Ring and nodular multiple sclerosis lesions: A retrospective natural history study

M. Davis, S. Auh, M. Riva, N. D. Richert, J. A. Frank, H. F. McFarland, F. Bagnato

Research output: Contribution to journalArticlepeer-review


Background: In patients with multiple sclerosis (MS), contrast-enhancing lesions (CELs) on postcontrast MRI are considered markers of the inflammatory responses associated with blood-brain barrier breakdown. Based upon shape, CELs may be defined as nodular (nCEL) or ring (rCEL) lesions. Several short-term studies pointed towards the assumption that rCELs represent areas of a more aggressive inflammatory process. Methods: In the present long-term (i.e., 2 years) retrospective natural history study, we used monthly imaging to follow rCEL and nCELs evolution in 16 patients with MS during the natural history. New CELs were identified monthly on month 4-9 MRIs, using month 1-3 MRIs to ensure that all CELs were not previously enhancing. Chronic black holes (cBHs) were counted monthly upon CEL disappearance up to the 24th MRI. Generalized estimating equation methods investigated within-patient differences between rCELs and nCELs in volume and likelihood to convert into cBHs. Kaplan-Meier survival curves estimated differences in the length of persistence between cBHs originating from nCELs and cBHs deriving from rCELs. Results: Fifty-two new rCELs and 281 nCELs were identified. rCELs had larger mean (z = 5.06, p ≤ 0.0001) volumes than nCELs. The proportion of cBHs from rCELs was similar (z = 1.81, p = 0.0710) to the proportion of cBHs from nCELs. Likewise, the length of persistence of cBHs deriving from rCELs was similar (χ1 = 2.339, p = 0.1262) to the duration of cBHs from nCELs. Conclusions: Our data suggest that worse radiologic characteristics associated with the acute phase of ring contrast-enhancing lesions and nodular contrast-enhancing lesions do not necessarily reflect a poorer lesion outcome over time.

Original languageEnglish (US)
Pages (from-to)851-856
Number of pages6
Issue number10
StatePublished - Mar 2010
Externally publishedYes

ASJC Scopus subject areas

  • Clinical Neurology

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