Association of serum total bilirubin levels with progressive renal decline and end-stage kidney disease: 10-year observational cohort study in Japanese patients with diabetes

被引:9
|
作者
Eto, Erina [1 ,4 ]
Maeda, Yasutaka [1 ,5 ]
Sonoda, Noriyuki [1 ,6 ]
Nakashima, Naoki [2 ]
Kobayashi, Kunihisa [1 ,7 ]
Takayanagi, Ryoichi [1 ,8 ]
Ogawa, Yoshihiro [1 ]
Inoguchi, Toyoshi [3 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Med & Bioregulatory Sci, Fukuoka, Japan
[2] Kyushu Univ Hosp, Med Informat Ctr, Fukuoka, Japan
[3] Fukuoka City Med Assoc, Fukuoka City Hlth Promot Support Ctr, Fukuoka, Japan
[4] Saga Ken Med Ctr Koseikan, Dept Endocrinol & Diabet, Saga, Japan
[5] Minami Diabet Clin Res Ctr, Fukuoka, Japan
[6] Sonoda Clin, Kagoshima, Japan
[7] Fukuoka Univ, Dept Endocrinol & Diabet Mellitus, Chikushi Hosp, Fukuoka, Japan
[8] Fukuoka Sanno Hosp, Fukuoka, Japan
来源
PLOS ONE | 2022年 / 17卷 / 07期
关键词
OXIDATIVE STRESS; GFR DECLINE; RISK; NEPHROPATHY; DNA; ANTIOXIDANT; DYSFUNCTION; DAMAGE; RATS;
D O I
10.1371/journal.pone.0271179
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective Previous reports have demonstrated the association of serum bilirubin levels with the progression of diabetic nephropathy. The objective of this study is to assess the association of basal bilirubin levels with progressive renal decline (PRD) and end-stage kidney disease (ESKD). Methods A total of 298 patients with diabetes who visited Kyushu University Hospital (Japan) were recruited and followed up for 10 years. PRD was defined as a negative change in estimated glomerular filtration ratio (eGFR) >3.7%/year, 2.5th percentile. Logistic regression analysis was performed to evaluate the association of total bilirubin levels with PRD and its cut-off point was determined by receiver operating characteristic (ROC) analysis. Kaplan-Meier method and Cox hazard regression analysis were used to evaluate the predictive ability of its cut-off point for ESKD. Results Logistic regression model showed that total bilirubin levels were significantly associated with PRD, and ROC analysis showed that its cut-off point was 0.5 mg/dL. Kaplan-Meier method showed that the percent of patients who reached two endpoints, composite endpoint (ESKD or doubling of creatinine level) or 30% eGFR decline, was significantly higher in the low bilirubin group than in the high bilirubin group (18.5% vs 11.0%, P = 0.045; 49.1% vs 42.1%, P = 0.045, respectively, log-rank test). Cox hazard regression models confirmed the independence of the predictive ability of its cut-off point. Conclusions Serum total bilirubin levels were negatively associated with PRD in diabetic nephropathy and its cut-off point was 0.5 mg/dL. It may be clinically useful for identifying patients at high risk of ESKD.
引用
收藏
页数:14
相关论文
共 50 条
  • [31] Serum Endocan Levels and Subclinical Atherosclerosis in Patients with Chronic Kidney and End-Stage Renal Diseases
    El-Senosy, Fatma M.
    Abd El Aziz, Rasha Elsayed Mohamed
    Kasim, Sammar Ahmed
    Gad, Lamia Abdulbary
    Hassan, Donia Ahmed
    Sabry, Seham
    El Mancy, Ismail Mohamed
    Shawky, Taiseer Ahmed
    Mohamed, Ibrahim Ghounim Ramadan
    Elmonier, Rady
    Kotb, Essam
    Abdul-Mohymen, Abeer Mohammed
    INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2022, 2022
  • [32] Sugammadex use in patients with end-stage renal disease: a historical cohort study
    Paredes, Stephania
    Porter, Steven B.
    Porter, Ivan E., II
    Ross Renew, J.
    CANADIAN JOURNAL OF ANESTHESIA-JOURNAL CANADIEN D ANESTHESIE, 2020, 67 (12): : 1789 - 1797
  • [33] Clinical study of kidney transplantation in diabetic patients with end-stage renal disease
    Sato, S
    Babazono, T
    Tomonaga, O
    Nakamura, M
    Hoshino, T
    Sageshima, J
    Tojimbara, T
    Fujita, S
    Nakajima, I
    Fuchinoue, S
    Teraoka, S
    Agishi, T
    TRANSPLANTATION PROCEEDINGS, 1998, 30 (07) : 3097 - 3098
  • [34] Simultaneous pancreas-kidney transplants in type I and type II diabetic patients with end-stage renal disease: Similar 10-year outcomes
    Light, JA
    Barhyte, DY
    TRANSPLANTATION PROCEEDINGS, 2005, 37 (02) : 1283 - 1284
  • [35] Serum albumin fragmentation in end-stage renal disease patients - a pilot study
    Donadio, Elena
    Piccolomini, Francesco
    Dimuccio, Veronica
    Felicioli, Antonio
    Balestreri, Ettore
    Cianti, Riccardo
    Armini, Alessandro
    Bini, Luca
    Felicioli, Romano
    Donadio, Carlo
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2009, 47 (11) : 1373 - 1379
  • [36] Progression to end-stage kidney disease in Japanese children with chronic kidney disease: results of a nationwide prospective cohort study
    Ishikura, Kenji
    Uemura, Osamu
    Hamasaki, Yuko
    Ito, Shuichi
    Wada, Naohiro
    Hattori, Motoshi
    Ohashi, Yasuo
    Tanaka, Ryojiro
    Nakanishi, Koichi
    Kaneko, Tetsuji
    Honda, Masataka
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2014, 29 (04) : 878 - 884
  • [37] Association between kidney function and mortality in type 2 diabetes patients: a 10-year prospective cohort study
    He, J.
    Fan, X.
    Yu, H.
    Qin, Y.
    Jian, S.
    Zhou, J.
    Lu, Y.
    Pan, E.
    Hang, D.
    Shen, C.
    Wu, M.
    DIABETOLOGIA, 2024, 67 : S199 - S200
  • [38] Increased end-stage renal disease risk in age-related macular degeneration: a nationwide cohort study with 10-year follow-up
    Jung, Wonyoung
    Park, Junhee
    Jang, Hye Ryoun
    Jeon, Junseok
    Han, Kyungdo
    Kim, Bongseong
    Yoon, Je Moon
    Lim, Dong Hui
    Shin, Dong Wook
    SCIENTIFIC REPORTS, 2023, 13 (01):
  • [39] Increased end-stage renal disease risk in age-related macular degeneration: a nationwide cohort study with 10-year follow-up
    Wonyoung Jung
    Junhee Park
    Hye Ryoun Jang
    Junseok Jeon
    Kyungdo Han
    Bongseong Kim
    Je Moon Yoon
    Dong Hui Lim
    Dong Wook Shin
    Scientific Reports, 13 (1)
  • [40] Comparison of mortality and end-stage renal disease (ESRD) between patients in one diabetes center and others in Japanese DERI cohort
    Uchigata, Y
    Asao, K
    Matsushima, M
    Otani, T
    Matsuura, N
    Tajima, N
    Iwamoto, Y
    DIABETOLOGIA, 2000, 43 : A256 - A256