C2 - 25476409
AN - SCOPUS:84928237474
SN - 1346-9843
VL - 79
SP - 351
EP - 359
JO - Circulation Journal
JF - Circulation Journal
IS - 2
ER -