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1 confidence interval, 1.05-1.85 per decade of hyperlipidemia).
2 y complications (diabetes, hypertension, and hyperlipidemia).
3 c abnormalities (diabetes, hypertension, and hyperlipidemia).
4 abetes mellitus, ischaemic heart disease and hyperlipidemia.
5 ght constitute a novel approach for treating hyperlipidemia.
6 in increased hepatic de novo lipogenesis and hyperlipidemia.
7 lerate thrombosis in mice in the settings of hyperlipidemia.
8 or the treatment of hypercholesterolemia and hyperlipidemia.
9      HE is not significantly associated with hyperlipidemia.
10 osis, and atherosclerosis in the settings of hyperlipidemia.
11 patients with chronic periodontitis (CP) and hyperlipidemia.
12 rowth of breast cancer using mouse models of hyperlipidemia.
13 ecreased atherosclerotic plaque formation in hyperlipidemia.
14  1.64; 95% CI, 1.02-2.68) but not obesity or hyperlipidemia.
15 ditions, such as diabetes, hypertension, and hyperlipidemia.
16 cluding hyperglycemia, hyperinsulinemia, and hyperlipidemia.
17 tolerance, weight gain, hepatosteatosis, and hyperlipidemia.
18  Zealand White (NZW) rabbits on diet-induced hyperlipidemia.
19  animal models of acute and high-fat-induced hyperlipidemia.
20 tor class B type 1 may account for alcoholic hyperlipidemia.
21 CCD36 and accelerated thrombosis observed in hyperlipidemia.
22 M2 patients and patients with statin-treated hyperlipidemia.
23 tes control and remission, hypertension, and hyperlipidemia.
24 ses the polyol pathway, AGEs production, and hyperlipidemia.
25 optosis of vascular smooth muscle cells, and hyperlipidemia.
26 n type 9 (PCSK9) has been developed to treat hyperlipidemia.
27 s a chronic inflammatory disease promoted by hyperlipidemia.
28 (n = 121), ascertained for familial combined hyperlipidemia.
29 egarding periodontal status of patients with hyperlipidemia.
30 thus a promising target for the treatment of hyperlipidemia.
31 velopment of obesity, insulin resistance and hyperlipidemia.
32 de transfer protein (MTP), can contribute to hyperlipidemia.
33  loss (38% versus 26%) after the reversal of hyperlipidemia.
34  syndrome with proteinuria, weight gain, and hyperlipidemia.
35 s were found for patients without history of hyperlipidemia.
36 D) for 28 weeks, resulting in steatosis with hyperlipidemia.
37 th that of brain CD36 to stroke pathology in hyperlipidemia.
38  were found for duration of hypertension and hyperlipidemia.
39 sened metrics of diabetes, hypertension, and hyperlipidemia.
40 olic disorders such as obesity, diabetes and hyperlipidemia.
41 ed thrombosis specifically in the setting of hyperlipidemia.
42 ies that have been extensively used to treat hyperlipidemia.
43 emia, kidney donor risk index, and recipient hyperlipidemia.
44 valent HRP prevalence as older patients with hyperlipidemia.
45 f lipid droplets in hepatocytes and systemic hyperlipidemia.
46 on of remnant lipoproteins, and postprandial hyperlipidemia.
47 responding lipid levels and risk of incident hyperlipidemia.
48 isk factors for lipids increase and incident hyperlipidemia.
49 s of treatment of hypertension (0-2 points), hyperlipidemia (0-2 points), and atrial fibrillation (0-
50 r hypertension, 0.97 (95% CI: 0.88-1.08) for hyperlipidemia, 1.01 (95% CI: 0.89-1.15) for diabetes me
51 .6%]; hypertension, 3.2% [CI, 2.2% to 4.2%]; hyperlipidemia, 1.5% [CI, 0.6% to 2.5%]).
52 smoking, diabetes mellitus, hypertension, or hyperlipidemia), 1036 subjects had 1 to 2 RF, and 1253 h
53 hotic; hazard ratio=1.63, 95% CI=0.98-2.70), hyperlipidemia (12.9% for clozapine vs. 8.5% for standar
54            We also found high prevalences of hyperlipidemia (24.5%), hypertension (21.9%), and gastro
55 ion (31.4%, 39.3%, and 76.2%, respectively), hyperlipidemia (29.2%, 22.1%, and 49.6%), and endocrine
56              Of the 524 109 individuals with hyperlipidemia, 316 182 (60%) had >/=1 outpatient prescr
57 this cross-sectional study, 94 patients with hyperlipidemia (50 receiving statins and 44 receiving no
58 , hypertension (47.1% vs 45.4%; P = .73), or hyperlipidemia (52.3% vs 63.4%; P = .45).
59 ange, 53-71], 87% men, 85% hypertension, 51% hyperlipidemia, 56% smokers).
60 y, was less than 10%, with the exceptions of hyperlipidemia (6.1% vs 11.2%), hypertension (9.8% vs 18
61 rted rates of medication discontinuation for hyperlipidemia (60.7% vs 43.2%, P < .001), diabetes (ins
62 the most prevalent risk factor for NAION was hyperlipidemia (62.9%); for diabetic patients, NAION ris
63 an 90% of patients; agreement was lowest for hyperlipidemia (68%; kappa = 0.36) and arthritis (66%; k
64 pe 2 diabetes (22.51%; 95% CI: 17.92-27.89), hyperlipidemia (69.16%; 95% CI: 49.91-83.46%), hypertens
65  hypertension; 5) coronary heart disease; 6) hyperlipidemia; 7) alcohol abuse; 8) tobacco use disorde
66  risk factors included hypertension (83.3%), hyperlipidemia (83.3%), and small cup-to-disc ratio (63.
67  levels and displayed prolonged postprandial hyperlipidemia accompanied by increased granulocyte numb
68                  We stratified patients with hyperlipidemia according to the risk categories outlined
69 zin-induced diabetic mice, hyperglycemia and hyperlipidemia acted reciprocally, accentuating renal in
70 d liver accumulation of glycogen and develop hyperlipidemia, adiposity as well as insulin resistance
71 e inhibited lesion formation and ameliorated hyperlipidemia after vascular injury and during atherosc
72 drome components (diabetes mellitus [DM] and hyperlipidemia; aHR, 1.44; CI, 1.12-1.84; P = 0.005) had
73 her with previous reports demonstrating that hyperlipidemia also impairs lung innate defense, these r
74 e younger and female but less likely to have hyperlipidemia, although other cardiovascular risk facto
75 ins) are widely prescribed for patients with hyperlipidemia and are generally well tolerated.
76                  It is highly upregulated in hyperlipidemia and atherosclerosis in a CX3CR1-independe
77 expression of microRNA-30c (miR-30c) reduced hyperlipidemia and atherosclerosis in mice without causi
78 ther a miR-30c mimic can be used to mitigate hyperlipidemia and atherosclerosis without inducing stea
79  prevents the development of hyperglycaemia, hyperlipidemia and atherosclerosis.
80 of hepatic miR-30c by anti-miR-30c increased hyperlipidemia and atherosclerosis.
81 ge- and sex-matched groups: 18 patients with hyperlipidemia and CP (HLp), 18 periodontally healthy pa
82 itions such as coronary heart disease (CHD), hyperlipidemia and diabetes mellitus (DM).
83 besity-associated metabolic disorders (e.g., hyperlipidemia and diabetes) and periodontitis has been
84 ic Ces1/Ces1g in Apoe (-/-) mice resulted in hyperlipidemia and exacerbated Western diet-induced athe
85 to have diabetes mellitus, hypertension, and hyperlipidemia and have higher discharge blood pressures
86 ked HFD-induced obesity, insulin resistance, hyperlipidemia and hepatic steatosis.
87 diovascular risk but with a low frequency of hyperlipidemia and high intake of n-3 (omega-3) fatty ac
88 been associated with metabolic toxicities of hyperlipidemia and hyperglycemia.
89 ies such as fatty liver, insulin resistance, hyperlipidemia and hyperinsulinemia.
90 estimated national control of hyperglycemia, hyperlipidemia and hypertension (especially for young me
91 bid cardiovascular disease risk factors like hyperlipidemia and hypertension in low- and middle-incom
92  with diabetes had controlled hyperglycemia, hyperlipidemia and hypertension, respectively.
93   In this respect, although obesity promotes hyperlipidemia and hypothalamic injury, MC4R agonists ar
94      His medical history was significant for hyperlipidemia and hypothyroidism.
95 ed atherosclerosis through the generation of hyperlipidemia and increased adiposity.
96 ry-low density lipoproteins), which leads to hyperlipidemia and increased fat deposition in periphera
97         Increased lipogenesis, together with hyperlipidemia and increased fat deposition, contribute
98 peroxidation, accumulating in circulation in hyperlipidemia and inducing platelet activation by promo
99  muscle insulin resistance in aging promotes hyperlipidemia and NAFLD by altering the pattern of post
100 rapeutic strategies, especially for treating hyperlipidemia and obesity, and other drugs are in devel
101 s IL-6 expression, is upregulated by LPS and hyperlipidemia and patients with familial hypercholester
102 harmful oxidative status in association with hyperlipidemia and periodontitis.
103 reas the available therapy primarily targets hyperlipidemia and prevention of thrombosis.
104 cells might serve as a possible link between hyperlipidemia and psoriasis.
105 ly hypermethylated in Mvarphis isolated from hyperlipidemia and T2DM ischemic muscles compared with c
106 lammatory, proangiogenic M2-Mvarphi genes in hyperlipidemia and T2DM ischemic muscles.
107 nflammatory and proangiogenic M2-Mvarphis in hyperlipidemia and T2DM ischemic muscles.
108                  Compared with the controls, hyperlipidemia and T2DM mice showed impaired perfusion r
109 s the periodontal status among patients with hyperlipidemia and users of statins.
110 g miR-30c levels might be useful in treating hyperlipidemias and associated disorders.
111 pathways linking diet-induced changes (e.g., hyperlipidemia) and the ensuing inflammation have remain
112 , hypertension, metabolic syndrome, smoking, hyperlipidemia, and a sedentary lifestyle are the major
113  and selected effects on glucose regulation, hyperlipidemia, and adipose pathology; but may not be as
114 a (PLA2g2a) is associated with inflammation, hyperlipidemia, and atherogenesis.
115 nd leader in the field of diabetes, obesity, hyperlipidemia, and atherosclerosis.
116 nd leader in the field of diabetes, obesity, hyperlipidemia, and atherosclerosis.
117                          Insulin resistance, hyperlipidemia, and cardiovascular complications are com
118 r risk factors, including diabetes mellitus, hyperlipidemia, and cigarette smoking to cases.
119 rior to conception caused maternal and fetal hyperlipidemia, and consequently larger fetuses.
120 , geographic region, hypertension, diabetes, hyperlipidemia, and coronary heart disease, the hazard r
121 28% to 31% of US patients with hypertension, hyperlipidemia, and diabetes, may be improved by electro
122  barrier and is associated with proteinuria, hyperlipidemia, and edema.
123 mice develop severe lipodystrophy, diabetes, hyperlipidemia, and fatty liver disease within the first
124 ate lipogenesis, resulting in hyperglycemia, hyperlipidemia, and hepatic steatosis.
125                                    Diabetes, hyperlipidemia, and hypertension are modifiable risk fac
126 e achieved through modification of diabetes, hyperlipidemia, and hypertension by summarizing current
127 de advanced age, smoking, diabetes mellitus, hyperlipidemia, and hypertension.
128  carcinoma, comorbidity index, hypertension, hyperlipidemia, and obesity by Cox's proportional hazard
129                      Diabetes, hypertension, hyperlipidemia, and obesity were all found to be risk fa
130 Charlson comorbidity scores, history of CVA, hyperlipidemia, and other cerebrovascular diseases.
131 rs (such as smoking, diabetes, hypertension, hyperlipidemia, and overweight) and encouraging healthy
132 bidity present among hypertension, diabetes, hyperlipidemia, and smoking (OR, 2.13, 95% CI, 1.51-2.99
133                   Increased duration of ART, hyperlipidemia, and smoking contributed to proximal RCA
134 emographics, cohort, hypertension, diabetes, hyperlipidemia, and tobacco use, risk differences compar
135 etermine whether simvastatin consumption and hyperlipidemia are associated with a worse periodontal c
136          Oxidative stress, inflammation, and hyperlipidemia are common factors involved in the pathop
137 ive to the general population, patients with hyperlipidemia are more prone to periodontal disease.
138 ane biophysical changes due to infection and hyperlipidemia are one of the key mechanisms by which C.
139                                        Serum hyperlipidemias are common human diseases that could be
140 ls were determined to be sensitive to plasma hyperlipidemia, as evidenced by its approximately 3-fold
141 tory of smoking, hypertension, diabetes, and hyperlipidemia, as well as personal and family history o
142 on of miR-155-5p expression in beta-cells by hyperlipidemia-associated endotoxemia improves the adapt
143           In this study, we demonstrate that hyperlipidemia-associated endotoxemia upregulates miR-15
144 mine the role of CD1-autoreactive T cells in hyperlipidemia-associated inflammatory diseases.
145 rotein (MTP) inhibitors is limited to severe hyperlipidemias because of associated hepatosteatosis an
146 hronic diseases (diabetes, hypertension, and hyperlipidemia) between 2011 and 2013.
147 hronic diseases (diabetes, hypertension, and hyperlipidemia) between 2011 and 2013.
148 ase for diagnoses of NIDDM, hypertension, or hyperlipidemia; body mass index (BMI); lipid profile; an
149 ession was induced in response to injury and hyperlipidemia but was absent at later time points, and
150                        She had no history of hyperlipidemia, but multiple blood samples were grossly
151                                              Hyperlipidemia, but not hyperglycemia, led to increased
152 ertension, cardiac conditions, diabetes, and hyperlipidemia, but not with whether patients had receiv
153 R-24 promotes hepatic lipid accumulation and hyperlipidemia by repressing Insig1, and suggest the use
154 nd the prothrombotic state in the setting of hyperlipidemia by sensing a wide range of endogenous lip
155 /- 6 [standard deviation]) with asymptomatic hyperlipidemia by using a 320-detector row scanner (Aqui
156 s the role of cafeteria diet-induced obesity/hyperlipidemia (CAF) on alveolar bone loss (ABL) in rats
157 ups: control, periodontitis (PERIO), obesity/hyperlipidemia (CAF), and obesity/hyperlipidemia plus pe
158 ss proteinuria, hypoalbuminaemia, edema, and hyperlipidemia, can be clinically divided into steroid-s
159 mmation of presence/absence of hypertension, hyperlipidemia, cardiac arrhythmias, coronary artery dis
160 e diabetes [prediabetes or type 2 diabetes], hyperlipidemia, cardiovascular events, and chronic kidne
161                                          For hyperlipidemia (cholesterol <200 mg/dL, high-density lip
162 ble analyses adjusting for Elixhauser index, hyperlipidemia, confounding drugs, and surgery type, odd
163         Obesity, diabetes, hypertension, and hyperlipidemia constitute risk factors for morbidity and
164  contributes to the development of diabetes, hyperlipidemia, coronary artery disease, and cancer.
165               Among patients with history of hyperlipidemia, countries in the highest tertile of gros
166 pendent of age, sex, diabetes, hypertension, hyperlipidemia, current smoking, left anterior descendin
167 tory included prostate cancer, hypertension, hyperlipidemia, deep-vein thrombosis, and stroke.
168     Resident participation; hypertension and hyperlipidemia detection, treatment, and control; smokin
169  lipid deposition to accentuate diet-induced hyperlipidemia, diabetes, and obesity.
170 therapy, including measures of hypertension, hyperlipidemia, diabetes, bone disease, and hematologic
171 nd stroke mortality, including hypertension, hyperlipidemia, diabetes, coronary heart disease, and ce
172        At baseline, women had lower rates of hyperlipidemia, diabetes, smoking, and renal disease but
173              Many young adults with moderate hyperlipidemia do not meet statin treatment criteria und
174 increases hepatic triglyceride synthesis and hyperlipidemia due to increased fatty acid esterificatio
175  failure, diabetes, asthma, hypertension, or hyperlipidemia) during the first six years of the study.
176 tients with psoriasis (n=105), patients with hyperlipidemia eligible for statin therapy under Nationa
177                                              Hyperlipidemia exacerbates ischemic stroke outcome and i
178              Elderly patients and those with hyperlipidemia experienced fewer typical symptoms than t
179 icantly elevated among adults with prolonged hyperlipidemia exposure by 55 years of age: 4.4% for tho
180 eridemias are diagnosed as familial combined hyperlipidemia (FCHL) and primary isolated hypertriglyce
181 rs (PPARs), has been generally used to treat hyperlipidemia for decades.
182                                              Hyperlipidemia found in CnAbeta(-/-) mice is, in part, d
183 es (hypertension, sleep apnea, diabetes, and hyperlipidemia), functional status, and patient satisfac
184 ions for 6 chronic conditions (hypertension, hyperlipidemia, gastroesophageal reflux disease, thyroid
185 ween 8-OHdG and MDA was also observed in the hyperlipidemia group.
186 tributed to lipid levels change and incident hyperlipidemia &gt;8.1-year follow-up among 6428 individual
187 ascular health, specifically the presence of hyperlipidemia, had a significant direct impact on ERC-t
188  we reveal that each rexinoid, which induced hyperlipidemia, had methyl groups that interacted with h
189                                              Hyperlipidemia has been extensively studied in the conte
190 ls with diabetes mellitus, hypertension, and hyperlipidemia have difficulty achieving control of all
191 ith better long-term %WL, while preoperative hyperlipidemia, higher body mass index, and older age we
192 HLp), 18 periodontally healthy patients with hyperlipidemia (HLh), 19 systemically healthy individual
193  the most common drugs for old patients with hyperlipidemia, hypercholesterolemia and atherosclerotic
194  diets, male LDLR(-/-) mice develop obesity, hyperlipidemia, hyperglycemia, and arteriosclerotic calc
195                Nod2 (-/-) HFD mice developed hyperlipidemia, hyperglycemia, glucose intolerance, incr
196 5 and HR = 2.70, 95% CI 1.81-4.03), although hyperlipidemia, hypertension, and COPD did not.
197 6-2011 evaluated MU in relation to diabetes, hyperlipidemia, hypertension, chronic obstructive pulmon
198 tory seem to be risk factors for MU, but not hyperlipidemia, hypertension, or COPD.
199 .5 g/24 h along with hypoalbuminemia, edema, hyperlipidemia (hypertriglyceridemia and hypercholestero
200  in the liver leads to hepatic steatosis and hyperlipidemia in animals under prolonged fasting.
201 I) guidelines on screening and management of hyperlipidemia in children and to discuss the critics co
202 anced perspective for screening and managing hyperlipidemia in children.
203 (-/-) dams developed glucose intolerance and hyperlipidemia in late pregnancy.
204   The molecular link between proteinuria and hyperlipidemia in nephrotic syndrome is not known.
205 ased use of medications for hypertension and hyperlipidemia in patients with no gap coverage and gene
206 y identify the influence of hyperglycemia or hyperlipidemia in producing specific cellular changes, s
207  but only the 7-methyl-9cUAB30 caused severe hyperlipidemia in rats.
208    Hepatic overexpression of miR-30c reduced hyperlipidemia in Western diet-fed mice by decreasing li
209 t association between cumulative exposure to hyperlipidemia in young adulthood and subsequent CHD ris
210                       Cumulative exposure to hyperlipidemia in young adulthood increases the subseque
211 ted metabolic dysregulation characterized by hyperlipidemia, increased adiposity, and insulin resista
212                           Atherosclerosis, a hyperlipidemia-induced chronic inflammatory process of t
213  inhibitors led to a significant decrease in hyperlipidemia-induced IL-1beta and IL-18 production, lo
214 lar diseases, presumably via amelioration of hyperlipidemia-induced monocytosis, and can be augmented
215 ased serum cholesterol levels and subsequent hyperlipidemia-induced monocytosis.
216                  Such diets lead to obesity, hyperlipidemia, insulin resistance, and steatosis that m
217                                              Hyperlipidemia is a major risk factor for cardiovascular
218                   Atherosclerosis, for which hyperlipidemia is a major risk factor, is the leading ca
219                                              Hyperlipidemia is a risk factor for various cardiovascul
220                                              Hyperlipidemia is frequent in DM2 patients, but the trea
221 systemic inflammatory state of patients with hyperlipidemia is indicated by their increased erythrocy
222 f miR-155-5p in the islet stress response to hyperlipidemia is unclear.
223 aired in diabetes and suggests that treating hyperlipidemia is vital for proper cardiac signaling and
224            Elevated plasma lipid content, or hyperlipidemia, is a significant risk factor for cardiov
225  history of hypertension, diabetes mellitus, hyperlipidemia, ischemic heart disease, stroke, total ch
226 ulin and adiponectin, severe lipoatrophy and hyperlipidemia lead to lethality.
227 gement of comorbidities such as diabetes and hyperlipidemia may help to limit late vascular complicat
228                            Among obesity and hyperlipidemia measures no factors were related to perio
229  This review describes mechanisms underlying hyperlipidemia-mediated neutrophilia and how neutrophils
230 score, inherited aortopathies, hypertension, hyperlipidemia, medications, aortic regurgitation, and r
231                                  Obesity and hyperlipidemia modulate the host response to challenges
232 groups: 1) simvastatin-treated patients with hyperlipidemia (n = 29); 2) patients with hyperlipidemia
233 g antihypertensive medications), and 60% had hyperlipidemia, nearly half of whom were receiving lipid
234 the association between duration of moderate hyperlipidemia (non-high-density lipoprotein cholesterol
235 etabolic diseases including atherosclerosis, hyperlipidemia, obesity, and diabetes.
236 o lower lipid absorption in order to control hyperlipidemia, obesity, metabolic syndrome, steatosis,
237 es, including sex, statin use, hypertension, hyperlipidemia, obesity, self-reported race, smoking, an
238  cells in the human body under conditions of hyperlipidemia/obesity, OA-treated cells gain or reduce
239 duce lipoprotein particles, exacerbating the hyperlipidemia of fasting and postprandial states.
240                                 Preoperative hyperlipidemia, older age, and higher body mass index we
241 DM2 patients and controls with patients with hyperlipidemia on statin therapy.
242  of VI, obesity, hypertension, diabetes, and hyperlipidemia on the EQ-5D index score using linear reg
243 nt improvement in the prediction of incident hyperlipidemia on top of traditional risk factors includ
244 ion (P = .023), hypertension (P = .021), and hyperlipidemia or obesity (P = .0004) were more common i
245 sis showed diabetes mellitus (P = .0001) and hyperlipidemia or obesity (P = .0142) were more common i
246 ues from donors either with diabetes or with hyperlipidemia or obesity reduced the failure rate from
247 donors either with diabetes mellitus or with hyperlipidemia or obesity reduced the failure rate.
248 especially with longer disease duration) and hyperlipidemia or obesity were associated with higher fa
249 4.0% +/- 3.4%) with no significant impact of hyperlipidemia or smoking.
250 0; 95% confidence interval [CI], 1.28-5.27), hyperlipidemia (OR, 3.42; 95% CI, 1.55-7.56), and curren
251             Obesity (odds ratio [OR]: 2.13), hyperlipidemia (OR, 4.13), hypertension (OR, 3.67), high
252 nd CVD risk factors (diabetes, hypertension, hyperlipidemia) or subclinical CVD measures (coronary ar
253 a known diagnosis of hypertension, diabetes, hyperlipidemia, or CVD.
254 y in adults without known CVD, hypertension, hyperlipidemia, or diabetes.
255 x, education level, oral hygiene habits, and hyperlipidemia (P = 0.049).
256 demia than in the diet-treated patients with hyperlipidemia (P = 0.05).
257 nificant strongest associations for incident hyperlipidemia (P range from 1.20x10(-3) to 4.67x10(-16)
258 at lower traditional risk than patients with hyperlipidemia, patients with psoriasis had increased NC
259 ), obesity/hyperlipidemia (CAF), and obesity/hyperlipidemia plus periodontitis (CAF+PERIO).
260                  New data suggest that diet, hyperlipidemia, pollutants, commensal microbes, and path
261 coronary artery disease, diabetes type 2 and hyperlipidemia presented with no symptoms of mitral valv
262 coronary artery disease, diabetes type 2 and hyperlipidemia presented with vertigo, headaches, mainly
263  models of atherosclerosis, normalization of hyperlipidemia promotes macrophage emigration and regres
264 be two novel immunodeficient mouse models of hyperlipidemia (Rag1(-/)(-)/LDLR(-/)(-) and Rag1(-/)(-)/
265 exhibited apparent phenotypes of obesity and hyperlipidemia regardless of exposure to casein injectio
266 reases over time and the incidence of future hyperlipidemia remains largely unknown.
267 pertension, coronary heart disease, obesity, hyperlipidemia, renal disease, hypothyroidism, and the n
268                The approach to management of hyperlipidemia should take two forms.
269 ients, the simvastatin-treated patients with hyperlipidemia showed a mean reduction of 0.8 mm (95% co
270                  The presence of obesity and hyperlipidemia significantly increased ABL in the CAF+PE
271 s (obesity, diabetes mellitus, hypertension, hyperlipidemia, smoking) with >/=1 risk factors in 58% o
272 users (n = 1,272; 33.9%) had higher rates of hyperlipidemia, smoking, a history of percutaneous coron
273 ents' glycated hemoglobin A1c, hypertension, hyperlipidemia, smoking, and renal impairment.
274 ion exists that controls for factors such as hyperlipidemia, smoking, medication, and disease stage,
275 glucagon and T3 actions synergize to correct hyperlipidemia, steatohepatitis, atherosclerosis, glucos
276       This study demonstrates that oxLDL and hyperlipidemia stimulate the generation of NOX2-derived
277  a mouse model of combined hyperglycemia and hyperlipidemia (streptozotocin-induced diabetic apolipop
278 ensates for the antiproliferative effects of hyperlipidemia, such that atherosclerosis was exacerbate
279 her in the simvastatin-treated patients with hyperlipidemia than in the diet-treated patients with hy
280 was higher in the diet-treated patients with hyperlipidemia than in the normolipidemic controls (P =
281  including diuretics, blood lead levels, and hyperlipidemia, the odds ratios of gout and hyperuricemi
282 nate immunity in endothelium synergizes with hyperlipidemia to cause topographical distribution of at
283 the activated form of SREBP2 synergized with hyperlipidemia to increase atherosclerosis in the athero
284 groups, including populations without marked hyperlipidemia (total cholesterol level <200 mg/dL); abs
285 th hyperlipidemia (n = 29); 2) patients with hyperlipidemia treated by diet alone (n = 28); and 3) no
286 may provide a novel strategy for obesity and hyperlipidemia treatment.
287 creening of persons with a family history of hyperlipidemia vs. general screening) in younger adults.
288 tory of diabetes mellitus, hypertension, and hyperlipidemia was associated with greater intima-media
289                     Midlife hypertension and hyperlipidemia were associated with 29% (prevalence rati
290 lacks only, whereas midlife hypertension and hyperlipidemia were associated with late-life ICAD in bo
291  triglyceride transfer activity might reduce hyperlipidemia while protecting liver from excess lipid
292                             Individuals with hyperlipidemia who took statins continuously for 2 years
293 I were significantly higher in patients with hyperlipidemia who were non-statin users compared with t
294 lowering trials enrolling 4300 patients with hyperlipidemia who were randomly assigned to receive 150
295                             However, whereas hyperlipidemia will enhance renal immune complex-mediate
296 s for devising novel strategies to attenuate hyperlipidemia, with the potential for cardiovascular di
297 nonalcoholic fatty liver disease (NAFLD) and hyperlipidemia, with their associated risks of endstage
298 n patients with coronary artery diseases and hyperlipidemia without effect on LDL level.
299                        In mice, induction of hyperlipidemia worsened diaphragmatic oxidative stress d
300  Overall, 85% of young adults with prolonged hyperlipidemia would not have been recommended for stati

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