ISSN 1662-4009 (online)

ey0017.6-15 | Transgender Medicine: Reviews and Position Statements | ESPEYB17

6.15. Gender-affirming hormones and surgery in transgender children and adolescents

S Mahfouda , JK Moore , A Siafarikas , T Hewitt , U Ganti , A Lin , FD Zepf

To read the full abstract: Lancet Diabetes Endocrinol. 2019, Jun; 7: 484–98. doi: https://www.ncbi.nlm.nih.gov/pubmed/30528161This review overviews the published literature on mental and physical health outcomes and treatment effects after gender-affirming hormone therapy and surgery in transgender adolescents and highlights important evidence gaps.There is tr...

ey0017.6-16 | Transgender Medicine: Reviews and Position Statements | ESPEYB17

6.16. European society for sexual medicine position statement [ldquo]assessment and hormonal management in adolescent and adult trans people, with attention for sexual function and satisfaction[rdquo]

G T’Sjoen , J Arcelus , ALC De Vries , AD Fisher , TO Nieder , M Ozer , J Motmans

To read the full abstract: J Sex Med. 2020, Apr; 17: 570–84. doi: https://www.ncbi.nlm.nih.gov/pubmed/32111534This position statement provides an update for health-care professionals on recommended basic principles for care of transgender people, including male, female and nonbinary. It uses a developmental approach to describe the best care for prepubescent, pubescent and adolescen...

ey0017.8-15 | New Concerns | ESPEYB17

8.15. Altered gray matter structure and white matter microstructure in patients with congenital adrenal hyperplasia: Relevance for working memory performance

Westeinde A Van’t , L Karlsson , Sandberg M Thomsen , A Nordenstrom , N Padilla , S Lajic

To read the full abstract: Cereb Cortex. 2020; 30(5): 2777–2788. PMID: 31819952.Congenital adrenal hyperplasia (CAH), most commonly caused by 21-hydroxylase deficiency, is an autosomal recessively inherited life-threatening impairment in cortisol and, in the severe salt wasting form, aldosterone synthesis. The implementation of neonatal screening programs for CAH and the continuous imp...

ey0017.10-7 | (1) | ESPEYB17

10.7. Real world hybrid closed-loop discontinuation: Predictors and perceptions of youth discontinuing the 670G system in the first 6 months

LH Messer , C Berget , T Vigers , L Pyle , C Geno , PR Wadwa , KA Driscoll , GP Forlenza

To read the full abstract: Pediatr Diabetes. 2020 Mar;21(2):319–327. doi: 10.1111/pedi.12971. Epub 2020 Jan 3. PMID: 31885123Dissatisfaction with technologies, discontinuation of use and inappropriate adjustments of insulin pump settings pose important areas of concern in adolescents using diabetes technologies. This study searched for predictors of hybrid closed loop (HCL) discontinuation...

ey0017.12-9 | Metabolic Syndrome | ESPEYB17

12.9. Variabilities in childhood cardiovascular risk factors and incident diabetes in adulthood: The Bogalusa Heart Study

T Du , C Fernandez , R Barshop , V Fonseca , W Chen , LA Bazzano

To read the full abstract: Diabetes Care. 2019;42(9):1816–23. doi: 10.2337/dc19-0430Short summary: In this longstanding cohort study (n =1718), high intraindividual variability over time in BMI and in HDL-C during childhood, independent of their mean levels, conferred an increased risk of later-life diabetes.Comment: Intraindividual variabil...

ey0017.15-6 | (1) | ESPEYB17

15.6. Primary prevention of cow’s milk sensitization and food allergy by avoiding supplementation with cow’s milk formula at birth: A randomized clinical trial

M Urashima , H Mezawa , M Okuyama , T Urashima , D Hirano , N Gocho , H Tachimoto

To read the full abstract: JAMA Pediatr. 2019 Oct 21;173(12):1137–45. doi: 10.1001/jamapediatrics.2019.3544.The authors describe a randomised controlled trial to decrease risks of sensitization to cow’s milk protein by avoiding supplementation with cow’s milk formula at birth. The trial included 330 newborns in Japan, where the practice of supplementing breastfeedin...

ey0016.1-7 | Updates on Kisspeptin | ESPEYB16

1.7. Genetic dissection of the different roles of hypothalamic kisspeptin neurons in regulating female reproduction

L Wang , C Vanacker , LL Burger , T Barnes , YM Shah , MG Myers , SM Moenter

To read the full abstract: Elife 2019;8:e43999.Two populations of Kisspeptin neurons are described in the hypothalamus. One population is located in the rostral part of the hypothalamus (the anteroventral periventricular nucleus, AVPV); the other is in the arcuate nucleus (ARC). The major difference between these populations is the opposing effects of 17b-estradiol (E2) on Kiss1...

ey0016.3-8 | Congenital Hypothyroidism | ESPEYB16

3.8. Newborn screening for primary congenital hypothyroidism: estimating test performance at different TSH thresholds

RL Knowles , J Oerton , T Cheetham , G Butler , C Cavanagh , L Tetlow , C Dezateux

To read the full abstract: J Clin Endocrinol Metab. 2018;103:3720–28.This nationwide prospective surveillance study aimed to estimate the performance of the current UK recommended TSH threshold (10 mU/L on day 5 after birth) for newborn blood spot screening compared to lower thresholds: 8 mU/L and 6 mU/L. Over a 12-month period, the authors included all patients with positive TSH ba...

ey0016.5-3 | New Therapies and Novel Therapeutic Strategies | ESPEYB16

5.3. ENPP1 enzyme replacement therapy improves blood pressure and cardiovascular function in a mouse model of generalized arterial calcification of infancy

T Khan , KW Sinkevicius , S Vong , A Avakian , MC Leavitt , H Malanson , A Marozsan , KL Askew

Abstract: Dis Model Mech. 2018 Oct 1; 11(10): dmm035691.In brief: Generalized arterial calcification of infancy (GACI) is a severe, rare disease characterized by excessive calcification of large and medium sized arteries caused by homozygous loss-of-function mutations in ENPP1. Here, in Enpp1 deficient mice, treatment with recombinant hu...

ey0016.10-10 | (1) | ESPEYB16

10.10. Sex as a determinant of type 1 diabetes at diagnosis

M Turtinen , T Harkonen , A Parkkola , J Ilonen , M Knip , Pediatric Diabetes Register Finnish

To read the full abstract: Pediatr Diabetes. 2018 Nov;19(7):1221–1228Despite good metabolic control some patients with type 1 diabetes (T1D) may develop comorbidities early while others despite high HbA1c levels remain free of complications for long durations. Risk factors for T1D complications are both of intrinsic (e.g. genetic) and extrinsic (e.g. environmental) origin. Amongst t...