izpis_h1_title_alt

Hypercholesterolemia in two siblings with resistance to thyroid hormones due to disease-causing variant in thyroid hormone receptor (THRB) gene
ID Pajek, Maja (Author), ID Avbelj Stefanija, Magdalena (Author), ID Trebušak Podkrajšek, Katarina (Author), ID Šuput Omladič, Jasna (Author), ID Žerjav-Tanšek, Mojca (Author), ID Battelino, Tadej (Author), ID Grošelj, Urh (Author)

.pdfPDF - Presentation file, Download (480,09 KB)
MD5: DD88A265AD996C4153B4C2FA201E2356
URLURL - Source URL, Visit https://www.mdpi.com/1648-9144/56/12/699 This link opens in a new window

Abstract
Resistance to thyroid hormone beta (RTHβ) is a syndrome characterized by a reduced response of target tissues to thyroid hormones. In 85% of cases, a pathogenic mutation in the thyroid hormone receptor beta (THRB) gene is found. The clinical picture of RTHβ is very diverse; the most common findings are goiter and tachycardia, but the patients might be clinically euthyroid. The laboratory findings are almost pathognomonic with elevated free thyroxin (fT4) levels and high or normal thyrotropin (TSH) levels; free triiodothyronin (fT3) levels may also be elevated. We present three siblings with THRB mutation (heterozygous disease-variant c.727C>T, p.Arg243Trp); two of them also had hypercholesterolemia, while all three had several other clinical characteristics of RTHβ. This is the first description of the known Slovenian cases with RTHβ due to the pathogenic mutation in the THRB gene. Hypercholesterolemia might be etiologically related with RTHβ, since the severity of hormonal resistance varies among different tissues and hypercholesterolemia in patients with THRB variants might indicate the relatively hypothyroid state of the liver. We suggest that cholesterol levels are measured in all RTHβ patients.

Language:English
Keywords:thyroid, resistance to thyroid hormones, RTHβ, thyroid hormone receptor, THRB, hypothyroidism, hypercholesterolemia
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
Publication status:Published
Publication version:Version of Record
Year:2020
Number of pages:6 str.
Numbering:Vol. 56, iss. 12, art. 699
PID:20.500.12556/RUL-134843 This link opens in a new window
UDC:616-053.2ž
ISSN on article:1648-9144
DOI:10.3390/medicina56120699 This link opens in a new window
COBISS.SI-ID:45814787 This link opens in a new window
Publication date in RUL:04.02.2022
Views:1043
Downloads:137
Metadata:XML DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Record is a part of a journal

Title:Medicina
Publisher:MDPI
ISSN:1648-9144
COBISS.SI-ID:6754623 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:15.12.2020

Projects

Funder:ARRS - Slovenian Research Agency
Project number:J3-2356
Name:Izražanje in funkcionalna analiza nekodirajočih RNA pri parkinsonovi bolezni

Funder:ARRS - Slovenian Research Agency
Project number:P3-0343
Name:Etiologija, zgodnje odkrivanje in zdravljenje bolezni pri otrocih in mladostnikih

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back