Prevalence of asymptomatic vasogenic edema in pretreatment Alzheimer's disease study cohorts from phase 3 trials of semagacestat and solanezumab

被引:63
作者
Carlson, Christopher [1 ]
Estergard, Wahiba [1 ]
Oh, Joonmi [2 ]
Suhy, Joyce [2 ]
Jack, Clifford R., Jr. [3 ]
Siemers, Eric [1 ]
Barakos, Jerome [2 ,4 ]
机构
[1] Eli Lilly & Co, Indianapolis, IN 46285 USA
[2] Synarc, San Francisco, CA USA
[3] Mayo Clin, Dept Radiol, Rochester, MN USA
[4] Calif Pacific Med Ctr, Dept Radiol, San Francisco, CA USA
关键词
Alzheimer's disease; Clinical trials; Magnetic resonance imaging; Vasogenic edema; Cerebral microhemorrhage; CEREBRAL AMYLOID ANGIOPATHY; REVERSIBLE ENCEPHALOPATHY SYNDROME; BETA-RELATED ANGIITIS; INFLAMMATION; MICROBLEEDS;
D O I
10.1016/j.jalz.2011.05.2353
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Cerebral vasogenic edema (VE) has been reported to occur during antiamyloid immunotherapy. VE may be associated with central nervous system pathology with blood brain barrier disruptions; however, less is known about the prevalence of naturally occurring VE in patients with Alzheimer's disease (AD). Methods: Fluid-attenuated inversion recovery imaging sequences were obtained from four ongoing multicenter, randomized, double-blind, placebo-controlled, phase 3 trials in patients with mild-to-moderate AD. The first set of baseline scans was from patients in volumetric magnetic resonance imaging addenda in the Interrupting Alzheimer's Dementia by EvaluatiNg Treatment of Amyloid PaThologY (IDENTITY) studies examining semagacestat, a gamma-secretase inhibitor (cohort 1, n = 621). The second set of baseline scans was from the EXPanding alzhEimer's Disease InvestigaTIONs (EXPEDITION) studies examining solanezumab, an anti-A beta monoclonal antibody (cohort 2, n = 2141). Readers were blinded to patient-identifying information and future treatment. A third set of baseline scans was from the first 700 patients who underwent protocol-specified magnetic resonance imaging before randomization in the EXPEDITION studies (cohort 3). The analysis used three neuroradiologists: two performed independent primary interpretations and the third was the adjudicator. Readers were blinded to patient information, treatment, protocol, and time point. Results: Four cases of asymptomatic VE were detected at baseline/screening. Two VE cases were due to underlying extra-axial mass lesions. The third VE case was associated with numerous microhemorrhages in keeping with cerebral amyloid angiopathy-related inflammation or A beta-related angiitis. The final VE case demonstrated localized sulcal fluid-attenuated inversion recovery imaging hyperintensity. No VE was detected in cohort 3 by readers blinded to patient baseline status. Conclusions: VE seems to be rare at baseline in patients with AD in clinical trials, 2 of 2762 associated with AD. Additional cohorts should be evaluated to support these findings. (C) 2011 The Alzheimer's Association. All rights reserved.
引用
收藏
页码:396 / 401
页数:6
相关论文
共 12 条
  • [1] Amyloid-β-related angiitis:: a rare cause of recurrent transient neurological symptoms
    Amick, Amy
    Joseph, Jeff
    Silvestri, Nicholas
    Selim, Magdy
    [J]. NATURE CLINICAL PRACTICE NEUROLOGY, 2008, 4 (05): : 279 - 283
  • [2] Posterior reversible encephalopathy syndrome, part 1: Fundamental imaging and clinical features
    Bartynski, W. S.
    [J]. AMERICAN JOURNAL OF NEURORADIOLOGY, 2008, 29 (06) : 1036 - 1042
  • [3] Posterior reversible encephalopathy syndrome, part 2: Controversies surrounding pathophysiology of vasogenic edema
    Bartynski, W. S.
    [J]. AMERICAN JOURNAL OF NEURORADIOLOGY, 2008, 29 (06) : 1043 - 1049
  • [4] Clinical manifestations of cerebral amyloid angiopathy-related inflammation
    Eng, JA
    Frosch, MP
    Choi, KC
    Rebeck, GW
    Greenberg, SM
    [J]. ANNALS OF NEUROLOGY, 2004, 55 (02) : 250 - 256
  • [5] Incidence of cerebral microbleeds A longitudinal study in a memory clinic population
    Goos, J. D. C.
    Henneman, W. J. P.
    Sluimer, J. D.
    Vrenken, H.
    Sluimer, I. C.
    Barkhof, F.
    Blankenstein, M. A.
    Scheltens, P. H.
    van der Flier, W. M.
    [J]. NEUROLOGY, 2010, 74 (24) : 1954 - 1960
  • [6] Cerebral microbleeds: a guide to detection and interpretation
    Greenberg, Steven M.
    Vernooij, Meike W.
    Cordonnier, Charlotte
    Viswanathan, Anand
    Salman, Rustorn Al-Shahi
    Warach, Steven
    Launer, Lenore J.
    Van Buchem, Mark A.
    Breteler, Monique M. B.
    [J]. LANCET NEUROLOGY, 2009, 8 (02) : 165 - 174
  • [7] Water homeostasis in the brain: Basic concepts
    Kimelberg, HK
    [J]. NEUROSCIENCE, 2004, 129 (04) : 851 - 860
  • [8] Course of cerebral amyloid angiopathy - related inflammation
    Kinnecom, C.
    Lev, M. H.
    Wendell, L.
    Smith, E. E.
    Rosand, J.
    Frosch, M. P.
    Greenberg, S. M.
    [J]. NEUROLOGY, 2007, 68 (17) : 1411 - 1416
  • [9] Cerebral microbleeds on MRI - Prevalence, associations, and potential clinical implications
    Koennecke, HC
    [J]. NEUROLOGY, 2006, 66 (02) : 165 - 171
  • [10] A phase 2 multiple ascending dose trial of bapineuzumab in mild to moderate Alzheimer disease
    Salloway, S.
    Sperling, R.
    Gilman, S.
    Fox, N. C.
    Blennow, K.
    Raskind, M.
    Sabbagh, M.
    Honig, L. S.
    Doody, R.
    van Dyck, C. H.
    Mulnard, R.
    Barakos, J.
    Gregg, K. M.
    Liu, E.
    Lieberburg, I.
    Schenk, D.
    Black, R.
    Grundman, M.
    [J]. NEUROLOGY, 2009, 73 (24) : 2061 - 2070