Objective: Reciprocal interaction between bone and glucose metabolism might play a pivotal role in the development of type 2 diabetes. We recently demonstrated that osteocalcin is increased in women with gestational diabetes (GDM) compared to healthy pregnant women and related to enhanced insulin secretion. Here, we aimed to investigate the role of the bone resorption marker CTX and osteopontin (OPN), a key molecule in subclinical inflammation underlying insulin resistance, in gestational diabetes. Methods: Insulin sensitivity and secretion (derived from OGTT) as well as CTX and osteopontin were investigated in 26 GDM and 52 women with normal glucose tolerance during pregnancy [CON] between 24th and 28th gestational weeks; 24 women also underwent postpartum examination. Results: CTX was significantly higher in GDM compared to CON (0.44±0.20 vs.0.28±0.12 ng/ml, p <0.007) and liver enzymes. Twelve weeks after delivery CTX and OPN were increased compared to pregnancy (both p
CITATION STYLE
Winhofer, Y., Kiefer, F. W., Handisurya, A., Tura, A., Klein, K., Schneider, B., … Kautzky-Willer, A. (2012). CTX (Crosslaps) rather than Osteopontin is associated with disturbed glucose metabolism in gestational diabetes. PLoS ONE, 7(7). https://doi.org/10.1371/journal.pone.0040947
Mendeley helps you to discover research relevant for your work.