Greater White Matter Hyperintensity Volume Is Associated with the Number of Microhemorrhages in Preclinical Alzheimer’s Disease - 21/11/24

Doi : 10.14283/jpad.2024.139 
Zahra Shirzadi 1, , A.P. Schultz 1, M. Properzi 1, R. Yaari 2, W.-Y. W. Yau 1, A.M. Brickman 3, M.S. Rafii 4, M.C. Donohue 4, K. Ernstrom 4, S. Wang 4, C.R. Jack 5, S.M. Greenberg 1, R. Raman 4, P. Aisen 4, R.A. Sperling 1, J.P. Chhatwal 1

A4 Study teams

1 Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA 
2 Eli Lilly and Company, Indianapolis, Indiana, USA 
3 Taub Institute for Research on Alzheimer’s Disease and the Aging Brain, Department of Neurology, Columbia University, New York, NY, USA 
4 Alzheimer’s Therapeutic Research Institute, University of Southern California, San Diego, CA, USA 
5 Mayo Clinic, Radiology, Rochester, MN, USA 

a drentz@bwh.harvard.edu drentz@bwh.harvard.edu

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Abstract

Background

Increased white matter hyperintensity (WMH) volume visible on MRI is a common finding in Alzheimer’s disease (AD). We hypothesized that WMH in preclinical AD is associated with the presence of advanced vessel amyloidosis manifested as microhemorrhages (MCH).

Objectives

1) To assess the relationship between baseline WMH volume and baseline MCH. 2) To assess the relationship between longitudinal WMH accumulation and last MRI MCH during the double-blind phase of the A4 trial.

Design

A multicenter, randomized, double-blind, placebo-controlled, Phase 3 study comparing solanezumab with placebo given as infusions once every 4 weeks over 4.5 years in subjects with preclinical AD, defined as having evidence of elevated brain amyloid before the stage of clinically evident cognitive impairment, with an optional open-label extension period.

Setting

Anti-Amyloid Treatment in Asymptomatic Alzheimer’s Disease (A4) study.

Participants

A sample of 1157 cognitively unimpaired older adults (mean age = 71.9 years [SD = 4.8 years], 59% women, 59% APOE ε4 carriers).

Measurements

A linear regression model was used to assess the impact of baseline MCH amount (0, 1, 2+) on WMH volume. A linear mixed-effects model was used to assess the impact of last MRI MCH on longitudinal WMH. All models were corrected for age, sex, grey matter volume, cortical amyloid PET, APOE ε4 status, and treatment group.

Results

Baseline WMH volume was greater in individuals with more than one MCH compared to those with no MCH (t=4.8, p<0.001). The longitudinal increase in WMH amongst individuals with one (t=2.3, p=0.025) and more than one MCH (t=6.7, p<0.001) at the last MRI was greater than those with no MCH.

Conclusion

These results indicate a strong association between WMH and MCH, a common manifestation of cerebral amyloid angiopathy and ARIA-H. These results suggest that increased WMH volume may represent an early sign of vessel amyloidosis, likely prior to the emergence of MCH.

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Key words : White matter hyperintensity, microhemorrhages, cerebral amyloid angiopathy, amyloid related imaging abnormalities, preclinical AD


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Vol 11 - N° 4

P. 869-873 - Agosto 2024 Ritorno al numero
Articolo precedente Articolo precedente
  • Safety Profile of a Cognitively Unimpaired Older Population with Elevated Cerebral Amyloid in a 4.5-Year Clinical Trial
  • Roy Yaari, K.C. Holdridge, M. Mancini, M.S. Rafii, M. Case, C. Battioui, J.R. Sims, P.S. Aisen, R.A. Sperling, A4 Study Team
| Articolo seguente Articolo seguente
  • Pre-Randomization Predictors of Study Discontinuation in a Preclinical Alzheimer’s Disease Randomized Controlled Trial
  • Rema Raman, K. Hussen, M.C. Donohue, K. Ernstrom, K.C. Holdridge, O. Langford, D.P. Molina-Henry, A.L. Pierce, J.R. Sims, A. Smith, R. Yaari, P.S. Aisen, R. Sperling, J.D. Grill, A4 Study Team

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