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. 2023 May 8;108(10):e923–e936. doi: 10.1210/clinem/dgad255

Table 4.

Serum markers with potential role for fracture risk assessment in diabetes

Marker Tissue of origin Role in diabetic bone Potential use for fracture prediction
Glycemia
(HbA1c)
Erythrocytes Collagen glycosylation
Fracture risk prediction
Yes (fracture data)
Bone turnover marker (PINP, CTX) Collagen formation/degradation State of low turnover
Evaluation of treatment efficacy
No predictive value
AGEs (pentosidine) Collagen cross-linking Impair bone properties by accumulation in bone collagen Potentially (limited fracture data)
Sclerostin Osteocyte Higher sclerostin gene expression in DM Potentially (no fracture data)
IGF-1 Hepatocyte Osteoblast stimulation Yes (fracture data)
Calciotropic hormones (eg, PTH) Parathyroid cells Calcium homeostasis Potentially (limited fracture data)
Proinflammatory cytokines
(eg, TNFα, IL-1, -6, -11, CRP)
Inflammation Alteration of bone remodeling Potentially (limited fracture data)
Vascular markers (eg, VEGF) Bone marrow Bone marrow cell apoptosis No fracture data
Adipokines
(eg, leptin, adiponectin)
Adipose tissue Regulation of osteoblast function No fracture data

Abbreviations: AGEs, advanced glycation end products; CRP, C-reactive protein; CTX, C-terminal telopeptide of type I collagen; DM, diabetes mellitus; HbA1c, glycated hemoglobin A1c; IGF-1, insulin-like growth factor-1; IL, interleukin; PINP, procollagen type 1 amino-terminal propeptide; PTH, parathyroid hormone; TNFα, tumor necrosis factor α; VEGF, vascular endothelial growth factor.