TY - JOUR
T1 - Growth curves for children with X-linked hypophosphatemia
AU - Mao, Meng
AU - Carpenter, Thomas O.
AU - Whyte, Michael P.
AU - Skrinar, Alison
AU - Chen, Chao Yin
AU - Martin, Javier San
AU - Rogol, Alan D.
N1 - Publisher Copyright:
© Endocrine Society 2020.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Context: We characterized linear growth in infants and children with X-linked hypophosphatemia (XLH). Objective: Provide linear growth curves for children with XLH from birth to early adolescence. Design: Data from 4 prior studies of XLH were pooled to construct growth curves. UX023-CL002 was an observational, retrospective chart review. Pretreatment data were collected from 3 interventional trials: two phase 2 trials (UX023-CL201, UX023-CL205) and a phase 3 trial (UX023-CL301). Setting: Medical centers with expertise in treating XLH. Patients: Children with XLH, 1-14 years of age. Intervention: None. Main Outcome Measure: Height-for-age linear growth curves, including values for the 5th, 10th, 25th, 50th, 75th, 90th, and 95th percentiles for children with XLH compared to population norms. Results: A total of 228 patients (132 girls, 96 boys) with 2381 height measurements were included. Nearly all subjects (> 99%) reported prior management with supplementation therapy. Compared to the Center for Disease Control and Prevention growth curves, boys at age 3 months, 6 months, 9 months, 1 year, and 2 years had median height percentiles of 46%, 37%, 26%, 18%, and 5%, respectively; for girls the median height percentiles were 52%, 37%, 25%, 18%, and 7%, respectively. Annual growth in children with XLH fell below that of healthy children near 1 year of age and progressively declined during early childhood, with all median height percentiles < 8% between 2 and 12 years old. Conclusion: Children with XLH show decreased height gain by 1 year of age and remain below population norms thereafter. These data will help evaluate therapeutic interventions on linear growth for pediatric XLH.
AB - Context: We characterized linear growth in infants and children with X-linked hypophosphatemia (XLH). Objective: Provide linear growth curves for children with XLH from birth to early adolescence. Design: Data from 4 prior studies of XLH were pooled to construct growth curves. UX023-CL002 was an observational, retrospective chart review. Pretreatment data were collected from 3 interventional trials: two phase 2 trials (UX023-CL201, UX023-CL205) and a phase 3 trial (UX023-CL301). Setting: Medical centers with expertise in treating XLH. Patients: Children with XLH, 1-14 years of age. Intervention: None. Main Outcome Measure: Height-for-age linear growth curves, including values for the 5th, 10th, 25th, 50th, 75th, 90th, and 95th percentiles for children with XLH compared to population norms. Results: A total of 228 patients (132 girls, 96 boys) with 2381 height measurements were included. Nearly all subjects (> 99%) reported prior management with supplementation therapy. Compared to the Center for Disease Control and Prevention growth curves, boys at age 3 months, 6 months, 9 months, 1 year, and 2 years had median height percentiles of 46%, 37%, 26%, 18%, and 5%, respectively; for girls the median height percentiles were 52%, 37%, 25%, 18%, and 7%, respectively. Annual growth in children with XLH fell below that of healthy children near 1 year of age and progressively declined during early childhood, with all median height percentiles < 8% between 2 and 12 years old. Conclusion: Children with XLH show decreased height gain by 1 year of age and remain below population norms thereafter. These data will help evaluate therapeutic interventions on linear growth for pediatric XLH.
KW - FGF23
KW - Growth curve
KW - PHEX
KW - Rickets
KW - X-linked hypophosphatemia
UR - http://www.scopus.com/inward/record.url?scp=85090078757&partnerID=8YFLogxK
U2 - 10.1210/clinem/dgaa495
DO - 10.1210/clinem/dgaa495
M3 - Article
C2 - 32721016
AN - SCOPUS:85090078757
SN - 0021-972X
VL - 105
SP - 3243
EP - 3249
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 10
ER -