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The prognostic legacy of left ventricular hypertrophy: cumulative evidence after the MAVI study
Fabio Angeli1, Gianpaolo Reboldi, Cristina Poltronieri
1aDepartment of Cardiology and Cardiovascular Pathophysiology, Hospital 'S.M. della Misericordia' bDepartment of Medicine, University of Perugia, Perugia cDepartment of Medicine, Hospital of Assisi, Assisi, Italy.
Insights
Cardiovascular risk remains elevated even after left ventricular hypertrophy (LVH) regression. Preventing LVH development is crucial for better patient outcomes and reduced cardiovascular events.
Area of Science:
- Cardiology
- Hypertension Research
- Echocardiography
Background:
- Left ventricular hypertrophy (LVH) regression offers prognostic benefits.
- However, the comparative cardiovascular risk in patients with regressed LVH versus those with persistently normal left ventricular mass is not well-established.
Purpose of the Study:
- To determine if cardiovascular risk in patients with regressed LVH is comparable to those who never developed LVH.
- To investigate the prognostic implications of different left ventricular mass phenotypes.
Main Methods:
- Analysis of the prospective 'Massa Ventricolare sinistra nell'Ipertensione' (MAVI) study.
- Serial echocardiographic measurements of left ventricular mass and association with cardiovascular events.
- Cumulative meta-analysis of MAVI and six comparable studies (2954 patients).
Main Results:
- Persistence or new development of LVH increased cardiovascular event risk (OR 1.96).
- LVH regression was associated with a 56% higher risk of cardiovascular events compared to persistently normal mass (OR 1.56).
- Evidence for adverse outcomes with persistent LVH remained consistent.
Conclusions:
- Cardiovascular risk is significantly higher in patients experiencing LVH regression compared to those with persistently normal left ventricular mass.
- Preventing the development of LVH is a critical therapeutic target.
Objective:
Although regression of left ventricular hypertrophy (LVH) confers a marked prognostic benefit, it is unknown whether cardiovascular risk in these patients is comparable to those who never developed LVH.
Methods:
We analyzed the 'Massa Ventricolare sinistra nell'Ipertensione' (MAVI) study, a prospective study in which serial changes in left ventricular mass at echocardiography were associated with subsequent cardiovascular events. We also conducted a cumulative meta-analysis in order to investigate how evidence progressed in this field. We defined three phenotypes: persistently normal left ventricular mass; LVH regression; persistence/new development of LVH.
Results:
Left ventricular mass was measured at baseline and 2 years after the initial assessment in 374 patients (64% women). Clinical outcomes were ascertained after the 2-year echocardiographic evaluation (mean follow-up 3.2 years). Persistence or new development of LVH was associated with an increased risk of cardiovascular events (odds ratio 1.96, 95% confidence interval 1.07-3.57, P = 0.029). In a cumulative meta-analyses that included MAVI and six comparable studies for a total of 2954 patients and 339 cardiovascular events, when a persistently normal left ventricular mass was taken as reference, regression of LVH was associated with 56% higher risk of cardiovascular events (odds ratio 1.56, 95% confidence interval 1.04-2.36, absolute risk increase 3%, P = 0.033). Conversely, evidence accrued from previous studies that persistence or new development of LVH predicts an adverse outcome did not change after MAVI.
Conclusions:
Cardiovascular risk is higher in patients with LVH regression than in those with persistently normal left ventricular mass. Preventing development of LVH is thus an important target.
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