Vertebral body reshaping after fractures: an important index of recovery in glucocorticoid-treated children.
children
glucocorticoid
spinal deformity index
vertebral body reshaping
vertebral fracture
Journal
The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362
Informations de publication
Date de publication:
16 Oct 2023
16 Oct 2023
Historique:
received:
19
07
2023
revised:
20
09
2023
accepted:
12
10
2023
medline:
16
10
2023
pubmed:
16
10
2023
entrez:
16
10
2023
Statut:
aheadofprint
Résumé
In this 6-year study we identified factors associated with spontaneous vertebral body reshaping in glucocorticoid (GC)-treated children with leukemia, rheumatic disorders, and nephrotic syndrome. Subjects were 79 children (mean age 7.4 years) who had VF evaluation on lateral spine radiographs at least one year after VF detection. VF were graded using the modified Genant semi-quantitative method and fracture burden for individuals was quantified using the spinal deformity index (SDI; sum of grades from T4 to L4). Sixty-five children (82.3%) underwent complete vertebral body reshaping (median time from VF detection to complete reshaping 1.3 years by Cox proportional hazard modeling). Of 237 VF, the majority (83.1%) ultimately reshaped, with 87.2% reshaping in the thoracic region versus 70.7% in the lumbar region (p=0.004). Cox models showed that: (1) every g/m2 increase in GC exposure in the first year after VF detection was associated with a 19% decline in the probability of reshaping; (2) each unit increase in the SDI at the time of VF detection was associated with a 19% decline in the probability of reshaping (hazard ratio [HR]=0.81; 95% confidence interval [CI]=0.71, 0.92; p=0.001); (3) each additional VF present at the time of VF detection reduced reshaping by 25% (HR=0.75; 95% CI=0.62, 0.90; p=0.002); and (4) each higher grade of VF severity decreased reshaping by 65% (HR=0.35; 95% CI=0.21, 0.57; p<0.001). After experiencing a VF, children with higher GC exposure, higher SDI, more severe fractures, or lumbar VF were at increased risk for persistent vertebral deformity.
Identifiants
pubmed: 37843393
pii: 7318157
doi: 10.1210/clinem/dgad611
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.