Evidence map›Paper›PMID 17854483›Full record

ArticleGenome biology2007

Social regulation of gene expression in human leukocytes.

Steve W Cole, Louise C Hawkley, Jesusa M Arevalo, Caroline Y Sung, Robert M Rose, John T Cacioppo

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 392 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
392citing papers in PubMed, 8 pooled it
11.4field-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

392 citing papers in PubMed, 8 syntheses or guidelines pooled it, 732 citations in OpenAlex.

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  7. The Relationship Between Multidimensional Motivation and Endocrine-Related Responses: A Systematic Review.Perspectives on psychological science : a journal of the Association for Psychological Science · 2021
    Pooled it
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  13. Loneliness and Plasma Biomarkers of Neurodegeneration in Community-Dwelling Older Adults: Cross-Sectional and Longitudinal Analyses.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2026
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332 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

6 authors at 2 institutions in 1 country.

Steve W ColeDepartment of Medicine, Division of Hematology-Oncology, UCLA School of Medicine, Los Angeles, CA 90095-1678, USA. coles@ucla.edu
Louise C Hawkley
Jesusa M Arevalo
Caroline Y Sung
Robert M Rose
John T Cacioppo
UCLA Health · USUniversity of California, Los Angeles · US

Funding

Integrative Biology:The Brain, Inflammation/Asthma (RMI)P20RR020645 · NCRR · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI ROSE, ROBERT M. · 2004 to 2006
$1.7M
Combinatorial Genomics in CancerR01CA116778 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COLE, STEVE W · 2006 to 2010
$1.5M
Autonomic nervous system control of HIV-1 replicationR01AI052737 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COLE, STEVE W · 2002 to 2005
$1.1M
NCI NIH HHS R01 CA116778NCRR NIH HHS P20 RR020645NIAID NIH HHS R01 AI052737NIAID NIH HHS R01 AI52737NIA NIH HHS P01 AG19811
6 · The paper itself

Abstract

backgroundSocial environmental influences on human health are well established in the epidemiology literature, but their functional genomic mechanisms are unclear. The present study analyzed genome-wide transcriptional activity in people who chronically experienced high versus low levels of subjective social isolation (loneliness) to assess alterations in the activity of transcription control pathways that might contribute to increased adverse health outcomes in social isolates.

resultsDNA microarray analysis identified 209 genes that were differentially expressed in circulating leukocytes from 14 high- versus low-lonely individuals, including up-regulation of genes involved in immune activation, transcription control, and cell proliferation, and down-regulation of genes supporting mature B lymphocyte function and type I interferon response. Promoter-based bioinformatic analyses showed under-expression of genes bearing anti-inflammatory glucocorticoid response elements (GREs; p = 0.032) and over-expression of genes bearing response elements for pro-inflammatory NF-kappaB/Rel transcription factors (p = 0.011). This reciprocal shift in pro- and anti-inflammatory signaling was not attributable to differences in circulating cortisol levels, or to other demographic, psychological, or medical characteristics. Additional transcription control pathways showing differential activity in bioinformatic analyses included the CREB/ATF, JAK/STAT, IRF1, C/EBP, Oct, and GATA pathways.

conclusionThese data provide the first indication that human genome-wide transcriptional activity is altered in association with a social epidemiological risk factor. Impaired transcription of glucocorticoid response genes and increased activity of pro-inflammatory transcription control pathways provide a functional genomic explanation for elevated risk of inflammatory disease in individuals who experience chronically high levels of subjective social isolation.

Indexed as

Gene Expression RegulationInterpersonal RelationsAgedComputational BiologyC-Reactive ProteinFemaleGenome, HumanGlucocorticoidsHumansLeukocytesMaleMiddle AgedModels, BiologicalPromoter Regions, GeneticSignal TransductionC-Reactive ProteinGlucocorticoids

Identifiers

PMID17854483
PMCPMC2375027
OpenAlexW2170607802

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.