Literature DB >> 24423288

Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system.

Valerie F Sidhoum1, Yee-Ming Chan, Margaret F Lippincott, Ravikumar Balasubramanian, Richard Quinton, Lacey Plummer, Andrew Dwyer, Nelly Pitteloud, Frances J Hayes, Janet E Hall, Kathryn A Martin, Paul A Boepple, Stephanie B Seminara.   

Abstract

CONTEXT: A subset of patients diagnosed with idiopathic hypogonadotropic hypogonadism (IHH) later achieves activation of their hypothalamic-pituitary-gonadal axis with normalization of steroidogenesis and/or gametogenesis, a phenomenon termed reversal.
OBJECTIVE: The objective of this study was to determine the natural history of reversal and to identify associated phenotypes and genotypes. DESIGN, SETTING, AND
SUBJECTS: This was a retrospective review of clinical, biochemical, and genetic features of patients with IHH evaluated at an academic medical center. MAIN OUTCOME MEASURES: History of spontaneous fertility, regular menses, testicular growth, or normalization of serum sex steroids, LH secretory profiles, brain imaging findings, and sequences of 14 genes associated with IHH were reviewed.
RESULTS: Of 308 patients with IHH, 44 underwent reversal. Time-to-event analysis estimated a lifetime incidence of reversal of 22%. There were no differences in the rates of cryptorchidism, micropenis, or partial pubertal development in patients with reversal vs IHH patients without reversal. Fifteen patients with reversal (30%) had Kallmann syndrome (IHH and anosmia); one had undetectable olfactory bulbs on a brain magnetic resonance imaging scan. Subjects with reversal were enriched for mutations affecting neurokinin B signaling compared with a cohort of IHH patients without reversal (10% vs 3%, P = .044), had comparable frequencies of mutations in FGFR1, PROKR2, and GNRHR, and had no mutations in KAL1. Five men did not sustain their reversal and again developed hypogonadotropism.
CONCLUSIONS: Reversal of IHH may be more widespread than previously appreciated and occurs across a broad range of genotypes and phenotypes. Enrichment for mutations that disrupt neurokinin B signaling in patients who reversed indicates that, despite the importance of this signaling pathway for normal pubertal timing, its function is dispensable later in life. The occurrence of reversal in a patient with no olfactory bulbs demonstrates that these structures are not essential for normal reproductive function. Patients with IHH require lifelong monitoring for reversal and, if reversal occurs, subsequent relapse also may occur.

Entities:  

Mesh:

Year:  2013        PMID: 24423288      PMCID: PMC3942233          DOI: 10.1210/jc.2013-2809

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


  50 in total

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2.  Olfactory phenotypic spectrum in idiopathic hypogonadotropic hypogonadism: pathophysiological and genetic implications.

Authors:  Hilana M Lewkowitz-Shpuntoff; Virginia A Hughes; Lacey Plummer; Margaret G Au; Richard L Doty; Stephanie B Seminara; Yee-Ming Chan; Nelly Pitteloud; William F Crowley; Ravikumar Balasubramanian
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3.  Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene.

Authors:  Nelly Pitteloud; James S Acierno; Astrid U Meysing; Andrew A Dwyer; Frances J Hayes; William F Crowley
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4.  The long-term clinical follow-up and natural history of men with adult-onset idiopathic hypogonadotropic hypogonadism.

Authors:  Andrew A Dwyer; Frances J Hayes; Lacey Plummer; Nelly Pitteloud; William F Crowley
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Authors:  Janne Tornberg; Gerasimos P Sykiotis; Kimberly Keefe; Lacey Plummer; Xuan Hoang; Janet E Hall; Richard Quinton; Stephanie B Seminara; Virginia Hughes; Guy Van Vliet; Stan Van Uum; William F Crowley; Hiroko Habuchi; Koji Kimata; Nelly Pitteloud; Hannes E Bülow
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8.  The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism.

Authors:  Nelly Pitteloud; Frances J Hayes; Paul A Boepple; Suzzunne DeCruz; Stephanie B Seminara; David T MacLaughlin; William F Crowley
Journal:  J Clin Endocrinol Metab       Date:  2002-01       Impact factor: 5.958

9.  Evidence for the Bauman variant in Kallmann's syndrome.

Authors:  A Kadva; W L Di; O Djahanbakhch; J Monson; R Silman
Journal:  Clin Endocrinol (Oxf)       Date:  1996-01       Impact factor: 3.478

10.  Episodic luteinizing hormone secretion in man. Pulse analysis, clinical interpretation, physiologic mechanisms.

Authors:  R J Santen; C W Bardin
Journal:  J Clin Invest       Date:  1973-10       Impact factor: 14.808

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1.  Hypothalamic Reproductive Endocrine Pulse Generator Activity Independent of Neurokinin B and Dynorphin Signaling.

Authors:  Margaret F Lippincott; Silvia León; Yee-Ming Chan; Chrysanthi Fergani; Rajae Talbi; I Sadaf Farooqi; Christopher M Jones; Wiebke Arlt; Susan E Stewart; Trevor R Cole; Ei Terasawa; Janet E Hall; Natalie D Shaw; Victor M Navarro; Stephanie Beth Seminara
Journal:  J Clin Endocrinol Metab       Date:  2019-10-01       Impact factor: 5.958

2.  Fatness and fertility: which direction?

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Journal:  J Clin Invest       Date:  2014-06-17       Impact factor: 14.808

3.  KISS1R signals independently of Gαq/11 and triggers LH secretion via the β-arrestin pathway in the male mouse.

Authors:  Maryse Ahow; Le Min; Macarena Pampillo; Connor Nash; Junping Wen; Kathleen Soltis; Rona S Carroll; Christine A Glidewell-Kenney; Pamela L Mellon; Moshmi Bhattacharya; Stuart A Tobet; Ursula B Kaiser; Andy V Babwah
Journal:  Endocrinology       Date:  2014-08-22       Impact factor: 4.736

4.  Do Substance P and Neurokinin A Play Important Roles in the Control of LH Secretion in Ewes?

Authors:  Chrysanthi Fergani; Leanne Mazzella; Lique M Coolen; Richard B McCosh; Steven L Hardy; Nora Newcomb; Pasha Grachev; Michael N Lehman; Robert L Goodman
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Review 5.  Paediatric and adult-onset male hypogonadism.

Authors:  Andrea Salonia; Giulia Rastrelli; Geoffrey Hackett; Stephanie B Seminara; Ilpo T Huhtaniemi; Rodolfo A Rey; Wayne J G Hellstrom; Mark R Palmert; Giovanni Corona; Gert R Dohle; Mohit Khera; Yee-Ming Chan; Mario Maggi
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6.  Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

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7.  Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome.

Authors:  Ravikumar Balasubramanian; Sheena Chew; Sarah E MacKinnon; Peter B Kang; Caroline Andrews; Wai-Man Chan; Elizabeth C Engle
Journal:  J Clin Endocrinol Metab       Date:  2015-01-05       Impact factor: 5.958

8.  CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism.

Authors:  Ihsan Turan; B Ian Hutchins; Bulent Hacihamdioglu; L Damla Kotan; Fatih Gurbuz; Ayca Ulubay; Eda Mengen; Bilgin Yuksel; Susan Wray; A Kemal Topaloglu
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Review 9.  Delayed and Precocious Puberty: Genetic Underpinnings and Treatments.

Authors:  Anisha Gohil; Erica A Eugster
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10.  Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay.

Authors:  Daiane Beneduzzi; Ericka B Trarbach; Le Min; Alexander A L Jorge; Heraldo M Garmes; Alessandra Covallero Renk; Marta Fichna; Piotr Fichna; Karina A Arantes; Elaine M F Costa; Anna Zhang; Oluwaseun Adeola; Junping Wen; Rona S Carroll; Berenice B Mendonça; Ursula B Kaiser; Ana Claudia Latronico; Letícia F G Silveira
Journal:  Fertil Steril       Date:  2014-07-10       Impact factor: 7.329

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