Evidence map›Paper›PMID 35618524›Full record

ArticleTransplantation proceedings

Association Between Total Cell Free DNA and SARS-CoV-2 In Kidney Transplant Patients: A Preliminary Study.

Jose Otto Reusing, Jongwon Yoo, Amishi Desai, Katya Brossart, Sarah McCormick, Allyson Koyen Malashevich, Michelle S Bloom, Gordon Fehringer, Roseann White, Paul R Billings and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Transplantation proceedings. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

15 authors at 3 institutions in 2 countries.

Jose Otto ReusingRenal Transplant Service, Hospital das Clinicas, University of São Paulo School of Medicine, São Paulo, Brazil.
Jongwon YooLoyola University Medical Center, Maywood, Illinois.
Amishi DesaiLoyola University Medical Center, Maywood, Illinois.
Katya BrossartNatera, Inc., San Carlos, California.
Sarah McCormickNatera, Inc., San Carlos, California.
Allyson Koyen MalashevichNatera, Inc., San Carlos, California.
Michelle S BloomNatera, Inc., San Carlos, California.
Gordon FehringerNatera, Inc., San Carlos, California.
Roseann WhiteNatera, Inc., San Carlos, California.
Paul R BillingsNatera, Inc., San Carlos, California.
Hossein TabrizianiNatera, Inc., San Carlos, California.
Zachary P DemkoNatera, Inc., San Carlos, California.
Philippe GauthierNatera, Inc., San Carlos, California.
Sanjeev K AkkinaLoyola University Medical Center, Maywood, Illinois. Electronic address: sanjeev.akkina@lumc.edu.
Elias David-NetoRenal Transplant Service, Hospital das Clinicas, University of São Paulo School of Medicine, São Paulo, Brazil. Electronic address: elias@davidneto.com.br.
Natera (United States) · USLoyola University Medical Center · USHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKidney transplant (KT) recipients are at high risk for developing severe COVID-19. Lowering immunosuppression levels in KT recipients with COVID-19 encourages native immune responses but can raise the risk of rejection. Donor-derived cell-free DNA (dd-cfDNA), reported as a fraction of total cfDNA, is a proven biomarker for KT rejection. Total cfDNA levels are elevated in patients with COVID-19, which may depress dd-cfDNA fractions, potentially leading to missed rejections.

methodsA retrospective analysis of 29 KT recipients hospitalized with COVID-19 between April and November 2020 examined total and dd-cfDNA levels. Blood samples were collected after onset of COVID-19, with follow-up samples collected from a subset of patients, when infection had likely subsided.

resultsAfter COVID-19 diagnosis, the median total cfDNA level was elevated (7.9 multiples of median [MoM]). A significant decrease in total cfDNA levels was observed between the first and second time points (6.2 MoM, 1.0 MoM; P <001). A significant positive association was identified between total cfDNA levels and COVID-19 severity (P = .02; R

conclusionsIn this preliminary study, total cfDNA levels were elevated in KT patients with COVID-19, subsiding after resolution of infection. High total cfDNA levels may confound dd-cfDNA results, leading to failure to identify rejection. Considering total cfDNA levels is important in interpretation of dd-cfDNA tests for assessment of rejection in KT patients with COVID-19 or other infection.

Indexed as

Cell-Free Nucleic AcidsCOVID-19Kidney TransplantationBiomarkersCOVID-19 TestingGraft RejectionHumansRetrospective StudiesSARS-CoV-2Tissue DonorsBiomarkersCell-Free Nucleic Acids

Identifiers

PMID35618524
PMCPMC8920956
OpenAlexW4221104227

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.