Evidence map›Paper›PMID 42432533›Full record

ArticleBMC nephrology2026

Bile acids as a predictor for all-cause mortality in peritoneal dialysis patients: a retrospective cohort study.

Siyuan Zhao, Xiaoxiao Wang, Qiong Bai, Wen Tang

Abstract read
In one paragraph

Article in BMC nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Siyuan ZhaoDepartment of Nephrology, Peking University Third Hospital, 49 North Garden Rd, Haidian District, 100191, Beijing, P. R. China.
Xiaoxiao WangResearch Center of Clinical Epidemiology, Peking University Third Hospital, Beijing, China.
Qiong BaiDepartment of Nephrology, Peking University Third Hospital, 49 North Garden Rd, Haidian District, 100191, Beijing, P. R. China. baiqiong@bjmu.edu.cn.
Wen TangDepartment of Nephrology, Peking University Third Hospital, 49 North Garden Rd, Haidian District, 100191, Beijing, P. R. China. tanggwen@126.com.

Funding

Clinical Cohort Construction Program of Peking University Third Hospital BYSYDL2023004Key Clinical Program of Peking University Third Hospital No. BYSYZD2021036National Natural Science Foundation of China 82470774
6 · The paper itself

Abstract

backgroundBile acids (BAs) are now recognized as endocrine hormones involved in glucose and lipid metabolism regulation and inflammation control. Recent studies have also shown the association of BAs level in chronic kidney disease progression and hemodialysis patients' prognosis. However, their role in peritoneal dialysis (PD) is unknown. Therefore, based on a longitudinal cohort, this study aims to explore the relationship of BAs and all-cause mortality in PD patients.

methodsA retrospective cohort study was conducted involving 517 PD patients. Serum BAs level prior to PD catheterization were collected. Restricted cubic spline (RCS) analysis with full adjustment was used to characterize the dose-response relationship between serum BAs and all-cause mortality. Cox proportional hazards regression models were performed to assess the independent association between BAs levels and all-cause mortality.

resultsA total of 517 patients were included. During a median follow-up of 3.65 (1.36, 5.46) years, death occurred in 210 of 517 (40.6%) patients. The relationship between BAs levels and the risk of all-cause mortality was fitted using multivariate RCS adjusted for clinical relevant factors showing that BAs levels were linearly associated with all-cause mortality (p for non-linearity = 0.589). Further Kaplan-Meier survival analysis revealed a significantly higher all-cause mortality risk in the high BAs group (log rank score 13.04, p < 0.001). Cox regression showed that elevated BAs levels were an independent risk factor for all-cause mortality in PD patients (HR = 1.056, 95% CI: 1.005-1.109, p = 0.031) after adjusting for confounding factors.

conclusionElevated pre-dialysis serum BAs levels are independently associated with increased all-cause mortality in PD patients. Serum BAs may represent a potential prognostic indicator, although further validation is required before clinical application.

Indexed as

Bile Acids and SaltsKidney Failure, ChronicPeritoneal DialysisAgedBiomarkersCause of DeathCohort StudiesFemaleHumansLongitudinal StudiesMaleMiddle AgedPredictive Value of TestsPrognosisProportional Hazards ModelsRetrospective StudiesBile Acids and SaltsBiomarkersBile acidsMortalityPeritoneal dialysis

Identifiers

PMID42432533
PMCPMC13640373

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.