Evidence map›Paper›PMID 40623774›Full record

ArticleClinical and experimental pharmacology & physiology2025

Potential Kidney Risks Associated With Clinical Doses of Omeprazole: In Vivo and In Vitro Studies.

Zibo Xiong, Zhiwei Lai, Sanmu Li, Hua Zhang, Yongqiang Wang, Lishan Tan, Guang Yang, Zuying Xiong

Abstract read
In one paragraph

Article in Clinical and experimental pharmacology & physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Zibo XiongDepartment of Nephrology, School of Clinical Medicine, Peking University Shenzhen Hospital, Anhui Medical University, Shenzhen, Guangdong, China.
Zhiwei LaiDivision of Nephrology, Peking University Shenzhen Hospital, Peking University, Shenzhen, China.
Sanmu LiDivision of Nephrology, Peking University Shenzhen Hospital, Peking University, Shenzhen, China.
Hua ZhangDivision of Nephrology, Peking University Shenzhen Hospital, Peking University, Shenzhen, China.
Yongqiang WangDepartment of Laboratory Medicine, Peking University Shenzhen Hospital, Peking University, Shenzhen, China.
Lishan TanDivision of Nephrology, Peking University Shenzhen Hospital, Peking University, Shenzhen, China.
Guang YangDivision of Nephrology, Peking University Shenzhen Hospital, Peking University, Shenzhen, China.ORCID 0000-0001-5271-7079
Zuying XiongDepartment of Nephrology, School of Clinical Medicine, Peking University Shenzhen Hospital, Anhui Medical University, Shenzhen, Guangdong, China.

Funding

Guangdong Basic and Applied Basic Research Foundation 2020A1515110970Guangdong Basic and Applied Basic Research Foundation 2023A1515111112National Natural Science Foundation of China 82100726Shenzhen Clinical Research Center for Urology and Nephrology LCYSSQ20220823091403008Shenzhen High-level Hospital Construction Fund and Peking University Shenzhen Hospital Scientific Research Fund KYQD2024366Shenzhen Science and Technology Innovation Commission JCYJ20210324110403011Shenzhen Science and Technology Innovation Commission JCYJ20220530150412026
6 · The paper itself

Abstract

Omeprazole is a widely used proton pump inhibitor and anti-Helicobacter pylori drug; however, its nephrotoxicity has been controversial. This study aimed to explore the effects and mechanisms of omeprazole on the kidney. In HK2, HPC, NRK and 293 T cells, omeprazole-induced alterations in cell morphology, density and viability in a concentration-dependent manner. Excessively high concentrations (> 50 μM) led to a significant increase in cell death. Interestingly, NRK seemed insensitive to omeprazole. RNA sequencing revealed significant alterations in the genomic expression profile when HK2 cells were incubated at a concentration of 5 μM, including the inhibition of proliferative, metabolic and cytokine receptor gene expression. This alteration augments the environmental susceptibility of HK2 when exposed to H

Indexed as

KidneyOmeprazoleProton Pump InhibitorsAnimalsCell LineCell ProliferationCell SurvivalDose-Response Relationship, DrugGene Expression RegulationHumansMaleRatsOmeprazoleProton Pump Inhibitorsdrug dosagedrug safetyenvironmental susceptibilitykidneysproton pump inhibitors

Identifiers

PMID40623774
PMCPMC12234212

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.