Adiponectin Is Associated with Changes in Bone Markers during Glycemic Control in Type 2 Diabetes Mellitus

被引:75
作者
Kanazawa, Ippei [1 ]
Yamaguchi, Toru [1 ]
Yamauchi, Mika [1 ]
Yamamoto, Masahiro [1 ]
Kurioka, Soichi [1 ]
Yano, Shozo [1 ]
Sugimoto, Toshitsugu [1 ]
机构
[1] Shimane Univ, Dept Internal Med 1, Fac Med, Izumo, Shimane 6938501, Japan
关键词
SERUM UNDERCARBOXYLATED OSTEOCALCIN; GLYCATION END-PRODUCTS; OSTEOBLASTIC MC3T3-E1 CELLS; MINERAL DENSITY; ELDERLY-WOMEN; POSTMENOPAUSAL WOMEN; VERTEBRAL FRACTURES; HIP FRACTURE; VITAMIN-K; GAMMA-CARBOXYLATION;
D O I
10.1210/jc.2008-2187
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Although several experiments show that adiponectin is associated with bone metabolism, a relationship between adiponectin and bone markers is still unclear. We monitored chronological changes in hyperglycemia, serum adiponectin, and bone markers during glycemic control in type 2 diabetes and analyzed relationships among these parameters. Subjects and Results: A total of 50 Japanese patients with poorly controlled type 2 diabetes [initial hemoglobin A(1c) (HbA(1c)) = 10.0 +/- 2.5%] were recruited, and biochemical data were collected before and after glycemic control for a month. Of bone formation markers, bone-specific alkaline phosphatase was decreased with a mean change of -3.11 [95% confidence interval (CI), -5.03 to -1.20; P < 0.01], whereas osteocalcin (OC) was increased with a mean change of 1.94 (95% CI, 1.45-2.42; P < 0.001) and undercarboxylated OC (ucOC)/OC ratio was decreased with a mean change of -0.15 (95% CI, -0.27 to -0.03; P < 0.01). Although adiponectin level was not significantly different before and after glycemic control, baseline adiponectin level, but not HbA1c, was positively correlated with changes in OC, ucOC, and urinary N-terminal cross-linked telopeptide of type I collagen (uNTX) (r = 0.30, P = 0.04; r = 0.32, P = 0.03; and r = 0.36, P = 0.01, respectively). Changes in adiponectin were also negatively correlated with changes in OC and uNTX (r = -0.42, P < 0.01; and r = -0.38, P < 0.01, respectively). Changes in HbA(1c) were negatively correlated with changes in OC (r = -0.30, P = 0.03). Conclusion: These findings show that treatments for hyperglycemia enhance OC level and suggest that serum adiponectin level before starting to compensate poorly controlled diabetics could predict the subsequent improvement of bone remodeling markers during glycemic control. (J Clin Endocrinol Metab 94: 3031-3037, 2009)
引用
收藏
页码:3031 / 3037
页数:7
相关论文
共 53 条
[1]   Advanced glycation end products stimulate osteoblast apoptosis via the MAP kinase and cytosolic apoptotic pathways [J].
Alikhani, Mani ;
Alikhani, Zoubin ;
Boyd, Coy ;
MacLellan, Christine M. ;
Raptis, Markos ;
Liu, Rongkun ;
Pischon, Nicole ;
Trackman, Philip C. ;
Gerstenfeld, Louis ;
Graves, Dana T. .
BONE, 2007, 40 (02) :345-353
[2]   Glucose-induced inhibition of in vitro bone mineralization [J].
Balint, E ;
Szabo, P ;
Marshall, CF ;
Sprague, SM .
BONE, 2001, 28 (01) :21-28
[3]   Adiponectin and its receptors are expressed in bone-forming cells [J].
Berner, HS ;
Lyngstadaas, SP ;
Spahr, A ;
Monjo, M ;
Thommesen, L ;
Drevon, CA ;
Syversen, U ;
Reseland, JE .
BONE, 2004, 35 (04) :842-849
[4]   Chronic hyperglycemia modulates osteoblast gene expression through osmotic and non-osmotic pathways [J].
Botolin, Sergiu ;
McCabe, Laura R. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2006, 99 (02) :411-424
[5]   DEFECTIVE STIMULATION OF PROLIFERATION AND COLLAGEN BIOSYNTHESIS OF HUMAN BONE-CELLS BY SERUM FROM DIABETIC-PATIENTS [J].
BRENNER, RE ;
RIEMENSCHNEIDER, B ;
BLUM, W ;
MORIKE, M ;
TELLER, WM ;
PIRSIG, W ;
HEINZE, E .
ACTA ENDOCRINOLOGICA, 1992, 127 (06) :509-514
[6]   Rosiglitazone promotes development of a novel adipocyte population from bone marrow-derived circulating progenitor cells [J].
Crossno, Joseph T., Jr. ;
Majka, Susan M. ;
Grazia, Todd ;
Gill, Ronald G. ;
Klemm, Dwight J. .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (12) :3220-3228
[7]   Osteocalcin differentially regulates β cell and adipocyte gene expression and affects the development of metabolic diseases in wild-type mice [J].
Ferron, Mathieu ;
Hinoi, Eiichi ;
Karsenty, Gerard ;
Ducy, Patricia .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (13) :5266-5270
[8]  
Fujimoto WY, 1996, DIABETIC MED, V13, pS7
[9]  
FURIE B, 1990, BLOOD, V75, P1753
[10]   Increased bone density and decreased bone turnover, but no evident alteration of fracture susceptibility in elderly women with diabetes mellitus [J].
Gerdhem, P ;
Isaksson, A ;
Åkesson, K ;
Obrant, KJ .
OSTEOPOROSIS INTERNATIONAL, 2005, 16 (12) :1506-1512