Evolution of Biomarkers of Atherogenic Risk in Liver Transplantation Recipients
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | LINHARES, L. M. C. | |
dc.contributor.author | OLIVEIRA, C. P. | |
dc.contributor.author | ALVARES-DA-SILVA, M. R. | |
dc.contributor.author | STEFANO, J. T. | |
dc.contributor.author | BARBEIRO, H. V. | |
dc.contributor.author | BARBEIRO, D. F. | |
dc.contributor.author | TERRABUIO, D. R. B. | |
dc.contributor.author | ABDALA, E. | |
dc.contributor.author | SORIANO, F. G. | |
dc.contributor.author | CARRILHO, F. J. | |
dc.contributor.author | FARIAS, A. Q. | |
dc.contributor.author | SIDDIQUI, M. S. | |
dc.contributor.author | D'ALBUQUERQUE, L. A. C. | |
dc.date.accessioned | 2019-02-21T17:24:15Z | |
dc.date.available | 2019-02-21T17:24:15Z | |
dc.date.issued | 2018 | |
dc.description.abstract | Background. Cardiovascular disease is a major contributing factor to long-term mortality after liver transplantation (LT). Methods. This study evaluated the evolution of atherogenic risk in liver transplant recipients (LTRs). Thirty-six subjects were prospectively enrolled at 12 months and followed for 48 months after liver transplantation. Serum biomarkers of endothelial dysfunction (sICAM-1 and sVCAM-1), chronic inflammation (serum amyloid A), and oxidative stress (myeloperoxidase) were measured at 12 and 48 months after LT. Additionally, at 12 months all patients underwent a cardiac computed tomography (CT) scan and a coronary artery calcium score (CACS). Results. The prevalence of risk factors of metabolic syndrome (MS) increased over the course of the study. The patients' sVCAM-1 and sICAM-1 increased from 1.82 +/- 0.44 ng/mL to 9.10 +/- 5.82 ng/mL (P < .001) and 0.23 +/- 0.09 ng/mL to 2.7 +/- 3.3 ng/mL, respectively from month 12 to 48. Serum myeloperoxidase increased from 0.09 +/- 0.07 ng/mL to 3.46 +/- 3.92 ng/mL (P < .001) over the course of the study. Serum amyloid A also increased from 21.4 +/- 40.7 ng/mL at entry to 91.5 +/- 143.6 ng/mL at end of study (P < .001). Conclusion. No association between these biomarkers and MS was noted. The cardiac CT revealed mild and moderate disease in 19% and 25% of the cohort, respectively. No association between serum biomarkers and CACS was noted. Serum biomarkers of atherogenic risk increase rapidly in LTRs and precede coronary plaques. | eng |
dc.description.index | MEDLINE | eng |
dc.description.sponsorship | Coordination for the Improvement of Higher Education Personnel at the University of Sao Paulo | |
dc.identifier.citation | TRANSPLANTATION PROCEEDINGS, v.50, n.10, p.3650-3655, 2018 | |
dc.identifier.doi | 10.1016/j.transproceed.2018.04.030 | |
dc.identifier.eissn | 1873-2623 | |
dc.identifier.issn | 0041-1345 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/30850 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER SCIENCE INC | eng |
dc.relation.ispartof | Transplantation Proceedings | |
dc.rights | restrictedAccess | eng |
dc.rights.holder | Copyright ELSEVIER SCIENCE INC | eng |
dc.subject.other | c-reactive protein | eng |
dc.subject.other | computed-tomography | eng |
dc.subject.other | metabolic syndrome | eng |
dc.subject.other | outcomes | eng |
dc.subject.other | quantification | eng |
dc.subject.other | association | eng |
dc.subject.other | prediction | eng |
dc.subject.other | mortality | eng |
dc.subject.other | disease | eng |
dc.subject.wos | Immunology | eng |
dc.subject.wos | Surgery | eng |
dc.subject.wos | Transplantation | eng |
dc.title | Evolution of Biomarkers of Atherogenic Risk in Liver Transplantation Recipients | eng |
dc.type | article | eng |
dc.type.category | original article | eng |
dc.type.version | publishedVersion | eng |
dspace.entity.type | Publication | |
hcfmusp.affiliation.country | Estados Unidos | |
hcfmusp.affiliation.countryiso | us | |
hcfmusp.author.external | ALVARES-DA-SILVA, M. R.:Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Div Gastroenterol, Porto Alegre, RS, Brazil | |
hcfmusp.author.external | SIDDIQUI, M. S.:Virginia Commonwealth Univ, Div Gastroenterol & Hepatol, Med Coll Virginia Campus, Richmond, VA 23284 USA | |
hcfmusp.citation.scopus | 6 | |
hcfmusp.contributor.author-fmusphc | LIVIA MELO CARONE LINHARES | |
hcfmusp.contributor.author-fmusphc | CLAUDIA PINTO MARQUES SOUZA DE OLIVEIRA | |
hcfmusp.contributor.author-fmusphc | JOSE TADEU STEFANO | |
hcfmusp.contributor.author-fmusphc | HERMES VIEIRA BARBEIRO | |
hcfmusp.contributor.author-fmusphc | DENISE FREDIANI BARBEIRO | |
hcfmusp.contributor.author-fmusphc | DEBORA RAQUEL BENEDITA TERRABUIO | |
hcfmusp.contributor.author-fmusphc | EDSON ABDALA | |
hcfmusp.contributor.author-fmusphc | FRANCISCO GARCIA SORIANO | |
hcfmusp.contributor.author-fmusphc | FLAIR JOSE CARRILHO | |
hcfmusp.contributor.author-fmusphc | ALBERTO QUEIROZ FARIAS | |
hcfmusp.contributor.author-fmusphc | LUIZ AUGUSTO CARNEIRO D ALBUQUERQUE | |
hcfmusp.description.beginpage | 3650 | |
hcfmusp.description.endpage | 3655 | |
hcfmusp.description.issue | 10 | |
hcfmusp.description.volume | 50 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 30586839 | |
hcfmusp.origem.scopus | 2-s2.0-85055567779 | |
hcfmusp.origem.wos | WOS:000454972000120 | |
hcfmusp.publisher.city | NEW YORK | eng |
hcfmusp.publisher.country | USA | eng |
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hcfmusp.scopus.lastupdate | 2024-05-10 | |
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