Literature DB >> 16352691

Hypothalamic and gonadal components of hypogonadism in boys with Prader-Labhart- Willi syndrome.

Urs Eiholzer1, Dagmar l'Allemand, Valentin Rousson, Michael Schlumpf, Theo Gasser, Jürg Girard, Annette Grüters, Manuela Simoni.   

Abstract

CONTEXT: The specific form of hypogonadism in Prader-Labhart-Willi syndrome (PWS), central or peripheral, remains unexplained.
OBJECTIVES: The objectives of this study were to investigate the cause of hypogonadism in PWS and determine whether human chorionic gonadotropin (hCG) treatment can restore pubertal development.
DESIGN: This was a clinical follow-up study, divided into two samples, over a duration of 1.5 and 4.5 yr. PATIENTS: Eight male infants and six peripubertal boys (age at start of observation, 0.06-0.93 and 8.1-10.8 yr, respectively) with genetically confirmed PWS were studied. INTERVENTION: hCG (500-1500 U twice weekly) was given from age 13.5 yr to the present. MAIN OUTCOME MEASURES: Serum FSH, LH, inhibin B, and testosterone levels and pubertal development were the main outcome measures.
RESULTS: Infants with PWS presented normal LH (2.3 +/- 0.7 U/liter) and testosterone (2.5 +/- 0.9 nmol/liter) levels (mean +/- sem at 5 months) compared with the reference range. However, two thirds of the boys displayed cryptorchidism. Inhibin B levels were at the lowest level of the normal range and decreased significantly between infancy and puberty (at 13 yr, 72 +/- 17 pg/ml), whereas FSH secretion increased (9.9 +/- 2.6 U/liter). Pubertal maturation stopped at an average bone age of 13.9 yr. hCG therapy increased testosterone (11 +/- 2 nmol/liter) and reduced FSH (at 16 yr, 1.1 +/- 0.9 U/liter) levels. Testicular volume (5.6 +/- 1 ml) and inhibin B (26.5 +/- 11.9 pg/ml) remained low.
CONCLUSION: Children with PWS display a specific form of combined hypothalamic (low LH) and peripheral (low inhibin B and high FSH) hypogonadism, suggesting a primary defect in Sertoli and/or germ cell maturation or an early germ cell loss. hCG therapy stimulates testosterone production and virilization.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16352691     DOI: 10.1210/jc.2005-0902

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  25 in total

1.  Follicle stimulating and leutinizing hormones, estradiol and testosterone in Prader-Willi syndrome.

Authors:  Duane T Brandau; Mariana Theodoro; Uttam Garg; Merlin G Butler
Journal:  Am J Med Genet A       Date:  2008-03-01       Impact factor: 2.802

Review 2.  Review of Prader-Willi syndrome: the endocrine approach.

Authors:  Ryan Heksch; Manmohan Kamboj; Kathryn Anglin; Kathryn Obrynba
Journal:  Transl Pediatr       Date:  2017-10

3.  Coexpression profiles reveal hidden gene networks.

Authors:  Konstantina Chachlaki; Vincent Prévot
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-23       Impact factor: 11.205

Review 4.  Mendelian genetics of male infertility.

Authors:  Kathleen Hwang; Alexander N Yatsenko; Carolina J Jorgez; Sarmistha Mukherjee; Roopa Lata Nalam; Martin M Matzuk; Dolores J Lamb
Journal:  Ann N Y Acad Sci       Date:  2010-12       Impact factor: 5.691

Review 5.  Prader- Willi syndrome: An uptodate on endocrine and metabolic complications.

Authors:  Giovanna Muscogiuri; Gloria Formoso; Gabriella Pugliese; Rosaria Maddalena Ruggeri; Elisabetta Scarano; Annamaria Colao
Journal:  Rev Endocr Metab Disord       Date:  2019-06       Impact factor: 6.514

6.  Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.

Authors:  Nichol L G Miller; Rachel Wevrick; Pamela L Mellon
Journal:  Hum Mol Genet       Date:  2008-10-17       Impact factor: 6.150

7.  Central precocious puberty and growth hormone deficiency in a boy with Prader-Willi syndrome.

Authors:  Antonino Crinò; Girolamo Di Giorgio; Riccardo Schiaffini; Alessandra Fierabracci; Sabrina Spera; Andrea Maggioni; Guido Castelli Gattinara
Journal:  Eur J Pediatr       Date:  2008-02-27       Impact factor: 3.183

8.  Genome-wide coexpression of steroid receptors in the mouse brain: Identifying signaling pathways and functionally coordinated regions.

Authors:  Ahmed Mahfouz; Boudewijn P F Lelieveldt; Aldo Grefhorst; Lisa T C M van Weert; Isabel M Mol; Hetty C M Sips; José K van den Heuvel; Nicole A Datson; Jenny A Visser; Marcel J T Reinders; Onno C Meijer
Journal:  Proc Natl Acad Sci U S A       Date:  2016-01-25       Impact factor: 11.205

9.  The FSH-inhibin axis in prader-willi syndrome: heterogeneity of gonadal dysfunction.

Authors:  Varda Gross-Tsur; Harry J Hirsch; Fortu Benarroch; Talia Eldar-Geva
Journal:  Reprod Biol Endocrinol       Date:  2012-05-06       Impact factor: 5.211

10.  Prader-Willi Syndrome with Angelman Syndrome in the Offspring.

Authors:  Donatella Greco; Luigi Vetri; Letizia Ragusa; Mirella Vinci; Angelo Gloria; Paola Occhipinti; Angela Antonia Costanzo; Giuseppe Quatrosi; Michele Roccella; Serafino Buono; Corrado Romano
Journal:  Medicina (Kaunas)       Date:  2021-05-08       Impact factor: 2.430

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.