Evidence map›Paper›PMID 31206565›Full record

ArticlePloS one2019

Levels of islet amyloid polypeptide in cerebrospinal fluid and plasma from patients with Alzheimer's disease.

Nina Schultz, Shorena Janelidze, Elin Byman, Lennart Minthon, Katarina Nägga, Oskar Hansson, Malin Wennström

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  11. Amylin antibodies frequently display cross-reactivity with CGRP: characterization of eight amylin antibodies.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    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

7 authors at 2 institutions in 1 country.

Nina SchultzClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.ORCID 0000-0001-8202-6455
Shorena JanelidzeClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Elin BymanClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Lennart MinthonClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Katarina NäggaClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Oskar HanssonClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Malin WennströmClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.ORCID 0000-0002-9957-1801
Lund University · SELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biologically active pancreatic hormone peptide islet amyloid polypeptide (IAPP) regulates brain functions such as appetite and cognition. It also plays a role in clearance of amyloid beta (Aβ), a peptide implicated in the dementia disorder Alzheimer's disease (AD). If IAPP becomes modified, it loses its biological activity and starts to aggregate. Such aggregations have been found in the AD brain and decreased plasma levels of the unmodified IAPP (uIAPP) have been shown in the same patients. In the current study, we analyze levels of uIAPP and total IAPP (unmodified and modified) in cerebrospinal fluid (CSF) to investigate its potential as a biomarker for AD. We found no differences in neither CSF nor plasma levels of uIAPP or total IAPP in AD patients compared to cognitive healthy individuals (NC). The levels of uIAPP in CSF of NC were positively correlated with uIAPP in plasma, Q-albumin and albumin levels in CSF, but negatively correlated with CSF levels of t-tau and p-tau. These findings were not seen in AD patients. Levels of total CSF IAPP correlated positively with total Q-albumin and albumin levels in CSF in both AD and NC. In addition, total plasma IAPP correlated positively with CSF t-tau and p-tau in NC and negatively with CSF Aβ42 in AD patients. To conclude, our studies did not find evidence supporting the use of CSF IAPP as an AD biomarker. However, our findings, indicating a compromised translocation of uIAPP in and out of the brain in AD patients as well as the correlations between total plasma IAPP and AD biomarkers, encourage further research on the role for IAPP in AD.

Indexed as

BiomarkersAgedAged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesEnzyme-Linked Immunosorbent AssayFemaleHumansIslet Amyloid PolypeptideMaleMiddle AgedPrognosistau ProteinsAmyloid beta-PeptidesBiomarkersIslet Amyloid Polypeptidetau Proteins

Identifiers

PMID31206565
PMCPMC6576764
OpenAlexW2949247513

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.