Hepatocyte growth factor as indicator for subclinical atherosclerosis.
Philip SommerMichael SchreinlechnerMaria NoflatscherClarisse EnglDaniela LenerMarkus TheurlRudolf KirchmairPeter MarschangPublished in: VASA. Zeitschrift fur Gefasskrankheiten (2024)
Background: Hepatocyte growth factor (HGF) is a pleiotropic cytokine mainly produced by mesenchymal cells. After endothelial damage by oxidized low-density lipoprotein (LDL), HGF is produced and released into the circulation in response. Due to this mechanism HGF has been proposed as possible clinical biomarker for clinical as well as subclinical atherosclerosis. Patients and methods: The conducted study is an observational, single centre, cohort study, including 171 patients with at least one cardiovascular risk factor or already established cardiovascular disease (CVD). Each patient underwent 3D plaque volumetry of the carotid and femoral arteries as well as physical examination and record of the medical history. Additionally, plasma HGF and further laboratory parameters like high sensitivity C-reactive protein and LDL-cholesterol were determined. Results: 169 patients were available for statistical analysis. In bivariate correlation, HGF showed a highly significant correlation with total plaque volume (TPV, r=0.48; p<0.001). In receiver operating characteristic (ROC) analysis for high TPV, HGF showed an area under the curve (AUC) of 0.68 (CI 95%: 0.59-0.77, p<0.001) with a sensitivity of 78% and a specificity of 52% to predict high TPV at a cut-off of 959 ng/ml. In the ROC-analysis for the presence of CVD, HGF demonstrated an AUC of 0.65 (95% CI 0.55-0.73; p=0.01) with a sensitivity of 77% and a specificity of 52%. Conclusions: Higher plasma levels of HGF are associated with higher atherosclerotic plaque volume as measured by 3D-ultrasound.
Keyphrases
- growth factor
- low density lipoprotein
- cardiovascular disease
- end stage renal disease
- ejection fraction
- newly diagnosed
- coronary artery disease
- healthcare
- type diabetes
- peritoneal dialysis
- risk factors
- bone marrow
- patient reported outcomes
- mental health
- metabolic syndrome
- liver injury
- cell proliferation
- endoplasmic reticulum stress