CARD8 and IL1B Polymorphisms Influence MRI Brain Patterns in Newborns with Hypoxic-Ischemic Encephalopathy Treated with Hypothermia.
Katarina EsihKatja GoričarZvonka Rener-PrimecVita DolžanAneta Soltirovska ŠalamonPublished in: Antioxidants (Basel, Switzerland) (2021)
Inflammation and oxidative stress are recognized as important contributors of brain injury in newborns due to a perinatal hypoxic-ischemic (HI) insult. Genetic variability in these pathways could influence the response to HI and the outcome of brain injury. The aim of our study was to evaluate the impact of common single-nucleotide polymorphisms in the genes involved in inflammation and response to oxidative stress on brain injury in newborns after perinatal HI insult based on the severity and pattern of magnetic resonance imaging (MRI) findings. The DNA of 44 subjects was isolated from buccal swabs. Genotyping was performed for NLRP3 rs35829419, CARD8 rs2043211, IL1B rs16944, IL1B rs1143623, IL1B rs1071676, TNF rs1800629, CAT rs1001179, SOD2 rs4880, and GPX1 rs1050450. Polymorphism in CARD8 was found to be protective against HI brain injury detected by MRI overall findings. Polymorphisms in IL1B were associated with posterior limb of internal capsule, basal ganglia, and white matter brain patterns determined by MRI. Our results suggest a possible association between genetic variability in inflammation- and antioxidant-related pathways and the severity of brain injury after HI insult in newborns.
Keyphrases
- brain injury
- oxidative stress
- subarachnoid hemorrhage
- magnetic resonance imaging
- cerebral ischemia
- pregnant women
- white matter
- contrast enhanced
- dna damage
- gestational age
- cord blood
- low birth weight
- diffusion weighted imaging
- genome wide
- single molecule
- diabetic rats
- multiple sclerosis
- high throughput
- gene expression
- dna methylation
- preterm infants
- signaling pathway
- endoplasmic reticulum stress
- newly diagnosed
- single cell
- anti inflammatory
- circulating tumor cells