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Relationship between kidney function, hemodynamic variables and circulating big endothelin levels in patients with severe refractory heart failure
Thomas Kos, Richard Pacher, Andreas Wimmer, Anda Bojic, Martin Hulsmann, Behnhard Frey, Gerd Mayer, Nylgrin Yilmaz, Lea Skvarilova, Jindrich Spinar, Jiri Vitovec, Jiri Toman, Wolfgang Woloszcuk, Brigitte Stanek
Jazyk angličtina Země Rakousko
Grantová podpora
IZ4298
MZ0
CEP - Centrální evidence projektů
PubMed
9553203
Knihovny.cz E-zdroje
- MeSH
- cévní rezistence fyziologie MeSH
- endotelin-1 MeSH
- endoteliny * krev MeSH
- funkce levé komory srdeční fyziologie MeSH
- funkce pravé komory srdeční fyziologie MeSH
- hemodynamika * fyziologie MeSH
- hodnoty glomerulární filtrace fyziologie MeSH
- ischemie patofyziologie MeSH
- ledviny krevní zásobení MeSH
- lidé středního věku MeSH
- lidé MeSH
- plicní oběh fyziologie MeSH
- plicní tlak v zaklínění fyziologie MeSH
- proteinové prekurzory * krev MeSH
- renální insuficience * patofyziologie MeSH
- srdeční selhání * patofyziologie MeSH
- vodní a elektrolytová rovnováha fyziologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
UNLABELLED: Fluid retention is a major characteristic of symptomatic, progressive heart failure when a main factor implicated in the pathogenesis of renal dysfunction is renal hypoperfusion. This may be a consequence of forward cardiac failure, resulting in a low cardiac output integrating poor left ventricular function secondary to myocardial impairment and increased resistance in the regional renal vasculature secondary to locally released vasoconstrictors, e.g. endothelin. So far, the role of the pulmonary circulation in perpetuating renal dysfunction in heart failure is unclear. METHODS: We investigated the relationship of hemodynamic variables obtained during right heart catheterization and plasma big endothelin levels to renal function variables in 18 male patients aged 52 +/- 3 years, with heart failure in the NYHA function class III-IV, based on idiopathic causes in 8 and ischemic causes in 10 patients. Renal plasma flow (RPF) was established by paraaminohippurate (PAH) clearance and the glomerular filtration rate (GFR) was measured by iothalamate clearance. RESULTS: Plasma big endothelin (ET) levels were increased above the upper normal range (1.8 fmol/ml) in 16 out of 18 patients, averaging 5.0 +/- 0.8 fmol/ml (1.7-11.9 fmol/ml). Positive correlations to big ET plasma levels were detected with mean pulmonary pressure (r = 0.73, p < 0.001) pulmonary capillary wedge pressure (r = 0.56, p < 0.05) and pulmonary vascular resistance index (r = 0.69, p < 0.01). Glomerular filtration rate (70 +/- 7 ml/min) and renal plasma flow (358 +/- 36 ml/min) were considerably reduced and exhibited a tendency to correlate inversely with big ET levels (r = -0.46, p = 0.056 and r = -0.44, p = 0.069, respectively). Contrary to expectations, RPF did not correlate significantly with cardiac index, systemic vascular resistance index or arterial blood pressure. In contrast, significant correlations were detected of RPF with pulmonary capillary wedge pressure (r = -0.69, p < 0.01), mean pulmonary artery pressure (r = -0.65, p < 0.01), right atrial pressure (r = -0.47, p < 0.05) and right ventricular ejection fraction (r = 0.49, p < 0.05). CONCLUSION: The findings suggest a role for endothelin in renal vasoconstriction and accord well with the concept that in severe heart failure renal hypoperfusion--by volume retention--as well as increased endothelin synthesis--by pulmonary vasoconstriction--play a part in the increased pulmonary filling pressures.
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- $a Kos, Thomas $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
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- $a Relationship between kidney function, hemodynamic variables and circulating big endothelin levels in patients with severe refractory heart failure / $c Thomas Kos, Richard Pacher, Andreas Wimmer, Anda Bojic, Martin Hulsmann, Behnhard Frey, Gerd Mayer, Nylgrin Yilmaz, Lea Skvarilova, Jindrich Spinar, Jiri Vitovec, Jiri Toman, Wolfgang Woloszcuk, Brigitte Stanek
- 520 9_
- $a UNLABELLED: Fluid retention is a major characteristic of symptomatic, progressive heart failure when a main factor implicated in the pathogenesis of renal dysfunction is renal hypoperfusion. This may be a consequence of forward cardiac failure, resulting in a low cardiac output integrating poor left ventricular function secondary to myocardial impairment and increased resistance in the regional renal vasculature secondary to locally released vasoconstrictors, e.g. endothelin. So far, the role of the pulmonary circulation in perpetuating renal dysfunction in heart failure is unclear. METHODS: We investigated the relationship of hemodynamic variables obtained during right heart catheterization and plasma big endothelin levels to renal function variables in 18 male patients aged 52 +/- 3 years, with heart failure in the NYHA function class III-IV, based on idiopathic causes in 8 and ischemic causes in 10 patients. Renal plasma flow (RPF) was established by paraaminohippurate (PAH) clearance and the glomerular filtration rate (GFR) was measured by iothalamate clearance. RESULTS: Plasma big endothelin (ET) levels were increased above the upper normal range (1.8 fmol/ml) in 16 out of 18 patients, averaging 5.0 +/- 0.8 fmol/ml (1.7-11.9 fmol/ml). Positive correlations to big ET plasma levels were detected with mean pulmonary pressure (r = 0.73, p < 0.001) pulmonary capillary wedge pressure (r = 0.56, p < 0.05) and pulmonary vascular resistance index (r = 0.69, p < 0.01). Glomerular filtration rate (70 +/- 7 ml/min) and renal plasma flow (358 +/- 36 ml/min) were considerably reduced and exhibited a tendency to correlate inversely with big ET levels (r = -0.46, p = 0.056 and r = -0.44, p = 0.069, respectively). Contrary to expectations, RPF did not correlate significantly with cardiac index, systemic vascular resistance index or arterial blood pressure. In contrast, significant correlations were detected of RPF with pulmonary capillary wedge pressure (r = -0.69, p < 0.01), mean pulmonary artery pressure (r = -0.65, p < 0.01), right atrial pressure (r = -0.47, p < 0.05) and right ventricular ejection fraction (r = 0.49, p < 0.05). CONCLUSION: The findings suggest a role for endothelin in renal vasoconstriction and accord well with the concept that in severe heart failure renal hypoperfusion--by volume retention--as well as increased endothelin synthesis--by pulmonary vasoconstriction--play a part in the increased pulmonary filling pressures.
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- $a Pacher, Richard $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
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- $a Wimmer, Andreas $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
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- $a Bojic, Anda $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
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- $a Hulsmann, Martin $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
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- $a Frey, Bernhard $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
- 700 1_
- $a Mayer, Gerd $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
- 700 1_
- $a Yilmaz, Nylgrin $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
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- $a Skvarilova, Lea $u Department of Internal Medicineand Cardioangiology, University of Brno, Czech Republic
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- $a Spinar, Jindrich $u Department of Internal Medicineand Cardioangiology, University of Brno, Czech Republic
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- $a Vitovec, Jiri $u Department of Internal Medicineand Cardioangiology, University of Brno, Czech Republic
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- $a Toman, Jiri $u Department of Internal Medicineand Cardioangiology, University of Brno, Czech Republic
- 700 1_
- $a Woloszcuk, Wolfgang $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
- 700 1_
- $a Stanek, Brigitte $u Department of Cardiology and Nephrology and LB1 for Experimental Endocrinology, University of Vienna, Austria
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- $t Wiener Klinische Wochenschrift $x 0043-5325 $g Roč. 110, č. 3 (1998), s. 89-95 $p Wien Klin Wochenschr $w MED00010762
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