1998
DOI: 10.1042/cs0940591
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How Does Treatment Influence Endocrine Mechanisms in Acute Severe Heart Failure? Effects on Cardiac Natriuretic Peptides, the Renin System, Neuropeptide Y and Catecholamines

Abstract: 1. Hormones involved in cardiovascular regulation are influenced by drug treatment. It is therefore difficult to study endocrine mechanisms in heart failure as most patients are already on treatment by the time they reach hospital. 2. We studied nine hospital in-patients before and after treatment of acute New York Heart Association class IV heart failure. 3. Before treatment, plasma brain and atrial natriuretic peptides were markedly elevated (BNP 121 +/- 26 pg/ml, ANP 163 +/- 33 pg/ml; normal range: BNP 3.9 … Show more

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Cited by 44 publications
(36 citation statements)
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“…[16][17][18][19] In contrast with other studies, they were not influenced by gender nor by the use of renin-angiotensin system blockers. [20][21][22] A limitation of the study is the small population of 103 nursing home residents, in one centre, which could lead to a selection bias in arriving at the prevalence of CHF of 23%. On the other hand, our prevalence of chronic heart failure is in line with the prevalence in other nursing home residents and in the elderly.…”
Section: Discussionmentioning
confidence: 99%
“…[16][17][18][19] In contrast with other studies, they were not influenced by gender nor by the use of renin-angiotensin system blockers. [20][21][22] A limitation of the study is the small population of 103 nursing home residents, in one centre, which could lead to a selection bias in arriving at the prevalence of CHF of 23%. On the other hand, our prevalence of chronic heart failure is in line with the prevalence in other nursing home residents and in the elderly.…”
Section: Discussionmentioning
confidence: 99%
“…Before immunization, the peptide immunogens NT-proANP [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20] , NTproBNP , NT-proBNP [5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24] , NT-proBNP 10 -29 , NTproBNP [41][42][43][44][45][46][47][48][49][50][51][52][53][54]…”
Section: Antiseraunclassified
“…The following assay buffer was used for all dilutions: 0.04 mol/L sodium hydrogen phosphate, 0.01 mol/L sodium dihydrogen phosphate, 0.1 mol/L NaCl, 1 g/L gelatin, 0.5 mL/L Triton X-100, pH 7.4. Calibrators (60 -6000 pmol/L) or plasma or serum samples were pipetted in duplicates of 25 L and incubated for 16 -24 h at 4°C with 100 L of antiserum solution (1:20 000 dilution for antiserum to NT-proANP 46 -79 and 1:40 000 dilution for antiserum to NT-proANP [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20] ) and 100 L of tracer solution containing ϳ8000 cpm of the appropriate radioiodinated peptide. Bound and free fractions were separated by precipitation with donkey anti-goat IgG (Scantibodies Laboratory, Inc., and Linco Research, Inc.) in 0.5 mL of 80 g/L polyethylene glycol 6000 containing normal goat serum as a carrier.…”
Section: Assay Proceduresmentioning
confidence: 99%
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