OR28-07 Negative Impact of Childhood Obesity and Type 2 Diabetes (T2D) on Bone Accrual and Strength: A Longitudinal Study

Abstract Disclosure: F. Bacha: None. P. Saha: None. R. Villareal: None. S. Musaad: None. R. Shypailo: None. M. Puyau: None. X. Zhang: None. Y. Mirabile: None. The impact of childhood obesity and youth-onset T2D on skeletal health (bone quality and strength) is not clear. We examined the longitudinal changes in bone microarchitecture (quality and strength) in youth across the glycemia spectrum. 48 adolescents (26 females); mean age 15.51 ± 1.33, 27% normal weight (NW), 31% overweight-normal glucose tolerance (OW), 42% OW-impaired glucose regulation (IGR) including prediabetes (n=4) or T2D (n=16), underwent baseline measurement of anthropometrics, body composition (DXA), cardiorespiratory fitness (VO2max), glucose tolerance test with glycemia and insulin indices; bone microarchitecture (HRpQCT) at the distal tibia and radius was measured at baseline (n=48), 6 month [Time 1 (T1)] (n=36) and 12 month (T2) (n=29). We examined longitudinal changes in bone quality and strength among the 3 subject categories, using generalized linear mixed models accounting for repeated subject data, adjusted for age, sex, baseline lean mass, fat mass, VO2max, HbA1c, fasting insulin, subject category, time and time by category interaction. At the tibia, there was a time by category interaction for tibia volumetric (v) BMD with estimate± SEM of -10.97±6.1, p=0.08 for IGR vs. NW and -13.34±6.1, p=0.04 for OW vs. NW, at T2 vs. baseline. Similarly, there was a negative time per category interaction for trabecular (Tb) inner BMD (-10.36±5.5, p=0.068), and Tb transverse BMD (-5.5±2.5, p=0.033) in IGR vs. NW; and for whole bone modulus (-222.47±115.30, p=0.06) in OW vs. NW, at T2 vs. baseline. Baseline fasting insulin contributed negatively to tibial whole bone modulus (-12.52±7.14, p=0.087). At the radius, there was a positive effect of time on vBMD and whole bone modulus, and a time by category interaction for radius vBMD -23.7±10.9, p=0.035 in IGR vs. NW and -20.7±10.9, p=0.066 in OW vs. NW; and for whole bone modulus -390.9±179.4, p=0.035 in IGR vs. NW and -377.02±179.9, p=0.04 in OW vs. NW, at T2 vs. baseline. Our results support a negative effect of childhood obesity and T2D on bone accrual, quality and strength at both the distal tibia and radius after accounting for age, sex, lean mass, fat mass and cardiorespiratory fitness. Insulin resistance contributes to lower bone strength at the distal tibia. This raises concern about long-term bone health in youth with obesity and dysglycemia. Presentation: Monday, July 14, 2025

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Journal of the Endocrine Society
Published
2025-10-01
DOI
https://doi.org/10.1210/jendso/bvaf149.1748
Primary Topic
Bone health and osteoporosis research
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article
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article

OR28-07 Negative Impact of Childhood Obesity and Type 2 Diabetes (T2D) on Bone Accrual and Strength: A Longitudinal Study

Punam K. Saha, Zhang Xiao-liu, Salma Musaad, Fida Bacha et al.
Journal of the Endocrine Society
Bone health and osteoporosis research
article

OR28-07 Negative Impact of Childhood Obesity and Type 2 Diabetes (T2D) on Bone Accrual and Strength: A Longitudinal Study

Punam K. Saha, Zhang Xiao-liu, Salma Musaad, Fida Bacha, Maurice R. Puyau, Roman J. Shypailo, Yiming Mirabile, Reina Villareal
article en

Abstract

Abstract Disclosure: F. Bacha: None. P. Saha: None. R. Villareal: None. S. Musaad: None. R. Shypailo: None. M. Puyau: None. X. Zhang: None. Y. Mirabile: None. The impact of childhood obesity and youth-onset T2D on skeletal health (bone quality and strength) is not clear. We examined the longitudinal changes in bone microarchitecture (quality and strength) in youth across the glycemia spectrum. 48 adolescents (26 females); mean age 15.51 ± 1.33, 27% normal weight (NW), 31% overweight-normal glucose tolerance (OW), 42% OW-impaired glucose regulation (IGR) including prediabetes (n=4) or T2D (n=16), underwent baseline measurement of anthropometrics, body composition (DXA), cardiorespiratory fitness (VO2max), glucose tolerance test with glycemia and insulin indices; bone microarchitecture (HRpQCT) at the distal tibia and radius was measured at baseline (n=48), 6 month [Time 1 (T1)] (n=36) and 12 month (T2) (n=29). We examined longitudinal changes in bone quality and strength among the 3 subject categories, using generalized linear mixed models accounting for repeated subject data, adjusted for age, sex, baseline lean mass, fat mass, VO2max, HbA1c, fasting insulin, subject category, time and time by category interaction. At the tibia, there was a time by category interaction for tibia volumetric (v) BMD with estimate± SEM of -10.97±6.1, p=0.08 for IGR vs. NW and -13.34±6.1, p=0.04 for OW vs. NW, at T2 vs. baseline. Similarly, there was a negative time per category interaction for trabecular (Tb) inner BMD (-10.36±5.5, p=0.068), and Tb transverse BMD (-5.5±2.5, p=0.033) in IGR vs. NW; and for whole bone modulus (-222.47±115.30, p=0.06) in OW vs. NW, at T2 vs. baseline. Baseline fasting insulin contributed negatively to tibial whole bone modulus (-12.52±7.14, p=0.087). At the radius, there was a positive effect of time on vBMD and whole bone modulus, and a time by category interaction for radius vBMD -23.7±10.9, p=0.035 in IGR vs. NW and -20.7±10.9, p=0.066 in OW vs. NW; and for whole bone modulus -390.9±179.4, p=0.035 in IGR vs. NW and -377.02±179.9, p=0.04 in OW vs. NW, at T2 vs. baseline. Our results support a negative effect of childhood obesity and T2D on bone accrual, quality and strength at both the distal tibia and radius after accounting for age, sex, lean mass, fat mass and cardiorespiratory fitness. Insulin resistance contributes to lower bone strength at the distal tibia. This raises concern about long-term bone health in youth with obesity and dysglycemia. Presentation: Monday, July 14, 2025

Journal of the Endocrine SocietyVol. 9(Supplement_1)
University of Iowa (US), Baylor College of Medicine (US)
Openalex Percentile: Top 61%
Bone health and osteoporosis research
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