COMT rs4818, pain sensitivity and duration, and alveolar bone grafting of oral clefts.

Oral Maxillofac Surg

Post-graduate Program in Dentistry and Center for Treatment of Cleft Lip and Palate, University Hospital Lauro Wanderley, Universidade Federal da Paraíba, João Pessoa, PB, Brazil.

Published: June 2021

Purpose: Verifying whether the mutation in COMT rs4818 could be involved in pain modulation.

Methods: Thirty-two individuals born with cleft lip and palate that underwent bone graft from the iliac crest bone were assessed at 12, 24, 48, 72 h, and 7 days regarding their pain experience using a visual analogic scale. DNA from each participant was collected from saliva samples, and genotyping of rs4818 was performed using TaqMan chemistry. Overrepresentation of rs4818 alleles was tested using chi-square or Fisher's exact tests with an alpha of 0.05.

Results: Of the 32 individuals, eighteen reported long pain duration, nine reported high pain intensity, and fourteen low pain intensity up to 48 h. No differences were found in the distribution of individuals depending on the reported pain by sex (p = 0.12), age (p = 0.42), or cleft type (p = 0.5). The distribution of COMT r4818 alleles was different depending on the intensity and duration of pain. Carriers of the C wild-type allele were four times more likely to show high pain intensity and duration (odds ratio = 4.29, 95% confidence interval 1.13-16.18), meaning that the G variant allele is protective.

Conclusion: COMT rs4818 is associated with postoperative pain after alveolar bone grafting.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10006-020-00912-0DOI Listing

Publication Analysis

Top Keywords

comt rs4818
12
pain intensity
12
pain
10
alveolar bone
8
bone grafting
8
high pain
8
intensity duration
8
comt
4
rs4818 pain
4
pain sensitivity
4

Similar Publications

Background/objective: Raloxifene, a selective estrogen receptor modulator (SERM), may improve symptoms and cognition in schizophrenia spectrum disorders (SSD). Studies have shown inconsistent efficacy, especially in men with SSD. We assessed whether single nucleotide polymorphisms (SNPs) on genes involved in the pharmacodynamics (ESR1 and COMT) and pharmacokinetics (UGT1A8) of raloxifene can explain the heterogeneous treatment response to raloxifene augmentation in patients with SSD.

View Article and Find Full Text PDF

Schizophrenia is a multifaceted psychiatric disorder characterized by hallucinations, delusions, cognitive impairments, and behavioral disturbances. Genetic factors significantly contribute to its pathogenesis, accounting for approximately 80% of the heritability. Globally, about 1% of the population is affected by schizophrenia, with 45,054 individuals in Kazakhstan receiving medical treatment for the condition, indicating a prevalence rate of 238,6 per 100,000 people.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates how specific genetic variations (SNPs) in the COMT and OPRM1 genes affect treatment responses in patients suffering from temporomandibular disorders (TMDp), particularly focusing on pain intensity, mouth opening, and anxiety levels.
  • In a group of 60 TMDp patients who received standardized treatment over six months, those with minor allele variants showed less improvement in pain reduction and anxiety compared to those with dominant homozygous variants.
  • The results suggest that genetic factors may help predict treatment outcomes in TMDp patients, implying that genotype assessment could be valuable in tailoring treatment strategies.
View Article and Find Full Text PDF

Purpose: Neurocognitive impairment is a common and debilitating complication of sickle cell disease (SCD) resulting from a combination of biological and environmental factors. The catechol-O-methyltransferase (COMT) gene modulates levels of dopamine availability in the prefrontal cortex. COMT has repeatedly been implicated in the perception of pain stimuli and frequency of pain crises in patients with SCD and is known to be associated with neurocognitive functioning in the general population.

View Article and Find Full Text PDF

Aim: Polymorphisms in the COMT gene can alter enzymatic functions, raising levels of endogenous catecholamines, which stimulates beta-adrenergic receptors related to pain. This study aimed to evaluate whether a polymorphism in the COMT gene (rs4818) is associated with dental pain in children.

Methodology: A cross-sectional study was conducted with a representative sample of 731 pairs of children and parents randomly selected from a population-based sample of eight-year-old children.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!