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Bone mineral density in diabetes mellitus
A Giacca1, A Fassina, F Caviezel
1Chair of Clinical Medicine, University of Milan, Italy.
Bone
|January 1, 1988
Summary
Bone mineral content (BMC) in diabetic individuals falls within normal ranges, unaffected by diabetes type or metabolic control. However, inverse correlations were observed with urinary calcium and phosphorus in non-insulin-dependent diabetic women and men.
Area of Science:
- Endocrinology
- Metabolic Bone Disease
- Diabetes Mellitus Research
Background:
- Diabetes mellitus is a complex metabolic disorder with potential systemic effects.
- Bone mineral density (BMD) and content (BMC) can be influenced by hormonal and metabolic factors.
- Understanding bone health in diabetic populations is crucial for comprehensive patient care.
Purpose of the Study:
- To investigate bone mineral content (BMC) in adult diabetic subjects.
- To compare BMC levels in diabetic patients with age- and sex-matched non-diabetic controls.
- To explore correlations between BMC and various endocrine, metabolic, and diabetes control parameters.
Main Methods:
- Bone mineral content (BMC) was measured using single photon absorptiometry at the distal radius.
- Diabetic subjects (n=100) were compared to a large control group (n=500).
- Subgroup analyses were performed based on diabetes type (IDD/NIDD), age, and menopausal status, with matched controls.
Main Results:
- Diabetic subjects exhibited normal BMC ranges relative to sex and age.
- No statistically significant differences in BMC were found between diabetic and control groups across subgroups.
- BMC showed no correlation with plasma hormone levels, calcium, phosphorus, or alkaline phosphatase.
- Inverse correlations were noted between BMC and urinary calcium/phosphorus in non-insulin-dependent diabetes.
Conclusions:
- Bone mineral content is generally preserved in adult diabetic individuals.
- Diabetes type, age, and menopausal status do not significantly alter BMC compared to controls.
- Urinary calcium and phosphorus excretion may be linked to bone mineral content in specific diabetic subgroups.