Evidence map›Paper›PMID 38672416›Full record

ReviewBiomolecules2024

Biomarkers for Managing Neurodegenerative Diseases.

Lara Cheslow, Adam E Snook, Scott A Waldman

Abstract readReview
In one paragraph

Review in Biomolecules, 2024. 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
–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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Unraveling Molecular Targets for Neurodegenerative Diseases ThroughInternational journal of molecular sciences · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. 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

3 authors.

Lara CheslowDepartment of Pharmacology, Physiology and Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.ORCID 0000-0003-0880-5957
Adam E SnookDepartment of Pharmacology, Physiology and Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.ORCID 0000-0001-9216-4560
Scott A WaldmanDepartment of Pharmacology, Physiology and Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.ORCID 0000-0001-6619-175X

Funding

Targeting visceral pain through intestinal neuropod cell GUCY2C signalingR01DK138834 · NIDDK · THOMAS JEFFERSON UNIVERSITY · PI MANUEL L COVARRUBIAS, Scott A. Waldman · 2023 to 2026
$3.4M
(PQ1) GUCY2C hormone loss translates APC-Beta-catenin mutations into epithelial transformationR01CA206026 · NCI · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A · 2016 to 2020
$1.8M
Neuroprotection by the GUCY2C gut-brain axis in Parkinson's diseaseR21NS130388 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A · 2023 to 2023
$429k
Off-the-shelf CAR-T Therapy via Tumor-Selective Immuno-engagersR21CA267087 · NCI · LEHIGH UNIVERSITY · PI SNOOK, ADAM, THEVENIN, DAMIEN · 2022 to 2023
$402k
Ligand-Induced Recruitment of CAR-T Cells to Colorectal CancersR21CA286339 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KIM, SANGWON VINCENT, SNOOK, ADAM · 2024 to 2025
$401k
Parkinson's disease therapies targeting GUCY2CF30NS125921 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI CHESLOW, LARA · 2022 to 2025
$179k
NCI NIH HHS R01 CA206026NCI NIH HHS R21 CA267087NCI NIH HHS R21 CA286339NIDDK NIH HHS R01 DK138834NIH HHS 1R01 CA204881, 1R01 CA206026, 1R21 1NS130388, 1R01 DK1388341NINDS NIH HHS F30 NS125921NINDS NIH HHS R21 NS130388
6 · The paper itself

Abstract

Neurological disorders are the leading cause of cognitive and physical disability worldwide, affecting 15% of the global population. Due to the demographics of aging, the prevalence of neurological disorders, including neurodegenerative diseases, will double over the next two decades. Unfortunately, while available therapies provide symptomatic relief for cognitive and motor impairment, there is an urgent unmet need to develop disease-modifying therapies that slow the rate of pathological progression. In that context, biomarkers could identify at-risk and prodromal patients, monitor disease progression, track responses to therapy, and parse the causality of molecular events to identify novel targets for further clinical investigation. Thus, identifying biomarkers that discriminate between diseases and reflect specific stages of pathology would catalyze the discovery and development of therapeutic targets. This review will describe the prevalence, known mechanisms, ongoing or recently concluded therapeutic clinical trials, and biomarkers of three of the most prevalent neurodegenerative diseases, including Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), and Parkinson's disease (PD).

Indexed as

Alzheimer DiseaseBiomarkersNeurodegenerative DiseasesAmyotrophic Lateral SclerosisAnimalsHumansParkinson DiseaseBiomarkersAlzheimer’s diseaseamyotrophic lateral sclerosisbiomarkersParkinson’s disease

Identifiers

PMID38672416
PMCPMC11048498

What OpenQuestion 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 OpenQuestion graph.