Evidence map›Paper›PMID 35704681›Full record

ArticleGut microbes

Gut dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus.

Robert M Clancy, Miranda C Marion, Hannah C Ainsworth, Miao Chang, Timothy D Howard, Peter M Izmirly, Mala Masson, Jill P Buyon, Carl D Langefeld

Open access · goldAbstract read
In one paragraph

Article in Gut microbes. 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
1.7field-weighted citation impact, top 16% 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, 10 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.

Robert M ClancyDepartment of Medicine, Division of Rheumatology, NYU Grossman School of Medicine, New York, NY, USA.
Miranda C MarionDepartment of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Hannah C AinsworthDepartment of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Miao ChangDepartment of Medicine, Division of Rheumatology, NYU Grossman School of Medicine, New York, NY, USA.
Timothy D HowardCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Peter M IzmirlyDepartment of Medicine, Division of Rheumatology, NYU Grossman School of Medicine, New York, NY, USA.
Mala MassonDepartment of Medicine, Division of Rheumatology, NYU Grossman School of Medicine, New York, NY, USA.
Jill P BuyonDepartment of Medicine, Division of Rheumatology, NYU Grossman School of Medicine, New York, NY, USA.
Carl D LangefeldDepartment of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC, USA.
New York University · USWake Forest University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Translational Center of Molecular Profiling in Preclinical and Established Lupus (COMPEL)P50AR070591 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUYON, JILL P · 2017 to 2021
$6.7M
Genetics and the Microbiome in Anti-Ro Preclinical and Established AutoimmunityR21AR071106 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUYON, JILL P, LANGEFELD, CARL D · 2017 to 2018
$406k
NCI NIH HHS P30 CA016087NIAMS NIH HHS P50 AR070591NIAMS NIH HHS R21 AR071106
6 · The paper itself

Abstract

Anti-SSA/Ro antibodies, while strongly linked to fetal cardiac injury and neonatal rash, can associate with a spectrum of disease in the mother, ranging from completely asymptomatic to overt Systemic Lupus Erythematosus (SLE) or Sjögren's Syndrome (SS). This study was initiated to test the hypothesis that the microbiome, influenced in part by genetics, contributes to disease state. The stool microbiome of healthy controls (HC) was compared to that of anti-SSA/Ro positive women whose children had neonatal lupus. At the time of sampling, these women were either asymptomatic (Asym), had minor rheumatic symptoms or signs considered as an undifferentiated autoimmune syndrome (UAS), or were diagnosed with SLE or SS. Differences in microbial relative abundances among these three groups were tested assuming an ordering in clinical severity (HC<Asym/UAS<SS/SLE) and then again without the ordinal assumption. Those taxa that showed differential relative abundances were then tested for whether the effect size differed depending on the women's HLA SLE-risk allele genotype (DRB1*03:01, DRB1*15:01, DQB1*02:01 and DQB1*06:02) or anti-SSA/Ro autoantibody levels. Multiple genera within the families

Indexed as

Gastrointestinal MicrobiomeLupus Erythematosus, SystemicSjogren's SyndromeChildDysbiosisFemaleHumansInfant, NewbornMothersAutoantibodiesautoimmunityhumanmicrobiome

Identifiers

PMID35704681
PMCPMC9225419
OpenAlexW4282963484

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.