Association of Lower Serum Bilirubin With Loss of Residual Kidney Function in Peritoneal Dialysis Patients.


Journal

Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy
ISSN: 1744-9987
Titre abrégé: Ther Apher Dial
Pays: Australia
ID NLM: 101181252

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 06 02 2019
revised: 08 05 2019
accepted: 12 06 2019
pubmed: 18 6 2019
medline: 15 12 2020
entrez: 18 6 2019
Statut: ppublish

Résumé

Bilirubin is recognized as an endogenous antioxidant, and low serum bilirubin is reported to be associated with the progression of kidney disease. However, it is unclear whether serum bilirubin levels are associated with the loss of residual kidney function (RKF) in peritoneal dialysis (PD) patients. This study investigated the relationship between serum total bilirubin and loss of RKF. We prospectively followed 94 PD patients who started PD in our hospital between June 2006 and May 2016. Ten patients who had chronic liver disease or cirrhosis were excluded. Patients were divided into three groups based on serum total bilirubin concentration tertiles: tertile 1 (T1) < 0.3, T2 = 0.3, and T3 ≥ 0.4 mg/dL. We estimated the relationship between serum bilirubin and loss of RKF, defined as daily urine volume (<100 mL) within 3 years after starting PD, using a Cox proportional hazards model. During the 3-year observation period, 22 patients lost RKF. The incidence rate of loss of RKF increased linearly with the decrease in serum total bilirubin levels (P for trend < 0.05). After adjusting for confounding factors, low serum total bilirubin level was shown to be an independent predictor of loss of RKF (hazard ratio [HR] for every 0.1 mg/dL decrease, 1.50; 95% confidence interval [CI], 1.01-2.51; HR [95%CI] for T2 and T1 [vs. T3] 2.03 [0.65-7.88] and 3.70 [1.00-15.9]). This study suggests that low serum total bilirubin levels are associated with the loss of RKF in PD patients.

Identifiants

pubmed: 31207066
doi: 10.1111/1744-9987.12865
doi:

Substances chimiques

Bilirubin RFM9X3LJ49

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

202-207

Informations de copyright

© 2019 International Society for Apheresis, Japanese Society for Apheresis, and Japanese Society for Dialysis Therapy.

Références

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Auteurs

Hiroaki Tsujikawa (H)

Department of Medicine and Clinical Science, Kyushu University, Fukuoka, Japan.

Shigeru Tanaka (S)

Fukuoka Dental College, Fukuoka, Japan.

Masatoshi Hara (M)

Department of Medicine and Clinical Science, Kyushu University, Fukuoka, Japan.

Yasuhiro Kawai (Y)

Department of Medicine and Clinical Science, Kyushu University, Fukuoka, Japan.

Yuta Matsukuma (Y)

Department of Medicine and Clinical Science, Kyushu University, Fukuoka, Japan.

Kumiko Torisu (K)

Department of Medicine and Clinical Science, Kyushu University, Fukuoka, Japan.
Department of Integrated Therapy for Chronic Kidney Disease, Kyushu University, Fukuoka, Japan.

Toshiaki Nakano (T)

Department of Medicine and Clinical Science, Kyushu University, Fukuoka, Japan.

Kazuhiko Tsuruya (K)

Department of Integrated Therapy for Chronic Kidney Disease, Kyushu University, Fukuoka, Japan.
Department of Nephrology, Nara Medical University, Nara, Japan.

Takanari Kitazono (T)

Department of Medicine and Clinical Science, Kyushu University, Fukuoka, Japan.

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