Increased levels of MMP-3, MMP-9 and MPO represent predictors of in-stent restenosis, while increased levels of ADMA, LCAT, ApoE and ApoD predict bare metal stent patency
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26365933
DOI
10.5507/bp.2015.037
Knihovny.cz E-zdroje
- Klíčová slova
- apolipoproteins D, apolipoproteins E, asymmetric dimethylarginine, in-stent restenosis, lecitin-cholesterol acyltransferase, matrix metalloproteinases, myeloperoxidase,
- MeSH
- apolipoproteiny D metabolismus MeSH
- apolipoproteiny E metabolismus MeSH
- arginin analogy a deriváty metabolismus MeSH
- biologické markery metabolismus MeSH
- koronární angioplastika MeSH
- koronární restenóza diagnóza patofyziologie MeSH
- lecitincholesterolacyltransferasa metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipoprotein (a) metabolismus MeSH
- matrixová metaloproteinasa 3 metabolismus MeSH
- matrixová metaloproteinasa 9 metabolismus MeSH
- okluze cévního štěpu diagnóza patofyziologie MeSH
- peroxidasa metabolismus MeSH
- průchodnost cév fyziologie MeSH
- senioři MeSH
- stenty * MeSH
- studie případů a kontrol MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- apolipoproteiny D MeSH
- apolipoproteiny E MeSH
- arginin MeSH
- biologické markery MeSH
- lecitincholesterolacyltransferasa MeSH
- lipoprotein (a) MeSH
- matrixová metaloproteinasa 3 MeSH
- matrixová metaloproteinasa 9 MeSH
- N,N-dimethylarginine MeSH Prohlížeč
- peroxidasa MeSH
AIMS: We sought to identify biochemical predictors that indicate susceptibility to in-stent restenosis (ISR) after coronary artery bare-metal stenting. METHODS: A total of 111 consecutive patients with post-percutaneous coronary intervention (PCI) in-stent restenosis of a target lesion within 12 months were matched for age, sex, vessel diameter, and diabetes with 111 controls without post-PCI ISR. Plasma or serum levels of biochemical markers were measured: matrix metalloproteinases (MMP) 2, 3, 9; myeloperoxidase (MPO); asymmetric dimethylarginine (ADMA); lipoprotein (a) (Lp[a]); apolipoproteins E and D (ApoE and D); and lecitin-cholesterol acyltransferase (LCAT). Multivariable logistic regression association tests were performed. RESULTS: Increased plasma MMP-3 (OR: 1.013; 95% CI: 1.004-1.023; P = 0.005), MMP-9 (OR: 1.014; 95% CI: 1.008-1.020; P < 0.0001) or MPO (OR: 1,003; 95% CI: 1.001-1.005; P = 0.002) was significantly associated with increased risk of ISR. Increased levels of ADMA (OR: 0.212; 95% CI: 0.054-0.827; P = 0.026), ApoE (OR: 0.924; 95% CI: 0.899-0.951; P < 0.0001), ApoD (OR: 0.919; 95% CI: 0.880-0.959; P = 0.0001), or LCAT (OR: 0.927; 95% CI: 0.902-0.952; P < 0.0001) was associated with risk reduction. No correlation was found between plasma MMP-2 or Lp (a) and ISR risk. CONCLUSIONS: Increased levels of MMP-3, MMP-9, and MPO represent predictors of ISR after bare-metal stent implantation. In contrast, increased ADMA, LCAT, and Apo E and D indicate a decreased in-stent restenosis occurrence.
Blood Center University Hospital of Ostrava
Department of Biomedical Sciencies Faculty of Medicine University of Ostrava
Department of Cardiovascular Diseases University Hospital Ostrava
Department of Clinical Studies Faculty of Medicine University of Ostrava Czech Republic
Department of Laboratory Medicine University Hospital Ostrava
Department of Medical Biophysics Faculty of Medicine and Dentistry Palacky University Olomouc
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