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Prognostic Relevance of Gene-Environment Interactions in Patients With Dilated Cardiomyopathy: Applying the MOGE(S)
Mark R Hazebroek1, Suzanne Moors1, Robert Dennert1
1Department of Cardiology, Maastricht University Medical Centre, Maastricht, the Netherlands.
Insights
The MOGE(S) classification effectively stratifies dilated cardiomyopathy (DCM) patients. Multiple MOGE(S) attributes indicate a higher risk of adverse outcomes, guiding personalized treatment strategies.
Area of Science:
- Cardiology
- Genetics
- Pathophysiology
Background:
- Dilated cardiomyopathy (DCM) presents complex multifactorial pathogenesis, hindering patient stratification.
- The MOGE(S) (morphofunctional, organ involvement, genetic or familial, etiology, stage) classification offers a structured approach to DCM assessment.
Purpose of the Study:
- To evaluate the clinical applicability of the MOGE(S) classification in DCM patients.
- To determine the prognostic relevance of the MOGE(S) classification in predicting outcomes for DCM patients.
Main Methods:
- Utilized data from the Maastricht Cardiomyopathy Registry, excluding specific heart disease types.
- Conducted comprehensive diagnostic work-up, including genetic evaluation and endomyocardial biopsy.
- Included 213 consecutive DCM patients in the analysis.
Main Results:
- Organ involvement (16%) and genetic/familial DCM (33%) were identified. A cause was found in 73% of patients, with 23% having multiple etiologies.
- Left ventricular reverse remodeling was more frequent in non-genetic/non-familial DCM.
- Higher MOGE(S) attribute counts (≥2) and organ involvement predicted adverse outcomes (p=0.007 and p<0.001, respectively). Gene-environment interactions also correlated with worse prognosis (p=0.03).
Conclusions:
- The MOGE(S) classification is applicable and prognostic in DCM.
- Each MOGE(S) attribute and gene-environment interactions are linked to patient outcomes.
- The presence of multiple MOGE(S) attributes strongly predicts adverse outcomes, supporting classification adaptation for multiple etiologies.
Background:
The multifactorial pathogenesis leading to dilated cardiomyopathy (DCM) makes stratification difficult. The recent MOGE(S) (morphofunctional, organ involvement, genetic or familial, etiology, stage) classification addresses this issue.
Objectives:
The purpose of this study was to investigate the applicability and prognostic relevance of the MOGE(S) classification in patients with DCM.
Methods:
This study used patients from the Maastricht Cardiomyopathy Registry in the Netherlands and excluded patients with ischemic, valvular, hypertensive, and congenital heart disease. All other patients underwent a complete diagnostic work-up, including genetic evaluation and endomyocardial biopsy.
Results:
A total of 213 consecutive patients with DCM were included: organ involvement was demonstrated in 35 (16%) and genetic or familial DCM in 70 (33%) patients, including 16 (8%) patients with a pathogenic mutation. At least 1 cause was found in 155 (73%) patients, of whom 48 (23%) had more than 1 possible cause. Left ventricular reverse remodeling was more common in patients with nongenetic or nonfamilial DCM than in patients with genetic or familial DCM (40% vs. 25%; p = 0.04). After a median follow-up of 47 months, organ involvement and higher New York Heart Association functional class were associated with adverse outcome (p < 0.001 and p = 0.02, respectively). Genetic or familial DCM per se was of no prognostic significance, but when it was accompanied by additional etiologic-environmental factors such as significant viral load, immune-mediated factors, rhythm disturbances, or toxic triggers, a worse outcome was revealed (p = 0.03). A higher presence of MOGE(S) attributes (≥2 vs. ≤1 attributes) showed an adverse outcome (p = 0.007).
Conclusions:
The MOGE(S) classification in DCM is applicable, and each attribute or the gene-environment interaction is associated with outcome. Importantly, the presence of multiple attributes was a strong predictor of adverse outcome. Finally, adaptation of the MOGE(S) involving multiple possible etiologies is recommended.
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