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10.1016/j.diabres.2004.08.006

http://scihub22266oqcxt.onion/10.1016/j.diabres.2004.08.006
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15860239!ä!15860239

suck abstract from ncbi


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pmid15860239      Diabetes+Res+Clin+Pract 2005 ; 68 (2): 117-25
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  • Osteoclastic function is accelerated in male patients with type 2 diabetes mellitus: the preventive role of osteoclastogenesis inhibitory factor/osteoprotegerin (OCIF/OPG) on the decrease of bone mineral density #MMPMID15860239
  • Suzuki K; Kurose T; Takizawa M; Maruyama M; Ushikawa K; Kikuyama M; Sugimoto C; Seino Y; Nagamatsu S; Ishida H
  • Diabetes Res Clin Pract 2005[May]; 68 (2): 117-25 PMID15860239show ga
  • To clarify the pathogenesis of altered bone metabolism in diabetic state and its underlying mechanisms, the bone mineral content and fasting levels of serum intact parathyroid hormone (i-PTH), intact osteocalcin (i-OC), tartrate-resistant acid phosphatase (TRAP) and osteoclastgenesis inhibitory factor/osteoprotegerin (OCIF/OPG) were measured in male type 2 diabetic patients and their age-matched controls. In addition, urine levels of osteoclastic markers, C-telopeptide of type I collagen (CTx), deoxypyridinoline (DPD), and N-telopeptide of type I collagen (NTx) were simultaneously determined. Serum levels of i-PTH and i-OC in diabetic patients were significantly lower than those in the controls. Conversely, serum concentrations of TRAP were significantly elevated in diabetic patients. However, no clear correlation was observed between serum i-OC and TRAP. It was also observed that urinary excretion of CTx, DPD, and NTx was significantly increased in the diabetics as compared with the controls. Unexpectedly, serum levels of OCIF/OPG tended to be higher in the diabetic group, and these values exhibited a significantly positive correlation with those of serum TRAP. There was found a significantly negative correlation between serum TRAP and bone mineral density (BMD) and also between serum OCIF/OPG and bone mineral density. It seems probable that OCIF/OPG has a suppressive role on the increased bone resorption to prevent further loss of the skeletal bone mass in type 2 diabetic patients.
  • |Acid Phosphatase/blood[MESH]
  • |Amino Acids/urine[MESH]
  • |Biomarkers/blood[MESH]
  • |Bone Density/*drug effects[MESH]
  • |C-Peptide/chemistry/urine[MESH]
  • |Calcitriol/blood[MESH]
  • |Calcium/blood[MESH]
  • |Collagen Type I[MESH]
  • |Collagen/urine[MESH]
  • |Data Interpretation, Statistical[MESH]
  • |Diabetes Mellitus, Type 2/*blood/*physiopathology/urine[MESH]
  • |Glycoproteins/chemistry/metabolism/*pharmacology/physiology[MESH]
  • |Humans[MESH]
  • |Insulin/blood[MESH]
  • |Isoenzymes/blood[MESH]
  • |Magnesium/blood[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Osteocalcin/blood[MESH]
  • |Osteoclasts/*physiology[MESH]
  • |Osteoprotegerin[MESH]
  • |Parathyroid Hormone/blood[MESH]
  • |Peptides/urine[MESH]
  • |Phosphorus/blood[MESH]
  • |Receptors, Cytoplasmic and Nuclear/chemistry/metabolism/physiology[MESH]
  • |Receptors, Tumor Necrosis Factor/chemistry/metabolism/physiology[MESH]
  • |Sex Factors[MESH]


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