Evidence map›Paper›PMID 24675478›Full record

Observational studyTransplantation2014

The role of donor-specific antibodies in acute cardiac allograft dysfunction in the absence of cellular rejection.

Nowell M Fine, Richard C Daly, Nisha Shankar, Soon J Park, Sudhir S Kushwaha, Manish J Gandhi, Naveen L Pereira

Abstract readObservational Study
In one paragraph

Observational study in Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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

7 authors at 2 institutions in 1 country.

Nowell M Fine1 Division of Cardiovascular Diseases, Department of Medicine, William J. von Liebig Transplant Center, Mayo Clinic, Rochester, MN. 2 Division of Cardiovascular Surgery, Department of Surgery, William J. von Liebig Transplant Center, Mayo Clinic, Rochester, MN. 3 Department of Laboratory Medicine and Pathology, William J. von Liebig Transplant Center, Mayo Clinic, Rochester, MN. 4 Address correspondence to: Naveen L. Pereira, M.D., Division of Cardiovascular Diseases, Department of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55901.
Richard C Daly
Nisha Shankar
Soon J Park
Sudhir S Kushwaha
Manish J Gandhi
Naveen L Pereira
Mayo Clinic · USMayo Clinic in Arizona · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
NCATS NIH HHS UL1 TR000135
6 · The paper itself

Abstract

backgroundAcute allograft dysfunction (AAD) is an important cause of morbidity among heart transplant recipients. The role of donor-specific antibodies (DSAs) in AAD, with the increasing use of single antigen bead (SAB) assays that have improved the ability to detect DSA, remains unclear.

methodsWe retrospectively reviewed 329 heart transplant recipients followed up at our institution. AAD was defined as an acute decline in left ventricular ejection fraction to less than 50% and a decrement of 10% or higher compared to baseline in the absence of cellular rejection. Patients with AAD were compared with matched 30 heart transplant controls.

resultsThere were 10 (3%) patients with AAD, 4 (40%) had DSA detectable by SAB assay compared to 16 (53%) controls (P=0.43). Peak DSA mean fluorescent intensity (MFI) levels were significantly higher at baseline (class I and class II) in AAD compared to controls. DSA MFI values increased at the time of AAD and returned to baseline values during follow-up for these patients with AAD (P<0.05) but remained unchanged over time for controls. Six (60%) patients with AAD and 1 (3%) control had antibody-mediated rejection (AMR) by endomyocardial biopsy (P<0.01). There were 4 (40%) patients with AAD with no DSA or AMR.

conclusionsAAD after heart transplant is a heterogeneous process characterized by 1) AMR and DSA, 2) AMR but no DSA, and 3) no AMR or DSA. The presence of DSA is not associated with AAD, but the quantity assessed by MFI levels may play a role.

Indexed as

Acute DiseaseAdultAgedAllograftsBiomarkersBiopsyCoronary AngiographyFemaleGraft RejectionHeart TransplantationHumansImmunosuppressive AgentsIsoantibodiesMaleMiddle AgedMinnesotaBiomarkersImmunosuppressive AgentsIsoantibodies

Identifiers

PMID24675478
PMCPMC4101052
OpenAlexW1966020049

What OpenQuestion holds

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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.