Evidence map›Paper›PMID 31282542›Full record

Trial reportThe Journal of infectious diseases2020

A Randomized, Placebo-Controlled, Pilot Clinical Trial of Dipyridamole to Decrease Human Immunodeficiency Virus-Associated Chronic Inflammation.

Bernard J C Macatangay, Edwin K Jackson, Kaleab Z Abebe, Diane Comer, Joshua Cyktor, Cynthia Klamar-Blain, Luann Borowski, Delbert G Gillespie, John W Mellors, Charles R Rinaldo and 1 more

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04410328 (A Randomized Controlled Trial to Evaluate the Outcomes With Aggrenox in Patients With SARS-CoV-2 Infection), which is not on this map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% 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.

NCT04410328 phase3completednot on this map

A Randomized Controlled Trial to Evaluate the Outcomes With Aggrenox in Patients With SARS-CoV-2 Infection

TypeinterventionalSponsorRutgers, The State University of New JerseyRan2020 to 2021Enrolled98ConditionsCovid19ArmsDipyridamole ER 200mg/ Aspirin 25mg orally/enterally AND Standard of care, Standard of care
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Adjunct Therapy for CD4Frontiers in immunology · 2021
    Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Neuroinflammation and Neuropathology.Neuroscience and behavioral physiology · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. COVID-19-associated coagulopathy: An exploration of mechanisms.Vascular medicine (London, England) · 2020
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Bernard J C MacatangayDepartment of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
Edwin K JacksonDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pennsylvania.
Kaleab Z AbebeDepartment of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
Diane ComerDepartment of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
Joshua CyktorDepartment of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
Cynthia Klamar-BlainDepartment of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
Luann BorowskiDepartment of Infectious Diseases and Microbiology, University of Pittsburgh Graduate School of Public Health, Pennsylvania.
Delbert G GillespieDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pennsylvania.
John W MellorsDepartment of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
Charles R RinaldoDepartment of Infectious Diseases and Microbiology, University of Pittsburgh Graduate School of Public Health, Pennsylvania.
Sharon A RiddlerDepartment of Medicine, University of Pittsburgh School of Medicine, Pennsylvania.
University of Pittsburgh · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Single Nephron and MetabolomicsP30DK079307 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLEYMAN, THOMAS R · 2008 to 2022
$13.4M
Dipyridamole as a Modulator of HIV-1 Inflammation by Adenosine RegulationU01AI110410 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MACATANGAY, BERNARD JONAS C, RIDDLER, SHARON · 2014 to 2017
$3.2M
NCATS NIH HHS UL1 TR000005NCI NIH HHS P30 CA047904NIAID NIH HHS U01 AI110410NIDDK NIH HHS P30 DK079307
6 · The paper itself

Abstract

backgroundAdenosine is a potent immunoregulatory nucleoside produced during inflammatory states to limit tissue damage. We hypothesized that dipyridamole, which inhibits cellular adenosine uptake, could raise the extracellular adenosine concentration and dampen chronic inflammation associated with human immunodeficiency virus (HIV) type 1.

methodsVirally suppressed participants receiving antiretroviral therapy were randomized 1:1 for 12 weeks of dipyridamole (100 mg 4 times a day) versus placebo capsules. All participants took open-label dipyridamole during weeks 12-24. Study end points included changes in markers of systemic inflammation (soluble CD163 and CD14, and interleukin 6) and levels of T-cell immune activation (HLA-DR+CD38+).

resultsOf 40 participants who were randomized, 17 dipyridamole and 18 placebo recipients had baseline and week 12 data available for analyses. There were no significant changes in soluble markers, apart from a trend toward decreased levels of soluble CD163 levels (P = .09). There was a modest decrease in CD8+ T-cell activation (-17.53% change for dipyridamole vs +13.31% for placebo; P = .03), but the significance was lost in the pooled analyses (P = .058). Dipyridamole also reduced CD4+ T-cell activation (-11.11% change; P = .006) in the pooled analyses. In post hoc analysis, detectable plasma dipyridamole levels were associated with higher levels of inosine, an adenosine surrogate, and of cyclic adenosine monophosphate.

conclusionDipyridamole increased extracellular adenosine levels and decreased T-cell activation significantly among persons with HIV-1 infection receiving virally suppressive therapy.

Indexed as

AdolescentAdultBiomarkersChronic DiseaseDipyridamoleDouble-Blind MethodHIV-1HIV InfectionsHumansInflammationMiddle AgedPhosphodiesterase InhibitorsPilot ProjectsYoung AdultBiomarkersDipyridamolePhosphodiesterase InhibitorsadenosinedipyridamoleHIVinflammation

Identifiers

PMID31282542
PMCPMC7184919
OpenAlexW2958570702

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.