Evidence map›Paper›PMID 26168044›Full record

ArticlePloS one2015

Measuring Compounds in Exhaled Air to Detect Alzheimer's Disease and Parkinson's Disease.

Jan-Philipp Bach, Maike Gold, David Mengel, Akira Hattesohl, Dirk Lubbe, Severin Schmid, Björn Tackenberg, Jürgen Rieke, Sasidhar Maddula, Jörg Ingo Baumbach and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-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

25 citing papers in PubMed, 76 citations in OpenAlex.

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  19. Human Breathomics Database.Database : the journal of biological databases and curation · 2020
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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

21 authors at 6 institutions in 1 country.

Jan-Philipp BachDepartment of Neurology, RWTH Aachen, 52074 Aachen, Germany.
Maike GoldDepartment of Neurology, Philipps-University Marburg, 35043 Marburg, Germany.
David MengelDepartment of Neurology, Philipps-University Marburg, 35043 Marburg, Germany.
Akira HattesohlDepartment of Internal Medicine, Division of Pulmonary Diseases, Philipps-University Marburg, 35043 Marburg, Germany.
Dirk LubbeDepartment of Psychology, Division of Methodology and Statistics of the University of Giessen, 35394 Giessen, Germany.
Severin SchmidDepartment of Internal Medicine, Division of Pulmonary Diseases, Philipps-University Marburg, 35043 Marburg, Germany.
Björn TackenbergDepartment of Neurology, Philipps-University Marburg, 35043 Marburg, Germany.
Jürgen RiekeDepartment of Neurology, Philipps-University Marburg, 35043 Marburg, Germany.
Sasidhar MaddulaFaculty of Applied Chemistry, Reutlingen University, 72762 Reutlingen, Germany.
Jörg Ingo BaumbachFaculty of Applied Chemistry, Reutlingen University, 72762 Reutlingen, Germany.
Christoph NellDepartment of Internal Medicine, Division of Pulmonary Diseases, Philipps-University Marburg, 35043 Marburg, Germany.
Tobias BoeseltDepartment of Internal Medicine, Division of Pulmonary Diseases, Philipps-University Marburg, 35043 Marburg, Germany.
Joan MichelisClinical Neuroscience Unit, Department of Neurology, University of Bonn, 53105 Bonn, Germany; Department of Psychiatry, University of Bonn, 53105 Bonn, Germany.
Judith AlferinkDepartment of Psychiatry, University of Bonn, 53105 Bonn, Germany; Department of Psychiatry, University of Münster, 48149 Münster, Germany.
Michael HenekaClinical Neuroscience Unit, Department of Neurology, University of Bonn, 53105 Bonn, Germany; German Centre for Neurodegenerative Disease (DZNE), 53105 Bonn, Germany.
Wolfgang OertelDepartment of Neurology, Philipps-University Marburg, 35043 Marburg, Germany.
Frank JessenDepartment of Psychiatry, University of Bonn, 53105 Bonn, Germany; German Centre for Neurodegenerative Disease (DZNE), 53105 Bonn, Germany.
Sabina JanciauskieneDepartment of Internal Medicine, University of Hannover, 30625 Hannover, Germany.
Claus VogelmeierDepartment of Internal Medicine, Division of Pulmonary Diseases, Philipps-University Marburg, 35043 Marburg, Germany.
Richard DodelDepartment of Neurology, Philipps-University Marburg, 35043 Marburg, Germany.
Andreas Rembert KoczullaDepartment of Internal Medicine, Division of Pulmonary Diseases, Philipps-University Marburg, 35043 Marburg, Germany.
Philipps University of Marburg · DEUniversity of Bonn · DEReutlingen University · DEGerman Center for Neurodegenerative Diseases · DERWTH Aachen University · DEUniversity of Giessen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is diagnosed based upon medical history, neuropsychiatric examination, cerebrospinal fluid analysis, extensive laboratory analyses and cerebral imaging. Diagnosis is time consuming and labour intensive. Parkinson's disease (PD) is mainly diagnosed on clinical grounds.

objectiveThe primary aim of this study was to differentiate patients suffering from AD, PD and healthy controls by investigating exhaled air with the electronic nose technique. After demonstrating a difference between the three groups the secondary aim was the identification of specific substances responsible for the difference(s) using ion mobility spectroscopy. Thirdly we analysed whether amyloid beta (Aβ) in exhaled breath was causative for the observed differences between patients suffering from AD and healthy controls.

methodsWe employed novel pulmonary diagnostic tools (electronic nose device/ion-mobility spectrometry) for the identification of patients with neurodegenerative diseases. Specifically, we analysed breath pattern differences in exhaled air of patients with AD, those with PD and healthy controls using the electronic nose device (eNose). Using ion mobility spectrometry (IMS), we identified the compounds responsible for the observed differences in breath patterns. We applied ELISA technique to measure Aβ in exhaled breath condensates.

resultsThe eNose was able to differentiate between AD, PD and HC correctly. Using IMS, we identified markers that could be used to differentiate healthy controls from patients with AD and PD with an accuracy of 94%. In addition, patients suffering from PD were identified with sensitivity and specificity of 100%. Altogether, 3 AD patients out of 53 participants were misclassified. Although we found Aβ in exhaled breath condensate from both AD and healthy controls, no significant differences between groups were detected.

conclusionThese data may open a new field in the diagnosis of neurodegenerative disease such as Alzheimer's disease and Parkinson's disease. Further research is required to evaluate the significance of these pulmonary findings with respect to the pathophysiology of neurodegenerative disorders.

Indexed as

Breath TestsAgedAlzheimer DiseaseAmyloid beta-PeptidesAnimalsBiomarkersBlotting, WesternCase-Control StudiesEnzyme-Linked Immunosorbent AssayFemaleHumansLungMaleMiceMice, Inbred C3HMice, Inbred C57BLAmyloid beta-Peptidesamyloid beta-protein (1-40)amyloid beta-protein (1-42)BiomarkersPeptide Fragments

Identifiers

PMID26168044
PMCPMC4500505
OpenAlexW1911269782

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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.