Cardiac sympathetic innervation and mortality risk scores in patients with heart failure

Leonardo Bencivenga1,2, Klara Komici3, Stefania Paolillo1

  • 1Department of Advanced Biomedical Sciences, University of Naples "Federico II", Naples, Italy.

Insights

Clinical risk scores and cardiac sympathetic innervation show a weak association in heart failure patients. Integrating both arrhythmic and general mortality risk tools is suggested for device implantation decisions.

Area of Science:

  • Cardiology
  • Nuclear Medicine
  • Medical Imaging

Background:

  • 123I-meta-IodineBenzylGuanidine (123I-mIBG) scintigraphy assesses cardiac adrenergic innervation for heart failure (HF) risk stratification.
  • Clinical risk scores identify HF patients at risk of all-cause mortality, potentially impacting device implantation benefits.
  • The relationship between arrhythmic risk indicators (innervation) and general mortality risk scores needs investigation.

Purpose of the Study:

  • To evaluate the correlation between established mortality risk scores and cardiac sympathetic innervation in HF patients.
  • To determine if risk scores can predict cardiac adrenergic impairment assessed by 123I-mIBG imaging.

Main Methods:

  • The study included 269 HF patients who underwent 123I-mIBG scintigraphy.
  • Eight risk stratification models (AAACC, FADES, MADIT, etc.) were assessed.
  • Cardiac adrenergic impairment was defined by a late heart-to-mediastinum ratio (H/M) <1.6.

Main Results:

  • A significant, though generally weak, negative correlation was found between late H/M ratio and all assessed mortality risk scores (r ranging from -0.15 to -0.32).
  • Risk scores demonstrated poor discrimination for cardiac innervation, with AUC values between 0.546 and 0.621.
  • The FADES score showed the strongest correlation (r=-0.32) and discrimination (AUC=0.621) among the models evaluated.

Conclusions:

  • A weak association exists between mortality risk scores and cardiac sympathetic innervation in HF patients.
  • Clinical practice should consider integrating tools assessing both arrhythmic and general mortality risks for device implantation decisions in HF.
  • Further research may refine the combined use of these tools for optimal patient selection.
Abstract

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