Reduced attenuation of bone resorption after oral glucose in type 2 diabetes

被引:24
作者
Chailurkit, La-or [1 ]
Chanprasertyothin, Suwannee [2 ]
Rajatanavin, Rajata [1 ]
Ongphiphadhanakul, Boonsong [1 ]
机构
[1] Mahidol Univ, Div Endocrinol & Metab, Dept Med, Fac Med,Ramathibodi Hosp, Rama 6th Rd, Bangkok 10400, Thailand
[2] Mahidol Univ, Ramathibodi Hosp, Fac Med, Res Ctr, Bangkok 10400, Thailand
关键词
D O I
10.1111/j.1365-2265.2007.03159.x
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective To investigate the effect of oral glucose on bone resorption and osteoprotegerin (OPG) in subjects with varying degrees of glucose tolerance. Design and Patients In a cross-sectional study, 163 postmenopausal women aged 50-88 years without previous history of diabetes, impaired fasting glucose (IFG) or impaired glucose tolerance (IGT) were recruited. All subjects underwent a 75-g oral glucose tolerance test (OGTT) and were then classified as having normal glucose tolerance (NGT), IFG, IGT or diabetes according to American Diabetes Association (ADA) criteria. Measurements Plasma glucose, serum insulin, C-terminal telopeptide of type I collagen (CTX-I) and OPG were measured. Results Fasting insulin levels increased progressively from subjects with NGT, IFG/IGT to diabetes. After adjusted for age and body mass index (BMI), there was no significant difference in fasting CTX-I and OPG levels across the various degrees of glucose tolerance. After oral glucose, there was a significant decrease in serum CTX-I and OPG (P < 0.001) except for serum OPG in diabetic subjects. In addition, the percentages of change from baseline for both serum CTX-I and OPG were significantly less in diabetic subjects when compared to those in NGT subjects (-40.9% and 0.6% for diabetes and -50.2% and -10.6% for NGT, respectively). Conclusions Oral glucose intake causes suppression of serum CTX-I and OPG in postmenopausal women. The effect is attenuated in women with type 2 diabetes.
引用
收藏
页码:858 / 862
页数:5
相关论文
共 30 条
[1]
American Diabetes Association, 2004, Diabetes Care, V27 Suppl 1, pS5, DOI 10.2337/diacare.27.2007.S5
[2]
Mechanism of circadian variation in bone resorption [J].
Bjarnason, NH ;
Henriksen, EEG ;
Alexandersen, P ;
Christgau, S ;
Henriksen, DB ;
Christiansen, C .
BONE, 2002, 30 (01) :307-313
[3]
Associations of serum osteoprotegerin levels with diabetes, stroke, bone density, fractures, and mortality in elderly women [J].
Browner, WS ;
Lui, LY ;
Cummings, SR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (02) :631-637
[4]
Sketetal involvement in patients with diabetes mettitus [J].
Carnevale, V ;
Romagnoli, E ;
D'Erasmo, E .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2004, 20 (03) :196-204
[5]
Octreotide abolishes the acute decrease in bone turnover in response to oral glucose [J].
Clowes, JA ;
Allen, HC ;
Prentis, DM ;
Eastell, R ;
Blumsohn, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (10) :4867-4873
[6]
Diabetes mellitus and the incidence of hip fracture:: results from the Nord-Trondelag Health Survey [J].
Forsén, L ;
Meyer, HE ;
Midthjell, K ;
Edna, TH .
DIABETOLOGIA, 1999, 42 (08) :920-925
[7]
Circulating osteoprotegerin is correlated with lipid profile, insulin sensitivity, adiponectin and sex steroids in an ageing male population [J].
Gannage-Yared, Marie-Helene ;
Fares, Florence ;
Semaan, Michelle ;
Khalife, Simon ;
Jambart, Selim .
CLINICAL ENDOCRINOLOGY, 2006, 64 (06) :652-658
[8]
Diabetes and incidence of functional disability in older women [J].
Gregg, EW ;
Mangione, CM ;
Cauley, JA ;
Thompson, TJ ;
Schwartz, AV ;
Ensrud, KE ;
Nevitt, MC .
DIABETES CARE, 2002, 25 (01) :61-67
[9]
Effects of dietary improvement on bone metabolism in elderly underweight women with osteoporosis: a randomised controlled trial [J].
Hampson, G ;
Martin, FC ;
Moffat, K ;
Vaja, S ;
Sankaralingam, S ;
Cheung, J ;
Blake, GM ;
Fogelman, I .
OSTEOPOROSIS INTERNATIONAL, 2003, 14 (09) :750-756
[10]
The changes in circulating osteoprotegerin after hormone therapy in postmenopausal women and their relationship with oestrogen responsiveness on bone [J].
Han, KO ;
Choi, JT ;
Choi, HA ;
Moon, IG ;
Yim, CH ;
Park, WK ;
Yoon, HK ;
Han, IK .
CLINICAL ENDOCRINOLOGY, 2005, 62 (03) :349-353