Quality of life and socioeconomic and educational status in patients with congenital hypothyroidism

dc.contributor.authorDanner Emmi
dc.contributor.authorSund Reijo
dc.contributor.authorSintonen Harri
dc.contributor.authorNiuro Laura
dc.contributor.authorNiinikoski Harri
dc.contributor.authorHuopio Hanna
dc.contributor.authorViikari Liisa A.
dc.contributor.authorJääskeläinen Jarmo
dc.contributor.organizationfi=lastentautioppi|en=Paediatrics and Adolescent Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40612039509
dc.converis.publication-id387535617
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/387535617
dc.date.accessioned2025-08-27T23:10:40Z
dc.date.available2025-08-27T23:10:40Z
dc.description.abstract<p>Background<br>The aim of this study was to investigate the influence of primary congenital hypothyroidism (CH) on quality of life, level of education and socioeconomic status (SES).</p><p>Methods<br>Two independent study cohorts, a national and a regional, were collected from Finnish national registers and patient records. Data on social security benefits, SES, marital status, and education were collected from Statistics Finland. Health-related quality of life (HRQoL) was studied in the regional patient cohort with the standardized 15D and 16D instruments.</p><p>Results<br>There were no statistically significant differences in education level, marital status, or SES between CH patients (n = 40) and their matched controls at the age of 25 years. The mean 15D score was both statistically significantly and clinically importantly lower in CH patients (n = 29) than controls (0.904 vs. 0.953, p = 0.008). CH patients reported significantly lower scores across various dimensions of physical and mental HRQoL, including breathing, sleeping, speech, excretion, mental function, distress, and vitality. The mean 16D score was lower in CH patients compared to controls (0.917, vs. 0.947), but without statistical significance.</p><p>Conclusion<br>SES of CH patients did not differ from matched controls. Thus, most CH patients integrate well into society, but their HRQoL is impaired.</p>
dc.identifier.eissn1530-0447
dc.identifier.jour-issn0031-3998
dc.identifier.olddbid203544
dc.identifier.oldhandle10024/186571
dc.identifier.urihttps://www.utupub.fi/handle/11111/38752
dc.identifier.urlhttps://www.nature.com/articles/s41390-024-03170-y
dc.identifier.urnURN:NBN:fi-fe2025082790148
dc.language.isoen
dc.okm.affiliatedauthorNiuro, Laura
dc.okm.affiliatedauthorNiinikoski, Harri
dc.okm.affiliatedauthorViikari, Liisa
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3142 Public health care science, environmental and occupational healthen_GB
dc.okm.discipline5141 Sociologyen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.discipline3142 Kansanterveystiede, ympäristö ja työterveysfi_FI
dc.okm.discipline5141 Sosiologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSpringer Nature
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1038/s41390-024-03170-y
dc.relation.ispartofjournalPediatric Research
dc.source.identifierhttps://www.utupub.fi/handle/10024/186571
dc.titleQuality of life and socioeconomic and educational status in patients with congenital hypothyroidism
dc.year.issued2024

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