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Metabolic bone markers can be related to preserved insulin secretion in children with newly diagnosed type 1 diabetes
Małgorzata Szymańska1, Izabela Michałus2, Marcin Kaszkowiak3
1Department of Paediatrics, Oncology, and Haematology, Medical University of Lodz, Poland.
Insights
Type 1 diabetes (T1D) in children is linked to bone metabolism changes, with markers improving as metabolic control is achieved. Preserved insulin secretion appears most crucial in managing these bone complications.
Area of Science:
- Pediatric Endocrinology
- Metabolic Bone Disease
- Diabetes Mellitus
Background:
- Type 1 diabetes (T1D) is associated with bone metabolism disorders.
- Evaluating bone metabolism markers in children with newly diagnosed T1D is crucial for understanding disease progression and complications.
Purpose of the Study:
- To assess bone metabolism markers in children with newly diagnosed T1D.
- To track changes in these markers after an average of seven months of diabetes duration.
- To correlate bone metabolism markers with clinical parameters of diabetes.
Main Methods:
- Evaluated osteocalcin (OC), osteoprotegerin (OPG), sRANKL, and deoxypyridoline (DPD) in 100 T1D patients and 52 controls.
- Performed DXA examinations for bone mineral density.
- Assessed markers at diagnosis and during follow-up.
Main Results:
- Lower OC and higher OPG at T1D onset compared to controls; OC increased, OPG decreased during follow-up.
- sRANKL and urine DPD increased during follow-up and were higher than controls.
- BMD-TBLH was lower in T1D patients than controls.
- OPG correlated with HbA1c, C-peptide, and BMI Z-score; sRANKL correlated with C-peptide levels.
Conclusions:
- Bone metabolism disorders in children with T1D are evident at diagnosis and modify with metabolic control.
- These bone changes are strongly associated with preserved insulin secretion.
Introduction:
Type 1 diabetes (T1D) may be associated with numerous complications including bone metabolism disorders. The aim of the study was to evaluate the bone metabolism markers twice in children with a newly diagnosed T1D and after an average of seven months of its duration in relation to parameters of the clinical course of diabetes.
Material And Methods:
In 100 T1D patients and 52 control subjects, the following bone turnover markers were evaluated: osteocalcin - OC, osteoprotegerin - OPG, sRANKL, and deoxypyridoline in urine - DPD and DXA examination was also performed.
Results:
Lower OC concentration at T1D onset in comparison to controls (p < 0.001) and its increase during follow-up (p < 0.001) was ob-served. The OPG concentration was elevated at T1D onset as compared to the control group (p = 0.024) and decreased thereafter (p < 0.001). The s-RANKL level increased during follow-up (p < 0.001) and was lower than in controls (p < 0.001). Urine DPD con-centration also increased during follow-up in the T1D patient group (p < 0.001) and was higher in comparison to the control group (p = 0.021). BMD-TBLH was higher in the control group as compared to patients both at T1D onset (p = 0.025) and in follow-up ob-servation (p = 0.034). Moreover, OPG correlated positively with glycated haemoglobin (HbA1c) (p = 0.004) and negatively with fasting C-peptide level (p = 0.046) and BMI Z-score (p = 0.003), whereas s-RANKL correlated positively with both fasting (p < 0.001) and stimulated C-peptide levels (p < 0.001).
Conclusions:
Bone metabolism disorders observed at T1D onset in children and modified after reaching the metabolic control of the disease seem to be most strongly associated with preserved insulin secretion.
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