Delays in maturation among adolescents with hemophilia and a history of inhibitors

Author:

Donfield Sharyne M.1,Lynn Henry S.2,Lail Alice E.1,Hoots W. Keith3,Berntorp Erik4,Gomperts Edward D.5

Affiliation:

1. Department of Biostatistics, Rho, Chapel Hill, NC;

2. Department of Biostatistics, Fudan University, Shanghai, China;

3. Gulf States Hemophilia and Thrombophilia Center, Houston Medical Center, Houston, TX;

4. Department for Coagulation Disorders, Malmö University Hospital, Malmö, Sweden; and

5. Saban Research Institute, Childrens Hospital, Los Angeles, CA

Abstract

Abstract Inhibitory antibodies to factors VIII or IX have the potential to affect a broad range of outcomes among people with hemophilia; however, their possible effect on growth and maturation has not been explored. We evaluated skeletal maturation (bone age), pubertal progression, serum testosterone levels, height velocity, and stature in the multicenter Hemophilia Growth and Development Study. A total of 333 children and adolescents (mean age, 12.4 years) were enrolled from 1989 to 1990 and followed for 7 years. Of these, 18% (n = 60) had a history of inhibitors. Bone age among HIV− adolescents with a history of inhibitors lagged 9 or more months behind those without inhibitors at every age from 12 to 15 years. Those with a history of inhibitors were older at every Tanner stage transition, attained a lower maximum growth velocity, and their serum testosterone levels were significantly lower compared with those without inhibitors. Delays were greater among HIV+ patients with a history of inhibitors compared with those without inhibitors; however, the differences were generally small and not statistically significant. The results of this investigation underscore the importance of monitoring the growth and maturation of children and adolescents with hemophilia, particularly those with inhibitors.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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