| Literature DB >> 25624340 |
Takeshi Matsumoto1, Kenji Oki1, Masato Kajikawa1, Ayumu Nakashima1, Tatsuya Maruhashi1, Yumiko Iwamoto1, Akimichi Iwamoto1, Nozomu Oda1, Takayuki Hidaka1, Yasuki Kihara1, Nobuoki Kohno1, Kazuaki Chayama1, Chikara Goto1, Yoshiki Aibara1, Kensuke Noma1, James K Liao1, Yukihito Higashi2.
Abstract
The purpose of this study was to evaluate vascular function and activity of Rho-associated kinases (ROCKs) in patients with primary aldosteronism. Vascular function, including flow-mediated vasodilation (FMD) and nitroglycerine-induced vasodilation, and ROCK activity in peripheral leukocytes were evaluated in 21 patients with aldosterone-producing adenoma (APA), 23 patients with idiopathic hyperaldosteronism (IHA), and 40 age-, sex-, and blood pressure-matched patients with essential hypertension (EHT). FMD was significantly lower in the APA group than in the IHA and EHT groups (3.2±2.0% versus 4.6±2.3% and 4.4±2.2%; P<0.05, respectively), whereas there was no significant difference in FMD between the IHA and EHT groups. There was no significant difference in nitroglycerine-induced vasodilation in the 3 groups. ROCK activity was higher in the APA group than in the IHA and EHT groups (1.29±0.57 versus 1.00±0.46 and 0.81±0.36l; P<0.05, respectively), whereas there was no significant difference in ROCK activity between the IHA and EHT groups. FMD correlated with age (r=-0.31; P<0.01), plasma aldosterone concentration (r=-0.35; P<0.01), and aldosterone:renin ratio (r=-0.34; P<0.01). ROCK activity correlated with age (r=-0.24; P=0.04), plasma aldosterone concentration (r=0.33; P<0.01), and aldosterone:renin ratio (r=0.46; P<0.01). After adrenalectomy, FMD and ROCK activity were restored in patients with APA. APA was associated with both endothelial dysfunction and increased ROCK activity compared with those in IHA and EHT. APA may have a higher risk of future cardiovascular events.Entities:
Keywords: Rho-associated kinases; aldosterone; hyperaldosteronism; hypertension
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Year: 2015 PMID: 25624340 PMCID: PMC4917381 DOI: 10.1161/HYPERTENSIONAHA.114.05001
Source DB: PubMed Journal: Hypertension ISSN: 0194-911X Impact factor: 10.190