ReviewJournal of inflammation research2026
The Interaction Between Ferroptosis and Necroptosis in Acute and Chronic Kidney Diseases.
Review in Journal of inflammation research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
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Who cites it
1 citing paper in PubMed.
- The associations among iron metabolism markers, iron supplementation regimen, and sepsis-induced myocardial injury: a retrospective study.Frontiers in nutrition · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Kidney disease represents a major non-communicable disease characterized by complex pathogenesis and limited therapeutic options. Current research has revealed multiple underlying mechanisms, including ferroptosis and necroptosis, which play important roles in acute kidney injury (AKI) and chronic kidney disease (CKD). Ferroptosis is an iron-dependent form of programmed cell death caused by the accumulation of lipid reactive oxygen species and is characterized by iron ion aggregation, lipid peroxidation, and excessive oxidative stress. Necroptosis is a regulated form of necrosis mediated by RIPK1-RIPK3 and is characterized by the recruitment and phosphorylation of the pseudokinase mixed lineage kinase domain-like protein (MLKL). Ferroptosis and necroptosis play important roles in various diseases such as tissue injury, cancer, and neurodegenerative diseases. Due to the intricate architecture of the kidney, the convergence of multiple systemic pathogenic factors, and the interactive regulation of intercellular signaling pathways, renal diseases exhibit complex pathogenesis and present limited therapeutic interventions. Exploring cell death and the interactions between different forms of cell death is highly important for understanding the occurrence and development of kidney diseases and for finding new treatment strategies. Ferroptosis and necroptosis influence renal cell viability and contribute to the exacerbation of kidney injury via inflammatory responses and additional mechanisms. They share common initiating factors and intersecting signaling pathways in the context of kidney diseases, thereby synergistically intensifying the pathological progression of renal damage. This article describes the pathogenesis and pathophysiological roles of ferroptosis, necroptosis, and their interactions in kidney diseases such as AKI and CKD and elucidates the potential of inhibiting ferroptosis and necroptosis, or their combined inhibition, in the prevention and treatment of kidney diseases such as AKI and CKD.
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Registered trials
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.