Matches in SemOpenAlex for { <https://semopenalex.org/work/W6587459> ?p ?o ?g. }
- W6587459 endingPage "215" @default.
- W6587459 startingPage "211" @default.
- W6587459 abstract "Extracellular Matrix Alterations in Patients With Paroxysmal and Persistent Atrial Fibrillation: Biochemical Assessment of Collagen Type-I Turnover Eleftherios M. Kallergis, Emmanuel G. Manios, Emmanuel M. Kanoupakis, Hercules E. Mavrakis, Dimitris A. Arfanakis, Niki E. Maliaraki, Chrisovalantis E. Lathourakis, Gregory I. Chlouverakis, Panos E. Vardas Serum markers of collagen type-I turnover differed significantly both between patients with atrial fibrillation (AF) and sinus rhythm and between paroxysmal and persistent AF patients, suggesting that the intensity of the extracellular synthesis and degradation of collagen type-I may be related to the burden or type of AF. Although cardiac biopsy is the gold standard for documenting and monitoring myocardial fibrosis, the development of noninvasive methods to indicate the presence of myocardial fibrosis in AF and in other clinical conditions is particularly attractive and could have a broader application. We investigated whether the serum markers of collagen turnover differed in various forms of atrial fibrillation (AF) and in sinus rhythm (SR) in humans. Structural alterations and fibrosis have been implicated in the generation and perpetuation of AF. Serum C-terminal propeptide of collagen type-I (CICP), C-terminal telopeptide of collagen type-I (CITP), matrix metalloproteinase-1, and tissue inhibitor of matrix metalloproteinases-1 were measured as markers of collagen synthesis and degradation in 70 patients with AF and 20 healthy control subjects in SR. C-terminal propeptide of collagen type-I and CITP were significantly higher in AF patients than in control subjects (91 ± 27 ng/ml vs. 67 ± 11 ng/ml, p < 0.001 and 0.38 ± 0.20 ng/ml vs. 0.25 ± 0.08 ng/ml, p < 0.001, respectively). Persistent AF patients had higher levels of CICP (105 ± 28 ng/ml vs. 80 ± 21 ng/ml, p < 0.001), but not CITP, compared with those with paroxysmal AF. Patients with persistent AF had lower levels of matrix metalloproteinase-1 but increased levels of tissue inhibitor of matrix metalloproteinases-1 compared with patients with paroxysmal AF (11.90 ± 4.79 ng/ml vs. 14.98 ± 6.28 ng/ml, p = 0.03 and 155 ± 45 ng/ml vs. 130 ± 38 ng/ml, p < 0.001, respectively). Tissue inhibitor of matrix metalloproteinases-1 levels were significantly lower in control subjects compared with those in both paroxysmal and persistent AF patients (102 ± 15 ng/ml vs. 130 ± 38 ng/ml vs. 155 ± 45 ng/ml, respectively, p < 0.001). Serum markers of collagen type-I turnover differed significantly between patients with AF and SR. Furthermore, these markers also differed significantly between paroxysmal and persistent AF patients, suggesting that the intensity of the extracellular synthesis and degradation of collagen type-I may be related to the burden or type of AF." @default.
- W6587459 created "2016-06-24" @default.
- W6587459 creator A5026735378 @default.
- W6587459 creator A5041401849 @default.
- W6587459 creator A5044099294 @default.
- W6587459 creator A5050611431 @default.
- W6587459 creator A5051456917 @default.
- W6587459 creator A5060071363 @default.
- W6587459 creator A5073928642 @default.
- W6587459 creator A5082310755 @default.
- W6587459 creator A5090204383 @default.
- W6587459 date "2008-07-01" @default.
- W6587459 modified "2023-09-26" @default.
- W6587459 title "Extracellular Matrix Alterations in Patients With Paroxysmal and Persistent Atrial Fibrillation" @default.
- W6587459 cites W1965037150 @default.
- W6587459 cites W1967255096 @default.
- W6587459 cites W1976468747 @default.
- W6587459 cites W1987436612 @default.
- W6587459 cites W2017179259 @default.
- W6587459 cites W2023844858 @default.
- W6587459 cites W2043659211 @default.
- W6587459 cites W2060379181 @default.
- W6587459 cites W2089940123 @default.
- W6587459 cites W2105809486 @default.
- W6587459 cites W2133554780 @default.
- W6587459 cites W2164168171 @default.
- W6587459 cites W2169679878 @default.
- W6587459 doi "https://doi.org/10.1016/j.jacc.2008.03.045" @default.
- W6587459 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18617070" @default.
- W6587459 hasPublicationYear "2008" @default.
- W6587459 type Work @default.
- W6587459 sameAs 6587459 @default.
- W6587459 citedByCount "94" @default.
- W6587459 countsByYear W65874592012 @default.
- W6587459 countsByYear W65874592013 @default.
- W6587459 countsByYear W65874592014 @default.
- W6587459 countsByYear W65874592015 @default.
- W6587459 countsByYear W65874592016 @default.
- W6587459 countsByYear W65874592017 @default.
- W6587459 countsByYear W65874592018 @default.
- W6587459 countsByYear W65874592019 @default.
- W6587459 countsByYear W65874592020 @default.
- W6587459 countsByYear W65874592021 @default.
- W6587459 countsByYear W65874592022 @default.
- W6587459 countsByYear W65874592023 @default.
- W6587459 crossrefType "journal-article" @default.
- W6587459 hasAuthorship W6587459A5026735378 @default.
- W6587459 hasAuthorship W6587459A5041401849 @default.
- W6587459 hasAuthorship W6587459A5044099294 @default.
- W6587459 hasAuthorship W6587459A5050611431 @default.
- W6587459 hasAuthorship W6587459A5051456917 @default.
- W6587459 hasAuthorship W6587459A5060071363 @default.
- W6587459 hasAuthorship W6587459A5073928642 @default.
- W6587459 hasAuthorship W6587459A5082310755 @default.
- W6587459 hasAuthorship W6587459A5090204383 @default.
- W6587459 hasConcept C109523444 @default.
- W6587459 hasConcept C125870589 @default.
- W6587459 hasConcept C126322002 @default.
- W6587459 hasConcept C131075544 @default.
- W6587459 hasConcept C134018914 @default.
- W6587459 hasConcept C160160445 @default.
- W6587459 hasConcept C164705383 @default.
- W6587459 hasConcept C181199279 @default.
- W6587459 hasConcept C189165786 @default.
- W6587459 hasConcept C207886595 @default.
- W6587459 hasConcept C2775914520 @default.
- W6587459 hasConcept C2779161974 @default.
- W6587459 hasConcept C2780559512 @default.
- W6587459 hasConcept C2780644872 @default.
- W6587459 hasConcept C3018763269 @default.
- W6587459 hasConcept C55493867 @default.
- W6587459 hasConcept C71924100 @default.
- W6587459 hasConcept C86803240 @default.
- W6587459 hasConceptScore W6587459C109523444 @default.
- W6587459 hasConceptScore W6587459C125870589 @default.
- W6587459 hasConceptScore W6587459C126322002 @default.
- W6587459 hasConceptScore W6587459C131075544 @default.
- W6587459 hasConceptScore W6587459C134018914 @default.
- W6587459 hasConceptScore W6587459C160160445 @default.
- W6587459 hasConceptScore W6587459C164705383 @default.
- W6587459 hasConceptScore W6587459C181199279 @default.
- W6587459 hasConceptScore W6587459C189165786 @default.
- W6587459 hasConceptScore W6587459C207886595 @default.
- W6587459 hasConceptScore W6587459C2775914520 @default.
- W6587459 hasConceptScore W6587459C2779161974 @default.
- W6587459 hasConceptScore W6587459C2780559512 @default.
- W6587459 hasConceptScore W6587459C2780644872 @default.
- W6587459 hasConceptScore W6587459C3018763269 @default.
- W6587459 hasConceptScore W6587459C55493867 @default.
- W6587459 hasConceptScore W6587459C71924100 @default.
- W6587459 hasConceptScore W6587459C86803240 @default.
- W6587459 hasIssue "3" @default.
- W6587459 hasLocation W65874591 @default.
- W6587459 hasLocation W65874592 @default.
- W6587459 hasOpenAccess W6587459 @default.
- W6587459 hasPrimaryLocation W65874591 @default.
- W6587459 hasRelatedWork W1558008960 @default.
- W6587459 hasRelatedWork W1967255096 @default.