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1 , high levels of triglycerides and decreased high-density lipoprotein).
2 the anti-atherogenic functions attributed to high density lipoprotein.
3 poprotein A-I (ApoA-I), a major component of high-density lipoprotein.
4 in duplicate for glucose, triglyceride, and high-density lipoprotein.
5 result of compensatory increases in ApoE on high-density lipoprotein.
6 nd APOE, respectively) and the generation of high density lipoproteins.
7 form lipid-protein particles reminiscent of high-density lipoproteins.
8 ome to control body mass, triglycerides, and high-density lipoproteins.
9 nd low-density lipoproteins whereas increase high-density lipoproteins.
10 teolysis and misfolding by binding to plasma high-density lipoproteins.
11 n, very-low-density lipoprotein (VLDL), LDL, high-density lipoprotein].
12 cholesterol efflux to apolipoprotein A-I and high-density lipoprotein-3 were qualitatively and quanti
13 des (84 versus 77 mg/dL, P = 0.01) and lower high-density lipoprotein (46 versus 60 mg/dL, P = 0.004)
14 ycerides (-53.7 +/- 116.4 mg/dL, P < 0.001), high-density lipoprotein (8.2 +/- 12.9 mg/dL, P < 0.001)
15 tly associated with higher concentrations of high-density lipoprotein (9%) and sex-hormone binding gl
17 n under shear stress can be modulated by the high-density lipoprotein and apolipoprotein A-I (HDL/Apo
18 ce, triglycerides, type-2 diabetes mellitus, high-density lipoprotein and low-density lipoprotein cho
20 17 coincided with a significant QTL for HDL (high-density lipoprotein) and a suggestive QTL for non-H
21 ts and increase in hsCRP, total cholesterol, high-density lipoprotein, and low-density lipoprotein le
22 n E levels were also measured in serum, LDL, high-density lipoprotein, and red blood cell membranes a
23 ure, triglycerides, low-density lipoprotein, high-density lipoprotein, and total cholesterol were not
24 Total cholesterol, low-density lipoprotein, high-density lipoprotein, and triglyceride levels all si
25 C-reactive protein, low-density lipoprotein, high-density lipoprotein, and triglyceride single-nucleo
26 , low-density lipoprotein (LDL) cholesterol, high-density lipoprotein, and triglycerides], lipoprotei
27 ) low-density lipoprotein oxidizability, (2) high-density lipoprotein antioxidant/anti-inflammatory c
28 tion to previously reported triglyceride and high-density lipoprotein associations, the variant was a
29 xed to glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) on
31 (Apo)A-I, the major lipid-binding protein of high-density lipoprotein, can prevent autoimmunity and s
32 triglycerides, but was associated with lower high density lipoprotein cholesterol (-0.014 standard de
34 nterestingly, significantly higher levels of high density lipoprotein cholesterol (HDLc) were observe
35 enzymatic activity and a 35% increase of the high density lipoprotein cholesterol that was observed u
36 een duration of moderate hyperlipidemia (non-high-density lipoprotein cholesterol >/= 160 mg/dL) in e
38 events and control of 6 RFs (no smoking, non-high-density lipoprotein cholesterol <130 mg/dl, triglyc
39 lesterol (1.6 [1.1-2.1]), and borderline low high-density lipoprotein cholesterol (1.4 [1.0-1.8]) rem
40 lipoprotein cholesterol (27.9 to 60.0%), non-high-density lipoprotein cholesterol (10.0 to 36.6%), ap
41 statistically significantly increased serum high-density lipoprotein cholesterol (13 trials; net cha
42 showed nominal significant association with high-density lipoprotein cholesterol (2 SNPs), low-densi
43 e saw a small increase in rate of change for high-density lipoprotein cholesterol (beta = 0.28 mg/dL;
44 associated in opposite directions with both high-density lipoprotein cholesterol (beta coefficient=-
45 carriers, carriers of PTV at CETP had higher high-density lipoprotein cholesterol (effect size, 22.6
46 s of total cholesterol (TC) (>/= 200 mg/dL), high-density lipoprotein cholesterol (HDL-C) (<40 mg/dL)
47 rs have been shown to substantially increase high-density lipoprotein cholesterol (HDL-C) and apolipo
48 Although the inverse association between high-density lipoprotein cholesterol (HDL-C) and risk of
49 y artery disease (CAD), but the relevance of high-density lipoprotein cholesterol (HDL-C) and triglyc
52 LDL-c from 155 to 128 mg/dL (P < .001), and high-density lipoprotein cholesterol (HDL-c) from 50.3 t
53 ational epidemiologic studies, higher plasma high-density lipoprotein cholesterol (HDL-C) has been as
54 cause of ischemic stroke, and a low level of high-density lipoprotein cholesterol (HDL-C) is also con
55 diet only), red wine significantly increased high-density lipoprotein cholesterol (HDL-C) level by 0.
56 ubfamily A, member 1 (ABCA1) and circulating high-density lipoprotein cholesterol (HDL-C) levels in v
57 -density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C) were either
59 ol levels, including total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-densit
64 vels of TRAP, was positively associated with high-density lipoprotein cholesterol (HDL-C; beta = 8.36
65 ated locus associated with triglycerides and high-density lipoprotein cholesterol (HDL-C; cg27243685;
67 lesterol (decreased in LFHC group only), and high-density lipoprotein cholesterol (increased in VHFLC
68 cholesterol (LDL-C), triglycerides, and non-high-density lipoprotein cholesterol (non-HDL-C) present
69 t also LDL-related biomarkers, including non-high-density lipoprotein cholesterol (non-HDL-C), apolip
71 ith >/= 5 births had the highest odds of low high-density lipoprotein cholesterol (OR, 1.5; 95% confi
72 lipoprotein cholesterol, and HbA1c and lower high-density lipoprotein cholesterol (P < 0.001 for all)
73 sedentary time was associated with decreased high-density lipoprotein cholesterol (P=0.04), and incre
74 and years of schooling (rG=0.18, s.e.=0.03), high-density lipoprotein cholesterol (rG=0.28, s.e.=0.05
75 CI, 1.11-1.94]), an elevated serum level of high-density lipoprotein cholesterol (RR per 1-SD increa
77 notypes: V(G)/V(p)=31.4%, P<3.1x10(-11)) and high-density lipoprotein cholesterol (V(G)/V(p)=26.4%, P
78 low-density lipoprotein cholesterol [LDL-C], high-density lipoprotein cholesterol [HDL-C], and trigly
79 asting lipid fractions (triglycerides [TGs], high-density lipoprotein cholesterol [HDL-C], low-densit
80 ed for LDL-C were observed with achieved non-high-density lipoprotein cholesterol and apolipoprotein
81 t association was found for higher levels of high-density lipoprotein cholesterol and decreased preva
82 adjusted models, women had higher levels of high-density lipoprotein cholesterol and high-density li
83 cational attainment, exercise, levels of non-high-density lipoprotein cholesterol and high-sensitivit
84 e MetS components and CA, except for reduced high-density lipoprotein cholesterol and nonfasting gluc
85 oprotein cholesterol, and ratios of total to high-density lipoprotein cholesterol and triglycerides t
86 terol; lipoprotein(a), apolipoprotein B, and high-density lipoprotein cholesterol are largely unaffec
87 for other cardiac risk factors including non-high-density lipoprotein cholesterol at 55 years of age
89 re, body mass index, apolipoprotein A-1, and high-density lipoprotein cholesterol concentration (beta
90 ted fasting blood glucose concentration, low high-density lipoprotein cholesterol concentration, hype
91 rapy, body mass index, heart rate, total and high-density lipoprotein cholesterol concentrations, smo
92 pectroscopy and a validated ex vivo assay of high-density lipoprotein cholesterol efflux capacity.
95 exposure to even moderate elevations in non-high-density lipoprotein cholesterol have elevated risk
96 ansaminase, white blood cell count and lower high-density lipoprotein cholesterol in men, and with hi
97 ), triglyceride level (-40%, -29%, and -8%), high-density lipoprotein cholesterol level (32%, 30%, an
98 f at least 70 mg/dL or a final screening non-high-density lipoprotein cholesterol level of at least 1
99 physical activity, total cholesterol level, high-density lipoprotein cholesterol level, systolic blo
102 ice lacking T39 (T39(-/-)) display increased high-density lipoprotein cholesterol levels associated w
103 iglyceride levels greater than 204 mg/dL and high-density lipoprotein cholesterol levels less than 34
104 s were also more likely to smoke, have lower high-density lipoprotein cholesterol levels, and have hi
105 rglycemia, elevated triglyceride levels, low high-density lipoprotein cholesterol levels, high blood
106 s in total, low-density lipoprotein, and non-high-density lipoprotein cholesterol levels, in triglyce
107 ompared with controls, despite no changes in high-density lipoprotein cholesterol or other circulatin
108 leukin-10 remained persistently elevated and high-density lipoprotein cholesterol persistently depres
109 h ARIC metabolic phenotypes, including total:high-density lipoprotein cholesterol ratio (rG=-0.44, P=
110 vents, digoxin use, and total cholesterol to high-density lipoprotein cholesterol ratio were associat
111 ded risk factors were body mass index, total:high-density lipoprotein cholesterol ratio, and systolic
113 gene, TEAD2, is found to be associated with high-density lipoprotein cholesterol through gene-based
114 than in WT mice (2.6 versus 0.4 mmol/L), and high-density lipoprotein cholesterol was significantly l
116 lipoprotein cholesterol and triglycerides to high-density lipoprotein cholesterol were calculated.
117 of higher systolic blood pressure and lower high-density lipoprotein cholesterol with Carotid artery
118 nce, blood pressure, triglycerides, glucose, high-density lipoprotein cholesterol) at 15 (n=512), 16
119 7 (low-density lipoprotein cholesterol), 8 (high-density lipoprotein cholesterol), 14 (triglycerides
120 epatitis A), biochemical (e.g., carotenoids, high-density lipoprotein cholesterol), physiological (e.
121 largely explained by lowering of non-HDL-C (high-density lipoprotein cholesterol), rather than incre
123 rol, 109.23 mg/dL (103.68-114.79 mg/dL); for high-density lipoprotein cholesterol, 42.80 mg/dL (39.84
124 erol, 71 single-nucleotide polymorphisms for high-density lipoprotein cholesterol, and 40 single-nucl
125 olesterol, the ratio of total cholesterol to high-density lipoprotein cholesterol, and 8-OHdG levels.
126 e relationship between additional LDL-C, non-high-density lipoprotein cholesterol, and apolipoprotein
127 r age, sex, hypertension, smoking, diabetes, high-density lipoprotein cholesterol, and body mass inde
128 c biomarkers, including glycated hemoglobin, high-density lipoprotein cholesterol, and C-reactive pro
129 diastolic blood pressure, total cholesterol, high-density lipoprotein cholesterol, and glucose levels
130 lic abnormalities (high fasting glucose, low high-density lipoprotein cholesterol, and high triglycer
131 Low-density lipoprotein cholesterol, non-high-density lipoprotein cholesterol, and ratios of tota
132 ia, neuroticism, educational attainment, and high-density lipoprotein cholesterol, and significant ne
135 were also observed in total cholesterol, non-high-density lipoprotein cholesterol, apolipoprotein B,
136 ding hypertension, hypertriglyceridemia, low high-density lipoprotein cholesterol, central obesity, a
137 -regression for various covariates including high-density lipoprotein cholesterol, each 1 unit of nat
138 ssure, ratio of fasting total cholesterol to high-density lipoprotein cholesterol, estimated glomerul
139 abolic biomarkers (diastolic blood pressure, high-density lipoprotein cholesterol, fasting and 2-hour
140 dominal obesity, elevated triglycerides, low high-density lipoprotein cholesterol, high blood pressur
141 ent for low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, lipoprotein(a), tr
143 ture mapping analysis for total cholesterol, high-density lipoprotein cholesterol, low-density lipopr
144 e-mapping analysis that were associated with high-density lipoprotein cholesterol, low-density lipopr
145 -wide DNA methylation and blood lipid levels high-density lipoprotein cholesterol, low-density lipopr
146 rs, carriers of PTV at CETP displayed higher high-density lipoprotein cholesterol, lower low-density
147 ences were found for fasting plasma glucose, high-density lipoprotein cholesterol, or triglycerides w
148 s such as waist circumference, triglyceride, high-density lipoprotein cholesterol, systolic and diast
149 and fasting blood sample (total cholesterol, high-density lipoprotein cholesterol, triglycerides, glu
150 actors: low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, typ
151 rable objective biomarkers (concentration of high-density lipoprotein cholesterol, vitamin D and C-re
160 ity lipoprotein cholesterol; lower levels of high-density lipoprotein cholesterol; and, to a lesser e
161 or remnant cholesterol, and -8 mg/dl for non-high-density lipoprotein cholesterol; lipoprotein(a), ap
162 s of total, low-density lipoprotein, and non-high-density lipoprotein cholesterol; lower levels of hi
163 ntly associated with total cholesterol (TC), high-density-lipoprotein cholesterol (HDL-C), low-densit
164 d alcohol and was positively associated with high-density-lipoprotein cholesterol and intakes of poly
165 lin resistance), serum-triglyceride-to-serum-high-density lipoprotein-cholesterol ratio TG/HDL-C, or
166 sterol, low-density lipoprotein-cholesterol, high-density lipoprotein-cholesterol, or triglyceride, 4
167 ypes of MDD with changes of fasting glucose, high-density lipoprotein-cholesterol, triglycerides, sys
168 tion between CCR2 and CX3CR1 expressions and high-density lipoprotein-cholesterol, whereas CCR5 expre
171 ciated with very low-density lipoprotein and high-density lipoprotein composition measures, other cho
172 .30 and 0.14, respectively; both p < 0.001), high-density lipoprotein (correlation coefficient 0.16 a
173 We validate our method using a real mouse high-density lipoprotein data (HDL) and show that CAVIAR
174 (-/-)) show decreased fatty liver, increased high-density lipoprotein, decreased low-density lipoprot
175 es mellitus, serum potassium, serum albumin, high-density lipoprotein, estimated glomerular filtratio
176 )particles to indicate their relationship to high-density lipoproteins formed by human apolipoprotein
178 omain protein 39B (Ttc39b, C9orf52) (T39), a high-density lipoprotein gene discovered in human genome
179 resistance, insulin, hemoglobin A1c, and low high-density lipoprotein had significant shared gene eff
180 resistance, insulin, hemoglobin A1c, and low high-density lipoprotein had significant shared gene eff
182 ed from the circulation and transferred from high density lipoprotein (HDL) - a main carrier of chole
183 ups and assessed for total cholesterol (TC), high density lipoprotein (HDL) and low density lipoprote
184 body fat -0.00516 (95% CI -0.00761--0.0027), high density lipoprotein (HDL) cholesterol 0.00179 (95%
187 all to the liver) is terminated by selective high density lipoprotein (HDL)-cholesteryl ester (CE) up
189 s designed for the analysis of lipoproteins, high density lipoproteins (HDL), apoproteins, and lipid
190 and function of the potent anti-inflammatory high-density lipoprotein (HDL) and accelerated atheroscl
191 A1 (apoA1) is the major protein component of high-density lipoprotein (HDL) and has well documented a
193 1, is a lipoprotein receptor that binds both high-density lipoprotein (HDL) and low-density lipoprote
196 ng of apolipoprotein A-I (apoA1) and nascent high-density lipoprotein (HDL) assembly is not well unde
197 6, 0.154; P = 0.007) and the ratio of TGs to high-density lipoprotein (HDL) cholesterol (beta = 2.689
198 eceptor BI (SR-BI) is the major receptor for high-density lipoprotein (HDL) cholesterol (HDL-C).
199 = 16.4 mg/dL, 95% CI: 11.2, 21.5), and lower high-density lipoprotein (HDL) cholesterol (MD = -2.1 mg
200 tein B were higher after VA than after iTFA; high-density lipoprotein (HDL) cholesterol and apolipopr
202 observing associations between low levels of high-density lipoprotein (HDL) cholesterol and cardiovas
204 l attainment, openness to new experience and high-density lipoprotein (HDL) cholesterol levels are mo
207 known to have effects on serum levels of non-high-density lipoprotein (HDL) cholesterol that alter th
208 iglycerides were 13% lower and the levels of high-density lipoprotein (HDL) cholesterol were 7% highe
209 rease in total, low-density lipoprotein, and high-density lipoprotein (HDL) cholesterol, but not in t
210 d body mass index (BMI), C-reactive protein, high-density lipoprotein (HDL) cholesterol, forced expir
211 e cardiometabolic risk-factor profile [lower high-density lipoprotein (HDL) cholesterol, higher total
212 ed circulating lipid profiles, in particular high-density lipoprotein (HDL) cholesterol, in overweigh
213 fasting glucose, insulin, total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density
214 ns of abnormal values for total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density
215 f low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, or triglycer
216 the median (n = 83) was older and had lower high-density lipoprotein (HDL) cholesterol, phospholipid
217 s such as waist circumference, triglyceride, high-density lipoprotein (HDL) cholesterol, systolic and
218 , low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triacylglyce
219 mass index (BMI), waist circumference (WC), high-density lipoprotein (HDL) cholesterol, triglyceride
222 ents whether obesity-induced endothelial and high-density lipoprotein (HDL) dysfunction is rapidly im
228 othesis that cholesterol efflux capacity and high-density lipoprotein (HDL) particle concentration pr
229 P is bound to apolipoprotein M (ApoM) in the high-density lipoprotein (HDL) particle, the immunologic
234 that functions as a physiologically relevant high-density lipoprotein (HDL) receptor whose primary ro
235 Twenty-four hours post-MI measurements of high-density lipoprotein (HDL) triglycerides (HDL-TG) pr
236 line (PBS) without significant interference: high-density lipoprotein (HDL) yields 4-6% of the LDL si
237 ified AH is 4%-23% in eQTLs, 35% in GWASs of high-density lipoprotein (HDL), and 23% in GWASs of schi
238 rides, and strong negative associations with high-density lipoprotein (HDL), HDL-diameter, HDL-C, HDL
239 ared with the SSGWAS for blood lipid traits (high-density lipoprotein (HDL), low-density lipoprotein
242 r HCV entry) and also blocks SR-BI-dependent high-density lipoprotein (HDL)-mediated enhancement of v
243 LPS binding protein, competitively inhibits high-density lipoprotein (HDL)-mediated LPS association
247 to cholesterol, promoting the maturation of high-density lipoproteins (HDL) from discoidal to spheri
250 gosine-1-phosphate (S1P) is a constituent of high-density lipoproteins (HDL) that contributes to thei
251 holesterol esters (CE) from atheroprotective high-density lipoproteins (HDL) to atherogenic low-densi
254 justed follow-up blood lipid concentrations (high-density lipoprotein [HDL] and low-density lipoprote
255 cholesterol, low-density lipoprotein [LDL], high-density lipoprotein [HDL], and triglycerides [TGs])
256 eins including brain (apoE) and circulating (high-density lipoprotein, HDL) synergize to facilitate A
259 h a genetic variant previously correlated to high-density lipoprotein in a human genome-wide associat
261 lectrochemical responses of purified low and high density lipoproteins (LDL and HDL, respectively) we
262 predicting height, body mass index (BMI) and high-density lipoprotein level (HDL) in two data cohorts
263 ounder population sequences: chr16:70790626 (high-density lipoprotein levels beta -1.71 (SE 0.25), P=
265 either prevalent CVD or CVD risk factors and high-density lipoprotein levels less than 50 mg/dL (<55
266 glyceride, very low-density lipoprotein, and high-density lipoprotein levels, as well as risk of coro
267 ating adiponectin was associated with higher high-density lipoprotein lipids and lower very-low-densi
268 trong inverse associations were observed for high-density lipoprotein measures, e.g., high-density li
269 tein A-I (apoA-I) has been shown to increase high-density lipoprotein-mediated cholesterol efflux cap
272 oriasis (OR, 3.90; 95% CI, 1.57-9.66); lower high-density lipoprotein (OR, 0.99; 95% CI, 0.98-0.99);
273 of high-density lipoprotein cholesterol and high-density lipoprotein particle concentration, leptin,
274 logical samples, with a special focus on non-high-density-lipoprotein particle concentrations (non-HD
276 s (72.4 vs. 64.6; P = 0.02), decreased large high-density lipoprotein particles (5.3 vs. 6.7; P < 0.0
278 hway as well as the extracellular matrix and high-density lipoprotein pathways in the aetiology of AM
280 ved as danger signals; efflux cholesterol to high-density lipoprotein; proliferate and migrate; under
281 g/dL; 95% CI: 0.9, 9.7 mg/dL) and the LDL to high-density lipoprotein ratio (5 trials; net change: 0.
282 tatus; alcohol intake; SBP; DBP; cholesterol:high-density lipoprotein ratio; diabetes; body mass inde
283 er receptors BI (SR-BI) and BII (SR-BII) are high-density lipoprotein receptors that recognize variou
285 otein cholesterol ratio (rG=-0.44, P=0.005), high-density lipoprotein (rG=-0.48, P=0.005), systolic b
286 we describe the development of reconstituted high-density lipoprotein (rHDL)-facilitated TAM PET imag
287 ree clinically relevant nanomedicines, i.e., high-density lipoprotein ([S]-HDL), polymeric micelles (
288 eptide nanoparticles that mimic native human high density lipoproteins significantly increases peptid
289 for high-density lipoprotein measures, e.g., high-density lipoprotein size (OR = 0.36, 0.30-0.42) and
290 tal (standardized estimate, 0.06; P = .050), high-density lipoprotein (standardized estimate, 0.07; P
291 ipoprotein subclasses, with the exception of high-density lipoprotein subclasses, which displayed a m
293 density lipoprotein/low-density lipoprotein, high-density lipoprotein, triglycerides, cytokines or bi
294 D and at least 1 of low-density lipoprotein, high-density lipoprotein, triglycerides, type 2 diabetes
295 ir association with low-density lipoprotein, high-density lipoprotein, triglycerides, type 2 diabetes
296 ng the gut microbiome explained </= 25.9% of high-density lipoprotein variance, significantly outperf
297 her (95% confidence interval, 1.71-2.97) and high-density lipoprotein was 1.62 mg/dL lower (95% confi
298 micelles, and nanocrystal-core reconstituted high-density lipoproteins, we have shown the approach's
300 rary's nanoparticles are based on endogenous high-density lipoprotein, which can preferentially deliv
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