Evidence map›Paper›PMID 38429112›Full record

ArticleGut2024

Absence of a pancreatic microbiome in intraductal papillary mucinous neoplasm.

Marie-Madlen Pust, Darío Missael Rocha Castellanos, Kara Rzasa, Andrea Dame, Gleb Pishchany, Charnwit Assawasirisin, Andrew Liss, Carlos Fernandez-Del Castillo, Ramnik J Xavier

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Marie-Madlen PustBroad Institute of MIT and Harvard, Cambridge, Massachusetts, USA xavier@molbio.mgh.harvard.edu mpust@mgh.harvard.edu cfernandez@mgh.harvard.edu.ORCID 0000-0001-6870-2488
Darío Missael Rocha CastellanosDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0002-6227-9161
Kara RzasaBroad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.ORCID 0000-0002-5753-7517
Andrea DameBroad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
Gleb PishchanyBroad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
Charnwit AssawasirisinDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Andrew LissDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Carlos Fernandez-Del CastilloDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA xavier@molbio.mgh.harvard.edu mpust@mgh.harvard.edu cfernandez@mgh.harvard.edu.
Ramnik J XavierBroad Institute of MIT and Harvard, Cambridge, Massachusetts, USA xavier@molbio.mgh.harvard.edu mpust@mgh.harvard.edu cfernandez@mgh.harvard.edu.
Broad Institute · USHarvard University · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

objectiveThis study aims to validate the existence of a microbiome within intraductal papillary mucinous neoplasm (IPMN) that can be differentiated from the taxonomically diverse DNA background of next-generation sequencing procedures.

designWe generated 16S rRNA amplicon sequencing data to analyse 338 cyst fluid samples from 190 patients and 19 negative controls, the latter collected directly from sterile syringes in the operating room. A subset of samples (n=20) and blanks (n=5) were spiked with known concentrations of bacterial cells alien to the human microbiome to infer absolute abundances of microbial traces. All cyst fluid samples were obtained intraoperatively and included IPMNs with various degrees of dysplasia as well as other cystic neoplasms. Follow-up culturing experiments were conducted to assess bacterial growth for microbiologically significant signals.

resultsMicrobiome signatures of cyst fluid samples were inseparable from those of negative controls, with no difference in taxonomic diversity, and microbial community composition. In a patient subgroup that had recently undergone invasive procedures, a bacterial signal was evident. This outlier signal was not characterised by higher taxonomic diversity but by an increased dominance index of a gut-associated microbe, leading to lower taxonomic evenness compared with the background signal.

conclusionThe 'microbiome' of IPMNs and other pancreatic cystic neoplasms does not deviate from the background signature of negative controls, supporting the concept of a sterile environment. Outlier signals may appear in a small fraction of patients following recent invasive endoscopic procedures. No associations between microbial patterns and clinical or cyst parameters were apparent.

Indexed as

MicrobiotaPancreatic Intraductal NeoplasmsPancreatic NeoplasmsRNA, Ribosomal, 16SAdenocarcinoma, MucinousAdultAgedAged, 80 and overCarcinoma, Pancreatic DuctalCyst FluidFemaleHumansMaleMiddle AgedPancreasRNA, Ribosomal, 16SENDOSCOPIC PROCEDURESINFLAMMATIONINTESTINAL MICROBIOLOGYPANCREATIC DISEASEPANCREATIC TUMOURS

Identifiers

PMID38429112
PMCPMC11187374
OpenAlexW4392386935

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.