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Meta-Analysis
. 2025 Jan;67(1):109-124.
doi: 10.1007/s00234-024-03457-1. Epub 2024 Sep 4.

Perfusion-weighted MRI patterns in neuropsychiatric systemic lupus erythematosus: a systematic review and meta-analysis

Affiliations
Meta-Analysis

Perfusion-weighted MRI patterns in neuropsychiatric systemic lupus erythematosus: a systematic review and meta-analysis

Narges Azizi et al. Neuroradiology. 2025 Jan.

Abstract

Background: Neuropsychiatric Systemic Lupus Erythematosus (NPSLE) is a complex manifestation of Systemic Lupus Erythematosus (SLE) characterized by a wide range of neurological and psychiatric symptoms. This study aims to elucidate the patterns of Perfusion-Weighted MRI (PWI) in NPSLE patients compared to SLE patients without neuropsychiatric manifestations (non-NPSLE) and healthy controls (HCs).

Material and methods: A systematic search was conducted in PubMed/Medline, Embase, Web of Science, and Scopus for studies utilizing PWI in NPSLE patients published through April 14, 2024. Cerebral blood flow (CBF) data from NPSLE, non-NPSLE patients, and HCs were extracted for meta-analysis, using standardized mean difference (SMD) as an estimate measure. For studies lacking sufficient data for inclusion, CBF, cerebral blood volume (CBV), and mean transit time (MTT) were reviewed qualitatively.

Results: Our review included eight observational studies employing PWI techniques, including dynamic susceptibility contrast (DSC) and arterial spin labeling (ASL). The meta-analysis of NPSLE compared to non-NPSLE incorporated four studies, encompassing 104 NPSLE patients and 90 non-NPSLE patients. The results revealed an SMD of -1.42 (95% CI: -2.85-0.00, I2: 94%) for CBF in NPSLE compared to non-NPSLE.

Conclusion: PWI reveals informative patterns of cerebral perfusion, showing a significant reduction in mean CBF in NPSLE patients compared to non-NPSLE patients. Our qualitative synthesis highlights these changes, particularly in the frontal and temporal lobes. However, the existing data exhibits considerable heterogeneity and limitations.

Keywords: Arterial spin labeling; Cerebral blood flow; Dynamic susceptibility contrast; Neuropsychiatric systemic lupus erythematosus; Perfusion-weighted MRI; Systemic lupus erythematosus.

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Conflict of interest statement

Declarations. Ethics approval: This manuscript does not involve clinical studies or contain any patient data. Informed consent: As this study is a systematic review and meta-analysis, it does not require informed consent. Competing Interests: The authors have no competing interests to declare that are relevant to the content of this article.

References

    1. Sarwar S et al (2021) Neuropsychiatric systemic lupus erythematosus: a 2021 update on diagnosis, management, and current challenges. Cureus 13(9):e17969 - PubMed - PMC
    1. Nikolopoulos D, Fanouriakis A, Bertsias G (2021) Treatment of neuropsychiatric systemic lupus erythematosus: clinical challenges and future perspectives. Expert Rev Clin Immunol 17(4):317–330 - PubMed - DOI
    1. Bărbulescu AL et al (2019) Neuroinflammation in systemic lupus erythematosus - a review. Rom J Morphol Embryol 60(3):781–786 - PubMed
    1. Duarte-Delgado NP, Vásquez G, Ortiz-Reyes BL (2019) Blood-brain barrier disruption and neuroinflammation as pathophysiological mechanisms of the diffuse manifestations of neuropsychiatric systemic lupus erythematosus. Autoimmun Rev 18(4):426–432 - PubMed - DOI
    1. Liu Y et al (2022) Pathogenesis and treatment of neuropsychiatric systemic lupus erythematosus: a review. Front Cell Dev Biol 10:998328 - PubMed - PMC - DOI

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