Searchable abstracts of presentations at key conferences on calcified tissues

ba0001pp357 | Osteoporosis: pathophysiology and epidemiology | ECTS2013

The prevalence of osteoporosis and risk factors for bone demineralization in Italy: first results from the firmo study

Fossi Caterina , Cavalli Loredana , Giusti Francesca , Metozzi Alessia , Parri Simone , Guazzini Andrea , Maria Luisa Brandi

Objective(s): We aimed to determine the prevalence of osteoporosis and risk factors for bone demineralization in the Italian population.Material and methods: 3090 consecutive subjects were screened for osteoporosis by using calcaneal quantitative ultrasounds (QUS) in 16 Italian cities (women: 2635; men: 455) during the extension of the FIRMO study carried out in 2011 on about 7000 people. Anamnestic data were collected to assess the presence of recognize...

ba0001pp409 | Osteoporosis: treatment | ECTS2013

25-OH vitamin D and γ-δ TCR lymphocyte interplay in the pathogenesis of acute phase reaction after zoledronic acid infusion for osteoporosis treatment

Crotti Chiara , Cavaciocchi Francesca , De Santis Maria , Ceribelli Angela , Fabbriciani Gianluigi , Selmi Carlo

Background: Zoledronic acid (ZA) for the treatment of osteoporosis (OP) is associated with a transient post-infusional acute phase reaction (APR) due to ZA-mediated activation of γ-δ TCR lymphocytes (γ-δTCR) and production of cytokines.Primary objective: To investigate if OP patients developing APR (APR+) after ZA infusion have lower 25-OH vitamin D (25-OHvD) levels and a higher percentage of γ-δTCR compared to patients with...

ba0002oc9 | Biology | ICCBH2013

EPO signaling and hematopoietic expansion as causes of osteoporosis in a thalassemia mouse model

Vogiatzi Maria , Yang Zhiwei , Oikonomidou Rea , Rivella Stefano , Boskey Adele , Ross F Paddy

Thalassemia is a chronic anemia associate with high rates of osteoporosis. To determine how erythropoiesis leads to bone loss in thalassemia, we used the th3/+ thalassemia mouse to study the role of erythropoietin (EPO) and hematopoietic progenitors (HP), since they are both increased in thalassemia.Methods: Bone marrow mesenchymal stem cells (MSCs) cultures and MSC cocultures with various HP from wild type (wt) and th3/+ mice were diff...

ba0002p13 | (1) | ICCBH2013

Bone turnover compensates for the delayed growth in small for gestational age neonates

Tenta Roxane , Bourgiezi Ifigeneia , Aliferis Evangelos , Papadopoulou Magda , Gounaris Antonis , Skouroliakou Maria

Objectives: To investigate the possible relationship between neonatal anthropometric characteristics and bone turnover and growth markers in a sample of neonates and their mothers, taking into account the size for the gestational age.Methods: A sample which consisted of 20 small for the gestational age (SGA), appropriate for the gestational age (AGA), and large for the gestational age (LGA) randomly selected term neonates and their 20 mothers were analyz...

ba0002p32 | (1) | ICCBH2013

The effect of vitamin D supplementation on calcium excretion in thalassemia

Balachandar Sadana , Vogiatzi Maria , Giardina Patricia , Sheth Sujit , Kleinert Dorothy , Randolph Rachel

Objective: Transfusion dependent thalassemia (TM) patients have routinely been placed on vitamin D supplementation due to their increased risk of osteoporosis, as well as their high rates of vitamin D deficiency (serum 25 hydroxyvitamin D (25-OHD) <11 ng/ml) and insufficiency (25-OHD <30 ng/ml). Furthermore, recent studies have linked 25-OHD levels to hypercalciuria and nephrolithiasis in TM. The objective of this study is to determine the effect of vitamin D supplemen...

ba0002p130 | (1) | ICCBH2013

‘Bone in bone' sign in juvenile osteoporosis in a 13-year-old girl

Sakalidou Maria , Atsali Eri , Bizimi Vasiliki , Skaradavos Gregory , Balanika Alexia , Athanasakos Athanasios , Alexopoulou Efthymia , Papakonstantinou Olymbia

Background: We present an interesting case of a young child under bisphosphonates, for the treatment of juvenile osteoporosis (IJO), that developed a ‘bone in bone sign’, in several vertebral bodies, evident both on radiographs (CRX) and on magnetic resonance (MR) studies.Presenting problem: A 13-year-old girl was admitted in our hospital complaining with thoracolumbar pain. The patient had been diagnosed with IJO 2 years ago because of.a histo...

ba0002p162 | (1) | ICCBH2013

Low bone mass and fractures in young patients with chronic diseases

Bianchi Maria Luisa , Vai Silvia , Colombo Carla , Corona Fabrizia , Ghio Luciana , Morandi Lucia , Nebbia Gabriella

We performed a prospective study on 440 young patients (aged 3–20 years), affected by various chronic diseases (cystic fibrosis; juvenile idiopathic arthritis; nephrotic syndrome; systemic lupus erythematosus; Duchenne muscular dystrophy; autoimmune hepatitis; transplants; etc.), with periodical bone mineral density (BMD) evaluations with DXA, for 3–14 years (7.8±6.2).266 patients were on long-term treatment with glucocorticoids (GCs); amo...

ba0002p187 | (1) | ICCBH2013

Juvenile idiopathic osteoporosis responsive to intravenous alendronate

Guagnelli Miguel Angel , Yeste Diego , Clemente Maria , Garrido Marta , Carrascosa Antonio

Background: Osteoporosis in otherwise healthy children demands thorough study as it may be the first manifestation of an occult illness. When other diseases can be ruled out, juvenile idiopathic osteoporosis (JIO) is the purported diagnosis.PresentationWe report the case of an 8-year -old boy with no personal or family history of chronic disease who presented with sudden ankle pain unrelated to trauma and not responsive to rest and...

ba0002p191 | (1) | ICCBH2013

Long-term follow-up in Stuve–Wiedemann syndrome: a case report

Sabrina Buonuomo Paola , Macchiaiolo Marina , Cambiaso Paola , Capolino Rossella , Digilio Maria Cristina , Andrea Bartuli

Background: Stuve–Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition characterized by bowing of the lower limbs with cortical thickening, wide metaphyses, abnormal trabecular pattern and camptodactyly. Additional features include dysautonomia symptoms with temperature instability, respiratory distress and sucking/swallowing difficulties in the first months of life.Most SWS cases do not survive beyond the first y...

ba0003oc2.5 | Osteoporosis epidemiology | ECTS2014

IGFBP1 as a predictor of hip fractures

Lundin Hans , Saaf Maria , Strender Lars-Erik , Nyren Sven , Johansson Sven-Erik , Salminen Helena

Insulin-like growth factor 1 (IGF-1) is known to be a predictor of future osteoporotic fractures. Insulin-like growth factor binding protein 1 (IGFBP1) regulates the bioavailability of IGF-1 and thus in reason IGFBP1 also could be a fracture predictor. To our knowledge there are no previous studies published on the relation between the serum concentration of IGFBP1 and fractures.This is a population-based prospective cohort study on 351 Swedish women age...