Searchable abstracts of presentations at key conferences on calcified tissues

ba0003pp256 | Osteoporosis: pathophysiology and epidemiology | ECTS2014

Sarcopenia increased mortality among elderly men

Fujiwara Sako , Masunari Naomi , Takahashi Ikuno , Ohishi Waka

Sarcopenia has been indicated as one of the important markers of frailty among the elderly. This study aims to evaluate mortality risk among Japanese elderly persons with sarcopenia, taking into account lifestyle and physical factors.From among a population-based community cohort, the Adult Health Study conducted at RERF, 1880 subjects (626 men and 1 254 women) aged 47–95 years old were enrolled in a prospective and longitudinal cohort study in Hiro...

ba0007oc23 | (1) | ICCBH2019

Effects of the FGF2 aptamer on growth plate cartilage development of achondroplasia patient-specific iPS cells in a xenograft model

Kimura Takeshi , Yasuda Kie , Nakano Yukako , Takeyari Shinji , Kitabatake Yasuji , Kubota Takuo , Miyoshi Yoko , Ozono Keiichi , Nonaka Yosuke , Fujiwara Masatoshi , Nakamura Yoshikazu

Objectives: Endochondral ossification in the growth plate cartilage (GPC) plays a crucial role in the determination of the length and shape of long bones. Many skeletal dysplasias are caused by GPC dysfunction, associated with short stature. We have already reported that human iPS cell-derived cartilage (hiPSC-Cart), when implanted into the subcutaneous spaces of the SCID mice for 4 weeks, formed skeletal tissue like GPC. This model could also recapitulate the pathology of FGF...

ba0004p16 | (1) | ICCBH2015

Genotype in patients with osteogenesis imperfecta using a targeted exome sequencing: correlation with phenotype

Kubota Takuo , Ohata Yasuhisa , Bizaoui-Auffret Varoona , Nawa Nobutoshi , Nakayama Hirofumi , Yamamoto Keiko , Fujiwara Makoto , Kitaoka Taichi , Takakuwa Satoshi , Namba Noriyuki , Ozono Keiichi

Objectives: Osteogenesis imperfecta (OI) is a relatively common skeletal dysplasia characterized by bone fragility, mainly resulting from mutations in the COL1A1 and COL1A2 genes. Phenotype–genotype correlation is not fully uncovered in OI. Additionally, more than ten genes have been found to be responsible for OI. In the current study, we determine mutations in patients with OI using a targeted exome sequencing and examine a phenotype–genotype correlation.<p cla...

ba0007p61 | (1) | ICCBH2019

Biochemical and genetic analysis in patients with odontohypophosphatasia in Japan

Kubota Takuo , Ohata Yasuhisa , Ishihara Yasuki , Fujiwara Makoto , Takeyari Shinji , Yamamoto Kenichi , Nakano Yukako , Miyata Kei , Nakayama Hirofumi , Kitaoka Taichi , Okawa Rena , Nakano Kazuhiko , Akiyama Tomoyuki , Ozono Keiichi

Background: Hypophosphatasia (HPP) is characterized by defective mineralization of bone and/or teeth in the presence of low serum alkaline phosphatase (ALP) activity and caused by mutations in the ALPL gene encoding tissue-nonspecific ALP. Odontohypophosphatasia (odonto HPP) is the mildest form of hypophosphatasia and characterized by dental complications without abnormalities of the skeleton system.Objectives: We aimed to investigate biochemical and gen...