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dc.contributor.authorSerdengecti, S
dc.contributor.authorArun, B
dc.contributor.authorErzin, Y
dc.contributor.authorDemir, G
dc.contributor.authorDemirelli, F
dc.contributor.authorMandel, NM
dc.contributor.authorBuyukunal, E
dc.contributor.authorBerkarda, B
dc.contributor.authorOzduroglu, M
dc.date.accessioned2021-03-03T14:51:06Z
dc.date.available2021-03-03T14:51:06Z
dc.date.issued1999
dc.identifier.citationOzduroglu M., Arun B., Erzin Y., Demir G., Demirelli F., Mandel N., Buyukunal E., Serdengecti S., Berkarda B., "Serum cardiolipin antibodies in cancer patients with thromboembolic events", CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, cilt.5, sa.3, ss.181-184, 1999
dc.identifier.issn1076-0296
dc.identifier.othervv_1032021
dc.identifier.otherav_3bd2be6b-1b7c-4169-99ec-38f3235d97cd
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44156
dc.identifier.urihttps://doi.org/10.1177/107602969900500307
dc.description.abstractThis study was undertaken to investigate a possible association of anticardiolipin antibodies (ACLAs) in cancer patients with thromboembolic events. Twenty-five patients with solid tumors complicated with acute thrombosis, 36 cancer patients without any thrombotic events, and a group of 20 healthy volunteers without thrombosis or malignancy were included. The mean age of the cancer patients with and without thrombosis and healthy subjects were 50 years (range 20-75), 45 years (range 23-66), and 40 years (range 20-68), respectively Deep venous thrombosis (n = 16) and thrombosis of the central venous port-catheter systems (n = 9) were confirmed by Doppler sonography in all patients. Ige and IgM isotypes of ACLAs were: quantitated by enzyme-linked immunosorbent assay with normal levels of <23 GPL and <11 MPL, respectively. Mean values of IgG ACLAs were found similar in cancer patients with acute thrombosis (13.8 +/- 4.9 GPL), without thrombosis (12.8 +/- 5.4 GPL) or in healthy subjects (14.8 +/- 5.5 GPL). Although the mean values of IgM ACLAs were within normal limits in all groups, cancer patients with thrombotic events had higher levels of IgM ACLAs (mean = 10.5 +/- 2.2 MPL) than cancer patients without thrombosis (mean = 4.6 +/- 2.3 MPL) (p = .01). Healthy subjects also had lower levels of IgM ACLAs (mean = 7.1 +/- 3.2 MPL) than cancer patients with thrombosis (p = .16). In addition, a higher percentage of cancer patients with or without thrombosis had IgM and IgG ACLA levels above normal limits compared with healthy controls. In conclusion, our study suggests an association between ACLAs or Ige and particularly IgM isotypes and venous thrombosis in malignancy. Identification of cancer patients who are at higher risk for developing thromboembolic events might lead to a better selection of patients for prophylactic anticoagulant therapy.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectHEMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPERİFERAL VASKÜLER HASTALIĞI
dc.titleSerum cardiolipin antibodies in cancer patients with thromboembolic events
dc.typeMakale
dc.relation.journalCLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
dc.contributor.department, ,
dc.identifier.volume5
dc.identifier.issue3
dc.identifier.startpage181
dc.identifier.endpage184
dc.contributor.firstauthorID44252


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