Evidence map›Paper›PMID 41593886›Full record

ArticleRenal failure2026

Biochemical phenotypes of acute kidney injury and their association with major adverse kidney events.

Pablo Maggiani-Aguilera, Guillermo Navarro-Blackaller, Pedro A Rodriguez-Peña, Yohevana García-Barrón, Edgar Saldaña-Rocha, Jose A Gómez, Jonathan S Chávez-Iñiguez

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Article in Renal failure, 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

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.

2 · The registry

The trial behind it

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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

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Pablo Maggiani-AguileraInternal Medicine Department, Hospital General de Mazatlan, Sinaloa, Mexico.
Guillermo Navarro-BlackallerNephrology Service, Hospital Civil de Guadalajara "Fray Antonio Alcalde", Guadalajara, Jalisco, Mexico.
Pedro A Rodriguez-PeñaInternal Medicine Department, Hospital General de Mazatlan, Sinaloa, Mexico.
Yohevana García-BarrónNephrology Service, Hospital General de Mazatlan, Sinaloa, Mexico.
Edgar Saldaña-RochaInternal Medicine Department, Hospital General de Mazatlan, Sinaloa, Mexico.
Jose A GómezInternal Medicine Department, Hospital General de Mazatlan, Sinaloa, Mexico.
Jonathan S Chávez-IñiguezNephrology Service, Hospital Civil de Guadalajara "Fray Antonio Alcalde", Guadalajara, Jalisco, Mexico.ORCID 0000-0003-2786-6667

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute kidney injury (AKI) is a heterogeneous syndrome in which conventional stratification based on serum creatinine and urine output may fail to capture the full spectrum of underlying metabolic disturbances. In a retrospective cohort study of hospitalized adults with AKI admitted to Hospital General de Mazatlán between January 2022 and July 2025, we sought to identify biochemical phenotypes associated with major adverse kidney events (MAKE). Demographic, clinical, and biochemical variables, including urea, creatinine, calcium, phosphorus, potassium, hemoglobin, albumin, and pH, were standardized using z-scores and clustered using k-means analysis. The primary outcome was MAKE, defined as in-hospital mortality or new requirement for kidney replacement therapy (KRT). Among 797 patients, three distinct biochemical phenotypes were identified: Phenotype 1, characterized by relatively preserved biochemical parameters; Phenotype 2, defined by anemia and hypocalcemia; and Phenotype 3, marked by severe metabolic derangements. Phenotype 3 exhibited the most severe kidney dysfunction and metabolic instability, including anemia, hyperkalemia, hyperphosphatemia, hypocalcemia, and acidosis, and was strongly associated with MAKE (odds ratio [OR] 3.39, 95% confidence interval [CI] 2.12-5.40;

Indexed as

Acute Kidney InjuryRenal Replacement TherapyAgedAnemiaCreatinineFemaleHospital MortalityHumansHypocalcemiaMaleMiddle AgedPhenotypeRetrospective StudiesCreatinineAcute kidney injurykidney replacement therapymajor adverse kidney eventsMAKEmortalityphenotypes

Identifiers

PMID41593886
PMCPMC12854221

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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.