Evidence map›Paper›PMID 42256042›Full record

ArticleJournal of general and family medicine2026

COVID-19 as a Potential Trigger for Tuberculosis: Insights From a Large-Scale Japanese Insurance Database Analysis.

Daisuke Miyamori, Kotaro Ikeda, Sachi Nagasaka, Masanori Ito

Abstract read
In one paragraph

Article in Journal of general and family medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Daisuke MiyamoriDepartment of General Internal Medicine Hiroshima University Hospital Hiroshima Japan.ORCID https://orcid.org/0000-0002-1352-3738
Kotaro IkedaDepartment of General Internal Medicine Hiroshima University Hospital Hiroshima Japan.ORCID https://orcid.org/0000-0002-8099-9074
Sachi NagasakaDepartment of General Internal Medicine Hiroshima University Hospital Hiroshima Japan.
Masanori ItoDepartment of General Internal Medicine Hiroshima University Hospital Hiroshima Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The long-term impact of COVID-19 on tuberculosis (TB) is concerning. This study assessed whether COVID-19 was associated with an increased risk of active TB treatment risk in Japan using a nationwide propensity score-matched cohort design. Methods: A retrospective cohort study used Japan's National Insurance Database from January 2020 to December 2022. COVID-19 patients were matched 1:1 with controls using propensity scores based on age, sex, immunosuppressants use, Charlson comorbidity index, related medical conditions, healthcare utilization and prior TB history. The primary outcome was initiation of isoniazid-based therapy plus rifampin with a TB-related ICD-10 diagnosis code. Cox proportional hazards models estimated hazard ratios (HRs) for COVID-19's effect on TB treatment initiation. Results: After matching, 3,097,422 individuals were included per group. During 8-month median follow-up, 886 participants initiated TB treatment. The HR among COVID-19 infected individuals was 4.14 (95% CI: 3.51-4.89) versus matched controls. Subgroup analyses showed interaction between prior TB history and COVID-19, with HR of 14.7 (5.35-40.2) in those with prior TB history, versus those without (HR 3.84, 95% CI 3.24-4.54). Risk remained elevated in participants without hospitalization (HR 3.96, 95% CI 3.35-4.68). Conclusions: This study provides robust population-based evidence demonstrating a moderate association between prior COVID-19 and subsequent initiation of active tuberculosis treatment, particularly in those with prior TB history.

Indexed as

COVID‐19National Insurance Databasepropensity score matchingtuberculosis

Identifiers

PMID42256042
PMCPMC13240490

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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.