How the MTHFR Mutation Affects Pregnancy
Women with certain MTHFR genetic variants who are planning a pregnancy may have questions about miscarriage, preeclampsia, and birth defects. Some research has reported associations between common MTHFR mutations, folate status, homocysteine, and adverse pregnancy outcomes. It’s important to note that these findings are often linked to folate deficiency, which can be prevented.1
Folate (vitamin B9) is essential during early pregnancy because it is involved in DNA synthesis, cell division, and methylation reactions in rapidly dividing tissues. Adequate folate before conception and in early pregnancy lowers the risk of neural tube defects affecting the baby’s brain and spinal cord.2
The MTHFR gene encodes the methylenetetrahydrofolate reductase enzyme, which converts 5,10‑methylenetetrahydrofolate to 5‑methyltetrahydrofolate (5‑MTHF), the main circulating form of folate used in the body. Certain MTHFR mutations reduce enzyme activity, which can lower 5‑MTHF availability and lead to increased homocysteine.
In pregnancy, low folate levels and elevated homocysteine have been linked to a higher risk of neural tube defects and other complications.3