Evidence map›Paper›PMID 37088544›Full record

ArticleAnnals of clinical and translational neurology2023

Multimodal investigation of melanopsin retinal ganglion cells in Alzheimer's disease.

Chiara La Morgia, Micaela Mitolo, Martina Romagnoli, Michelangelo Stanzani Maserati, Stefania Evangelisti, Maddalena De Matteis, Sabina Capellari, Claudio Bianchini, Claudia Testa, Gilles Vandewalle and 12 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  8. Alzheimer's disease pathophysiology in the Retina.Progress in retinal and eye research · 2024
    Review
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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

22 authors at 8 institutions in 2 countries.

Chiara La Morgia *IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.ORCID 0000-0002-4639-8929
Micaela Mitolo *IRCCS Istituto delle Scienze Neurologiche di Bologna, Programma Neuroimmagini Funzionali e Molecolari, Bologna, Italy.
Martina RomagnoliIRCCS Istituto delle Scienze Neurologiche di Bologna, Programma di Neurogenetica, Bologna, Italy.ORCID 0000-0003-1995-558X
Michelangelo Stanzani MaseratiIRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.
Stefania EvangelistiDipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.ORCID 0000-0003-4556-8233
Maddalena De MatteisIRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.
Sabina CapellariIRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.
Claudio BianchiniDipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
Claudia TestaIRCCS Istituto delle Scienze Neurologiche di Bologna, Programma Neuroimmagini Funzionali e Molecolari, Bologna, Italy.
Gilles VandewalleSleep and Chronobiology Lab, GIGA-Cyclotron Research Centre-In Vivo Imaging, University of Liège, Liège, Belgium.ORCID 0000-0003-2483-2752
Aurelia SantoroDipartimento di Medicina Specialistica Diagnostica e Sperimentale, Università di Bologna, Bologna, Italy.
Michele CarbonelliDipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
Pietro D'AgatiIRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.
Marco FilardiDipartimento di Medicina di Base, Neuroscienze e degli Organi di Senso, Università di Bari Aldo Moro, Bari, Italy.
Pietro AvanziniCNR, Istituto di Neuroscienze, Parma, Italy.
Piero BarboniIRCCS San Raffaele, Milan, Italy.
Corrado ZenesiniIRCCS Istituto delle Scienze Neurologiche di Bologna, Unità di Epidemiologia e Statistica, Bologna, Italy.
Flavia BaccariIRCCS Istituto delle Scienze Neurologiche di Bologna, Unità di Epidemiologia e Statistica, Bologna, Italy.
Rocco LiguoriIRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.ORCID 0000-0002-1815-1013
Caterina TononDipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
Raffaele Lodi *Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
Valerio Carelli *Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
Istituto delle Scienze Neurologiche di Bologna · ITUniversity of Bologna · ITIstituto Nanoscienze · ITOsservatorio astronomico di Bologna · ITUniversity of Bari Aldo Moro · ITUniversity of Liège · BEUniversity of Parma · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn Alzheimer's disease (AD), the presence of circadian dysfunction is well-known and may occur early in the disease course. The melanopsin retinal ganglion cell (mRGC) system may play a relevant role in contributing to circadian dysfunction. In this study, we aimed at evaluating, through a multimodal approach, the mRGC system in AD at an early stage of disease.

methodsWe included 29 mild-moderate AD (70.9 ± 11 years) and 26 (70.5 ± 8 years) control subjects. We performed an extensive neurophtalmological evaluation including optical coherence tomography with ganglion cell layer segmentation, actigraphic evaluation of the rest-activity rhythm, chromatic pupillometry analyzed with a new data-fitting approach, and brain functional MRI combined with light stimuli assessing the mRGC system.

resultsWe demonstrated a significant thinning of the infero-temporal sector of the ganglion cell layer in AD compared to controls. Moreover, we documented by actigraphy the presence of a circadian-impaired AD subgroup. Overall, circadian measurements worsened by age. Chromatic pupillometry evaluation highlighted the presence of a pupil-light response reduction in the rod condition pointing to mRGC dendropathy. Finally, brain fMRI showed a reduced occipital cortex activation with blue light particularly for the sustained responses.

interpretationOverall, the results of this multimodal innovative approach clearly document a dysfunctional mRGC system at early stages of disease as a relevant contributing factor for circadian impairment in AD providing also support to the use of light therapy in AD.

Indexed as

Alzheimer DiseaseRetinal Ganglion CellsHumansMelanopsinRetinaRod OpsinsMelanopsinRod Opsins

Identifiers

PMID37088544
PMCPMC10270274
OpenAlexW4366777256

What OpenQuestion holds

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LicenceCC BY
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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.