Evidence map›Paper›PMID 19564875›Full record

ArticleInternational journal of obesity (2005)2009

Depot-specific differences in inflammatory mediators and a role for NK cells and IFN-gamma in inflammation in human adipose tissue.

R W O'Rourke, M D Metcalf, A E White, A Madala, B R Winters, I I Maizlin, B A Jobe, C T Roberts, M K Slifka, D L Marks

Abstract read
In one paragraph

Article in International journal of obesity (2005), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

104 citing papers in PubMed, 196 citations in OpenAlex.

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  5. Total and abdominal adiposity are associated with inflammation in older adults using a factor analysis approach.The journals of gerontology. Series A, Biological sciences and medical sciences · 2012
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  16. TetraSODNutrients · 2022
    Article
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44 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

10 authors at 2 institutions in 1 country.

R W O'RourkeDepartment of Surgery, Oregon Health and Science University, Portland, OR 97239-3098, USA. orourkro@ohsu.edu
M D Metcalf
A E White
A Madala
B R Winters
I I Maizlin
B A Jobe
C T Roberts
M K Slifka
D L Marks
Oregon Health & Science University · USUniversity of Pittsburgh · US

Funding

YR 50 PROJ- ROBERTS PRIMATE ISLETP51RR000163 · NCRR · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI FRUH, KLAUS J · 1985 to 2011
$140.8M
OREGON CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024140 · NCRR · OREGON HEALTH & SCIENCE UNIVERSITY · PI ORWOLL, ERIC S. · 2006 to 2011
$61.1M
Hypothalamic Mechanisms in CachexiaR01DK070333 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI MARKS, DANIEL L. · 2004 to 2013
$2.6M
Cytokine-mediated T cell activationR01AI054458 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI SLIFKA, MARK K · 2004 to 2008
$1.6M
Oregon Clinical and Translational Science InstituteTL1RR024159 · NCRR · OREGON HEALTH & SCIENCE UNIVERSITY · PI ORWOLL, ERIC S. · 2006 to 2011
$852k
LIGHT and Adipose Tissue Inflammation in Human ObesityK08DK074397 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI O'ROURKE, ROBERT W · 2008 to 2012
$744k
Screening for Barrett's in Otolaryngology PatientsK23DK066165 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOBE, BLAIR ANDERSON · 2004 to 2008
$666k
REPRODUCTIVE STEROIDS AND EXPERIMENTAL STROKEK01RR000163 · NCRR · OREGON HEALTH AND SCIENCE UNIVERSITY · PI MURPHY, STEPHANIE J · 2000 to 2004
$479k
The Prevalence of Barrett's Esophagus in Patients with *R03CA105959 · NCI · OREGON HEALTH AND SCIENCE UNIVERSITY · PI JOBE, BLAIR ANDERSON · 2003 to 2004
$151k
NCI NIH HHS R03 CA105959NCRR NIH HHS K01 RR000163NCRR NIH HHS P51 RR000163NCRR NIH HHS RR00163NCRR NIH HHS TL1 RR024159NCRR NIH HHS UL1 RR024140NIAID NIH HHS AI054458NIAID NIH HHS R01 AI054458NIDDK NIH HHS K08 DK074397NIDDK NIH HHS K23 DK066165NIDDK NIH HHS R01 DK070333
6 · The paper itself

Abstract

backgroundAdipose tissue is a primary in vivo site of inflammation in obesity. Excess visceral adipose tissue (VAT), when compared to subcutaneous adipose tissue (SAT), imparts an increased risk of obesity-related comorbidities and mortality, and exhibits differences in inflammation. Defining depot-specific differences in inflammatory function may reveal underlying mechanisms of adipose-tissue-based inflammation.

methodsStromovascular cell fractions (SVFs) from VAT and SAT from obese humans undergoing bariatric surgery were studied in an in vitro culture system with transcriptional profiling, flow cytometric phenotyping, enzyme-linked immunosorbent assay and intracellular cytokine staining.

resultsTranscriptional profiling of SVF revealed differences in inflammatory transcript levels in VAT relative to SAT, including elevated interferon-gamma (IFN-gamma) transcript levels. VAT demonstrated a broad leukocytosis relative to SAT that included macrophages, T cells and natural killer (NK) cells. IFN-gamma induced a proinflammatory cytokine expression pattern in SVF and adipose tissue macrophages (ATM). NK cells, which constitutively expressed IFN-gamma, were present at higher frequency in VAT relative to SAT. Both T and NK cells from SVF expressed IFN-gamma on activation, which was associated with tumor necrosis factor-alpha expression in macrophages.

conclusionThese data suggest involvement of NK cells and IFN-gamma in regulating ATM phenotype and function in human obesity and a potential mechanism for the adverse physiologic effects of VAT.

Indexed as

AdultBariatric SurgeryFemaleGene Expression RegulationHumansImmunohistochemistryInflammation MediatorsInterferon-gammaIntra-Abdominal FatKiller Cells, NaturalObesityPanniculitisSubcutaneous FatInflammation MediatorsInterferon-gamma

Identifiers

PMID19564875
PMCPMC3150185
OpenAlexW2080640170

What OpenQuestion holds

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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.