High levels of factor VIII activity in patients with acquired hemophilia A in remission are associated with unusually low coagulation potentials

被引:1
|
作者
Shibasaki, Fumitaka [1 ]
Takeyama, Masahiro [2 ]
Ogiwara, Kenichi [2 ]
Furukawa, Shoko [2 ]
Nakajima, Yuto [2 ]
Shimonishi, Naruto [2 ]
Nogami, Keiji [2 ]
机构
[1] Nara Med Univ, Kashihara, Nara, Japan
[2] Nara Med Univ, Dept Pediat, 840 Shijo Cho, Kashihara, Nara 6348522, Japan
关键词
Acquired hemophilia A; Factor VIII; Anti-factor VIII antibody; Blood coagulation test; Factor VIII activity; VON-WILLEBRAND-FACTOR; HIGH PLASMA-LEVELS; THROMBIN GENERATION; VENOUS THROMBOEMBOLISM; 1ST REPORT; THROMBOMODULIN; RISK; ENDOTHELIUM; BINDING;
D O I
10.1007/s12185-022-03528-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Elevated factor VIII activity (FVIII:C) is often observed in patients with acquired hemophilia A (PwAHA) in remission. However, comprehensive coagulation potentials in this patient group remain to be investigated.Aim To evaluate comprehensive coagulation potentials in PwAHA.Methods We investigated coagulation function in eleven PwAHA with high FVIII:C (> 150 IU/dL) using thrombin generation assay (TGA) and/or rotational thromboelastometry (ROTEM), and compared findings with results obtained from contrived samples generated by spiking recombinant FVIII.Results The median FVIII:C and FVIII inhibitor titers during remission in enrolled PwAHA were 206 IU/dL and 0.44 BU/mL, respectively. In all patients, lag time and time to peak were either prolonged or normal compared to contrived samples corresponding to their FVIII:C. However, higher values of peak thrombin and endogenous thrombin potentials compared to contrived samples were observed in two patients. ROTEM parameters were within normal ranges in all cases. One patient (FVIII:C 171 IU/dL) developed venous thrombosis and pulmonary embolism, but TGA parameters showed low or normal coagulation potential compared to contrived samples corresponding to his FVIII:C.Conclusion PwAHA with high FVIII:C could exhibit lower coagulation potentials than those corresponding to their FVIII:C.
引用
收藏
页码:669 / 677
页数:9
相关论文
共 50 条
  • [21] Modeling to Predict Factor VIII Levels Associated with Zero Bleeds in Patients with Severe Hemophilia A Initiated on Tertiary Prophylaxis
    Chowdary, Pratima
    Fischer, Kathelijn
    Collins, Peter W.
    Cotterill, Amy
    Konkle, Barbara A.
    Blanchette, Victor
    Pipe, Steven W.
    Berntorp, Erik
    Wolfsegger, Martin
    Engl, Werner
    Spotts, Gerald
    THROMBOSIS AND HAEMOSTASIS, 2020, 120 (05) : 728 - 736
  • [22] High levels of coagulation factors and venous thrombosis risk: strongest association for factor VIII and von Willebrand factor
    Rietveld, I. M.
    Lijfering, W. M.
    le Cessie, S.
    Bos, M. H. A.
    Rosendaal, F. R.
    Reitsma, P. H.
    Cannegieter, S. C.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2019, 17 (01) : 99 - 109
  • [23] A limited sampling strategy for estimating individual pharmacokinetic parameters of coagulation factor VIII in patients with hemophilia A
    Bolon-Larger, Magali
    Chamouard, Valerie
    Bressolle, Francoise
    Boulieu, Roselyne
    THERAPEUTIC DRUG MONITORING, 2007, 29 (01) : 20 - 26
  • [24] High coagulation factor VIII and von Willebrand factor in patients with lymphoma and leukemia
    Martin Mohren
    Kathleen Jentsch-Ullrich
    Michael Koenigsmann
    Siegfried Kropf
    Enrico Schalk
    Gerd Lutze
    International Journal of Hematology, 2016, 103 : 189 - 195
  • [25] Immunological characterization of factor VIII autoantibodies in patients with acquired hemophilia A in the presence or absence of underlying disease
    Matsumoto, T
    Shima, M
    Fukuda, K
    Nogami, K
    Giddings, JC
    Murakami, T
    Tanaka, I
    Yoshioka, A
    THROMBOSIS RESEARCH, 2001, 104 (06) : 381 - 388
  • [26] Coagulation factor XII, XI, and VIII activity levels and secondary events after first ischemic stroke
    Rohmann, Jessica L.
    Huo, Shufan
    Sperber, Pia S.
    Piper, Sophie K.
    Rosendaal, Frits R.
    Heuschmann, Peter U.
    Endres, Matthias
    Liman, Thomas G.
    Siegerink, Bob
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2020, 18 (12) : 3316 - 3324
  • [27] Familial clustering of high factor VIII levels in patients with venous thromboembolism
    Schambeck, CM
    Hinney, K
    Haubitz, I
    Taleghani, BM
    Wahler, D
    Keller, F
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (02) : 289 - 292
  • [28] High factor VIII antigen levels increase the risk of venous thrombosis but are not associated with polymorphisms in the von Willebrand factor and factor VIII gene
    Kamphuisen, PW
    Eikenboom, JCJ
    Rosendaal, FR
    Koster, T
    Blann, AD
    Vos, HL
    Bertina, RM
    BRITISH JOURNAL OF HAEMATOLOGY, 2001, 115 (01) : 156 - 158
  • [29] Partial F8 gene duplication (factor VIII Padua) associated with high factor VIII levels and familial thrombophilia
    Simioni, Paolo
    Cagnin, Stefano
    Sartorello, Francesca
    Sales, Gabriele
    Pagani, Luca
    Bulato, Cristiana
    Gavasso, Sabrina
    Nuzzo, Francesca
    Chemello, Francesco
    Radu, Claudia M.
    Tormene, Daniela
    Spiezia, Luca
    Hackeng, Tilman M.
    Campello, Elena
    Castoldi, Elisabetta
    BLOOD, 2021, 137 (17) : 2383 - 2393
  • [30] T cell recognition of the A2 domain of coagulation factor VIII in hemophilia patients and healthy subjects
    Hu, GL
    Okita, DK
    Conti-Fine, BM
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (11) : 1908 - 1917