4.7 Article

Physiological instability is linked to mortality in primary central nervous system lymphoma: A case-control fMRI study

期刊

HUMAN BRAIN MAPPING
卷 43, 期 13, 页码 4030-4044

出版社

WILEY
DOI: 10.1002/hbm.25901

关键词

brain pulsation; functional imaging; lymphoma; malignancy; mortality

资金

  1. Academy of Finland [338599, TERVA 314497, TERVA 335720]
  2. Instrumentarium Science Foundation
  3. Jane ja Aatos Erkko Foundation
  4. Maire Taponen Foundation
  5. Medical Research Center Oulu
  6. Orion Research Foundation
  7. Finnish Brain Foundation
  8. Finnish Medical Foundation

向作者/读者索取更多资源

This study used physiological magnetic resonance encephalography to quantify the impact of (peri)vascular primary central nervous system lymphoma (PCNSL) involvement on the stability of physiological brain pulsations. The study found that the levels of CV were associated with short-term mortality risk, and abnormal clusters extended spatially beyond routine neuroimaging findings.
Primary central nervous system lymphoma (PCNSL) is an aggressive brain disease where lymphocytes invade along perivascular spaces of arteries and veins. The invasion markedly changes (peri)vascular structures but its effect on physiological brain pulsations has not been previously studied. Using physiological magnetic resonance encephalography (MREG(BOLD)) scanning, this study aims to quantify the extent to which (peri)vascular PCNSL involvement alters the stability of physiological brain pulsations mediated by cerebral vasculature. Clinical implications and relevance were explored. In this study, 21 PCNSL patients (median 67y; 38% females) and 30 healthy age-matched controls (median 63y; 73% females) were scanned for MREG(BOLD) signal during 2018-2021. Motion effects were removed. Voxel-by-voxel Coefficient of Variation (CV) maps of MREG(BOLD) signal was calculated to examine the stability of physiological brain pulsations. Group-level differences in CV were examined using nonparametric covariate-adjusted tests. Subject-level CV alterations were examined against control population Z-score maps wherein clusters of increased CV values were detected. Spatial distributions of clusters and findings from routine clinical neuroimaging were compared [contrast-enhanced, diffusion-weighted, fluid-attenuated inversion recovery (FLAIR) data]. Whole-brain mean CV was linked to short-term mortality with 100% sensitivity and 100% specificity, as all deceased patients revealed higher values (n = 5, median 0.055) than surviving patients (n = 16, median 0.028) (p < .0001). After adjusting for medication, head motion, and age, patients revealed higher CV values (group median 0.035) than healthy controls (group median 0.024) around arterial territories (p <= .001). Abnormal clusters (median 1.10 x 10(5)mm(3)) extended spatially beyond FLAIR lesions (median 0.62 x 10(5)mm(3)) with differences in volumes (p = .0055).

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