Evidence map›Paper›PMID 26621352›Full record

ArticleActa neuropathologica communications2015

Differential expression of galanin in the cholinergic basal forebrain of patients with Lewy body disorders.

Athanasios Alexandris, Alan King Lun Liu, Raymond Chuen-Chung Chang, Ronald K B Pearce, Steve M Gentleman

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Article in Acta neuropathologica communications, 2015. 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
1.0field-weighted citation impact, top 28% 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, 17 citations in OpenAlex.

  1. Neuropeptidergic systems in psychiatric disorders.Frontiers in endocrinology · 2025
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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

5 authors at 3 institutions in 2 countries.

Athanasios AlexandrisDivision of Brain Sciences, Department of Medicine, Imperial College London, Burlington Danes Building, Hammersmith Hospital Campus, London, W12 0NN, UK. a.s.alexandris@gmail.com.
Alan King Lun LiuDivision of Brain Sciences, Department of Medicine, Imperial College London, Burlington Danes Building, Hammersmith Hospital Campus, London, W12 0NN, UK.
Raymond Chuen-Chung ChangLaboratory of Neurodegenerative Diseases, School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Ronald K B PearceDivision of Brain Sciences, Department of Medicine, Imperial College London, Burlington Danes Building, Hammersmith Hospital Campus, London, W12 0NN, UK.
Steve M GentlemanDivision of Brain Sciences, Department of Medicine, Imperial College London, Burlington Danes Building, Hammersmith Hospital Campus, London, W12 0NN, UK. s.gentleman@imperial.ac.uk.
Imperial College London · GBHammersmith Hospital · GBUniversity of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDepletion of cholinergic neurons within the nucleus basalis of Meynert (nbM) is thought to contribute to the development of cognitive impairments in both Alzheimer's disease (AD) and Lewy body disorders (LBD). It has been reported that, in late stage AD, a network of fibres that contain the neuropeptide galanin displays significant hypertrophy and 'hyperinnervates' the surviving cholinergic neurons. Galanin is considered as a highly inducible neuroprotective factor and in AD this is assumed to be part of a protective tissue response. The aim of this study was to determine if a similar galanin upregulation is present in the nbM in post-mortem tissue from patients with LBD. Gallatin immunohistochemistry was carried out on anterior nbM sections from 76 LBD cases (27 PD, 15 PD with mild cognitive impairment (MCI), 34 PD with dementia (PDD) and 4 aged-matched controls. Galaninergic innervation of cholinergic neurons was assessed on a semi-quantitative scale.

resultsThe LBD group had significantly higher galaninergic innervation scores (p = 0.016) compared to controls. However, this difference was due to increased innervation density only in a subgroup of LBD cases and this correlated positively with choline acetyltransferase-immunopositive neuron density.

conclusionGalanin upregulation within the basal forebrain cholinergic system in LBD, similar to that seen in AD, may represent an intrinsic adaptive response to neurodegeneration that is consistent with its proposed roles in neurogenesis and neuroprotection.

Indexed as

AgedAged, 80 and overCholinergic AgentsCognitive DysfunctionCohort StudiesFemaleGalaninGlial Fibrillary Acidic ProteinHumansLewy Body DiseaseMaleMicroscopy, ConfocalProsencephalonStatistics, NonparametricCholinergic AgentsGalaninGlial Fibrillary Acidic Protein

Identifiers

PMID26621352
PMCPMC4666186
OpenAlexW2185900262

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Registered trials

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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.