ReviewJornal brasileiro de nefrologia
Methanol intoxication and acute kidney injury: pathophysiological mechanisms and therapeutic approaches.
Review in Jornal brasileiro de nefrologia. 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 lactate gap as a diagnostic clue in ethylene glycol poisoning and a tool for differentiating methanol intoxication.Jornal brasileiro de nefrologiaArticle
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Methanol intoxication is a potentially lethal condition that primarily affects the central nervous system, but it can also induce significant renal damage. Acute kidney injury (AKI) in this context is often underestimated, despite being an important prognostic marker associated with increased mortality and morbidity. This review aims to elucidate the pathophysiological mechanisms linking methanol intoxication to AKI, describe the cellular and metabolic pathways involved, and discuss current therapeutic approaches for renal protection and recovery. A descriptive and analytical review was conducted through searches in the PubMed, Embase, and Cochrane Library databases, including studies published between 2000 and 2025. Eligible articles addressed methanol-related nephrotoxicity, AKI mechanisms, or treatment strategies involving fomepizole, hemodialysis, and renal support. The nephrotoxic effects of methanol are mediated by the accumulation of formic acid, which inhibits mitochondrial cytochrome oxidase, leading to tissue hypoxia, oxidative stress, and cellular apoptosis. The main renal alterations include osmotic nephrosis and acute tubular necrosis, frequently associated with metabolic acidosis, rhabdomyolysis, or hemolysis. Risk factors such as anemia, sepsis, volume depletion, and acute pancreatitis exacerbate renal injury. AKI is linked to higher rates of multiple organ failure and in-hospital mortality. Methanol-induced AKI results from multifactorial mechanisms involving mitochondrial dysfunction, oxidative stress, and hemodynamic instability.
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