Searchable abstracts of presentations at key conferences in endocrinology

ea0016p480 | Neuroendocrinology | ECE2008

Hypopituitarism following traumatism brain injury in the West Indies: a pilot study between July 2005 and July 2006

Morineaux Sabine , Do Laurent , Simonetti Maurice , Salin Jacques , Foucan Patrick , Donnet Jean-Paul , Lalanne-Mistrih Marie-Laure

Sixty patients with traumatic brain injury are newly diagnosed every year in our island, particularly in patients with addictive behaviours. In France, it is the 4th rank of health expenses, as a major issue of public health care. In order to perform a first endocrine assessment, we performed a pilot study to diagnose traumatic brain injury induced hypopituitarism, assessed at least 6 months after injury, in moderate to severe traumatic brain injuries patients, hospitalized in...

ea0063s17.1 | Where do pituitary tumours come from? | ECE2019

Specification of pituitary cell fates

Drouin Jacques

The pituitary derives from an invagination of the oral ectoderm, Rathke’s pouch, where pituitary progenitors are specified during early development. These progenitors are marked by expression of Sox2 and their entry into differentiation involves a switch from Sox2 to expression of other transcription factors implementing each of the lineage-specific differentiation programs. This switch is also accompanied by a switch in cell cycle control mechanisms that may be disrupted...

ea0032s12.1 | Male reproductive endocrinology | ECE2013

Semaphorin 3A: a new gene involved in Kallmann syndrome

Young Jacques

Kallmann syndrome (KS) is a genetic disorder associating pubertal failure with congenital absent or impaired sense of smell. KS is related to defective neuronal development affecting both the migration of olfactory nerve endings and GnRH neurons. The discovery of several genetic mutations responsible for KS led to the identification of signaling pathways involved in these processes, but the mutations so far identified account for only 30–40% of cases of KS. We attempted t...

ea0026s23.3 | Optimising thyroid hormone replacement | ECE2011

Failure of thyroxin replacement to suppress TSH: what to do now?

Orgiazzi Jacques

Persistence of elevated TSH levels despite large doses of L-thyroxin is not uncommon, although thyroxin substitution is usually easy and convenient. The first cause to be considered is thyroxin malabsorption, whether organic, due to concomitant gastric or intestinal disease, or bariatric surgery, or, more frequently, related to dietary or drug interference. Proton-pump inhibitors, antacids and a long list of drugs may decrease thyroxin absorption. Drugs and thyr...

ea0078p17 | Diabetes | BSPED2021

Do hospital admissions improve outcomes for children and young people with poor diabetes control?

Jacques John E , Ferguson Elspeth C

Introduction: Achieving an HbA1c of less than 48 mmol/mol minimises the risk of complications in children and young people with type one diabetes. Elective admissions to hospital are one option employed to improve glycaemic control in patients with an HbA1c above target. There is however limited evidence to support such admissions. We aimed to retrospectively compare glycaemic control between patients electively admitted to hospital to stabilise their dia...

ea0028p238 | Pituitary | SFEBES2012

Ultrastructural changes in somatotrophs and gonadotrophs in TPit null mice

Yick Lok , Khetchoumian Konstantin , Drouin Jacques , Christian Helen

Tpit is a pituitary-specific transcription factor that is important for corticotroph terminal differentiation. In TPit null mice corticotroph cells do not differentiate and cells immunopositive for SF1, LH and FSH are observed in the intermediate lobe (Pulichino et al. 2003 Genes Dev). As the anterior lobe in TPit null mice showed a 50% decrease in cell number compared to wild-type (WT), and corticotrophs comprise only 5–7% of anterior lobe cells, we investigated c...

ea0022p772 | Thyroid | ECE2010

Vitamin D deficiency contributes to post-thyroidectomy hypocalcemia

Jacques Aurelie , Page Cyril , Justinien Etienne , Strunski Vladimir , Desailloud Rachel

Hypocalcemia is a classic complication after total thyroidectomy, mostly due to post-operative hypoparathyroidism. However others factors, like vitamin D deficiency, may contribute to this hypocalcemia.Objective: To determine if vitamin D preoperative status influence early postoperative serum calcium levels after total thyroidectomy.Patients and methods: Seventy-nine patients (65 women/14 men), mean age 52.8 (±12.7), were inc...

ea0020p291 | Clinical case reports and clinical reports | ECE2009

The R106C mutation of the V2 vasopressor receptor gene (AVPR2) causing X linked congenital nephrogenic diabetes insipidus is responsive to short term desmopressin challenge

Fysekidis Marinos , Boffa Jean-Jacques , Baud Laurent , Haymann Jean-Philippe

Background and aims: Patients with AVPR2 gene mutations present nephrogenic diabetes insipidus (NDI) resulting to a severe deficit in urine concentration despite high levels of circulating Antidiuretic Hormone (ADH). The mutation in codon 106 of the AVPR2 gene leading to the substitution of arginine by cysteine (R106C) is known to produce a mild disease while in vitro characterization revealed a complete loss of function. We report the case of a 24-year-old male member ...

ea0014s14.1 | Trojan horses for steroids | ECE2007

Alpha-fetoprotein protects the developing female brain from estrogens

Bakker Julie , De Mees Christelle , Balthazart Jacques , Szpirer Claude

The classic view of sexual differentiation in mammalian species holds that sex differences in the brain and behavior develop under the influence of estrogens derived from the neural aromatization of testosterone: the brain develops as male in the presence of estrogens and as female in their absence. In agreement with this view, it has been proposed that the female brain needs to be protected from estrogens produced by the placenta and that alpha-fetoprotein (AFP) - a major fet...