We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us

Download Mobile App




Events

10 Feb 2026 - 13 Feb 2026
17 Apr 2026 - 21 Apr 2026

British Genomics Study Looks at Hereditary Thyroid Hormone Variations

By LabMedica International staff writers
Posted on 15 Mar 2015
Data accumulated during the intense study of two population groups in the United Kingdom has been mined for information related to the hereditary basis of thyroid hormone variations.

Normal thyroid function is essential for health, but its genetic architecture remains poorly understood. More...
To increase understanding of this factor for the heritable thyroid hormones thyrotropin (TSH) and free thyroxine (FT4), investigators linked to the Wellcome Trust Sanger Institute's (Hinxton, United Kingdom) UK10K project analyzed whole-genome sequence data from two well-studied population groups.

The Avon Longitudinal Study of Parents and Children (ALSPAC) includes more than 14,000 mothers enrolled during pregnancy in 1991 and 1992, and the health and development of their children has been followed in great detail ever since. The ALSPAC families have provided a vast amount of genetic and environmental information over the years. The TwinsUK Adult Twin Registry is cited as being the most detailed clinical adult register in the world. It comprises 11,000 identical and non-identical twins between the ages of 16 and 85 years who have generated a database used to study the genetic and environmental etiology of age-related complex traits and diseases.

Meta-analysis results for common variants associated with TSH and FT4 led to the identification of a novel variant in the SYN2 (synapsin II) gene linked to TSH, as well as a new independent variant in the PDE8B (phosphodiesterase 8B) gene. For FT4, the investigators identified a low-frequency variant near B4GALT6 (B-N-acetylglucosaminyl-glycopeptide b-1,4-galactosyltransferase)/SLC25A52 (solute carrier family 25, member 52) and a rare TTR (transthyretin, a serum and cerebrospinal fluid carrier of the thyroid hormone thyroxine) variant. All common variants explained about 20% of the variance in TSH and FT4.

Contributing author Dr. Nicholas Timpson, reader in genetic epidemiology at the University of Bristol (United Kingdom) and co-chair of the UK10K whole genome sequencing initiative, said, “This work is another example of how extending gene studies to include whole genome sequencing can identify new clinically informative variants and enhance our understanding of key biological processes. The UK10K project has been essential to this endeavor and we are now beginning to realize its potential."

Related Links:

Wellcome Trust Sanger Institute
University of Bristol



Gold Member
Hematology Analyzer
Medonic M32B
POC Helicobacter Pylori Test Kit
Hepy Urease Test
Autoimmune Liver Diseases Assay
Microblot-Array Liver Profile Kit
Pipette
Accumax Smart Series
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Immunology

view channel
Image: Circulating tumor cells isolated from blood samples could help guide immunotherapy decisions (Photo courtesy of Shutterstock)

Blood Test Identifies Lung Cancer Patients Who Can Benefit from Immunotherapy Drug

Small cell lung cancer (SCLC) is an aggressive disease with limited treatment options, and even newly approved immunotherapies do not benefit all patients. While immunotherapy can extend survival for some,... Read more

Microbiology

view channel
Image: New evidence suggests that imbalances in the gut microbiome may contribute to the onset and progression of MCI and Alzheimer’s disease (Photo courtesy of Adobe Stock)

Comprehensive Review Identifies Gut Microbiome Signatures Associated With Alzheimer’s Disease

Alzheimer’s disease affects approximately 6.7 million people in the United States and nearly 50 million worldwide, yet early cognitive decline remains difficult to characterize. Increasing evidence suggests... Read more

Technology

view channel
Image: Vitestro has shared a detailed visual explanation of its Autonomous Robotic Phlebotomy Device (photo courtesy of Vitestro)

Robotic Technology Unveiled for Automated Diagnostic Blood Draws

Routine diagnostic blood collection is a high‑volume task that can strain staffing and introduce human‑dependent variability, with downstream implications for sample quality and patient experience.... Read more

Industry

view channel
Image: Roche’s cobas® Mass Spec solution enables fully automated mass spectrometry in routine clinical laboratories (Photo courtesy of Roche)

New Collaboration Brings Automated Mass Spectrometry to Routine Laboratory Testing

Mass spectrometry is a powerful analytical technique that identifies and quantifies molecules based on their mass and electrical charge. Its high selectivity, sensitivity, and accuracy make it indispensable... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.