Searchable abstracts of presentations at key conferences on calcified tissues

ba0006oc21 | (1) | ICCBH2017

Scoliosis in fibrous dysplasia/McCune-albright syndrome

Berglund Jason , Tella Sri Harsha , Kim Lauren , Stanton Robert , Collins Michael , Boyce Alison

Objectives: Fibrous dysplasia is a rare bone and endocrine disorder resulting from somatic activating mutations in GNAS. In the skeleton, proliferation of undifferentiated stromal cells results in osseous lesions that are prone to deformity, fracture, and pain. Lesions may affect one bone or many, and may occur in isolation or in association with hyperfunctioning endocrinopathies, termed McCune-Albright syndrome (MAS). Scoliosis is a potentially serious, even lethal c...

ba0006p064 | (1) | ICCBH2017

Extensive periosteal new bone formation secondary to copper deficiency in a 2 year-old boy with arterial tortuosity syndrome

Bowden Sasigarn , Adler Brent , Shaikhkhalil Ala , Hor Kan , McBride Kim , Steingass Katherine

Background: Periosteal reaction can be a manifestation of various underlying medical conditions, including tumor, infection, trauma, metabolic or genetic diseases.Presenting problem: A 2 year-old male presented for evaluation of periosteal bone formation in symmetrical distribution of proximal humerus, radius, ulnar, femur, and clavicles, noted after having persistent fussiness, irritability and inability to bear weight and use arms for 3 weeks. He had a...

ba0003pp221 | Osteoporosis: evaluation and imaging | ECTS2014

Comparison of diagnostic strategies to detect prevalent vertebral fracture for adults over age 50: use of vertebral fracture assessment or spine radiography

Kim Deog-Yoon , Oh Sung-Hee , Ahn Jeonghoon , Lee Young Eun , Lee Yu Kyung , Hwang Jin-Seub , Yoo Na Eun , Lee Joo-Hyun , Pyo Junhee , Kim Dam , Choi Yun Young , Bae Sang-Cheol , Sung Yoon-Kyoung

Background: The prevalent vertebral fracture (VF) is a risk factor for future VF, which can be decreased with drug therapy. However, most VFs are not recognized clinically. VFA by DXA and spine X-ray can be performed to detect these prevalent VFs.Objectives: This study aimed to estimate the costs, effectiveness, and radiation exposure of VF diagnostic strategies.Methods: Markov model over a 10-year period was used to calculate the ...

ba0002p65 | (1) | ICCBH2013

Improvement in morphological properties of trabecular bones and longitudinal growth in tibia for growing rats through an impact stimulation

Eom Sinae , Ko Chang-Yong , Park Ji Hyung , Seo Dong-Hyun , Jung Young Jin , Kim Han Sung

Mechanical stress and strain generated by physical exercises or the other passive stimulations are well known to have a positive effect on the growing musculoskeletal system. Especially, when the impact stimulation which evokes high magnitude of strain in a second is applied to bone, it improves bone qualities. Thus, to verify the effect of impact stimulation, we conducted longitudinal study on morphological properties of the tibia in growing rats. Free falls from designated h...

ba0003pp117 | Cell biology: osteoblasts and bone formation | ECTS2014

EGF inhibits Wnt/β-catenin-induced osteoblast differentiation in a Smurf1-dependent manner

Kwon Arang , Boonanantanasarn Kanitsak , Lee Hye-Lim , Woo Kyung Mi , Ryoo Hyun-Mo , Kim Gwan-Shik , Baek Jeong-Hwa

BMPs and canonical Wnts are the representative developmental signals that enhance osteoblast differentiation and bone formation. Previously, we demonstrated that EGF inhibits BMP2-induced osteoblast differentiation through the induction of Smurf1 expression. However, the regulatory role of EGF in Wnt/β-catenin-induced osteoblast differentiation has not been elucidated. In this study, we investigated the effect of EGF on Wnt/β-catenin signaling-induced osteoblast diff...

ba0003pp362 | Other diseases of bone and mineral metabolism | ECTS2014

Osteogenesis imperfecta in adults: a cross sectional trial

Hald Jannie Dahl , Folkestad Lars , Andersen Jane , Harslof Torben , Lund Allan , Jens-Erik Beck Jensen , Brixen Kim , Langdahl Bente

Osteogenesis imperfecta (OI) is a hereditary disease with a generalized involvement of the connective tissue caused by collagen type 1 mutations. The clinical appearance is broad with fractures as the key symptom. Only few genotype–phenotype correlations have been established. We aim to characterize the Danish OI population thoroughly including DXA and HRpQCT, anthropometry, patient history, and genetic background.This cross-sectional study includes...

ba0004p142 | (1) | ICCBH2015

The mechanical multi-stimulation for musculoskeletal disease

Park Ji Hyung , Cho Seungkwan , Seo Dong-Hyun , Hwang Dong-Hyun , Han Tae-Young , Kim Han Sung

Osteoporosis takes the form of porous bone loss which is due to aging, insufficient exercise and unbalanced nutrition and so on. A number of treatments were developed to treat the osteoporosis, which were categorized by pharmacological and non-pharmacological methods. However, it is generally accepted that taking too much pharmacological medication may be harmful to the health. Thus, non-pharmacological treatments are considered as the alternative ways to overcome the side eff...

ba0005p223 | Energy metabolism and bone, fat and bone | ECTS2016

Cyclic AMP/protein kinase A signalling downregulates Dlx5 expression via inducing C/Ebpβ in 3T3-L1 preadipocytes

Baek Jeong-Hwa , Lee Hye-Lim , Qadir Abdul , Kim Hyun Jeong , Chung Jin , Woo Kyung Mi , Ryoo Hyun-Mo

Distal-less homeobox 5 (Dlx5) is a transcription factor that enhances osteogenic differentiation of mesenchymal stem cells via upregulating the expression of Runx2 and other osteoblast phenotypic genes. We have previously demonstrated that Dlx5 also downregulates adipogenic differentiation of mesenchymal stem cells and that insulin decreases expression levels of Dlx5 via increasing expression levels of miR-124, a microRNA targeting 3′UTR of Dlx5. However, the mechanism o...

ba0005p247 | Genetics and Epigenetics | ECTS2016

Common variants in Rspo 1,2 and 3 do not associate with BMD in stratified subpopulations of the Odense Androgen Study and mutations in these genes are not a common cause of craniotubular hyperostosis

Fijalkowski Igor , Hendrickx Gretl , Boudin Eveline , Szilagyi Ingrid , Nielsen Torben , Andersen Marianne , Brixen Kim , Van Hul Wim

The R-spondins are a family of four small, secreted agonists of the Wnt signaling pathway. Growing evidence from both in vitro studies and in vivo models supports the major role of these proteins in the skeletal development processes. In humans, common genetic variation in the RSPO3 gene has been associated with BMD in large scale GWAS study.This study aimed at further investigation of the genetic and functional contributions of the R-s...