Evidence map›Paper›PMID 41251950›Full record

ArticleJournal of endocrinological investigation2026

Thyroid peroxidase antibodies and coronary artery calcification: results from the ELSA-Brasil cohort study.

Vandrize Meneghini, William R Tebar, Giuliano Generoso, Carolina Cps Janovsky, Paulo A Lotufo, Márcio S Bittencourt, Alexandre C Pereira, Isabela M Bensenor

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Article in Journal of endocrinological investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

8 authors.

Vandrize MeneghiniCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-2787-6841
William R TebarCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil.
Giuliano GenerosoCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil.
Carolina Cps JanovskyCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil.
Paulo A LotufoCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil.
Márcio S BittencourtCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil.
Alexandre C PereiraCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil.
Isabela M BensenorCenter for Clinical and Epidemiological Research, Universidade de São Paulo, Av. Lineu Prestes 2565, 3° andar, CEP 05508-000, São Paulo, Brazil. isabensenor@gmail.com.

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2011/12256-4Fundação de Amparo à Pesquisa do Estado de São Paulo 2021/04416-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2021/06798-0
6 · The paper itself

Abstract

purposeThis study explored the association between TPOAb levels and the incidence and progression of coronary artery calcification (CAC) among participants from the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil).

methodsWe included individuals with no prior cardiovascular disease who underwent two CAC measurements within the ELSA-Brasil cohort from the São Paulo Research Center. Fasting serum TPOAb levels were analyzed as continuous data, categorized in quartiles, and as detectable and positive levels. Incident CAC was defined as a baseline CAC = 0 followed by a CAC > 0 in the second measurement. CAC progression was assessed using the Hokanson method only for participants with CAC > 0 at baseline. We performed Poisson regression models with robust variance and logistic regression models using the first quartile of TPOAb as the reference.

resultsA total of 3013 individuals were included (57.2% women, age 49.3 ± 8.1 years, 55.2% white). The third (IRR = 1.38, 95% CI = 1.03-1.85) and the fourth (IRR = 1.43, 95% CI = 1.07-1.91) quartiles of TPOAb were associated with a higher risk of CAC incidence, even after adjusting for sociodemographic variables, cardiovascular risk factors, and thyroid function. These associations remained consistent in sensitivity analyses for euthyroid individuals (Q3: IRR = 1.49, 95% CI = 1.07-2.06 and Q4: IRR = 1.60, 95% CI = 1.15-2.22). Sex-stratified analyses revealed a stronger association between the fourth quartile of TPOAb and CAC incidence in men, while the third quartile was significantly associated with CAC incidence in women. There was a statistically significant association between high detectable TPOAb and CAC progression (OR = 1.50, 95% CI = 1.01-2.24).

conclusionOur findings indicate that individuals with higher levels of TPOAb were at higher risk of developing CAC over a 5-year follow-up period, suggesting an atherogenic role of TPOAb independent of thyroid function.

Indexed as

AutoantibodiesCoronary Artery DiseaseIodide PeroxidaseVascular CalcificationAdultBiomarkersBrazilCohort StudiesFemaleFollow-Up StudiesHumansIncidenceLongitudinal StudiesMaleMiddle AgedPrognosisAutoantibodiesBiomarkersIodide PeroxidaseAutoimmune thyroiditisCohort studiesCoronary atherosclerosisIodide peroxidase

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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.