TY - JOUR
T1 - The bleeding phenotype in people with nonsevere hemophilia
AU - Kloosterman, Fabienne R.
AU - Zwagemaker, Anne-Fleur
AU - Bagot, Catherine N.
AU - Beckers, Erik A. M.
AU - Castaman, Giancarlo
AU - Cnossen, Marjon H.
AU - Collins, Peter W.
AU - Hay, Charles
AU - Hof, Michel
AU - Gorkom, Britta Laros-Van
AU - Leebeek, Frank W. G.
AU - Male, Christoph
AU - Meijer, Karina
AU - Pabinger, Ingrid
AU - Shapiro, Susan
AU - Coppens, Michiel
AU - Fijnvandraat, Karin
AU - Gouw, Samantha C.
AU - Fijnvandraat, Karin
AU - Coppens, Michiel
AU - Gouw, Samantha C.
AU - Leebeek, Frank W. G.
AU - Kruip, Marieke
AU - Cnossen, Marjon H.
AU - Meijer, Karina
AU - Eikenboom, Jeroen
AU - Smiers, Frans J. W.
AU - Beckers, Erik A. M.
AU - Nieuwenhuizen, Laurens
AU - Brons, Paul
AU - Gorkom, Britta Laros-Van
AU - Castaman, Giancarlo
AU - Collins, Peter
AU - Bagot, Catherine N.
AU - Hay, Charles
AU - Shapiro, Susan
AU - Boyce, Sara
AU - Male, Christoph
AU - Pabinger, Ingrid
AU - the DYNAMO study group
AU - Jackson, Shannon
N1 - Funding Information: This work was funded by a grant from Novo Nordisk and supported by the Parelsnoer clinical biobank Hemophilia at the Health-RI (funded by the Ministry of Health, Welfare and Sport). The funding sponsor had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; or preparation, review, and approval of the manuscript. Funding Information: Conflict-of-interest disclosure: G.C. is a speaker at company symposia during scientific meetings for Bayer, Grifols, LFB, Roche, Sobi, Novo Nordisk, Werfen, and Kedrion; has received research funding directly to his institution from CSL Behring, Pfizer, and Sobi; and, during the last 2 years, has participated in advisory boards of Bayer, Takeda, CSL Behring, Novo Nordisk, Pfizer, Roche, Sanofi, SOBI, and UniQure. M.H.C. has received investigator-initiated research and travel grants as well as speaker fees over the years from the Netherlands Organisation for Scientific Research, the Netherlands Organization for Health Research and Development, the Dutch “Innovatiefonds Zorgverzekeraars,” Baxter/Baxalta/Shire/ Takeda, Pfizer, Bayer Schering Pharma, CSL Behring, Sobi Biogen, Novo Nordisk, Novartis, and Nordic Pharma; and has served as a steering board member for Roche, Bayer and Novartis (all grants, awards, and fees go to the Erasmus MC). P.W.C. had received research support from CSL Behring; and consultancy fees from CSL Behring, Novo Nordisk, Sobi, and Roche. F.W.G.L. received unrestricted research grants from CSL Behring, Shire/Takeda, Sobi, and uniQure; is a consultant for CSL Behring, Shire/Takeda, Bio-Marin, and uniQure, of which the fees go to the University; and was a Data and Safety Monitoring Board member of a study sponsored by Roche. C.M. reports consultancy or speaker for Bayer, Biotest, CSL Behring, Grifols, Novo Nordisk, Roche, and Takeda; has received travel support from Bayer, Biotest, CSL Behring, and Novo Nordisk; and his institution has received research support from Bayer, Baxalta/Shire/Takeda, Biotest, CSL Behring, Novo Nordisk, and Sobi. K.M. received speaker fees from Alexion, Bayer, and CSL Behring; fees for participation in trial steering committee for Bayer; consulting fees from UniQure; and fees for participation in data monitoring and end point adjudication committee for Octapharma (all fees paid to her institution). I.P. has received honoraria for lectures and/or advisory boards from Bayer, Biotest, CSL Behring, Sobi, Roche, Takeda, Pfizer, and Novo Nordisk; and her institution has received research grants from CSL Behring, Novo Nordisk, Sobi, and Takeda. M.C. has received financial support for research from Bayer, CSL Behring, Daiichi Sankyo, Portola/Alexion, Roche, Sanquin Blood Supply, and UniQure; and consultancy or lecturing Publisher Copyright: © 2022 by The American Society of Hematology.
PY - 2022/7/26
Y1 - 2022/7/26
N2 - Detailed information on the onset, frequency, and severity of bleeding in nonsevere hemophilia is limited. We aimed to assess the bleeding phenotype of persons with nonsevere hemophilia and to analyze the association between baseline factor VIII/IX (FVIII/IX) levels and the joint bleeding rate. In the DYNAMO (Dynamic Interplay Between Bleeding Phenotype and Baseline Factor Level in Moderate and Mild Hemophilia A and B) study, an international multicenter cohort, we included males with nonsevere hemophilia (FVIII/IX, 0.02-0.35 IU/mL) aged 12 to 55 years. Information on age at first treated (joint) bleed, annual bleeding rates (ABRs), and annual joint bleeding rates (AJBRs) was collected from the medical files. The association between baseline FVIII/IX levels and the joint bleeding rate was assessed by using a frailty model for recurrent events. In total, 304 persons (70 with moderate hemophilia and 234 with mild hemophilia) were included. The median age was 38 years (interquartile range [IQR], 25-49 years), and the median baseline FVIII/IX level was 0.12 IU/mL (IQR, 0.05-0.21 IU/mL). In total, 245 (81%) persons had experienced at least 1 bleed, and 156 (51%) had experienced at least 1 joint bleed. The median age at first bleed and first joint bleed was 8 and 10 years, respectively. The median ABR and AJBR was 0.2 (IQR, 0.1-0.5) and 0.0 (IQR, 0.0-0.2). From baseline FVIII/IX levels 0.02 to 0.05 IU/mL to >0.25 IU/mL, the median ABR decreased from 0.6 (IQR, 0.2-1.4) to 0.1 (IQR, 0.0-0.2) and the AJBR from 0.2 (IQR, 0.0-0.4) to 0.0 (IQR, 0.0-0.0). Baseline FVIII/IX was inversely associated with the joint bleeding rate (P < .001). Low bleeding rates were observed in persons with nonsevere hemophilia. However, one-half of all adolescents and adults had experienced a joint bleed.
AB - Detailed information on the onset, frequency, and severity of bleeding in nonsevere hemophilia is limited. We aimed to assess the bleeding phenotype of persons with nonsevere hemophilia and to analyze the association between baseline factor VIII/IX (FVIII/IX) levels and the joint bleeding rate. In the DYNAMO (Dynamic Interplay Between Bleeding Phenotype and Baseline Factor Level in Moderate and Mild Hemophilia A and B) study, an international multicenter cohort, we included males with nonsevere hemophilia (FVIII/IX, 0.02-0.35 IU/mL) aged 12 to 55 years. Information on age at first treated (joint) bleed, annual bleeding rates (ABRs), and annual joint bleeding rates (AJBRs) was collected from the medical files. The association between baseline FVIII/IX levels and the joint bleeding rate was assessed by using a frailty model for recurrent events. In total, 304 persons (70 with moderate hemophilia and 234 with mild hemophilia) were included. The median age was 38 years (interquartile range [IQR], 25-49 years), and the median baseline FVIII/IX level was 0.12 IU/mL (IQR, 0.05-0.21 IU/mL). In total, 245 (81%) persons had experienced at least 1 bleed, and 156 (51%) had experienced at least 1 joint bleed. The median age at first bleed and first joint bleed was 8 and 10 years, respectively. The median ABR and AJBR was 0.2 (IQR, 0.1-0.5) and 0.0 (IQR, 0.0-0.2). From baseline FVIII/IX levels 0.02 to 0.05 IU/mL to >0.25 IU/mL, the median ABR decreased from 0.6 (IQR, 0.2-1.4) to 0.1 (IQR, 0.0-0.2) and the AJBR from 0.2 (IQR, 0.0-0.4) to 0.0 (IQR, 0.0-0.0). Baseline FVIII/IX was inversely associated with the joint bleeding rate (P < .001). Low bleeding rates were observed in persons with nonsevere hemophilia. However, one-half of all adolescents and adults had experienced a joint bleed.
UR - http://www.scopus.com/inward/record.url?scp=85134796985&partnerID=8YFLogxK
U2 - https://doi.org/10.1182/bloodadvances.2022007620
DO - https://doi.org/10.1182/bloodadvances.2022007620
M3 - Article
C2 - 35533261
SN - 2473-9529
VL - 6
SP - 4256
EP - 4265
JO - Blood advances
JF - Blood advances
IS - 14
ER -