Data on body mass, glucose tolerance and bone phenotype of mice with osteogenesis imperfecta on long-term low-fat and high-fat diets

Data Brief. 2022 Feb 16:41:107961. doi: 10.1016/j.dib.2022.107961. eCollection 2022 Apr.

Abstract

Male and female mice with a dominant severe bone fragility disorder, osteogenesis imperfecta, and their wild-type littermates (FVB background) were challenged with a long-term (26 weeks) high-fat diet to evaluate the development of obesity and glucose intolerance. Here we present data for the measurements of body mass, the outcome of glucose tolerance tests during the long-term diet, as well as organ weights and bone phenotype at the end of the study. Interpretation of the data and further in-depth analysis can be found in the article "Male but not female mice with severe osteogenesis imperfecta are partially protected from high-fat diet-induced obesity." by Tauer JT, Boraschi-Diaz I, Al Rifai O, Rauch F, Ferron M, Komarova SV, published in Molecular Genetics and Metabolism. The data presented here demonstrate individual mouse outcomes of long-term diet experiments that can be reused for comparative studies of diet-induced changes in wild-type mice on different backgrounds and different mouse models of osteogenesis imperfecta.

Keywords: AUC, Area under the curve; Animal model; BAT, Brown adipose tissue; BMD, Bone mineral density; BV/TV, bone volume/tissue volume; Body mass; Bone phenotype; CT, Computed tomography; FVB; GTT, Glucose tolerance test; Glucose intolerance; HFD, High-fat/low-sugar diet; High-fat diet; LFD, Low-fat/low-sugar diet; OI, Osteogenesis imperfecta; Osteogenesis imperfecta; PBS, phosphate-buffered saline; SEM, Standard error of mean; Tb.Sp., Trabecular separation; Trab.BMD, Trabecular bone mineral density; WAT, White adipose tissue; WT, Wild-type.