High
leptin concentration, low-grade
inflammation, and
insulin resistance often coexist in obese subjects; this adverse metabolic milieu may be the main culprit for increased fracture risk and impaired bone quality seen in patients with
type 2 diabetes. We examined the associations of
leptin, hs (high sensitivity)- CRP and
insulin resistance with bone turnover markers (BTMs) and bone characteristics in 55 young obese adults (median BMI 40 kg/m2) and 65 non-obese controls. Mean age of the subjects was 19.5 ± 2.5 years (mean ± SD). Concentrations of
leptin,
adiponectin,
hs-CRP, MMP-8 and
TIMP-1, fasting plasma
glucose and
insulin (to calculate HOMA), BTMs (BAP, P1NP, CTX-1, and TRAC5b) were measured. Bone characteristics were determined with pQCT at radius and tibia, and with DXA for central sites.
Leptin,
hs-CRP and HOMA correlated inversely with BTMs: the partial coefficients were 1.5-1.9 fold higher in males than in females. After adjusting for age, BMI, and other endocrine factors,
leptin displayed an independent effect in males on radial bone mass (p = 0.019), tibial trabecular density (p = 0.025) and total hip BMD (p = 0.043), with lower densities in males with high
leptin. In females, the model adjusting for age, BMI, and other endocrine factors, revealed that
hs-CRP had independent effects on radial bone mass (p = 0.034) and lumbar spine BMD (p = 0.016), women with high
hs-CRP having lower values. Partial correlations of
adiponectin and
TIMP-1 with bone characteristics were discrepant; MMP-8 showed no associations. In conclusion, in young obese adults and their controls,
leptin,
hs-CRP and HOMA associate inversely with BTMs and bone characteristics.
Leptin appears to be the key independent effector in males, whereas
hs-CRP displayed a predominant role in females.