TY - JOUR
T1 - Lower levels of proteinuria are associated with elevated mortality in incident dialysis patients
AU - Hishida, Manabu
AU - Shafi, Tariq
AU - Appel, Lawrence J.
AU - Maruyama, Shoichi
AU - Inaguma, Daijo
AU - Matsushita, Kunihiro
N1 - Funding Information:
Manabu Hishida reports grants from the Kaikoukai Healthcare Group. The Aichi Kidney Foundation partially provided funding for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Shoichi Maruyama received research funding from Otsuka Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co.,Ltd., Pfizer Inc., Kyowa Hakko Kirin Co.,Ltd., MSD KK, Astellas Pharma Inc., Torii Pharmaceutical Co.,Ltd., Daiichi Sankyo Co.,Ltd., Sumitomo Dainippon Pharma Co., Ltd., Alexion Pharmaceuticals,Inc., and Sanwa Kagaku Kenkyusho Co.,Ltd. Kunihiro Matsushita received research funding and personal fee from Kyowa Kirin and personal fee from Akebia outside of the work. These do not alter the adherence to all PLOS ONE policies on sharing data and materials. We acknowledge the support provided by the following members of the Aichi Cohort study of Prognosis in Patients Newly Initiated into Dialysis (AICOPP), who participated in this study: Yasuhiro Otsuka, Asami Takeda (Japanese Red Cross Nagoya Daiichi Hospital), Hirofumi Tamai (Anjo Kosei Hospital), Tomohiko Naruse (Kasugai Municipal Hospital), Kei Kurata (Tosei General Hospital), Hideto Oishi (Komaki City Hospital), Isao Aoyama (Japanese Community Healthcare Organization Chukyo Hospital), Hiroshi Ogawa (Shinseikai Daiichi Hospital), Hiroko ushimoto (Chita City Hospital), Hideaki Shimizu (Chubu-Rosai Hospital), Junichiro amamoto (Tsushima City Hospital), Hisashi Kurata (Toyota Kosei Hospital), Taishi Yamakawa (Toyohashi unicipal Hospital), Takaaki Yaomura (Nagoya Medical Center), Hirotake asuga (Nagoya Kyouritsu Hospital), Shizunori Ichida (Japanese Red Cross Nagoya Daiichi Hospital), Shoichi Maruyama (Nagoya University Graduate School of Medicine), Seiichi Matsuo (Nagoya University Graduate School of Medicine), Noritoshi Kato (Nagoya University Graduate Schoolof Medicine), Shigehisa Koide (Fujita Health University Hospital), and Yukio Yuzawa (Fujita Health University Hospital)
Publisher Copyright:
© 2019 Hishida et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2019/12
Y1 - 2019/12
N2 - Introduction Proteinuria is a potent predictor of adverse events in general, although a few large studies have reported a J-shaped association between proteinuria and mortality in individuals with glomerular filtration rate <30 ml/min/1.73m2. However, this association has not been specifically evaluated among incident dialysis patients. Methods Among 1,380 Japanese patients who initiated dialysis, we quantified the association of pre-dialysis dipstick proteinuria (negative/trace, 1+, 2+, and ≥3+) with mortality using Cox models adjusting for potential confounders, such as age, gender, clinical history of hypertension, diabetes, and cardiovascular disease. Results Mean age of study participants was 67.4 (SD 13.0) years, and 67.6% were men. The most common dipstick proteinuria category was ≥3+ (55.4%), followed by 2+ (31.2%), 1+ (9.9%), and negative or trace (3.5%). Patients with lower proteinuria level were older than those with higher proteinuria. Lower proteinuria was significantly associated with a higher risk of all-cause mortality, even after accounting for potential confounders (p for trend <0.001). In those with negative/trace dipstick proteinuria compared to those with dipstick proteinuria ≥3+, the adjusted hazard ratio was 2.60 [95% CI: 1.62–4.17] in the fully adjusted model. Similar findings were observed when analyses were restricted to patients older than 70 years, and when cardiovascular mortality and non-cardiovascular mortality were analyzed separately. Conclusions In incident dialysis patients, pre-dialysis proteinuria was inversely associated with mortality risk. Although future studies are needed to identify mechanisms, our findings suggest the need to carefully interpret proteinuria in patients with incident dialysis.
AB - Introduction Proteinuria is a potent predictor of adverse events in general, although a few large studies have reported a J-shaped association between proteinuria and mortality in individuals with glomerular filtration rate <30 ml/min/1.73m2. However, this association has not been specifically evaluated among incident dialysis patients. Methods Among 1,380 Japanese patients who initiated dialysis, we quantified the association of pre-dialysis dipstick proteinuria (negative/trace, 1+, 2+, and ≥3+) with mortality using Cox models adjusting for potential confounders, such as age, gender, clinical history of hypertension, diabetes, and cardiovascular disease. Results Mean age of study participants was 67.4 (SD 13.0) years, and 67.6% were men. The most common dipstick proteinuria category was ≥3+ (55.4%), followed by 2+ (31.2%), 1+ (9.9%), and negative or trace (3.5%). Patients with lower proteinuria level were older than those with higher proteinuria. Lower proteinuria was significantly associated with a higher risk of all-cause mortality, even after accounting for potential confounders (p for trend <0.001). In those with negative/trace dipstick proteinuria compared to those with dipstick proteinuria ≥3+, the adjusted hazard ratio was 2.60 [95% CI: 1.62–4.17] in the fully adjusted model. Similar findings were observed when analyses were restricted to patients older than 70 years, and when cardiovascular mortality and non-cardiovascular mortality were analyzed separately. Conclusions In incident dialysis patients, pre-dialysis proteinuria was inversely associated with mortality risk. Although future studies are needed to identify mechanisms, our findings suggest the need to carefully interpret proteinuria in patients with incident dialysis.
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U2 - 10.1371/journal.pone.0226866
DO - 10.1371/journal.pone.0226866
M3 - Article
C2 - 31869391
AN - SCOPUS:85077210034
SN - 1932-6203
VL - 14
JO - PLoS ONE
JF - PLoS ONE
IS - 12
M1 - e0226866
ER -