Evidence map›Paper›PMID 27184740›Full record

ArticleScientific reports2016

Modified serpinA1 as risk marker for Parkinson's disease dementia: Analysis of baseline data.

Steffen Halbgebauer, Magdalena Nagl, Hans Klafki, Ute Haußmann, Petra Steinacker, Patrick Oeckl, Jan Kassubek, Elmar Pinkhardt, Albert C Ludolph, Hilkka Soininen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  9. CSF SerpinA1 in Creutzfeldt-Jakob disease and frontotemporal lobar degeneration.Annals of clinical and translational neurology · 2020
    Article
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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

13 authors at 4 institutions in 2 countries.

Steffen HalbgebauerDepartment of Neurology, University of Ulm, Germany.
Magdalena NaglDepartment of Neurology, University of Ulm, Germany.
Hans KlafkiLVR-Klinikum Essen, Department of Psychiatry and Psychotherapy, Faculty of Medicine, University of Duisburg-Essen, Germany.
Ute HaußmannLVR-Klinikum Essen, Department of Psychiatry and Psychotherapy, Faculty of Medicine, University of Duisburg-Essen, Germany.
Petra SteinackerDepartment of Neurology, University of Ulm, Germany.
Patrick OecklDepartment of Neurology, University of Ulm, Germany.
Jan KassubekDepartment of Neurology, University of Ulm, Germany.
Elmar PinkhardtDepartment of Neurology, University of Ulm, Germany.
Albert C LudolphDepartment of Neurology, University of Ulm, Germany.
Hilkka SoininenDepartment of Neurology, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland.
Sanna-Kaisa HerukkaDepartment of Neurology, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland.
Jens WiltfangDepartment of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.
Markus OttoDepartment of Neurology, University of Ulm, Germany.
Universität Ulm · DEKuopio University Hospital · FIUniversity of Göttingen · DEUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early detection of dementia in Parkinson disease is a prerequisite for preventive therapeutic approaches. Modified serpinA1 in cerebrospinal fluid (CSF) was suggested as an early biomarker for differentiation between Parkinson patients with (PDD) or without dementia (PD). Within this study we aimed to further explore the diagnostic value of serpinA1. We applied a newly developed nanoscale method for the detection of serpinA1 based on automated capillary isoelectric focusing (CIEF). A clinical sample of 102 subjects including neurologically healthy controls (CON), PD and PDD patients was investigated. Seven serpinA1 isoforms of different charge were detected in CSF from all three diagnostic groups. The mean CSF signals of the most acidic serpinA1 isoform differed significantly (p < 0.01) between PDD (n = 29) and PD (n = 37) or CON (n = 36). Patients above the cut-off of 6.4 have a more than six times higher risk for an association with dementia compared to patients below the cut off. We propose this serpinA1 CIEF-immunoassay as a novel tool in predicting cognitive impairment in PD patients and therefore for patient stratification in therapeutic trials.

Indexed as

AgedAged, 80 and overalpha 1-AntitrypsinBiomarkersDementiaFemaleHumansIsoelectric FocusingMaleMiddle AgedParkinson DiseasePrognosisRisk Assessmentalpha 1-AntitrypsinBiomarkersSERPINA1 protein, human

Identifiers

PMID27184740
PMCPMC4868992
OpenAlexW2405913244

What OpenQuestion holds

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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.