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Bone: Another potential target to treat, prevent and predict diabetes
Dong-Mei Liu1, Ioanna Mosialou2, Jian-Min Liu3
1Department of Rheumatology, ZhongShan Hospital, FuDan University, Shanghai, China.
Bone-derived molecules like osteocalcin influence glucose metabolism, impacting type 2 diabetes treatment. Understanding this bone-glucose axis offers new therapeutic strategies for diabetes prevention and management.
Area of Science:
- Endocrinology
- Metabolism
- Bone Biology
Background:
- Type 2 diabetes mellitus (T2DM) is a growing global health concern.
- Emerging evidence links bone-derived molecules to glucose metabolism regulation.
- Existing T2DM treatments require novel therapeutic targets.
Purpose of the Study:
- To review the current understanding of the bone-glucose metabolism interplay.
- To highlight bone-derived molecules modulating glucose homeostasis.
- To explore skeletal intervention as a potential T2DM therapeutic strategy.
Main Methods:
- Literature review of preclinical and clinical studies.
- Analysis of identified bone-derived factors and their mechanisms.
- Synthesis of evidence on the bone-glucose axis.
Main Results:
- Osteocalcin (OCN), particularly undercarboxylated OCN (ucOC), enhances insulin secretion and sensitivity.
- Lipocalin 2 suppresses appetite via hypothalamic action.
- Osteocytes secrete factors (BMP7, sclerostin) affecting adipose tissue and energy expenditure.
- Bone resorption factors also influence glucose homeostasis.
Conclusions:
- Bone-derived molecules play a significant role in regulating glucose metabolism.
- Targeting the bone-glucose axis presents promising avenues for T2DM treatment and prevention.
- Further research into bone-derived factors could lead to innovative diabetes therapies.
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