2016
Thrombosis in thrombocythemic Ph-myeloproliferations is associated with higher platelet count prior to the event: results of analyses of prothrombotic risk factors from a registry of patients treated with anagrelide
SCHWARZ, Jiří, Petra OVESNÁ, Olga ČERNÁ, Jarmila KISSOVÁ, Jacqueline SOUKUPOVÁ MAALOUFOVÁ et. al.Základní údaje
Originální název
Thrombosis in thrombocythemic Ph-myeloproliferations is associated with higher platelet count prior to the event: results of analyses of prothrombotic risk factors from a registry of patients treated with anagrelide
Autoři
SCHWARZ, Jiří (203 Česká republika), Petra OVESNÁ (203 Česká republika, domácí), Olga ČERNÁ (203 Česká republika), Jarmila KISSOVÁ (203 Česká republika, domácí), Jacqueline SOUKUPOVÁ MAALOUFOVÁ (203 Česká republika), Yvona BRYCHTOVÁ (203 Česká republika), Michael DOUBEK (203 Česká republika, domácí), Libor ČERVINEK (203 Česká republika, domácí), Eduard CMUNT (203 Česká republika), Petr DULÍČEK (203 Česká republika), Vít CAMPR (203 Česká republika), Leoš KŘEN (203 Česká republika, domácí) a Miroslav PENKA (203 Česká republika, garant, domácí)
Vydání
European Journal of Haematology, Hoboken, Wiley-Blackwell, 2016, 0902-4441
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.653
Kód RIV
RIV/00216224:14110/16:00089657
Organizační jednotka
Lékařská fakulta
UT WoS
000367920800016
EID Scopus
2-s2.0-84955193963
Klíčová slova anglicky
myeloproliferative disorders; platelets; JAK2; thrombophilia; thrombosis; anagrelide
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 4. 8. 2016 16:32, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Controversies still exist regarding definition of the thrombotic risks in Ph-(BCR/ABL1-) myeloproliferative disorders with thrombocythemia (MPD-T). Platelet counts at diagnosis are currently not taken as a risk factor of thrombosis. In our cohort of 1179 patients with MPD-T, prospectively registered for anagrelide treatment, we found that the median platelet count prior to the thrombotic event was significantly higher than at time points without any ensuing thrombosis (453 vs. 400 9 10(9)/L, P < 0.001), albeit higher platelet counts at diagnosis tended to be connected with fewer thrombotic events (in contrast to WBC counts at diagnosis). The JAK2(V617F) mutation predicted both arterial and venous events, while age >65 yr, hypertension, diabetes mellitus, smoking, elevated triglyceride and homocysteine levels predicted arterial events only. For venous events, the specific thrombophilic risk factors (factor V `Leiden' and others), antiphospholipid antibodies, and elevated factor VIII levels played a major role. During anagrelide treatment (+/- aspirin), we documented a decrease in both venous (6.7-fold) and arterial events (1.8-fold), while bleeding (mostly minor events) increased twofold compared to history. Our results suggest that keeping platelet counts at low levels may be a meaningful therapeutic measure to prevent thrombosis, although their counts at diagnosis lack any prognostic value.