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Published on: April 8, 2013
Left Ventricular Hypertrophy: Etiology-Based Therapeutic Options
1Department of Cardiology, Memorial Ankara Hospital, Ankara, Turkey.
Insights
Left ventricular hypertrophy (LVH) presents diagnostic challenges due to varied causes and presentations. Early identification of treatable conditions like Fabry disease or cardiac amyloidosis is crucial for preventing heart failure and improving patient outcomes.
Area of Science:
- Cardiology
- Internal Medicine
- Pathophysiology
Background:
- Left ventricular hypertrophy (LVH) diagnosis is complex due to overlapping clinical and morphological features.
- LVH progression can lead to heart failure, arrhythmias, and increased mortality.
- Differentiating physiological (athletic heart) from pathological LVH is vital.
Purpose of the Study:
- To systematically review treatments for diverse patterns of cardiac hypertrophy.
- To highlight advances in managing LVH caused by specific conditions like Fabry disease, cardiac amyloidosis, and hypertrophic cardiomyopathy.
- To guide clinicians in preventing cardiovascular events and mortality associated with LVH.
Main Methods:
- Systematic review of current literature on LVH etiologies and treatments.
- Analysis of treatment impacts on outcomes for various hypertrophy patterns.
- Focus on specific conditions: Fabry disease, cardiac amyloidosis, and hypertrophic cardiomyopathy.
Main Results:
- Common LVH causes include hypertension, aortic valve stenosis, and infiltrative diseases.
- Management strategies encompass lifestyle changes, medications, surgery, and devices.
- Specific treatments for Fabry disease, amyloidosis, and hypertrophic cardiomyopathy offer improved prognoses.
Conclusions:
- Accurate diagnosis of LVH etiology is essential for effective management.
- Targeted therapies for specific causes of LVH can prevent disease progression and improve survival.
- Continued research into novel treatments is necessary for optimizing patient care.
Abstract:
Determining the etiologies of left ventricular hypertrophy (LVH) can be challenging due to the similarities of the different manifestations in clinical presentation and morphological features. Depending on the underlying cause, not only left ventricular mass but also left ventricular cavity size, or both, may increase. Patients with LVH remain asymptomatic for a few years, but disease progression will lead to the development of systolic or diastolic dysfunction and end-stage heart failure. As hypertrophied cardiac muscle disrupts normal conduction, LVH predisposes to arrhythmias. Distinguishing individuals with treatable causes of LVH is important for prevention of cardiovascular events and mortality. Athletic's heart with physiological LVH does not require treatment. Frequent causes of hypertrophy include etiologies due to pressure/volume overload, such as systemic hypertension, hypertrophic cardiomyopathy, or infiltrative cardiac processes such as amyloidosis, Fabry disease, and sarcoidosis. Hypertension and aortic valve stenosis are the most common causes of LVH. Management of LVH involves lifestyle changes, medications, surgery, and implantable devices. In this review we systematically summarize treatments for the different patterns of cardiac hypertrophy and their impacts on outcomes while informing clinicians on advances in the treatment of LVH due to Fabry disease, cardiac amyloidosis, and hypertrophic cardiomyopathy.
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