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




Genetic Clue to Irritable Bowel Syndrome Found

By LabMedica International staff writers
Posted on 03 Apr 2014
Irritable bowel syndrome (IBS) may be caused by genetics, diet, past trauma, anxiety and all are thought to play a role, but now, for the first time, a defined genetic defect that causes a subset of IBS has been reported. More...


IBS is a common disorder that affects the large intestine and most patients with the disorder commonly experience symptoms of cramping, abdominal pain, bloating gas, diarrhea and constipation and most treatments for IBS target these symptoms. One of the risk factors for IBS is a family history of the syndrome where those who have a first-degree relative, such as a parent or sibling, with IBS are at increased risk of the condition.

An international team of scientists led by those at the Mayo Clinic (Rochester, MN, USA) studied the sodium channel of people with IBS and control subjects. Many of the patients with cardiac arrhythmias which are caused by mutations in the gene sodium channel, voltage-gated, type V, alpha subunit (SCN5A) also have symptoms of IBS. The team investigated whether patients with IBS have SCN5A variants that affect the function of the sodium ion channel protein Nav1.5.

The investigators performed genotype analysis of SCN5A in 584 persons with IBS and 1,380 control subjects. Mutant forms of SCN5A were expressed in Human Embryonic Kidney (HEK)-293 cells, and functions were assessed by voltage clamp analysis. A genome-wide association study (GWAS) was analyzed for an association signal for the SCN5A gene and replicated in 1,745 patients in four independent cohorts of IBS patients and controls.

Missense mutations were found in SCN5A in 13/584 patients (2.2%). Diarrhea-predominant IBS (IBS-D) was the most prevalent form of IBS in the overall study population (25%). However, a significantly greater percentage of individuals with SCN5A mutations had constipation-predominant IBS (IBS-C, 31%) than IBS-D (10%). In the GWAS and four replicated studies, the SCN5A locus was strongly associated with IBS.

The scientists were able to restore function to a patient with constipation predominant IBS with a defective SCN5A gene and resulting abnormally functioning sodium channel. They used a drug called mexiletine, which restored the function of the channel and reversed the patient's symptoms of constipation and abdominal pain. Gianrico Farrugia, MD, a lead study author, said, “This gives us hope that from only treating symptoms of the disease, we can now work to find disease-modifying agents, which is where we really want to be to affect long-term treatment of IBS.” The study was published on March 5, 2014, in the journal Gastroenterology.

Related Links:

Mayo Clinic



New
Gold Member
Hematology Analyzer
Medonic M32B
POC Helicobacter Pylori Test Kit
Hepy Urease Test
New
Pipette
Accumax Smart Series
New
Gel Cards
DG Gel Cards
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

Hematology

view channel
Image: The microfluidic device for passive separation of platelet-rich plasma from whole blood (Photo courtesy of University of the Basque Country)

Portable and Disposable Device Obtains Platelet-Rich Plasma Without Complex Equipment

Platelet-rich plasma (PRP) plays a crucial role in regenerative medicine due to its ability to accelerate healing and repair tissue. However, obtaining PRP traditionally requires expensive centrifugation... Read more

Immunology

view channel
Image: The new technology could predict who will benefit from immunotherapy (Photo courtesy of Max Delbrück Center)

New Technology Deciphers Immune Cell Communication to Predict Immunotherapy Response

A healthy immune system depends on complex communication between specialized cell types that detect, alert, and eliminate harmful threats. When these immune signaling pathways break down, the result can... Read more

Microbiology

view channel
Image: MycoMEIA Aspergillus Assay is the first FDA-cleared urine-based test for invasive aspergillosis (Photo courtesy of Pearl Diagnostics)

Urine-Based Assay Diagnoses Common Lung Infection in Immunocompromised People

Invasive Aspergillosis (IA), a life-threatening fungal infection, poses a serious threat to immunocompromised individuals, especially those with hematologic malignancies, transplants, or severe lung diseases.... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.