Evidence mapPaperPMID 34276349Full record

ArticleFrontiers in aging neuroscience2021

Mechanistic Analysis of Age-Related Clinical Manifestations in Down Syndrome.

Xu-Qiao Chen, Zhuo Xing, Quang-Di Chen, Richard J Salvi, Xuming Zhang, Benjamin Tycko, William C Mobley, Y Eugene Yu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.3field-weighted citation impact, top 8% of its field
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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Kynurenine pathway metabolite alterations in Down syndrome and Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  6. Article
  7. Article
  8. Protein Oxidation in Aging and Alzheimer's Disease Brain.Antioxidants (Basel, Switzerland) · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
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 at 4 institutions in 1 country.

Xu-Qiao ChenDepartment of Neurosciences, University of California San Diego, La Jolla, CA, United States.
Zhuo XingThe Children's Guild Foundation Down Syndrome Research Program, Genetics and Genomics Program and Department of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.
Quang-Di ChenDepartment of Communicative Disorders and Sciences and Center for Hearing and Deafness, University at Buffalo, Buffalo, NY, United States.
Richard J SalviDepartment of Communicative Disorders and Sciences and Center for Hearing and Deafness, University at Buffalo, Buffalo, NY, United States.
Xuming ZhangDepartment of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Benjamin TyckoHackensack-Meridian Health Center for Discovery and Innovation, Nutley, NJ, United States.
William C MobleyDepartment of Neurosciences, University of California San Diego, La Jolla, CA, United States.
Y Eugene YuThe Children's Guild Foundation Down Syndrome Research Program, Genetics and Genomics Program and Department of Cancer Genetics and Genomics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.
Cancer Genetics (United States) · USUniversity of California, San Diego · USHackensack Meridian Health · USUniversity of Arkansas for Medical Sciences · US

Funding

Antisense Oligonucleotides targeting APP to prevent neurodegeneration in models of Down Syndrome and Alzheimer's diseaseR01AG061151 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI William C Mobley · 2022 to 2023
$1.3M
Treating with Gamma-Secretase Modulators to Prevent Neurodegeneration in Mouse Models of Down Syndrome and Alzheimer DiseaseR01AG055523 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI William C Mobley · 2022 to 2022
$516k
NIA NIH HHS R01 AG055523NIA NIH HHS R01 AG061151
6 · The paper itself

Abstract

Down syndrome (DS) is the most common genetic cause of Alzheimer's disease (AD) due to trisomy for all or part of human chromosome 21 (Hsa21). It is also associated with other phenotypes including distinctive facial features, cardiac defects, growth delay, intellectual disability, immune system abnormalities, and hearing loss. All adults with DS demonstrate AD-like brain pathology, including amyloid plaques and neurofibrillary tangles, by age 40 and dementia typically by age 60. There is compelling evidence that increased

Indexed as

Alzheimer’s diseaseCOVID-19Down syndromehearing lossinfectionmechanisms

Identifiers

PMID34276349
PMCPMC8281234
OpenAlexW3179432282

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.