TY - JOUR
T1 - Japan Renal Biopsy Registry and Japan Kidney Disease Registry
T2 - Committee report for 2009 and 2010
AU - Sugiyama, Hitoshi
AU - Yokoyama, Hitoshi
AU - Sato, Hiroshi
AU - Saito, Takao
AU - Kohda, Yukimasa
AU - Nishi, Shinichi
AU - Tsuruya, Kazuhiko
AU - Kiyomoto, Hideyasu
AU - Iida, Hiroyuki
AU - Sasaki, Tamaki
AU - Higuchi, Makoto
AU - Hattori, Motoshi
AU - Oka, Kazumasa
AU - Kagami, Shoji
AU - Kawamura, Tetsuya
AU - Takeda, Tetsuro
AU - Hataya, Hiroshi
AU - Fukasawa, Yuichiro
AU - Fukatsu, Atsushi
AU - Morozumi, Kunio
AU - Yoshikawa, Norishige
AU - Shimizu, Akira
AU - Kitamura, Hiroshi
AU - Yuzawa, Yukio
AU - Matsuo, Seiichi
AU - Kiyohara, Yutaka
AU - Joh, Kensuke
AU - Nagata, Michio
AU - Taguchi, Takashi
AU - Makino, Hirofumi
N1 - Funding Information:
T. Saito was supported by Novartis Pharma Co. and Kyowa-Kirin Co. Other authors declare no competing interests.
Funding Information:
The authors greatly acknowledge the help and assistance of many colleagues in centers and affiliate hospitals with collection of data for the J-RBR/J-KDR. We also sincerely thank Ms. M. Irie of the UNIN-INDICE and Ms. Y. Saito of the JSN for supporting the registration system and Ms. K. Fukuda of the JSN for submitting the manuscript. This study was supported by the committee grant from the Japanese Society of Nephrology and by a grant-in-aid from the Research Group on Progressive Renal Disease from the Ministry of Health, Labor and Welfare, Japan.
PY - 2013/4
Y1 - 2013/4
N2 - The Japan Renal Biopsy Registry (J-RBR) was started in 2007 and the Japan Kidney Disease Registry (J-KDR) was then started in 2009 by the Committee for Standardization of Renal Pathological Diagnosis and the Committee for the Kidney Disease Registry of the Japanese Society of Nephrology. The purpose of this report is to describe and summarize the registered data from 2009 and 2010. For the J-KDR, data were collected from 4,016 cases, including 3,336 (83.1 %) by the J-RBR and 680 (16.9 %) other cases from 59 centers in 2009, and from 4,681 cases including 4,106 J-RBR cases (87.7 %) and 575 other cases (12.3 %) from 94 centers in 2010, including the affiliate hospitals. In the J-RBR, 3,165 native kidneys (94.9 %) and 171 renal grafts (5.1 %) and 3,869 native kidneys (94.2 %) and 237 renal grafts (5.8 %)were registered in 2009 and 2010, respectively. Patients younger than 20 years of age comprised 12.1 % of the registered cases, and those 65 years and over comprised 24.5 % of the cases with native kidneys in 2009 and 2010. The most common clinical diagnosis was chronic nephritic syndrome (55.4 % and 50.0 % in 2009 and 2010, respectively), followed by nephrotic syndrome (22.4 % and 27.0 %); the most frequent pathological diagnosis as classified by the pathogenesis was IgA nephropathy (31.6 % and 30.4 %), followed by primary glomerular diseases (except IgA nephropathy) (27.2 % and 28.1 %). Among the primary glomerular diseases (except IgA nephropathy) in the patients with nephrotic syndrome, membranous nephropathy was the most common histopathology in 2009 (40.3 %) and minor glomerular abnormalities (50.0 %) were the most common in 2010 in native kidneys in the J-RBR. Five new secondary and longitudinal research studies by the J-KDR were started in 2009 and one was started in 2010.
AB - The Japan Renal Biopsy Registry (J-RBR) was started in 2007 and the Japan Kidney Disease Registry (J-KDR) was then started in 2009 by the Committee for Standardization of Renal Pathological Diagnosis and the Committee for the Kidney Disease Registry of the Japanese Society of Nephrology. The purpose of this report is to describe and summarize the registered data from 2009 and 2010. For the J-KDR, data were collected from 4,016 cases, including 3,336 (83.1 %) by the J-RBR and 680 (16.9 %) other cases from 59 centers in 2009, and from 4,681 cases including 4,106 J-RBR cases (87.7 %) and 575 other cases (12.3 %) from 94 centers in 2010, including the affiliate hospitals. In the J-RBR, 3,165 native kidneys (94.9 %) and 171 renal grafts (5.1 %) and 3,869 native kidneys (94.2 %) and 237 renal grafts (5.8 %)were registered in 2009 and 2010, respectively. Patients younger than 20 years of age comprised 12.1 % of the registered cases, and those 65 years and over comprised 24.5 % of the cases with native kidneys in 2009 and 2010. The most common clinical diagnosis was chronic nephritic syndrome (55.4 % and 50.0 % in 2009 and 2010, respectively), followed by nephrotic syndrome (22.4 % and 27.0 %); the most frequent pathological diagnosis as classified by the pathogenesis was IgA nephropathy (31.6 % and 30.4 %), followed by primary glomerular diseases (except IgA nephropathy) (27.2 % and 28.1 %). Among the primary glomerular diseases (except IgA nephropathy) in the patients with nephrotic syndrome, membranous nephropathy was the most common histopathology in 2009 (40.3 %) and minor glomerular abnormalities (50.0 %) were the most common in 2010 in native kidneys in the J-RBR. Five new secondary and longitudinal research studies by the J-KDR were started in 2009 and one was started in 2010.
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U2 - 10.1007/s10157-012-0746-8
DO - 10.1007/s10157-012-0746-8
M3 - Article
C2 - 23385776
AN - SCOPUS:84891444188
SN - 1342-1751
VL - 17
SP - 155
EP - 173
JO - Clinical and Experimental Nephrology
JF - Clinical and Experimental Nephrology
IS - 2
ER -