Evidence map›Paper›PMID 33970408›Full record

ArticlePurinergic signalling2021

Cystic fibrosis improves COVID-19 survival and provides clues for treatment of SARS-CoV-2.

Edward H Abraham, Guido Guidotti, Eliezer Rapaport, David Bower, Jack Brown, Robert J Griffin, Andrew Donnelly, Ellen D Waitzkin, Kenon Qamar, Mark A Thompson and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Purinergic signalling, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Mechanisms by which the cystic fibrosis transmembrane conductance regulator may influence SARS-CoV-2 infection and COVID-19 disease severity.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  6. Article
  7. Article
  8. The Impact of COVID-19 in Cystic Fibrosis.Archivos de bronconeumologia · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Reply to Eisenhut.American journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  15. 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

12 authors at 7 institutions in 1 country.

Edward H AbrahamSaint Francis Health System, Tulsa, OK, USA. edwardhabraham@gmail.com.ORCID 0000-0002-4429-2389
Guido GuidottiDepartment of Molecular and Cell Biology, Harvard University, Cambridge, MA, USA.
Eliezer RapaportATP Therapeutics, LLC, Cambridge, MA, USA.
David BowerHorizon Medical Services, Tamarac, FL, USA.
Jack BrownSt. John Medical Center, Tulsa, OK, USA.
Robert J GriffinUniversity of Arkansas for Medical Sciences, Little Rock, AR, USA.
Andrew DonnellySaint Francis Health System, Tulsa, OK, USA.
Ellen D Waitzkin, Boston, MA, USA.
Kenon QamarKansas City Urology Care, Kansas City, KS, USA.
Mark A ThompsonKansas City Urology Care, Kansas City, KS, USA.
Sukumar EthirajanKansas City Urology Care, Kansas City, KS, USA.
Kent RobinsonBayer GU Oncology, St. Louis, MO, USA.
Kansas City CARE Clinic · USATP Clinical Research (United States) · USBayer (United States) · USHarvard University · USSaint Francis Health System · USSt. John Medical Center · USUniversity of Arkansas for Medical Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic pools of ATP are elevated in individuals homozygous for cystic fibrosis (CF) as evidenced by elevated blood and plasma ATP levels. This elevated ATP level seems to provide benefit in the presence of advanced solid tumors (Abraham et al., Nature Medicine 2(5):593-596, 1996). We published in this journal a paper showing that IV ATP can elevate the depleted ATP pools of advanced cancer patients up to levels found in CF patients with subsequent clinical, biochemical, and quality of life (QOL) improvements (Rapaport et al., Purinergic Signalling 11(2): 251-262, 2015). We hypothesize that the elevated ATP levels seen in CF patients may be benefiting CF patients in another way: by improving their survival after contracting COVID-19. We discuss here the reasoning behind this hypothesis and suggest how these findings might be applied clinically in the general population.

Indexed as

COVID-19Adenosine TriphosphateCystic FibrosisHumansSARS-CoV-2Adenosine TriphosphateAdenosineAdenosine triphosphateATPCFCFTRCoronavirusCOVID-19Cystic fibrosisCytokine stormPannexinSARS-CoV-2

Identifiers

PMID33970408
PMCPMC8107773
OpenAlexW3162786892

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.