Searchable abstracts of presentations at key conferences in endocrinology

ea0029p679 | Diabetes | ICEECE2012

No influence of the chronic poor clycaemic control on ANP levels in diabetics with microvascular illness

Villar M. , Alameda C. , Becerra A. , Menacho M. , Lopez-Perez G.

Introduction: Atrial natriuretic peptide (ANP), a member of the natriuretic peptide family, regulates several physiologic parameters including diuresis and natriuresis, and lowers arterial, blood pressure.It has been reported that plasma concentrations of ANP rise in response to acute hyperglycaemia in diabetes (1) (2) and this may indicate a neurohormonal response to limit target organ damage (3).We investigate if in situation chr...

ea0029p680 | Diabetes | ICEECE2012

Nephropathy could be a main factor in the increased levels of ANP in diabetes

Villar M. , Becerra A. , Alameda C. , Lopez-Perez G. , Menacho M.

Introduction: Its has been suggested that atrial natriuretic peptide (ANP) may contribuye to the development of microalbuminuria in diabetes mellitus.Plasma ANP concentration have been reported to be elevated in association with microalbuminuria, all of wich predict the future development of overt nephropathy in diabetes (1).Key players in neurohormonal activation include neuropeptides and their receptors wich include the ANP (2).<...

ea0029p957 | Female Reproduction | ICEECE2012

Prevalence of hyperandrogenism, polycystic ovary syndrome and metabolic syndrome in female-to-male transsexuals

Becerra Fernandez A. , Villar R. , Perez Lopez G. , Menacho Roman M.

Introduction: Gender identity disorder (GID) is a disagreement between biological sexual differentiation and self-declared gender identity. The aetiology of GID remains unclear, although endocrinological, neuroanatomical and psychosocial factors are all thought to be causally involved. Polycystic ovary syndrome (PCOS) is characterized by chronic anovulation, polycystic ovarian morphology, and biochemical and/or biological signs of hyperandrogenism. Most women with PCOS also ex...

ea0016p318 | Endocrine tumours | ECE2008

Cushing's syndrome due to a pigmented nodular adrenocortical disease and a acromegaly corresponding to a Carney complex (CNC)

Sanabria Concha , Perez-Ferre Natalia , Diaz Jose Angel

The CNC is a dominantly syndrome, characterized by spotty skin pigmentation, endocrine overactivity and myxomas (Carney & Young 1992), associated with lentigines and blue naevi; the disease links to 17q22-24, and its mutations have been identified in the genes PRKAR1α. The most common endocrine manifestations affect two o more endocrine glands, including acromegaly, thyroid and testicular tumours and ACTH-independent Cushing’s syndrome due to primary pigmented no...

ea0006p30 | Endocrine tumours and neoplasia | SFE2003

Extracts from the Marine Sponges Anthosigmella varians (AV) and Spongia barbara (SB) Lower Cyclin B1 Levels, Cause a G2/M Cell Cycle Block and Trigger Apoptosis in SW-13 Human Adrenal Carcinoma Cultures

Brown J , Cappell S , Perez-Stable C , Fishman L

Many marine sponges have been shown to produce metabolites with cell growth and endocrine altering activities. We tested crude extracts (1.0 mg/ml) from two species (AV and SB) for effects on levels of an important cell cycle regulatory protein, cyclin B1; cell cycle growth-phase (sub-G1/Apoptosis, G1, S, and G2/M), as well as on cell survival in SW-13 human adrenal carcinoma cultures. Polyacrylamide gel electrophoresis studies of cyclin B1 levels indicate a 60-90 % reduction ...

ea0099ep4 | Calcium and Bone | ECE2024

Involvement of age, obesity and genetic polymorphisms in the increment of 25(OH)D levels after 12-month treatment with calcifediol and cholecalciferol

Jodar Esteban , Arranz-Gutierrez Paula , Luis Perez-Castrillon Jose

Introduction: Vitamin D deficiency is a prevalent condition worldwide. Low serum 25(OH)D levels are associated with several diseases, being age and obesity strongly related to hypovitaminosis D. In addition, several genetic variants have also been associated with lower and/or higher 25(OH)D levels.Objective: We aimed to assess the potential influence of age, BMI, waist circumference and genetic variants on the efficacy of 12-month treatment with calcifed...

ea0032p319 | Clinical case reports - Thyroid / Others | ECE2013

Everolimus. a new therapeutic target in the metastatic neuroendocrine carcinoma

Rodriguez Jose Perez , Hernandez Tomas Martin , Hernandez Cristina , Baz David Vicente , Manzano Virginia Martin , Baldrich Alfonso Gentil , Perez Angel Sendon

Introduction: Everolimus is a drug selective inhibitor of mTOR and approved by the FDA in 2011 for treatment of neuroendocrine tumors of pancreatic origin unresectable. Our objective was to evaluate the efficacy and safety of everolimus in a patient with malignant pancreatic head insulinoma.Case: This is a 31 year old man who complains of epigastric pain, dizziness, sweating and syncope related to exercise. During admission is objectively severe hypoglyc...

ea0032p479 | Diabetes | ECE2013

Insulinator: a computer program to help in the insulin therapy

Rodriguez Jose Perez , Portillo Cristobal Morales , Jimenez Virginia Hernando , Cobos Manuel Malagon , Olmedo Isabel Serrano , Perez Angel Sendon

Introduction and objectives: In clinical practice many professionals are involved in the diabetes treatment. To facilitate this work, we present a computer program, based in recommended guidelines, to improve the management of insulin therapy, called insulinator. We evaluated the correlation between these and clinical practice.Materials and methods: Insulinator has been made so that using a number of variables (weight, HbA1c and glycemic control) offer a...

ea0020p232 | Bone/Calcium | ECE2009

Clinical and molecular characterization of Spanish patients with pseudohypoparathyroidism

Moure Maria Dolores , Fernandez-Rebollo Eduardo , Gaztambide Sonia , Perez-Nanclares Gustavo , Castano Luis , de Nanclares Guiomar Perez , Spanish PHP Group

Pseudohypoparathyroidism (PHP) is a term applied to a heterogeneous group of disorders whose common feature is resistance to parathyroid hormone. Most of the PHP forms are caused by defects in GNAS: PHP-Ia (characterized by PTH and TSH resistance with Albright Hereditary Osteodystrophy) is caused by heterozygous inactivating mutations in those exons of GNAS encoding the α subunit of the stimulatory G-protein, and the autosomal dominant form of PHP-Ib (PTH an...

ea0041ep624 | Endocrine tumours and neoplasia | ECE2016

Inferior petrosal sinus sampling in the differential diagnosis of ACTH-dependent Cushing’s syndrome

Sanchez Beatriz Lardies , Aznar Pablo Trincado , Fernandez Leticia Perez , Monreal Isabel Azcona , Garcia Maria Martinez , Sanz Guayente Verdes , Paris Alejandro Sanz , Perez Javier Acha

Introduction: Bilateral sampling of the inferior petrosal sinuses is an accurate test to diagnose Cushing’s disease and distinguish it with the ectopic ACTH syndrome. The aim of the study was to review the petrosal sinus samplings carried out during last 10 years in our hospital.Methods and material: The medical histories of patients admitted for suspected Cushing’s disease in the last 10 years (from 2005 till 2015) were reviewed. There were se...