Evidence map›Paper›PMID 31591382›Full record

ArticleTranslational psychiatry2019

A combined miRNA-piRNA signature to detect Alzheimer's disease.

Gaurav Jain, Anne Stuendl, Pooja Rao, Tea Berulava, Tonatiuh Pena Centeno, Lalit Kaurani, Susanne Burkhardt, Ivana Delalle, Johannes Kornhuber, Michael Hüll and 11 more

Abstract readMulticenter Study
In one paragraph

Article in Translational psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 2 pooled it
–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

78 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  19. piRNA associates with immune diseases.Cell communication and signaling : CCS · 2024
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18 more citing papers are in PubMed but not listed here.

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

21 authors.

Gaurav JainDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075, Göttingen, Germany.
Anne StuendlTranslational Dementia Research, German Center for Neurodegenerative Diseases (DZNE), 53127, Bonn, Germany.
Pooja RaoDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075, Göttingen, Germany.
Tea BerulavaDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075, Göttingen, Germany.
Tonatiuh Pena CentenoDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075, Göttingen, Germany.ORCID http://orcid.org/0000-0002-9329-8912
Lalit KauraniDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075, Göttingen, Germany.
Susanne BurkhardtDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075, Göttingen, Germany.
Ivana DelalleDepartment of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Johannes KornhuberDepartment of Psychiatry and Psychotherapy, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054, Erlangen, Germany.
Michael HüllCenter for Geriatric Medicine and Gerontology, University Medical Center Freiburg, 79106, Freiburg, Germany.
Wolfgang MaierDepartment of Neurodegenerative Diseases and Geriatric Psychiatry, University of Bonn, 53127, Bonn, Germany.
Oliver PetersDepartment of Psychiatry, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 12200, Berlin, Germany.
Hermann EsselmannDepartment of Psychiatry and Psychotherapy, University Medical Center Göttingen (UMG), 37075, Göttingen, Germany.ORCID http://orcid.org/0000-0001-5484-9710
Claudia SchulteCenter of Neurology, Department of Neurodegeneration and Hertie-Institute for Clinical Brain Research, University of Tuebingen, 72076, Tuebingen, Germany.
Christian DeuschleCenter of Neurology, Department of Neurodegeneration and Hertie-Institute for Clinical Brain Research, University of Tuebingen, 72076, Tuebingen, Germany.
Mathis SynofzikCenter of Neurology, Department of Neurodegeneration and Hertie-Institute for Clinical Brain Research, University of Tuebingen, 72076, Tuebingen, Germany.
Jens WiltfangDepartment of Psychiatry and Psychotherapy, University Medical Center Göttingen (UMG), 37075, Göttingen, Germany.ORCID http://orcid.org/0000-0003-1492-5330
Brit MollenhauerDepartment of Neurology, University Medical Center Göttingen (UMG), 37075, Göttingen, Germany.
Walter MaetzlerCenter of Neurology, Department of Neurodegeneration and Hertie-Institute for Clinical Brain Research, University of Tuebingen, 72076, Tuebingen, Germany.
Anja SchneiderTranslational Dementia Research, German Center for Neurodegenerative Diseases (DZNE), 53127, Bonn, Germany. anja.scheider@dzne.de.
Andre FischerDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075, Göttingen, Germany. andre.fischer@dzne.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common neurodegenerative disorder causing huge emotional and economic burden to our societies. An effective therapy has not been implicated yet, which is in part also due to the fact that pathological changes occur years before clinical symptoms manifest. Thus, there is a great need for the development of a translatable biomarker. Recent evidence highlights microRNAs as candidate biomarkers. In this study, we use next-generation sequencing to study the small noncoding RNAome (sncRNAome) in exosomes derived from human cerebrospinal fluid (CSF). We show that the sncRNAome from CSF-derived exosomes is dominated not only by microRNAs (miRNAs) but also by PIWI-interacting RNAs (piRNAs). We define a combined signature consisting of three miRNAs and three piRNAs that are suitable to detect AD with an AUC of 0.83 in a replication cohort and furthermore predict the conversion of mild-cognitive impaired (MCI) patients to AD dementia with an AUC of 0.86 for the piRNA signature. When combining the smallRNA signature with pTau and Aβ 42/40 ratio the AUC reaches 0.98. Our study reports a novel exosomal small noncoding RNA signature to detect AD pathology and provides the first evidence that in addition to miRNAs, piRNAs should also be considered as a candidate biomarker for AD.

Indexed as

AdultAgedAlzheimer DiseaseAmyloid beta-PeptidesArea Under CurveBiomarkersCognitive DysfunctionCohort StudiesFemaleGermanyHumansMaleMicroRNAsMiddle AgedPeptide FragmentsRNA, Small InterferingAmyloid beta-Peptidesamyloid beta-protein (40-42)BiomarkersMicroRNAsPeptide FragmentsRNA, Small Interfering

Identifiers

PMID31591382
PMCPMC6779890

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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.