scholarly journals Is ambulatory arterial stiffness index a marker of large-artery stiffness? Evidence from intervention studies

2015 ◽  
Vol 38 (12) ◽  
pp. 799-801 ◽  
Author(s):  
Giuseppe Schillaci ◽  
Giacomo Pucci
2022 ◽  
pp. 174749302110664
Author(s):  
Weishi Liu ◽  
Luyang Zhang ◽  
Yuan Gao ◽  
Kai Liu ◽  
Yanan Li ◽  
...  

Background: Arterial stiffness index (ASI) is a potential risk factor for cerebrovascular and cardiometabolic diseases, but the causal links between them are inconclusive. The aim is to evaluate the causal effects of ASI on cerebrovascular and cardiometabolic diseases by Mendelian randomization (MR). Methods: Two-sample MR analysis was performed to infer causal links. Genetic variants significantly associated with ASI were extracted. The inverse variance weighted method was used for estimating the effects. Sensitivity analysis was performed to test heterogeneity or pleiotropy. Results: MR analysis indicated an effect of genetically predicted ASI on the risk of ischemic stroke (IS) of all causes (OR = 1.894, 95% CI 1.210–2.965, p = 0.005). No links were identified between genetically predicted ASI and other cerebrovascular or cardiometabolic diseases (all p > 0.05). Subgroup analysis of IS etiologies found a suggestive association between genetically predicted ASI and large artery atherosclerosis stroke (LAS) (OR = 3.726, 95% CI 1.230–11.286, p = 0.020). There were no effects of ASI on IS due to cardioembolism or small vessel occlusion. Conclusion: The current MR analysis suggested that genetically predicted ASI was associated with higher risk of IS of all causes. The results and the underlying pathways or mechanisms between ASI and IS needs further investigation.


2018 ◽  
Vol 36 (Supplement 1) ◽  
pp. e179
Author(s):  
A. Merezhanova ◽  
E. Tarlovskaya ◽  
K. Mazalov ◽  
M. Mazalova ◽  
N. Kamardina ◽  
...  

2006 ◽  
Vol 24 (11) ◽  
pp. 2247-2253 ◽  
Author(s):  
Tine W Hansen ◽  
Jan A Staessen ◽  
Christian Torp-Pedersen ◽  
Susanne Rasmussen ◽  
Yan Li ◽  
...  

2008 ◽  
Vol 26 (6) ◽  
pp. 1268-1269 ◽  
Author(s):  
Benjamin Gavish ◽  
Iddo Z Ben-Dov ◽  
Michael Bursztyn

Hypertension ◽  
2007 ◽  
Vol 49 (5) ◽  
pp. 986-991 ◽  
Author(s):  
Giuseppe Schillaci ◽  
Gianfranco Parati ◽  
Matteo Pirro ◽  
Giacomo Pucci ◽  
Massimo R. Mannarino ◽  
...  

2018 ◽  
Vol 36 (7) ◽  
pp. 1604-1605 ◽  
Author(s):  
Thomas Okon ◽  
Karl Fengler ◽  
Karl-Philipp Rommel ◽  
Philipp Lurz

2017 ◽  
Vol 64 (4) ◽  
pp. 279-283
Author(s):  
Alexandru Minca ◽  
◽  
Mihai Comsa ◽  
Maria Mirabela Manea ◽  
Maria Daniela Tanasescu ◽  
...  

Chronic kidney disease (CKD) affects approximately two million people (in a population of 20 million) in Romania. Hypertension is often associated with CKD and both (hypertension and CKD) are risk factors for cardiovascular (CV) events. Ambulatory blood pressure monitoring (ABPM) is increasingly used all around the world for the diagnosis and monitoring of BP (blood pressure) because it is proven that the ABPM is superior to office BP measurements in evaluating patients with hypertension, with or without CKD. Reduced nocturnal BP fall (non-dipping or reverse-dipping patterns) is associated with target organ damage, especially kidney disease and the proportion of non-dippers and reverse-dippers patients increases progressively with the reduction of glomerular filtration rate (GFR). Another ABPM parameter, ambulatory arterial stiffness index (AASI), is an index which was recently proposed for the evaluation of arterial stiffness (a better tool than PP). It has prognostic value for cardiac death and stroke and several studies have showed that is negatively related to eGFR and is positively related to albuminuria. Hyperbaric area index (HBI) might be considered a novel sensitive marker [independent of patterns of NBPC (nocturnal BP change)] for the reduction of kidney function. These facts suggest that ABPM offers multiple useful data with impact, not only in future CV and renal outcomes assessment, but also in the treatment and management of hypertensive patients with CKD.


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