LDL-oxidation, serum uric acid, kidney function and pulse-wave velocity: Data from the Brisighella Heart Study cohort

2018 ◽  
Vol 261 ◽  
pp. 204-208 ◽  
Author(s):  
Arrigo F.G. Cicero ◽  
Masanari Kuwabara ◽  
Richard Johnson ◽  
Marilisa Bove ◽  
Federica Fogacci ◽  
...  
2017 ◽  
Vol 35 ◽  
pp. e348
Author(s):  
A.F. G. Cicero ◽  
M. Bove ◽  
M. Rosticci ◽  
F. Fogacci ◽  
M. Giovannini ◽  
...  

2015 ◽  
Vol 28 (8) ◽  
pp. 966-970 ◽  
Author(s):  
Cristina Pellegrino Baena ◽  
Paulo Andrade Lotufo ◽  
José Geraldo Mill ◽  
Roberto de Sa Cunha ◽  
Isabela J Benseñor

2020 ◽  
Vol 16 (6) ◽  
pp. 931-937
Author(s):  
S. V. Nedogoda ◽  
T. N. Sanina ◽  
V. V. Tsoma ◽  
A. A. Ledyaeva ◽  
E. V. Chumachek ◽  
...  

Aim. To evaluate the single pill combination with lisinopril, amlodipine and indapamide ability in additional angioprotection achievement in patients with arterial hypertension and high pulse wave velocity (PWV) regardless on previous antihypertensive therapy (AHT).Material and methods. To the open non-randomized study duration 12 weeks 40 patients were included taking triple AHT during 6 months. All participants underwent ambulatory 24 hour blood pressure (BP) monitoring, applanation tonometry (augmentation index and central BP), pulse wave velocity assessment, laboratory tests (HbA1c, serum uric acid, high sensitive C-reactive protein [hsCRP], serum uric acid).Results. We observed additional systolic BP (SBP) and diastolic BP (DBP) reduction by 16.9% and 22.11% on lisinopril, amlodipine and indapamide single pill combination. Lisinopril, amlodipine and indapamide single pill combination decreased 24 h mean SBP by 16.77%, and 24 h mean DBP -23.5% (ABPM data), PWV by 19.7%, augmentation index by 14.81%, central SBP by 11.9% (p<0,05). There were positive changes in hsCRP level (-13.0%, p<0.05) and serum uric acid (-9.0%, p<0.05).Conclusion. Lisinopril, amlodipine and indapamide single pill combination provided control BP, arterial elastic properties improving (augmentation index, PWV, central BP) and favorable influence on inflammation and serum uric acid level.


Hypertension ◽  
2020 ◽  
Vol 76 (5) ◽  
pp. 1616-1624 ◽  
Author(s):  
Rosa Maria Bruno ◽  
Peter M. Nilsson ◽  
Gunnar Engström ◽  
Benjamin Nilsson Wadström ◽  
Jean-Philippe Empana ◽  
...  

Pulse wave velocity is an established marker of early vascular aging but may also help identifying individuals with supernormal vascular aging. We tested the hypothesis that individuals with the largest difference (Δ-age) between chronological and vascular age show the lowest rate of cardiovascular events and may thus be defined as supernormal vascular aging. Vascular age was defined as the predicted age in the best fitting multivariable regression model including classical risk factors and treatment and pulse wave velocity, in a subset of the Reference Values for Arterial Stiffness Collaboration Database (n=3347). Δ-age was then calculated as chronological age minus vascular age, and the 10th and 90th percentiles were used to define early (Δ-age<−5.7 years), normal (Δ-age −5.7 to 6.8 years) and supernormal vascular aging (Δ-age>6.8 years). The risk for fatal and nonfatal cardiovascular events associated with vascular aging categories was investigated in the Malmö Diet and Cancer Study cohort (n=2642). In the Malmö Diet and Cancer Study Cohort (6.6-year follow-up, 286 events), Δ-age was significantly ( P <0.01) and inversely associated with cardiovascular events. Compared with normal vascular aging, supernormal vascular aging had lower risk (hazard ratio, 0.59 [95% CI, 0.41–0.85]), whereas early vascular aging had higher risk (hazard ratio, 2.70 [95% CI, 1.55–4.70]) of cardiovascular events, in particular coronary events. There was no significant association with all-cause mortality. This study represents the first validation of the clinical significance of the supernormal vascular aging concept, based on prospective data. Its further characterization may help discovering novel protective molecular pathways and providing preventive strategies for successful vascular aging.


2019 ◽  
Vol 32 (6) ◽  
pp. 547-556 ◽  
Author(s):  
Changwei Li ◽  
Jiang He ◽  
Shengxu Li ◽  
Wei Chen ◽  
Lydia Bazzano ◽  
...  

2008 ◽  
Vol 27 (6) ◽  
pp. 1382-1387 ◽  
Author(s):  
Samuel W. Fielden ◽  
Brandon K. Fornwalt ◽  
Michael Jerosch-Herold ◽  
Robert L. Eisner ◽  
Arthur E. Stillman ◽  
...  

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