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Lipoprotein(a) is associated with DNA damage in patients with heterozygous familial hypercholesterolemia.
Wozniak, Ewelina; Broncel, Marlena; Wozniak, Agnieszka; Satala, Joanna; Pawlos, Agnieszka; Bukowska, Bozena; Gorzelak-Pabis, Paulina.
Afiliación
  • Wozniak E; Laboratory of Tissue Immunopharmacology, Department of Internal Diseases and Clinical Pharmacology, Medical University of Lodz, Lodz, Poland. ewelina.wozniak@umed.lodz.pl.
  • Broncel M; Laboratory of Tissue Immunopharmacology, Department of Internal Diseases and Clinical Pharmacology, Medical University of Lodz, Lodz, Poland.
  • Wozniak A; Laboratory of Tissue Immunopharmacology, Department of Internal Diseases and Clinical Pharmacology, Medical University of Lodz, Lodz, Poland.
  • Satala J; Laboratory of Tissue Immunopharmacology, Department of Internal Diseases and Clinical Pharmacology, Medical University of Lodz, Lodz, Poland.
  • Pawlos A; Laboratory of Tissue Immunopharmacology, Department of Internal Diseases and Clinical Pharmacology, Medical University of Lodz, Lodz, Poland.
  • Bukowska B; Department of Biophysics of Environmental Pollution, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
  • Gorzelak-Pabis P; Laboratory of Tissue Immunopharmacology, Department of Internal Diseases and Clinical Pharmacology, Medical University of Lodz, Lodz, Poland.
Sci Rep ; 14(1): 2564, 2024 01 31.
Article en En | MEDLINE | ID: mdl-38297066
ABSTRACT
Heterozygous familial hypercholesterolemia (HeFH) is a common autosomal-dominant inherited disorder associated with atherosclerotic cardiovascular disease (ASCVD). HeFH subjects have a higher lipoprotein(a), i.e. Lp(a), concentration than the general population. Patients with FH are exposed to elevated levels of LDL from birth and ox-LDL may induce other oxidation pathways. The aim of the study was to determine the levels of markers of oxidative stress and DNA damage in patients with HeFH and describe the effect of Lp(a) on the resulting damage. Higher DNA damage was identified in patients with HeFH compared to the normolipidemic ones, and ASCVD was associated with greater damage. Oxidative stress markers were elevated in HeFH patients; however, only ox-LDL was higher in the ASCVD group and its level correlated with DNA damage. A positive correlation was found between DNA damage and Lp(a) concentration in the HeFH patients. Higher levels of Lp(a) were associated with greater DNA damage, especially in patients with HeFH and ASCVD. In HeFH patients, the optimal Lp(a) cut-off point associated with ASCVD is > 23.45 nmol/L, i.e. much lower than for the general population; however this cut-off point needs validation in a larger group of HeFH patients.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Aterosclerosis / Hipercolesterolemia / Hiperlipoproteinemia Tipo II Tipo de estudio: Risk_factors_studies Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Aterosclerosis / Hipercolesterolemia / Hiperlipoproteinemia Tipo II Tipo de estudio: Risk_factors_studies Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article