Evidence map›Paper›PMID 25426069›Full record

ArticleFrontiers in aging neuroscience2014

Amyloid Beta1-42 and the Phoshorylated Tau Threonine 231 in Brains of Aged Cynomolgus Monkeys (Macaca fascicularis).

Huda Shalahudin Darusman, Albert Gjedde, Dondin Sajuthi, Steven J Schapiro, Otto Kalliokoski, Yuli P Kristianingrum, Ekowati Handaryani, Jann Hau

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Article
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  4. Experimental modeling of Alzheimer's disease: Translational lessons from cross-taxon analyses.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
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  16. Diet, psychosocial stress, and Alzheimer's disease-related neuroanatomy in female nonhuman primates.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2021
    Article
  17. Article
  18. A nonhuman primate model of early Alzheimer's disease pathologic change: Implications for disease pathogenesis.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2019
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Huda Shalahudin DarusmanDepartment of Experimental Medicine, Faculty of Health Science, University of Copenhagen , Copenhagen , Denmark ; Department of Anatomy, Physiology and Pharmacology, Faculty of Veterinary Medicine, Bogor Agricultural University , Bogor , Indonesia.
Albert GjeddeDepartment of Neuroscience and Pharmacology, Faculty of Health Science, University of Copenhagen , Copenhagen , Denmark ; Center for Functionally Integrative Neuroscience, University of Aarhus , Aarhus , Denmark ; Department of Radiology and Radiological Science, Johns Hopkins University , Baltimore, MD , USA ; Department of Neurology and Neurosurgery, McGill University , Montréal, QC , Canada.
Dondin SajuthiPrimate Research Center, Bogor Agricultural University , Bogor , Indonesia.
Steven J SchapiroDepartment of Experimental Medicine, Faculty of Health Science, University of Copenhagen , Copenhagen , Denmark ; Department of Veterinary Sciences, The University of Texas MD Anderson Cancer Center , Bastrop, TX , USA.
Otto KalliokoskiDepartment of Experimental Medicine, Faculty of Health Science, University of Copenhagen , Copenhagen , Denmark.
Yuli P KristianingrumDepartment of Pathology, Faculty of Veterinary Medicine, University of Gajah Mada , Yogyakarta , Indonesia.
Ekowati HandaryaniDivision of Pathology, Department of Clinic, Reproduction and Pathology, Faculty of Veterinary Medicine, Bogor Agricultural University , Bogor , Indonesia.
Jann HauDepartment of Experimental Medicine, Faculty of Health Science, University of Copenhagen , Copenhagen , Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological hallmarks indicative of Alzheimer's disease (AD), which are the plaques of amyloid beta1-42 and neurofibrillary tangles, were found in brain of aged cynomolgus monkey. The aim of this study was to investigate if aged monkeys exhibiting spatial memory impairment and levels of biomarkers indicative of AD, had brain lesions similar to human patients suffering from senile dementia. Generating immunohistochemistry technique to biomarkers of amyloid beta1-42 and the phosphorylated tau 231, our study assessed the amyloidopathy, such as indicative to the senile plaques and cerebral amyloid angiopathy, and the tauopathy, to possible neurofibrillary tangles. Six aged monkeys were selected based on their spatial memory performance and profile of biomarkers of AD, divided equally to affected aged subject - with Memory-affected and low amyloid level, and aged with higher performance in memory and amyloid, as the age-matched subjects. Using immunohistochemistry, plaques of amyloid beta1-42 were observed in two out of three brains of aged subjects with memory impairment and biomarkers indicative of AD. The cerebral amyloid angiopathy was observed in both aged monkey groups, and unlike in the human, the amyloids were found to deposit in the small veins and capillaries. In one of the affected individuals, phosphorylated tau was positively stained intracellularly of the neurons, indicating a possibility of an early stage of the formation of tangles. These findings add to the body of evidence of the utility of the aged cynomolgus monkeys as a spontaneous model for Alzheimer-related disease.

Indexed as

cerebral amyloid angiopathydegenerative diseaseimmunohistochemistryneurofibrillary tanglessenile plaques

Identifiers

PMID25426069
PMCPMC4225838

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.