4.6 Article

Cortical superficial siderosis in the general population: The Framingham Heart and Rotterdam studies

Journal

INTERNATIONAL JOURNAL OF STROKE
Volume 16, Issue 7, Pages 798-808

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1747493020984559

Keywords

Brain microbleeds; cerebral amyloid angiopathy; cerebral hemorrhage; community; cortical superficial siderosis; stroke facilities

Funding

  1. Framingham Heart Study's National Heart, Lung, and Blood Institute contract [N01-HC-25195, HHSN268201500001I]
  2. National Institute of Neurological Disorders and Stroke [R01 NS17950]
  3. National Institute on Aging [R01 AG008122, R01 AG16495, K23AG038444, R03 AG04818001A1, AG033193]
  4. NIH [1RO1 HL64753, R01 HL076784, 1 R01 AG028321, P30 AG010129, NS017950]
  5. NHLBI [HL67288, 2K24HL04334]
  6. Erasmus Medical Center Rotterdam
  7. Netherlands Organisation for Scientific Research (NWO)
  8. Netherlands Organisation for Health Research and Development (ZonMW)
  9. Research Institute for Diseases in the Elderly (RIDE)
  10. Netherlands Genomics Initiative (NGI)
  11. Ministry of Education, Culture and Science
  12. Ministry of Health, Welfare and Sports
  13. European Commission (DG XII)
  14. Municipality of Rotterdam
  15. Erasmus University Rotterdam

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In community-dwelling older adults, cortical superficial siderosis is associated with cerebral amyloid angiopathy, indicating that individuals with this condition may be at a higher risk for intracerebral hemorrhage and future neurological events.
Objective We aimed to characterize cortical superficial siderosis, its determinants and sequel, in community-dwelling older adults. Methods The sample consisted of Framingham (n = 1724; 2000-2009) and Rotterdam (n = 4325; 2005-2013) study participants who underwent brain MRI. In pooled individual-level analysis, we compared baseline characteristics in patients with cortical superficial siderosis to two reference groups: (i) persons without hemorrhagic MRI markers of cerebral amyloid angiopathy (no cortical superficial siderosis and no microbleeds) and (ii) those with presumed cerebral amyloid angiopathy based on the presence of strictly lobar microbleeds but without cortical superficial siderosis. Results Among a total of 6049 participants, 4846 did not have any microbleeds or cortical superficial siderosis (80%), 401 had deep/mixed microbleeds (6.6%), 776 had strictly lobar microbleeds without cortical superficial siderosis (12.8%) and 26 had cortical superficial siderosis with/without microbleeds (0.43%). In comparison to participants without microbleeds or cortical superficial siderosis and to those with strictly lobar microbleeds but without cortical superficial siderosis, participants with cortical superficial siderosis were older (OR 1.09 per year, 95% CI 1.05, 1.14; p < 0.001 and 1.04, 95% CI 1.00, 1.09; p = 0.058, respectively), had overrepresentation of the APOE e4 allele (5.19, 2.04, 13.25; p = 0.001 and 3.47, 1.35, 8.92; p = 0.01), and greater prevalence of intracerebral hemorrhage (72.57, 9.12, 577.49; p < 0.001 and 81.49, 3.40, >999.99; p = 0.006). During a mean follow-up of 5.6 years, 42.4% participants with cortical superficial siderosis had a stroke (five intracerebral hemorrhage, two ischemic strokes and four undetermined strokes), 19.2% had transient neurological deficits and 3.8% developed incident dementia. Conclusion Our study adds supporting evidence to the association between cortical superficial siderosis and cerebral amyloid angiopathy within the general population. Community-dwelling persons with cortical superficial siderosis may be at high risk for intracerebral hemorrhage and future neurological events.

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