Searchable abstracts of presentations at key conferences in endocrinology

ea0011p84 | Clinical case reports | ECE2006

Hypopituitarism in an adult thalassemic patient. Effects of different replacement therapies

Danesi L , Cattaneo A , Lavezzi E , Scacchi M , Cavagnini F

In a small but not negligible proportion of thalassemic patients, a true growth hormone deficiency (GHD), not secondary to pubertal delay, can be documented. Among the features of adult GHD syndrome, osteoporosis leads to a 2.5-fold increase in fracture risk. Thalassemia is characterized by a peculiar bone disease leading to osteopenia. The effectiveness of GH treatment in GHD adult thalassemic patients has not been explored yet. We report here the case of such a patient, disp...

ea0032p808 | Paediatric endocrinology | ECE2013

Sex steroid priming in differential diagnosis between idiopathic GH deficiency and constitutional delay of growth and puberty

Radin Raffaella , Moro Mirella , Scacchi Massimo , Cavagnini Francesco , Danesi Leila , Persani Luca

Priming with sex steroids prior to stimulation tests for the diagnosis of GH deficiency (GHD) in peripubertal years remains controversial, though some evidence suggests its utility in improving the specificity of GH testing for the distinction between idiopathic GHD (IGHD) and constitutional delay of growth and puberty (CDGP). However, few data are available on the final height (FH) of untreated CDGP patients. In order to better understand the usefulness of priming, we analyze...

ea0011p83 | Clinical case reports | ECE2006

Endocrine evaluation in a man with restrictive eating behaviour

Moro M , Danesi L , Polli N , Rasi E , Filippini B , Andrioli M , Scacchi M , Cavagnini F

Eating disorders are less common in men than in women. Furthermore, in males, a restrictive eating behaviour is frequently secondary to other psychiatric disorders. In case of suspected primary anorexia nervosa (AN), in male patients it is obviously impossible to rely on a typical clinical sign as is amenorrhea.Case description: A 23-yr old man came to our observation because of an important weight loss in the last two years (from 60 to 48 kg, body mass ...

ea0020p242 | Bone/Calcium | ECE2009

Peculiar features of bone disease in thalassemia: comparison with anorexia nervosa

Cattaneo Agnese , Danesi Leila , Scacchi Massimo , Carzaniga Chaiara , Vai Silvia , Ortolani Sergio , Cappellini Maria Domenica , Cavagnini Francesco

In thalassemic patients individual values of BMD measured by traditional DEXA are lower than those determined by QCT. The reason for this discrepancy is still controversial.Aim: To investigate bone features in a large group of thalassemic patients, compared with patients with anorexia nervosa, also characterized by precocious osteoporosis.Study design: Forty-six adult thalassemic subjects and 25 anorectic women were studied. In all...

ea0032p1081 | Thyroid cancer | ECE2013

A novel multi-target pyrazolopyrimidine derivative with anti-neoplastic properties, CLM29, is active against medullary thyroid cancer in vitro and in vivo

Fallahi Poupak , Ferrari Silvia Martina , Bocci Guido , La Motta Concettina , Ruffilli Ilaria , Di Domenicantonio Andrea , Corrado Alda , Mancusi Caterina , Danesi Romano , Da Settimo Federico , Miccoli Paolo , Antonelli Alessandro

Introduction: CLM29, a pyrazolo[3,4-d]pyrimidine compound, inhibits several targets (including the RET tyrosine kinase, epidermal growth factor receptor, vascular endothelial growth factor receptor and has an anti-angiogenic effect). Recently it has been shown to inhibit proliferation and migration in primary papillary dedifferentiated thyroid cancer cells. The aim of this study is to evaluate the anti-tumor activity of CLM29 in medullary thyroid cancer (MTC).<p c...

ea0026p132 | Growth factors | ECE2011

Bone turnover and mineral density in thalassemia: relationships with gh secretory status and circulating somatomedins

Danesi Leila , Cattaneo Agnese , Scacchi Massimo , Sciortino Giovanna , Vitale Giovanni , Domenica Cappellini Maria , Arvigo Marica , Ferone Diego , Minuto Francesco , Cavagnini Francesco

Introduction: Previous data from our group suggested a role for the GH/IGF1 axis in the pathophysiology of osteoporosis in thalassemia (Clin Endocrinol 69:202, 2008). The present study was aimed at evaluating the relationships between circulating IGFs and bone metabolism and density in a very large series of adult thalassemic patients.Study design: One hundred and thirty-nine patients affected by thalassemia major (mean age 32.3±7.87 years) underwen...

ea0016p66 | Bone and calcium | ECE2008

Osteopenia/osteoporosis in adult thalassemic patients: contribution of growth hormone - insulin-like growth factor I deficiency

Scacchi Massimo , Danesi Leila , Cattaneo Agnese , Valassi Elena , Pecori Giraldi Francesca , Argento Crocetta , D'Angelo Emanuela , Mirra Nadia , Zanaboni Laura , Tampieri Benedetta , Cappellini Maria Domenica , Cavagnini Francesco

GH and IGF-I exert an important role in the control of bone formation. Osteopenia and osteoporosis are a frequent recurrence in patients with thalassemia. Due to the high prevalence of GH deficiency (GHD) in adult thalassemic patients (Scacchi et al., Clin Endocrinol 2007), we investigated the possible role of GH - IGF-I abnormalities in the pathogenesis of the osteopenia/osteoporosis of this disease.Study: Sixty-four adult thalassemic pati...

ea0014p181 | (1) | ECE2007

The growth hormone – insulin-like growth factor-I axis in adult thalassemic patients

Danesi Leila , Cattaneo Agnese , Valassi Elena , Scacchi Massimo , D’Angelo Emanuela , Mirra Nadia , Zanaboni Laura , Cappellini Maria Domenica , Cavagnini Francesco

GH deficiency (GHD) can be recognized in a not negligible proportion of thalassemic children, while data on the prevalence of this disorder in adult patients are lacking. Therefore, we elected to study the GH – IGF-I axis in a large group of adult thalassemic subjects.Study design: Ninety-four patients (69 with thalassemia major and 25 with thalassemia intermedia on stable transfusional regimen, 39 men and 55 women, aged 31.5±6.8 years, receivi...

ea0037ep1036 | Thyroid (non-cancer) | ECE2015

Prevalence of hypothyroidism in a large series of adult thalassemic patients

Radin Raffaella , Danesi Leila , Ambrogio Alberto , Cassinerio Elena , Zanaboni Laura , Cappellini Maria Domenica , Baldini Marina , Poggi Maurizio , Ottaviani Chiara , Toscano Vincenzo , Zavattaro Marco , Cavagnini Francesco , Persani Luca , Scacchi Massimo

Hypothyroidism has been traditionally described as a frequent endocrine complication of thalassemic children: in these patients hypothyroidism is mainly of primary origin and not linked to autoimmunity (Mariotti et al., Pediatr Endocrinol Rev 2011). Fewer data are available on the prevalence and nature of this complication in adult age thalassemia. Therefore, we elected to evaluate thyroid function and autoimmunity in a large series of adult patients.<p class="abs...