Gene expression of iron transporters, markers of vascularization and structural integrity in placenta of mothers with and without anemia

Mol Biol Rep. 2024 May 11;51(1):652. doi: 10.1007/s11033-024-09609-z.

Abstract

Objective: To compare the mRNA expression of placental iron transporters (TfR-1 and FPN), markers of placental vascularization (VEGF and sFLT1) and marker of structural integrity (LMN-A) in term women with and without iron deficiency anemia.

Materials and methods: A total of 30 pregnant women were enrolled; 15 cases of iron deficiency anemia (Hb 7-10.9 gm/dL) and 15 gestational age matched healthy controls (Hb ≥ 11 gm/dL). Peripheral venous blood was collected for assessment of hemoglobin levels and serum iron profile. Placental tissue was used for assessing the mRNA expression of TfR-1, FPN, VEGF, sFLT-1 and LMN-A via real time PCR.

Results: Placental expression of TfR-1, VEGF and LMN-A was increased in pregnant women with anemia compared to healthy pregnant controls. Placental expression of sFLT-1 was decreased in pregnant women with anemia compared to healthy pregnant controls. There was no change in the placental expression of FPN.

Conclusion: The increased expression of TfR-1, VEGF and LMN-A in cases of iron deficiency anemia are most likely to be compensatory in nature to help maintain adequate fetal iron delivery.

What does this study adds to the clinical work: Compensatory changes in the placenta aimed at buffering transport of iron to the fetus are seen in pregnant women with anemia compared to healthy pregnant controls.

Keywords: Anemia in pregnancy; Angiogenesis-antiangiogenesis; Iron transport; LMN-A; Placental hemodynamics.

MeSH terms

  • Adult
  • Anemia, Iron-Deficiency* / genetics
  • Anemia, Iron-Deficiency* / metabolism
  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Biomarkers* / blood
  • Biomarkers* / metabolism
  • Case-Control Studies
  • Cation Transport Proteins* / genetics
  • Cation Transport Proteins* / metabolism
  • Female
  • Gene Expression / genetics
  • Humans
  • Iron* / metabolism
  • Placenta* / metabolism
  • Pregnancy
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Transferrin* / genetics
  • Receptors, Transferrin* / metabolism
  • Vascular Endothelial Growth Factor A* / genetics
  • Vascular Endothelial Growth Factor A* / metabolism
  • Vascular Endothelial Growth Factor Receptor-1 / genetics
  • Vascular Endothelial Growth Factor Receptor-1 / metabolism

Substances

  • Receptors, Transferrin
  • Vascular Endothelial Growth Factor A
  • Cation Transport Proteins
  • Iron
  • Biomarkers
  • Vascular Endothelial Growth Factor Receptor-1
  • CD71 antigen
  • FLT1 protein, human
  • VEGFA protein, human
  • Antigens, CD
  • RNA, Messenger
  • metal transporting protein 1