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  1. Article ; Online: Impact of neutrophil extracellular trap formation on thromboembolic events and prognosis in patients with newly-diagnosed lymphoproliferative disorders.

    Hoppe, Anna / Wojtasińska, Ewelina / Rupa-Matysek, Joanna

    Polish archives of internal medicine

    2023  Volume 134, Issue 1

    MeSH term(s) Humans ; Extracellular Traps ; Prognosis
    Language English
    Publishing date 2023-12-22
    Publishing country Poland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 123500-x
    ISSN 1897-9483 ; 0032-3772
    ISSN (online) 1897-9483
    ISSN 0032-3772
    DOI 10.20452/pamw.16648
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Evaluation of the prevalence of hepatitis C virus infection in patients with hemophilia treated in a single hemophilia center in Poland.

    Schneider, Anna / Wojtasińska, Ewelina / Pielaszkiewicz, Katarzyna / Joks, Monika / Gil, Lidia / Rupa-Matysek, Joanna

    Polish archives of internal medicine

    2023  Volume 133, Issue 5

    MeSH term(s) Humans ; Hepacivirus ; Hemophilia A/therapy ; Prevalence ; Poland/epidemiology ; Hepatitis C
    Language English
    Publishing date 2023-02-20
    Publishing country Poland
    Document type Journal Article
    ZDB-ID 123500-x
    ISSN 1897-9483 ; 0032-3772
    ISSN (online) 1897-9483
    ISSN 0032-3772
    DOI 10.20452/pamw.16438
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The Profile of Markers of Bone Turnover, Inflammation and Extracellular Neutrophil Traps on Bone Mass in Haemophilia and the Development of Haemophilic Arthropathy.

    Czajkowska, Sylwia / Rupa-Matysek, Joanna / Wojtasińska, Ewelina / Nijakowski, Kacper / Surdacka, Anna / Gil, Lidia

    Journal of clinical medicine

    2022  Volume 11, Issue 16

    Abstract: Background: The aim of the study is to evaluate selected biomarkers of bone turnover, inflammation, neutrophil trap and factors predisposing haemophiliacs to bone loss, and to analyse their relationship with clinical features, treatment and ... ...

    Abstract Background: The aim of the study is to evaluate selected biomarkers of bone turnover, inflammation, neutrophil trap and factors predisposing haemophiliacs to bone loss, and to analyse their relationship with clinical features, treatment and complications.
    Methods: The levels of interleukin 6 (IL-6); citrullinated histone (CH3); osteocalcin (BGLAP); bone alkaline phosphatase (BALP); N-terminal procollagen type I propeptide (P1NP); and C-terminal collagen type I telopeptide (C1CP) were examined in 60 patients with haemophilia.
    Results: The cut-off value for BGLAP is 26.41 ng/mL, and 929.7 pg/mL for CH3. There is a statistically significant difference between BGLAP, BALP, C1CP and CH3 concentrations, depending on the prophylaxis used. The median concentration of BGLAP in patients taking the factor on demand is 28.0 ng/mL, BALP 322.5 U/L, C1CP 191.2 ng/mL and CH3 1114.4 pg/mL. In patients taking recombinant coagulation factor VIII/IX as prophylaxis of bleeding, the median BGLAP concentrations are 35.9 ng/mL, BALP 280.9 U/L, C1CP 161.6 ng/mL and CH3 952.5 pg/mL. BGLAP and BALP concentrations are dependent on the development of haemophilic arthropathic.
    Conclusions: The concentrations of selected markers of bone turnover and NETs may help to identify patients at particular risk of developing haemophilic arthropathy and bone metabolic turnover abnormalities.
    Language English
    Publishing date 2022-08-12
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm11164711
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Potential Biochemical Markers and Radiomorphometric Indices as Predictors of Reduced Bone Mass in Patients with Congenital Hemophilia.

    Czajkowska, Sylwia / Rupa-Matysek, Joanna / Wojtasińska, Ewelina / Nijakowski, Kacper / Gil, Lidia / Surdacka, Anna / Kulczyk, Tomasz

    Journal of clinical medicine

    2022  Volume 11, Issue 12

    Abstract: Background: The study aimed to evaluate radiomorphometric indices derived from panoramic X-rays and selected blood markers of bone turnover and neutrophil extracellular traps, with a view to identifying hemophilic patients at risk of developing ... ...

    Abstract Background: The study aimed to evaluate radiomorphometric indices derived from panoramic X-rays and selected blood markers of bone turnover and neutrophil extracellular traps, with a view to identifying hemophilic patients at risk of developing osteoporosis. Methods: The study consisted of 50 adult men with hemophilia A and B (mild, moderate, and severe). The control group consisted of 25 healthy adult men. In both groups, blood samples were collected to determine concentrations of citrullinated histone H3 (CH3) and osteocalcin (BGLAP) with ELISA tests, and panoramic X-rays were obtained. Images were imported into AudaXCeph software to calculate two radiomorphometric indices: mental index (MI) and panoramic mandibular index (PMI). Concentrations of BGLAP and CH3 were compared with MI and PMI values in patients with and without hemophilia. Results: There were statistically significant differences in BGLAP, CH3, and PMI between the study and the control group (p < 0.05). Multivariate logistic regression analysis showed a predictive value for PMI, BGLAP, and CH3.The ROC curve with cutoff point (Youden index) at 0.40—PMI was calculated. No correlation was observed for the PMI index in any particular subgroup of patients. No correlation between MI and BGLAP/CH3 was observed. Conclusions: Simultaneous use of PMI value and BGLAP and CH3 levels may allow the identification of patients with hemophilia who requirea detailed diagnosis of osteoporosis with DXA.
    Language English
    Publishing date 2022-06-13
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm11123391
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  5. Article ; Online: Evaluation of thromboelastometry parameters as predictive markers for sinusoidal obstruction syndrome in patients undergoing allogeneic stem cell transplantation for acute leukaemia.

    Rupa-Matysek, Joanna / Gil, Lidia / Wojtasińska, Ewelina / Kanduła, Zuzanna / Nowicki, Adam / Matuszak, Magdalena / Komarnicki, Mieczysław

    Oncotarget

    2017  Volume 8, Issue 35, Page(s) 60001–60014

    Abstract: Hepatic sinusoidal obstruction syndrome (previously named veno-occlusive disease, SOS/VOD) is a serious complication of allogeneic stem cell transplantation (HSCT). Early identification of patients at risk of SOS/VOD may possibly improve the outcome and ... ...

    Abstract Hepatic sinusoidal obstruction syndrome (previously named veno-occlusive disease, SOS/VOD) is a serious complication of allogeneic stem cell transplantation (HSCT). Early identification of patients at risk of SOS/VOD may possibly improve the outcome and reduce mortality. Rotation thromboelastometry (ROTEM) is global assay allowing for the precise assessment of both bleeding and thrombotic conditions, however, its usefulness in patients undergoing HSCT for acute leukaemia has not been studied. We evaluated the thromboelastometry parameters in patients undergoing allogeneic HSCT for acute leukaemia to identify candidate biomarkers of SOS/VOD occurrence. ROTEM assays (INTEM, EXTEM, FIBTEM, APTEM) were performed on day -10, on the day of stem cell infusion (day 0) and on days +12 and +28 post-HSCT. The diagnosis of SOS/VOD was based on the Baltimore criteria. Seven patients (26%) developed SOS/VOD. On day +12, the patients with SOS/VOD had statistically significant longer INTEM-CT (clotting time, 199 ± 33.41vs166 ± 23.65s,
    Language English
    Publishing date 2017-08-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2560162-3
    ISSN 1949-2553 ; 1949-2553
    ISSN (online) 1949-2553
    ISSN 1949-2553
    DOI 10.18632/oncotarget.18499
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The relationship between mean platelet volume and thrombosis recurrence in patients diagnosed with antiphospholipid syndrome.

    Rupa-Matysek, Joanna / Gil, Lidia / Wojtasińska, Ewelina / Ciepłuch, Katarzyna / Lewandowska, Maria / Komarnicki, Mieczysław

    Rheumatology international

    2014  Volume 34, Issue 11, Page(s) 1599–1605

    Abstract: Increased mean platelet volume (MPV) is associated with platelet reactivity and is a predictor of cardiovascular risk and unprovoked venous thromboembolism. The aim of our study was to evaluate MPV in patients with confirmed antiphospholipid antibody ... ...

    Abstract Increased mean platelet volume (MPV) is associated with platelet reactivity and is a predictor of cardiovascular risk and unprovoked venous thromboembolism. The aim of our study was to evaluate MPV in patients with confirmed antiphospholipid antibody syndrome (APS) and to identify the correlation between the value of MPV and the recurrence of thrombosis. The studied group consists of 247 patients with a history of thrombosis and/or pregnancy loss (median age 38, range 18-66 years) classified as APS group (n = 70) or APS negative patients (n = 177) according to the updated Sapporo criteria. The control group consisted of 98 healthy subjects. MPV was significantly higher in the group of patients with clinically and laboratory confirmed APS (median 7.85, range 4.73-12.2 fl) in comparison with the controls. It was also higher than in APS negative patients (7.61, range 5.21-12.3 fl). APS patients with triple positivity for antiphospholipid antibodies with respect to Miyakis classification categories had higher MPV values than other APS patients (9.69 ± 1.85 vs. 7.29 ± 1.3 fl, p = 0.001). Recurrent thrombotic episodes were observed in 83 patients, but among the triple positive high-risk patients with APS in 80 % cases (p = 0.0046). In receiver operating characteristic curve analysis, the value of MPV level for thrombosis recurrence prediction in the APS group with sensitivity of 86 % and specificity of 82 % was 7.4 fl. In the multivariate logistic regression model, MPV above 7.4 fl (OR 3.65; 95 % CI 1.38-9.64, p = 0.009) significantly predicts thrombosis recurrence. Our results identify the value of MPV as a prognostic factor of thrombosis recurrence in patients with APS.
    MeSH term(s) Abortion, Spontaneous/blood ; Abortion, Spontaneous/etiology ; Adolescent ; Adult ; Aged ; Antiphospholipid Syndrome/blood ; Antiphospholipid Syndrome/complications ; Antiphospholipid Syndrome/diagnosis ; Area Under Curve ; Biomarkers/blood ; Case-Control Studies ; Chi-Square Distribution ; Female ; Humans ; Logistic Models ; Male ; Mean Platelet Volume ; Middle Aged ; Multivariate Analysis ; Odds Ratio ; Platelet Activation ; Predictive Value of Tests ; Pregnancy ; ROC Curve ; Recurrence ; Risk Factors ; Thrombosis/blood ; Thrombosis/diagnosis ; Thrombosis/etiology ; Young Adult
    Chemical Substances Biomarkers
    Language English
    Publishing date 2014-03-27
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 8286-7
    ISSN 1437-160X ; 0172-8172
    ISSN (online) 1437-160X
    ISSN 0172-8172
    DOI 10.1007/s00296-014-2996-0
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  7. Article ; Online: Coagulation profile in patients with H1N1 influenza A infection undergoing treatment for haematological malignancies.

    Rupa-Matysek, Joanna / Gil, Lidia / Wojtasińska, Ewelina / Zajdel, Katarzyna / Ciepłuch, Katarzyna / Komarnicki, Mieczysław

    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

    2014  Volume 25, Issue 8, Page(s) 912–915

    Abstract: Patients with haematological malignancies receiving concurrent treatment or after allogeneic stem cell transplantation (HSCT) are considered to be at increased risk for acquiring influenza A (H1N1) infection (pH1N1) and influenza-associated complications ...

    Abstract Patients with haematological malignancies receiving concurrent treatment or after allogeneic stem cell transplantation (HSCT) are considered to be at increased risk for acquiring influenza A (H1N1) infection (pH1N1) and influenza-associated complications leading to increased mortality. We report of a series of haematological patients with severe course of laboratory-confirmed pH1N1, including two patients after HSCT. Coagulation assays were conducted and the association between coagulation activation and poor outcome pH1N1 infection was found in the analyzed group.
    MeSH term(s) Adult ; Aged ; Antineoplastic Agents/therapeutic use ; Biomarkers/blood ; Blood Coagulation ; Blood Coagulation Tests ; Female ; Hematologic Neoplasms/blood ; Hematologic Neoplasms/complications ; Hematologic Neoplasms/mortality ; Hematologic Neoplasms/therapy ; Hematopoietic Stem Cell Transplantation ; Humans ; Influenza A Virus, H1N1 Subtype/physiology ; Influenza, Human/blood ; Influenza, Human/complications ; Influenza, Human/mortality ; Influenza, Human/therapy ; Male ; Middle Aged ; Prognosis ; Survival Analysis ; Transplantation, Homologous
    Chemical Substances Antineoplastic Agents ; Biomarkers
    Language English
    Publishing date 2014-12
    Publishing country England
    Document type Journal Article
    ZDB-ID 1033551-1
    ISSN 1473-5733 ; 0957-5235
    ISSN (online) 1473-5733
    ISSN 0957-5235
    DOI 10.1097/MBC.0000000000000139
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Assessment of coagulation profile by thromboelastometry in adult patients with cyanotic congenital heart disease.

    Rupa-Matysek, Joanna / Trojnarska, Olga / Gil, Lidia / Szczepaniak-Chicheł, Ludwina / Wojtasińska, Ewelina / Tykarski, Andrzej / Grajek, Stefan / Komarnicki, Mieczysław

    International journal of cardiology

    2016  Volume 202, Page(s) 556–560

    Abstract: Background: Patients with cyanotic congenital heart disease (CCHD) have an increased risk of bleeding and thrombotic complications. Prolonged conventional coagulation screening parameters, such as activated partial thromboplastin time or prothrombin ... ...

    Abstract Background: Patients with cyanotic congenital heart disease (CCHD) have an increased risk of bleeding and thrombotic complications. Prolonged conventional coagulation screening parameters, such as activated partial thromboplastin time or prothrombin time, are reported in less than 20% of CCHD patients.
    Methods: The aim of this study was to determine the haemostatic abnormalities in 32 adult patients with CCHD by rotation thromboelastometry (ROTEM) with assessment of coagulation dynamic properties, as a guide for perioperative prophylaxis or haemostatic therapy. The control group consisted of 35 healthy subjects.
    Results: Our results suggest that CCHD patients, in comparison to healthy controls, had a tendency to hypocoagulate with delayed activation of haemostasis and clot formation, initiated by both intrinsic and extrinsic activators. The growth of the clot was slower and the clot firmness was decreased, which may additionally contribute to bleeding diathesis. Moreover, the clot lysis readings suggest higher clot stability in the CCHD group. All velocity parameters were markedly lower in the CCHD patients, indicating a decreased rate of clot formation. Although coagulation tests and platelet count were normal, the usefulness of rotation thromboelastometry in monitoring or guiding therapy in CCHD patients is demonstrated.
    Conclusion: In conclusion, our results provide new insights into the data on hypocoagulation with impaired clot lysis in adult CCHD patients as determined by ROTEM. Our findings may assist in determining the optimal management of patients with CCHD undergoing surgery.
    MeSH term(s) Adult ; Aged ; Anticoagulants/therapeutic use ; Blood Coagulation/physiology ; Blood Coagulation Tests/methods ; Cyanosis/blood ; Cyanosis/complications ; Cyanosis/pathology ; Female ; Fibrinogen/physiology ; Fibrinolysis/physiology ; Heart Diseases/blood ; Heart Diseases/complications ; Heart Diseases/congenital ; Heart Diseases/pathology ; Hemorrhage/blood ; Hemorrhage/complications ; Hemorrhage/pathology ; Hemostatic Techniques ; Humans ; Male ; Middle Aged ; Partial Thromboplastin Time/methods ; Perioperative Care ; Prothrombin Time ; Thrombelastography/methods ; Thrombosis/blood ; Thrombosis/complications ; Thrombosis/pathology ; Warfarin/therapeutic use ; Young Adult
    Chemical Substances Anticoagulants ; Warfarin (5Q7ZVV76EI) ; Fibrinogen (9001-32-5)
    Language English
    Publishing date 2016-01-01
    Publishing country Netherlands
    Document type Letter
    ZDB-ID 779519-1
    ISSN 1874-1754 ; 0167-5273
    ISSN (online) 1874-1754
    ISSN 0167-5273
    DOI 10.1016/j.ijcard.2015.09.082
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  9. Article ; Online: Bleeding complications after arthroscopy in a JAK2V617F-positive patient with essential thrombocythemia and acquired von Willebrand syndrome (AVWS).

    Rupa-Matysek, Joanna / Lewandowski, Krzysztof / Lewandowska, Maria / Wojtasińska, Ewelina / Wojtaszewska, Marzena Liliana / Walczak, Michał / Bykowska, Ksenia / Komarnicki, Mieczysław

    International journal of hematology

    2015  Volume 101, Issue 4, Page(s) 405–410

    Abstract: Acquired von Willebrand syndrome (AVWS) is an acquired bleeding disorder with clinical and laboratory features similar to those of the inherited form of the disease. AVWS is reported in many disorders, most frequently in myeloproliferative neoplasms and ... ...

    Abstract Acquired von Willebrand syndrome (AVWS) is an acquired bleeding disorder with clinical and laboratory features similar to those of the inherited form of the disease. AVWS is reported in many disorders, most frequently in myeloproliferative neoplasms and in, among others, essential thrombocythemia (ET). Interestingly, ET is associated with both the thrombotic and haemorrhagic complications, which occur in 20 % and 5-30 % of patients, respectively. The present report concerns a 38-year-old man, suffering from ET, who presented with two episodes of post-arthroscopic joint bleeding after synovectomy required for the treatment of synovial hypertrophy and chronic left knee joint synovitis. We discuss the current diagnostic approaches, as well as the risk factors predisposing to bleeding and its management, in patients with essential thrombocythemia.
    MeSH term(s) Adult ; Arthroscopy/adverse effects ; Hemorrhage/diagnosis ; Hemorrhage/etiology ; Hemorrhage/genetics ; Humans ; Janus Kinase 2/genetics ; Knee Joint/surgery ; Male ; Platelet Count ; Point Mutation ; Synovitis/complications ; Synovitis/diagnosis ; Synovitis/genetics ; Synovitis/surgery ; Thrombocythemia, Essential/complications ; Thrombocythemia, Essential/diagnosis ; Thrombocythemia, Essential/genetics ; von Willebrand Diseases/complications ; von Willebrand Diseases/diagnosis ; von Willebrand Diseases/genetics ; von Willebrand Factor/analysis
    Chemical Substances von Willebrand Factor ; JAK2 protein, human (EC 2.7.10.2) ; Janus Kinase 2 (EC 2.7.10.2)
    Language English
    Publishing date 2015-04
    Publishing country Japan
    Document type Case Reports ; Journal Article
    ZDB-ID 1076875-0
    ISSN 1865-3774 ; 0917-1258 ; 0925-5710
    ISSN (online) 1865-3774
    ISSN 0917-1258 ; 0925-5710
    DOI 10.1007/s12185-014-1707-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Inhibitory effects of bortezomib on platelet aggregation in patients with multiple myeloma.

    Rupa-Matysek, Joanna / Gil, Lidia / Wojtasińska, Ewelina / Nowicki, Adam / Dytfeld, Dominik / Kaźmierczak, Maciej / Komarnicki, Mieczysław

    Thrombosis research

    2014  Volume 134, Issue 2, Page(s) 404–411

    Abstract: Introduction: Multiple myeloma (MM) therapy affects prothrombotic and anticoagulant processes. Patients receiving thalidomide, especially in combination with steroids, are at increased risk of venous thromboembolism (VTE), while the incidence of VTE on ... ...

    Abstract Introduction: Multiple myeloma (MM) therapy affects prothrombotic and anticoagulant processes. Patients receiving thalidomide, especially in combination with steroids, are at increased risk of venous thromboembolism (VTE), while the incidence of VTE on bortezomib is low. In vitro studies indicate that bortezomib causes a reduction in ADP-induced platelet aggregation.
    Objectives: To analyse the influence of bortezomib on platelet aggregation induced by various agonists in patients with MM.
    Patients and methods: A total of 30 patients (median age 57.5years) with relapsed/refractory MM receiving bortezomib-based regimens were analysed. Optical platelet aggregometry was performed with the agonists collagen, ADP and ristocetin and measured over two 21-day cycles. The results from two groups: those treated with bortezomib and thalidomide (BT group, n=11) and those without thalidomide (B group, n=19) were analysed.
    Results: During the second cycle, significantly decreased platelet aggregation was observed in the B group: 5μM ADP (p=0.0285, day 1 versus 8); 3.5μM ADP (p=0.0005, day 1 versus 8 and day 1 versus 11), collagen (p=0.0014, day 4 versus 8, day 4 versus 11), 1.25mg/ml ristocetin (p=0.0017, day 1 versus 8 and day 1 versus 11). Agonist-induced platelet aggregation tended to be reduced over time during the 1st cycle in group B. In the thalidomide group, significant platelet aggregation inhibition by collagen only was found. Transient reduction in platelet count was observed in all patients, but more prominently in group B.
    Conclusion: The inhibitory effects of prolonged exposure of bortezomib on platelet aggregation were demonstrated in relapsed/refractory MM patients, but antithrombotic activity of bortezomib should be clarified in further prospective studies.
    MeSH term(s) Adult ; Aged ; Angiogenesis Inhibitors/adverse effects ; Angiogenesis Inhibitors/therapeutic use ; Antineoplastic Agents/pharmacology ; Antineoplastic Agents/therapeutic use ; Boronic Acids/pharmacology ; Boronic Acids/therapeutic use ; Bortezomib ; Female ; Humans ; Male ; Middle Aged ; Multiple Myeloma/blood ; Multiple Myeloma/drug therapy ; Platelet Aggregation/drug effects ; Platelet Function Tests ; Prospective Studies ; Pyrazines/pharmacology ; Pyrazines/therapeutic use ; Thalidomide/adverse effects ; Thalidomide/therapeutic use ; Venous Thromboembolism/chemically induced
    Chemical Substances Angiogenesis Inhibitors ; Antineoplastic Agents ; Boronic Acids ; Pyrazines ; Thalidomide (4Z8R6ORS6L) ; Bortezomib (69G8BD63PP)
    Language English
    Publishing date 2014-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 121852-9
    ISSN 1879-2472 ; 0049-3848
    ISSN (online) 1879-2472
    ISSN 0049-3848
    DOI 10.1016/j.thromres.2014.05.032
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