Evidence map›Paper›PMID 37304077›Full record

ArticleFrontiers in aging neuroscience2023

The ANeED study - ambroxol in new and early dementia with Lewy bodies (DLB): protocol for a phase IIa multicentre, randomised, double-blinded and placebo-controlled trial.

Luiza Jadwiga Chwiszczuk, Monica Haraldseid Breitve, Bjørn-Eivind Bordewick Kirsebom, Per Selnes, John Chr Fløvig, Anne-Brita Knapskog, Ragnhild E Skogseth, Jessica Hubbers, Elin Holst-Larsen, Arvid Rongve

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Sphingolipidoses: expanding the spectrum of α-synucleinopathies.Journal of neural transmission (Vienna, Austria : 1996) · 2026
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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

10 authors at 7 institutions in 1 country.

Luiza Jadwiga ChwiszczukDepartment of Old Age Related Medicine, Haugesund Hospital, Helse Fonna Trust, Haugesund, Norway.
Monica Haraldseid BreitveDepartment of Research and Innovation, Haugesund Hospital, Helse Fonna Trust, Haugesund, Norway.
Bjørn-Eivind Bordewick KirsebomDepartment of Neurology, University Hospital of North Norway, Tromsø, Norway.
Per SelnesDepartment of Neurology, Akershus University Hospital, Lørenskog, Norway.
John Chr FløvigSant Olavs Hospital, Trondheim, Norway.
Anne-Brita KnapskogDepartment of Geriatric Medicine, Oslo University Hospital, Oslo, Norway.
Ragnhild E SkogsethDepartment of Internal Medicine, Haraldsplass Deaconess Hospital, Bergen, Norway.
Jessica HubbersDepartment of Research and Innovation, Haugesund Hospital, Helse Fonna Trust, Haugesund, Norway.
Elin Holst-LarsenSenior Clinical Research Associate in ProToCall, Haugesund, Norway.
Arvid RongveDepartment of Research and Innovation, Haugesund Hospital, Helse Fonna Trust, Haugesund, Norway.
Privatsykehuset Haugesund · NOSt Olav's University Hospital · NOAkershus University Hospital · NOFonna Hospital TrustHaraldsplass Diakonale Sykehus · NOOslo University Hospital · NOUniversity Hospital of North Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Currently, there are no disease-modifying pharmacological treatment options for dementia with Lewy bodies (DLB). The hallmark of DLB is pathological alpha-synuclein (aS) deposition. There are growing amounts of data suggesting that reduced aS clearance is caused by failure in endolysosomal and authophagic pathways, as well as and glucocerebrosidase (GCase) dysfunction and mutations in the GCase gene (GBA). The population's studies demonstrated that the incidence of GBA mutations is higher among Parkinson's disease (PD) patients, and carriers of such mutations have a higher risk of developing PD. The incidence of GBA mutations is even higher in DLB and a genome-wide association study (GWAS) confirmed the correlation between GBA mutations and DLB. Methods: This is a multicentre, phase IIa, double-blinded, randomised and placebo-controlled clinical trial, using a parallel arm design for 18 months' follow-up. The allocation ratio is 1:1 (treatment:placebo). Discussion: The ANeED study is an ongoing clinical drug trial with ABX. The unique, but not fully understood mechanism of ABX on the enhancement of lysosomal aS clearance may be promising as a possible modifying treatment in DLB. Trial Registration: The clinical trial is registered in the international trials register - clinicaltrials.com (NCT0458825) and nationally at the Current Research Information System in Norway (CRISTIN 2235504).

Indexed as

alpha-synucleinambroxolclinical trial in DLBdementia with Lewy bodies (DLB)DLBtreatment

Identifiers

PMID37304077
PMCPMC10250712
OpenAlexW4378472324

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.