Association of left ventricular diastolic dysfunction with inflammatory activity, renal dysfunction, and liver-related mortality in patients with cirrhosis and ascites

Eur J Gastroenterol Hepatol. 2024 Jun 1;36(6):775-783. doi: 10.1097/MEG.0000000000002762. Epub 2024 Mar 19.

Abstract

Left ventricular diastolic dysfunction (LVDD) is the predominant cardiac abnormality in cirrhosis. We investigated the association of LVDD with systemic inflammation and its impact on renal function, occurrence of hepatorenal syndrome (HRS) and survival in patients with cirrhosis and ascites. We prospectively enrolled 215 patients with cirrhosis and ascites. We evaluated the diagnosis and grading of LVDD by Doppler echocardiography, inflammatory markers, systemic hemodynamics, vasoactive factors, radioisotope-assessed renal function and blood flow, HRS development and liver-related mortality. LVDD was diagnosed in 142 (66%) patients [grade 2/3: n = 61 (43%)]. Serum lipopolysaccharide-binding protein (LBP), plasma renin activity (PRA) and glomerular filtration rate (GFR) were independently associated with the presence of grade 2/3 LVDD and the severity of diastolic dysfunction. Serum tumor necrosis factor-α, cardiac output and plasma noradrenaline were also independently associated with the presence of grade 2/3 LVDD. The diastolic function marker E / e ' was strongly correlated with serum LBP ( r = 0.731; P < 0.001), PRA ( r = 0.714; P < 0.001) and GFR ( r = -0.609; P < 0.001) among patients with LVDD. The 5-year risk of HRS development and death was significantly higher in patients with grade 2/3 LVDD compared to those with grade 1 (35.5 vs. 14.4%; P = 0.01 and 53.3 vs. 28.2%; P = 0.03, respectively). The occurrence and severity of LVDD in patients with cirrhosis and ascites is closely related to inflammatory activity. Advanced LVDD is associated with baseline circulatory and renal dysfunction, favoring HRS development, and increased mortality.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins*
  • Adult
  • Aged
  • Ascites* / etiology
  • Ascites* / mortality
  • Ascites* / physiopathology
  • Biomarkers* / blood
  • Carrier Proteins / blood
  • Diastole
  • Echocardiography, Doppler
  • Female
  • Glomerular Filtration Rate*
  • Hepatorenal Syndrome* / etiology
  • Hepatorenal Syndrome* / mortality
  • Hepatorenal Syndrome* / physiopathology
  • Humans
  • Inflammation / blood
  • Inflammation Mediators / blood
  • Kidney / physiopathology
  • Liver Cirrhosis* / complications
  • Liver Cirrhosis* / mortality
  • Liver Cirrhosis* / physiopathology
  • Male
  • Membrane Glycoproteins*
  • Middle Aged
  • Prognosis
  • Prospective Studies
  • Renin / blood
  • Risk Factors
  • Severity of Illness Index
  • Ventricular Dysfunction, Left* / mortality
  • Ventricular Dysfunction, Left* / physiopathology

Substances

  • Biomarkers
  • lipopolysaccharide-binding protein
  • Inflammation Mediators
  • Carrier Proteins
  • Renin
  • Acute-Phase Proteins
  • Membrane Glycoproteins