Evidence map›Paper›PMID 41368586›Full record

ArticleDrug design, development and therapy2025

Enhanced Nutritional Support May Ameliorate Rivaroxaban-Related Rapid Renal Function Decline: New Insights from a Real-World Study.

Cheng Meng, Linjie Li, Ying Han, Xinxin Zhang, Yujia Lin, Hangkuan Liu, Shichen Jiang, Tiekun Yan, Lirong Zhang, Baocheng Chang and 2 more

Abstract read
In one paragraph

Article in Drug design, development and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Cheng Meng *Department of Nephrology, Kidney Disease Medical Center, General Hospital, Tianjin Medical University, National Key Clinical Specialty, Tianjin Key Medical Discipline, Tianjin, People's Republic of China.
Linjie Li *Department of Cardiology, Tianjin Medical University General Hospital, Tianjin, 300052, People's Republic of China.
Ying Han *Department of Cardiology, Tianjin Medical University General Hospital, Tianjin, 300052, People's Republic of China.
Xinxin ZhangDepartment of Nephrology, Kidney Disease Medical Center, General Hospital, Tianjin Medical University, National Key Clinical Specialty, Tianjin Key Medical Discipline, Tianjin, People's Republic of China.
Yujia LinDepartment of Nephrology, Kidney Disease Medical Center, General Hospital, Tianjin Medical University, National Key Clinical Specialty, Tianjin Key Medical Discipline, Tianjin, People's Republic of China.
Hangkuan LiuDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, 300052, People's Republic of China.ORCID 0009-0006-2322-6354
Shichen JiangDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, 300052, People's Republic of China.
Tiekun YanDepartment of Nephrology, Kidney Disease Medical Center, General Hospital, Tianjin Medical University, National Key Clinical Specialty, Tianjin Key Medical Discipline, Tianjin, People's Republic of China.
Lirong ZhangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, People's Republic of China.
Baocheng ChangNHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin, 300134, People's Republic of China.
Xin ZhouDepartment of Cardiology, Tianjin Medical University General Hospital, Tianjin, 300052, People's Republic of China.
Junya JiaDepartment of Nephrology, Kidney Disease Medical Center, General Hospital, Tianjin Medical University, National Key Clinical Specialty, Tianjin Key Medical Discipline, Tianjin, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: Aim to compare the effects of rivaroxaban and warfarin on rapid renal function decline. Methods: 8842 patients from the Tianjin Health and Medical Data Platform, with a 2.3 years median follow-up (interquartile range,1.5-3.4), were assigned to either the warfarin group (n = 3913) or rivaroxaban group (n = 4929). Logistic models, inverse probability of treatment weighting(IPTW), and propensity score-matched (PSM) analyses were employed to compare the risk of rapid renal function decline associated with rivaroxaban versus warfarin. The multivariable fractional polynomial interaction(MFPI) was used to investigate interactions between continuous variables and the adverse outcome. Restricted cubic splines(RCS) were applied to assess the relationship between the prognostic nutritional index (PNI) score and the adverse outcome. Results: Rivaroxaban was associated with an increased risk of rapid renal function decline compared with warfarin in both the univariate (odds ratio [OR], 1.24; 95% confidence interval [CI], 1.14-1.36; Conclusion: Rivaroxaban was associated with a higher risk of rapid renal function decline than warfarin. Enhanced nutritional support may help mitigate this adverse outcome.

Indexed as

Factor Xa InhibitorsKidneyNutritional SupportRivaroxabanWarfarinAgedFemaleHumansMaleMiddle AgedFactor Xa InhibitorsRivaroxabanWarfarinnutritional supportrapid renal function declinerivaroxabanwarfarin

Identifiers

PMID41368586
PMCPMC12683164

What Socratic holds

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Registered trials

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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.