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Cytokeratin 18 as a Novel Biomarker in Patients with Hypertrophic Cardiomyopathy.
Fragkiadakis, Konstantinos; Ktena, Niki; Kalantidou, Aikaterini; Dermitzaki, Eirini; Anastasiou, Ioannis; Papathanassiou, Stamatis; Kontaraki, Joanna; Kalomoirakis, Petros; Kanoupakis, Emmanuel; Patrianakos, Alexandros; Papadomanolakis, Antonis; Daskalaki, Efsevia; Kiousi, Theodora; Kouraki, Katerina; Kranioti, Elena; Tzardi, Maria; Venihaki, Maria; Karagogeos, Domna; Capetanaki, Yassemi; Kardassis, Dimitris; Kochiadakis, Georgios; Parthenakis, Fragkiskos; Marketou, Maria.
Afiliação
  • Fragkiadakis K; Cardiology Department, Heraklion University General Hospital, 71110 Heraklion, Greece.
  • Ktena N; Cardiology Department, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Kalantidou A; Division of Basic Sciences, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Dermitzaki E; Clinical Chemistry, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Anastasiou I; Clinical Chemistry, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Papathanassiou S; Cardiology Department, Heraklion University General Hospital, 71110 Heraklion, Greece.
  • Kontaraki J; Institute of Molecular Biology, 55128 Mainz, Germany.
  • Kalomoirakis P; Cardiology Department, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Kanoupakis E; Cardiology Department, Heraklion University General Hospital, 71110 Heraklion, Greece.
  • Patrianakos A; Cardiology Department, Heraklion University General Hospital, 71110 Heraklion, Greece.
  • Papadomanolakis A; Cardiology Department, Heraklion University General Hospital, 71110 Heraklion, Greece.
  • Daskalaki E; Forensic Medicine Unit, Department of Forensic Sciences, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Kiousi T; Forensic Medicine Unit, Department of Forensic Sciences, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Kouraki K; Forensic Medicine Unit, Department of Forensic Sciences, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Kranioti E; Laboratory of Pathology, University General Hospital of Heraklion, 71110 Heraklion, Greece.
  • Tzardi M; Forensic Medicine Unit, Department of Forensic Sciences, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Venihaki M; Laboratory of Pathology, University General Hospital of Heraklion, 71110 Heraklion, Greece.
  • Karagogeos D; Clinical Chemistry, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Capetanaki Y; Division of Basic Sciences, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Kardassis D; Center of Basic Research, Biomedical Research Foundation, Academy of Athens, 11527 Athens, Greece.
  • Kochiadakis G; Laboratory of Biochemistry, School of Medicine, University of Crete, 71003 Heraklion, Greece.
  • Parthenakis F; Cardiology Department, Heraklion University General Hospital, 71110 Heraklion, Greece.
  • Marketou M; Cardiology Department, School of Medicine, University of Crete, 71003 Heraklion, Greece.
Cells ; 13(16)2024 Aug 09.
Article em En | MEDLINE | ID: mdl-39195218
ABSTRACT
Hypertrophic cardiomyopathy (HCM) is a heart muscle disease associated with an increased risk for sudden cardiac death (SCD). Cytokeratin 18-based proteins, such as M30 and M65 antigens, are known cell-death biomarkers. M30 antigen is released from cells during apoptosis, and M65 antigen is released during cell death from any cause, such as apoptosis or necrosis. We aimed to study the expression of M30 and M65 antigens in peripheral blood obtained by 46 HCM patients and compare with 27 age- and sex-matched patients without HCM. We also investigated the CK18 expression in myocardium from postmortem HCM hearts. M30 and M65 antigens were significantly increased in the HCM vs. non-HCM group (Μ30 338 ± 197 U/uL vs. 206 ± 166 U/uL, p = 0.003; M65 428 ± 224 U/uL vs. 246 ± 214 U/uL, p = 0.001), and HCM patients with a higher expression of these markers (M30 417 ± 208 vs. 271 ± 162 U/uL, p = 0.011; M65 518 ± 242 vs. 351 ± 178 U/uL, p = 0.011) had a higher risk for SCD. In HCM, both apoptosis and necrosis are increased, but particularly necrosis (M30/M65 ratio 0.75 ± 0.09 vs. 0.85 ± 0.02, p < 0.001). CK18 is expressed in the HCM myocardium (1.767 ± 0.412 vs. 0.537 ± 0.383, % of area, p = 0.0058). Therefore, M30 and M65 antigens may be novel biomarkers in HCM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Biomarcadores / Queratina-18 Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Biomarcadores / Queratina-18 Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article