Systemic Chemotherapy Interferes in Homocysteine Metabolism in Breast Cancer Patients
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | YAMASHITA, Eliana K. | |
dc.contributor.author | TEIXEIRA, Bianca M. | |
dc.contributor.author | YOSHIHARA, Renata N. | |
dc.contributor.author | KUNIYOSHI, Renata K. | |
dc.contributor.author | ALVES, Beatriz C. A. | |
dc.contributor.author | GEHRKE, Flavia S. | |
dc.contributor.author | VILAS-BOAS, Viviane A. | |
dc.contributor.author | CORREIA, Joao A. | |
dc.contributor.author | AZZALIS, Ligia A. | |
dc.contributor.author | JUNQUEIRA, Virginia B. C. | |
dc.contributor.author | PEREIRA, Edimar Cristiano | |
dc.contributor.author | FONSECA, Fernando L. A. | |
dc.date.accessioned | 2014-09-30T14:46:31Z | |
dc.date.available | 2014-09-30T14:46:31Z | |
dc.date.issued | 2014 | |
dc.description.abstract | Background Hyperhomocysteinemia in breast cancer (BC) patients can be a risk factor for thromboembolic events. This study aimed to evaluate homocysteine and its cofators (folic acid and vitamin B12) concentrations and platelet count at diagnosis of BC, 3 and 6 months after the beginning of chemotherapy treatment and to correlate them with clinical data. Methods Thirty-five BC patients were included; blood samples were obtained by venipuncture. Plasmatic Hcy and cofactors concentrations were measured by competitive chemiluminescent enzyme immunoassay method. Platelet count was done using an automated analyzer. Statistical analysis was performed using the software SPSS. Results During chemotherapy, homocysteine (P = 0.032) and vitamin B12 (P < 0.001) concentrations increased, while folate and platelets decreased (P < 0.001). Among the clinical data, the menopausal status showed significant positive correlation (P = 0.022) with homocysteine concentration increase. Conclusions Evaluation of homocysteine concentrations during chemotherapy is extremely important because their levels increase during chemotherapy treatment, thus increasing the risk of thromboembolism development. | |
dc.description.index | MEDLINE | |
dc.description.sponsorship | FAPESP [2009/54343-0 2009/54342-4] | |
dc.identifier.citation | JOURNAL OF CLINICAL LABORATORY ANALYSIS, v.28, n.2, p.157-162, 2014 | |
dc.identifier.doi | 10.1002/jcla.21660 | |
dc.identifier.eissn | 1098-2825 | |
dc.identifier.issn | 0887-8013 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/7732 | |
dc.language.iso | eng | |
dc.publisher | JOHN WILEY & SONS INC | |
dc.relation.ispartof | Journal of Clinical Laboratory Analysis | |
dc.rights | restrictedAccess | |
dc.rights.holder | Copyright JOHN WILEY & SONS INC | |
dc.subject | homocysteine | |
dc.subject | folic acid | |
dc.subject | vitamin B 12 | |
dc.subject | breast neoplasms | |
dc.subject | chemotherapy and thromboembolism | |
dc.subject.other | circulating tumor-cells | |
dc.subject.other | venous thromboembolism | |
dc.subject.other | peripheral-blood | |
dc.subject.other | adjuvant therapy | |
dc.subject.other | thrombosis | |
dc.subject.other | risk | |
dc.subject.wos | Medical Laboratory Technology | |
dc.title | Systemic Chemotherapy Interferes in Homocysteine Metabolism in Breast Cancer Patients | |
dc.type | article | |
dc.type.category | original article | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.author.external | YAMASHITA, Eliana K.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil | |
hcfmusp.author.external | TEIXEIRA, Bianca M.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil | |
hcfmusp.author.external | YOSHIHARA, Renata N.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil | |
hcfmusp.author.external | ALVES, Beatriz C. A.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil | |
hcfmusp.author.external | GEHRKE, Flavia S.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil | |
hcfmusp.author.external | VILAS-BOAS, Viviane A.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil | |
hcfmusp.author.external | CORREIA, Joao A.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil | |
hcfmusp.author.external | AZZALIS, Ligia A.:Univ Fed Sao Paulo, Dept Biol Sci, BR-09972270 Diadema, SP, Brazil | |
hcfmusp.author.external | JUNQUEIRA, Virginia B. C.:Univ Fed Sao Paulo, Dept Biol Sci, BR-09972270 Diadema, SP, Brazil | |
hcfmusp.author.external | PEREIRA, Edimar Cristiano:Univ Fed Sao Paulo, Dept Biol Sci, BR-09972270 Diadema, SP, Brazil | |
hcfmusp.author.external | FONSECA, Fernando L. A.:ABC, Sch Med, Dept Hematol & Oncol, Santo Andre, SP, Brazil; Univ Fed Sao Paulo, Dept Biol Sci, BR-09972270 Diadema, SP, Brazil | |
hcfmusp.citation.scopus | 18 | |
hcfmusp.contributor.author-fmusphc | RENATA KELLY KUNIYOSHI | |
hcfmusp.description.beginpage | 157 | |
hcfmusp.description.endpage | 162 | |
hcfmusp.description.issue | 2 | |
hcfmusp.description.volume | 28 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 24395112 | |
hcfmusp.origem.scopus | 2-s2.0-84896105774 | |
hcfmusp.origem.wos | WOS:000332840500013 | |
hcfmusp.publisher.city | HOBOKEN | |
hcfmusp.publisher.country | USA | |
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hcfmusp.remissive.sponsorship | FAPESP | |
hcfmusp.scopus.lastupdate | 2024-05-17 | |
relation.isAuthorOfPublication | 9f912ef6-3621-47a3-8652-9beaf473b391 | |
relation.isAuthorOfPublication.latestForDiscovery | 9f912ef6-3621-47a3-8652-9beaf473b391 |
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