Hyperthyrotropinaemia in untreated subjects with down's syndrome aged 6 months to 64 years: a comparative analysis
Objectives To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a feature in a subset of patients with Down's syndrome. Design Comparative analysis. Setting Major health maintenance org...
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Published in | Archives of disease in childhood Vol. 97; no. 7; pp. 595 - 598 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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London
BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
01.07.2012
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Abstract | Objectives To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a feature in a subset of patients with Down's syndrome. Design Comparative analysis. Setting Major health maintenance organisation (3.8 million insured). Patients A data warehouse search identified all subjects with Down's syndrome who attended Clalit Health Services in 2006 and were tested for TSH and free thyroxine (T4) level on the day of diagnosis (intention-to-treat population). The study group consisted of patients who were not diagnosed with thyroid disease or did not receive thyroid-modulating medication (n=428). Their findings were compared with a control group of healthy age- and sex-matched subjects who were randomly selected from the general population. Main outcome measures Distribution of free T4, TSH and total T3 levels. Results The distribution plot for TSH showed a significant shift of the curve to higher values in the study group compared with the controls (p≤0.0001). This finding held true on further analysis of the whole intention-to-treat population (p<0.006). The free T4 distribution curve also shifted significantly to higher levels in patients with Down's syndrome (p≤0.0001). Conclusions Down's syndrome is associated with higher TSH levels. The results suggest that hyperthyrotropinaemia is an innate attribute of chromosome 21 trisomy. Therefore, T4 treatment should not be contemplated in Down's Syndrome unless the TSH is >95th centile in the presence of normal-range free T4 levels. |
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AbstractList | Objectives To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a feature in a subset of patients with Down's syndrome. Design Comparative analysis. Setting Major health maintenance organisation (3.8 million insured). Patients A data warehouse search identified all subjects with Down's syndrome who attended Clalit Health Services in 2006 and were tested for TSH and free thyroxine (T4) level on the day of diagnosis (intention-to-treat population). The study group consisted of patients who were not diagnosed with thyroid disease or did not receive thyroid-modulating medication (n=428). Their findings were compared with a control group of healthy age- and sex-matched subjects who were randomly selected from the general population. Main outcome measures Distribution of free T4, TSH and total T3 levels. Results The distribution plot for TSH showed a significant shift of the curve to higher values in the study group compared with the controls (p≤0.0001). This finding held true on further analysis of the whole intention-to-treat population (p<0.006). The free T4 distribution curve also shifted significantly to higher levels in patients with Down's syndrome (p≤0.0001). Conclusions Down's syndrome is associated with higher TSH levels. The results suggest that hyperthyrotropinaemia is an innate attribute of chromosome 21 trisomy. Therefore, T4 treatment should not be contemplated in Down's Syndrome unless the TSH is >95th centile in the presence of normal-range free T4 levels. To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a feature in a subset of patients with Down's syndrome. Comparative analysis. Major health maintenance organisation (3.8 million insured). A data warehouse search identified all subjects with Down's syndrome who attended Clalit Health Services in 2006 and were tested for TSH and free thyroxine (T4) level on the day of diagnosis (intention-to-treat population). The study group consisted of patients who were not diagnosed with thyroid disease or did not receive thyroid-modulating medication (n=428). Their findings were compared with a control group of healthy age- and sex-matched subjects who were randomly selected from the general population. Distribution of free T4, TSH and total T3 levels. The distribution plot for TSH showed a significant shift of the curve to higher values in the study group compared with the controls (p≤0.0001). This finding held true on further analysis of the whole intention-to-treat population (p<0.006). The free T4 distribution curve also shifted significantly to higher levels in patients with Down's syndrome (p≤0.0001). Down's syndrome is associated with higher TSH levels. The results suggest that hyperthyrotropinaemia is an innate attribute of chromosome 21 trisomy. Therefore, T4 treatment should not be contemplated in Down's Syndrome unless the TSH is >95th centile in the presence of normal-range free T4 levels. Objectives To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a feature in a subset of patients with Down's syndrome. Design Comparative analysis. Setting Major health maintenance organisation (3.8 million insured). Patients A data warehouse search identified all subjects with Down's syndrome who attended Clalit Health Services in 2006 and were tested for TSH and free thyroxine (T4) level on the day of diagnosis (intention-to-treat population). The study group consisted of patients who were not diagnosed with thyroid disease or did not receive thyroid-modulating medication (n=428). Their findings were compared with a control group of healthy age- and sex-matched subjects who were randomly selected from the general population. Main outcome measures Distribution of free T4, TSH and total T3 levels. Results The distribution plot for TSH showed a significant shift of the curve to higher values in the study group compared with the controls (pâ[per thousand]¤0.0001). This finding held true on further analysis of the whole intention-to-treat population (p<0.006). The free T4 distribution curve also shifted significantly to higher levels in patients with Down's syndrome (pâ[per thousand]¤0.0001). Conclusions Down's syndrome is associated with higher TSH levels. The results suggest that hyperthyrotropinaemia is an innate attribute of chromosome 21 trisomy. Therefore, T4 treatment should not be contemplated in Down's Syndrome unless the TSH is >95th centile in the presence of normal-range free T4 levels. To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a feature in a subset of patients with Down's syndrome.OBJECTIVESTo determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a feature in a subset of patients with Down's syndrome.Comparative analysis.DESIGNComparative analysis.Major health maintenance organisation (3.8 million insured).SETTINGMajor health maintenance organisation (3.8 million insured).A data warehouse search identified all subjects with Down's syndrome who attended Clalit Health Services in 2006 and were tested for TSH and free thyroxine (T4) level on the day of diagnosis (intention-to-treat population). The study group consisted of patients who were not diagnosed with thyroid disease or did not receive thyroid-modulating medication (n=428). Their findings were compared with a control group of healthy age- and sex-matched subjects who were randomly selected from the general population.PATIENTSA data warehouse search identified all subjects with Down's syndrome who attended Clalit Health Services in 2006 and were tested for TSH and free thyroxine (T4) level on the day of diagnosis (intention-to-treat population). The study group consisted of patients who were not diagnosed with thyroid disease or did not receive thyroid-modulating medication (n=428). Their findings were compared with a control group of healthy age- and sex-matched subjects who were randomly selected from the general population.Distribution of free T4, TSH and total T3 levels.MAIN OUTCOME MEASURESDistribution of free T4, TSH and total T3 levels.The distribution plot for TSH showed a significant shift of the curve to higher values in the study group compared with the controls (p≤0.0001). This finding held true on further analysis of the whole intention-to-treat population (p<0.006). The free T4 distribution curve also shifted significantly to higher levels in patients with Down's syndrome (p≤0.0001).RESULTSThe distribution plot for TSH showed a significant shift of the curve to higher values in the study group compared with the controls (p≤0.0001). This finding held true on further analysis of the whole intention-to-treat population (p<0.006). The free T4 distribution curve also shifted significantly to higher levels in patients with Down's syndrome (p≤0.0001).Down's syndrome is associated with higher TSH levels. The results suggest that hyperthyrotropinaemia is an innate attribute of chromosome 21 trisomy. Therefore, T4 treatment should not be contemplated in Down's Syndrome unless the TSH is >95th centile in the presence of normal-range free T4 levels.CONCLUSIONSDown's syndrome is associated with higher TSH levels. The results suggest that hyperthyrotropinaemia is an innate attribute of chromosome 21 trisomy. Therefore, T4 treatment should not be contemplated in Down's Syndrome unless the TSH is >95th centile in the presence of normal-range free T4 levels. |
Audience | Professional Academic |
Author | Bar-Tal, Ornit Antebi, Felice Greenberg-Dotan, Sari Hochberg, Ze'ev Meyerovitch, Joseph |
Author_xml | – sequence: 1 givenname: Joseph surname: Meyerovitch fullname: Meyerovitch, Joseph email: josephm@post.tau.ac.il organization: The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel – sequence: 2 givenname: Felice surname: Antebi fullname: Antebi, Felice email: josephm@post.tau.ac.il organization: Chief Medicine Offi ce, Clalit Health Services, Tel Aviv, Israel – sequence: 3 givenname: Sari surname: Greenberg-Dotan fullname: Greenberg-Dotan, Sari email: josephm@post.tau.ac.il organization: Chief Medicine Offi ce, Clalit Health Services, Tel Aviv, Israel – sequence: 4 givenname: Ornit surname: Bar-Tal fullname: Bar-Tal, Ornit email: josephm@post.tau.ac.il organization: Chief Medicine Offi ce, Clalit Health Services, Tel Aviv, Israel – sequence: 5 givenname: Ze'ev surname: Hochberg fullname: Hochberg, Ze'ev email: josephm@post.tau.ac.il organization: Division of Endocrinology, Meyer Children's Hospital, Rambam Medical Center, and Rappaport Faculty of Medicine and Research Institute, Technion, Israel Institute of Technology, Haifa, Israel |
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CitedBy_id | crossref_primary_10_3390_genes12020222 crossref_primary_10_1586_17446651_2015_1063995 crossref_primary_10_1111_cen_15236 crossref_primary_10_1159_000362450 crossref_primary_10_1002_ajmg_a_38219 crossref_primary_10_4103_ijem_IJEM_422_20 crossref_primary_10_3389_fendo_2020_00543 crossref_primary_10_1097_MED_0000000000000382 crossref_primary_10_1016_j_jpeds_2014_12_035 crossref_primary_10_1016_j_ejmhg_2014_01_007 crossref_primary_10_1089_thy_2022_0320 crossref_primary_10_3389_fendo_2021_782865 crossref_primary_10_1297_cpe_2022_0063 crossref_primary_10_1210_clinem_dgad333 crossref_primary_10_18273_revmed_v35n3_2022010 crossref_primary_10_1089_thy_2013_0248 crossref_primary_10_1530_EJE_15_0484 crossref_primary_10_1159_000457952 |
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Snippet | Objectives To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone... To determine whether an altered hypothalamic-pituitary-thyroid axis is inherent to Down's syndrome or if a high level of thyroid-stimulating hormone (TSH) is a... |
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SubjectTerms | Adolescent Adult Age Distribution Biological and medical sciences Care and treatment Case-Control Studies Child Child, Preschool Chromosome aberrations Comparative Analysis Control Groups Down Syndrome Down Syndrome - blood Down Syndrome - complications Down Syndrome - physiopathology Drug Therapy Flow Charts General aspects Genetic aspects Health aspects Humans Hypothalamic-pituitary-adrenal axis Hypothalamo-Hypophyseal System - physiopathology Hypothyroidism Infant Laboratories Medical genetics Medical research Medical sciences Middle Aged Miscellaneous Neonates Patients Physiological aspects Population Pregnancy Prevention and actions Public health. Hygiene Public health. Hygiene-occupational medicine Regression (Statistics) Statistical analysis Thyroid Thyroid diseases Thyroid Diseases - blood Thyroid Diseases - etiology Thyroid Diseases - physiopathology Thyroid Gland - physiopathology Thyrotropin Thyrotropin - blood Thyroxine - blood Triiodothyronine - blood Young Adult |
Title | Hyperthyrotropinaemia in untreated subjects with down's syndrome aged 6 months to 64 years: a comparative analysis |
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