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.
Abstract

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