Related Experiment Video
Updated: Oct 20, 2025

Calcification of Vascular Smooth Muscle Cells and Imaging of Aortic Calcification and Inflammation
Published on: May 31, 2016
Atherosclerosis and Cardiovascular Diseases in Progeroid Syndromes
Hisaya Kato1,2, Yoshiro Maezawa1,2
1Department of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine.
Insights
Hutchinson-Gilford progeria syndrome (HGPS) and Werner syndrome (WS) are rare genetic disorders that model human aging. Studying these conditions offers insights into cardiovascular disease development and potential treatments.
Area of Science:
- Gerontology
- Genetics
- Cardiovascular Medicine
Background:
- Hutchinson-Gilford progeria syndrome (HGPS) and Werner syndrome (WS) are distinct genetic progeroid syndromes.
- HGPS presents in childhood with premature aging and early death from cardiovascular disease (CVD).
- WS manifests after puberty with accelerated aging, leading to death in the 50s from CVD and cancer.
Purpose of the Study:
- To review the pathogenesis of atherosclerotic diseases in HGPS and WS.
- To discuss current and emerging treatments for these conditions.
- To leverage insights from progeroid syndromes for understanding human aging and CVD.
Main Methods:
- Review of existing literature on HGPS and WS.
- Analysis of pathogenesis mechanisms for atherosclerotic diseases in both syndromes.
- Synthesis of latest findings on treatment strategies.
Main Results:
- Both HGPS and WS serve as critical models for studying age-associated cardiovascular disease.
- Shared and distinct pathways contribute to accelerated atherosclerosis in these syndromes.
- Recent research provides novel therapeutic targets for managing CVD in progeroid conditions.
Conclusions:
- Understanding progeroid syndromes deepens our knowledge of normal human aging processes.
- Targeting specific molecular pathways in HGPS and WS may offer broader applications for CVD prevention and treatment.
- Further research into these rare diseases is crucial for advancing geriatric and cardiovascular medicine.
Abstract:
Hutchinson-Gilford progeria syndrome (HGPS) and Werner syndrome (WS) are two of the representative genetic progeroid syndromes and have been widely studied in the field of aging research. HGPS is a pediatric disease in which premature aging symptoms appear in early childhood, and death occurs at an average age of 14.5 years, mainly due to cardiovascular disease (CVD). Conversely, WS patients exhibit accelerated aging phenotypes after puberty and die in their 50s due to CVD and malignant tumors. Both diseases are models of human aging, leading to a better understanding of the aging-associated development of CVD. In this review, we discuss the pathogenesis and treatment of atherosclerotic diseases presented by both progeroid syndromes with the latest findings.
More Related Videos
09:06Quantitative Analysis of Cellular Composition in Advanced Atherosclerotic Lesions of Smooth Muscle Cell Lineage-Tracing Mice
Published on: February 20, 2019
07:36Induction of Atherosclerotic Plaques Through Activation of Mineralocorticoid Receptors in Apolipoprotein E-deficient Mice
Published on: September 26, 2018
Related Concept Videos
Atherosclerosis I: Introduction
Atherosclerosis II: Clinical Manifestations and Diagnostic Tests
Atherosclerosis III: Management
Coronary Artery Disease I: Introduction
Coronary Artery Disease II: Pathophysiology
Rheumatic Heart Disease I: Introduction