Published online before print April 8, 2004, doi: 10.1161/01.STR.0000126807.69758.0e
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2004;35:1415.)
© 2004 American Heart Association, Inc.
Original Contributions |
Hemorrhage Burden Predicts Recurrent Intracerebral Hemorrhage After Lobar Hemorrhage
From the Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, Mass.
Correspondence to Steven M. Greenberg, MD, PhD, Clinical Trials Unit, Wang Building ACC 836, Massachusetts General Hospital, Boston, MA 02114. E-mail greenberg{at}helix.mgh.harvard.edu
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsDiscussionReferences |
|---|
Background and Purpose— Small asymptomatic cerebral hemorrhages detectable by gradient-echo MRI are common in patients with intracerebral hemorrhage (ICH), particularly lobar ICH related to cerebral amyloid angiopathy (CAA). We sought to determine whether hemorrhages detected at the time of lobar ICH predict the major clinical complications of CAA: recurrent ICH or decline in cognition and function.
Methods— Ninety-four consecutive survivors of primary lobar ICH (age 
55) with gradient-echo MRI at presentation were followed in a prospective cohort study for 32.9±24.0 months. A subset of 34 subjects underwent a second MRI after a stroke-free interval of 15.8±6.5 months. Study endpoints were recurrent symptomatic ICH or clinical decline, defined as onset of cognitive impairment, loss of independent functioning, or death.
Results— The total number of hemorrhages at baseline predicted risk of future symptomatic ICH (3-year cumulative risks 14%, 17%, 38%, and 51% for subjects with 1, 2, 3 to 5, or 6 baseline hemorrhages, P=0.003). Higher numbers of hemorrhages at baseline also predicted increased risk for subsequent cognitive impairment, loss of independence, or death (P=0.002) among subjects not previously demented or dependent. For subjects followed after a second MRI, new microhemorrhages appeared in 17 of 34 and predicted increased risk of subsequent symptomatic ICH (3-year cumulative risks 19%, 42%, and 67% for subjects with 0, 1 to 3, or 4 new microhemorrhages, P=0.02), but not subsequent clinical decline.
Conclusions— Hemorrhages identified by MRI predict clinically important events in survivors of lobar ICH. Detection of microhemorrhages may be useful for assessing risk in ICH patients and as a surrogate marker for clinical studies.
Key Words: hemorrhage • amyloid • magnetic resonance imaging, gradient echo • dementia
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Growing evidence has implicated deposition of ß-amyloid in cerebral vessels, defined as cerebral amyloid angiopathy (CAA), as an important cause of both intracerebral hemorrhage (ICH)1 and cognitive impairment.2,3 ICH associated with CAA often recurs, with highest risk among individuals with the apolipoprotein E (APOE)
2 or 4 alleles.4 In the absence of noninvasive methods for detecting cerebrovascular amyloid, these multiple CAA-related hemorrhages in lobar brain regions serve as the primary means for diagnosing CAA during life.5 Cerebral hemorrhages associated with CAA can be relatively large and symptomatic or small and clinically silent. The small "microhemorrhages" consist pathologically of collections of hemosiderin-laden macrophages, often associated with diseased blood vessels.6 Microhemorrhages in CAA and other cerebrovascular disorders can be sensitively imaged by gradient-echo or T2*-weighted MRI.7 Using gradient-echo MRI, we have demonstrated that microhemorrhages are common in patients with CAA-related symptomatic ICH8 and that new microhemorrhages occur in approximately half of lobar ICH patients over a 17-month follow-up even in the absence of new clinical symptoms.9
The high frequency of microhemorrhages in CAA raises questions about the clinical importance of these lesions, either as direct contributors to CAA-related impairment or indirect markers of the disease’s course and prognosis. Therefore, we undertook a prospective cohort study of survivors of lobar ICH with gradient-echo MRI at presentation. We sought to address (1) whether microhemorrhages and larger symptomatic ICHs share a similar distribution in the brain or risk factors such as APOE genotype, and (2) whether the number of old hemorrhages or the incident appearance of new microhemorrhages predict future events such as recurrent symptomatic ICH, cognitive impairment, or functional decline.
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Patient Recruitment and Follow-Up
Subjects were prospectively enrolled in a longitudinal cohort study of survivors of primary lobar hemorrhage as described4 (Figure 1). Briefly, subjects were recruited from consecutive patients age
55 years admitted to Massachusetts General Hospital (MGH) for lobar ICH between July 1994 and March 2002. Subjects were excluded for hemorrhages in deep hemispheric regions such as basal ganglia, or thalamus, or definite secondary cause of ICH. Survivors of lobar ICH who underwent MRI with gradient-echo sequences within 90 days of their index ICH were considered eligible. Of 213 potentially eligible patients who survived at least 30 days after primary lobar ICH, 127 underwent gradient-echo MRI. Fourteen of these patients were excluded for MRI occurring more than 90 days after presentation; 5 because MRI images were not available or interpretable, and 11 because the patient or family could not be reached for clinical follow-up information. An additional 3 subjects with CAA-related perivascular inflammation were excluded because of the markedly different course associated with this syndrome, 10 leaving a final prospective cohort of 94 survivors of primary lobar ICH with available baseline gradient-echo MRI and follow-up clinical data. Of the 94 subjects, 90 were white and 4, African American.
|
Baseline clinical information was obtained as described4,11 without knowledge of radiographic or genetic results. Clinical data collected and recorded at the time of index presentation included demographic information, history of hypertension, diabetes mellitus, coronary artery disease or previous symptomatic ICH or ischemic stroke. Data on prior history of cognitive impairment or inability to live independently were determined by interviews with patients and caregivers (see below) as well as review of medical records. DNA was prepared from blood samples and APOE genotype determined by the polymerase chain reaction/restriction enzyme method.4 DNA samples were available from 81 of the 94 subjects in the cohort (including all 34 subjects who underwent a follow-up MRI scan as described under MRI Detection of Hemorrhages); subjects without DNA samples declined consent for genotyping or were not available for blood draw during their hospitalization.
Follow-up clinical data were obtained by systematic telephone interviews4 performed at 6-month intervals through June 2003 for a mean follow-up period from presentation to last interview or study endpoint of 32.9±24.0 months. During the interview, the patient, caregiver, or both were questioned regarding the appearance of symptoms suggestive of incident stroke, decline in memory, language or other cognitive functions, or loss of independent functional status over the previous 6-month interval. Questions on functional status followed the structured interview proposed for the modified Rankin Scale12 with a modified Rankin Scale score of 3 considered to represent functional dependence. Cognitive status was systematically assessed by asking informants to compare the subject’s ability to perform a list of daily cognitive tasks involving memory, praxis, calculation, or reasoning with his or her baseline 5 to 10 years prior to the index event. Cognitive impairment was defined as the presence of deficits in memory or other cognitive areas sufficient to interfere with tasks of daily living.
This study was performed with approval and in accord with guidelines of the institutional review boards of MGH and with informed consent of all participating subjects or family members.
MRI Detection of Hemorrhages
MRI with axial gradient-echo images (TR 750/TE 50/5 to 6-mm slice thickness/1 mm interslice gap) was performed as described8,9 using a 1.5-T superconductive magnet. Hemorrhages (defined as rounded foci hypointense on gradient-echo sequences and distinct from vascular flow voids, leptomeningeal hemosiderosis, or nonhemorrhagic subcortical mineralization) were recorded according to size (microhemorrhages defined as 
5 mm in diameter, macrohemorrhages >5 mm in diameter) and cortical lobe in which they were centered. We have previously demonstrated high interrater reliability (intraclass correlation coefficient 0.97) for counting hemorrhagic lesions.9 All MRI analyses were performed and recorded without knowledge of clinical or genetic information.
Participants were encouraged to return for additional research MRI scans 12 to 18 month following their baseline scans. Of 36 subjects who returned for follow-up MRI, 1 was excluded from analysis because of a symptomatic ICH prior to the second MRI and 1 because of absent clinical follow-up information, leaving 34 subjects to be analyzed for the effects of new microhemorrhages without clinical recurrent ICH. These 34 subjects were younger (71.0 versus 75.7 years, P<0.005) and had more hemorrhages at baseline (median 3 versus median 2, P=0.02) than the remainder of the cohort, but did not differ by sex, hypertension, APOE genotype, previous cognitive impairment, or the occurrence of preindex symptomatic ICH. The mean interval between the baseline and follow-up MRI in the 34 subjects was 15.8±6.5 months. New microhemorrhages were identified by comparison of initial and follow-up scans without knowledge of clinical or genetic information as described9 and their locations recorded.
Statistical Methods
The total number of hemorrhagic lesions (microhemorrhages plus macrohemorrhages) was displayed in categories defined by cut-points (1, 2, 3 to 5, and 6) chosen at the beginning of the statistical analysis to divide the 94 subjects approximately into quartiles. Significance testing for these lesions was performed with the nonparametric Wilcoxon rank sum test because of their skewed distributions. Similarly, categories for the number of new hemorrhagic lesions were initially defined with cut-points of 0, 1 to 3, and 4 new hemorrhages and the rank sum test used for statistical significance. The relationship between hemorrhages at baseline and appearance of new hemorrhages was examined with a nonparametric rank sum test for trend across categories of baseline hemorrhages.13 Age at index ICH was analyzed as both a continuous variable and a dichotomous variable categorized by the median age of the cohort (<75 versus 75). APOE genotype was analyzed as a categorical variable according to the presence or absence of the 2 or 4 alleles, the 3/3 genotype serving as reference. Multivariable analysis of the presence or absence of new hemorrhages was performed using multiple logistic regression to control for the time interval between the baseline and follow-up scans and the category of baseline hemorrhages.
We used the Kaplan-Meier method to estimate the cumulative proportion of patients with 2 prespecified outcomes during follow-up: (1) recurrent symptomatic ICH, and (2) clinical decline, defined as incident cognitive impairment, loss of functional independence, or death among subjects not cognitively impaired or dependent prior to or within 30 days after their index ICH. Survival time was calculated from date of initial MRI scan for analysis of baseline hemorrhages or from date of follow-up MRI for analysis of new hemorrhages. Survival was calculated until the date of recurrent hemorrhage or the last known date without recurrence for analysis of recurrent ICH, or till date of death, estimated date of incident cognitive impairment, or estimated loss of independent functioning for analysis of clinical decline. Significance testing was performed by the log-rank test for dichotomous variables. Significance testing for outcome as a function of baseline or new hemorrhages was performed by Cox proportional hazards regression model, with the categories of hemorrhage counts chosen as the independent variable in order to limit the effect of outlying values of hemorrhage counts on the analysis. Hazard ratios (HR) with 95% CI were calculated by Cox regression model; analyses of new hemorrhages also included a term for the length of interval between the baseline and follow-up MRIs.
All analyses were performed with Stata software (Stata Corporation). All significance tests were 2-tailed.
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Correlates of Baseline and New Hemorrhages
The total number of macrohemorrhagic and microhemorrhagic lesions identified by gradient-echo MRI in consecutive elderly survivors of lobar ICH ranged from 1 to 35. Even in this cohort selected for the presence of symptomatic ICH, microhemorrhages were nearly 2.5-fold more common than macrohemorrhages (Table 1). The distribution among the cortical lobes for the 2 classes of hemorrhages was similar (Table 1). Among potential predictors of total hemorrhages at baseline, there was no association with age, sex, APOE genotype, or the presence of vascular risk factors such as hypertension (Table 2), diabetes, coronary disease, or previous stroke (data not shown). Individuals with cognitive impairment prior to their index ICH showed a trend (P=0.066) toward more hemorrhages at baseline (median 3, interquartile range 2 to 7) than those without prior cognitive impairment (median 2, interquartile range 1 to 4).
|
|
Among 34 subjects who underwent a follow-up research MRI scan after an approximately 16 month stroke-free interval, 17 (50%) demonstrated between 1 and 16 new microhemorrhages (Table 3). Larger numbers of hemorrhages at baseline and the presence of the APOE 2 or 4 allele significantly predicted the appearance of new hemorrhages. New hemorrhages appeared in 13 of 19 (68%) carriers of APOE 2 or 4 compared with only 4 of 15 (26%) of those with the 3/ 3 genotype (odds ratio 6.6, 95% CI 1.2 to 38.3, controlling for baseline hemorrhages and duration between scans). Age, sex, and vascular risk factors, again, showed no association with appearance of new microhemorrhages.
|
Risk of Recurrent ICH or Clinical Decline
Recurrent lobar ICH occurred in 27 of 94 (28%) subjects in the cohort, a mean of 20.8±16.7 months following index presentation. The number of hemorrhages on the baseline scan was a significant predictor of time until recurrence (Figure 2A). The cumulative risk of recurrent ICH at 3 years of follow-up increased from 14% for subjects with only 1 hemorrhage at baseline to 17% for those with 2 hemorrhages, 37% for 3 to 5 hemorrhages, and 51% for 6 or more hemorrhages (HR 1.7, 95% CI 1.2 to 2.4 for each increase in category). This association remained independent in multivariable analysis controlling for previously defined risk factors for recurrent ICH: APOE genotype and history of previous ICH4 (HR 1.5, 95% CI 1.1 to 2.2, P=0.03). Among the 34 subjects with follow-up MRI scans following a stroke-free interval, recurrent ICH occurred in 11 (32%), a mean of 16.1±10.4 months after the second MRI. Subjects with new hemorrhages on the follow-up scan also demonstrated increased risk for early recurrence (Figure 2B). Cumulative risk of recurrent ICH 3 years after the follow-up scan was 19% for those with no new hemorrhages, 42% for 1 to 3 new hemorrhages, and 67% for 4 or more new hemorrhages (HR 3.0, 95% CI 1.2 to 7.3 for each increase in category controlling for the interval between MRI scans; HR 2.6, 95% CI 1.0 to 6.7 controlling in addition for APOE genotype and history of prior ICH).
|
We also examined the effect of baseline hemorrhages on the incidence of cognitive impairment, functional dependence or death among the 53 subjects in the cohort who survived their index ICH without the immediate occurrence of 1 of these events. During subsequent follow-up, 19 of the 53 (36%) developed cognitive impairment, loss of functional independence, or death at a mean 27.9±17.1 month. Greater numbers of hemorrhages at baseline predicted increased hazard for these clinical events as well (Figure 3A; HR 1.9, 95% CI 1.2 to 2.8 for each increase in category). Baseline hemorrhages were associated with clinical decline even among subjects without recurrent ICH (HR 2.3, 95% CI 1.3 to 4.2, P=0.005), indicating that this association was not primarily driven by risk of subsequent ICH. The number of new hemorrhages during follow-up was not predictive of clinical decline in the subset of 24 subjects with serial MRI scans not rendered cognitively impaired or dependent by their index events (Figure 3B).
|
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
A major finding from this analysis is that hemorrhages detected by MRI predict risk of future symptomatic ICH in survivors of an initial lobar hemorrhage. Early recurrence was associated with both the number of hemorrhages at baseline and the rate of new hemorrhage appearance over a follow-up interval. The most plausible interpretation of these data are that MRI-detectable hemorrhages are a marker of the severity and aggressiveness of the underlying vascular disease and, thereby, predict risk of recurrent ICH.
The number of total hemorrhages was also marginally associated with previous cognitive impairment and a significant predictor of subsequent clinical decline in subjects not disabled or cognitively impaired by their index ICH. It is unclear whether these findings reflect a direct effect of hemorrhage burden on neurologic function, or if microhemorrhages are instead a marker of other pathologies associated with CAA such as neuritic plaques, 14 white matter damage, 15,16 or ischemic infarction17,18 that themselves impair cognition. Several large studies have indicated that cerebrovascular lesions in general19,20 and CAA in particular2,3 are risk factors for cognitive impairment, especially in the setting of concomitant Alzheimer disease (AD) pathology. Our study raises the possibility that microhemorrhages may be one of the manifestations of advanced CAA that contribute to clinical impairment. The rate of new microhemorrhage emergence did not predict decline, suggesting a role for total lesion burden, rather than rate of appearance as the determinant of their effects on cognitive and behavioral function.
We found that new microhemorrhages, like recurrent symptomatic lobar ICH,4 occur with increased frequency in carriers of the APOE 2 or 4 alleles. Previous studies of APOE and CAA have identified an association between APOE 4 and extent of vascular amyloid,21–23 and between APOE 2 and CAA-related vessel breakdown.24,25 It is therefore plausible that these alleles mark lobar ICH patients with more severe CAA pathology and, therefore, increased risk for new vessel rupture.
A potential weakness in this study is the uncertainty of the diagnosis of cognitive impairment. The proportion of patients diagnosed with dementia varies sharply according to how it is defined;26 studies also indicate that cognitive impairment presents with different clinical characteristics in vascular disease compared with AD.27 Because of the further limitations of a telephone-based rather than in-person follow-up scheme, we chose to prespecify a broad clinical endpoint that included loss of functional independence and death in addition to cognitive impairment. We note that any errors in classification according to these endpoints should bias toward a null result rather than a spurious association. The mechanism for the association between multiple hemorrhages and clinical decline remains to be determined, but does not appear to require recurrent symptomatic ICH, as the association remained present among subjects without clinical recurrence.
Our results have potential implications for the treatment of patients with lobar ICH. The decision to prescribe antiplatelet or anticoagulant treatment for prevention of thromboembolism, for example, depends substantially on the patient’s risk for ICH.28 It is therefore plausible that information from gradient-echo MRI might affect the risk-benefit calculation for anticoagulation or antiplatelet treatment in specific clinical situations.
These findings also offer support for use of hemorrhages detected by MRI as a surrogate outcome marker in studies of CAA. All available evidence suggests that microhemorrhages occur by the same mechanisms as larger symptomatic hemorrhages: the 2 types of hemorrhages demonstrate similar vascular pathologies6 and, in this study of lobar ICH, show similar distributions (Table 1) and dependence on APOE genotype (Table 3). Further, we find that the cumulative number or incident appearance of hemorrhages predicts the likelihood of symptomatic ICH (Figure 2), suggesting that microhemorrhages reflect essentially the same underlying pathological process as symptomatic ICH. These findings raise the possibility that interventions found to reduce the rate of MRI-detectable hemorrhage would also be effective in preventing symptomatic ICH, and that gradient-echo MRI might, thus, emerge as a useful technique for evaluating potential treatments for CAA.
|
Acknowledgments |
|---|
We are grateful to Dr Rebecca Betensky for assistance with and critical review of the biostatistical analysis. This work was supported by the National Institutes of Health grant NS041409 and the Harvard Center for Neurodegeneration and Repair.
Received January 20, 2004; accepted February 10, 2004.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
1. Greenberg SM. Cerebral amyloid angiopathy. Prospects for clinical diagnosis and treatment. Neurology. 1998; 51: 690–694.
2. Neuropathology Group of the Medical Research Council Cognitive Function and Ageing Study. Pathological correlates of late-onset dementia in a multicentre, community-based population in England and Wales. Neuropathology group of the medical research council cognitive function and ageing study (MRC CFAS). Lancet. 2001; 357: 169–175.[CrossRef][Medline] [Order article via Infotrieve]
3. Pfeifer LA, White LR, Ross GW, Petrovitch H, Launer LJ. Cerebral amyloid angiopathy and cognitive function: the HAAS autopsy study. Neurology. 2002; 58: 1629–1634.
4. O’Donnell HC, Rosand J, Knudsen KA, Furie KL, Segal AZ, Chiu RI, Ikeda D, Greenberg SM. Apolipoprotein E genotype and the risk of recurrent lobar intracerebral hemorrhage. N Engl J Med. 2000; 342: 240–245.
5. Knudsen KA, Rosand J, Karluk D, Greenberg SM. Clinical diagnosis of cerebral amyloid angiopathy: validation of the Boston criteria. Neurology. 2001; 56: 537–539.
6. Fazekas F, Kleinert R, Roob G, Kleinert G, Kapeller P, Schmidt R, Hartung HP. Histopathologic analysis of foci of signal loss on gradient-echo T2*-weighted MR images in patients with spontaneous intracerebral hemorrhage: evidence of microangiopathy-related microbleeds. AJNR Am J Neuroradiol. 1999; 20: 637–642.
7. Atlas SW, Mark AS, Grossman RI, Gomori JM. Intracranial hemorrhage: gradient-echo MR imaging at 1.5 t. Comparison with spin-echo imaging and clinical applications. Radiology. 1988; 168: 803–807.
8. Greenberg SM, Finklestein SP, Schaefer PW. Petechial hemorrhages accompanying lobar hemorrhage: detection by gradient-echo MRI. Neurology. 1996; 46: 1751–1754.
9. Greenberg SM, O’Donnell HC, Schaefer PW, Kraft E. MRI detection of new hemorrhages: potential marker of progression in cerebral amyloid angiopathy. Neurology. 1999; 53: 1135–1138.
10. Eng JA, Frosch MP, Choi K, Rebeck GW, Greenberg SM. Clinical manifestations of cerebral amyloid angiopathy-related inflammation. Ann Neurol. 2004; 55: 246–252.
11. Rosand J, Eckman MH, Knudsen KA, Singer DE, Greenberg SM. Outcome of warfarin-related intracerebral hemorrhage. Arch Intern Med. In press.
12. Wilson JT, Hareendran A, Grant M, Baird T, Schulz UG, Muir KW, Bone I. Improving the assessment of outcomes in stroke: use of a structured interview to assign grades on the modified Rankin scale. Stroke. 2002; 33: 2243–2246.
13. Cuzick J. A Wilcoxon-type test for trend. Statistics in Medicine. 1985; 4: 87–90.[Medline] [Order article via Infotrieve]
14. Gilbert JJ, Vinters HV. Cerebral amyloid angiopathy: incidence and complications in the aging brain. I. Cerebral hemorrhage. Stroke. 1983; 14: 915–923.
15. Haglund M, Englund E. Cerebral amyloid angiopathy, white matter lesions and Alzheimer encephalopathy—a histopathological assessment. Dement Geriatr Cogn Disord. 2002; 14: 161–166.[Medline] [Order article via Infotrieve]
16. Smith EE, Eng JA, Rosand J, Greenberg SM. Presence of leukoaraiosis predicts recurrent lobar hemorrhage. Stroke. 2003; 34: 242. Abstract.
17. Olichney JM, Hansen LA, Hofstetter CR, Grundman M, Katzman R, Thal LJ. Cerebral infarction in Alzheimer’s disease is associated with severe amyloid angiopathy and hypertension. Arch Neurol. 1995; 52: 702–708.
18. Cadavid D, Mena H, Koeller K, Frommelt RA. Cerebral beta amyloid angiopathy is a risk factor for cerebral ischemic infarction. A case control study in human brain biopsies. J Neuropathol Exp Neurol. 2000; 59: 768–773.[Medline] [Order article via Infotrieve]
19. Snowdon DA, Greiner LH, Mortimer JA, Riley KP, Greiner PA, Markesbery WR. Brain infarction and the clinical expression of Alzheimer disease. The nun study. JAMA. 1997; 277: 813–817.
20. Vermeer SE, Prins ND, den Heijer T, Hofman A, Koudstaal PJ, Breteler MM. Silent brain infarcts and the risk of dementia and cognitive decline. N Engl J Med. 2003; 348: 1215–1222.
21. Schmechel DE, Saunders AM, Strittmatter WJ, Crain BJ, Hulette CM, Joo SH, Pericak-Vance MA, Goldgaber D, Roses AD. Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease. Proc Natl Acad Sci U S A. 1993; 90: 9649–9653.
22. Greenberg SM, Rebeck GW, Vonsattel JPV, Gomez-Isla T, Hyman BT. Apolipoprotein E epsilon 4 and cerebral hemorrhage associated with amyloid angiopathy. Ann Neurol. 1995; 38: 254–259.[CrossRef][Medline] [Order article via Infotrieve]
23. Premkumar DR, Cohen DL, Hedera P, Friedland RP, Kalaria RN. Apolipoprotein E-epsilon4 alleles in cerebral amyloid angiopathy and cerebrovascular pathology associated with Alzheimer’s disease. Am J Pathol. 1996; 148: 2083–2095.[Abstract]
24. Greenberg SM, Vonsattel JP, Segal AZ, Chiu RI, Clatworthy AE, Liao A, Hyman BT, Rebeck GW. Association of apolipoprotein E epsilon2 and vasculopathy in cerebral amyloid angiopathy. Neurology. 1998; 50: 961–965.
25. McCarron MO, Nicoll JA, Stewart J, Ironside JW, Mann DM, Love S, Graham DI, Dewar D. The apolipoprotein E epsilon2 allele and the pathological features in cerebral amyloid angiopathy-related hemorrhage. J Neuropathol Exp Neurol. 1999; 58: 711–718.[Medline] [Order article via Infotrieve]
26. Erkinjuntti T, Ostbye T, Steenhuis R, Hachinski V. The effect of different diagnostic criteria on the prevalence of dementia. N Engl J Med. 1997; 337: 1667–1674.
27. O’Brien JT, Erkinjuntti T, Reisberg B, Roman G, Sawada T, Pantoni L, Bowler JV, Ballard C, DeCarli C, Gorelick PB, Rockwood K, Burns A, Gauthier S, DeKosky ST. Vascular cognitive impairment. Lancet Neurol. 2003; 2: 89–98.[CrossRef][Medline] [Order article via Infotrieve]
28. Eckman MH, Rosand J, Knudsen KA, Singer DE, Greenberg SM. Can patients be anticoagulated after intracerebral hemorrhage? A decision analysis. Stroke. 2003; 34: 1710–1716.
This article has been cited by other articles:
 |
|
 |
|
  S. -B. Jeon, S. U. Kwon, A. -H. Cho, S. -C. Yun, J. S. Kim, and D. -W. Kang Rapid appearance of new cerebral microbleeds after acute ischemic stroke Neurology, November 17, 2009; 73(20): 1638 - 1644. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. D.C. Goos, M.I. Kester, F. Barkhof, M. Klein, M. A. Blankenstein, P. Scheltens, and W. M. van der Flier Patients With Alzheimer Disease With Multiple Microbleeds: Relation With Cerebrospinal Fluid Biomarkers and Cognition Stroke, November 1, 2009; 40(11): 3455 - 3460. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. N. Orken, G. Kenangil, E. Uysal, and H. Forta Cerebral Microbleeds in Ischemic Stroke Patients on Warfarin Treatment Stroke, November 1, 2009; 40(11): 3638 - 3640. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. M. Greenberg, R. N. K. Nandigam, P. Delgado, R. A. Betensky, J. Rosand, A. Viswanathan, M. P. Frosch, and E. E. Smith Microbleeds Versus Macrobleeds: Evidence for Distinct Entities * Supplemental Materials and Methods Stroke, July 1, 2009; 40(7): 2382 - 2386. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
W. T. Kimberly, A. Gilson, N. S. Rost, J. Rosand, A. Viswanathan, E. E. Smith, and S. M. Greenberg Silent ischemic infarcts are associated with hemorrhage burden in cerebral amyloid angiopathy Neurology, April 7, 2009; 72(14): 1230 - 1235. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 R.N.K. Nandigam, A. Viswanathan, P. Delgado, M.E. Skehan, E.E. Smith, J. Rosand, S.M. Greenberg, and B.C. Dickerson MR Imaging Detection of Cerebral Microbleeds: Effect of Susceptibility-Weighted Imaging, Section Thickness, and Field Strength AJNR Am. J. Neuroradiol., February 1, 2009; 30(2): 338 - 343. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. Mittal, Z. Wu, J. Neelavalli, and E.M. Haacke Susceptibility-Weighted Imaging: Technical Aspects and Clinical Applications, Part 2 AJNR Am. J. Neuroradiol., February 1, 2009; 30(2): 232 - 252. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
W. J.P. Henneman, J. D. Sluimer, C. Cordonnier, M. M.E. Baak, P. Scheltens, F. Barkhof, and W. M. van der Flier MRI Biomarkers of Vascular Damage and Atrophy Predicting Mortality in a Memory Clinic Population Stroke, February 1, 2009; 40(2): 492 - 498. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S.-H. Lee, W.-S. Ryu, and J.-K. Roh Cerebral microbleeds are a risk factor for warfarin-related intracerebral hemorrhage Neurology, January 13, 2009; 72(2): 171 - 176. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P. V. Patel, E. FitzMaurice, R. N. K. Nandigam, P. Auluck, A. Viswanathan, J. N. Goldstein, J. Rosand, S. M. Greenberg, and E. E. Smith Association of Subdural Hematoma With Increased Mortality in Lobar Intracerebral Hemorrhage Arch Neurol, January 1, 2009; 66(1): 79 - 84. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Yakushiji, M. Nishiyama, S. Yakushiji, T. Hirotsu, A. Uchino, J. Nakajima, M. Eriguchi, Y. Nanri, M. Hara, E. Horikawa, et al. Brain Microbleeds and Global Cognitive Function in Adults Without Neurological Disorder Stroke, December 1, 2008; 39(12): 3323 - 3328. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. H. Eckman, L. K.S. Wong, Y. O.Y. Soo, W. Lam, S. R. Yang, S. M. Greenberg, and J. Rosand Patient-Specific Decision-Making for Warfarin Therapy in Nonvalvular Atrial Fibrillation: How Will Screening With Genetics and Imaging Help? * Supplemental Appendix Stroke, December 1, 2008; 39(12): 3308 - 3315. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
B. R. Copenhaver, A. W. Hsia, J. G. Merino, R. E. Burgess, J. T. Fifi, L. Davis, S. Warach, and C. S. Kidwell Racial differences in microbleed prevalence in primary intracerebral hemorrhage Neurology, October 7, 2008; 71(15): 1176 - 1182. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S-H Lee, B-S Kang, N Kim, and J-K Roh Does microbleed predict haemorrhagic transformation after acute atherothrombotic or cardioembolic stroke? J. Neurol. Neurosurg. Psychiatry, August 1, 2008; 79(8): 913 - 916. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Viswanathan, P. Patel, R. Rahman, R. N. K. Nandigam, C. Kinnecom, L. Bracoud, J. Rosand, H. Chabriat, S. M. Greenberg, and E. E. Smith Tissue Microstructural Changes Are Independently Associated With Cognitive Impairment in Cerebral Amyloid Angiopathy Stroke, July 1, 2008; 39(7): 1988 - 1992. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
B. S. Jacobs and S. M. Greenberg Statins, low cholesterol, and hemorrhagic stroke: An uncertain triangle Neurology, June 10, 2008; 70(24_Part_2): 2355 - 2356. [Full Text] [PDF]
|
|
|
|
|
|
J. A. Pettersen, G. Sathiyamoorthy, F.-Q. Gao, G. Szilagyi, N. K. Nadkarni, P. St George-Hyslop, E. Rogaeva, and S. E. Black Microbleed Topography, Leukoaraiosis, and Cognition in Probable Alzheimer Disease From the Sunnybrook Dementia Study Arch Neurol, June 1, 2008; 65(6): 790 - 795. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. Tatsumi, T. Ayaki, M. Shinohara, and T. Yamamoto Type of Gradient Recalled-Echo Sequence Results in Size and Number Change of Cerebral Microbleeds AJNR Am. J. Neuroradiol., April 1, 2008; 29(4): e13 - e13. [Full Text] [PDF]
|
|
|
|
|
|
K. Vahedi, M. Boukobza, P. Massin, D. B. Gould, E. Tournier-Lasserve, and M. -G. Bousser Clinical and brain MRI follow-up study of a family with COL4A1 mutation Neurology, October 16, 2007; 69(16): 1564 - 1568. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. Broderick, S. Connolly, E. Feldmann, D. Hanley, C. Kase, D. Krieger, M. Mayberg, L. Morgenstern, C. S. Ogilvy, P. Vespa, et al. REPRINT: Guidelines for the Management of Spontaneous Intracerebral Hemorrhage in Adults: 2007 Update: A Guideline From the American Heart Association/American Stroke Association Stroke Council, High Blood Pressure Research Council, and the Quality of Care and Outcomes in Research Interdisciplinary Working Group: The American Academy of Neurology affirms the value of this guideline as an educational tool for neurologists. Circulation, October 16, 2007; 116(16): e391 - e413. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
H C Hanger, T J Wilkinson, N Fayez-Iskander, and R Sainsbury The risk of recurrent stroke after intracerebral haemorrhage J. Neurol. Neurosurg. Psychiatry, August 1, 2007; 78(8): 836 - 840. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. Cordonnier, R. Al-Shahi Salman, and J. Wardlaw Spontaneous brain microbleeds: systematic review, subgroup analyses and standards for study design and reporting Brain, August 1, 2007; 130(8): 1988 - 2003. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Viswanathan, A. Gschwendtner, J. -P. Guichard, F. Buffon, R. Cumurciuc, M. O'Sullivan, M. Holtmannspotter, C. Pachai, M. -G. Bousser, M. Dichgans, et al. Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL Neurology, July 10, 2007; 69(2): 172 - 179. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. Broderick, S. Connolly, E. Feldmann, D. Hanley, C. Kase, D. Krieger, M. Mayberg, L. Morgenstern, C. S. Ogilvy, P. Vespa, et al. Guidelines for the Management of Spontaneous Intracerebral Hemorrhage in Adults: 2007 Update: A Guideline From the American Heart Association/American Stroke Association Stroke Council, High Blood Pressure Research Council, and the Quality of Care and Outcomes in Research Interdisciplinary Working Group: The American Academy of Neurology affirms the value of this guideline as an educational tool for neurologists. Stroke, June 1, 2007; 38(6): 2001 - 2023. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
E.M. Haacke, Z.S. DelProposto, S. Chaturvedi, V. Sehgal, M. Tenzer, J. Neelavalli, and D. Kido Imaging Cerebral Amyloid Angiopathy with Susceptibility-Weighted Imaging AJNR Am. J. Neuroradiol., February 1, 2007; 28(2): 316 - 317. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. S. Jeret, C . Cordonnier, W .M. van der Flier, J .D. Sluimer, F . Barkhof, and P . Scheltens Prevalence and severity of microbleeds in a memory clinic setting Neurology, January 30, 2007; 68(5): 391 - 391. [Full Text] [PDF]
|
|
|
|
 |
|
 B. Thanvi and T. Robinson Sporadic cerebral amyloid angiopathy--an important cause of cerebral haemorrhage in older people Age Ageing, November 1, 2006; 35(6): 565 - 571. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Viswanathan, J.-P. Guichard, A. Gschwendtner, F. Buffon, R. Cumurcuic, C. Boutron, E. Vicaut, M. Holtmannspotter, C. Pachai, M.-G. Bousser, et al. Blood pressure and haemoglobin A1c are associated with microhaemorrhage in CADASIL: a two-centre cohort study Brain, September 1, 2006; 129(9): 2375 - 2383. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. P. Chao, A. L. Kotsenas, and D. F. Broderick Cerebral Amyloid Angiopathy: CT and MR Imaging Findings RadioGraphics, September 1, 2006; 26(5): 1517 - 1531. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. W. Chen, M. E. Gurol, J. Rosand, A. Viswanathan, S. M. Rakich, T. R. Groover, S. M. Greenberg, and E. E. Smith Progression of white matter lesions and hemorrhages in cerebral amyloid angiopathy. Neurology, July 11, 2006; 67(1): 83 - 87. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. H. Salat, E. E. Smith, D. S. Tuch, T. Benner, V. Pappu, K. M. Schwab, M. E. Gurol, H. D. Rosas, J. Rosand, and S. M. Greenberg White Matter Alterations in Cerebral Amyloid Angiopathy Measured by Diffusion Tensor Imaging Stroke, July 1, 2006; 37(7): 1759 - 1764. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Viswanathan and H. Chabriat Cerebral Microhemorrhage Stroke, February 1, 2006; 37(2): 550 - 555. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
H.-C. Koennecke Cerebral microbleeds on MRI: Prevalence, associations, and potential clinical implications Neurology, January 24, 2006; 66(2): 165 - 171. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Viswanathan, S. M. Rakich, C. Engel, R. Snider, J. Rosand, S. M. Greenberg, and E. E. Smith Antiplatelet use after intracerebral hemorrhage Neurology, January 24, 2006; 66(2): 206 - 209. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. J. Werring, L. J. Coward, N. A. Losseff, H. R. Jager, and M. M. Brown Cerebral microbleeds are common in ischemic stroke but rare in TIA Neurology, December 27, 2005; 65(12): 1914 - 1918. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. Hanley and W. Hacke Critical Care and Emergency Medicine Neurology in Stroke Stroke, February 1, 2005; 36(2): 205 - 207. [Full Text] [PDF]
|
|
|
|
|
|
E. E. Smith, M. E. Gurol, J. A. Eng, C. R. Engel, T. N. Nguyen, J. Rosand, and S. M. Greenberg White matter lesions, cognition, and recurrent hemorrhage in lobar intracerebral hemorrhage Neurology, November 9, 2004; 63(9): 1606 - 1612. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. M. Greenberg, M. E. Gurol, J. Rosand, and E. E. Smith Amyloid Angiopathy-Related Vascular Cognitive Impairment Stroke, November 1, 2004; 35(11_suppl_1): 2616 - 2619. [Abstract] [Full Text] [PDF]
|
|
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||