Determination of Serum Progranulin in Patients with Untreated Familial Hypercholesterolemia

• Published in: Biomedicines Vol. 10; no. 4; p. 771
• Main Authors: Nádró, Bíborka, Lőrincz, Hajnalka, Juhász, Lilla, Szentpéteri, Anita, Sztanek, Ferenc, Varga, Éva, Páll, Dénes, Paragh, György, Harangi, Mariann
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 25.03.2022; MDPI
• Subjects: Arteriosclerosis; Atherosclerosis; Cholesterol; Disease; Enzymes; familial hypercholesterolemia; Growth factors; High density lipoprotein; high-density lipoprotein subfraction; Hypercholesterolemia; Inflammation; Laboratories; Lipids; Lipoproteins; Low density lipoprotein; Outpatient care facilities; Oxidative stress; Population studies; progranulin; tumor necrosis factor alpha; Tumor necrosis factor-α; Hungary; United Kingdom > UK; United States > US; Redondo Beach California; Europe; Germany; progranulin; tumor necrosis factor alpha; inflammation; high-density lipoprotein subfraction; familial hypercholesterolemia
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10040771

Familial hypercholesterolemia (FH) is an autosomal dominant trait characterized by elevated LDL-C concentrations and is associated with an increased risk of premature atherosclerosis. Progranulin (PGRN) is a multifunctional protein that is known to have various anti-atherogenic effects. To date, the use of serum PGRN in patients with FH has not been studied. In total, 81 untreated patients with heterozygous FH (HeFH) and 32 healthy control subjects were included in this study. Serum PGRN, sICAM-1, sVCAM-1, oxLDL and TNFα concentrations were determined by ELISA. Lipoprotein subfractions were detected by Lipoprint. We diagnosed FH using the Dutch Lipid Clinic Network criteria. We could not find a significant difference between the PGRN concentrations of the HeFH patients and controls (37.66 ± 9.75 vs. 38.43 ± 7.74 ng/mL, ns.). We found significant positive correlations between triglyceride, TNFα, sVCAM-1, the ratio of small HDL subfraction and PGRN, while significant negative correlations were found between the ratio of large HDL subfraction and PGRN both in the whole study population and in FH patients. PGRN was predicted by sVCAM-1, logTNFα and the ratio of small HDL subfraction. The strong correlations between HDL subfractions, inflammatory markers and PGRN suggest that PGRN may exert its anti-atherogenic effect in HeFH through the alteration of HDL composition and the amelioration of inflammation rather than through decreasing oxidative stress.