Evidence map›Paper›PMID 37614163›Full record

ArticleObesity (Silver Spring, Md.)2023

Visceral adipose microbial and inflammatory signatures in metabolically healthy and unhealthy nonhuman primates.

Alistaire D Ruggiero, Ravichandra Vemuri, Darla DeStephanis, Ashlynn Brock, Masha R Block, Jeff Chou, Swapan K Das, Abigail G Williams, Kylie Kavanagh

Open access · hybridAbstract read
In one paragraph

Article in Obesity (Silver Spring, Md.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 6 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 2 countries.

Alistaire D RuggieroDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0002-1942-2751
Ravichandra VemuriDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Darla DeStephanisDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Ashlynn BrockDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Masha R BlockDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Jeff ChouDepartment of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Swapan K DasDepartment of Endocrinology and Metabolism, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0002-2197-8855
Abigail G WilliamsDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Kylie KavanaghDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0001-8772-6186
Wake Forest University · USUniversity of Tasmania · AU

Funding

Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
Vervet Research Colony as a Biomedical ResourceP40OD010965 · OD · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Matthew Jorgensen · 2012 to 2026
$14.6M
TRAINING PROGRAM IN IMMUNOLOGY AND PATHOGENESIST32AI007401 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Martha Ann Alexander-Miller · 1991 to 2026
$4.4M
Adipose Mitochondial Quality Control and Cardiovascular Function in Metabolically Healthy and Unhealthy Obese MonkeysR01HL142930 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KAVANAGH, KYLIE · 2019 to 2023
$3.4M
NCATS NIH HHS UL1 TR001420NHLBI NIH HHS R01 HL142930NIAID NIH HHS T32 AI007401NIH HHS P40 OD010965
6 · The paper itself

Abstract

objectiveObesity is a key risk factor for metabolic syndrome (MetS); however, >10% of lean individuals meet MetS criteria. Visceral adipose tissue (VAT) disproportionately contributes to inflammation and insulin resistance compared with subcutaneous fat depots. The primary aim of this study was to profile tissue microbiome components in VAT over a wide range of metabolic statuses in a highly clinically relevant model.

methodsVAT was profiled from nonhuman primates that naturally demonstrate four distinct health phenotypes despite consuming a healthy diet, namely metabolically healthy lean and obese and metabolically unhealthy lean and obese.

resultsVAT biopsied from unhealthy lean and obese nonhuman primates demonstrated upregulation of immune signaling pathways, a tissue microbiome enriched in gram-negative bacteria including Pseudomonas, and deficiencies in anti-inflammatory adipose tissue M2 macrophages. VAT microbiomes were distinct from fecal microbiomes, and fecal microbiomes did not differ by metabolic health group, which was in contrast to the VAT bacterial communities.

conclusionsImmune activation with gram-negative VAT microbial communities is a consistent feature in elevated MetS risk in both lean and obesity states.

Indexed as

Metabolic SyndromeObesityAdipose TissueAnimalsBiopsyPrimates

Identifiers

PMID37614163
PMCPMC10783165
OpenAlexW4386117276

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.