Natural course of subclinical hypothyroidism in Down's syndrome : prospective study results and therapeutic considerations
Pathogenesis, natural course and therapeutic management of subclinical hypothyroidism (SH) in Down's syndrome (DS) remain object of debate in literature. In the present study thyroid function, antithyroid antibody (ATA) prevalence and serum lipid concentrations were investigated in a group of 3...
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Veröffentlicht in: | Journal of endocrinological investigation 1995, Vol.18 (1), p.35-40 |
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creator | RUBELLO, D POZZAN, G. B CASARA, D GIRELLI, M. E BOCCATO, S RIGON, F BACCICHETTI, C PICCOLO, M BETTERLE, C BUSNARDO, B |
description | Pathogenesis, natural course and therapeutic management of subclinical hypothyroidism (SH) in Down's syndrome (DS) remain object of debate in literature. In the present study thyroid function, antithyroid antibody (ATA) prevalence and serum lipid concentrations were investigated in a group of 344 Down patients (DP) and data were compared with those obtained from a control group of 257 age and sex matched healthy subjects. Thyroid function and ATA prevalence were also studied in 120 parents of DP. SH prevalence was clearly higher in DP (32.5% of cases) than in controls (1.1%) and parents (0%). Similarly, ATA prevalence was higher in DP (18% of cases) than in controls (5.8%) and parents (6.6%). In spite of this, no correlation was found in DP between SH and ATA prevalences, since ATA were detected in 18.7% of SH-DP and in 15.8% of euthyroid DP. Thus, circulating ATA were not detected in the majority of SH-DP. No significant differences regarding T4, FT4, T3 and serum lipid levels among SH and euthyroid DP and controls were found. Moreover, TSH levels were only slightly increased, generally less than 10 microU/ml, in most cases of SH-DP. Follow-up was longer than 24 months (range 2-7 years, mean 3.1) in a group of 201 DP: two different patterns of SH course were observed, mainly depending on the presence or the absence of circulating ATA. In particular, 35.7% of ATA-positive SH-DP developed a clinically evident thyroid disease (overt hypothyroidism or hyperthyroidism), while no similar case was recorded among ATA-negative SH-DP. |
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B ; CASARA, D ; GIRELLI, M. E ; BOCCATO, S ; RIGON, F ; BACCICHETTI, C ; PICCOLO, M ; BETTERLE, C ; BUSNARDO, B</creator><creatorcontrib>RUBELLO, D ; POZZAN, G. B ; CASARA, D ; GIRELLI, M. E ; BOCCATO, S ; RIGON, F ; BACCICHETTI, C ; PICCOLO, M ; BETTERLE, C ; BUSNARDO, B</creatorcontrib><description>Pathogenesis, natural course and therapeutic management of subclinical hypothyroidism (SH) in Down's syndrome (DS) remain object of debate in literature. In the present study thyroid function, antithyroid antibody (ATA) prevalence and serum lipid concentrations were investigated in a group of 344 Down patients (DP) and data were compared with those obtained from a control group of 257 age and sex matched healthy subjects. Thyroid function and ATA prevalence were also studied in 120 parents of DP. SH prevalence was clearly higher in DP (32.5% of cases) than in controls (1.1%) and parents (0%). Similarly, ATA prevalence was higher in DP (18% of cases) than in controls (5.8%) and parents (6.6%). In spite of this, no correlation was found in DP between SH and ATA prevalences, since ATA were detected in 18.7% of SH-DP and in 15.8% of euthyroid DP. Thus, circulating ATA were not detected in the majority of SH-DP. No significant differences regarding T4, FT4, T3 and serum lipid levels among SH and euthyroid DP and controls were found. Moreover, TSH levels were only slightly increased, generally less than 10 microU/ml, in most cases of SH-DP. Follow-up was longer than 24 months (range 2-7 years, mean 3.1) in a group of 201 DP: two different patterns of SH course were observed, mainly depending on the presence or the absence of circulating ATA. In particular, 35.7% of ATA-positive SH-DP developed a clinically evident thyroid disease (overt hypothyroidism or hyperthyroidism), while no similar case was recorded among ATA-negative SH-DP.</description><identifier>ISSN: 0391-4097</identifier><identifier>EISSN: 1720-8386</identifier><identifier>DOI: 10.1007/BF03349694</identifier><identifier>PMID: 7759782</identifier><identifier>CODEN: JEIND7</identifier><language>eng</language><publisher>Milano: Kurtis</publisher><subject>Adolescent ; Adult ; Autoantibodies - blood ; Biological and medical sciences ; Child ; Child, Preschool ; Chromosome aberrations ; Down Syndrome - complications ; Female ; Graves Disease - complications ; Graves Disease - immunology ; Graves Disease - physiopathology ; Humans ; Hypothyroidism - complications ; Hypothyroidism - immunology ; Hypothyroidism - physiopathology ; Infant ; Lipids - blood ; Male ; Medical genetics ; Medical sciences ; Middle Aged ; Prospective Studies ; Thyroid Gland - immunology ; Thyroiditis, Autoimmune - complications ; Thyroiditis, Autoimmune - immunology ; Thyroiditis, Autoimmune - physiopathology</subject><ispartof>Journal of endocrinological investigation, 1995, Vol.18 (1), p.35-40</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-9d1f89e982c19bf9cb75a5ca480976cb6f6c25e63d05c191817efca76c231c2e3</citedby><cites>FETCH-LOGICAL-c311t-9d1f89e982c19bf9cb75a5ca480976cb6f6c25e63d05c191817efca76c231c2e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3450085$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7759782$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RUBELLO, D</creatorcontrib><creatorcontrib>POZZAN, G. B</creatorcontrib><creatorcontrib>CASARA, D</creatorcontrib><creatorcontrib>GIRELLI, M. E</creatorcontrib><creatorcontrib>BOCCATO, S</creatorcontrib><creatorcontrib>RIGON, F</creatorcontrib><creatorcontrib>BACCICHETTI, C</creatorcontrib><creatorcontrib>PICCOLO, M</creatorcontrib><creatorcontrib>BETTERLE, C</creatorcontrib><creatorcontrib>BUSNARDO, B</creatorcontrib><title>Natural course of subclinical hypothyroidism in Down's syndrome : prospective study results and therapeutic considerations</title><title>Journal of endocrinological investigation</title><addtitle>J Endocrinol Invest</addtitle><description>Pathogenesis, natural course and therapeutic management of subclinical hypothyroidism (SH) in Down's syndrome (DS) remain object of debate in literature. In the present study thyroid function, antithyroid antibody (ATA) prevalence and serum lipid concentrations were investigated in a group of 344 Down patients (DP) and data were compared with those obtained from a control group of 257 age and sex matched healthy subjects. Thyroid function and ATA prevalence were also studied in 120 parents of DP. SH prevalence was clearly higher in DP (32.5% of cases) than in controls (1.1%) and parents (0%). Similarly, ATA prevalence was higher in DP (18% of cases) than in controls (5.8%) and parents (6.6%). In spite of this, no correlation was found in DP between SH and ATA prevalences, since ATA were detected in 18.7% of SH-DP and in 15.8% of euthyroid DP. Thus, circulating ATA were not detected in the majority of SH-DP. No significant differences regarding T4, FT4, T3 and serum lipid levels among SH and euthyroid DP and controls were found. Moreover, TSH levels were only slightly increased, generally less than 10 microU/ml, in most cases of SH-DP. Follow-up was longer than 24 months (range 2-7 years, mean 3.1) in a group of 201 DP: two different patterns of SH course were observed, mainly depending on the presence or the absence of circulating ATA. In particular, 35.7% of ATA-positive SH-DP developed a clinically evident thyroid disease (overt hypothyroidism or hyperthyroidism), while no similar case was recorded among ATA-negative SH-DP.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Autoantibodies - blood</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chromosome aberrations</subject><subject>Down Syndrome - complications</subject><subject>Female</subject><subject>Graves Disease - complications</subject><subject>Graves Disease - immunology</subject><subject>Graves Disease - physiopathology</subject><subject>Humans</subject><subject>Hypothyroidism - complications</subject><subject>Hypothyroidism - immunology</subject><subject>Hypothyroidism - physiopathology</subject><subject>Infant</subject><subject>Lipids - blood</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Thyroid Gland - immunology</subject><subject>Thyroiditis, Autoimmune - complications</subject><subject>Thyroiditis, Autoimmune - immunology</subject><subject>Thyroiditis, Autoimmune - physiopathology</subject><issn>0391-4097</issn><issn>1720-8386</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtP3TAQhS1URC-33bCv5EUFUqW0dpzENju4LQ8JtRtYR44z0TXKC48NSn89rojoah7n0zwOISecfeeMyR-XV0yIQle6OCAbLnOWKaGqD2TDhOZZwbT8SI4RHxkTUih5RI6kLLVU-Yb8_W1C9KandooegU4dxdjY3o3Opu5-maewX_zkWocDdSP9Ob2MZ0hxGVs_DUDP6ewnnMEG9wwUQ2wX6gFjH5CasaVhD97MEIOzaceIrk11cCn7RA470yN8XuOWPFz9ut_dZHd_rm93F3eZFZyHTLe8Uxq0yi3XTadtI0tTWlOo9Fdlm6qrbF5CJVpWJoIrLqGzJkm54DYHsSWnb3PToU8RMNSDQwt9b0aYItZS5lrpiiXw2xto00fooatn7wbjl5qz-p_R9X-jE_xlnRqbAdp3dHU26V9X3WBysvNmtA7fMVGUjKlSvAIZ-ogO</recordid><startdate>1995</startdate><enddate>1995</enddate><creator>RUBELLO, D</creator><creator>POZZAN, G. B</creator><creator>CASARA, D</creator><creator>GIRELLI, M. E</creator><creator>BOCCATO, S</creator><creator>RIGON, F</creator><creator>BACCICHETTI, C</creator><creator>PICCOLO, M</creator><creator>BETTERLE, C</creator><creator>BUSNARDO, B</creator><general>Kurtis</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1995</creationdate><title>Natural course of subclinical hypothyroidism in Down's syndrome : prospective study results and therapeutic considerations</title><author>RUBELLO, D ; POZZAN, G. B ; CASARA, D ; GIRELLI, M. E ; BOCCATO, S ; RIGON, F ; BACCICHETTI, C ; PICCOLO, M ; BETTERLE, C ; BUSNARDO, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-9d1f89e982c19bf9cb75a5ca480976cb6f6c25e63d05c191817efca76c231c2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Autoantibodies - blood</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chromosome aberrations</topic><topic>Down Syndrome - complications</topic><topic>Female</topic><topic>Graves Disease - complications</topic><topic>Graves Disease - immunology</topic><topic>Graves Disease - physiopathology</topic><topic>Humans</topic><topic>Hypothyroidism - complications</topic><topic>Hypothyroidism - immunology</topic><topic>Hypothyroidism - physiopathology</topic><topic>Infant</topic><topic>Lipids - blood</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Thyroid Gland - immunology</topic><topic>Thyroiditis, Autoimmune - complications</topic><topic>Thyroiditis, Autoimmune - immunology</topic><topic>Thyroiditis, Autoimmune - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RUBELLO, D</creatorcontrib><creatorcontrib>POZZAN, G. B</creatorcontrib><creatorcontrib>CASARA, D</creatorcontrib><creatorcontrib>GIRELLI, M. E</creatorcontrib><creatorcontrib>BOCCATO, S</creatorcontrib><creatorcontrib>RIGON, F</creatorcontrib><creatorcontrib>BACCICHETTI, C</creatorcontrib><creatorcontrib>PICCOLO, M</creatorcontrib><creatorcontrib>BETTERLE, C</creatorcontrib><creatorcontrib>BUSNARDO, B</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of endocrinological investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RUBELLO, D</au><au>POZZAN, G. B</au><au>CASARA, D</au><au>GIRELLI, M. E</au><au>BOCCATO, S</au><au>RIGON, F</au><au>BACCICHETTI, C</au><au>PICCOLO, M</au><au>BETTERLE, C</au><au>BUSNARDO, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natural course of subclinical hypothyroidism in Down's syndrome : prospective study results and therapeutic considerations</atitle><jtitle>Journal of endocrinological investigation</jtitle><addtitle>J Endocrinol Invest</addtitle><date>1995</date><risdate>1995</risdate><volume>18</volume><issue>1</issue><spage>35</spage><epage>40</epage><pages>35-40</pages><issn>0391-4097</issn><eissn>1720-8386</eissn><coden>JEIND7</coden><abstract>Pathogenesis, natural course and therapeutic management of subclinical hypothyroidism (SH) in Down's syndrome (DS) remain object of debate in literature. In the present study thyroid function, antithyroid antibody (ATA) prevalence and serum lipid concentrations were investigated in a group of 344 Down patients (DP) and data were compared with those obtained from a control group of 257 age and sex matched healthy subjects. Thyroid function and ATA prevalence were also studied in 120 parents of DP. SH prevalence was clearly higher in DP (32.5% of cases) than in controls (1.1%) and parents (0%). Similarly, ATA prevalence was higher in DP (18% of cases) than in controls (5.8%) and parents (6.6%). In spite of this, no correlation was found in DP between SH and ATA prevalences, since ATA were detected in 18.7% of SH-DP and in 15.8% of euthyroid DP. Thus, circulating ATA were not detected in the majority of SH-DP. No significant differences regarding T4, FT4, T3 and serum lipid levels among SH and euthyroid DP and controls were found. Moreover, TSH levels were only slightly increased, generally less than 10 microU/ml, in most cases of SH-DP. Follow-up was longer than 24 months (range 2-7 years, mean 3.1) in a group of 201 DP: two different patterns of SH course were observed, mainly depending on the presence or the absence of circulating ATA. In particular, 35.7% of ATA-positive SH-DP developed a clinically evident thyroid disease (overt hypothyroidism or hyperthyroidism), while no similar case was recorded among ATA-negative SH-DP.</abstract><cop>Milano</cop><pub>Kurtis</pub><pmid>7759782</pmid><doi>10.1007/BF03349694</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Autoantibodies - blood Biological and medical sciences Child Child, Preschool Chromosome aberrations Down Syndrome - complications Female Graves Disease - complications Graves Disease - immunology Graves Disease - physiopathology Humans Hypothyroidism - complications Hypothyroidism - immunology Hypothyroidism - physiopathology Infant Lipids - blood Male Medical genetics Medical sciences Middle Aged Prospective Studies Thyroid Gland - immunology Thyroiditis, Autoimmune - complications Thyroiditis, Autoimmune - immunology Thyroiditis, Autoimmune - physiopathology |
title | Natural course of subclinical hypothyroidism in Down's syndrome : prospective study results and therapeutic considerations |
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