Evidence map›Paper›PMID 39495677›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2025

Tuberculosis and Increased Incidence of Cardiovascular Disease: Cohort Study Using United States and United Kingdom Health Records.

Julia A Critchley, Elizabeth S Limb, Anjali Khakharia, Iain M Carey, Sara C Auld, Stephen De Wilde, Tess Harris, Lawrence S Phillips, Derek G Cook, Mary K Rhee and 3 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

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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

13 authors.

Julia A CritchleyPopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.ORCID 0000-0002-5248-4188
Elizabeth S LimbPopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.ORCID 0000-0003-0830-7376
Anjali KhakhariaClinical Studies Center, Atlanta VA Health Care System, Decatur, Georgia, USA.ORCID 0000-0001-7401-0058
Iain M CareyPopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.ORCID 0000-0003-1099-8460
Sara C AuldDivision of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Department of Medicine, Emory School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0002-8972-3736
Stephen De WildePopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.ORCID 0000-0002-4238-4474
Tess HarrisPopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.ORCID 0000-0002-8671-1553
Lawrence S PhillipsClinical Studies Center, Atlanta VA Health Care System, Decatur, Georgia, USA.
Derek G CookPopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.ORCID 0000-0002-9723-5759
Mary K RheeClinical Studies Center, Atlanta VA Health Care System, Decatur, Georgia, USA.
Umar A R ChaudhryPopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.ORCID 0000-0002-2618-9257
Liza BowenPopulation Health Research Institute, St George's School of Health and --Medical Sciences, City St George's, University of London, London, United Kingdom.
Matthew J MageeDepartments of Global Health and Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.

Funding

Emory/Georgia TB Research Advancement Center (TRAC)P30AI168386 · NIAID · EMORY UNIVERSITY · PI Neel Rajnikant Gandhi, Jyothi Rengarajan · 2022 to 2026
$5.8M
CHANGING THE NATURAL HISTORY OF TYPE 2 DIABETES – “CHANGE” STUDYR01DK127083 · NIDDK · EMORY UNIVERSITY · PI PHILLIPS, LAWRENCE S · 2021 to 2025
$1.7M
The Role of Tuberculosis Disease on Non-Communicable Disease Risk: Comparative Analysis of Large Healthcare DatabasesR21AI156161 · NIAID · EMORY UNIVERSITY · PI CRITCHLEY, JULIA ALISON, MAGEE, MATTHEW JAMES · 2021 to 2022
$372k
BLRD VA I01 BX005831Cystic Fibrosis Foundation PHILLI12A0European Union RIA2018CO-2514-PROTIDNational Institute of Allergy and Infectious DiseasesNCCDPHP CDC HHS U18 DP006711NIAID NIH HHS P30 AI168386NIAID NIH HHS R21 AI156161NIDDK NIH HHS R01 DK127083NIH HHS R21AI156161
6 · The paper itself

Abstract

backgroundLimited evidence suggests elevated risks of cardiovascular disease (CVD) among people diagnosed with tuberculosis (TB) disease, though studies have not adjusted for preexisting CVD risk. We carried out a cohort study using 2 separate datasets, estimating CVD incidence in people with TB versus those without.

methodsUsing data from the United States (Veterans Health Administration) and the United Kingdom (Clinical Practice Research Datalink) for 2000-2020, we matched adults with incident TB disease and no CVD history 2 years before TB diagnosis (US, n = 2121; UK, n = 15 820) with up to 10 people without TB on the basis of age, sex, race/ethnicity and healthcare practice. Participants were followed beginning 2 years before TB diagnosis and for 2 years subsequently. The acute period was defined as 3 months before/after TB diagnosis. TB, CVD, and covariates were identified from electronic routinely collected data (primary and secondary care; mortality). Poisson models estimated incident rate ratios for CVD events in people with TB compared to those without.

resultsCVD incidence was consistently higher in people with TB, including during the baseline period (pre-TB) and particularly in the acute period: incident rate ratios were US, 3.5 (95% confidence interval, 2.7-4.4), and UK, 2.7 (2.2-3.3). Rate ratios remained high after adjusting for differences in preexisting CVD risk: US, 3.2 (2.2-4.4); UK, 1.6 (1.2-2.1).

conclusionsIncreased CVD incidence was observed in people with TB versus those without, especially within months of TB diagnosis, persistent after adjustment for differences in preexisting risk. Enhancing CVD screening and risk management may improve long-term outcomes in people with TB.

Indexed as

Cardiovascular DiseasesTuberculosisAdultAgedCohort StudiesFemaleHumansIncidenceMaleMiddle AgedRisk FactorsUnited KingdomUnited Statescardiovascular diseasescohort studyelectronic health recordspost-TBtuberculosis

Identifiers

PMID39495677
PMCPMC11848252

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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.