TY - JOUR
T1 - Randomized trial of an intensified, multifactorial intervention in patients with advanced-stage diabetic kidney disease
T2 - Diabetic Nephropathy Remission and Regression Team Trial in Japan (DNETT-Japan)
AU - the Diabetic Nephropathy Remission and Regression Team Trial in Japan (DNETT-Japan) collaborative group
AU - Shikata, Kenichi
AU - Haneda, Masakazu
AU - Ninomiya, Toshiharu
AU - Koya, Daisuke
AU - Suzuki, Yoshiki
AU - Suzuki, Daisuke
AU - Ishida, Hitoshi
AU - Akai, Hiroaki
AU - Tomino, Yasuhiko
AU - Uzu, Takashi
AU - Nishimura, Motonobu
AU - Maeda, Shiro
AU - Ogawa, Daisuke
AU - Miyamoto, Satoshi
AU - Makino, Hirofumi
N1 - Funding Information:
DNETT-Japan was supported in part by a Grant-in-Aid for Scientific Research (200624010B to H Makino) from the Ministry of Health, Labor and Welfare of Japan from 2006 to 2009. This trial was also supported by Okayama Medical Foundation, Asahi Kasei Pharma, Astellas, AstraZeneca, Otsuka, Kowa Pharmaceutical, Daiichi Sankyo, Sanwa Kagaku, Sanofi Aventis, Sumitomo Dainippon Pharma, Takeda, Mitsubishi Tanabe Pharma, Chugai, Terumo, Eli Lilly, Novartis Pharma, MSD, Bayer, Boehringer Ingelheim, Eizai and Teijin Pharma. We thank Professor Michihiro Yoshida, Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan, for reviewing the paper.
Funding Information:
KS received speaker fees from MSD, Eli Lilly Japan, Nippon Boehringer Ingelheim, Novo Nordisk Pharma, Mitsubishi Tanabe and Kyowa Hakko Kirin; research support from Takeda, MSD, Kyowa Hakko Kirin and Mitsubishi Tanabe; and a consulting fee from Daiichi Sankyo. MH has received speaker fees from Astellas, Taisho‐Toyama, Tanabe‐Mitsubishi, Boehringer Ingelheim, Taisho, Kowa, Ono, MSD, Novartis and Novo‐Nordisk; and research support from Novo‐Nordisk, Ono, Shionogi and Johnson & Johnson. DK received speaker fees from MSD, Astellas Pharma Inc., Ono, Taisho, Mitsubishi Tanabe, Eli Lilly Japan, Boehringer‐Ingelheim Japan and Novo Nordisk Pharma; and research support from Ono., Taisho, Mitsubishi Tanabe and Boehringer‐Ingelheim Japan. HA received a research grant from Ono and Boehringer Ingelheim GmbH. MN received speaker fees from Mitsubishi Tanabe, Takeda, Kyowa Kirin, Taisho, Novo Nordisk Pharma and Daiichi Sankyo. HM is a consultant for AbbVie, Teijin and Boehringer‐Ingelheim Japan. TN, YS, SM, DS, TY, TU, DO and SM declare no conflict of interest.
Funding Information:
DNETT‐Japan was supported in part by a Grant‐in‐Aid for Scientific Research (200624010B to H Makino) from the Ministry of Health, Labor and Welfare of Japan from 2006 to 2009. This trial was also supported by Okayama Medical Foundation, Asahi Kasei Pharma, Astellas, AstraZeneca, Otsuka, Kowa Pharmaceutical, Daiichi Sankyo, Sanwa Kagaku, Sanofi Aventis, Sumitomo Dainippon Pharma, Takeda, Mitsubishi Tanabe Pharma, Chugai, Terumo, Eli Lilly, Novartis Pharma, MSD, Bayer, Boehringer Ingelheim, Eizai and Teijin Pharma. We thank Professor Michihiro Yoshida, Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan, for reviewing the paper.
Publisher Copyright:
© 2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd
PY - 2021/2
Y1 - 2021/2
N2 - Aims/Introduction: We evaluated the efficacy of multifactorial intensive treatment (IT) on renal outcomes in patients with type 2 diabetes and advanced-stage diabetic kidney disease (DKD). Materials and Methods: The Diabetic Nephropathy Remission and Regression Team Trial in Japan (DNETT-Japan) is a multicenter, open-label, randomized controlled trial with a 5-year follow-up period. We randomly assigned 164 patients with advanced-stage diabetic kidney disease (urinary albumin-to-creatinine ratio ≥300 mg/g creatinine, serum creatinine level 1.2–2.5 mg/dL in men and 1.0–2.5 mg/dL in women) to receive either IT or conventional treatment. The primary composite outcome was end-stage kidney failure, doubling of serum creatinine or death from any cause, which was assessed in the intention-to-treat population. Results: The IT tended to reduce the risk of primary end-points as compared with conventional treatment, but the difference between treatment groups did not reach the statistically significant level (hazard ratio 0.69, 95% confidence interval 0.43–1.11; P = 0.13). Meanwhile, the decrease in serum low-density lipoprotein cholesterol level and the use of statin were significantly associated with the decrease in primary outcome (hazard ratio 1.14; 95% confidence interval 1.05–1.23, P < 0.001 and hazard ratio 0.53, 95% confidence interval 0.28–0.998, P < 0.05, respectively). The incidence of adverse events was not different between treatment groups. Conclusions: The risk of kidney events tended to decrease by IT, although it was not statistically significant. Lipid control using statin was associated with a lower risk of adverse kidney events. Further follow-up study might show the effect of IT in patients with advanced diabetic kidney disease.
AB - Aims/Introduction: We evaluated the efficacy of multifactorial intensive treatment (IT) on renal outcomes in patients with type 2 diabetes and advanced-stage diabetic kidney disease (DKD). Materials and Methods: The Diabetic Nephropathy Remission and Regression Team Trial in Japan (DNETT-Japan) is a multicenter, open-label, randomized controlled trial with a 5-year follow-up period. We randomly assigned 164 patients with advanced-stage diabetic kidney disease (urinary albumin-to-creatinine ratio ≥300 mg/g creatinine, serum creatinine level 1.2–2.5 mg/dL in men and 1.0–2.5 mg/dL in women) to receive either IT or conventional treatment. The primary composite outcome was end-stage kidney failure, doubling of serum creatinine or death from any cause, which was assessed in the intention-to-treat population. Results: The IT tended to reduce the risk of primary end-points as compared with conventional treatment, but the difference between treatment groups did not reach the statistically significant level (hazard ratio 0.69, 95% confidence interval 0.43–1.11; P = 0.13). Meanwhile, the decrease in serum low-density lipoprotein cholesterol level and the use of statin were significantly associated with the decrease in primary outcome (hazard ratio 1.14; 95% confidence interval 1.05–1.23, P < 0.001 and hazard ratio 0.53, 95% confidence interval 0.28–0.998, P < 0.05, respectively). The incidence of adverse events was not different between treatment groups. Conclusions: The risk of kidney events tended to decrease by IT, although it was not statistically significant. Lipid control using statin was associated with a lower risk of adverse kidney events. Further follow-up study might show the effect of IT in patients with advanced diabetic kidney disease.
KW - Diabetic Nephropathy Remission and Regression Team Trial in Japan
KW - Diabetic kidney disease
KW - Diabetic nephropathy
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U2 - 10.1111/jdi.13339
DO - 10.1111/jdi.13339
M3 - Article
C2 - 32597548
AN - SCOPUS:85089074111
SN - 2040-1116
VL - 12
SP - 207
EP - 216
JO - Journal of Diabetes Investigation
JF - Journal of Diabetes Investigation
IS - 2
ER -