Samih Abed Odhaib, Miaad Jassim Mohammed, Mahmood Thamer Altemimi, Abbas Ali Mansour
{"title":"Thyroid Function Screening among First- and Second-Degree Healthy\nAsymptomatic Relatives of Patients with Hashimoto’s Thyroiditis","authors":"Samih Abed Odhaib, Miaad Jassim Mohammed, Mahmood Thamer Altemimi, Abbas Ali Mansour","doi":"10.2174/0102506882249988231205102133","DOIUrl":null,"url":null,"abstract":"\n\nAssessment of thyroid dysfunction among relatives of patients diagnosed with Hashimoto’s thyroiditis is controversial due to the lack of evidence.\nScreening and prediction of thyroid dysfunction among first- and second-degree relatives (FDRs and SDRs) of patients were diagnosed with\nHashimoto’s thyroiditis.\n\n\n\nThree hundred and forty-six asymptomatic relatives of 97 patients diagnosed with Hashimoto’s thyroiditis were enrolled in mixed cross-sectional\nand prospective assessments for thyroid dysfunction over more than two years (September 2018-December 2020).\nBoth FDR and SDR were evaluated by thyrotropin (TSH) and thyroid ultrasound at enrollment. Individuals with abnormal TSH were thoroughly\nevaluated biochemically and were subsequently classified as euthyroid, subclinical, and overt thyroid dysfunctional. The future reversion of\nenrolled individuals with normal and subclinical thyroid function to overt dysfunction was predicted by using the Thyroid Event Amsterdam\n(THEA) score.\n\n\n\nThree-quarters of the participants were non-smoking married women. Thyroid dysfunction was diagnosed among 43% of the participants (n=150),\nof whom two-thirds (74%) were having overt dysfunction (n=111). Neither the demographic elements nor the initial thyroid function could predict\nthe future thyroid function among those participants. Two out of ten (16%) were having autoimmune thyroid disease (AITD) as part of familial\nclustering (n=56). Four participants with subclinical hypothyroidism were treated accordingly due to their high THEA score despite the global\nlower THEA score (5.00±0.44).\n\n\n\nScreening of asymptomatic relatives of patients diagnosed with Hashimoto's thyroiditis could help identify the familial background of thyroid\ndiseases in 43% of FDRs and SDRs. One-third may have an underlying autoimmune basis.\n","PeriodicalId":110816,"journal":{"name":"New Emirates Medical Journal","volume":"11 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Emirates Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0102506882249988231205102133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Assessment of thyroid dysfunction among relatives of patients diagnosed with Hashimoto’s thyroiditis is controversial due to the lack of evidence.
Screening and prediction of thyroid dysfunction among first- and second-degree relatives (FDRs and SDRs) of patients were diagnosed with
Hashimoto’s thyroiditis.
Three hundred and forty-six asymptomatic relatives of 97 patients diagnosed with Hashimoto’s thyroiditis were enrolled in mixed cross-sectional
and prospective assessments for thyroid dysfunction over more than two years (September 2018-December 2020).
Both FDR and SDR were evaluated by thyrotropin (TSH) and thyroid ultrasound at enrollment. Individuals with abnormal TSH were thoroughly
evaluated biochemically and were subsequently classified as euthyroid, subclinical, and overt thyroid dysfunctional. The future reversion of
enrolled individuals with normal and subclinical thyroid function to overt dysfunction was predicted by using the Thyroid Event Amsterdam
(THEA) score.
Three-quarters of the participants were non-smoking married women. Thyroid dysfunction was diagnosed among 43% of the participants (n=150),
of whom two-thirds (74%) were having overt dysfunction (n=111). Neither the demographic elements nor the initial thyroid function could predict
the future thyroid function among those participants. Two out of ten (16%) were having autoimmune thyroid disease (AITD) as part of familial
clustering (n=56). Four participants with subclinical hypothyroidism were treated accordingly due to their high THEA score despite the global
lower THEA score (5.00±0.44).
Screening of asymptomatic relatives of patients diagnosed with Hashimoto's thyroiditis could help identify the familial background of thyroid
diseases in 43% of FDRs and SDRs. One-third may have an underlying autoimmune basis.