Association between the MTHFR (rs1801133) gene variation and serum trace elements levels (Copper and Zinc) in individuals diagnosed with neural tube defects

Clin Chim Acta. 2024 Aug 15:562:119856. doi: 10.1016/j.cca.2024.119856. Epub 2024 Jul 6.

Abstract

Background and aims: Neural tube defects (NTDs) occur when the neural tube fails to close within 28 days of human embryonic development. This results in central nervous system disorders like anencephaly, spina bifida, and encephalocele. Early diagnosis and treatment are crucial to minimize their impact on an individual's health and well-being. The present study aims to define the association between prenatal exposure to trace elements (Cu and Zn) and the single nucleotide polymorphism (SNP) of the MTHFR gene involved in folate metabolism pathways in neural tube defects in children and their mothers.

Material and methods: A cross-sectional study involving 331 participants (90 NTD cases, 88 healthy mothers, 85 NTD children, and 68 healthy children) from antenatal check-ups in Obstetrics and Gynaecology and Pediatric Surgery for Neural Tube Defects in the Outpatient Department (OPD) and Inpatient Department (IPD). Assessed Cu and Zn concentrations and their associations. Genomic DNA was extracted, and real-time PCR was used to determine genotypes. Atomic absorption spectrophotometry measured trace elements. Statistical analyses included Chi-Square tests, odds ratios, and Mann-Whitney U tests.

Results: Significant associations were found between MTHFR C677T genotypes and NTD risk in mothers (p = 0.0491) and children (p = 0.0297). Allelic frequency analysis indicated a T allele association with NTD risk in children (p = 0.0107). Recessive models showed significant associations in mothers (p = 0.0169) and children (p = 0.1678). Cu levels differed significantly between NTD cases and controls (p < 0.0001), with MTHFR genotypes influencing Cu levels. Zinc levels also varied significantly (p < 0.0001).

Conclusion: This study reveals complex associations between MTHFR C677T genotypes, trace element concentrations, and NTD risk in mothers and children. This targeted approach allows healthcare providers to identify at-risk pregnancies early, enabling personalised interventions like folic acid supplementation and counselling to moderate neural tube defect (NTD) risk in a future pregnancy.

MeSH terms

  • Adult
  • Child
  • Copper* / blood
  • Cross-Sectional Studies
  • Female
  • Humans
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2)* / genetics
  • Neural Tube Defects* / blood
  • Neural Tube Defects* / diagnosis
  • Neural Tube Defects* / genetics
  • Polymorphism, Single Nucleotide
  • Pregnancy
  • Trace Elements / blood
  • Zinc* / blood

Substances

  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Copper
  • MTHFR protein, human
  • Zinc
  • Trace Elements