Evidence map›Paper›PMID 34889081›Full record

ArticleAnnals of clinical and translational neurology2021

The gut microbiota in pediatric multiple sclerosis and demyelinating syndromes.

Helen Tremlett, Feng Zhu, Douglas Arnold, Amit Bar-Or, Charles N Bernstein, Christine Bonner, Jessica D Forbes, Morag Graham, Janace Hart, Natalie C Knox and 9 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 3 pooled it
3.8field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 3 syntheses or guidelines pooled it, 66 citations in OpenAlex.

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  10. A narrative review of genetic and environmental factors and risk for multiple sclerosis. The design of the Italian multicentric PEDIGREE study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
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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

19 authors at 9 institutions in 2 countries.

Helen TremlettMedicine (Neurology), University of British Columbia and The Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, V6T 1Z3, Canada.ORCID 0000-0001-5804-2535
Feng ZhuMedicine (Neurology), University of British Columbia and The Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, V6T 1Z3, Canada.
Douglas ArnoldThe Montreal Neurological Institute, McGill University, Montreal, Quebec, H3A 2B4, Canada.ORCID 0000-0003-4266-0106
Amit Bar-OrCenter for Neuroinflammation and Experimental Therapeutics and Department of Neurology, Perleman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Charles N BernsteinDepartment of Internal Medicine, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba Inflammatory Bowel Disease Clinical and Research Centre, University of Manitoba, Winnipeg, Manitoba, R3E 3P4, Canada.
Christine BonnerNational Microbiology Laboratory, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, R3E 3R2, Canada.
Jessica D ForbesDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, M5S 1A8, Canada.
Morag GrahamNational Microbiology Laboratory, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, R3E 3R2, Canada.
Janace HartDepartment of Neurology, University of California San Francisco, San Francisco, California, 94158, USA.
Natalie C KnoxNational Microbiology Laboratory, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, R3E 3R2, Canada.
Ruth Ann MarrieDepartment of Internal Medicine, Max Rady College of Medicine, Rady Faculty of Health Sciences, Winnipeg, Manitoba, R3A 1R9, Canada.
Ali I MirzaMedicine (Neurology), University of British Columbia and The Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, V6T 1Z3, Canada.
Julia O'MahonyThe Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
Gary Van DomselaarNational Microbiology Laboratory, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, R3E 3R2, Canada.
E Ann YehThe Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
Yinshan ZhaoMedicine (Neurology), University of British Columbia and The Djavad Mowafaghian Centre for Brain Health, Vancouver, BC, V6T 1Z3, Canada.
Brenda BanwellDivision of Neurology, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Emmanuelle WaubantDepartment of Neurology, University of California San Francisco, San Francisco, California, 94158, USA.ORCID 0000-0001-5188-0157
US Network of Pediatric MS Centers, the Canadian Pediatric Demyelinating Disease Network
Public Health Agency of Canada · CAUniversity of British Columbia · CAUniversity of Toronto · CAUniversity of California, San Francisco · USChildren's Hospital of Philadelphia · USManitoba Health · CAMontreal Neurological Institute and Hospital · CATranslational Therapeutics (United States) · USUniversity of Manitoba · CA

Funding

the Multiple Sclerosis Scientific and Research Foundation 2636
6 · The paper itself

Abstract

objectiveTo examine the gut microbiota in individuals with and without pediatric-onset multiple sclerosis (MS).

methodsWe compared stool-derived microbiota of Canadian Pediatric Demyelinating Disease Network study participants ≤21 years old, with MS (disease-modifying drug [DMD] exposed and naïve) or monophasic acquired demyelinating syndrome [monoADS] (symptom onset <18 years), and unaffected controls. All were ≥30 days without antibiotics or corticosteroids. V4 region 16S RNA gene-derived amplicon sequence variants (Illumina MiSeq) were assessed using negative binomial regression and network analyses; rate ratios were age- and sex-adjusted (aRR).

resultsThirty-two MS, 41 monoADS (symptom onset [mean] = 14.0 and 6.9 years) and 36 control participants were included; 75%/56%/58% were female, with mean ages at stool sample = 16.5/13.8/15.1 years, respectively. Nine MS cases (28%) were DMD-naïve. Although microbiota diversity (alpha, beta) did not differ between participants (p > 0.1), taxa-level and gut community networks did. MS (vs. monoADS) exhibited > fourfold higher relative abundance of the superphylum Patescibacteria (aRR = 4.2;95%CI:1.6-11.2, p = 0.004, Q = 0.01), and lower abundances of short-chain fatty acid (SCFA)-producing Lachnospiraceae (Anaerosporobacter) and Ruminococcaceae (p, Q < 0.05). DMD-naïve MS cases were depleted for Clostridiales vadin-BB60 (unnamed species) versus either DMD-exposed, controls (p, Q < 0.01), or monoADS (p = 0.001, Q = 0.06) and exhibited altered community connectedness (p < 10

interpretationGut microbiota community structure, function and connectivity, and not just individual taxa, are of likely importance in MS.

Indexed as

Gastrointestinal MicrobiomeAdolescentCanadaCase-Control StudiesChildChild, PreschoolCohort StudiesComputational BiologyDemyelinating Autoimmune Diseases, CNSFemaleHumansMaleMultiple SclerosisRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

PMID34889081
PMCPMC8670321
OpenAlexW4200274519

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.