Literature DB >> 9612899

[Activity of renin-angiotensin-aldosterone system (RAAS) and vasopressin level in patients with primary pulmonary hypertension].

T V Martyniuk, I E Chazova, V P Masenko, V N Volkov, Iu N Belenkov.   

Abstract

AIM: Assessment of RAAS and vasopressin in patients with primary pulmonary hypertension (PPH).
MATERIALS AND METHODS: Activity of plasma renin (APR), angiotensin-converting enzyme (ACE), plasma levels of angiotensin II (AII) and vasopressin (VP), serum concentration of aldosteron (AS) were measured by radioimmunoassay and enzyme immunoassay in 21 PPH patients with circulatory failure (age 34.7 +/- 2.1 years), 11 patients with NYHA functional class II-III, 10 with class IV, and 10 control subjects (age 29.8 +/- 1.5 years).
RESULTS: Compared to controls, 21 PPH patients had elevated RAAS parameters: APR up to 3.52 ng/ml/h (p < 0.05), activity of ACE up to 43.13 units, AII level up to 33.93 ng/ml (p < 0.01), AS up to 468.86 ng/ml (p < 0.01), VP up to 5.26 ng/ml (p < 0.001). Circulatory failure progression resulted in activation of all the RAAS components. This and VP activation was the greatest in PPH patients with ACE > 5 ng/ml/h. PPH patients with mean pressure in the pulmonary artery higher than 60 mm Hg demonstrated higher ARP, AS, VP, AII, ACE than those who had this pressure under 60 mm Hg.
CONCLUSION: PPH patients display a noticeable activation of RAAS and VP. This activation seems to be secondary as the changes increase with elevation of the pressure in the pulmonary artery and aggravation of circulatory insufficiency. Plasma renin activity determines the degree of RAAS activation as a whole. The discovered activation of RAAS in PPH gives grounds for doubts in the validity of using ACE inhibitors in the treatment of PPH.

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Year:  1998        PMID: 9612899

Source DB:  PubMed          Journal:  Ter Arkh        ISSN: 0040-3660            Impact factor:   0.467


  7 in total

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Review 2.  Potential Contribution of Carotid Body-Induced Sympathetic and Renin-Angiotensin System Overflow to Pulmonary Hypertension in Intermittent Hypoxia.

Authors:  Rodrigo Iturriaga; Sebastian Castillo-Galán
Journal:  Curr Hypertens Rep       Date:  2019-10-10       Impact factor: 5.369

3.  Aldosterone inactivates the endothelin-B receptor via a cysteinyl thiol redox switch to decrease pulmonary endothelial nitric oxide levels and modulate pulmonary arterial hypertension.

Authors:  Bradley A Maron; Ying-Yi Zhang; Kevin White; Stephen Y Chan; Diane E Handy; Christopher E Mahoney; Joseph Loscalzo; Jane A Leopold
Journal:  Circulation       Date:  2012-07-11       Impact factor: 29.690

4.  Plasma aldosterone levels are elevated in patients with pulmonary arterial hypertension in the absence of left ventricular heart failure: a pilot study.

Authors:  Bradley A Maron; Alexander R Opotowsky; Michael J Landzberg; Joseph Loscalzo; Aaron B Waxman; Jane A Leopold
Journal:  Eur J Heart Fail       Date:  2012-10-30       Impact factor: 15.534

5.  Effectiveness of spironolactone plus ambrisentan for treatment of pulmonary arterial hypertension (from the [ARIES] study 1 and 2 trials).

Authors:  Bradley A Maron; Aaron B Waxman; Alexander R Opotowsky; Hunter Gillies; Christiana Blair; Reza Aghamohammadzadeh; Joseph Loscalzo; Jane A Leopold
Journal:  Am J Cardiol       Date:  2013-06-07       Impact factor: 2.778

6.  Pulmonary artery denervation: a novel treatment modality for pulmonary hypertension.

Authors:  Trixie Le; Christian Makar; Philip Morway; Nir Hoftman; Soban Umar
Journal:  J Thorac Dis       Date:  2019-04       Impact factor: 2.895

Review 7.  Autonomic nervous system involvement in pulmonary arterial hypertension.

Authors:  Mylène Vaillancourt; Pamela Chia; Shervin Sarji; Jason Nguyen; Nir Hoftman; Gregoire Ruffenach; Mansoureh Eghbali; Aman Mahajan; Soban Umar
Journal:  Respir Res       Date:  2017-12-04
  7 in total

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