Literature DB >> 24108313

The IGSF1 deficiency syndrome: characteristics of male and female patients.

S D Joustra1, N Schoenmakers, L Persani, I Campi, M Bonomi, G Radetti, P Beck-Peccoz, H Zhu, T M E Davis, Y Sun, E P Corssmit, N M Appelman-Dijkstra, C A Heinen, A M Pereira, A J Varewijck, J A M J L Janssen, E Endert, R C Hennekam, M P Lombardi, M M A M Mannens, B Bak, D J Bernard, M H Breuning, K Chatterjee, M T Dattani, W Oostdijk, N R Biermasz, J M Wit, A S P van Trotsenburg.   

Abstract

CONTEXT: Ig superfamily member 1 (IGSF1) deficiency was recently discovered as a novel X-linked cause of central hypothyroidism (CeH) and macro-orchidism. However, clinical and biochemical data regarding growth, puberty, and metabolic outcome, as well as features of female carriers, are scarce.
OBJECTIVE: Our objective was to investigate clinical and biochemical characteristics associated with IGSF1 deficiency in both sexes.
METHODS: All patients (n = 42, 24 males) from 10 families examined in the university clinics of Leiden, Amsterdam, Cambridge, and Milan were included in this case series. Detailed clinical data were collected with an identical protocol, and biochemical measurements were performed in a central laboratory.
RESULTS: Male patients (age 0-87 years, 17 index cases and 7 from family studies) showed CeH (100%), hypoprolactinemia (n = 16, 67%), and transient partial GH deficiency (n = 3, 13%). Pubertal testosterone production was delayed, as were the growth spurt and pubic hair development. However, testicular growth started at a normal age and attained macro-orchid size in all evaluable adults. Body mass index, percent fat, and waist circumference tended to be elevated. The metabolic syndrome was present in 4 of 5 patients over 55 years of age. Heterozygous female carriers (age 32-80 years) showed CeH in 6 of 18 cases (33%), hypoprolactinemia in 2 (11%), and GH deficiency in none. As in men, body mass index, percent fat, and waist circumference were relatively high, and the metabolic syndrome was present in 3 cases.
CONCLUSION: In male patients, the X-linked IGSF1 deficiency syndrome is characterized by CeH, hypoprolactinemia, delayed puberty, macro-orchidism, and increased body weight. A subset of female carriers also exhibits CeH.

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Year:  2013        PMID: 24108313     DOI: 10.1210/jc.2013-2743

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


  33 in total

1.  Is IGSF1 involved in human pituitary tumor formation?

Authors:  Fabio R Faucz; Anelia D Horvath; Monalisa F Azevedo; Isaac Levy; Beata Bak; Ying Wang; Paraskevi Xekouki; Eva Szarek; Evgenia Gourgari; Allison D Manning; Rodrigo Bertollo de Alexandre; Emmanouil Saloustros; Giampaolo Trivellin; Maya Lodish; Paul Hofman; Yvonne C Anderson; Ian Holdaway; Edward Oldfield; Prashant Chittiboina; Maria Nesterova; Nienke R Biermasz; Jan M Wit; Daniel J Bernard; Constantine A Stratakis
Journal:  Endocr Relat Cancer       Date:  2014-12-19       Impact factor: 5.678

Review 2.  Pediatric Hypothyroidism: Diagnosis and Treatment.

Authors:  Ari J Wassner
Journal:  Paediatr Drugs       Date:  2017-08       Impact factor: 3.022

3.  TRH Action Is Impaired in Pituitaries of Male IGSF1-Deficient Mice.

Authors:  Marc-Olivier Turgeon; Tanya L Silander; Denica Doycheva; Xiao-Hui Liao; Marc Rigden; Luisina Ongaro; Xiang Zhou; Sjoerd D Joustra; Jan M Wit; Mike G Wade; Heike Heuer; Samuel Refetoff; Daniel J Bernard
Journal:  Endocrinology       Date:  2017-04-01       Impact factor: 4.736

4.  IGSF1 variants in boys with familial delayed puberty.

Authors:  Sjoerd D Joustra; Karoliina Wehkalampi; Wilma Oostdijk; Nienke R Biermasz; Sasha Howard; Tanya L Silander; Daniel J Bernard; Jan M Wit; Leo Dunkel; Monique Losekoot
Journal:  Eur J Pediatr       Date:  2014-10-30       Impact factor: 3.183

Review 5.  Central hypothyroidism - a neglected thyroid disorder.

Authors:  Paolo Beck-Peccoz; Giulia Rodari; Claudia Giavoli; Andrea Lania
Journal:  Nat Rev Endocrinol       Date:  2017-05-26       Impact factor: 43.330

6.  Central hypothyroidism in adults: better understanding for better care.

Authors:  Solange Grunenwald; Philippe Caron
Journal:  Pituitary       Date:  2015-02       Impact factor: 4.107

Review 7.  Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

Authors:  Qing Fang; Akima S George; Michelle L Brinkmeier; Amanda H Mortensen; Peter Gergics; Leonard Y M Cheung; Alexandre Z Daly; Adnan Ajmal; María Ines Pérez Millán; A Bilge Ozel; Jacob O Kitzman; Ryan E Mills; Jun Z Li; Sally A Camper
Journal:  Endocr Rev       Date:  2016-11-09       Impact factor: 19.871

Review 8.  Molecular insights into the aetiology of female reproductive ageing.

Authors:  John R B Perry; Anna Murray; Felix R Day; Ken K Ong
Journal:  Nat Rev Endocrinol       Date:  2015-10-13       Impact factor: 43.330

9.  A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene

Authors:  Doğa Türkkahraman; Nimet Karataş Torun; Nadide Cemre Randa
Journal:  J Clin Res Pediatr Endocrinol       Date:  2020-08-10

10.  Dopaminergic organization of striatum is linked to cortical activity and brain expression of genes associated with psychiatric illness.

Authors:  Robert A McCutcheon; Kirsten Brown; Matthew M Nour; Stephen M Smith; Mattia Veronese; Fernando Zelaya; Martin Osugo; Sameer Jauhar; William Hallett; Mitul M Mehta; Oliver D Howes
Journal:  Sci Adv       Date:  2021-06-09       Impact factor: 14.136

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