Searchable abstracts of presentations at key conferences in endocrinology

ea0012p104 | Reproduction | SFE2006

Population reference ranges for plasma testosterone and calculated free testosterone in older men

Teoh YP , Wallace AM

ObjectiveTo establish a set of population derived reference ranges for plasma total testosterone, sex hormone binding globulin (SHBG) and calculated free testosterone (FT) values especially in older men.BackgroundThe age-related decline in testosterone concentrations in men is gradual and both cross-sectional and longitudinal data have shown that there was a small but significant decline in total and free tes...

ea0012p5 | Clinical case reports/Governance | SFE2006

Adrenoleukodystrophy presenting with hypoadrenalism: can it occur at any age?

Creedon H , Yogendra A , Jennings AM

X-linked adrenoleukodystrophy (ALD) is a rare condition affecting the nervous system and adrenal cortex that typically presents in childhood. It results from mutations in the ABCD1 gene. We describe two cases of ALD presenting with hypoadrenalism in adulthood.A 20 year old man presented with persistent vomiting. He was pigmented, blood pressure was 100/60 mmHg, and neurological examination was normal. Investigations showed serum sodium 125 mmol/L, urea 1...

ea0011p422 | Diabetes, metabolism and cardiovascular | ECE2006

Correlations between leptin, insulin resistance and lipid profile in postmenopausal women

Poiana C , Stoian L , Stefanescu AM

Leptin is a circulating hormone produced primarily by the adipose tissue, which controls food intake and energy homeostasis. Important peripheral actions of leptin involve inhibition of insulin biosynthesis and secretion in pancreatic ß-cells. In turn, insulin stimulates leptin secretion from adipose tissue, establishing a hormonal regulatory feedback loop: ‘adipo-insular axis’. The aim of our study was to determine the interrelations between leptin, insulin/ins...

ea0008p80 | Reproduction | SFE2004

Arterial viscoelastic properties and blood pressure in pregnant women with polycystic ovary syndrome

Hu S , Seifalian AM , Hardiman P

Objective: We previously reported that the reduced arterial elasticity in polycystic ovary syndrome (PCOS) women is present in the first trimester of pregnancy. Women with reduced arterial elasticity are more likely to develop pre eclampsia, which association with PCOS is still unproven. This study was designed to compare blood pressure (BP) and arterial elasticity in pregnant PCOS women and controls in second trimester.Methods: The subjects were 15 preg...

ea0013p260 | Reproduction | SFEBES2007

Serum anti-mullerian hormone is elevated in girls with exaggerated adrenarche

Paterson WF , Fleming R , Ahmed SF , Wallace AM

Anti-Mullerian hormone (AMH) is produced by the ovarian granulosa cells in immature follicles from around week 36 of gestation to the menopause. Expression is highest in pre-antral and early antral follicles. AMH has a generally inhibitory effect on early follicle development and possibly on the responsiveness of growing follicles to FSH. Serum AMH is markedly elevated in women with PCOS and increased concentrations have also been reported in the healthy prepubertal daughters ...

ea0012p25 | Clinical case reports/Governance | SFE2006

Infertility and osteopenia in a male patient with thyroid hormone resistance

Kisalu J , Davies E , Solomon AM , Bouloux P-M

We report the case of a 26 year old man who presented to his GP with infertility; biochemical investigations revealed elevated serum free thyroid hormones (FT4 41 pmol/l (12–22); FT3 13.4 pmol/l (2.8–7.1); and a normal TSH (2 pmol/l (0.27–4.2). He was referred to the endocrine department.On examination, he was found to be clinically well though thin (BMI 18), anxious and tremulous. His heart rate was 110 bpm and blood pressure was normal. ...

ea0012p35 | Cytokines, growth factors, growth and development | SFE2006

Effects of androgens on differentiation of human skeletal muscle-derived cells in vitro

Solomon AM , Sinanan ACM , Bouloux PMG , Lewis MP

IntroductionThe mechanism by which hypertrophy of skeletal muscle occurs in response to anabolic androgens is incompletely understood. This study used a cell culture model of human skeletal muscle-derived cells, with samples obtained from consenting subjects and local ethics committee approval. The objective was to determine changes in myogenicity upon exposure to exogenous androgen +/− IGF-1 and to see whether an additive effect would be observed....

ea0011p11 | Bone | ECE2006

PTH and phosphate circadian rhythms are altered in adult growth hormone deficient patients with low bone mineral density

White HD , Ahmad AM , Durham BH , Fraser WD , Vora JP

Adult Growth Hormone Deficiency (AGHD) is associated with osteoporosis. PTH is secreted in a circadian rhythm and temporal fluctuations in PTH concentration, particularly at night, appear to be important in the regulation of bone turnover. Serum phosphate is an important determinant of PTH, with changes in phosphate preceding fluctuations in PTH concentration. We examined the difference in PTH and phosphate circadian rhythmicity in AGHD patients with normal and reduced bone mi...

ea0011p12 | Bone | ECE2006

Oral phosphate therapy used as an adjunct to growth hormone in adult growth hormone deficiency results in greater changes in bone mineral density compared with growth hormone replacement alone

White HD , Ahmad AM , Durham BH , Fraser WD , Vora JP

Adult Growth Hormone Deficiency (AGHD) is associated with reduced bone mineral density (BMD) and bone turnover. Abnormalities in PTH circadian rhythmicity, including blunted nocturnal rise in PTH concentration have been reported in AGHD and may underlie the pathogenesis of osteoporosis. Serum phosphate is an important regulator of PTH, with changes in phosphate concentration preceding fluctuations in PTH. We examined the effect of oral phosphate therapy on PTH circadian rhythm...

ea0011p125 | Clinical case reports | ECE2006

Identification of two novel GALNT3 mutations in a patient with familial tumoral calcinosis (FTC)

Barbieri AM , Filopanti M , Bua G , Beck-Peccoz P

FTC (OMIM #211900) is a rare autosomal recessive disorder characterized by the presence of ectopic calcifications in the skin and subcutaneous tissues. These calcified masses look like irregular tumors which usually develop in a periarticular position, causing pain and often necessitating surgical excision. The majority of affected individuals have hyperphosphatemia due to increased renotubular reabsorption of phosphate and elevated levels of serum 1,25-dihydroxyvitamin D (cal...