Total-body skeletal muscle mass: estimation by dual-energy X-ray absorptiometry in children and adolescents

BACKGROUND: Skeletal muscle (SM) is an important compartment but is difficult to quantify in children and adolescents. OBJECTIVE: We investigated the potential of dual-energy X-ray absorptiometry (DXA) for measuring total-body SM in pediatric subjects. DESIGN: A previously published adult DXA SM pre...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The American journal of clinical nutrition 2006-11, Vol.84 (5), p.1014-1020
Hauptverfasser: Kim, Jaehee, Shen, Wei, Gallagher, Dympna, Jones, Alfredo Jr, Wang, ZiMian, Wang, Jack, Heshka, Stanley, Heymsfield, Steven B
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:BACKGROUND: Skeletal muscle (SM) is an important compartment but is difficult to quantify in children and adolescents. OBJECTIVE: We investigated the potential of dual-energy X-ray absorptiometry (DXA) for measuring total-body SM in pediatric subjects. DESIGN: A previously published adult DXA SM prediction formula was evaluated in children and adolescents aged 5-17 y (n = 99) who varied in pubertal maturation stage. SM estimated by whole-body magnetic resonance imaging (MRI) was used as the reference. The adult SM model was not accurate for subjects below Tanner stage 5 (n = 65; aged 5-14 y). New pediatric SM prediction models were therefore developed and validated in a separate group (n = 18). RESULTS: The adult DXA SM prediction model was valid in subjects at Tanner stage 5 but significantly (P < 0.001) overestimated SM in subjects below Tanner stage 5. New SM prediction formulas were developed with appendicular lean soft tissue (ALST) estimates by DXA as the main predictor variable (eg, model 1, ALST alone: R² = 0.982, SEE = 0.565 kg, P < 0.001). The new models were validated by the leave-one-out method and were cross-validated in a separate validation group. CONCLUSIONS: A previously reported adult DXA SM prediction model is applicable in children and adolescents late in pubertal development (Tanner stage 5). A new DXA SM prediction model was developed for prepubertal and pubertal subjects (Tanner stage =5 y. DXA thus provides an important opportunity for quantifying total-body SM mass across most of the human life span.
ISSN:0002-9165
1938-3207
DOI:10.1093/ajcn/84.5.1014