The Metabolic Vulnerability Index: A Novel Marker for Mortality Prediction in Heart Failure

JACC Heart Fail. 2024 Feb;12(2):290-300. doi: 10.1016/j.jchf.2023.06.013. Epub 2023 Jul 19.

Abstract

Background: Inflammation and protein energy malnutrition are associated with heart failure (HF) mortality. The metabolic vulnerability index (MVX) is derived from markers of inflammation and malnutrition and measured by nuclear magnetic resonance spectroscopy. MVX has not been examined in HF.

Objectives: The authors sought to examine the prognostic value of MVX in patients with HF.

Methods: The authors prospectively assembled a population-based cohort of patients with HF from 2003 to 2012 and measured MVX scores with a nuclear magnetic resonance scan from plasma collected at enrollment. Patients were divided into 4 MVX score groups and followed until March 31, 2021.

Results: The authors studied 1,382 patients (median age: 78 years; 48% women). The median MVX score was 64.6. Patients with higher MVX were older, more likely to be male, have atrial fibrillation, have higher NYHA functional class, and have HF duration of >18 months. Higher MVX was associated with mortality independent of Meta-analysis Global Group in Chronic Heart Failure score, ejection fraction, and other prognostic biomarkers. Compared to those with the lowest MVX, the HRs for MVX groups 2, 3, and 4 were 1.2 (95% CI: 0.9-1.4), 1.6 (95% CI: 1.3-2.0), and 1.8 (95% CI: 1.4-2.2), respectively (Ptrend < 0.001). Measures of model improvement document the added value of MVX in HF for classifying the risk of death beyond the Meta-analysis Global Group in Chronic Heart Failure score and other biomarkers.

Conclusions: In this HF community cohort, MVX was strongly associated with mortality independently of established clinical factors and improved mortality risk classification beyond clinically validated markers. These data underscore the potential of MVX to stratify risk in HF.

Keywords: NMR; heart failure; inflammation; malnutrition; metabolomics; mortality.

Publication types

  • Meta-Analysis

MeSH terms

  • Aged
  • Biomarkers
  • Chronic Disease
  • Female
  • Heart Failure*
  • Humans
  • Inflammation / complications
  • Male
  • Prognosis
  • Stroke Volume

Substances

  • Biomarkers