4.6 Article

Associations of cardiac injury biomarkers with risk of peripheral artery disease: The Multi-Ethnic Study of Atherosclerosis

期刊

INTERNATIONAL JOURNAL OF CARDIOLOGY
卷 344, 期 -, 页码 199-204

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ELSEVIER IRELAND LTD
DOI: 10.1016/j.ijcard.2021.09.055

关键词

Peripheral vascular disease; Biomarkers

资金

  1. National Heart, Lung, and Blood Institute [HHSN268201500003I, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC95167, N01-HC-95168, N01-HC-95169, R01-HL127659]
  2. NCATS [UL1-TR-000040, UL1-TR-001079, UL1-TR-001420]

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The study found that NT-proBNP and hs-cTnT are independently associated with the development of clinical PAD, with each log unit increment in hs-cTnT and NT-proBNP leading to a 30% and 50% higher risk of clinical PAD respectively. No significant associations were observed for incident low ABI.
Introduction: We investigated the associations of high-sensitivity cardiac Troponin T (hs-cTnT) and N-terminal pro B-type natriuretic peptide (NT-proBNP) levels with risk of developing clinical peripheral artery disease (PAD) or a low ankle-brachial index (ABI). Methods: Hs-cTnT and NT-proBNP were measured in 6692 and 5458 participants respectively without baseline PAD between 2000 and 2002 in the Multi-ethnic Study of Atherosclerosis. A significant number also had repeat biomarker measurement between 2004 and 2005. Incident clinical PAD was ascertained through 2017. Incident low ABI, defined as ABI <0.9 and decline of >= 0.15 from baseline, was assessed among 5920 eligible individuals who had an ABI >0.9 at baseline and at least one follow-up ABI measurement 3-10 years later. Multivariable Cox proportional hazards and logistic regression modeling were used to determine the association of these biomarkers with clinical PAD and low ABI, respectively. Results: Overall, 121 clinical PAD and 118 low ABI events occurred. Adjusting for demographic and clinical characteristics, each log unit increment in hs-cTnT and NT-proBNP was associated with a 30% (adjusted hazard ratio (HR) 1.3, 95% confidence interval (CI): 1.1, 1.6) and 50% (HR) 1.5, 95% CI: 1.2, 1.8) higher risk of clinical PAD respectively. No significant associations were observed for incident low ABI. Change in these biomarkers was not associated with either of the PAD outcomes. Conclusions: NT-proBNP and hs-cTnT are independently associated with the development of clinical PAD. Further study should determine whether these biomarkers can help to better identify those at higher risk for PAD.

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