TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young Adult

Background. For unknown reasons, the prevalence of thyroid autoimmune disorders is higher in patients with Down's syndrome than in the general population. The present case strongly supports a recent evaluation of propagating screening for thyroid disease in this group of patients to assure earl...

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Main Authors: Anne-Sophie Gauchez, Magali Pizzo, Dany Alcaraz-Galvain, Karim Chikh, Jacques Orgiazzi, Georg Brabant, Catherine Ronin, Anne Charrié
Format: Article
Language:English
Published: Hindawi Limited 2010-01-01
Series:Journal of Thyroid Research
Online Access:http://dx.doi.org/10.4061/2010/703978
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spelling doaj-2c9dd3fbc5c040629e94a66bb7f7aa152020-11-25T00:18:39ZengHindawi LimitedJournal of Thyroid Research2042-00722010-01-01201010.4061/2010/703978703978TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young AdultAnne-Sophie Gauchez0Magali Pizzo1Dany Alcaraz-Galvain2Karim Chikh3Jacques Orgiazzi4Georg Brabant5Catherine Ronin6Anne Charrié7Laboratoire du Service de Médecine Nucléaire, Centre Hospitalier de Chambéry, 73000 Chambéry, FranceNeurodiag, UMR 6149, CNRS et Université de Provence, 13331 Marseille, FranceSociété Française de Médecine Nucléaire, Groupe de Biologie Spécialisée, Centre Antoine Béclère, 45 rue des Saints Pères, 75270 Paris, FranceSociété Française de Médecine Nucléaire, Groupe de Biologie Spécialisée, Centre Antoine Béclère, 45 rue des Saints Pères, 75270 Paris, FranceService Endocrinologie, Diabète, Nutrition, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, 69495 Pierre-Bénite, FranceDepartment of Endocrinology, The Christie, Manchester M20 4BX, UKNeurodiag, UMR 6149, CNRS et Université de Provence, 13331 Marseille, FranceSociété Française de Médecine Nucléaire, Groupe de Biologie Spécialisée, Centre Antoine Béclère, 45 rue des Saints Pères, 75270 Paris, FranceBackground. For unknown reasons, the prevalence of thyroid autoimmune disorders is higher in patients with Down's syndrome than in the general population. The present case strongly supports a recent evaluation of propagating screening for thyroid disease in this group of patients to assure early diagnosis of hypothyroidism. Methods. In a 25-year-old man diagnosed with Down's syndrome, clinical manifestations of hypothyroidism were lacking, but profound biochemical abnormalities were found with particularly high levels of thyroid stimulating hormone (TSH). Antigenic properties of TSH were characterized using a panel of anti-TSH antibodies. Results. Technical problems not infrequently associated with TSH measurements are convincingly ruled out. Antigenic characterization of the patient's circulating TSH revealed circulating forms of TSH different from pituitary TSH which closely resembled TSH recombinant human hormone. Conclusions. It appears counterintuitive that the bioactivity of TSH decreases in the hypothyroid state as higher bioactivity of TSH is anticipated in hypothyroidism promoted by an increased hypothalamic TRH drive. In contrast, diminished negative thyroid hormone feedback will enhance posttranslational glycosylation of TSH subunits and increase sialylation of the carbohydrate side chains. Both exert a negative effect on TSH bioactivity, only compensated by the very high levels of the hormone as in the present case.http://dx.doi.org/10.4061/2010/703978
collection DOAJ
language English
format Article
sources DOAJ
author Anne-Sophie Gauchez
Magali Pizzo
Dany Alcaraz-Galvain
Karim Chikh
Jacques Orgiazzi
Georg Brabant
Catherine Ronin
Anne Charrié
spellingShingle Anne-Sophie Gauchez
Magali Pizzo
Dany Alcaraz-Galvain
Karim Chikh
Jacques Orgiazzi
Georg Brabant
Catherine Ronin
Anne Charrié
TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young Adult
Journal of Thyroid Research
author_facet Anne-Sophie Gauchez
Magali Pizzo
Dany Alcaraz-Galvain
Karim Chikh
Jacques Orgiazzi
Georg Brabant
Catherine Ronin
Anne Charrié
author_sort Anne-Sophie Gauchez
title TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young Adult
title_short TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young Adult
title_full TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young Adult
title_fullStr TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young Adult
title_full_unstemmed TSH Isoforms: About a Case of Hypothyroidism in a Down's Syndrome Young Adult
title_sort tsh isoforms: about a case of hypothyroidism in a down's syndrome young adult
publisher Hindawi Limited
series Journal of Thyroid Research
issn 2042-0072
publishDate 2010-01-01
description Background. For unknown reasons, the prevalence of thyroid autoimmune disorders is higher in patients with Down's syndrome than in the general population. The present case strongly supports a recent evaluation of propagating screening for thyroid disease in this group of patients to assure early diagnosis of hypothyroidism. Methods. In a 25-year-old man diagnosed with Down's syndrome, clinical manifestations of hypothyroidism were lacking, but profound biochemical abnormalities were found with particularly high levels of thyroid stimulating hormone (TSH). Antigenic properties of TSH were characterized using a panel of anti-TSH antibodies. Results. Technical problems not infrequently associated with TSH measurements are convincingly ruled out. Antigenic characterization of the patient's circulating TSH revealed circulating forms of TSH different from pituitary TSH which closely resembled TSH recombinant human hormone. Conclusions. It appears counterintuitive that the bioactivity of TSH decreases in the hypothyroid state as higher bioactivity of TSH is anticipated in hypothyroidism promoted by an increased hypothalamic TRH drive. In contrast, diminished negative thyroid hormone feedback will enhance posttranslational glycosylation of TSH subunits and increase sialylation of the carbohydrate side chains. Both exert a negative effect on TSH bioactivity, only compensated by the very high levels of the hormone as in the present case.
url http://dx.doi.org/10.4061/2010/703978
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