Evidence map›Paper›PMID 33843271›Full record

ArticleAmerican journal of physiology. Renal physiology2021

NMR-based serum and urine metabolomic profile reveals suppression of mitochondrial pathways in experimental sepsis-associated acute kidney injury.

Stephen W Standage, Shenyuan Xu, Lauren Brown, Qing Ma, Adeleine Koterba, Patrick Lahni, Prasad Devarajan, Michael A Kennedy

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

22 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  7. Fueling kidney recovery: boosting BCAA metabolism to overcome nephrotoxic AKI.American journal of physiology. Renal physiology · 2025
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  13. Statistical considerations and database limitations in NMR-based metabolic profiling studies.Metabolomics : Official journal of the Metabolomic Society · 2023
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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 at 2 institutions in 1 country.

Stephen W StandageDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.ORCID 0000-0002-0550-6532
Shenyuan XuDepartment of Chemistry and Biochemistry, Miami University, Oxford, Ohio.
Lauren BrownDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Qing MaDivision of Nephrology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Adeleine KoterbaDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Patrick LahniDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Prasad DevarajanDepartment of Pediatrics, University of Cincinnati, Cincinnati, Ohio.
Michael A KennedyDepartment of Chemistry and Biochemistry, Miami University, Oxford, Ohio.
Cincinnati Children's Hospital Medical Center · USMiami University · US

Funding

Proteomics CoreP50DK096418 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI DEVARAJAN, PRASAD · 2012 to 2021
$8.4M
The Role of PPARa in Cardiac Dysfunction in SepsisK08HL133377 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI STANDAGE, STEPHEN WADE · 2017 to 2021
$810k
NHLBI NIH HHS K08 HL133377NIDDK NIH HHS P50 DK096418
6 · The paper itself

Abstract

Sepsis-associated acute kidney injury (SA-AKI) is a significant problem in the critically ill that causes increased death. Emerging understanding of this disease implicates metabolic dysfunction in its pathophysiology. This study sought to identify specific metabolic pathways amenable to potential therapeutic intervention. Using a murine model of sepsis, blood and tissue samples were collected for assessment of systemic inflammation, kidney function, and renal injury. Nuclear magnetic resonance (NMR)-based metabolomics quantified dozens of metabolites in serum and urine that were subsequently submitted to pathway analysis. Kidney tissue gene expression analysis confirmed the implicated pathways. Septic mice had elevated circulating levels of inflammatory cytokines and increased levels of blood urea nitrogen and creatinine, indicating both systemic inflammation and poor kidney function. Renal tissue showed only mild histological evidence of injury in sepsis. NMR metabolomic analysis identified the involvement of mitochondrial pathways associated with branched-chain amino acid metabolism, fatty acid oxidation, and de novo NAD

Indexed as

Acute Kidney InjuryAnimalsBiomarkersBlood Urea NitrogenCreatinineCytokinesGene Expression RegulationInflammationMagnetic Resonance ImagingMaleMetabolomicsMiceMice, Inbred C57BLMitochondriaSepsisBiomarkersCreatinineCytokinesacute kidney injurymetabolic profilingmetabolomicsnuclear magnetic resonancesepsis

Identifiers

PMID33843271
PMCPMC8424559
OpenAlexW3156169807

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.