Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2007 Oct;28(9):1645-9.
doi: 10.3174/ajnr.A0645. Epub 2007 Sep 20.

Improved identification of intracortical lesions in multiple sclerosis with phase-sensitive inversion recovery in combination with fast double inversion recovery MR imaging

Affiliations

Improved identification of intracortical lesions in multiple sclerosis with phase-sensitive inversion recovery in combination with fast double inversion recovery MR imaging

F Nelson et al. AJNR Am J Neuroradiol. 2007 Oct.

Abstract

Background and purpose: Accurate detection and classification of purely intracortical lesions in multiple sclerosis (MS) are important in understanding their role in disease progression and impact on the clinical manifestations of the disease. However, detection of these lesions with conventional MR imaging remains a challenge. Although double inversion recovery (DIR) has been shown to improve the sensitivity of the detection of cortical lesions, this sequence has low signal-to-noise ratio (SNR), poor delineation of lesion borders, and is prone to image artifacts. We demonstrate that intracortical lesions can be identified and classified with greater confidence by the combination of DIR with phase-sensitive inversion recovery (PSIR) images.

Materials and methods: A total of 16 subjects with MS were included in this study. DIR, PSIR, and fluid-attenuated inversion recovery (FLAIR) images were acquired and inspected by 3 experts, with identification of lesions by consensus. PSIR and DIR images were jointly used to classify lesions as purely intracortical, mixed gray-white matter, and juxtacortical. The difference in the number of lesions detected in each category was compared between combined PSIR and DIR and conventional FLAIR.

Results: PSIR consistently allowed a clearer classification and delineation of lesions. Combined PSIR and DIR images showed a 337% improvement in the total number of lesions detected compared with FLAIR alone. Detection of intracortical lesions was improved by 417% compared with FLAIR. Detection of mixed gray-white matter and juxtacortical lesions was improved by 396% and 130%, respectively, compared with FLAIR.

Conclusion: Reliable detection and classification of intracortical lesions in MS are greatly improved by combined use of PSIR and DIR.

PubMed Disclaimer

Figures

Fig 1.
Fig 1.
DIR (A), PSIR (B), and FLAIR (C) images from a single patient with MS at the same section location. An intracortical lesion is evident in the left parietal area. Also note the excellent overall delineation of the gray-white matter border on PSIR.
Fig 2.
Fig 2.
Examples of cortical lesions on PSIR (left), DIR (center), and FLAIR (right). Lesions shown are (A) purely intracortical, (B) mixed, and (C) juxtacortical.
Fig 3.
Fig 3.
Example of flow artifact. On the DIR image (A), apparent cortical lesions (arrows) are visible. However, on the PSIR image (B), there are no corresponding hypointense signals. On PSIR, a flow artifact is seen more clearly (arrows), which is the likely source of the false-positive.
Fig 4.
Fig 4.
Example of RF inhomogeneity artifact. On the DIR image (A), an apparent cortical lesion is visible (white arrow). On the PSIR image (B), there is again no corresponding hypointensity. On DIR, the signal intensity is 38% higher for the apparent lesion than the contralateral area, compared with 14% for PSIR. The relative insensitivity of PSIR to the RF artifact allows rejection of the lesion on DIR as a false-positive.

Similar articles

Cited by

References

    1. Dawson JW. The histology of disseminated sclerosis. Trans Roy Soc Edinb 1916;50:517–740
    1. Brownell B, Hughes JT. The distribution of plaques in the cerebrum in multiple sclerosis. J Neurol Neurosurg Psychiatry 1962;25:315–20 - PMC - PubMed
    1. Lumsden CE. The neuropathology of multiple sclerosis. In: Vinken PJ, Bruyn GW, eds. Handbook of Clinical Neurology. Vol. 9. Amsterdam: Elsevier Science Publishers;1970. :217–309
    1. Bo L, Vedeler CA, Nyland HI, et al. Subpial demyelination in the cerebral cortex of multiple sclerosis patients. J Neuropathol Exp Neurol 2003;62:723–32 - PubMed
    1. Brink BP, Veerhuis R, Breij EC, et al. The pathology of multiple sclerosis is location-dependent: no significant complement activation is detected in purely cortical lesions. J Neuropathol Exp Neurol 2005;64:147–55 - PubMed

Publication types