Bone Turnover Markers in Patients With Nonalcoholic Fatty Liver Disease and/or Type 2 Diabetes During Oral Glucose and Isoglycemic Intravenous Glucose
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[1] M. Daleva,et al. Biochemical , 2020, Definitions.
[2] S. Upala,et al. Nonalcoholic fatty liver disease and osteoporosis: a systematic review and meta-analysis , 2017, Journal of Bone and Mineral Metabolism.
[3] A. Linneberg,et al. Comparison of two automated assays of BTM (CTX and P1NP) and reference intervals in a Danish population , 2017, Osteoporosis International.
[4] J. Holst,et al. Differential impact of glucose administered intravenously or orally on bone turnover markers in healthy male subjects. , 2017, Bone.
[5] P. Vestergaard,et al. Epidemiology of Fractures in Diabetes , 2017, Calcified Tissue International.
[6] S. Lee,et al. Association between bone mineral density and nonalcoholic fatty liver disease in Korean adults , 2016, Journal of Endocrinological Investigation.
[7] J. Tomlinson,et al. Non-alcoholic fatty liver disease and diabetes , 2016, Metabolism: clinical and experimental.
[8] Xin Gao,et al. The association of liver fat content and serum alanine aminotransferase with bone mineral density in middle-aged and elderly Chinese men and postmenopausal women , 2016, Journal of Translational Medicine.
[9] T. Vilsbøll,et al. Diabetic and nondiabetic patients with nonalcoholic fatty liver disease have an impaired incretin effect and fasting hyperglucagonaemia , 2016, Journal of internal medicine.
[10] S. Shim,et al. Association of nonalcoholic fatty liver disease with bone mineral density and serum osteocalcin levels in Korean men , 2016, European journal of gastroenterology & hepatology.
[11] H. Koistinen,et al. The effects of acute hyperinsulinemia on bone metabolism , 2015, Endocrine connections.
[12] B. Ferraz-de-Souza,et al. The role of enteric hormone GLP-2 in the response of bone markers to a mixed meal in postmenopausal women with type 2 diabetes mellitus , 2015, Diabetology & Metabolic Syndrome.
[13] M. Christensen,et al. Glucose-dependent insulinotropic polypeptide inhibits bone resorption in humans. , 2014, The Journal of clinical endocrinology and metabolism.
[14] S. Khosla,et al. In Vivo Assessment of Bone Quality in Postmenopausal Women With Type 2 Diabetes , 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[15] T. Hansen,et al. A functional amino acid substitution in the glucose-dependent insulinotropic polypeptide receptor (GIPR) gene is associated with lower bone mineral density and increased fracture risk. , 2014, The Journal of clinical endocrinology and metabolism.
[16] D. Chappard,et al. Glucose-dependent insulinotropic polypeptide (GIP) receptor deletion leads to reduced bone strength and quality. , 2013, Bone.
[17] D. Chappard,et al. Glucose-dependent insulinotropic polypeptide receptor deficiency leads to modifications of trabecular bone volume and quality in mice. , 2013, Bone.
[18] Yu Xu,et al. Association between nonalcoholic fatty liver disease (NAFLD) and osteoporotic fracture in middle-aged and elderly Chinese. , 2012, The Journal of clinical endocrinology and metabolism.
[19] J. Kanis,et al. FRAX underestimates fracture risk in patients with diabetes , 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[20] J. Holst,et al. Glucose-Dependent Insulinotropic Polypeptide , 2011, Diabetes.
[21] E. Vittinghoff,et al. Association of BMD and FRAX score with risk of fracture in older adults with type 2 diabetes. , 2011, JAMA.
[22] P. Hayes,et al. Prevalence of and Risk Factors for Hepatic Steatosis and Nonalcoholic Fatty Liver Disease in People With Type 2 Diabetes: the Edinburgh Type 2 Diabetes Study , 2011, Diabetes Care.
[23] S. Khosla,et al. Effects of physiological variations in circulating insulin levels on bone turnover in humans. , 2011, The Journal of clinical endocrinology and metabolism.
[24] K. Xiang,et al. Variants from GIPR, TCF7L2, DGKB, MADD, CRY2, GLIS3, PROX1, SLC30A8 and IGF1 Are Associated with Glucose Metabolism in the Chinese , 2010, PloS one.
[25] S. Majumdar,et al. High-resolution peripheral quantitative computed tomographic imaging of cortical and trabecular bone microarchitecture in patients with type 2 diabetes mellitus. , 2010, Journal of Clinical Endocrinology and Metabolism.
[26] Alex Doney,et al. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge , 2010, Nature Genetics.
[27] J. Holst,et al. Four-month treatment with GLP-2 significantly increases hip BMD: a randomized, placebo-controlled, dose-ranging study in postmenopausal women with low BMD. , 2009, Bone.
[28] S. Chanprasertyothin,et al. Reduced attenuation of bone resorption after oral glucose in type 2 diabetes , 2008, Clinical endocrinology.
[29] J. Holst,et al. Reduction in bone resorption by exogenous glucagon-like peptide-2 administration requires an intact gastrointestinal tract , 2008, Scandinavian journal of gastroenterology.
[30] J. Holst. The physiology of glucagon-like peptide 1. , 2007, Physiological reviews.
[31] Walter C Willett,et al. Systematic review of type 1 and type 2 diabetes mellitus and risk of fracture. , 2007, American journal of epidemiology.
[32] G. Targher,et al. Prevalence of Nonalcoholic Fatty Liver Disease and Its Association With Cardiovascular Disease Among Type 2 Diabetic Patients , 2007, Diabetes Care.
[33] P. Vestergaard,et al. Discrepancies in bone mineral density and fracture risk in patients with type 1 and type 2 diabetes—a meta-analysis , 2007, Osteoporosis International.
[34] Karen C Johnson,et al. Risk of fracture in women with type 2 diabetes: the Women's Health Initiative Observational Study. , 2006, The Journal of clinical endocrinology and metabolism.
[35] Jonathan C. Cohen,et al. Prevalence of hepatic steatosis in an urban population in the United States: Impact of ethnicity , 2004, Hepatology.
[36] J. Holst,et al. Role of Gastrointestinal Hormones in Postprandial Reduction of Bone Resorption , 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[37] R. Eastell,et al. Octreotide abolishes the acute decrease in bone turnover in response to oral glucose. , 2003, The Journal of clinical endocrinology and metabolism.
[38] J. Holst,et al. Both GLP-1 and GIP are insulinotropic at basal and postprandial glucose levels and contribute nearly equally to the incretin effect of a meal in healthy subjects , 2003, Regulatory Peptides.
[39] R. Eastell,et al. Acute changes of bone turnover and PTH induced by insulin and glucose: euglycemic and hypoglycemic hyperinsulinemic clamp studies. , 2002, The Journal of clinical endocrinology and metabolism.
[40] R. Eastell,et al. Effect of feeding on bone turnover markers and its impact on biological variability of measurements. , 2002, Bone.
[41] A. Folsom,et al. Type 1 and type 2 diabetes and incident hip fractures in postmenopausal women. , 2001, Diabetes care.
[42] W. Creutzfeldt,et al. Glucagon-like peptide-1 but not glucagon-like peptide-2 stimulates insulin release from isolated rat pancreatic islets , 1985, Diabetologia.
[43] P. Vestergaard,et al. Biochemical bone turnover markers in diabetes mellitus - A systematic review. , 2016, Bone.
[44] J. Holst,et al. Glucose-Dependent Insulinotropic Polypeptide A Bifunctional Glucose-Dependent Regulator of Glucagon and Insulin Secretion in Humans , 2011 .
[45] Joel Z Stengel,et al. Prevalence of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis among a largely middle-aged population utilizing ultrasound and liver biopsy: a prospective study. , 2011, Gastroenterology.
[46] Sesi Pengajian,et al. EFFECT OF FEEDING , 2023 .
[47] C. Christiansen,et al. Mechanism of circadian variation in bone resorption. , 2002, Bone.
[48] S. Cummings,et al. Older women with diabetes have an increased risk of fracture: a prospective study. , 2001, The Journal of clinical endocrinology and metabolism.