Evidence map›Paper›PMID 37534876›Full record

ArticleeLife2023

Association between bisphosphonate use and COVID-19 related outcomes.

Jeffrey Thompson, Yidi Wang, Tobias Dreischulte, Olga Barreiro, Rodrigo J Gonzalez, Pavel Hanč, Colette Matysiak, Harold R Neely, Marietta Rottenkolber, Thomas Haskell and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. 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
3.1field-weighted citation impact, top 8% 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, 12 citations in OpenAlex.

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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 4 institutions in 2 countries.

Jeffrey Thompson *Cerner Enviza, Malvern, United States.
Yidi Wang *Dept. of Immunology, Harvard Medical School, Boston, United States.
Tobias DreischulteInstitute of General Practice and Family Medicine, University Hospital of Ludwig Maximilians-University Munich, Munich, Germany.
Olga BarreiroDept. of Immunology, Harvard Medical School, Boston, United States.
Rodrigo J GonzalezDept. of Immunology, Harvard Medical School, Boston, United States.
Pavel HančDept. of Immunology, Harvard Medical School, Boston, United States.
Colette MatysiakDept. of Immunology, Harvard Medical School, Boston, United States.
Harold R NeelyDept. of Immunology, Harvard Medical School, Boston, United States.
Marietta RottenkolberInstitute of General Practice and Family Medicine, University Hospital of Ludwig Maximilians-University Munich, Munich, Germany.
Thomas HaskellCerner Enviza, Malvern, United States.
Stefan EndresCenter of Integrated Protein Science Munich and Division of Clinical Pharmacology, University Hospital, LMU Munich, Germany, Munich, Germany.ORCID 0000-0002-4703-537X
Ulrich H von AndrianDept. of Immunology, Harvard Medical School, Boston, United States.ORCID 0000-0003-4231-2283
Harvard University · USCerner (United States) · USLudwig-Maximilians-Universität München · DECenter for Integrated Protein Science Munich · DE

Funding

Intravascular Immune Surveillance by Anti-viral T CellsR01AI155865 · NIAID · HARVARD MEDICAL SCHOOL · PI VON ANDRIAN, ULRICH H · 2021 to 2025
$3.2M
Neutrophil Dynamics in Nasal MucosaR01AI175379 · NIAID · HARVARD MEDICAL SCHOOL · PI ULRICH H VON ANDRIAN · 2023 to 2026
$2.7M
Regulation of Skin Inflammation by Nociceptive Sensory NeuronsR01AR068383 · NIAMS · HARVARD MEDICAL SCHOOL · PI VON ANDRIAN, ULRICH H · 2015 to 2019
$1.9M
Cancer Research Institute CRI2453NIAID NIH HHS R01 AI155865NIAID NIH HHS R01 AI175379NIAMS NIH HHS AR068383NIAMS NIH HHS R01 AR068383
6 · The paper itself

Abstract

Background: Although there are several efficacious vaccines against COVID-19, vaccination rates in many regions around the world remain insufficient to prevent continued high disease burden and emergence of viral variants. Repurposing of existing therapeutics that prevent or mitigate severe COVID-19 could help to address these challenges. The objective of this study was to determine whether prior use of bisphosphonates is associated with reduced incidence and/or severity of COVID-19. Methods: A retrospective cohort study utilizing payer-complete health insurance claims data from 8,239,790 patients with continuous medical and prescription insurance January 1, 2019 to June 30, 2020 was performed. The primary exposure of interest was use of any bisphosphonate from January 1, 2019 to February 29, 2020. Bisphosphonate users were identified as patients having at least one bisphosphonate claim during this period, who were then 1:1 propensity score-matched to bisphosphonate non-users by age, gender, insurance type, primary-care-provider visit in 2019, and comorbidity burden. Main outcomes of interest included: (a) any testing for SARS-CoV-2 infection; (b) COVID-19 diagnosis; and (c) hospitalization with a COVID-19 diagnosis between March 1, 2020 and June 30, 2020. Multiple sensitivity analyses were also performed to assess core study outcomes amongst more restrictive matches between BP users/non-users, as well as assessing the relationship between BP-use and other respiratory infections (pneumonia, acute bronchitis) both during the same study period as well as before the COVID outbreak. Results: A total of 7,906,603 patients for whom continuous medical and prescription insurance information was available were selected. A total of 450,366 bisphosphonate users were identified and 1:1 propensity score-matched to bisphosphonate non-users. Bisphosphonate users had lower odds ratios (OR) of testing for SARS-CoV-2 infection (OR = 0.22; 95%CI:0.21-0.23; p<0.001), COVID-19 diagnosis (OR = 0.23; 95%CI:0.22-0.24; p<0.001), and COVID-19-related hospitalization (OR = 0.26; 95%CI:0.24-0.29; p<0.001). Sensitivity analyses yielded results consistent with the primary analysis. Bisphosphonate-use was also associated with decreased odds of acute bronchitis (OR = 0.23; 95%CI:0.22-0.23; p<0.001) or pneumonia (OR = 0.32; 95%CI:0.31-0.34; p<0.001) in 2019, suggesting that bisphosphonates may protect against respiratory infections by a variety of pathogens, including but not limited to SARS-CoV-2. Conclusions: Prior bisphosphonate-use was associated with dramatically reduced odds of SARS-CoV-2 testing, COVID-19 diagnosis, and COVID-19-related hospitalizations. Prospective clinical trials will be required to establish a causal role for bisphosphonate-use in COVID-19-related outcomes. Funding: This study was supported by NIH grants, AR068383 and AI155865, a grant from MassCPR (to UHvA) and a CRI Irvington postdoctoral fellowship, CRI2453 (to PH).

Indexed as

BronchitisCOVID-19Respiratory Tract InfectionsCOVID-19 TestingCOVID-19 VaccinesDiphosphonatesHumansProspective StudiesRetrospective StudiesSARS-CoV-2COVID-19 VaccinesDiphosphonatesBisphosphonateCOVID-19epidemiologyglobal healthhumanmedicineretrospective cohort study

Identifiers

PMID37534876
PMCPMC10691801
OpenAlexW4385514381

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.