PMID- 21437719 OWN - NLM STAT- MEDLINE DCOM- 20120817 LR - 20221207 IS - 1433-2965 (Electronic) IS - 0937-941X (Linking) VI - 23 IP - 2 DP - 2012 Feb TI - Serum undercarboxylated osteocalcin levels are inversely associated with glycemic status and insulin resistance in an elderly Japanese male population: Fujiwara-kyo Osteoporosis Risk in Men (FORMEN) Study. PG - 761-70 LID - 10.1007/s00198-011-1600-7 [doi] AB - SUMMARY: Recent animal studies have demonstrated that undercarboxylated osteocalcin upregulates insulin secretion via osteoblast-insulin signaling. However, it remains unclear whether such a pathway exists in humans. This study showed that serum undercarboxylated osteocalcin levels were inversely associated with fasting plasma glucose, hemoglobin A(1c), and homeostasis model assessment of insulin resistance (HOMA-IR) levels in community-dwelling elderly Japanese men. INTRODUCTION: Undercarboxylated osteocalcin (ucOC) was reported to increase insulin secretion and improve glucose tolerance via osteoblast-insulin signaling in animal-based studies. Whether this pathway also exists in humans is unknown. We aimed to clarify whether serum ucOC levels are associated with glycemic status and insulin resistance in the general Japanese population. METHODS: We included 2,174 Japanese men (>/=65 years) who were able to walk without aid from others and lived at home in four cities of Nara Prefecture. We excluded participants with a history of diseases or medications that affect bone metabolism, other than type 2 diabetes mellitus (T2DM). Fasting plasma glucose, glycated hemoglobin A(1c), and HOMA-IR levels were determined as outcome measures. RESULTS: Of the 1,597 participants included in the analysis, both intact OC (iOC) and ucOC levels showed significant inverse correlations with all outcome measures, even after adjusting for potential confounders. Mean values of outcome measures showed a significant decreasing trend with higher quintiles of iOC or ucOC after adjusting for confounders. This trend remained significant for ucOC quintiles after further adjustment for iOC levels, but was not significant for iOC quintiles after adjusting for ucOC levels. These results were attenuated, but still apparent, after excluding participants receiving drug therapy for T2DM. CONCLUSIONS: Levels of ucOC, but not iOC, were inversely associated with glycemic index and insulin resistance in a population of Japanese men. These findings will need to be confirmed with longitudinal studies. FAU - Iki, M AU - Iki M AD - Department of Public Health, Kinki University Faculty of Medicine, 377-2 Oono-higashi, Osaka-Sayama, Osaka 589-8511, Japan. masa@med.kindai.ac.jp FAU - Tamaki, J AU - Tamaki J FAU - Fujita, Y AU - Fujita Y FAU - Kouda, K AU - Kouda K FAU - Yura, A AU - Yura A FAU - Kadowaki, E AU - Kadowaki E FAU - Sato, Y AU - Sato Y FAU - Moon, J S AU - Moon JS FAU - Tomioka, K AU - Tomioka K FAU - Okamoto, N AU - Okamoto N FAU - Kurumatani, N AU - Kurumatani N LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110325 PL - England TA - Osteoporos Int JT - Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA JID - 9100105 RN - 0 (Blood Glucose) RN - 0 (Glycated Hemoglobin A) RN - 0 (Isoenzymes) RN - 0 (hemoglobin A1c protein, human) RN - 104982-03-8 (Osteocalcin) RN - EC 3.1.3.2 (Acid Phosphatase) RN - EC 3.1.3.2 (Tartrate-Resistant Acid Phosphatase) SB - IM CIN - Osteoporos Int. 2013 Oct;24(10):2733. PMID: 23860956 CIN - Osteoporos Int. 2013 Oct;24(10):2735. PMID: 23860957 MH - Acid Phosphatase/blood MH - Aged MH - Anthropometry/methods MH - Blood Glucose/*metabolism MH - Diabetes Mellitus, Type 2/blood/epidemiology MH - Glycated Hemoglobin/metabolism MH - Humans MH - Insulin Resistance/*physiology MH - Isoenzymes/blood MH - Japan/epidemiology MH - Life Style MH - Male MH - Osteocalcin/*blood MH - Signal Transduction/physiology MH - Tartrate-Resistant Acid Phosphatase EDAT- 2011/03/26 06:00 MHDA- 2012/08/18 06:00 CRDT- 2011/03/26 06:00 PHST- 2010/11/19 00:00 [received] PHST- 2011/02/08 00:00 [accepted] PHST- 2011/03/26 06:00 [entrez] PHST- 2011/03/26 06:00 [pubmed] PHST- 2012/08/18 06:00 [medline] AID - 10.1007/s00198-011-1600-7 [doi] PST - ppublish SO - Osteoporos Int. 2012 Feb;23(2):761-70. doi: 10.1007/s00198-011-1600-7. Epub 2011 Mar 25.