Searchable abstracts of presentations at key conferences on calcified tissues

ba0001pp433 | Osteoporosis: treatment | ECTS2013

Denosumab is associated with progressive improvements in hip cortical mass and thickness

Poole K , Treece G , Gee A , Brown J P , McClung M R , Wang A , Libanati C

Denosumab (DMAb) significantly improves bone strength at the hip, estimated by FEA from QCT scans, from baseline (B/L) and vs placebo (Pbo) (Keaveny ASBMR 2010). We determined the extent and distribution of mass and thickness changes at the proximal femur, a key skeletal site for fracture risk, using a novel cortical bone mapping technique on the same serial QCT scans. A FREEDOM substudy included 80 women who underwent hip QCT scanning at B/L and months 12, 24 and 36 during DM...

ba0003pp167 | Cell biology: osteoclasts and bone resorption | ECTS2014

Inhibitory effect of Crossostephium chinense extract on RANKL-activating osteoclastogenesis in patients with tophaceous gout

Wang Shih-Wei , Kuo Han-Chun , Hsu Hsia-Fen , Houng Jer-Yiing

Chronic tophaceous gout is the natural evolution of untreated gouty arthritis and is characterized by the deposition of solid monosodium urate crystal aggregated in a variety of tissue including joints, bursae and tendons. Tophaceous gout is well-known to cause bone erosions and is characterized by enhanced osteoclasts development. Peripheral blood mononuclear cells (PBMCs) from patients with severe erosive gout showed the preferential ability to transform into osteoclast-like...

ba0003pp367 | Other diseases of bone and mineral metabolism | ECTS2014

Blockade of Wnt inhibitor Dickkopf-1 improves bone mass and microstructure of osteogensis imperfecta

Wang Feng-Sheng , Su Wen-Hong , Chuang Pei-Chin , Kuo Su-Ren , Ko Jih-Yang

Osteogenesis imperfect (OI) is an inheritable bone disease with low bone mass, fragility, deformity and multiple fractures in skeletal tissues. Modulation of Wnt signalling components reportedly alleviates excessive bone and joint remodelling in various skeletal disorders. This study is undertaken to explore whether loss of Wnt inhibitor Dickkopf-1 (Dkk1) action affects bone formation or skeletal homeostasis in OI. In clinical vignettes, OI patients had severe osteoporosis (<e...

ba0005p12 | Biochemical testing | ECTS2016

Improvement on growth of osteoporotic bone tissue around screw and fixation strength of screw induced by stress force from the expanding pedicle screw: dynamic microstructural, histological and biomechanical studies in osteoporotic sheep lumbar vertebrae

Liu Da , Zhang Bo , Xie Qing-yun , Wang Cai-ru , Liao Dong-fa , Lei Wei

Objective: It was proved that expansive pedicle screw (EPS) could significantly enhance immediate screw stability through mechanical expanding and compressing. However, there were little researches on growth of bone tissue around screw and dynamic screw stability in vivo in osteoporotic vertebrae. This study was designed to evaluate growth and microstructure of bone tissue around screw and fixation strength of screw in osteoporotic sheep lumbar vertebrae.<p class=...

ba0005p92 | Calciotropic and phosphotropic hormones and mineral metabolism | ECTS2016

The analysis of missed diagnosis and misdiagnosis of 144 tumor-induced osteomalacia patients

Feng Juan , Jiang Yan , Wang Ou , Li Mei , Xing Xiao-ping , Meng Xun-wu , Xia Weibo

Introduction: Tumor-induced osteomalacia (TIO) is a rare acquired paraneoplastic syndrome which is usually induced by mesenchymal tissue tumor with excessive secretion of FGF23. The misdiagnosis of TIO is frequently seen in clinic. Therefore, this study is aimed to describe the misdiagnosed situation of TIO, explore the possible underlying reasons for missed diagnosis and misdiagnosis through the analysis of 144 TIO patients, and improve clinicians’ awareness of TIO.<...

ba0005p227 | Energy metabolism and bone, fat and bone | ECTS2016

The role of interleukin-6 and tumor necrosis factor alpha gene in fat and bone communication

Wang Chunyu , Tian Li , Zhang Kun , Chen Yaxi , Chen Xiang , Xie Ying , Zhao Qian , Yu Xijie

Objective: To comparing the role of interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) in fat and bone communication.Methods: Male wild type (WT) mice, IL-6 knockout (IL-6−/−) mice, and tumor necrosis factor alpha (TNF-α) were fed with either standard diet (SD) or high fat diet (HFD) for 12 weeks. Bone mass and bone microstructure were evaluated by micro-CT. Gene expression related to lipid and bone metabolisms ...

ba0005p296 | Osteoporosis: evaluation and imaging | ECTS2016

Predicting hip fracture type of elderly Asian patients with low-energy fall by volumetric BMD and femoral morphology from QCT

Su Yong-Bin , Cheng Xiao-Guang , Wang Ling , Ma Yi-Min

Introduction: Femoral neck fractures and trochanteric fractures are two major types of hip fractures. The BMD changing or hip strength analysis (HSA) of the two type fractures may be different. No research had focused on a large sample of Asian people. This study investigated the differences in BMD and morphologic features of the two type hip fractures of elderly Asian people from QCT.Methods: A total of 279 elderly Chinese patients with hip fractures du...

ba0005p453 | Other diseases of bone and mineral metabolism | ECTS2016

Two novel mutations of RUNX2 gene in two sporadic cleidocranial dysplasia patients

Zhang Cong , Jiang Yan , Xing Xiaoping , Li Mei , Wang Ou , Xia Weibo

Background: Cleidocranial dysplasia (CCD) is an autosomal-dominant skeletal dysplasia syndrome characterized by delayed closure of cranial sutures, remained-open fontanels, hypoplastic clavicles, abnormal dentition including retention of the primary teeth and delayed eruption of secondary dentition, and short stature. The responsible gene for CCD is RUNX2, which encodes an important transcription factor for osteoblast development and bone formation. CCD is caused by t...

ba0005p457 | Other diseases of bone and mineral metabolism | ECTS2016

Mutant TGFβ1 in Camurati-Engelamann disease causes systemic manifestations and reproductive disorders more often than previously thought: report of eight Chinese families

Jiajue Ruizhi , Zhao Zhen , Wu Bo , Jiang Yan , Wang Ou , Li Mei , Xing Xiaoping , Xia Weibo

Camurati-Engelmann disease (CED) is a rare autosomal dominant bone disease with transforming growth factor-β1 (TGFβ1) gene mutation. In order to expand our limited knowledge of Chinese CED patients, we reported eight Chinese families (11 patients) diagnosed with CED. The study was approved the Department of Scientific Research of Peking Union Medical College Hospital. All the patients were evaluated genetically, clinically, biochemically and radiographically...