@article{b57c3a0b0b6c42398b7cc3e5598d5d4b,
title = "Factor VIII prophylaxis effects outweigh other hemostasis contributors in predicting severe haemophilia A joint outcomes",
abstract = "Introduction: The Joint Outcome Study (JOS) demonstrated that previously untreated children with severe haemophilia A treated with prophylactic factor VIII (FVIII) concentrate had superior joint outcomes at age 6 years compared to those children treated episodically for bleeding. However, variation in joint outcome within each treatment arm was not well explained. Aim: In this study, we sought to better understand variation in joint outcomes at age 6 years in participants of the JOS. Methods: We evaluated the influence of FVIII half-life, treatment adherence, constitutional coagulant and anticoagulant proteins, and global assays on joint outcomes (number of joint bleeds, total number of bleeds, total MRI score and joint physical exam score). Logistic regression was used to evaluate the association of variables with joint failure status on MRI, defined as presence of subchondral cyst, surface erosion or joint-space narrowing. Each parameter was also correlated with each joint outcome using Spearman correlations. Results: Prophylaxis treatment arm and FVIII trough were each found to reduce risk of joint failure on univariate logistic regression analysis. When controlling for treatment arm, FVIII trough was no longer significant, likely because of the high level of covariation between these variables. We found no consistent correlation between any laboratory assay performed and any joint outcome parameter measured. Conclusion: In the JOS, the effect of prescribed prophylactic FVIII infusions on joint outcome overshadowed the contribution of treatment adherence, FVIII half-life, global assays of coagulation and constitutional coagulation proteins. (ClinicalTrials.gov number, NCT00207597).",
keywords = "blood coagulation factors, global assays, haemophilia, joints, paediatric, prophylaxis",
author = "{for the Joint Outcome Study Group Investigators} and Warren, {Beth Boulden} and Linda Jacobson and Christine Kempton and Buchanan, {George R.} and Michael Recht and Deborah Brown and Cindy Leissinger and Shapiro, {Amy D.} and Abshire, {Thomas C.} and Manco-Johnson, {Marilyn J.} and Brenda Riske and Hacker, {Michele R.} and Ray Kilcoyne and Ingram, {J. David} and Manco-Johnson, {Michael L.} and Sharon Funk and Valentino, {Leonard A.} and Hoots, {W. Keith} and Donna DiMichele and Shirley Bleak and Alan Cohen and Prasad Mathew and Alison Matsunaga and Desiree Medeiros and Diane Nugent and Thomas, {Gregory A.} and Thompson, {Alexis A.} and Kevin McRedmond and Soucie, {J. Michael} and Harlan Austin and Evatt, {Bruce L.}",
note = "Funding Information: The JOS was supported by grants from the Centers for Disease Control and Prevention (U27/CCU812106) and the National Institutes of Health (R00069). Bayer HealthCare donated the factor VIII (Kogenate) used in the study but had no role in study design, data accrual, data analysis or manuscript preparation. The Hemophilia and Thrombosis Research Society recruited sites for participation. Clinical research and laboratory personnel, laboratory reagents and study database management were funded in part by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) Maternal and Child Health Bureau 340B Program (2H30MC24049, Mountain States Hemophilia Network). For this analysis, BBW was funded by the HTRS/Novo Nordisk Clinical Fellowship Award and the Bayer Hemophilia Awards Program Fellowship Project Award. We would like to thank Dr. Alfonso Iorio and the WAPPS-Hemo team at McMaster University, Hamilton, Ontario, for use of the WAPPS-Hemo programme to calculate FVIII pharmacokinetic parameters. Publisher Copyright: {\textcopyright} 2019 John Wiley & Sons Ltd",
year = "2019",
month = sep,
day = "1",
doi = "10.1111/hae.13778",
language = "English (US)",
volume = "25",
pages = "867--875",
journal = "Haemophilia",
issn = "1351-8216",
publisher = "Wiley-Blackwell",
number = "5",
}