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ProMIS Neurosciences Inc PMN

ProMIS Neurosciences Inc. is a development stage biotechnology company. The Company is focused on generating and developing antibody therapeutics selectively targeting toxic misfolded proteins in neurodegenerative diseases such as Alzheimer’s disease (AD), amyotrophic lateral sclerosis (ALS) and multiple system atrophy (MSA), an alpha-synucleinopathy. Its proprietary target discovery engine applies a thermodynamic, computational discovery platform - ProMIS and Collective Coordinates - to predict novel targets known as Disease Specific Epitopes on the molecular surface of misfolded proteins. Using this approach, the Company is developing novel antibody therapeutics for AD, ALS and MSA. Its product portfolio includes PMN310 / Amyloid-beta, PMN267 / TDP-43, and PMN442 / Alpha-synuclein. The Company plans to investigate additional synucleinopathies, including Parkinson's disease (PD) and dementia with Lewy bodies (DLB). Its wholly owned subsidiary is ProMIS Neurosciences (US) Inc.


NDAQ:PMN - Post by User

Bullboard Posts
Post by retiredcopon May 25, 2018 11:41am
93 Views
Post# 28080976

Amyloid Positivity Increases Risk

Amyloid Positivity Increases Risk Amyloid-Positivity Increases Risk for Cognitive Impairment in Dementia-Free Patients
Amyloid-positive patients without dementia have a >2-fold increased risk for amnestic mild cognitive impairment (aMCI) compared with amyloid-negative dementia-free patients, according to a study published in JAMA Neurology.
In addition, amyloid-positive patients with mild cognitive impairment (MCI) and no cognitive impairment at baseline are at greater risk for progression to Alzheimer's disease (AD) compared with their amyloid-negative counterparts.
A total of 3894 dementia-free patients were randomly selected to undergo clinical and cognitive evaluation at baseline and every 15 months from 2008 to 2018.
Of these patients, a total of 1671 underwent carbon 11-Pittsburgh compound B positron emission tomography imaging (mean [SD] age, 71.3 [9.8]). Prevalent MCI was found in 10.7% (n=179) of participants. The primary study outcome was the prevalence of amyloid positivity and the risk for progression from normal cognition to incident aMCI and from MCI or aMCI to incident AD.
In patients age 50 to 59 and 80 to 89 at baseline, the prevalence of amyloid positivity in the absence of MCI increased from 2.7% (95% CI, 0.5%-4.9%) to 41.3% (95% CI, 33.4%-49.2%) during follow-up, respectively. In addition, the prevalence of amyloid-positive MCI in patients age 50 to 59 and 80 to 89 increased from 0% to 16.4% (95% CI, 10.3%-22.5%), respectively.
An analysis adjusted for age, sex, and education revealed a 2.3-fold increased risk for incident aMCI in amyloid-positive vs amyloid-negative participants (hazard ratio [HR] 2.26; 95% CI, 1.52-3.35; P <.001).
 

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