Good long-term glycemic compensation is associated with better trabecular bone score in postmenopausal women with type 2 diabetes
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
31842578
DOI
10.33549/physiolres.934304
PII: 934304
Knihovny.cz E-zdroje
- MeSH
- diabetes mellitus 2. typu krev farmakoterapie patologie MeSH
- glykovaný hemoglobin metabolismus MeSH
- hypoglykemika farmakologie terapeutické užití MeSH
- kombinovaná farmakoterapie MeSH
- kostní denzita * MeSH
- lidé středního věku MeSH
- lidé MeSH
- metformin farmakologie terapeutické užití MeSH
- postmenopauza MeSH
- průřezové studie MeSH
- sitagliptin fosfát farmakologie terapeutické užití MeSH
- trabekulární kostní tkáň účinky léků patologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- glykovaný hemoglobin MeSH
- hemoglobin A1c protein, human MeSH Prohlížeč
- hypoglykemika MeSH
- metformin MeSH
- sitagliptin fosfát MeSH
Osteoporosis is an increasingly widespread disease, as well as diabetes mellitus. It is now accepted that osteoporotic fractures are a serious co-morbidity and complication of diabetes. Despite of good bone mineral density in Type 2 Diabetes (T2DM) patients is the fracture risk elevated. It is due to reduced bone quality. To determine the effect of glycemic compensation on bone density and trabecular bone score (TBS) in T2DM. We analyzed a cohort of 105 postmenopausal women with T2DM. For all patients, central bone density (spinal and lumbar spine) was tested by DXA methodology, glycemic control parameters were assessed, and anthropometric parameters were measured. Bone quality was analyzed using TBS software. The results were statistically processed. Good glycemic compensation with glycated hemoglobin (A1c) value <7.0 % DCCT did not lead to BMD changes in patients with T2DM. However, patients with HbA1c <7 % DCCT had significantly better TBS (1.254±0.148 vs. 1.166±0.094, p=0.01). There was a negative correlation between TBS and glycated hemoglobin (r= -0,112, p<0.05) with glycemic fasting (r= -0.117, p<0.05). The optimal effect on TBS is achieved when all three markers of glycemic compensation (glycated hemoglobin, fasting plasma glucose and postprandial glycemia) are in optimal range. By using ROC curves glycated hemoglobin has the most significant effect on TBS. Optimal glycemic compensation, evaluated by glycated hemoglobin, does not lead to changes in BMD but has a beneficial effect on TBS in T2DM. Good glycemic control is required also for reduction of the risk of osteoporosis and osteoporotic fractures.
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