Single Nucleotides Polymorphisms in COX2 Gene and their Association with Signs and Symptoms of Teething - A Pilot Study
Pesqui. bras. odontopediatria clín. integr
; 23: e210244, 2023. tab, graf
Article
ي En
| LILACS, BBO
| ID: biblio-1529121
المكتبة المسؤولة:
BR1264.1
ABSTRACT
ABSTRACT Objective:
To investigate the association between single nucleotide polymorphisms in the COX2 gene (rs689466 and rs5275) and local and systemic signs and symptoms of teething. Material andMethods:
Forty-four pairs of mothers-babies/toddlers were included. Erupted primary teeth were evaluated during clinical examination. Local and systemic signs and symptoms of teething were obtained from mothers' reporting via anamnesis. Samples of buccal cells were retrieved for DNA genotyping using real-time PCR. The T-test, Chi-square test, logistic regression, and haplotype analyses were applied.Results:
Almost all mothers (95.5%) reported at least one local or systemic sign and symptom of teething. The most common was increased salivation (79.5%), diarrhea (72.3 %), and fever (70.5 %). The mean number of signs and symptoms per child was higher in boys than girls (mean = 5.1; SD= 1.5; p=0.008). Sleep disturbance (p=0.03) and loss of appetite (p=0.05) were more reported in boys. The rs689466 and rs5275 were not associated with signs and symptoms of teething (p>0.05).Conclusion:
The single nucleotide polymorphisms in the COX2 gene (rs689466 and rs5275) were not associated with local and systemic signs and symptoms of teething.Key words
النص الكامل:
1
الفهرس:
LILACS
الموضوع الرئيسي:
Sleep Wake Disorders
/
Tooth, Deciduous
/
Tooth Eruption
/
Polymorphism, Single Nucleotide
نوع الدراسة:
Diagnostic_studies
/
Risk_factors_studies
المحددات:
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
اللغة:
En
مجلة:
Pesqui. bras. odontopediatria clín. integr
موضوع المجلة:
ODONTOLOGIA
السنة:
2023
نوع:
Article