BONE DENSITOMETRY AND BIOCHEMICAL BONE REMODELING MARKERS IN TYPE-1 DIABETES-MELLITUS

Bone mineral density (BMD) at the lumbar spine, quantified by dual ene rgy X-ray absorptiometry, and biochemical bone remodeling markers (ser um alkaline phosphatase, osteocalcin, tartrate-resistant acid phosphat ase and urinary hydroxyproline) have been studied in 94 patients with diabetes mellitus aged 18-62 years. BMD was normal (1.13 +/- 0.02 g/cm (2) in patient vs. 1.16 +/- 0.12 g/cm(2) in controls), although it was found to be negatively correlated with HbA(1), microalbuminuria, age and the duration of the disease. Serum alkaline phosphatase(188 +/- 75 I.U./l vs. 168 +/- 42 I.U./l; P < 0.03), serum tartrate-resistant aci d phosphatase (14.3 +/- 4.3 I.U./l vs. 11.7 +/- 3.7 I.U./l; P < 0.0001 ) and urinary hydroxyproline (0.018 +/- 0.016 mmol/mmol creatinine vs. 0.011 +/- 0.008 mmol/mmol creatinine; P < 0.0001) were higher in diab etics than in controls. Serum osteocalcin was lower (2.5 +/- 1.3 ng/ml vs. 3:4 +/- 1.2 ng/ml; P < 0.0001). No relationship was found between bone remodeling markers and BMD. It is concluded that lumbar BMD is n ormal in type 1 diabetic patients, although the degree of metabolic co ntrol, age and duration of the disease may affect it. In the light of the biochemical markers, bone remodeling may be disturbed in diabetes, but such disturbance seems to be unimportant regarding BMD.