2014
DOI: 10.4158/ep13110.or
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Osteocalcin Levels on Oral Glucose Load in Women being Investigated for Polycystic Ovary Syndrome

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Cited by 14 publications
(11 citation statements)
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“…Previous reports have been consistent, and reported lower levels of BTM in subjects with T2DM compared to nondiabetic subjects [6,16,21,39]. In insulin resistant [40], obese [17], and healthy subjects [15], glucose-loading is reported to exhibit a suppressive effect on BTM. An oral glucose tolerance test suppressed PINP and CTX by two-fourfold, higher fasting serum levels of glucose were associated with lower PINP, and higher levels of insulin were associated with increased bone formation markers [15].…”
Section: Discussionmentioning
confidence: 53%
“…Previous reports have been consistent, and reported lower levels of BTM in subjects with T2DM compared to nondiabetic subjects [6,16,21,39]. In insulin resistant [40], obese [17], and healthy subjects [15], glucose-loading is reported to exhibit a suppressive effect on BTM. An oral glucose tolerance test suppressed PINP and CTX by two-fourfold, higher fasting serum levels of glucose were associated with lower PINP, and higher levels of insulin were associated with increased bone formation markers [15].…”
Section: Discussionmentioning
confidence: 53%
“…5 In addition, patients with type 2 diabetes and polycystic ovarian syndrome are characterised by hyperinsulinaemia; yet, they have low circulating levels of OC, P1NP and b-CTx. 2,3 These studies all suggest that glucose may affect osteoblast function. In the current study, the circulating glucose levels were maintained around 5 mmol l À 1 ; however, glucose was constantly infused to achieve this targeted blood glucose level.…”
Section: Discussionmentioning
confidence: 91%
“…Bone remodelling markers (BRMs) are suppressed after a meal or following a glucose load 1,2 and correlate inversely with fasting plasma glucose levels as well as with 2 h glucose levels during an oral glucose tolerance test, 3 suggesting that glucose and insulin may affect osteoblast and osteoclast function. It is plausible that impairment of glucose handling might contribute to alterations in BRMs, thereby contributing to the increased fracture risk observed in obese people and those with type 2 diabetes.…”
Section: Introductionmentioning
confidence: 99%
“…Insulin infused at high, intermediate and low doses neither affected the level of undercarboxylated osteocalcin in participants with type 2 diabetes nor in healthy individuals ( 9 ). Furthermore, OGTT has previously been shown to decrease osteocalcin as well as undercarboxylated osteocalcin ( 10 , 11 ) and osteocalcin levels decreased during a hyperinsulinemic, euglycemic clamp in obese people ( 12 ). Antiresorptive therapies are hypothesized to increase undercarboxylated osteocalcin and thereby decrease diabetes incidence, however, in a post-hoc analysis of three randomized controlled trials the antiresorptive therapy did not affect fasting plasma glucose, weight loss, or diabetes risk ( 13 ).…”
Section: Discussionmentioning
confidence: 99%