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DOI 10.1007/s10157-018-1579-x

Медицинская библиотека · Clinical and experimental nephrology · 2018

Regional variations in immunosuppressive therapy in patients with primary nephrotic syndrome: the Japan nephrotic syndrome cohort study.

Yamamoto Ryohei, Imai Enyu, Maruyama Shoichi, Yokoyama Hitoshi, Sugiyama Hitoshi, Nitta Kosaku, Tsukamoto Tatsuo, Uchida Shunya, Takeda Asami, Sato Toshinobu, Wada Takashi, Hayashi Hiroki, Akai Yasuhiro, Fukunaga Megumu, Tsuruya Kazuhiko, Masutani Kosuke, Konta Tsuneo, Shoji Tatsuya, Hiramatsu Takeyuki, Goto Shunsuke, Tamai Hirofumi, Nishio Saori, Shirasaki Arimasa, Nagai Kojiro, Yamagata Kunihiro, Hasegawa Hajime, Yasuda Hidemo, Ichida Shizunori, Naruse Tomohiko, Fukami Kei, Nishino Tomoya, Sobajima Hiroshi, Tanaka Satoshi, Akahori Toshiyuki, Ito Takafumi, Yoshio Terada, Katafuchi Ritsuko, Fujimoto Shouichi, Okada Hirokazu, Ishimura Eiji, Kazama Junichiro James, Hiromura Keiju, Mimura Tetsushi, Suzuki Satashi, Saka Yosuke, Sofue Tadashi, Suzuki Yusuke, Shibagaki Yugo, Kitagawa Kiyoki, Morozumi Kunio, Fujita Yoshiro, Mizutani Makoto, Shigematsu Takashi, Kashihara Naoki, Sato Hiroshi, Matsuo Seiichi, Narita Ichiei, Isaka Yoshitaka

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Аннотация

BACKGROUND

The lack of high-quality clinical evidences hindered broad consensus on optimal therapies for primary nephrotic syndromes. The aim of the present study was to compare prevalence of immunosuppressive drug use in patients with primary nephrotic syndrome across 6 regions in Japan.

METHODS

Between 2009 and 2010, 380 patients with primary nephrotic syndrome in 56 hospitals were enrolled in a prospective cohort study [Japan Nephrotic Syndrome Cohort Study (JNSCS)], including 141, 151, and 38 adult patients with minimal change disease (MCD), membranous nephropathy (MN), and focal segmental glomerulosclerosis (FSGS), respectively. Their clinical characteristics were compared with those of patients registered in a large nationwide registry of kidney biopsies [Japan Renal Biopsy Registry (J-RBR)]. The regional prevalence of use of each immunosuppressive drug was assessed among adult MCD, MN, and FSGS patients who underwent immunosuppressive therapy in the JNSCS (n = 139, 127, and 34, respectively). Predictors of its use were identified using multivariable-adjusted logistic regression models.

RESULTS

The clinical characteristics of JNSCS patients were comparable to those of J-RBR patients, suggesting that the JNSCS included the representatives in the J-RBR. The secondary major immunosuppressive drugs were intravenous methylprednisolone [n = 33 (24.6%), 24 (19.7%), and 9 (28.1%) in MCD, MN, and FSGS, respectively] and cyclosporine [n = 25 (18.7%), 62 (50.8%), and 16 (50.0%), respectively]. The region was identified as a significant predictor of use of intravenous methylprednisolone in MCD and MN patients.

CONCLUSION

Use of intravenous methylprednisolone for MCD and MN differed geographically in Japan. Its efficacy should be further evaluated in a well-designed trial.

Для цитирования: Yamamoto Ryohei, Imai Enyu, Maruyama Shoichi, Yokoyama Hitoshi, Sugiyama Hitoshi, Nitta Kosaku, Tsukamoto Tatsuo, Uchida Shunya, Takeda Asami, Sato Toshinobu, Wada Takashi, Hayashi Hiroki, Akai Yasuhiro, Fukunaga Megumu, Tsuruya Kazuhiko, Masutani Kosuke, Konta Tsuneo, Shoji Tatsuya, Hiramatsu Takeyuki, Goto Shunsuke, Tamai Hirofumi, Nishio Saori, Shirasaki Arimasa, Nagai Kojiro, Yamagata Kunihiro, Hasegawa Hajime, Yasuda Hidemo, Ichida Shizunori, Naruse Tomohiko, Fukami Kei, Nishino Tomoya, Sobajima Hiroshi, Tanaka Satoshi, Akahori Toshiyuki, Ito Takafumi, Yoshio Terada, Katafuchi Ritsuko, Fujimoto Shouichi, Okada Hirokazu, Ishimura Eiji, Kazama Junichiro James, Hiromura Keiju, Mimura Tetsushi, Suzuki Satashi, Saka Yosuke, Sofue Tadashi, Suzuki Yusuke, Shibagaki Yugo, Kitagawa Kiyoki, Morozumi Kunio, Fujita Yoshiro, Mizutani Makoto, Shigematsu Takashi, Kashihara Naoki, Sato Hiroshi, Matsuo Seiichi, Narita Ichiei, Isaka Yoshitaka. Regional variations in immunosuppressive therapy in patients with primary nephrotic syndrome: the Japan nephrotic syndrome cohort study.. Clinical and experimental nephrology. 2018. DOI: 10.1007/s10157-018-1579-x.

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