Searchable abstracts of presentations at key conferences on calcified tissues

ba0005p444 | Other diseases of bone and mineral metabolism | ECTS2016

Deep characterization of a zebrafish model for dominant osteogenesis imperfecta

Tonelli Francesca , Gioia Roberta , Biggiogera Marco , Fisher Shannon , Leikin Sergey , Schinke Thorsten , Rossi Antonio , Forlino Antonella

Dominant osteogenesis imperfecta (OI) is a bone disease mainly caused by collagen type I mutations and characterized by bone fragility and growth delay. Nowadays no definitive cure is available. A zebrafish OI model (Chihuahua) carrying an heterozygous G574D substitution in the α1 chain of collagen type I was generated by ENU mutagenesis and is available in our laboratory. Control (WT) and mutant (Chi+/−) fish growth was followed up from day 1 post fertilization to ...

ba0005p471 | Paediatric bone disease | ECTS2016

Bone involvement and intervertebral disc calcifications in beta-thalassemic patients: a retrospective study

de Sire Alessandro , Moretti Antimo , Bianco Massimiliano , Gimigliano Francesca , Iolascon Giovanni

Background: Bone involvement in patients with β-thalassemia is well known, but only few studies have analyzed bone microarchitecture and the prevalence of intervertebral disc calcifications (IDCs) in these patients. The aim of our study was to evaluate the bone quality in a group of patients with β-thalassemia in terms of geometry and microarchitecture properties; moreover, we evaluated the presence of IDCs in these patients.Material and method...

ba0007is10 | (1) | ICCBH2019

Endoplasmic reticulum stress in osteoblasts

Besio Roberta , Tonelli Francesca , Garibaldi Nadia , Leoni Laura , Cotti Silvia , Forlino Antonella

Bone tissue homeostasis requires the coordinated activity of osteoblasts, the bone forming cells, of osteoclasts, the bone resorbing cells, and of osteocytes, generally referred as the bone mechano-sensors. In this contest, osteoblasts are the mesenchymal cells secreting the extracellular matrix components on which hydroxyapatite crystals are then deposited. The most abundant protein of this organic matrix is type I collagen, a heterotrimeric secretory protein, synthesized as ...

ba0007p36 | (1) | ICCBH2019

ALPL gene mutation in a family

Vai Silvia , Broggi Francesca , Luisa Bianchi Maria , Ponti Emanuela , Mihalich Alessandra , Maria Di Blasio Anna

Introduction: The clinical diagnosis of mild forms of hypophosphatasia [HPP], a rare genetic bone disease, is often made in adulthood, on the basis of persistently low serum levels of alkaline phosphatase [ALP], often coupled with signs of poor bone/teeth mineralization.Case report: A 50-year-old male on treatment with vitamin D supplementation because of osteoporosis of lumbar spine (T-score –3.2) and femoral neck (T-score –2.4), was referred ...

ba0007p98 | (1) | ICCBH2019

The effect of vitamin D on bone health assessed by radiogrammetry: a double-blind placebo-controlled vitamin D supplementation trial in infants

Uday Suma , Crowe Francesca , Bowie Jessica , Mughal Zulf , Manaseki-Holland Semira , Hogler Wolfgang

Introduction: The effect of vitamin D± calcium supplementation in children has traditionally been assessed using growth parameters, biochemical markers and radiographs.Objectives: To evaluate the utility of Bone Health Index (BHI), obtained using automated hand radiogrammetry, in assessing treatment effect in children participating in a vitamin D supplementation trial.Methods: In this double-blind placebo-controlled trial, Afg...

ba0001pp11 | Clinical case posters | ECTS2013

Gorham disease: a case with severe cervical spine involvement

Terroso Georgina , Pinho Andre Rodrigues , Carvalho Manuel Santos , Freitas Joana , Serdoura Francisco , Veludo Vitorino

Introduction: Gorham disease (GD), also known as Gorham–Stout syndrome, massive osteolysis or disappearing bone disease, is a very rare disease characterized by spontaneous and progressive osteolysis of one or more bones. Its prognosis is highly variable and unpredictable, ranging from minimal disability to death, due to involvement of vital structures, such as the vertebral column and rib cage. Osteoclasts hyperactivity has been suggested as potential pathogenetic abnorm...

ba0004p116 | (1) | ICCBH2015

Osteopetrosis with uncommon final height: can only local IGF1 hold normal growth during pubertal spurt?

Milani Soraya Sader , Paula Francisco Jose , Liberatore Jr Raphael , Martinelli Jr Carlos Eduardo

Background: Final stature is a result of concomitant growth hormone (GH)-IGF1 axis integrity, a healthy environment and genetic background. Occasionally, growth occurs despite remarkable impairment in hormone profile. Presenting problem: An uncommon case of longitudinal growth in a boy with very low IGF1 concentrations and clinical diagnosis of osteopetrosis. Clinical management: We report on the case of a 19 year-old male patient with the diagnosis of osteopetrosis who had a ...

ba0003pp116 | Cell biology: osteoblasts and bone formation | ECTS2014

Inhibitory effect of GH on the adipogenic commitment of mesenchymal stromal cells derived from human trabecular bone

Bolamperti Simona , Spinello Alice , Sauer Aisha , GianLuigi Moro , Ometti Marco , Fraschini Gianfranco , Guidobono Francesca , Rubinacci Alessandro , Villa Isabella

Besides its well known effect on longitudinal bone growth, GH plays a role in the maintenance of adult bone mass. As aging progresses GH levels decline, bone mass decreases and mesenchymal precursors show a reduced osteogenic differentiation capacity resulting in an increase in bone marrow adipocytes. We investigated the effect of GH on MSC differentiation and the possible involvement of microRNA in this process. Human MSC derived from trabecular specimens, waste material of o...

ba0003pp311 | Osteoporosis: treatment | ECTS2014

Rates and reasons for lack of persistence with anti-osteoporotic drugs: analysis of the Campania Region Database

Iolascon Giovanni , Gimigliano Francesca , Moretti Antimo , Di Pietro Gioconda , Capaldo Annarita , Orlando Valentina , Monetti Valeria , Menditto Enrica

Background: Osteoporosis treatment involves several therapeutic tools, including long-term drug therapy. Subjects with chronic disorders are more likely to be non-adherent and/or non-persistent to treatment than those with other diseases. Adherence is the extent to which patients take medication as prescribed by their physicians, whereas persistence is the time from treatment initiation to discontinuation. Lack of persistence is common among subjects using oral anti-osteoporot...

ba0005p117 | Cancer and bone: basic, translational and clinical | ECTS2016

Contribution of multiple myeloma-derived exosomes to bone disease

Raimondi Lavinia , De Luca Angela , Carina Valeria , Agnese Valentina , Fontana Simona , Monteleone Francesca , Saieva Laura , Alessandro Riccardo , Giavaresi Gianluca

Bone disease is the most frequent complication in multiple myeloma (MM) resulting in pain, bone fractures, spinal cord compression and hypercalcemia. Within the bone marrow microenvironment (BMM), MM cells interact with bone cells to enhance bone resorption activity and compromise new bone formation mechanism; in turn, BMM provides a survival and drug resistance framework by interaction of MM cells with bone marrow components. Exosomes are important mediators of crosstalk betw...