Evidence map›Paper›PMID 29163474›Full record

ArticleFrontiers in immunology2017

Aged Gut Microbiota Contributes to Systemical Inflammaging after Transfer to Germ-Free Mice.

Floris Fransen, Adriaan A van Beek, Theo Borghuis, Sahar El Aidy, Floor Hugenholtz, Christa van der Gaast-de Jongh, Huub F J Savelkoul, Marien I De Jonge, Mark V Boekschoten, Hauke Smidt and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 241 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
241citing papers in PubMed, 1 pooled it
12.3field-weighted citation impact, top 1% 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

241 citing papers in PubMed, 1 synthesis or guideline pooled it, 379 citations in OpenAlex.

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181 more citing papers are in PubMed but not listed here.

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

12 authors at 6 institutions in 1 country.

Floris FransenTop Institute Food and Nutrition, Wageningen, Netherlands.
Adriaan A van BeekTop Institute Food and Nutrition, Wageningen, Netherlands.
Theo BorghuisTop Institute Food and Nutrition, Wageningen, Netherlands.
Sahar El AidyMicrobial Physiology, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, Groningen, Netherlands.
Floor HugenholtzTop Institute Food and Nutrition, Wageningen, Netherlands.
Christa van der Gaast-de JonghLaboratory of Pediatric Infectious Diseases, Radboud University Medical Center, Nijmegen, Netherlands.
Huub F J SavelkoulCell Biology and Immunology Group, Wageningen University, Wageningen, Netherlands.
Marien I De JongeLaboratory of Pediatric Infectious Diseases, Radboud University Medical Center, Nijmegen, Netherlands.
Mark V BoekschotenTop Institute Food and Nutrition, Wageningen, Netherlands.
Hauke SmidtTop Institute Food and Nutrition, Wageningen, Netherlands.
Marijke M FaasDepartment of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Paul de VosTop Institute Food and Nutrition, Wageningen, Netherlands.
TiFN · NLWageningen University & Research · NLUniversity of Groningen · NLRadboud University Medical Center · NLRadboud University Nijmegen · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced age is associated with chronic low-grade inflammation, which is usually referred to as inflammaging. Elderly are also known to have an altered gut microbiota composition. However, whether inflammaging is a cause or consequence of an altered gut microbiota composition is not clear. In this study, gut microbiota from young or old conventional mice was transferred to young germ-free (GF) mice. Four weeks after gut microbiota transfer immune cell populations in spleen, Peyer's patches, and mesenteric lymph nodes from conventionalized GF mice were analyzed by flow cytometry. In addition, whole-genome gene expression in the ileum was analyzed by microarray. Gut microbiota composition of donor and recipient mice was analyzed with 16S rDNA sequencing. Here, we show by transferring aged microbiota to young GF mice that certain bacterial species within the aged microbiota promote inflammaging. This effect was associated with lower levels of

Indexed as

aginggerm-free micegut microbiomeimmune systeminflammaging

Identifiers

PMID29163474
PMCPMC5674680
OpenAlexW2765279273

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.