Journals / Anatolian Current Medical Journal / 2026 / Volume: 8 Issue: 4

Maternal iron deficiency anemia is associated with reduced fetal thymic size in the early second trimester

Deniz Taşdemir(Department of Perinatology, Şanlıurfa Training and Research Hospital)0000-0002-0755-5338
Mehmet Akif İzgi(Department of Internal Medicine, Mehmet Akif Inan Training and Research Hospital)0009-0000-4200-4120
Bekir Kahveci(Department of Obstetrics and Gynecology, Sanliurfa Training and Research Hospital)0000-0002-8729-1669
Pages
—
Publication Date
2026-07-16
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Longitudinal studies incorporating postnatal immune outcomes are needed to determine the clinical significance of these findings.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Aims: To evaluate the association between maternal iron-deficiency anemia (IDA) and fetal thymic size in the early second trimester using standardized ultrasonographic measurements.
📊
Key Findings & Data:Methods: This prospective observational study included 78 pregnant women with IDA and 78 healthy controls with singleton pregnancies between 20+0 and 24+6 weeks of gestation.
💡
Conclusion & Impact:Longitudinal studies incorporating postnatal immune outcomes are needed to determine the clinical significance of these findings.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Iron deficiency anemia · fetal thymus · thymic-thoracic ratio

Abstract

Aims: To evaluate the association between maternal iron-deficiency anemia (IDA) and fetal thymic size in the early second trimester using standardized ultrasonographic measurements. Methods: This prospective observational study included 78 pregnant women with IDA and 78 healthy controls with singleton pregnancies between 20+0 and 24+6 weeks of gestation. A priori power analysis indicated that at least 126 participants (63 per group) were required to provide 80% power. Standardized fetal thoracic and thymic ultrasonography was performed in all participants. Thoracic and thymus anteroposterior (AP) diameters were measured, and the thymic-thoracic ratio (TTR) was calculated. Thymus volume, surface area, and gestational age-adjusted Z-scores were obtained from orthogonal measurements and reference charts. Intraobserver reliability was assessed using the intraclass correlation coefficient (ICC). Because the main ultrasound variables were not normally distributed, group comparisons were performed using the Mann-Whitney U test, and effect sizes were expressed as r. Adjusted linear regression analyses evaluated maternal IDA as the exposure and fetal thymic measurements as outcomes. Results: A total of 189 women were screened, 33 were excluded, and 156 were included in the final analysis. Intraobserver reliability was excellent (ICC=0.91). Maternal age, gestational age at examination, gravidity, and parity were similar between groups, whereas body-mass index was lower in the IDA group (p=0.006, r=0.219). Thoracic AP diameter did not differ significantly between groups (p=0.241). In contrast, fetuses of mothers with IDA had smaller thymus AP diameter (8.0 vs. 8.7 mm, p<0.001), lower TTR (0.38 vs. 0.40, p=0.001), lower thymus volume (6.8 vs. 7.5 cm³, p<0.001), smaller thymus surface area (148 vs. 161 mm², p=0.001), and lower gestational age-adjusted thymus Z-scores (-0.43 vs. -0.05, p<0.001). A graded reduction in fetal thymic measurements was observed from controls to mild and moderate IDA. In adjusted linear regression analyses, maternal IDA remained independently associated with lower fetal thymic measurements, whereas thoracic AP diameter was not significantly associated with IDA. Conclusion: Maternal IDA was associated with smaller fetal thymic measurements during the early second trimester despite preserved thoracic size. These findings support an association between maternal iron status and fetal thymic morphometry. Longitudinal studies incorporating postnatal immune outcomes are needed to determine the clinical significance of these findings.

🔖

Cite This Article

Taşdemir, D., İzgi, M. A., Kahveci, B. (2026). Maternal iron deficiency anemia is associated with reduced fetal thymic size in the early second trimester. Anatolian Current Medical Journal, Volume: 8 Issue: 4. https://doi.org/10.38053/acmj.1958101

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (18)

  1. World Health Organization. The global prevalence of anaemia in 2011. World Health Organization; 2015.
  2. Stevens GA, Finucane MM, De-Regil LM, et al. Global, regional, and national trends in haemoglobin concentration and prevalence of total and severe anaemia in children and pregnant and non-pregnant women for 1995-2011: a systematic analysis of population-representative data. Lancet Glob Health. 2013;1(1):e16-e25. doi:10.1016/S2214-109X(13)70001-9
  3. Rasmussen K. Is there a causal relationship between iron deficiency or iron-deficiency anemia and weight at birth, length of gestation and perinatal mortality? J Nutr. 2001;131(2S-2):590S-603S. doi:10.1093/jn/131.2.590S
  4. Scholl TO. Iron status during pregnancy: setting the stage for mother and infant. Am J Clin Nutr. 2005;81(5):1218S-1222S. doi:10.1093/ajcn/81.5.1218
  5. Georgieff MK. Iron deficiency in pregnancy. Am J Obstet Gynecol. 2020; 223(4):516-524. doi:10.1016/j.ajog.2020.03.006
  6. Oppenheimer SJ. Iron and its relation to immunity and infectious disease. J Nutr. 2001;131(2S-2):616S-633S. doi:10.1093/jn/131.2.616S
  7. Beard JL. Iron biology in immune function, muscle metabolism and neuronal functioning. J Nutr. 2001;131(2S-2):568S-580S. doi:10.1093/jn/131.2.568S
  8. Haynes BF, Heinly CS. Early human T cell development: analysis of the human thymus at the time of initial entry of hematopoietic stem cells into the fetal thymic microenvironment. J Exp Med. 1995;181(4):1445-1458. doi:10.1084/jem.181.4.1445
  9. Savino W. The thymus is a common target organ in infectious diseases. PLoS Pathog. 2006;2(6):e62. doi:10.1371/journal.ppat.0020062
  10. Cromi A, Ghezzi F, Raffaelli R, Bergamini V, Siesto G, Bolis P. Ultrasonographic measurement of thymus size in IUGR fetuses: a marker of the fetal immunoendocrine response to malnutrition. Ultrasound Obstet Gynecol. 2009;33(4):421-426. doi:10.1002/uog.6320
  11. El-Haieg DO, Zidan AA, El-Nemr MM. The relationship between sonographic fetal thymus size and the components of the systemic fetal inflammatory response syndrome in women with preterm prelabour rupture of membranes. BJOG. 2008;115(7):836-841. doi:10.1111/j.1471-0528.2008.01715.x
  12. de Felice C, Toti P, Musarò M, et al. Early activation of the hypothalamic-pituitary-adrenal-axis in very-low-birth-weight infants with small thymus at birth. J Matern Fetal Neonatal Med. 2008;21(4):251-254. doi:10.1080/14767050801927871
  13. Yinon Y, Zalel Y, Weisz B, et al. Fetal thymus size as a predictor of chorioamnionitis in women with preterm premature rupture of membranes. Ultrasound Obstet Gynecol. 2007;29(6):639-643. doi:10.1002/uog.4022
  14. Chaoui R, Heling KS, Lopez AS, Thiel G, Karl K. The thymic-thoracic ratio in fetal heart defects: a simple way to identify fetuses at high risk for microdeletion 22q11. Ultrasound Obstet Gynecol. 2011;37(4):397-403. doi:10.1002/uog.8952
  15. Gamez F, De Leon-Luis J, Pintado P, et al. Fetal thymus size in uncomplicated twin and singleton pregnancies. Ultrasound Obstet Gynecol. 2010;36(3):302-307. doi:10.1002/uog.7578
  16. Beard J. Iron deficiency alters brain development and functioning. J Nutr. 2003;133(5 Suppl 1):1468S-1472S. doi:10.1093/jn/133.5.1468S
  17. Hassan TH, Badr MA, Karam NA, et al. Impact of iron deficiency anemia on the function of the immune system in children. Medicine (Baltimore). 2016;95(47):e5395. doi:10.1097/MD.0000000000005395
  18. Tangshewinsirikul C, Panburana P. Sonographic measurement of fetal thymus size in uncomplicated singleton pregnancies. J Clin Ultrasound. 2017;45(3):150-159. doi:10.1002/jcu.22419