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Brain Iron in Nucleus Accumbens and Cognitive Function in Preeclampsia.

Created on 02 Jul 2026

Authors

Boyao Chen, Meng Li, Tao Chen, Qihao Zhang, Zhenyu Cheng, Xinxin Huo, Fushuai Zhang, Yiwen Chen, Pengcheng Liang, Yanli Li, Linfeng Yang, Lingfei Guo

Published in

Hypertension (Dallas, Tex. : 1979). Jul 02, 2026. Epub Jul 02, 2026.

Abstract

Preeclampsia is associated with long-term cognitive dysfunction, potentially linked to cerebral iron deposition. This study investigated striatal iron alterations using quantitative susceptibility mapping and their relationship with cognitive function in patients with preeclampsia.
This cross-sectional study enrolled 321 participants, including nonpregnant and pregnant healthy controls, and patients with preeclampsia. Participants underwent the Montreal Cognitive Assessment, Trail Making Test, and 1.5 T brain magnetic resonance imaging. Striatal iron content was quantified using quantitative susceptibility mapping reconstructed with a morphology-enabled dipole inversion algorithm.
Preeclampsia patients showed poorer executive function (Trail Making Test part [A+B]: partial η2=0.170; part B: partial η2=0.100) and elevated nucleus accumbens magnetic susceptibility (all P<0.001). Age (β=0.744, P<0.001) and hematocrit (β=0.846, P=0.011) were independently associated with iron levels. In addition, significant interactions between nucleus accumbens susceptibility values and preeclampsia status were observed for log-transformed Trail Making Test completion times (part [A+B]: interaction β=0.388, P=0.006; part B: interaction β=0.424, P=0.003), indicating that elevated iron specifically exacerbates executive vulnerability in preeclampsia.
Nucleus accumbens iron level is elevated in preeclampsia and correlates with executive performance. Although the cross-sectional design limits causal conclusions, these findings highlight nucleus accumbens iron deposition as a key pathological feature underlying preeclampsia-related cerebral involvement.

PMID:
42389781
Bibliographic data and abstract were imported from PubMed on 02 Jul 2026.

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