Quantitative and longitudinal assessment of human placental inflammation using diffusion basis spectrum imaging
2025

Assessing Placental Inflammation with MRI

Sample size: 82 publication Evidence: high

Author Information

Author(s): Sun Zhexian, Wu Wenjie, Xiang Zezhen, Gao Hansong, Ju Weina, Uhm Cherilyn, Hagemann Ian S., Woodard Pamela K., Zhong Nanbert, Cahill Alison G., Wang Qing, Wang Yong

Primary Institution: Washington University in St Louis

Hypothesis

Can diffusion basis spectrum imaging (DBSI) effectively measure immune cell infiltration in the placenta during pregnancy?

Conclusion

DBSI can detect elevated immune cell infiltration associated with placental inflammation, enabling early detection and monitoring throughout pregnancy.

Supporting Evidence

  • DBSI revealed significantly greater immune cell infiltration in inflammation placentas compared to non-inflammation placentas.
  • Immune cellularity increased from early to late pregnancy in both groups.
  • DBSI can detect differences in immune cell density as early as 11–13 weeks' gestation.
  • Linear regression showed significant correlations between DBSI and immunohistochemistry-derived immune cell densities.

Takeaway

Researchers used a special MRI technique to see how many immune cells are in the placenta, which helps doctors check for problems during pregnancy.

Methodology

The study used diffusion basis spectrum imaging (DBSI) to analyze 202 MRI scans from 82 patients, comparing placentas with and without inflammation.

Potential Biases

Potential bias due to reliance on CD4+ cells for validation and exclusion of other immune cell types.

Limitations

The study did not account for potential confounders such as comorbidities and medication use, and the method may overlook other immune cell types.

Participant Demographics

Participants included 91 patients with singleton pregnancies, aged approximately 29 years.

Statistical Information

P-Value

p<0.01

Statistical Significance

p<0.01

Digital Object Identifier (DOI)

10.1038/s44294-024-00049-5

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