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Clinicopathological analysis of biopsy-proven diabetic nephropathy based on the Japanese classification of diabetic nephropathy
Authors:Kengo Furuichi  Miho Shimizu  Yukio Yuzawa  Akinori Hara  Tadashi Toyama  Hiroshi Kitamura  Yoshiki Suzuki  Hiroshi Sato  Noriko Uesugi  Yoshifumi Ubara  Junichi Hohino  Satoshi Hisano  Yoshihiko Ueda  Shinichi Nishi  Hitoshi Yokoyama  Tomoya Nishino  Kentaro Kohagura  Daisuke Ogawa  Koki Mise  Yugo Shibagaki  Hirofumi Makino  Seiichi Matsuo  Takashi Wada  Research Group of Diabetic Nephropathy  Ministry of Health  Labour  Welfare of Japan  and Japan Agency for Medical Research  Development
Affiliation:1.Department of Nephrology,Kanazawa University Hospital,Kanazawa,Japan;2.Department of Nephrology,Fujita Health University Hospital,Toyoake,Japan;3.Department of Pathology, Clinical Research Center,National Hospital Organization Chiba East National Hospital,Chiba,Japan;4.Health Administration Center, Niigata University,Niigata,Japan;5.Clinical Pharmacology and Therapeutics,Tohoku University Graduate School of Pharmaceutical Sciences,Sendai,Japan;6.Department of Pathology, Faculty of Medicine,University of Tsukuba,Tsukuba,Japan;7.Nephrology Center, Toranomon Hospital,Minato,Japan;8.Department of Pathology, Faculty of Medicine,Fukuoka University,Fukuoka,Japan;9.Department of Pathology,Dokkyo Medical University Koshigaya Hospital,Koshigaya,Japan;10.Division of Nephrology and Kidney Center,Kobe University Graduate School of Medicine,Kobe,Japan;11.Department of Nephrology,Kanazawa Medical University School of Medicine,Uchinada,Japan;12.Second Department of Internal Medicine,Nagasaki University School of Medicine,Nagasaki,Japan;13.Department of Cardiovascular Medicine, Nephrology and Neurology,University of the Ryukyus School of Medicine,Okinawa,Japan;14.Department of Nephrology, Rheumatology, Endocrinology and Metabolism,Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences,Okayama,Japan;15.Division of Nephrology and Hypertension, Department of Internal Medicine,St. Marianna University School of Medicine,Kawasaki,Japan;16.Division of Nephrology, Department of Internal Medicine,Nagoya University Graduate School of Medicine,Nagoya,Japan;17.Department of Nephrology and Laboratory Medicine,Kanazawa University,Kanazawa,Japan
Abstract:

Background

The Japanese classification of diabetic nephropathy reflects the risks of mortality, cardiovascular events and kidney prognosis and is clinically useful. Furthermore, pathological findings of diabetic nephropathy are useful for predicting prognoses. In this study, we evaluated the characteristics of pathological findings in relation to the Japanese classification of diabetic nephropathy and their ability to predict prognosis.

Methods

The clinical data of 600 biopsy-confirmed diabetic nephropathy patients were collected retrospectively from 13 centers across Japan. Composite kidney events, kidney death, cardiovascular events, all-cause mortality, and decreasing rate of estimated GFR (eGFR) were evaluated based on the Japanese classification of diabetic nephropathy.

Results

The median observation period was 70.4 (IQR 20.9–101.0) months. Each stage had specific characteristic pathological findings. Diffuse lesions, interstitial fibrosis and/or tubular atrophy (IFTA), interstitial cell infiltration, arteriolar hyalinosis, and intimal thickening were detected in more than half the cases, even in Stage 1. An analysis of the impacts on outcomes in all data showed that hazard ratios of diffuse lesions, widening of the subendothelial space, exudative lesions, mesangiolysis, IFTA, and interstitial cell infiltration were 2.7, 2.8, 2.7, 2.6, 3.5, and 3.7, respectively. Median declining speed of eGFR in all cases was 5.61 mL/min/1.73 m2/year, and the median rate of declining kidney function within 2 years after kidney biopsy was 24.0%.

Conclusions

This study indicated that pathological findings could categorize the high-risk group as well as the Japanese classification of diabetic nephropathy. Further study using biopsy specimens is required to clarify the pathogenesis of diabetic kidney disease.
Keywords:
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