Create Account | Sign In: Author or Forum

 
 
News  |  Journals  |  Conferences  |  Blogs  |  Articles  |  Forums  |  Twitter    
 

 Headlines:

 

Category: Family Medicine | Internal Medicine | Neurology | Pediatrics | Psychiatry | Journal

Back to Journal Articles

Polygenic Component Linked to Risk of Schizophrenia

Last Updated: July 09, 2009.

 

Component involving thousands of alleles also appears to contribute to risk of bipolar disorder

Share |

Comments: (0)

Tell-a-Friend

 

  Related
 
Common polygenic variation may be responsible for a considerable portion of the total genetic variation involved in schizophrenia risk, according to research published online July 1 in Nature.

THURSDAY, July 9 (HealthDay News) -- Common polygenic variation may be responsible for a considerable portion of the total genetic variation involved in schizophrenia risk, according to research published online July 1 in Nature.

Pamela Sklar, M.D., of Massachusetts General Hospital in Boston, and colleagues writing on behalf of the International Schizophrenia Consortium sought to discover whether common variants have a substantial role en masse in schizophrenia.

The authors used more than 3,000 males and females with the disease and more than 3,000 controls, and assessed further samples to replicate their findings and investigate whether the polygenic component is also associated with bipolar disorder. The researchers found a polygenic basis to schizophrenia, involving thousands of common alleles, that explains one-third or more of the variation in liability and is also shared with bipolar disorder.

"A highly polygenic model suggests that genetically influenced individual differences across domains of brain development and function may form a diathesis for major psychiatric illness, perhaps as multiple growth and metabolic pathways influence human height. Our results may also reflect heterogeneity, such that some patients have aetiologically distinct diseases. The shared genetic liability between schizophrenia and bipolar disorder, previously suggested by clinical and genetic epidemiology, opens up the possibility of genetically based refinements in diagnosis," the authors write.

Abstract
Full Text (subscription or payment may be required)

Copyright © 2009 ScoutNews, LLC. All rights reserved.


Previous: Gender Disparities Seen in Research Grant Applications Next: Five Genes Implicated in Brain Tumor Risk

Reader comments on this article are listed below. Review our comments policy.


Submit your opinion:

Name:

Email:

Location:

URL:

Remember my personal information

Notify me of follow-up comments?

advertisement.gif (61x7 -- 0 bytes)
 

Are you a Doctor, Pharmacist, PA or a Nurse?

Join the Doctors Lounge online medical community

  • Editorial activities: Publish, peer review, edit online articles.

  • Ask a Doctor Teams: Respond to patient questions and discuss challenging presentations with other members.

Doctors Lounge Membership Application

 
     

 advertisement.gif (61x7 -- 0 bytes)

 

 

Useful Sites
MediLexicon
  Tools & Services: Follow DoctorsLounge on Twitter Follow us on Twitter | RSS News | Newsletter | Contact us
Copyright © 2001-2013
Doctors Lounge.
All rights reserved.

Medical Reference:
Diseases | Symptoms
Drugs | Labs | Procedures
Software | Tutorials

Advertising
Links | Humor
Forum Archive
CME | Conferences

Privacy Statement
Terms & Conditions
Editorial Board
About us | Email

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information:
verify here.