Ryosuke Hatano, Takahiro Doi, Satoshi Kimura, Rintaro Furuoka, Kosuke Uruno, Koki Morishita, Ken Masuda, Ryo Nishikawa, Kaoru Komuro, Hiroyuki Iwano, Daigo Nagahara, Satoshi Yuda, Akiyoshi Hashimoto, Tomoaki Nakata
Liver fibrosis parameters are also independent prognostic factors along with cardiac sympathetic nervous function and renal dysfunction in patients with HF, potentially enabling additive risk stratification of these patients.
BACKGROUND: This study aimed to determine the prognostic impact of liver fibrosis on cardiac sympathetic innervation and renal function in patients with heart failure (HF) compared with the well-established prognostic value of cardiorenal and hepatorenal linkage.
METHODS: In 525 consecutive patients with HF with left ventricular ejection fraction <50%, the fibrosis-5 index (Fib-5) was calculated to evaluate hepatic dysfunction and liver fibrosis. After 123I-metaiodobenzylguanidine (MIBG) scintigraphy, patient outcomes, with lethal cardiac events (CEs) as the primary endpoint, were evaluated for a mean interval of 36.1 ± 26.8 months. CEs were defined as sudden cardiac death, death from heart failure, detection of fatal ventricular arrhythmia, and appropriate implantable cardioverter defibrillator therapy for fatal ventricular arrhythmia.
RESULTS: During follow-up, CEs were documented in 139 patients with HF. Fib-5, estimated glomerular filtration rate (eGFR), and the standardized heart-to-mediastinum ratio of MIBG activity (sHMR) were significantly reduced in CEs group compared with those in the non-CEs group. The overall multivariate analysis revealed that these parameters were significant independent determinants of CEs. Combining the cut-off values of Fib-5 (<-13.6), eGFR (<41.0 mL/min/1.73 m2), and late sHMR (<1.83), determined by receiver operating characteristic curve analysis further successfully differentiated patients with HF at higher risk for CEs from other patients with HF.
CONCLUSIONS: Liver fibrosis parameters are also independent prognostic factors along with cardiac sympathetic nervous function and renal dysfunction in patients with HF, potentially enabling additive risk stratification of these patients.