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Microvascular Alterations in Hypertension and Vascular Aging
- Source :
- Current hypertension reviews. 13(1)
- Publication Year :
- 2017
-
Abstract
- Hypertension and aging are characterized by vascular remodelling and stiffness as well as endothelial dysfunction. Endothelial function declines with age, since aging is associated with senescence of the endothelium due to increased rate of apoptosis and reduced regenerative capacity of the endothelium. Different phenotypes of hypertension have been described in younger and adult subjects with hypertension. In younger patients, functional and structural alterations of resistance arteries occur as the earliest vascular alterations which have prognostic significance and may contribute to stiffness of large arteries through wave reflection. In individuals above age of 50 years as well as in subjects with long-lasting elevated blood pressure, vascular changes occur predominantly in conduit arteries which become stiffer. Activation of renin-angiotensin-aldosterone and endothelin systems plays a key role in endothelial dysfunction, vascular remodelling, and aging by inducing reactive oxygen species production, and promoting inflammation and cell growth.
- Subjects :
- 0301 basic medicine
Senescence
medicine.medical_specialty
Aging
Endothelium
vascular remodelling
media-to-lumen ratio
arterial stiffness
PWV
pulse pressure
endothelial dysfunction
Inflammation
Vascular remodelling in the embryo
03 medical and health sciences
Vascular Stiffness
Internal medicine
Internal Medicine
medicine
Humans
Regeneration
Endothelial dysfunction
business.industry
Age Factors
Arteries
Middle Aged
medicine.disease
030104 developmental biology
Endocrinology
medicine.anatomical_structure
Pathophysiology of hypertension
Hypertension
Microvessels
Arterial stiffness
Vascular resistance
Vascular Resistance
Endothelium, Vascular
medicine.symptom
business
Subjects
Details
- ISSN :
- 18756506
- Volume :
- 13
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Current hypertension reviews
- Accession number :
- edsair.doi.dedup.....baa28356caf0a64c6f3f75a3e62a57c3