Publication:
Thyroid antibody status, subclinical hypothyroidism, and the risk of coronary heart disease: an individual participant data analysis.

cris.virtualsource.author-orcid3bddaf43-d073-4769-bb3f-0a79526c4cae
cris.virtualsource.author-orciddcf039b3-51b9-457e-aa4f-439d935925b3
dc.contributor.authorCollet, Tinh-Hai
dc.contributor.authorBauer, Douglas C
dc.contributor.authorCappola, Anne R
dc.contributor.authorAsvold, Bjørn O
dc.contributor.authorWeiler, Stefan
dc.contributor.authorVittinghoff, Eric
dc.contributor.authorGussekloo, Jacobijn
dc.contributor.authorBremner, Alexandra
dc.contributor.authorden Elzen, Wendy P J
dc.contributor.authorMaciel, Rui M B
dc.contributor.authorVanderpump, Mark P J
dc.contributor.authorCornuz, Jacques
dc.contributor.authorDörr, Marcus
dc.contributor.authorWallaschofski, Henri
dc.contributor.authorNewman, Anne B
dc.contributor.authorSgarbi, José A
dc.contributor.authorRazvi, Salman
dc.contributor.authorVölzke, Henry
dc.contributor.authorWalsh, John P
dc.contributor.authorAujesky, Drahomir
dc.contributor.authorRodondi, Nicolas
dc.date.accessioned2024-10-23T17:26:14Z
dc.date.available2024-10-23T17:26:14Z
dc.date.issued2014-09
dc.description.abstractCONTEXT Subclinical hypothyroidism has been associated with increased risk of coronary heart disease (CHD), particularly with thyrotropin levels of 10.0 mIU/L or greater. The measurement of thyroid antibodies helps predict the progression to overt hypothyroidism, but it is unclear whether thyroid autoimmunity independently affects CHD risk. OBJECTIVE The objective of the study was to compare the CHD risk of subclinical hypothyroidism with and without thyroid peroxidase antibodies (TPOAbs). DATA SOURCES AND STUDY SELECTION A MEDLINE and EMBASE search from 1950 to 2011 was conducted for prospective cohorts, reporting baseline thyroid function, antibodies, and CHD outcomes. DATA EXTRACTION Individual data of 38 274 participants from six cohorts for CHD mortality followed up for 460 333 person-years and 33 394 participants from four cohorts for CHD events. DATA SYNTHESIS Among 38 274 adults (median age 55 y, 63% women), 1691 (4.4%) had subclinical hypothyroidism, of whom 775 (45.8%) had positive TPOAbs. During follow-up, 1436 participants died of CHD and 3285 had CHD events. Compared with euthyroid individuals, age- and gender-adjusted risks of CHD mortality in subclinical hypothyroidism were similar among individuals with and without TPOAbs [hazard ratio (HR) 1.15, 95% confidence interval (CI) 0.87-1.53 vs HR 1.26, CI 1.01-1.58, P for interaction = .62], as were risks of CHD events (HR 1.16, CI 0.87-1.56 vs HR 1.26, CI 1.02-1.56, P for interaction = .65). Risks of CHD mortality and events increased with higher thyrotropin, but within each stratum, risks did not differ by TPOAb status. CONCLUSIONS CHD risk associated with subclinical hypothyroidism did not differ by TPOAb status, suggesting that biomarkers of thyroid autoimmunity do not add independent prognostic information for CHD outcomes.
dc.description.numberOfPages10
dc.description.sponsorshipUniversitätsklinik für Allgemeine Innere Medizin, Kompetenzbereich für Allgemeine Innere Medizin
dc.identifier.pmid24915118
dc.identifier.publisherDOI10.1210/jc.2014-1250
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/128826
dc.language.isoen
dc.publisherThe Endocrine Society
dc.relation.ispartofThe Journal of clinical endocrinology and metabolism
dc.relation.issn1945-7197
dc.relation.organizationDCD5A442C17EE17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleThyroid antibody status, subclinical hypothyroidism, and the risk of coronary heart disease: an individual participant data analysis.
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage3362
oaire.citation.issue9
oaire.citation.startPage3353
oaire.citation.volume99
oairecerif.author.affiliationUniversitätsklinik für Allgemeine Innere Medizin, Kompetenzbereich für Allgemeine Innere Medizin
oairecerif.author.affiliationUniversitätsklinik für Allgemeine Innere Medizin, Kompetenzbereich für Allgemeine Innere Medizin
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.description.ispublishedpub
unibe.eprints.legacyId62472
unibe.journal.abbrevTitleJ. Clin. Endocrinol. Metab.
unibe.refereedTRUE
unibe.subtype.articlejournal

Files

Collections