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Incidence and Predictors of Progression to Chagas Cardiomyopathy: Long-Term Follow-Up of Trypanosoma cruzi –Seropositive Individuals
Author(s) -
Maria Carmo Pereira Nunes,
Lewis Buss,
Jose Luiz P. Silva,
Larissa Natany Almeida Martins,
Cláudia Di Lorenzo Oliveira,
Clareci Silva Cardoso,
Bruno Oliveira de Figueiredo Brito,
Ariela Mota Ferreira,
Léa Campos de Oliveira,
Ana Luiza Bierrenbach,
Fábio Fernandes,
Michael P. Busch,
Viviane Tiemi Hotta,
Luiz Mário Baptista Martinelli,
Maria Carolina F. Almeida Soeiro,
Adriana Brentegani,
Vera Maria Cury Salemi,
Márcia Mendes Menezes,
Antônio Luiz Pinho Ribeiro,
Éster Cerdeira Sabino
Publication year - 2021
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.121.055112
Subject(s) - medicine , cardiomyopathy , chagas disease , trypanosoma cruzi , ejection fraction , incidence (geometry) , heart failure , cardiology , immunology , parasite hosting , physics , world wide web , computer science , optics
Background: There are few contemporary cohorts ofTrypanosoma cruzi –seropositive individuals, and the basic clinical epidemiology of Chagas disease is poorly understood. Herein, we report the incidence of cardiomyopathy and death associated withT. cruzi seropositivity.Methods: Participants were selected in blood banks at 2 Brazilian centers. Cases were defined asT. cruzi –seropositive blood donors.T. cruzi –seronegative controls were matched for age, sex, and period of donation. Patients with established Chagas cardiomyopathy were recruited from a tertiary outpatient service. Participants underwent medical examination, blood collection, ECG, and echocardiogram at enrollment (2008–2010) and at follow-up (2018–2019). The primary outcomes were all-cause mortality and development of cardiomyopathy, defined as the presence of a left ventricular ejection fraction <50% or QRS complex duration ≥120 ms, or both. To handle loss to follow-up, a sensitivity analysis was performed using inverse probability weights for selection.Results: We enrolled 499T. cruzi –seropositive donors (age 48±10 years, 52% male), 488T. cruzi –seronegative donors (age 49±10 years, 49% male), and 101 patients with established Chagas cardiomyopathy (age 48±8 years, 59% male). The mortality in patients with established cardiomyopathy was 80.9 deaths/1000 person-years (py) (54/101, 53%) and 15.1 deaths/1000 py (17/114, 15%) inT. cruzi –seropositive donors with cardiomyopathy at baseline. AmongT. cruzi –seropositive donors without cardiomyopathy at baseline, mortality was 3.7 events/1000 py (15/385, 4%), which was no different fromT. cruzi –seronegative donors with 3.6 deaths/1000 py (17/488, 3%). The incidence of cardiomyopathy inT. cruzi –seropositive donors was 13.8 (95% CI, 9.5–19.6) events/1000 py (32/262, 12%) compared with 4.6 (95% CI, 2.3–8.3) events/1000 py (11/277, 4%) in seronegative controls, with an absolute incidence difference associated withT. cruzi seropositivity of 9.2 (95% CI, 3.6–15.0) events/1000 py.T. cruzi antibody level at baseline was associated with development of cardiomyopathy (adjusted odds ratio, 1.4 [95% CI, 1.1–1.8]).Conclusions: We present a comprehensive description of the natural history ofT. cruzi seropositivity in a contemporary patient population. The results highlight the central importance of anti–T. cruzi antibody titer as a marker of Chagas disease activity and risk of progression.

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