Evidence map›Paper›PMID 30374882›Full record

ArticleCell stress & chaperones2018

Might hyperbaric oxygen therapy (HBOT) reduce renal injury in diabetic people with diabetes mellitus? From preclinical models to human metabolomics.

Lauren E Harrison, Charles Giardina, Lawrence E Hightower, Caesar Anderson, George A Perdrizet

Open access · bronzeAbstract read
In one paragraph

Article in Cell stress & chaperones, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-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

12 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Lauren E HarrisonDepartment of Molecular and Cell Biology, University of Connecticut, 91 N Eagleville Road, U3125, Storrs, CT, 06269, USA. lauren.harrison@uconn.edu.ORCID http://orcid.org/0000-0002-7727-4873
Charles GiardinaDepartment of Molecular and Cell Biology, University of Connecticut, 91 N Eagleville Road, U3125, Storrs, CT, 06269, USA.
Lawrence E HightowerDepartment of Molecular and Cell Biology, University of Connecticut, 91 N Eagleville Road, U3125, Storrs, CT, 06269, USA.
Caesar AndersonDepartment of Emergency Medicine, UC San Diego Health System, Wound Care and Hyperbaric Medicine, Encinitas, CA, 92024, USA.
George A PerdrizetDepartment of Surgery, Hartford Health Care and the Hospital of Central Connecticut, Wound Care and Hyperbaric Medicine, New Britain, CT, 06050, USA.
University of Connecticut · USThe Hospital of Central Connecticut · USUC San Diego Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic kidney disease (DKD) is the leading cause of end-stage renal failure in the western world. Current treatment of diabetic kidney disease relies on nutritional management and drug therapies to achieve metabolic control. Here, we discuss the potential application of hyperbaric oxygen therapy (HBOT) for the treatment of diabetic kidney disease (DKD), a treatment which requires patients to breathe in 100% oxygen at elevated ambient pressures. HBOT has traditionally been used to diabetic foot ulcers (DFU) refractory to conventional medical treatments. Successful clinic responses seen in the DFU provide the underlying therapeutic rationale for testing HBOT in the setting of DKD. Both the DFU and DKD have microvascular endothelial disease as a common underlying pathologic feature. Supporting evidence for HBOT of DKD comes from previous animal studies and from our preliminary prospective clinical trial reported here. We report urinary metabolomic data obtained from patients undergoing HBOT for DFU, before and after exposure to 6 weeks of HBOT. The preliminary data support the concept that HBOT can reduce biomarkers of renal injury, oxidant stress, and mitochondrial dysfunction in patients receiving HBOT for DFU. Further studies are needed to confirm these initial findings and correlate them with simultaneous measures of renal function. HBOT is a safe and effective treatment for DFU and could also be for individuals with DKD.

Indexed as

AnimalsBiomarkersDiabetic FootDiabetic NephropathiesHumansHyperbaric OxygenationMetabolomicsMitochondriaModels, AnimalOxidative StressProspective StudiesTreatment OutcomeBiomarkersBiomarkersChronic kidney diseaseDiabetic kidney diseaseHeme oxygenaseHyperbaric oxygen therapyMitochondrial functionReactive oxygen species

Identifiers

PMID30374882
PMCPMC6237687
OpenAlexW2899032456

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.