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High-Sensitivity Cardiac Troponins I and T and Cardiovascular Outcomes: Findings from the Systolic Blood Pressure Intervention Trial (SPRINT).
Jia, Xiaoming; Nambi, Vijay; Berry, Jarett D; Dalmacy, Djhenne; Ascher, Simon B; Taylor, Addison A; Hoogeveen, Ron C; de Lemos, James A; Ballantyne, Christie M.
Afiliação
  • Jia X; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
  • Nambi V; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
  • Berry JD; Department of Medicine, Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, United States.
  • Dalmacy D; Department of Internal Medicine, The University of Texas at Tyler Health Science Center, Tyler, TX, United States.
  • Ascher SB; Department of Internal Medicine, The University of Texas at Tyler Health Science Center, Tyler, TX, United States.
  • Taylor AA; Department of Medicine, University of California-Davis, Sacramento, CA, United States.
  • Hoogeveen RC; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
  • de Lemos JA; Department of Medicine, Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, United States.
  • Ballantyne CM; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
Clin Chem ; 70(2): 414-424, 2024 02 07.
Article em En | MEDLINE | ID: mdl-38084941
ABSTRACT

BACKGROUND:

Cardiac troponins are associated with adverse cardiovascular disease (CVD) outcomes. The value of high-sensitivity cardiac troponin I (hs-cTnI) independently and in concert with troponin T (hs-cTnT) in the management of hypertension has not been well studied.

METHODS:

We assessed the utility of hs-cTnI independently and with hs-cTnT in identifying the highest risk individuals in the Systolic Blood Pressure Intervention Trial (SPRINT). Among 8796 eligible SPRINT participants, hs-cTnI was measured at baseline and 1 year. The association of baseline level and 1-year change in hs-cTnI with CVD events and all-cause death was evaluated using adjusted Cox regression models. We further assessed the complementary value of hs-cTnI and hs-cTnT by identifying concordant and discordant categories and assessing their association with outcomes.

RESULTS:

hs-cTnI was positively associated with composite CVD risk [myocardial infarction, other acute coronary syndrome, stroke, or cardiovascular death hazard ratio 1.23, 95% confidence interval 1.08-1.39 per 1-unit increase in log(troponin I)] independent of traditional risk factors, N-terminal pro-B-type natriuretic peptide, and hs-cTnT. Intensive blood pressure lowering was associated with greater absolute risk reduction (4.5% vs 1.7%) and lower number needed to treat (23 vs 59) for CVD events among those with higher baseline hs-cTnI (≥6 ng/L in men, ≥4 ng/L in women). hs-cTnI increase at 1 year was also associated with increased CVD risk. hs-cTnI and hs-cTnT were complementary, and elevations in both identified individuals with the highest risk for CVD and death.

CONCLUSIONS:

Baseline levels and change in hs-cTnI over 1 year identified higher-risk individuals who may derive greater cardiovascular benefit with intensive blood pressure treatment. hs-TnI and hs-TnT have complementary value in CVD risk assessment. ClinicalTrials.gov Registration Number NCT01206062.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Troponina I / Infarto do Miocárdio Limite: Female / Humans / Male Idioma: En Revista: Clin Chem Assunto da revista: QUIMICA CLINICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Troponina I / Infarto do Miocárdio Limite: Female / Humans / Male Idioma: En Revista: Clin Chem Assunto da revista: QUIMICA CLINICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos
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