Evidence map›Paper›PMID 30474860›Full record

ArticleJournal of neurochemistry2018

HDL mimetic peptides affect apolipoprotein E metabolism: equal supplement or functional enhancer?: An Editorial for 'High-density lipoprotein mimetic peptide 4F mitigates amyloid-β-induced inhibition of apolipoprotein E secretion and lipidation in primary astrocytes and microglia' on page 647.

Wenzhang Wang, Xiongwei Zhu

Erratum issuedOpen access · bronzeAbstract readEditorialComment
In one paragraph

Article in Journal of neurochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. HDL and Therapy.Advances in experimental medicine and biology · 2022
    Article
  4. Perspectives on the Role ofJournal of Alzheimer's disease reports · 2021
    Review
  5. Article
  6. Molecular Insight into the Therapeutic Promise of TargetingOxidative medicine and cellular longevity · 2020
    Review
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Wenzhang WangDepartment of Pathology, Case Western Reserve University, Cleveland, Ohio, USA.
Xiongwei ZhuDepartment of Pathology, Case Western Reserve University, Cleveland, Ohio, USA.ORCID 0000-0003-2092-6508
Case Western Reserve University · US

Funding

The Role of PGC-1alpha and Mitochondrial Biogenesis in the Pathogenesis of Alzheimer's DiseaseRF1AG056363 · NIA · CASE WESTERN RESERVE UNIVERSITY · PI ZHU, XIONGWEI · 2018 to 2018
$3.2M
Molecular Mechanisms Underlying Mitochondrial Dynamics Abnormalities in Alzheimer DiseaseRF1AG049479 · NIA · CASE WESTERN RESERVE UNIVERSITY · PI ZHU, XIONGWEI · 2016 to 2016
$2.6M
Abnormal Mitochondrial Dynamics and Mitochondrial Dysfunction in Alzheimer's DiseR01NS083385 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI ZHU, XIONGWEI · 2013 to 2017
$2.1M
Impaired mitochondrial proteostasis in Alzheimer?s diseaseR21AG058015 · NIA · CASE WESTERN RESERVE UNIVERSITY · PI WANG, WENZHANG · 2018 to 2019
$440k
The Pathogenic Mechanism of C19orf12 in Mitochondrial Membrane Protein Associated NeurodegenerationR03NS112782 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI WANG, WENZHANG · 2019 to 2020
$161k
The Role of Altered Mitochondrial Contact Site and Cristae Organizing System (MICOS) in Alzheimer's DiseaseR03AG063362 · NIA · CASE WESTERN RESERVE UNIVERSITY · PI WANG, WENZHANG · 2019 to 2020
$160k
Alzheimer's Association AARG-16-443584NIA NIH HHS R03 AG063362NIA NIH HHS R21 AG058015NIA NIH HHS RF1 AG049479NIA NIH HHS RF1 AG056363NIH HHS AG049479NIH HHS AG056363NIH HHS AG058015NIH HHS NS083385NINDS NIH HHS R01 NS083385NINDS NIH HHS R03 NS112782
6 · The paper itself

Abstract

ε4 allele of ApoE is the strongest genetic risk factor for late onset Alzheimer's disease (AD). Supplementation of ApoE proteins or mimetics has been pursued for drug developments against AD. A very low-density lipoprotein (HDL) mimetic peptide 4F was shown to alleviate AD-related deficits in APP transgenic mice, and this editorial highlights a study by Chernick et al. who use both mouse and human neuroglial cells to explore the mechanism underlying beneficial effects of this peptide. The authors demonstrate that 4F peptide significantly increased the secretion and lipidation of ApoE in the absence and presence of Aβ independent of de novo transcription/translation, but requiring ABCA1 and the integrity of the secretory pathway between ER and Golgi. This study reveals a novel mechanism of HDL mimetic peptide as a functional ApoE enhancer and support further development of ApoA-I 4F peptide as effective ApoE modulating agents against AD.

Indexed as

Alzheimer DiseaseAstrocytesAmyloid beta-PeptidesAnimalsApolipoproteins EBrainDietary SupplementsHumansLipoproteins, HDLMiceMice, TransgenicMicrogliaPeptidesAmyloid beta-Peptidesapolipoprotein A-I mimetic peptide 4FApolipoproteins ELipoproteins, HDLPeptides

Identifiers

PMID30474860
PMCPMC6309212
OpenAlexW2902335013

What OpenQuestion holds

Textmetadata
LicenceTDM
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.