Evidence map›Paper›PMID 34121475›Full record

ArticleASN neuro

Metabolism-Based Gene Differences in Neurons Expressing Hyperphosphorylated AT8- Positive (AT8+) Tau in Alzheimer's Disease.

Audra York, Angela Everhart, Michael P Vitek, Kirby W Gottschalk, Carol A Colton

Open access · goldAbstract read
In one paragraph

Article in ASN neuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Functional Diversity of HemN-like Proteins.ACS bio & med chem Au · 2022
    Review
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

5 authors at 1 institution in 1 country.

Audra YorkDivision of Translational Brain Sciences, Department of Neurology, Duke University Medical Center, Durham, North Carolina, United States.ORCID 0000-0003-1048-8962
Angela EverhartDivision of Translational Brain Sciences, Department of Neurology, Duke University Medical Center, Durham, North Carolina, United States.
Michael P VitekDivision of Translational Brain Sciences, Department of Neurology, Duke University Medical Center, Durham, North Carolina, United States.
Kirby W GottschalkDivision of Translational Brain Sciences, Department of Neurology, Duke University Medical Center, Durham, North Carolina, United States.
Carol A ColtonDivision of Translational Brain Sciences, Department of Neurology, Duke University Medical Center, Durham, North Carolina, United States.ORCID 0000-0003-3305-370X
Duke University · US

Funding

Sex and APOE genotype interact to alter immune regulated metabolism in ADRF1AG057895 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA, COLTON, CAROL ANNE · 2019 to 2019
$5.8M
Immune-based nutrient deprivation and neurodegenerative diseaseR01AG045422 · NIA · DUKE UNIVERSITY · PI COLTON, CAROL ANNE · 2013 to 2017
$2.3M
Sex and APOE genotype interact to alter immune regulated metabolism in ADR56AG057895 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA, COLTON, CAROL ANNE · 2017 to 2017
$1.1M
Immunosuppression in humans with ADR21AG051097 · NIA · DUKE UNIVERSITY · PI COLTON, CAROL ANNE · 2016 to 2017
$437k
NIA NIH HHS R01 AG045422NIA NIH HHS R21 AG051097NIA NIH HHS R56 AG057895NIA NIH HHS RF1 AG057895
6 · The paper itself

Abstract

Metabolic adaptations in the brain are critical to the establishment and maintenance of normal cellular functions and to the pathological responses to disease processes. Here, we have focused on specific metabolic pathways that are involved in immune-mediated neuronal processes in brain using isolated neurons derived from human autopsy brain sections of normal individuals and individuals diagnosed as Alzheimer's disease (AD). Laser capture microscopy was used to select specific cell types in immune-stained thin brain sections followed by NanoString technology to identify and quantify differences in mRNA levels between age-matched control and AD neuronal samples. Comparisons were also made between neurons isolated from AD brain sections expressing pathogenic hyperphosphorylated AT8- positive (AT8+) tau and non-AT8+ AD neurons using double labeling techniques. The mRNA expression data showed unique patterns of metabolic pathway expression between the subtypes of captured neurons that involved membrane based solute transporters, redox factors, and arginine and methionine metabolic pathways. We also identified the expression levels of a novel metabolic gene, Radical-S-Adenosyl Domain1 (

Indexed as

Alzheimer DiseaseApolipoprotein E4FemaleHumansMaleNeuronsPhosphorylationtau ProteinsApolipoprotein E4tau ProteinsAPOE and sex based changesbrain metabolismdifferential gene expressionhyperphosphorylated tauradical s-adenosyl domain 1

Identifiers

PMID34121475
PMCPMC8207264
OpenAlexW3170984191

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.