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1. |
Evidence Supporting a Beneficial Role for Long-Term L-Arginine Supplementation in High-Risk Pregnancies |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 1-1
Alfredo Germain,
Gloria Valdés,
Mary Romanik,
M. Reyes,
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ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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2. |
Correction |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 2-2
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PDF (20KB)
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ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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3. |
C-Reactive Protein: Risk Marker or Mediator in Atherothrombosis? |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 6-11
Ishwarlal Jialal,
Sridevi Devaraj,
Senthil Venugopal,
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摘要:
Abstract—Inflammation appears to be pivotal in all phases of atherosclerosis from the fatty streak lesion to acute coronary syndromes. An important downstream marker of inflammation is C-reactive protein (CRP). Numerous studies have shown that CRP levels predict cardiovascular disease in apparently healthy individuals. This has resulted in a position statement recommending cutoff levels of CRP <1.0, 1.0 to 3.0, and >3.0 mg/L equating to low, average, and high risk for subsequent cardiovascular disease. More interestingly, much in vitro data have now emerged in support of a role for CRP in atherogenesis. To date, studies largely in endothelial cells, but also in monocyte-macrophages and vascular smooth muscle cells, support a role for CRP in atherogenesis. The proinflammatory, proatherogenic effects of CRP that have been documented in endothelial cells include the following: decreased nitric oxide and prostacyclin and increased endothelin-1, cell adhesion molecules, monocyte chemoattractant protein-1 and interleukin-8, and increased plasminogen activator inhibitor-1. In monocyte-macrophages, CRP induces tissue factor secretion, increases reactive oxygen species and proinflammatory cytokine release, promotes monocyte chemotaxis and adhesion, and increases oxidized low-density lipoprotein uptake. Also, CRP has been shown in vascular smooth muscle cells to increase inducible nitric oxide production, increase NFκb and mitogen-activated protein kinase activities, and, most importantly, upregulate angiotensin type-1 receptor resulting in increased reactive oxygen species and vascular smooth muscle cell proliferation. Future studies should be directed at delineating the molecular mechanisms for these important in vitro observations. Also, studies should be directed at confirming these findings in animal models and other systems as proof of concept. In conclusion, CRP is a risk marker for cardiovascular disease and, based on future studies, could emerge as a mediator in atherogenesis.
ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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4. |
Is There a Rationale for Angiotensin Blockade in the Management of Obesity Hypertension? |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 12-19
Arya Sharma,
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摘要:
Obesity, currently affecting >20% of the adult population in most Western countries, is a major risk factor for the development of hypertension. Hypertension in obese patients is, in the majority of instances, further complicated by the concomitant presence of dyslipidemia and insulin resistance. The latter is reflected by derangement of glucose homeostasis, ranging from hyperinsulinemia to frank type 2 diabetes. Hypertension in obese patients is also associated with an increased risk for left ventricular hypertrophy, endothelial dysfunction, renal hyperfiltration, microalbuminuria, and elevated markers of inflammation. Sodium retention, volume expansion, and increased cardiac output are common findings in obese individuals. These changes are largely attributable to increased activity of the sympathetic nervous system and insufficient suppression of the renin-angiotensin system. Recent data show increased expression of angiotensin II–forming enzymes in adipose tissue, and increased activity of the renin-angiotensin system has recently been implicated in the development of insulin resistance and type 2 diabetes. Accordingly, antihypertensive agents that block the renin-angiotensin system might be a beneficial strategy for treatment of obesity-related hypertension. Both angiotensin-converting enzyme inhibitors and angiotensin type-1 receptor blockers have been associated with favorable metabolic properties and end-organ protection in addition to their antihypertensive effects. Data from ongoing large trials will provide an indication of the protective and preventive effects of these treatment strategies while offering insights into the mechanisms linking obesity, hypertension, and other facets of the metabolic syndrome.
ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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5. |
Preventing Dementia by Treating Hypertension and Preventing Stroke |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 20-21
J. Spence,
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ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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6. |
The Dietary Sodium–Blood Pressure Plot “Stiffens” |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 22-24
Alexei Bagrov,
Edward Lakatta,
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ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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7. |
C3 or Not C3That Is the Question |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 25-26
Stephanie Watts,
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ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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8. |
A Genetic Predisposition to Hypertension? |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 27-28
David Geller,
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ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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9. |
Midlife Blood Pressure and the Risk of Hippocampal AtrophyThe Honolulu Asia Aging Study |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 29-34
Esther Korf,
Lon White,
Philip Scheltens,
Lenore Launer,
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摘要:
Hippocampal atrophy (HA) is usually attributed to the neurofibrillary tangles and neuritic plaques of Alzheimer disease. However, the hippocampus is vulnerable to global ischemia, which may lead to atrophy. We investigated the association of midlife blood pressure (BP) and late-life HA in a sample of Japanese-American men born between 1900 and 1919. BP was measured on 3 occasions between 1965 and 1971. In 1994 to 1996 a subsample underwent magnetic resonance imaging (MRI) of the brain. Hippocampal volume was estimated by manually drawing regions of interest on relevant scan slices; HA was defined as the lowest quartile of hippocampal volume. Also assessed on the MRI were cortical and subcortical infarcts, lacunes, and white matter hyperintensities. The risk (OR, 95% CI) was estimated for HA associated with systolic (<140 versus ≥140 mm Hg) and diastolic (<90 versus ≥90 mm Hg) BP and with antihypertensive treatment. Analyses were adjusted for sociodemographic factors, other cardiovascular risk factors, apolipoprotein E allele, and correlated brain pathology. Those never treated with antihypertensive medication had a significantly increased risk for HA (OR 1.7; CI=1.12; 2.65). The nontreated subjects with high systolic BP had an increased risk (OR=1.98; CI=0.89; 4.39) for HA. Results were similar for untreated men with high diastolic BP (OR=3.51; CI=1.26; 9.74). In conclusion, treatment with antihypertensive treatment modifies the association of BP and HA, such that high levels of BP adversely affect the hippocampus in persons never treated with antihypertensives.
ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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10. |
Dietary Sodium Restriction Rapidly Improves Large Elastic Artery Compliance in Older Adults With Systolic Hypertension |
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Hypertension: Journal of The American Heart Association,
Volume 44,
Issue 1,
2004,
Page 35-41
Phillip Gates,
Hirofumi Tanaka,
William Hiatt,
Douglas Seals,
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摘要:
We determined the temporal effects of dietary sodium restriction on large elastic artery compliance and systolic blood pressure (SBP) in 12 untreated, older (64±2 years) men and women (6 each) with stage 1 systolic hypertension. After baseline measurements subjects were assigned to 4 weeks of low or normal sodium intake (randomized, crossover design). Urinary sodium excretion was reduced by 60% by the end of week 1 of sodium restriction (54±11 mmol/d,P< 0.01) versus baseline (135±14). Compared with baseline (0.11±0.01 mm/mm Hg), carotid artery compliance was increased by 27% (to 0.14±0.02,P< 0.05) at the end of week 1 of sodium restriction, attaining peak levels by week 2 (+46%, to 0.16±0.02,P< 0.01). Similarly, supine resting brachial artery SBP was reduced by >5 mm Hg by week 1 of sodium restriction, attaining peak reductions by week 2 (−12 mm Hg,P< 0.01 versus baseline). The 24-hour ambulatory SBP was ≈3 mm Hg lower at week 1 of sodium restriction and ≈6 mm Hg lower by week 2 (P< 0.01 versus baseline). The reductions in resting SBP from baseline to week 2 of sodium restriction were strongly related to the corresponding increases in carotid compliance (r= 0.80,P< 0.01). Urinary sodium excretion, carotid artery compliance, and SBP were not different during normal sodium intake versus baseline. Other subject characteristics were not different across conditions. Sodium restriction rapidly improves large elastic artery compliance in older adults with stage 1 systolic hypertension. These improvements in central arterial compliance appear to be a key mechanism in the rapid normalization of SBP by sodium restriction in these patients.
ISSN:0194-911X
出版商:OVID
年代:2004
数据来源: OVID
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