Hypertrophic cardiomyopathy: The time-synchronized relationship between ischemia and left ventricular dysfunction assessed by highly sensitive troponin i and NT-proBNP

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Abstract

The aim of this study was to compare NT-proBNP using the absolute values and NT-proBNP/ULN values that were standardized by age and gender between three subgroups: those without ischemia (negative hs-troponin I and no anginal pain (hsTnI-/AP-)), those with painless ischemia (hsTnI+/AP-), and those with painful ischemia (hsTnI+/AP+). Additionally, echocardiographic parameters were compared in these three subgroups. The absolute value of NT-proBNP was significantly higher in the painful ischemia subgroup (hsTnI-/AP- vs. hsTnI+/AP- vs. hsTnI+/AP+: 502 (174-833) vs. 969 (363-1346) vs. 2053 (323-3283) pg/ml; p = 0 018 for the whole-model analysis). The standardized value of NT-proBNP/ULN was gradually increased (hsTnI-/AP- vs. hsTnI+/AP- vs. hsTnI+/AP+: 3 61 + 0 63 vs. 6 90 + 1 31 vs. 9 35 + 1 87; p = 0 001 for the whole-model analysis). In the comparison between subgroups (hsTnI-/AP- vs. hsTnI+/AP- vs. hsTnI+/AP+), two echocardiographic parameters increased significantly. The left ventricular maximum wall thickness (LVMWT) at diastole was 1 99 ± 0 08 cm vs. 2 28 ± 0 13 cm vs. 2 49 ± 0 15 cm (p = 0 004 for the whole-model analysis). The maximal gradient of the provoked left ventricular outflow tract (LVOT) gradient increased significantly in only the painful-ischemia subgroup (11 (7-30) mmHg vs. 12 (9.35-31.5) mmHg vs. 100 (43-120) mmHg). In conclusion, both painless ischemia and painful ischemia are associated with a gradual, significant increase in NT-proBNP/ULN in comparison to the double-negative hsTnI/AP subgroup. In contrast, NT-proBNP is significantly higher in only the subgroup with painful ischemia.

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APA

Rajtar-Salwa, R., Gȩbka, A., Dziewierz, A., & Dimitrow, P. P. (2019). Hypertrophic cardiomyopathy: The time-synchronized relationship between ischemia and left ventricular dysfunction assessed by highly sensitive troponin i and NT-proBNP. Disease Markers, 2019. https://doi.org/10.1155/2019/6487152

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