Evidence map›Paper›PMID 41635189›Full record

ArticleDiagnostic and interventional radiology (Ankara, Turkey)2026

Microvascular dysfunction in patients with transthyretin cardiac amyloidosis evaluated by 13N-ammonia positron emission tomography-computed tomography: is it an early marker of the disease?

Aristóteles Neto, Caio Cafezeiro, Bruno Bueno, Cristhian Espinoza Romero, Vitor Emer Rosa, Viviane Hotta, Camila de Godoi Carneiro, Carlos Rochitte, Vagner Madrini, Jose Soares and 5 more

Abstract read
In one paragraph

Article in Diagnostic and interventional radiology (Ankara, Turkey), 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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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Aristóteles NetoHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-9524-0255
Caio CafezeiroHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0001-5960-2952
Bruno BuenoHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-6721-7779
Cristhian Espinoza RomeroHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0003-0191-7358
Vitor Emer RosaHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0001-6521-2870
Viviane HottaHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-9236-3815
Camila de Godoi CarneiroDepartment of Radiology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), São Paulo, Brazil.ORCID 0000-0002-6547-398X
Carlos RochitteHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0003-4505-3344
Vagner MadriniHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-1116-6554
Jose SoaresHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-2419-081X
William ChalelaHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0003-3751-0728
Marcos LimaDepartment of Radiology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), São Paulo, Brazil.ORCID 0009-0004-7358-776X
Carlos BuchpiguelDepartment of Radiology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), São Paulo, Brazil.ORCID 0000-0003-0956-2790
Edward MillerMedicine and Radiology in the Section of Cardiovascular Medicine in Yale New Heaven Hospital, Connecticut, United States.ORCID 0000-0002-2156-5962
Fabio FernandesHeart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID 0009-0006-6462-3196

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate coronary microvascular function using 13N-ammonia positron emission tomography/ computed tomography in individuals with pathogenic

methodsWe evaluated microvascular impairment by measuring CFR in 20 patients with and 20 patients without cardiac involvement due to TTR amyloidosis (ATTR), all presumed to be free from epicardial coronary artery disease and carrying

resultsThe study revealed a significantly reduced mean global CFR in the cardiac involvement group (1.849 ± 0.379 vs. 2.952 ± 0.7,

conclusionIn patients with ATTR CA, coronary microvascular dysfunction emerges as a clinically relevant marker of cardiac involvement, even in the absence of structural abnormalities or obstructive coronary disease. CLINICAL SIGNIFICANCE: CFR assessment may aid in diagnostic suspicion, risk stratification, and understanding of angina symptoms in this population.

Indexed as

Amyloid Neuropathies, FamilialMicrovesselsPositron Emission Tomography Computed TomographyAgedAmmoniaBiomarkersCoronary CirculationCoronary VesselsFemaleHumansMaleMiddle AgedNitrogen RadioisotopesSensitivity and SpecificityAmmoniaBiomarkersNitrogen-13Nitrogen RadioisotopesAmyloidosiscoronary arteriesmicrovascular blood flow

Identifiers

PMID41635189
PMCPMC13530596

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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.