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Age-Related Femoral Bone Loss in Men: Evidence for Hyperparathyroidism and Insulin-Like Growth Factor-1 Deficiency

¹ Centre de Gérontologie Clinique Antonin Balmès, CHU Montpellier, France.
² UPRES EA 3444, Ecole de Santé Publique, Université Henri Poincaré, Nancy, France.
³ Faculté du Sport, Université Henri Poincaré, Nancy, France.
⁴ Laboratoire de Biologie Cellulaire, Explorations Fonctionnelles Métaboliques, CHU-Brabois, Vandoeuvre-les-Nancy, France.
⁵ Laboratoire Central de Chimie, Hôpital Central, Nancy, France.

Address correspondence to Dr. Claude Jeandel, Service de Médecine Interne-Gériatrie, Centre de Prévention et de Traitement des Maladies du Vieillissement; 39 avenue Charles Flahault 34295 Montpellier Cedex 5, France. E-mail: c-jeandel{at}chu-montpellier.fr

Background. We sought to determine the extent to which the age-related decline of femoral neck (FN) bone mineral density (BMD) might be explained by the age-related change of body composition and biological parameters and the mechanisms by which these factors might influence FN BMD in men.

Methods. The relationships between FN BMD and anthropometric, hormonal, and biochemical parameters and bone turnover markers were studied in 82 men aged 25–86 years.

Results. Age was associated with a decline of FN BMD and osteocalcin (OC), bone alkaline phosphatase (bALP), and urinary C-telopeptide (p <.05). The significant relationship between FN BMD and OC (p <.01) did not remain after adjustment for age. With use of multiple linear regression and adjusting for all significant variables associated with FN BMD in univariate analysis (p <.01) (age, weight, lean and fat mass, height, and levels of dehydroepiandrosterone sulfate, insulin-like growth factor [IGF-1], testosterone, and parathyroid hormone [PTH]), age accounted for 29.5% of FN BMD variance. When age was excluded from the model, PTH accounted for 19.5% and IGF-1 for 10% of the FN BMD variance. Bone turnover markers were significantly intercorrelated, and levels of IGF-1 were positively associated with those of bALP and OC (p <.05).

Conclusions. These results show that age is a strong predictor of FN BMD in men, resulting in a decline of bone remodeling, especially of bone formation. The results also show that, after taking into account anthropometric and other biological factors possibly involved in bone aging, the major part of the effect of age on bone is explained by the age-related increase of PTH and decrease of IGF-1 in men, suggesting that all measures taken to limit these age-related changes may be effective in the prevention of the age-related decline of FN BMD in men.