Evidence map›Paper›PMID 26092111›Full record

ReviewJournal of neurovirology2016

Peripheral aetiopathogenic drivers and mediators of Parkinson's disease and co-morbidities: role of gastrointestinal microbiota.

Sylvia M Dobbs, R John Dobbs, Clive Weller, André Charlett, Aisha Augustin, David Taylor, Mohammad A A Ibrahim, Ingvar Bjarnason

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of neurovirology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Role ofJournal of clinical medicine · 2020
    Review
  11. Article
  12. Review
  13. Article
  14. Frontiers in microbiology · 2019
    Review
  15. Frontiers in medicine · 2019
    Article
  16. Review
  17. The nasal and gut microbiome in Parkinson's disease and idiopathic rapid eye movement sleep behavior disorder.Movement disorders : official journal of the Movement Disorder Society · 2018
    Article
  18. Microbiota-Brain-Gut Axis and Neurodegenerative Diseases.Current neurology and neuroscience reports · 2017
    Review
  19. Review
  20. Frontiers in cellular and infection microbiology · 2017
    Review
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

8 authors at 3 institutions in 1 country.

Sylvia M DobbsPharmaceutical Sciences, King's College London, London, UK. sylvia.dobbs@kcl.ac.uk.
R John DobbsPharmaceutical Sciences, King's College London, London, UK.
Clive WellerPharmaceutical Sciences, King's College London, London, UK.
André CharlettPharmaceutical Sciences, King's College London, London, UK.
Aisha AugustinPharmaceutical Sciences, King's College London, London, UK.
David TaylorPharmaceutical Sciences, King's College London, London, UK.
Mohammad A A IbrahimDiagnostic Immunology Laboratory, King's College and St Thomas's Hospitals, London, UK.
Ingvar BjarnasonDepartment of Gastroenterology, King's College Hospital, London, UK.
King's College London · GBKing's College Hospital · GBMaudsley Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We seek an aetiopathogenic model for the spectrum of Parkinson's disease (PD), functional bowel disease, depression and cognitive impairment. The adopted concept is that systemic immuno-inflammatory processes mediate neuro-inflammation. The model would be based on phenotype, exposome (including gastrointestinal microbiome), milieu (immuno-inflammatory and metabolome), human genetics and their interactions. It would enable a patient's position, to be understood in terms of drivers, perpetuators and mediators, and a future position, with and without intervention, predicted. Even the cardinal facets of PD may have different drivers: halting one may allow escape down subordinate pathways. Peptic ulceration is prodromal to PD. In our randomised placebo-controlled trial, hypokinesia improved over the year following biopsy-proven Helicobacter pylori eradication and rigidity worsened. This was independent of any (stable, long t½) antiparkinsonian medication. There are pointers to an autoimmune process: for example, surveillance-confirmed hypokinesia effect was indication specific. During surveillance, successive antimicrobial courses, other than for Helicobacter, were associated with cumulative increase in rigidity. Exhibiting laxatives appeared to stem the overall temporal increase, despite antiparkinsonian medication, in rigidity. Thus, intestinal dysbiosis may be a major source of bystander neuronal damage. There are biological gradients of objective measures of PD facets on circulating inflammatory markers and leucocyte subset counts. Moreover, lactulose hydrogen breath test positivity for small-intestinal bacterial overgrowth (present in two thirds of PD patients) is associated with the same subsets: higher natural killer and total CD4+ counts and lower neutrophils. With greater aetiopathogenic understanding, relatively low cost and on-the-shelf medication could have a major impact. A new generation of animal models, based on the gut microbiome, is envisaged.

Indexed as

Gastrointestinal MicrobiomeAnimalsCD4-Positive T-LymphocytesCognition DisordersComorbidityDepressionDysbiosisHelicobacter InfectionsHelicobacter pyloriHumansInflammationInflammatory Bowel DiseasesKiller Cells, NaturalNeutrophilsParkinson DiseasePeptic UlcerAetiologyAutoimmunityBystander damageHelicobacterIntestinal dysbiosisParkinson’s and overlap diseasesPathogenesis

Identifiers

PMID26092111
PMCPMC4729788
OpenAlexW1871710684

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.