Affiliation:
1. Medizinische Klinik und Poliklinik IV, LMU München, Munich,
Germany
Abstract
AbstractPatients with primary aldosteronism (PA) are at increased cardiovascular
risk, compared to patients with essential hypertension (EH). Cardiovascular
damage could depend on PA phenotype, potentially being lower in milder forms
of PA. Our aim was to assess atherosclerotic burden and arterial stiffness
in 88 prospectively recruited patients, including 44 patients with mild PA
and EH respectively. All patients underwent a structured study program,
including measurements of ankle-brachial index, oscillometric measurement of
central pulse wave velocity (cPWV) and vascular ultrasound examination of
the supraaortic arteries, the abdominal aorta, and the femoropopliteal
arteries. A plaque score was calculated to estimate atherosclerotic burden
for each patient. This is a prospective case-control study set at a tertiary
care hospital. Patients with PA and EH matched well for age, gender, blood
pressure, BMI, and cardiovascular risk factors such as diabetes mellitus and
smoking status. Common carotid intima-media thickness (0.77 vs.
0.75 mm; p=0.997) and cPWV (7.2 vs. 7.1 m/s;
p=0.372) were comparable between patients with PA and EH. The
atherosclerotic burden, as expressed by the plaque score, did not differ
between the two groups (p=0.159). However, after initiation of
treatment cPWV was significantly decreased in patients with PA
(p=0.017). This study shows that subclinical atherosclerotic burden
and arterial stiffness in patients with milder forms of PA is comparable to
patients with EH. Nevertheless, specific treatment for PA significantly
improved cPWV, which argues for a more liberal use of mineralocorticoid
receptor antagonists in patients with arterial hypertension.
Funder
German Conn’s Registry-Else-Kröner Hyperaldosteronism Registry
European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme
Central Relay in Health and Disease
Clinician Scientist PRogram In Vascular MEdicine
(PRIME
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
5 articles.
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