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1 abetes mellitus mainly led to an increase in calcified plaque.
2 ndent association with annual progression of calcified plaque.
3 o human peripheral arteries with substantial calcified plaque.
4 Only 1 ACS occurred in the absence of calcified plaque.
5 traclass correlation coefficients, >0.99) of calcified plaque.
6 ied plaque was noted or EBT- if there was no calcified plaque.
7 w-risk, quiescent, eccentric, nonobstructive calcified plaque.
8 with fewer mixed plaques and more often only calcified plaques.
9 scrimination between soft, intermediate, and calcified plaques.
10 (n = 10), mild (n = 10), or severe (n = 10) calcified plaques.
11 timated total plaque volume (-9.4 mm(3)) and calcified plaque (-11.4 mm(3)) and overestimated for non
12 , which comprised mostly fibrous (62.7%) and calcified plaque (23.6%), showed increasingly prominent
13 ; 95% CI, 0.15-0.85) and more often had only calcified plaques (38% versus 16%; ORadjusted=3.57; 95%
14 American patients had a lower prevalence of calcified plaque (39 [26%] vs 68 [45%] white patients, P
15 versus 54.6+/-19.2%; P<0.001) and partially calcified plaques (44.3+/-19.6 versus 54.9+/-20.0%; P<0.
16 Cluster 4 (n = 300), which comprised mostly calcified plaque (58.7%), demonstrated the greatest tota
19 aled fewer mixed plaques and more often only calcified plaques among athletes, suggesting a more beni
20 LDL-C is associated with higher risk of non-calcified plaque and with higher relative risk of future
21 DL-C) is associated with the presence of non-calcified plaques and future cardiovascular events in in
22 vels were associated with lower incidence of calcified plaques and plaques without high-risk features
23 e assessed the characteristics of individual calcified plaques and their relationship to other parame
24 92% and 88% for any plaque, 95% and 91% for calcified plaque, and 91% and 89% for noncalcified plaqu
25 cified plaque, a mixture of noncalcified and calcified plaque, and calcified plaque were significantl
26 t or supplements with any of our measures of calcified plaque, and no greater mortality risk was obse
27 spectively), and specifically with increased calcified plaques (aOR, 1.07 [1.00 to 1.15] per 10%; aOR
28 is, macrophage area, necrotic core area, and calcified plaque area was evaluated by using recursive p
29 ile mixed plaque at coronary CT angiography, calcified plaque at intravascular US, and lipid-rich pla
31 for uptake was significantly associated with calcified plaque burden (P < 0.0001) and cardiovascular
33 Younger diabetic individuals appear to have calcified plaque burden comparable to that of older indi
34 coronary plaque characteristics and overall calcified plaque burden confer an increased risk of coro
36 women 50 to 59 years old at enrollment, the calcified-plaque burden in the coronary arteries after t
37 he number of proximal segments with mixed or calcified plaques (C-index 0.64, p < 0.0001) and the num
38 The presence and severity of coronary artery calcified plaque (CAC) differs markedly between individu
39 l atherosclerosis imaging of coronary artery calcified plaque (CAC) to the primary prevention of coro
40 d computed tomography measurement of carotid calcified plaque (CarCP) and coronary calcified plaque (
41 ied plaque (CCP) and with or without carotid calcified plaque (CarCP) measured by electrocardiogram-g
42 est for an association among coronary artery calcified plaque, carotid artery calcified plaque, carot
43 nary artery calcified plaque, carotid artery calcified plaque, carotid IMT, and ACR while adjusting f
44 subjects with multiple (> or =3) individual calcified plaques, CC was heterogeneous within individua
45 are with or without the presence of coronary calcified plaque (CCP) and with or without carotid calci
46 posite, although nonsignificant, increase in calcified plaque (%change calcified volume/log2-fold cha
47 raphy showed a better agreement with ICA for calcified plaques compared with SR coronary CT angiograp
51 may reflect that the pathological process of calcified plaque formation and progression is the same i
53 f coronary artery calcium, mixed plaque, and calcified plaque; higher CCL2 levels were associated wit
55 orded in 188 (47%), any plaque in 214 (53%), calcified plaque in 151 (38%), and noncalcified/mixed pl
56 n after CAS, particularly in patients with a calcified plaque in the carotid bulb, but is easily trea
59 supplements and measures of subclinical CVD (calcified plaque in the coronary artery, carotid artery,
65 Accurate quantification of calcium in each calcified plaque may require that the threshold be set i
66 respecified endpoints were non-calcified and calcified plaque measures and high risk plaque features
68 alyzed separately: CAC score >0, any plaque, calcified plaque, noncalcified/mixed plaque, segment inv
69 included adjusted odds ratios (aOR) for non-calcified plaque on CCTA and adjusted hazard ratios (aHR
70 e, a proximal segment with either a mixed or calcified plaque or a stenosis >50% is equivalent to a 5
71 6 to 3.26], p < 0.0001) or the presence of a calcified plaque (OR 1.89 [range 1.25 to 2.84], p < 0.00
72 ) and of any plaque; noncalcified, mixed, or calcified plaque; or stenosis on coronary CT angiography
74 s, age was the only independent predictor of calcified plaque (p = 0.02) and remodeling (p = 0.005).
75 exercise was associated with greater CAC and calcified plaque progression, whereas vigorous intensity
76 -related risk of CHD (CASR), coronary artery calcified plaque (PTPRN2), and kidney function (CDH23, H
77 stprocessing techniques enhanced accuracy of calcified plaque quantification by reducing effects of t
78 1, P=0.002; fibrous plaque: r=0.54, P<0.001; calcified plaque: r=0.59, P<0.001; total plaque: r=0.62,
84 reas coronary artery calcification score and calcified plaque volume are more determined by genetics.
85 rtery calcification) score, noncalcified and calcified plaque volumes by coronary computed tomography
87 hile coronary artery calcification score and calcified plaque volumes had a relatively strong genetic
89 and 77%, respectively, and the prevalence of calcified plaque was 71%, 92%, and 85%, respectively, in
90 was good, and agreement for the presence of calcified plaque was high (kappa = 0.92, MESA; kappa = 0
93 es were higher in patients with CAV, whereas calcified plaque was not (median 0.0 vs 0.0, P = .510).
94 and HDLC > or =35 mg/dl; and 2) EBT+ if any calcified plaque was noted or EBT- if there was no calci
95 therosclerosis was regarded as definite if a calcified plaque was seen in the wall of an artery and p
96 correction factor was applied, the volume of calcified plaque was statistically better quantified wit
97 mmol/L higher LDL-C, the overall aOR for non-calcified plaques was 1.21 [95% confidence interval (CI)
101 re of noncalcified and calcified plaque, and calcified plaque were significantly higher among men wit
102 s prepared, and materials mimicking soft and calcified plaques were added to simulate stenosed corona
104 nel-volume CT by comparing measured areas of calcified plaque with respect to the reference standard