Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P01178 (
oxytocin
)
15,767
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Oxytocin
(OT) and a polymorphism (rs53576) in the oxytocin receptor gene (OXTR) have been independently associated with stress reactivity, whereas
oxytocin
's sister peptide, arginine vasopressin (AVP) and polymorphisms in the vasopressin receptor gene (AVPR1A) have been independently associated with aggressive behavior. In this study, 68 men and 98 women were genotyped for the OXTR rs53576 polymorphism and the AVPR1A
RS1
polymorphism. Baseline and poststressor levels of plasma OT, plasma AVP, positive affect, and anger were assessed. Women, but not men, with high levels of poststressor OT and the GG genotype of rs53576 felt the most positive affect after the stressor. Men, but not women, with high levels of poststressor AVP and the 320 allele of the
RS1
polymorphism reported more poststressor anger than noncarriers. These data constitute the first evidence that
oxytocin
and vasopressin receptor genes interact with levels of OT and AVP to predict sex-specific emotional stress responses.
...
PMID:Oxytocin and vasopressin receptor polymorphisms interact with circulating neuropeptides to predict human emotional reactions to stress. 2466 Jul 71
Background:
There are limited treatments available for autism spectrum disorder (ASD). Studies have reported significant associations between the receptor genes of
oxytocin
(OT) and vasopressin (AVP) and ASD diagnosis, as well as ASD-related phenotypes. Researchers have also found the manipulation of these systems affects social and repetitive behaviors, core characteristics of ASD. Consequently, research involving the
oxytocin
/vasopressin pathways as intervention targets has increased. Therefore, further examination into the relationship between these neuropeptides and ASD was undertaken. In this study, we examined associations between variants in the receptor genes of vasopressin (
AVPR1A, AVPR1B
),
oxytocin
(
OXTR
), and ASD diagnosis along with related subphenotypes.
Methods:
Probands were assessed using Autism Diagnostic Interview-Revised, Autism Diagnostic Observation Schedule, and clinical DSM-IV-TR criteria. Single nucleotide polymorphisms (SNPs) in
AVPR1B
and
OXTR
, and microsatellites in
AVPR1A
were genotyped in ~200 families with a proband with ASD. Family-based association testing (FBAT) was utilized to determine associations between variants and ASD. Haplotypes composed of
OXTR
SNPs (i.e., rs53576-rs2254298-rs2268493) were also analyzed due to previously published associations.
Results:
Using the additive inheritance model in FBAT we found associations between
AVPR1B
SNPs (rs28632197,
p
= 0.005, rs35369693,
p
= 0.025) and diagnosis. As in other studies,
OXTR
rs2268493 (
p
= 0.050) was associated with diagnosis. rs2268493 was also associated with ASD subphenotypes of social withdrawal (
p
= 0.013) and Insistence on Sameness (
p
= 0.039). Further analyses demonstrated that the haplotype, rs2254298-rs2268493 was found to be significantly associated with diagnosis (A-T;
p
= 0.026). FBAT was also used to analyze
AVPR1A
microsatellites (
RS1
and RS3). Both length variants were found to be associated with restrictive, repetitive behaviors, but not overall diagnosis. Correction for multiple comparisons was performed for SNPs tested in each gene region, only
AVPR1B
SNPs remained significantly associated with ASD diagnosis.
Conclusions:
Autism is a heterogeneous disorder with many genes and pathways that contribute to its development. SNPs and microsatellites in the receptor genes of OT and AVP are associated with ASD diagnosis and measures of social behavior as well as restricted repetitive behaviors. We reported a novel association with ASD and
AVPR1B
SNPs. Understanding of genotype-phenotype relationships may be helpful in the development of pharmacological interventions for the OT/AVP system.
...
PMID:ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-
AVPR1A, AVPR1B
, and
OXTR
. 2792 Jun 63