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Possibilities of T2*-Relaxometry and Diffusion-Weighted MRI for Fetal Brain and Placental Assessment

https://doi.org/10.52560/2713-0118-2026-1-107-120

Abstract

Hypoxia is one of the leading causes of impaired intrauterine development and adverse perinatal outcomes. The T2*-relaxometry method, based on the BOLD effect, enables noninvasive quantitative assessment of tissue oxygenation. Apparent diffusion coefficient (ADC) mapping is employed in the diagnosis of cerebral ischemia and serves as a quantitative biomarker of prenatal brain maturation.

Objective. To compare the utility of T2*-relaxometry and ADC mapping in assessing gestational characteristics, as well as hypoxic conditions of the fetal brain and placenta.

Materials and Methods. A retrospective cross-sectional analysis was conducted on 200 prenatal MRI examinations performed between 18 and 38 weeks of gestation (WG) from 2024 to 2025, using 1.5 T and 3 T Philips scanners at the MTC SB RAS (Novosibirsk, Russia). T2*- relaxometry was performed using a multi-echo single-shot echo-planar imaging (SS-EPI) sequence with TE ranging from 25 to 225 ms. ADC mapping was conducted using single-shot diffusion-weighted imaging (SSh DWI) with b-values of 0 and 700 s/mm². T2*-relaxation times (RT) and ADC values were obtained through ROI analysis of manually segmented regions of the brain and placenta. Statistical analysis included the Shapiro — Wilk test, Pearson and Spearman correlations, paired t-test, ANOVA, and Kruskal — Wallis test, with significance set at p < 0.05.

Results. T2*-mapping of the brain in 110 fetuses (66 scanned at 1.5 T; 44 at 3 T) and of the placenta in 50 cases (30 at 1.5 T; 20 at 3 T) demonstrated a decrease in T2*-RT with advancing gestational age (p = 0.0018 for the brain, p = 0.05 for the placenta). ADC values of the fetal brain (n = 126) were also inversely correlated with gestational age (p = 0.0135), whereas no significant gestational dependence was found for placental T2*-RT or ADC values (p > 0.209). Group analysis revealed a significant reduction in fetal brain T2*-RT after 29 WG compared to fetuses before 29 WG (p = 0.001).

Conclusions. Both T2*-RT and ADC values of the fetal brain are significantly influenced by gestational age, with more pronounced changes observed in the third trimester. T2*-relaxometry and ADC mapping are applicable for quantitative evaluation of fetal brain and placental deve- lopment and hold potential for early, noninvasive detection of hypoxic conditions.

About the Authors

A. M. Gornostaeva
International Tomography Center, SB RAS
Russian Federation

Alyona M. Gornostaeva - Junior Researcher, International Tomography Center, Siberian Branch, Russian Academy of Sciences; Radiologist at the Avicenna Medical Center of the Mother and Child Group of Companies.

Novosibirsk



V. D. Abramova
International Tomography Center, SB RAS; Novosibirsk State University
Russian Federation

Victoria D. Abramova - Junior Researcher, International Tomography Center, Siberian Branch, Russian Academy of Sciences; Postgraduate Student, Novosibirsk State University.

Novosibirsk



A. A. Savelov
International Tomography Center, SB RAS
Russian Federation

Andrey A. Savelov - Candidate of Physical and Mathematical Sciences, Senior Researcher, International Tomography Center, Siberian Branch, Russian Academy of Sciences.

Novosibirsk



K. A. Paraskun
International Tomography Center, SB RAS; Novosibirsk State University
Russian Federation

Kseniia A. Paraskun - Junior Researcher, International Tomography Center, Siberian Branch, Russian Academy of Sciences; Postgraduate Student, Novosibirsk State University.

Novosibirsk



A. M. Korostyshevskaya
International Tomography Center, SB RAS
Russian Federation

Aleksandra M. Korostyshevskaya - Doctor of Medical Sciences, Leading Researcher, International Tomography Center, Siberian Branch, Russian Academy of Sciences.

Novosibirsk



References

1. Makogon A. V., Andryushina I. V. Haemolytic disease of the fetus: monitoring, treatment of the fetus and delivery. Vopr. ginekol. akus. perinatol. (Gynecology, Ob­ stetrics and Perinatology). 2018;17(3):45-52. (In Russ). DOI

2. Arthurs O. J., Rega A., Guimiot F., Belarbi N., Rosenblatt J., Biran V., Elmaleh M., Sebag G., Alison M. Diffusion-weighted magnetic resonance imaging of the fetal brain in intrauterine growth restriction. Ultrasound Obstet Gynecol. 2017; 50(1):79-87. DOI

3. Capuani S., Guerreri M., Antonelli A., Bernardo S., Porpora M. G., Giancotti A., Catalano C., Manganaro L. Diffusion and perfusion quantified by Magnetic Resonance Imaging are markers of human placenta development in normal pregnancy. Placenta. 2017;58:33-39. DOI

4. Cromb D., Steinweg J., Aviles Verdera J., van Poppel M. P. M., Bonthrone A. F., Lloyd D. F. A., Pushparajah K., Simpson J., Razavi R., Rutherford M., Counsell S. J., Hutter J. T2*-Relaxometry MRI to Assess Third Trimester Placental and Fetal Brain Oxygenation and Placental Characteristics in Healthy Fetuses and Fetuses With Congenital Heart Disease. J. Magn. Reson. Imaging. 2025;61(3):1246-1255. DOI

5. Han R., Huang L., Sun Z., Zhang D., Chen X., Yang X., Cao Z. Assessment of apparent diffusion coefficient of normal fetal brain development from gestational age week 24 up to term age: a preliminary study. Fetal. Diagn. Ther. 2015;37(2):102-7. DOI

6. Hansen D. N., Sinding M., Petersen A., Christiansen O. B., Uldbjerg N., Peters D. A., Frøkjær J. B., Sørensen A. T2*-weighted placental magnetic resonance imaging: a biomarker of placental dysfunction in small-for-gestational-age pregnancies. Am. J. Obstet. Gynecol. MFM. 2022;4(3):100578. DOI

7. Ho A. E. P., Hutter J., Jackson L. H., Seed P. T., Mccabe L., Al-Adnani M., Marnerides A., George S., Story L., Hajnal J. V., Rutherford M. A., Chappell L. C. T2* Placental Magnetic Resonance Imaging in Preterm Preeclampsia: An Observational Cohort Study. Hyperten­ sion. 2020;75(6):1523-1531. DOI

8. Korostyshevskaya А. М., Prihod'ko I. Yu., Savelov А. А., Yarnykh V. L. Direct comparison between apparent diffusion coefficient and macromolecular proton fraction as quantitative biomarkers of the human fetal brain maturation. J. Magn. Reson. Imaging. 2019;50(1):52-61. DOI

9. Kotovich D., Guedalia J. S. B., Hoffmann C., Sze G., Eisenkraft A., Yaniv G. Apparent Diffusion Coefficient Value Changes and Clinical Correlation in 90 Cases of Cytomegalovirus-Infected Fetuses with Unremarkable Fetal MRI Results. AJNR Am. J. Neuroradiol. 2017;38(7):1443-1448. DOI

10. Kutuk M. S., Sahin M., Gorkem S. B., Doganay S., Ozturk A. Relationship between Doppler findings and fetal brain apparent diffusion coefficient in early-onset intra-uterine growth restriction. J. Matern. Fetal. Neonatal. Med. 2018; 31(23):3201-3208. DOI

11. Lauridsen M. H., Uldbjerg N., Henriksen T. B., Petersen O. B., Stausbøl-Grøn B., Matthiesen N. B., Peters D. A., Ringgaard S., Hjortdal V. E. Cerebral Oxygenation Measurements by Magnetic Resonance Imaging in Fetuses With and Without Heart Defects. Circ. Cardiovasc. Imaging. 2017;10(11):e006459. DOI

12. O’Connor J. P. B., Robinson S. P., Waterton J. C. Imaging tumour hypoxia with oxygen-enhanced MRI and BOLD MRI. Br. J. Radiol. 2019;92(1096):20180642. DOI

13. Schneider J. F., Confort-Gouny S., Le Fur Y., Viout P., Bennathan M., Chapon F., Fogliarini C., Cozzone P., Girard N. Diffusion-weighted imaging in normal fetal brain maturation. Eur. Radiol. 2007; 17(9):2422-9. DOI

14. Schönberg N., Weisstanner C., Wiest R., Bonél H. M., Piechowiak E. I., Cullmann J. L., Raio L., Pastore-Wapp M., Slavova N. The influence of various cerebral and extracerebral pathologies on apparent diffusion coefficient values in the fetal brain. J. Neuroimaging. 2020;30(4):477-485. DOI

15. Steinweg J. K., Hui G. T. Y., Pietsch M., Ho A., van Poppel M. P., Lloyd D., Colford K., Simpson J. M., Razavi R., Pushparajah K., Rutherford M., Hutter J. T2* placental MRI in pregnancies complicated with fetal congenital heart disease. Placenta. 2021;108:23-31. DOI

16. Vasylechko S., Malamateniou C., Nunes R. G., Fox M., Allsop J., Rutherford M., Rueckert D., Hajnal J. V. T2* relaxometry of fetal brain at 1.5 Tesla using a motion tolerant method. Magn. Reson. Med. 2015;73(5):1795-802. DOI

17. Vu C., Chai Y., Coloigner J., Nederveen A. J., Borzage M., Bush A., Wood J. C. Quantitative perfusion mapping with induced transient hypoxia using BOLD MRI. Magn. Reson. Med. 2021;85(1):168-181. DOI

18. Yaniv G., Hoffmann C., Weisz B., Lipitz S., Katorza E., Kidron D., Bergman D., Biegon A. Region-specific reductions in brain apparent diffusion coefficient in cytomegalovirus-infected fetuses. Ul­ trasound Obstet. Gynecol. 2016;47(5): 600-7. DOI

19. Yaniv G., Katorza E., Bercovitz R., Bergman D., Greenberg G., Biegon A., Hoffmann C. Region-specific changes in brain diffusivity in fetal isolated mild ventriculomegaly. Eur. Radiol. 2016;26 (3):840-8. DOI

20. Zheng W., Yan G., Jiang Y., Bao Z., Li K., Deng M., Li B., Zou Y. Diffusion-Weighted MRI of the Fetal Brain in Fetal Growth Restriction With Maternal Preeclampsia or Gestational Hypertension. J. Magn. Re­ son. Imaging. 2024;59(4):1384-1393. DOI


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For citations:


Gornostaeva A.M., Abramova V.D., Savelov A.A., Paraskun K.A., Korostyshevskaya A.M. Possibilities of T2*-Relaxometry and Diffusion-Weighted MRI for Fetal Brain and Placental Assessment. Radiology - Practice. 2026;(1):107-120. (In Russ.) https://doi.org/10.52560/2713-0118-2026-1-107-120

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ISSN 2713-0118 (Online)