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1 patients for troponin I and 25 patients for troponin T).
2 .e., NT-proBNP), and cardiac necrosis (i.e., Troponin T).
3 relate with log(concomitant high-sensitivity troponin-T).
4 tients with NSTE-ACS and an elevated cardiac troponin T.
5 tality, better than high-sensitivity cardiac troponin T.
6 terminal pro-B-type natriuretic peptide, and troponin T.
7 the case of chronic HF) to high-sensitivity troponin T.
8 by a positive test for cardiac troponin I or troponin T.
9 tions as determined by expression of cardiac troponin T.
10 ned changes in pre-dialysis highly sensitive troponin T.
11 syndrome (NSTE-ACS) and an elevated cardiac troponin T.
12 tients with NSTE-ACS and an elevated cardiac troponin T.
13 ated by the significantly reduced release of troponin-T.
14 detecting low concentrations of the protein troponin-T.
15 system was developed that used thresholds of troponin T (0.05 ng/ml) and N-terminal pro-B-type natriu
16 se without (n = 43) (mean +/- SD increase in troponin T, 0.011 +/- 0.009 vs. 0.003 +/- 0.006 mug/L, P
17 21.5% with elevated high-sensitivity cardiac troponin T; 17.7% with elevated NT-proBNP) with 825 inci
20 ity C-reactive protein, and high-sensitivity troponin T, Abeta40 independently predicted CV death and
25 expression of cardiomyogenic markers cardiac troponin T and alpha-smooth muscle actin in CPCedeltaB c
26 ins, including myosin light chain-2 slow and troponin T and carbonylation of myosin heavy chains.
27 easurement of the cardiac troponins, cardiac troponin T and cardiac troponin I, using sensitive metho
28 -enriched miRNAs with high-sensitive cardiac troponin T and cMyBP-C returned the highest area under t
29 the duration of such therapy, the levels of troponin T and creatine kinase, and the rates of bleedin
32 is of two meat tenderisation protein markers troponin T and desmin by the four proteases was detected
34 e 2222 patients with serial high-sensitivity troponin T and high-sensitivity troponin I measurements.
35 efficacy end point was postoperative plasma troponin T and I levels during the first 24 hours after
36 rent COVID-19 infection had higher levels of troponin T and lower lymphocyte count, but elevated D-di
37 and serial plasma levels of high-sensitivity troponin T and midregional proatrial natriuretic peptide
38 l-known biomarkers (high-sensitivity cardiac troponin T and N-terminal pro-brain natriuretic peptide)
39 pomyosin alpha-1 chain, fast myotomal muscle troponin T and parvalbumin beta 2 increased their intens
40 beating sheets of cells that express cardiac troponin T and show a full range of action potential mor
43 ssociated with high plasma concentrations of troponin-T and N-terminal brain natriuretic propeptide,
44 enhancement) and biomarkers (high-sensitive troponin-T and NT-proBNP [N-terminal Pro-B-type natriure
47 natriuretic peptide (NT-proBNP) and cardiac troponins T and I (TnT and TnI) for prognostication, but
48 omarkers of cardiac damage (high-sensitivity troponin T) and dysfunction (N-terminal pro-B-type natri
50 enaline, lipopolysaccharide binding protein, troponin T, and brain natriuretic peptide levels were me
51 d on clinical presentation, high-sensitivity troponin T, and cardiac magnetic resonance imaging, afte
53 N-terminal pro-brain natriuretic peptide and Troponin T, and functional assessment comprising the 6-m
54 atriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive protein sign
55 atriuretic peptide, high-sensitivity cardiac troponin T, and high-sensitivity C-reactive protein.
56 nalyses, including C-reactive protein, IL-6, troponin T, and N-terminal pro-B-type natriuretic peptid
57 n, procalcitonin, ferritin, D-dimer, cardiac troponin T, and N-terminal pro-B-type natriuretic peptid
58 F: N-terminal B-type natriuretic peptide and troponin T, and newly emergent biomarkers, angiopoietin-
60 Elevated levels of NT-proBNP, high-sensitive troponin-T, and growth-differentiation factor 15 identif
61 riuretic peptide (NT-proBNP), high-sensitive troponin-T, and growth-differentiation factor 15 with ca
62 arker measurement (NT-proBNP, high-sensitive troponin-T, and growth-differentiation factor 15) at the
64 f N-terminal pro-B-type natriuretic peptide, troponin-T, and urinary albumin excretion, increasing mo
65 iuretic peptide and high-sensitivity cardiac troponin T are frequently elevated in severe sepsis or s
67 rence limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independent cohort
68 The TRAPID-AMI trial study (High-Sensitivity Troponin-T Assay for Rapid Rule-Out of Acute Myocardial
69 the widespread use of high-sensitive cardiac troponin T assays, positive tests become frequent, but t
70 urve for the high-sensitivity assay of serum troponin T at 72 hours), inotrope score (calculated from
71 stable angina (28% of patients) and negative Troponin T at baseline to 3 groups: 2 groups received RI
72 h-sensitivity troponin I or high-sensitivity troponin T at presentation and after early or late seria
73 val incremental change of the ln-transformed troponin-T at 72 h was 0.79 +/- 1.54 in the xenon group
75 as by detecting different concentrations of Troponin T biomarkers (cTnT) through antibody-functional
76 reduced the heart recipient plasma levels of troponin T by 34% (14 900 +/- 12 100 ng/L to 9800 +/- 79
77 L and a perioperative high-sensitive cardiac troponin T change greater than or equal to 6.3 ng/L are
78 k predictive power of high-sensitive cardiac troponin T change in addition to the Revised Cardiac Ris
79 uretic peptide) and hs-TnT (high-sensitivity troponin T), circulating SN levels declined after resusc
80 osite end point in patients with an abnormal troponin T concentration (>/=14 ng per liter) as compare
82 We tested for an association between the troponin T concentration and a composite end point of de
84 integrate the high-sensitivity troponin I or troponin T concentration at emergency department present
86 7 (99.6%) had detectable (>/=3 ng per liter) troponin T concentrations and 897 (39.3%) had abnormal t
87 7.1% among the patients who had had abnormal troponin T concentrations at baseline, as compared with
90 osite end point among patients with abnormal troponin T concentrations was 1.85 (95% confidence inter
91 riuretic peptide or high-sensitivity cardiac troponin T concentrations were independently associated
96 log-transformed concomitant high-sensitivity troponin-T concentrations (mixed linear model: t = 3.8,
99 flammatory markers included high-sensitivity troponin T, creatine kinase, myoglobin, N-terminal B-typ
100 igh-sensitivity C-reactive protein (hs-CRP), Troponin-T, creatine kinase-MB, fibrinogen, and D-Dimer
101 c acute cardiac stress (by measuring cardiac troponin T (cTnT) and N-terminal prohormone of brain nat
102 However, it is not clear whether cardiac troponin T (cTnT) and troponin I (cTnI) are equivalent m
104 biological significance of elevated cardiac troponin T (cTnT) in patients with neuromuscular disease
106 assumption that chronically elevated cardiac troponin T (cTnT) levels fluctuate randomly around a hom
108 p device provides the capability for cardiac-troponin T (cTnT) measurements with co-existed 10 microg
109 hypertrophic cardiomyopathy-causing cardiac troponin T (cTnT) mutation Delta160Glu (Delta160E) is lo
111 udy was to evaluate whether elevated cardiac troponin T (cTnT) was independently associated with an i
112 ry are cardiac troponin I (cTnI) and cardiac troponin T (cTnT) which have been considered as 'gold st
114 of TNNT2, the gene that encodes for cardiac troponin T (cTnT), a biomarker of myocardial injury.
115 tion between LVH, low but detectable cardiac troponin T (cTnT), and elevated N-terminal pro-B-type na
118 For the first time, we show that cardiac troponin T (cTnT), in part through its intrinsically dis
120 eric/cooperative mechanism is cardiac muscle troponin T (cTnT), the central region (CR) and the T2 re
123 factor-15 (GDF-15), high-sensitivity cardiac troponin T (cTnT-hs) and haemoglobin, age, and previous
124 ing of cardiac Troponin-I (cTnI) and cardiac-Troponin-T (cTnT) in a point-of-care sensor format.
125 rix metalloproteinase-9 (MMP-9), and cardiac Troponin-T (cTnT) were evaluated by appropriate biochemi
128 ve, the area under the 72-h high-sensitivity troponin-T curve was lower in patients assigned to the h
132 utcomes among patients with newly recognized troponin T elevation will require an evolution in manage
133 1-h algorithm using high-sensitivity cardiac troponin T embedded in routine clinical care and its ass
136 gh impedance spectroscopy was used to detect troponin-T functionalized immunoassays on nanotextured Z
137 d syndrome and long-QT syndrome, and cardiac troponin T gene, tnnt2, affected in human cardiomyopathi
139 perienced an event associated with a cardiac troponin T >99th percentile of a normal reference popula
140 ension and a composite of myocardial injury (troponin T >= 0.03 ng/mL without nonischemic cause) and
141 al of 5460 patients had at least one cardiac troponin T >=0.01 ng/mL; 1365 of these patients were cla
142 myocardial injury (high-sensitivity cardiac troponin T >=6 ng/L] and stress (N-terminal pro-B-type n
143 proBNP (>14 pmol/L), elevated high-sensitive troponin-T (>14 ng/L), and elevated growth-differentiati
144 ro-B-type natriuretic peptide [>40 pg/mL] or troponin T [>0.6 pg/mL]) were recruited, along with 61 a
146 uretic peptide, and high-sensitivity cardiac troponin T, higher levels of Cp were associated with HF
147 r circulation and a high-sensitivity cardiac troponin T (hs-cTnT) acquired on the day of admission.
149 h small elevations of high-sensitive cardiac troponin T (hs-cTnT) are associated with incident heart
151 evel, with elevated high-sensitivity cardiac troponin T (hs-cTnT) concentrations (>/=14 ng/L) using P
152 ide (NT-proBNP) and high-sensitivity cardiac troponin T (hs-cTnT) concentrations were measured by ele
153 c value of baseline high-sensitivity cardiac troponin T (hs-cTnT) elevation in SCAD patients undergoi
154 o mental stress and high-sensitivity cardiac troponin T (hs-cTnT) in healthy older individuals withou
155 cremental prognostic value of high-sensitive troponin T (hs-cTnT) in heart failure (HF) beyond that o
156 ions of introducing high-sensitivity cardiac troponin T (hs-cTnT) into clinical practice and to defin
158 etectable (<5 ng/l) high-sensitivity cardiac troponin T (hs-cTnT) level and an electrocardiogram (ECG
159 that any detectable high-sensitivity cardiac troponin T (hs-cTnT) level is associated with adverse ou
160 eferable when using high-sensitivity cardiac troponin T (hs-cTnT) levels in the diagnosis of acute my
162 endpoints included high-sensitivity cardiac troponin T (hs-cTnT) on day 4, left ventricular (LV) rem
163 elevated levels of high-sensitivity cardiac troponin T (hs-cTnT) or N-terminal pro-B-type natriureti
164 ority of a 0/1-hour high-sensitivity cardiac troponin T (hs-cTnT) protocol in comparison with a 0/3-h
166 algorithm based on high-sensitivity cardiac troponin T (hs-cTnT) testing at presentation and again 1
167 we assessed whether high-sensitivity cardiac troponin T (hs-cTnT), a marker of subclinical myocardial
168 atriuretic peptide, high-sensitivity cardiac troponin T (hs-cTnT), and high-sensitivity cardiac tropo
169 eptide (NT-proBNP), high-sensitivity cardiac troponin T (hs-cTnT), and low-density lipoprotein choles
173 tic peptide (NT-proBNP) and high-sensitivity troponin T (hs-TnT) can be used as surrogate markers and
174 The prognostic value of high-sensitivity troponin T (hs-TnT) elevation after elective percutaneou
175 the prevalence of elevated high-sensitivity troponin T (hs-TnT) in 298 patients with heart failure w
176 ate the prognostic value of high-sensitivity troponin T (hs-TnT) in addition to clinical risk factors
177 trasensitive tests to measure high-sensitive troponin T (hs-TnT) serum levels revealed the presence o
178 elationship between OSA and high-sensitivity troponin T (hs-TnT), cardiac structure, and CV outcomes
179 he prognostic importance of high-sensitivity troponin T (hs-TnT), N-terminal pro-brain natriuretic pe
181 farction) evaluated high-sensitivity cardiac troponin-T (hs-cTnT) in a 1-hour acute myocardial infarc
182 rdial damage (using high-sensitivity cardiac troponin-T [hs-cTnT]) and with coronary heart disease (C
184 nknown if evaluation with a high-sensitivity troponin T (hsTnT) assay affects prognosis in this large
186 B-type natriuretic peptide, high sensitivity troponin T (hsTnT), beta-trace protein (BTP) and interle
187 atients, analyzing baseline high-sensitivity troponin T (hsTnT), NT-proBNP (N-terminal B-type natriur
189 to determine whether hsTnT (high-sensitivity troponin T) identifies emergency department acute heart
190 of the patients and high-sensitivity cardiac troponin T in 84.5%, with higher concentrations in those
192 mited to the use of natriuretic peptides and troponin-T in patients with increased cardiovascular ris
193 ined as an absolute high-sensitivity cardiac troponin T increase of >/=14 ng/L from preoperative to p
194 ease significantly over time, troponin I and troponin T increased moderately, and no consistent clini
198 confidence limits (CL): 1.52 to 12.30), peak troponin T level (OR: 1.20; 95% CL: 1.08 to 1.34), and u
200 vel, hemoglobin A1c level, phosphorus level, troponin T level, log N-terminal pro-B-type natriuretic
201 nd-point was the proportion of patients with Troponin T levels >3xULN postprocedure (at 6 or 18-24 ho
202 hest pain, elevated high-sensitivity cardiac troponin T levels (>14 ng/l), and inconclusive electroca
205 study was to examine the extent of change in troponin T levels in patients with non-ST-segment elevat
207 patients with NSTE-ACS and elevated cardiac troponin T levels, an early invasive strategy has no ben
208 nfarct size (P<0.005) and a 61% reduction in troponin-T levels (P<0.05) in comparison with saline con
210 iomarkers (hs-cTnT (high sensitivity cardiac troponin-T) <6 ng/L and NT-proBNP (N-terminal pro-B-type
212 edural increases of high-sensitivity cardiac troponin T (mean: 9.9 ng/ml, range: 2.7 to 19.0 ng/ml vs
214 rdiography, and concomitant high-sensitivity troponin-T measurement in patients with severe sepsis or
215 24-hour postoperative high-sensitive cardiac troponin T measurements and the respective changes were
216 tigations including high-sensitivity cardiac troponin T measurements at later time points or coronary
217 re- and postoperative high-sensitive cardiac troponin T measurements demonstrated a majority of patie
220 cardiograms and concomitant high-sensitivity troponin-T measurements were performed in a cohort of 10
222 in vivo, transgenic mice harboring the R92Q troponin-T mutation and wild-type littermates received a
223 f Drosophila cardiac tubes revealed that the troponin-T mutation prolongs systole and restricts diast
225 Measures: Concentrations of high-sensitivity troponin T, N-terminal pro-B-type natriuretic peptide, a
226 cacy International Trial]), high-sensitivity troponin T, N-terminal pro-B-type natriuretic peptide, g
227 biomarkers of cardiac damage were measured (troponin T, N-terminal pro-brain natriuretic peptide, an
228 white blood cell count, fibrinogen, D-dimer, troponin T, N-terminal pro-brain natriuretic peptide, an
229 out either elevated high-sensitivity cardiac troponin T or NT-proBNP had a 10-year CV incidence rate
232 erences in creatine kinase release (P=0.92), troponin T (P=0.85), or cardiac MRI-assessed infarct siz
234 In contrast, patients with NR had higher troponin T peak (P=0.006) but similar late gadolinium en
235 TPase, increased levels of phospholamban and troponin T phosphorylation, and reduced phosphorylation
237 lective expression of EcSOD from the cardiac troponin-T promoter after systemic administration of AAV
239 superoxide dismutase (EcSOD) via the cardiac troponin-T promoter would protect the mouse heart agains
244 ed 2 mouse models of sarcomeric HCM (cardiac troponin T R92L and R92W) with differential myocellular
246 ylprednisolone significantly reduced cardiac troponin T release and the number of allograft infiltrat
247 myocardial damage evidenced by serum cardiac troponin T release in the rat and mouse cardiac allograf
248 m21G6 significantly reduced infarct size and troponin-T release, and led to marked preservation of ca
250 markers of cardiac (high-sensitivity cardiac troponin T), renal (creatinine and cystatin-C), and hepa
252 n natriuretic peptide (pro-BNP), and cardiac troponin T showed significant linear trends for increase
254 he truncated slow skeletal muscle isoform of troponin T (ssTnT) encoded by the mutant TNNT1 gene is u
256 y more cardiomyocytes, determined by cardiac troponin-T staining, in the MI zone of the QHG213H hydro
257 dysfunction), age, injury (high-sensitivity troponin T), systemic involvement, and electrical abnorm
259 tween or near residues 112 to 136 of cardiac troponin-T, the crucial TnT1 (N-terminal domain of tropo
260 oding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) caused altered troponin protein stoic
261 cluding the Insulin Receptor (Insr), Cardiac Troponin T (Tnnt2), Lim Domain Binding 3 (Ldb3) RNAs in
262 roponin I (TNNI3p.98truncation ) and cardiac troponin T (TNNT2p.K217deletion ; also known as the p.K2
270 als also showed negligible interference from troponin T (TnT), bovine serum albumin (BSA) and urea un
272 ith a dilated cardiomyopathy (DCM) mutation, troponin T (TnT)-R173W, display sarcomere protein misali
275 ced expression of troponin I to 39% and 51%, troponin T to 64% and 53%, and troponin C to 73% and 97%
276 the binding of increasing concentrations of troponin-T to the immobilized antibodies on the ZnO surf
277 in-T, the crucial TnT1 (N-terminal domain of troponin-T)-tropomyosin-binding region, cause cardiomyop
278 -pro-B-type natriuretic peptide (NT-proBNP), troponin T (TropT) and C-reactive protein (CRP) predict
279 rrest of cardiomyocyte contraction either by troponin T type 2a (tnnt2a) MO or in weak atriumm58 (wea
281 diovascular disease in our study had cardiac troponin T values above the current myocardial infarctio
282 The effect of xenon on the change in the troponin-T values did not differ in patients with or wit
293 iuretic peptide and high-sensitivity cardiac troponin T were measured 1, 2, and 7 days after enrollme
295 ntricular structure and function and cardiac troponin-T were among the top predictors for incident he
297 e association of hs-TnI and high-sensitivity troponin T with incident CVD events was also evaluated.
298 ro-brain natriuretic peptide (NT-proBNP) and troponin T with liver involvement and the presence of ne
299 t patients would have had a negative cardiac troponin T with older assays); and Group 4, those with h
300 re- and postoperative high-sensitive cardiac troponin T with the occurrence of major adverse cardiac