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81. |
Endothelin and active renin levels in essential hypertension and hypertension with renal artery stenosis before and after percutaneous transluminal renal angioplasty |
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Journal of Hypertension,
Volume 15,
Issue 12,
1997,
Page 1791-1796
Kim Teunissen,
Cornelis Postma,
Brigit van Jaarsveld,
Frans Derkx,
Theo Thien,
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摘要:
ObjectiveTo determine whether active renin and endothelin levels in venous plasma differ between patients with renal artery stenosis and patients with primary hypertension. Among the patients with renal artery stenosis we also compared active renin and endothelin levels between subjects who had been cured or whose blood pressure had improved after treatment of the stenosis and those without a beneficial reaction after such treatment.MethodsWe measured immunoreactive endothelin and active renin levels in peripheral venous plasma before and 1 h after angiotensin converting enzyme inhibition in 25 patients with primary hypertension and in 27 patients with hypertension and renal artery stenosis. Percutaneous transluminal angioplasty was performed in 21 patients of the latter group. For 11 patients of this group, hypertension was cured or there was an improvement, whereas 10 other patients did not respond to this treatment. Baseline active renin and endothelin levels were compared between these groups, as were the clinical characteristics of the patients.ResultsBaseline endothelin levels were similar in members of the renal artery stenosis [median 3.6 pg/ml (range 1.4–11.7)] and in members of the no stenosis group [5.0 pg/ml (1.5–8.0)]. Also baseline endothelin levels did not differ between members of the successfully treated [3.6 pg/ml (1.8–8.9)] and unsuccessfully treated groups [3.75 pg/ml (1.4–8.3)]. Angiotensin converting enzyme (ACE) inhibition failed to cause a significant change in endothelin level in members of any of the patient groups. Although baseline renin levels differed significantly between members of the renal artery stenosis and no stenosis groups [40.2 μu/ml (0.9–543) versus 13.4 μu/ml (2.5–931), (P< 0.05)], there was no difference in baseline renin levels between the members of successful and unsuccessful groups [25.7 μu/ml (9.2–475.6) versus 65.3 μu/ml (12.3–542.6)]. ACE inhibition caused a significant increase in renin level in members of all groups except the unsuccessfully treated group.ConclusionsCirculating endothelin levels did not differ significantly among patients with essential hypertension, hypertension with renal artery stenosis and proven renovascular hypertension and, although the renin–angiotensin system was clearly activated in members of the renovascular hypertension group, ACE inhibition did not affect their endothelin levels. These results suggest that endothelin does not play a direct role in the pathophysiology of renovascular hypertension.
ISSN:0263-6352
出版商:OVID
年代:1997
数据来源: OVID
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82. |
Possible familial origin of multifocal renal artery fibromuscular dysplasia |
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Journal of Hypertension,
Volume 15,
Issue 12,
1997,
Page 1797-1801
Isabelle Pannier-Moreau,
Philippe Grimbert,
Béatrice Fiquet-Kempf,
Albert Vuagnat,
Xavier Jeunemaitre,
Pierre Corvol,
Pierre-François Plouin,
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摘要:
ObjectiveTo describe phenotypes and estimate the prevalence of familial cases of renal artery fibromuscular dysplasia (FMD).Patients and settingOne hundred and four unrelated hypertensive patients (94 women) with renal artery fibromuscular dysplasia documented on angiography and classified as having multifocal or unifocal lesions. Familial cases were defined as those with angiographic evidence of renal artery FMD in at least one sibling.ResultsEighty-one patients had multifocal and 16 had unifocal FMD. Both types of stenosis were present in seven patients. Fifty-four patients had bilateral FMD, including the seven patients with both unifocal and multifocal lesions. The 16 patients with unifocal FMD were younger, more likely to be men, and more commonly had unilateral stenoses, stenoses exceeding 75% and a small ischemic kidney than the 81 patients with multifocal lesions. Eleven cases were identified as familial on the basis of FMD having been documented in at least one sibling (eight sibling pairs and three trios). All probands were women and exhibited multifocal lesions. FMD was more often bilateral in familial than it was in apparently sporadic cases.ConclusionsMultifocal FMD was mostly found in women and unifocal FMD in young men with more severe stenosis and kidney ischemia. The documented prevalence of familial cases was 11% in this series, the true prevalence being probably higher because only a few siblings were examined by angiography. Familial cases all exhibited the multifocal type and were more commonly bilateral than were sporadic cases.
ISSN:0263-6352
出版商:OVID
年代:1997
数据来源: OVID
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83. |
The natriuretic effect of nifedipine gastrointestinal therapeutic system remains despite the presence of mild‐to‐moderate renal failure |
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Journal of Hypertension,
Volume 15,
Issue 12,
1997,
Page 1803-1808
Carlos Campo,
Olga Garcia-Vallejo,
Vivencio Barrios,
Vicente Lahera,
Montserrat Manero,
Esther Esteban,
Jose Rodicio,
Luis Ruilope,
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摘要:
BackgroundCalcium channel blockers facilitate the renal excretion of sodium and this effect is maintained during chronic administration of these drugs. However, it is unknown whether this natriuretic effect remains despite the presence of a decreased renal function.ObjectiveTo compare the natriuretic capacity of nifedipine gastrointestinal therapeutic system (GITS) and lisinopril in patients with mild-to-moderate chronic renal failure.MethodsAn open-label, randomized, comparative study was conducted to compare the natriuretic capacity of nifedipine GITS and lisinopril in the presence of mild-to-moderate renal failure (creatinine clearance 30–80 ml/min). After a wash-out period of 4 weeks an intravenous saline infusion (30 ml/kg of body weight of isotonic saline in 4 h) was performed and repeated after 4 weeks of active therapy. Two sex- and age-matched groups of hypertensive patients (n = 25) were included in the study. Renal failure was diagnosed as secondary to nephrosclerosis in all the patients.ResultsA significant increase in the renal capacity to excrete the sodium load was observed in patients receiving nifedipine GITS (n = 11) but not in those taking lisinopril (n = 13). Both drugs controlled blood pressure to a similar extent. No changes were observed in body weight, glomerular filtration rate and renal plasma flow (measured as inulin and paraaminohippurate clearances). A significant drop was observed in urinary albumin excretion after lisinopril, but not after nifedipine. Heart rate was higher in nifedipine group.ConclusionThe natriuretic capacity of nifedipine GITS remains despite the presence of mild-to-moderate chronic renal failure. Such an effect takes place in the absence of changes in renal hemodynamics, suggesting that it is caused by a direct tubular effect.
ISSN:0263-6352
出版商:OVID
年代:1997
数据来源: OVID
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84. |
Blood pressure and endocrine effects of single doses of CS‐866, a novel angiotensin II antagonist, in salt‐restricted hypertensive patients |
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Journal of Hypertension,
Volume 15,
Issue 12,
1997,
Page 1809-1812
Kurt Püchler,
Jürg Nussberger,
Petra Laeis,
Peter Witte,
Hans Brunner,
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摘要:
ObjectiveThis study was conducted to assess the dose-response relationship of the new angiotensin II (Ang II) antagonist CS-866 on blood pressure and on endocrine parameters in hypertensive patients with an activated renin–angiotensin system.DesignFollowing a four-way crossover protocol, two groups of eight patients with mild-to-moderate hypertension received a sodium-restricted diet (60 mmol daily) and ingested single doses of 2.5, 10 and 40 mg or 5, 20 and 80 mg of CS-866, respectively, or placebo. Twenty-four hour ambulatory blood pressure measurements, plasma renin activity (PRA), Ang II and concentrations of RNH-6270, the pharmacologically active metabolite of CS-866, were monitored up to 24 h after medication.ResultsCS-866 was well tolerated. There was a significant decrease in 24 h diastolic blood pressure (DBP) at all doses of CS-866 above 5 mg. Increasing doses of CS-866 from 2.5 to 10 mg and from 5 to 20 mg lowered the mean 24 h DBP and DBP AUC0-24h values considerably more than increasing doses from 10 to 40 mg and from 20 to 80 mg, respectively. The mean 24 h DBP was lowered by 6.9 and 8.4 mmHg after oral doses of 10 and 20 mg CS-866, respectively, compared with placebo and by 8.9 mmHg after 80 mg CS-866. The drug increased PRA and Ang II concentrations in plasma, maximum concentrations of which occurred within 3 h post-dose. The highest RNH-6270 concentrations were also found at the first post-dose measurement 3 h after administration of CS-866.ConclusionThe new Ang II receptor antagonist CS-866 is effective and well tolerated. In salt-restricted hypertensive patients, CS-866 lowered blood pressure and increased PRA and Ang II concentrations at low doses. A single oral dose of 10–20 mg CS-866 resulted in almost maximal effects.
ISSN:0263-6352
出版商:OVID
年代:1997
数据来源: OVID
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