HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The serotonin receptor HTR1B: gene polymorphisms in attention deficit hyperactivity disorder.

Abstract
Serotonin plays an essential role in cognition, locomotor activity, and the regulation of sleep, pain, mood, and aggression. Polymorphisms of the HTR1B gene have been implicated in a variety of psychiatric disorders including attention deficit hyperactivity disorder (ADHD) and obsessive-compulsive disorder (OCD). The objectives of this study were to: (i) expand our original investigation of the relationship between the HTR1B receptor gene and attention deficit/hyperactivity and; (ii) to investigate a possible association of obsessive behaviors/perfectionism and the HTR1B gene in a sample of 203 families with an ADHD proband. Six single nucleotide polymorphisms (SNPs) of the HTR1B receptor gene were genotyped using standard methods. Evidence for an association between the HTR1B gene and ADHD as a qualitative diagnosis, or the inattentive and hyperactive-impulsive quantitative traits was not supported by either TDT single marker analysis or haplotype analysis. In addition we did not find evidence to suggest an association between HTR1B and perfectionism in this sample of ADHD families.
AuthorsAbel Ickowicz, Yu Feng, Karen Wigg, Jennifer Quist, Tejasawe Pathare, Wendy Roberts, Molly Malone, Russell Schachar, Rosemary Tannock, James L Kennedy, Catyh L Barr
JournalAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (Am J Med Genet B Neuropsychiatr Genet) Vol. 144B Issue 1 Pg. 121-5 (Jan 05 2007) ISSN: 1552-4841 [Print] United States
PMID16958036 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA Primers
  • HTR1B protein, human
  • Receptor, Serotonin, 5-HT1B
Topics
  • Adolescent
  • Attention Deficit Disorder with Hyperactivity (genetics)
  • Base Sequence
  • Child
  • DNA Primers (genetics)
  • Female
  • Haplotypes
  • Humans
  • Linkage Disequilibrium
  • Male
  • Obsessive-Compulsive Disorder (genetics)
  • Polymorphism, Single Nucleotide
  • Receptor, Serotonin, 5-HT1B (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: