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1 that triglyceride levels causally influence low-density lipoprotein.
2 re typically present in oxidatively modified low-density lipoprotein.
3 inds both high-density lipoprotein (HDL) and low-density lipoprotein.
4 blood pressure 51.2%; body mass index 33.8%; low-density lipoprotein 31.4%; and waist-to-hip ratio 29
5 ces, -0.35 kg/m(2); 95% CI, -0.62 to -0.07), low-density lipoprotein (4 studies; mean differences, -0
7 preventing inflammation induced by oxidized low-density lipoprotein and promoting apoptotic cell cle
8 ned significant after adjusting for baseline low-density lipoprotein and statin dose (beta=-0.27; P=0
9 ss 6 to 12 months, including blood pressure, low-density lipoprotein and total cholesterol levels, an
10 tween noncoding rare variants in SLC22A3 and low-density lipoprotein and total cholesterol, associati
11 tiology via extensive associations with very-low-density lipoprotein and triglyceride metabolism.
13 tivity and total HDL antioxidant capacity on low-density lipoproteins), and HDL vasodilatory capacity
15 ciated with a significant increase in total, low-density lipoprotein, and high-density lipoprotein (H
16 Serum levels of total cholesterol (TC), TG, low-density lipoprotein, and high-density lipoprotein we
17 resulted in significant reductions in total, low-density lipoprotein, and non-high-density lipoprotei
18 ncreased high-density lipoprotein, decreased low-density lipoprotein, and reduced atherosclerosis.
19 IHD, systolic and diastolic blood pressure, low-density lipoprotein- and total cholesterol, triglyce
20 ocumab had no effects on FCRs or PRs of very low-density lipoproteins-apoB and very low-density lipop
21 is tempers triglyceride availabiity for very low density lipoprotein assembly and allows homeostatic
22 the CC-genotype was associated with elevated low density lipoprotein cholesterol (LDLc) and total cho
23 burden related to phenotypic FH, defined by low-density lipoprotein cholesterol >/=190 mg/dL, is lik
25 Children with HeFH (age, 6-<18 years) and low-density lipoprotein cholesterol >4.9 mmol/L or >4.1
26 ntion parameters-aspirin use, lipid control (low-density lipoprotein cholesterol <70 mg/dL or statin
28 d with the highest versus lowest quartile of low-density lipoprotein cholesterol (>/= 146 versus </=
29 idence interval, 18-27; P<1.0x10(-4)), lower low-density lipoprotein cholesterol (-12.2 mg/dL; 95% co
30 ipoprotein cholesterol (1.6 [1.2-2.2]), high low-density lipoprotein cholesterol (1.6 [1.1-2.1]), and
31 ]), obesity (3.7 [2.0-7.0]), borderline high low-density lipoprotein cholesterol (1.6 [1.2-2.2]), hig
32 63.1%), LDL cholesterol (1.3 to 32.9%), very-low-density lipoprotein cholesterol (27.9 to 60.0%), non
33 oach using only childhood lipid measures for low-density lipoprotein cholesterol (area under the rece
35 A and NPHSII, respectively; both p < 0.001), low-density lipoprotein cholesterol (correlation coeffic
36 t showed differential responses in total and low-density lipoprotein cholesterol (decreased in LFHC g
39 se <126 mg/dl, total cholesterol <240 mg/dl, low-density lipoprotein cholesterol (LDL-C) <160 mg/dl,
40 iglycerides (TGs), high-density (HDL-C), and low-density lipoprotein cholesterol (LDL-C) (n=627).
41 haracterized by extremely elevated levels of low-density lipoprotein cholesterol (LDL-C) and accelera
42 ma concentrations of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and apolipop
44 ontinuous relationship between reductions in low-density lipoprotein cholesterol (LDL-C) and major ad
46 oring nonfasting lipid assessment may affect low-density lipoprotein cholesterol (LDL-C) estimation.
47 elected individuals with increased levels of low-density lipoprotein cholesterol (LDL-C) have shown m
48 tients with elevated 10-year risk (>5%) or a low-density lipoprotein cholesterol (LDL-C) level of 4.9
49 y statins and targeting or using a threshold low-density lipoprotein cholesterol (LDL-C) level of les
50 cluding 511 adult patients with uncontrolled low-density lipoprotein cholesterol (LDL-C) levels and h
51 noclonal antibody against PCSK9 that reduces low-density lipoprotein cholesterol (LDL-C) levels by 55
52 itors in patients with persistently elevated low-density lipoprotein cholesterol (LDL-C) levels despi
53 ter transfer protein (CETP) inhibitors lower low-density lipoprotein cholesterol (LDL-C) levels witho
55 amination of the effects of lifetime reduced low-density lipoprotein cholesterol (LDL-C) on cardiovas
56 was shown that intraindividual variation in low-density lipoprotein cholesterol (LDL-C) predicts bot
58 exin type 9 monoclonal antibodies can reduce low-density lipoprotein cholesterol (LDL-C) to very low
60 vestigated whether the relative reduction in low-density lipoprotein cholesterol (LDL-c) was a good i
61 igh-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and triglyc
62 igh-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and triglyc
65 orin Efficacy International Trial, intensive low-density lipoprotein cholesterol (LDL-C)-reducing the
70 one of the scavenger receptors for oxidized low-density lipoprotein cholesterol (ox-LDL), plays a cr
71 l/L, LF = -0.31 +/- 0.10 mmol/L; P = 0.024), low-density lipoprotein cholesterol (PY = -0.35 +/- 0.10
72 patients after acute coronary syndrome with low-density lipoprotein cholesterol 50 to 125 mg/dL were
73 igh-density lipoprotein cholesterol [HDL-C], low-density lipoprotein cholesterol [LDL-C], total chole
74 e subtilisin/kexin type 9), markedly reduces low-density lipoprotein cholesterol across diverse patie
75 n/kexin type 9) inhibitor evolocumab reduced low-density lipoprotein cholesterol and cardiovascular e
76 me-wide significant variants associated with low-density lipoprotein cholesterol and coronary heart d
78 creased body mass index, active smoking, and low-density lipoprotein cholesterol and lipoprotein(a) l
79 nsistent relationship between lower achieved low-density lipoprotein cholesterol and lower risk of li
80 s and cumulative exposure to lower levels of low-density lipoprotein cholesterol are not associated w
81 atment to placebo in individuals with normal low-density lipoprotein cholesterol but increased C-reac
83 sult in lifelong exposure to lower levels of low-density lipoprotein cholesterol can provide informat
84 ificantly lower median time-weighted average low-density lipoprotein cholesterol compared with placeb
86 t-day humans, including variants involved in low-density lipoprotein cholesterol concentrations, schi
87 s for neurocognitive impairment per 20 mg/dL low-density lipoprotein cholesterol decrements were 1.02
88 s in the face of lower levels of circulating low-density lipoprotein cholesterol in mice lacking miR-
89 A1c was -0.022 +/- 0.53%; however, total and low-density lipoprotein cholesterol increased significan
90 CI, -0.82 to -0.16]; 23 trials [n = 58022]), low-density lipoprotein cholesterol level (-2.58 mg/dL [
91 , but approval rates did not vary by patient low-density lipoprotein cholesterol level nor statin use
93 ter publication) in the cohort with elevated low-density lipoprotein cholesterol levels (ie, >/=190 m
94 , including reductions in blood pressure and low-density lipoprotein cholesterol levels and improveme
95 atherosclerotic cardiovascular disease with low-density lipoprotein cholesterol levels of at least 7
96 counted net price of $10311 in patients with low-density lipoprotein cholesterol levels of at least 8
99 sment of the efficacy and safety of lowering low-density lipoprotein cholesterol levels with atorvast
103 on the potential long-term effects of lower low-density lipoprotein cholesterol on neurocognitive im
104 of early initiation of statin treatment for low-density lipoprotein cholesterol reduction in childre
105 NA that regulates LDLR and may contribute to low-density lipoprotein cholesterol response to statin t
106 eye examination, hemoglobin A1c testing, and low-density lipoprotein cholesterol testing), prescribin
107 eye examination, hemoglobin A1c testing, and low-density lipoprotein cholesterol testing), prescribin
108 sed on benefits estimated from reductions in low-density lipoprotein cholesterol that occurred in PCS
111 ing family history, more stringent age-based low-density lipoprotein cholesterol thresholds, or alter
112 herosclerotic Cardiovascular Risk in Adults, low-density lipoprotein cholesterol treatment thresholds
114 s coronary intervention, and higher level of low-density lipoprotein cholesterol were independent pre
117 (A), biomarkers (B) (NT-proBNP, hs-cTnT, and low-density lipoprotein cholesterol), and clinical varia
118 -8 mg/dl for total cholesterol, -8 mg/dl for low-density lipoprotein cholesterol, +8 mg/dl for remnan
119 ed on 58 single-nucleotide polymorphisms for low-density lipoprotein cholesterol, 71 single-nucleotid
120 nt of saturated with unsaturated fats lowers low-density lipoprotein cholesterol, a cause of atherosc
121 ype natriuretic peptide, and lower levels of low-density lipoprotein cholesterol, adiponectin, lipopr
122 with progressively higher levels of glucose, low-density lipoprotein cholesterol, and blood pressure.
123 ntrol subjects and had higher triglycerides, low-density lipoprotein cholesterol, and HbA1c and lower
124 pe 9 (PCSK9) inhibitors substantially reduce low-density lipoprotein cholesterol, but it is presently
125 nic profile scores for BMI, HDL cholesterol, low-density lipoprotein cholesterol, coronary artery dis
126 ng insulin, triglyceride, total cholesterol, low-density lipoprotein cholesterol, fasting glucose, di
127 diabetes duration, systolic blood pressure, low-density lipoprotein cholesterol, hemoglobin A1c, alb
128 ated to cardiovascular disease risk factors: low-density lipoprotein cholesterol, high-density lipopr
129 high-density lipoprotein cholesterol, lower low-density lipoprotein cholesterol, lower triglycerides
132 In multivariable analysis, older age, higher low-density lipoprotein cholesterol, pack per year of sm
134 Application of SCOPA to two GWAS of high-and low-density lipoprotein cholesterol, triglycerides and b
135 1 microbe intervention in rats reduced serum low-density lipoprotein cholesterol, triglycerides and t
136 ex, fasting plasma glucose, glycohemoglobin, low-density lipoprotein cholesterol, triglycerides, high
137 ensitivity cardiac troponin T (hs-cTnT), and low-density lipoprotein cholesterol, where NT-proBNP and
138 acebo, in addition to effective statin-based low-density lipoprotein cholesterol-lowering treatment.
139 is-methylation quantitative trait loci for a low-density lipoprotein cholesterol-related differential
146 igh-density-lipoprotein cholesterol (HDL-C), low-density-lipoprotein cholesterol (LDL-C), and/or trig
148 Plasma levels of total cholesterol (T-CHL), low density lipoprotein-cholesterol (LDL-CHL), and resis
149 and cardiovascular disease (CVD) context and low density lipoprotein-cholesterol concentrations withi
151 ed back into the cellular media, whereas the low-density lipoprotein component was localized to the l
152 n DCs on atherosclerosis were examined using low-density lipoprotein-deficient (Ldlr(-/-)) bone marro
156 with cholesterol concentrations in high- and low-density lipoproteins (HDL and LDL) particles measure
159 CAD as a function of their association with low-density lipoprotein, high-density lipoprotein, trigl
160 tein component, indicating their origin from low-density lipoprotein, intermediate-density lipoprotei
162 contributes to atherosclerosis by targeting low density lipoprotein (LDL) receptor (LDLR) degradatio
163 show that alpha2delta-1 is a ligand for the Low Density Lipoprotein (LDL) Receptor-related Protein-1
164 kinetics of key biological proteins, namely Low Density Lipoprotein (LDL), Tissue Necrosis Factor al
166 Although EC are in constant contact with low density lipoproteins (LDL), how EC process LDL and w
168 gnificantly lowers blood pressure as well as low-density lipoprotein (LDL) and high-density lipoprote
169 95% CI, 0.80-0.95, per mmol/l increase), and low-density lipoprotein (LDL) cholesterol (OR, 0.83; 95%
170 btilisin/kexin type 9 (PCSK9), lowers plasma low-density lipoprotein (LDL) cholesterol and apolipopro
171 e cardiometabolic risk-factor profile [lower low-density lipoprotein (LDL) cholesterol and triglyceri
172 e subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by appr
173 was found to produce sustained reductions in low-density lipoprotein (LDL) cholesterol levels over th
175 oncern that these drugs or the low levels of low-density lipoprotein (LDL) cholesterol that result fr
176 l3 mRNA, Angptl3 protein, triglycerides, and low-density lipoprotein (LDL) cholesterol, as well as re
177 mes were: blood pressure, total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density
178 nstrated to be associated with at least 1 of low-density lipoprotein (LDL) cholesterol, high-density
186 ly, hepatic vigilin knockdown decreases VLDL/low-density lipoprotein (LDL) levels and formation of at
190 isin/kexin type 9 (PCSK9) down-regulates the low-density lipoprotein (LDL) receptor, elevating LDL ch
191 iosynthesis thereby upregulating the hepatic low-density lipoprotein (LDL) receptors and increasing t
195 ins, such as high-density lipoprotein (HDL), low-density lipoprotein (LDL), and very-low density lipo
196 ther the most electronegative subfraction of low-density lipoprotein (LDL), L5, is correlated with QT
198 ipid traits (high-density lipoprotein (HDL), low-density lipoprotein (LDL), plasma concentrations of
199 9 (PCSK9), such as evolocumab, lower plasma low-density lipoprotein (LDL)-cholesterol concentrations
200 CDP) on the role of non-statin therapies for low-density lipoprotein (LDL)-cholesterol lowering in th
203 rin Efficacy International Trial by reducing low-density-lipoprotein (LDL) cholesterol levels more th
205 hages ingest high levels of damaged modified low-density lipoproteins (LDLs), generating macrophage f
208 (-250.19 g; 95% CI, -459.9 to -40.5 g), and low-density lipoprotein levels (-15.4 mg/dL; 95% CI, -23
209 n-1(Sort1), a known regulator of circulating low-density lipoprotein levels in humans, as a novel tar
212 gh-density lipoprotein lipids and lower very-low-density lipoprotein lipids, glucose levels, branched
213 tein, intermediate-density lipoprotein, very-low-density lipoprotein, lipoprotein (a), or chylomicron
215 ystemic treatment with anti-inflammatory and low-density lipoprotein-lowering drugs are currently bei
216 terol (MD -8.5 mg/dl, 95% CI -9.5, -7.4) and low-density lipoprotein (MD -2.4 mg/dl, 95% CI -3.4, -1.
217 % confidence interval 3.48-6.78), other very-low-density lipoprotein measures, and branched-chain ami
218 inhibition of PCSK9 has any effects on very low-density lipoprotein or intermediate-density lipoprot
219 induced by cholesterol crystals and oxidized low-density lipoproteins (ox-LDL), potentially by increa
220 xidative stress were measured in plasma: (1) low-density lipoprotein oxidizability, (2) high-density
222 d leads to the uptake of native and oxidized low-density lipoprotein (oxLDL) by macrophages (Mvarphis
224 CD36 recognizes oxidized lipids in oxidized low-density lipoprotein (oxLDL) particles, a process tha
227 Procollagens, pre-chylomicrons, and pre-very low-density lipoproteins (pre-VLDLs) are too big to fit
228 macrophage LKB1 reduction caused by oxidized low-density lipoprotein promotes foam cell formation and
229 icantly improved high-density lipoprotein to low-density lipoprotein ratios in high fat-fed mice with
230 n signals via the lipoprotein receptors very low density lipoprotein receptor (VLDLR) and apolipoprot
231 t mice (0.162 cm(2)+/-0.023 [n=9], P2X7(-/-) low density lipoprotein receptor(-/-) : 0.084 cm(2)+/-0.
232 xpression was analyzed in aortic arches from low density lipoprotein receptor(-/-) mice consuming a h
236 ent increases mRNA and protein expression of low density lipoprotein receptor-related protein 2 and a
237 ent and activation of beta1 integrin via the low density lipoprotein receptor-related protein-1 (LRP1
238 Mice fed a Western-type diet and lacking low-density lipoprotein receptor (Ldlr(-/-)T39(-/-)) sho
241 audin-1 (CLDN1), Occludin (OCLN), SR-BI, and low-density lipoprotein receptor (LDLR), function mainly
242 ertase subtilisin/kexin type 9 (PCSK9) binds low-density lipoprotein receptor (LDLR), preventing its
244 the inflamed aorta in atherosclerosis-prone low-density lipoprotein receptor deficient (Ldlr(-/-)) m
246 of atherogenesis by mPGES-1 deletion in the low-density lipoprotein receptor knockout mice (n=17-21)
250 clerotic lesion size was found in Ldlr(-/-) (low-density lipoprotein receptor null) mice transplanted
251 ion disrupts an interaction with VLDLR (very low-density lipoprotein receptor), while the APOER2 sign
252 arrow-restricted deletion of DNGR-1 in Ldlr (low-density lipoprotein receptor)-deficient mice (Ldlr(-
253 teraction with the RELN receptor VLDLR (very low-density lipoprotein receptor); this was confirmed by
255 Tet2-mutant cells in atherosclerosis-prone, low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
256 ate senescent cells in atherosclerosis-prone low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
257 od vessels invading photoreceptors: the very low-density lipoprotein receptor-deficient (Vldlr(-/-) )
259 results in decreased hepatic inflammation in low-density lipoprotein receptor-deficient mice on a Wes
260 ress as prime response pathways in livers of low-density lipoprotein receptor-deficient mice on a Wes
263 , the receptors for these secreted proteins, low-density lipoprotein receptor-related protein 1 (LRP1
264 ction with the endocytic scavenger receptor, low-density lipoprotein receptor-related protein 1 (LRP1
265 ctin, a protein acting downstream from agrin/low-density lipoprotein receptor-related protein 4 (LRP4
266 ancer have identified novel functions of the low-density lipoprotein receptor-related protein 4-muscl
267 ptions of tryptophan hydroxylase 1 (Tph1) or low-density lipoprotein receptor-related protein 5 (Lrp5
269 rocytic thrombospondin-1 (TSP1) and synaptic low-density lipoprotein receptor-related protein-1 (LRP1
271 (LPS) by a pathway that apparently requires low-density lipoprotein receptor-related protein-1 (LRP1
272 rocytic thrombospondin-1 (TSP1) and synaptic low-density lipoprotein receptor-related protein-1 (LRP1
273 receptors frizzled 1-10 and the co-receptors low-density lipoprotein receptor-related proteins 5 and
275 els through a mechanism that is dependent on low-density lipoprotein receptors (LDLRs) and LDLR-relat
276 ntiplatelet therapy, blood pressure control, low-density lipoprotein reduction, and lifestyle modific
281 (standardized estimate, 0.07; P = .003), and low-density lipoprotein (standardized estimate, 0.04; P
282 links to the apolipoprotein B component of a low-density lipoprotein through a disulfide bridge to fo
284 tions were observed for extremely large very-low-density lipoprotein triglycerides (odds ratio [OR] =
285 very low-density lipoproteins-apoB and very low-density lipoproteins triglycerides or on postprandia
286 sion of SRA (scavenger receptor A), modified low-density lipoprotein uptake and foam cell formation,
287 DL), low-density lipoprotein (LDL), and very-low density lipoprotein (VLDL), play a critical role in
290 tic triglycerides (TAG) associated with very-low-density lipoprotein (VLDL) play a major role in main
291 nuation of hepatic steatosis, increased very low-density lipoprotein (VLDL) secretion, and improved g
292 prevents fructose-induced increases in very-low-density lipoprotein (VLDL) triglycerides by decreasi
293 ) for 8 weeks on the plasma kinetics of very-low-density lipoprotein (VLDL)-apolipoprotein B-100 (apo
294 d proteomic profiles implicated these 3 very-low-density lipoprotein (VLDL)-associated apolipoprotein
295 ortant for HCV cell-to-cell spread, but very-low-density lipoprotein (VLDL)-containing mouse serum di
296 erved strong positive associations with very-low-density lipoprotein (VLDL)-lipoproteins, VLDL-choles
298 in (HDL) yields 4-6% of the LDL signal, very-low-density-lipoprotein (VLDL) yields 1-3%, and human se
299 lisin/kexin type 9 (PCSK9) selectively binds low-density lipoprotein; we hypothesized that it can als
300 d the hope that additional agents that lower low-density lipoprotein will decrease risk of atheroscle
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