Evidence map›Paper›PMID 32043112›Full record

ArticleBlood2020

Hemopexin deficiency promotes acute kidney injury in sickle cell disease.

Solomon F Ofori-Acquah, Rimi Hazra, Oluwaseun O Orikogbo, Danielle Crosby, Bethany Flage, Ezekiel B Ackah, Diane Lenhart, Roderick J Tan, Dario A Vitturi, Vivian Paintsil and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 41 citations in OpenAlex.

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  18. Sickle Cell Disease and CKD: An Update.American journal of nephrology · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 3 countries.

Solomon F Ofori-AcquahUniversity of Pittsburgh School of Medicine.
Rimi HazraUniversity of Pittsburgh School of Medicine.
Oluwaseun O OrikogboUniversity of Pittsburgh School of Medicine.
Danielle CrosbyUniversity of Pittsburgh School of Medicine.
Bethany FlageUniversity of Pittsburgh School of Medicine.
Ezekiel B AckahSchool of Public Health, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Diane LenhartUniversity of Pittsburgh School of Medicine.
Roderick J TanRenal-Electrolyte Division, Department of Medicine and.
Dario A VitturiPittsburgh Heart, Lung, and Blood Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA.
Vivian PaintsilKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Ellis Owusu-DaboSchool of Public Health, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Samit GhoshUniversity of Pittsburgh School of Medicine.
SickleGenAfrica Network
University of Pittsburgh · USKwame Nkrumah University of Science and Technology · GHKomfo Anokye Teaching Hospital · GHUniversity of Ghana · GH

Funding

SickleGenAfrica:Sickle Cell Disease Genomics Network of AfricaU54HL141011 · NHLBI · UNIVERSITY OF GHANA · PI MAKANI, JULIE · 2017 to 2021
$5.5M
Role of erythroid DAMP molecules in the pathogenesis of vascular injury in sepsisR01GM113816 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OFORI-ACQUAH, SOLOMON FIIFI, SHIVA, SRUTI · 2015 to 2019
$3.3M
Ghana-SPARCO: Ghana Sickle Pan-African Research ConsortiumU01HL157004 · NHLBI · KWAME NKRUMAH UNIVERSITY/SCIENCE/TECH · PI OFORI-ACQUAH, SOLOMON FIIFI, SARFO, FRED STEPHEN · 2021 to 2025
$1.4M
Protection against sickle cell disease nephropathy by nitrated fatty acidsK01HL133331 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VITTURI, DARIO A · 2016 to 2021
$848k
NHLBI NIH HHS K01 HL133331NHLBI NIH HHS U01 HL157004NHLBI NIH HHS U54 HL141011NIGMS NIH HHS R01 GM113816
6 · The paper itself

Abstract

Acute kidney injury (AKI) is a major clinical concern in sickle cell disease (SCD). Clinical evidence suggests that red cell alarmins may cause AKI in SCD, however, the sterile inflammatory process involved has hitherto not been defined. We discovered that hemopexin deficiency in SCD is associated with a compensatory increase in α-1-microglobulin (A1M), resulting in an up to 10-fold higher A1M-to-hemopexin ratio in SCD compared with healthy controls. The A1M-to-hemopexin ratio is associated with markers of hemolysis and AKI in both humans and mice with SCD. Studies in mice showed that excess heme is directed to the kidneys in SCD in a process involving A1M causing AKI, whereas excess heme in controls is transported to the liver as expected. Using genetic and bone marrow chimeric tools, we confirmed that hemopexin deficiency promotes AKI in sickle mice under hemolytic stress. However, AKI was blocked when hemopexin deficiency in sickle mice was corrected with infusions of purified hemopexin prior to the induction of hemolytic stress. This study identifies acquired hemopexin deficiency as a risk factor of AKI in SCD and hemopexin replacement as a potential therapy.

Indexed as

Disease SusceptibilityAcute Kidney InjuryAnemia, Sickle CellAnimalsBiopsyDisease Models, AnimalDisease ProgressionErythrocytesGlomerular Filtration RateHemeHemopexinHumansKidney Function TestsMiceModels, BiologicalHemeHemopexin

Identifiers

PMID32043112
PMCPMC7218735
OpenAlexW3005865582

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.