TY - JOUR
T1 - Improvements in bone density and structure during anti-TNF-α therapy in pediatric Crohn's disease
AU - Griffin, Lindsay M.
AU - Thayu, Meena
AU - Baldassano, Robert N.
AU - DeBoer, Mark D.
AU - Zemel, Babette S.
AU - Denburg, Michelle R.
AU - Denson, Lee A.
AU - Shults, Justine
AU - Herskovitz, Rita
AU - Long, Jin
AU - Leonard, Mary B.
N1 - Publisher Copyright:
Copyright © 2015 by the Endocrine Society.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - Context: Pediatric Crohn's Disease (CD) is associated with deficits in trabecularbonemineral density (BMD) and cortical structure, potentially related to TNF-α effects to decrease bone formation and promote bone resorption. Objective: This study aimed to examine changes in bone density and structure in children and adolescents with CD following initiation of anti-TNF-α therapy. Design and Participants: Participants (n = 74; age 5-21 years) with CD completed a 12-month prospective cohort study. Main Outcome Measures: Tibia peripheral quantitative computed tomography scans were obtained at initiation of anti-TNF-α therapy and 12 months later. Musculoskeletal outcomes were expressed as sex-and race-specific z scores relative to age, based on -650 reference participants. Results: At baseline, CD participants had lower height, trabecular BMD, cortical area (due to smaller periosteal and larger endocortical circumferences), and muscle area z scores, compared with reference participants (all P=.01). Pediatric CD activity index decreased during the 10-week induction (P=.001), in association with subsequent gains in height, trabecular BMD, cortical area (due to recovery of endocortical bone), and muscle area z scores over 12 months (height P=.05; others P=.001). Bone-specific alkaline phosphatase levels, a biomarker of bone formation, increased a median of 75% (P=.001) during induction with associated 12-month improvements in trabecularBMDand cortical area z scores (both P<001). Younger age was associated with greater increases in trabecular BMD z scores (P=.001) and greater linear growth with greater recovery of cortical area (P=.001). Conclusions: Anti-TNF-α therapy was associated with improvements in trabecularBMDand cortical structure. Improvements were greater in younger and growing participants, suggesting a window of opportunity for treatment of bone deficits.
AB - Context: Pediatric Crohn's Disease (CD) is associated with deficits in trabecularbonemineral density (BMD) and cortical structure, potentially related to TNF-α effects to decrease bone formation and promote bone resorption. Objective: This study aimed to examine changes in bone density and structure in children and adolescents with CD following initiation of anti-TNF-α therapy. Design and Participants: Participants (n = 74; age 5-21 years) with CD completed a 12-month prospective cohort study. Main Outcome Measures: Tibia peripheral quantitative computed tomography scans were obtained at initiation of anti-TNF-α therapy and 12 months later. Musculoskeletal outcomes were expressed as sex-and race-specific z scores relative to age, based on -650 reference participants. Results: At baseline, CD participants had lower height, trabecular BMD, cortical area (due to smaller periosteal and larger endocortical circumferences), and muscle area z scores, compared with reference participants (all P=.01). Pediatric CD activity index decreased during the 10-week induction (P=.001), in association with subsequent gains in height, trabecular BMD, cortical area (due to recovery of endocortical bone), and muscle area z scores over 12 months (height P=.05; others P=.001). Bone-specific alkaline phosphatase levels, a biomarker of bone formation, increased a median of 75% (P=.001) during induction with associated 12-month improvements in trabecularBMDand cortical area z scores (both P<001). Younger age was associated with greater increases in trabecular BMD z scores (P=.001) and greater linear growth with greater recovery of cortical area (P=.001). Conclusions: Anti-TNF-α therapy was associated with improvements in trabecularBMDand cortical structure. Improvements were greater in younger and growing participants, suggesting a window of opportunity for treatment of bone deficits.
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U2 - 10.1210/jc.2014-4152
DO - 10.1210/jc.2014-4152
M3 - Article
C2 - 25919459
AN - SCOPUS:84943746635
SN - 0021-972X
VL - 100
SP - 2630
EP - 2639
JO - Journal of clinical endocrinology and metabolism
JF - Journal of clinical endocrinology and metabolism
IS - 7
ER -