Evidence map›Paper›PMID 25452149›Full record

ArticleBrain, behavior, and immunity2015

Endogenous circadian regulation of pro-inflammatory cytokines and chemokines in the presence of bacterial lipopolysaccharide in humans.

Shadab A Rahman, Oscar Castanon-Cervantes, Frank A J L Scheer, Steven A Shea, Charles A Czeisler, Alec J Davidson, Steven W Lockley

Abstract read
In one paragraph

Article in Brain, behavior, and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

57 citing papers in PubMed, 81 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

7 authors at 3 institutions in 1 country.

Shadab A RahmanDivision of Sleep and Circadian Disorders, Department of Medicine, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep and Circadian Disorders, Department of Neurology, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep Medicine, Department of Medicine, Harvard Medical School, 164 Longwood Ave., Boston, MA 02115, United States. Electronic address: sarahman@rics.bwh.harvard.edu.
Oscar Castanon-CervantesNeuroscience Institute, Morehouse School of Medicine, 720 Westview Dr. S.W., Atlanta, GA 30310, United States.
Frank A J L ScheerDivision of Sleep and Circadian Disorders, Department of Medicine, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep and Circadian Disorders, Department of Neurology, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep Medicine, Department of Medicine, Harvard Medical School, 164 Longwood Ave., Boston, MA 02115, United States.
Steven A SheaDivision of Sleep and Circadian Disorders, Department of Medicine, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep and Circadian Disorders, Department of Neurology, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep Medicine, Department of Medicine, Harvard Medical School, 164 Longwood Ave., Boston, MA 02115, United States; Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, 3181 S.W. Sam Jackson Park Rd., Portland, OR 97239, United States.
Charles A CzeislerDivision of Sleep and Circadian Disorders, Department of Medicine, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep and Circadian Disorders, Department of Neurology, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep Medicine, Department of Medicine, Harvard Medical School, 164 Longwood Ave., Boston, MA 02115, United States.
Alec J DavidsonNeuroscience Institute, Morehouse School of Medicine, 720 Westview Dr. S.W., Atlanta, GA 30310, United States.
Steven W LockleyDivision of Sleep and Circadian Disorders, Department of Medicine, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep and Circadian Disorders, Department of Neurology, Brigham and Women's Hospital, 221 Longwood Ave., Boston, MA 02115, United States; Division of Sleep Medicine, Department of Medicine, Harvard Medical School, 164 Longwood Ave., Boston, MA 02115, United States.
Brigham and Women's Hospital · USHarvard University · USOregon Health & Science University · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
Zoledronic Acid in Treatment of Osteoporosis in PostmenoM01RR002635 · NCRR · BRIGHAM AND WOMEN'S HOSPITAL · PI GARBER, JUDY E. · 1985 to 2008
$48.4M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025008 · NCRR · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2007 to 2011
$29.0M
Atlanta Clinical and Translational Science Institute (ACTSI) RenewalUL1TR000454 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$25.8M
TRAINING IN SLEEP, CIRCADIAN &RESPIRATORY NEUROBIOLOGYT32HL007901 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Charles A Czeisler · 1998 to 2026
$18.5M
Training and knowledge transferU54NS060659 · NINDS · MOREHOUSE SCHOOL OF MEDICINE · PI FORD, BYRON D. · 2008 to 2012
$6.9M
Atlanta Clinical and Translational Science Institute (ACTSI) RenewalKL2TR000455 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$2.9M
Atlanta Clinical and Translational Science Institute (KL2)KL2RR025009 · NCRR · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2007 to 2011
$2.9M
Mechanisms underlying adverse health consequences of shift workR01HL094806 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHEER, FRANK A · 2009 to 2013
$1.6M
Chronobiology of cardiovascular and pulmonary diseaseK24HL076446 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SHEA, STEVEN A · 2004 to 2013
$1.5M
Human circadian sensitivity to very short light pulsesRC2HL101340 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI KLERMAN, ELIZABETH B. · 2009 to 2010
$1.3M
Atlanta Clinical and Translational Science Institute (ACTSI) RenewalTL1TR000456 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$1.2M
NCATS NIH HHS KL2 TR000455NCATS NIH HHS TL1 TR000456NCATS NIH HHS UL1 TR000454NCRR NIH HHS KL2 RR025009NCRR NIH HHS M01 RR002635NCRR NIH HHS M01 RR02635NCRR NIH HHS TL1 RR025010NCRR NIH HHS UL1 RR025008NCRR NIH HHS UL1RR025008NCRR NIH HHS UL1 RR025758NCRR NIH HHS UL1RR025758NHLBI NIH HHS 1RC2HL101340-01NHLBI NIH HHS K24 HL076446NHLBI NIH HHS K24-HL076446NHLBI NIH HHS R01 HL094806NHLBI NIH HHS RC2 HL101340NHLBI NIH HHS T32 HL007901NINDS NIH HHS U54 NS060659NINDS NIH HHS U54NS060659
6 · The paper itself

Abstract

Various aspects of immune response exhibit 24-h variations suggesting that infection susceptibility and treatment efficacy may vary by time of day. Whether these 24-h variations are endogenous or evoked by changes in environmental or behavioral conditions is not known. We assessed the endogenous circadian control and environmental and behavioral influences on ex-vivo lipopolysaccharide stimulation of whole blood in thirteen healthy participants under 48h of baseline conditions with standard sleep-wake schedules and 40-50h of constant environmental and behavioral (constant routine; CR) conditions. Significant 24-h rhythms were observed under baseline conditions in Monocyte Chemotactic Protein, Granulocyte-Macrophage Colony-Stimulating Factor and Interleukin 8 but not Tumor Necrosis Factor alpha whereas significant 24-h rhythms were observed in all four immune factors under CR conditions. The rhythm amplitudes, expressed as a percentage of mean, were comparable between immune factors and across conditions. In contrast, the acrophase time (time of the fitted peak) was different between immune factors, and included daytime and nighttime peaks and changes across behavioral conditions. These results suggest that the endogenous circadian system underpins the temporal organization of immune responses in humans with additional effects of external environmental and behavioral cycles. These findings have implications for understanding the adverse effects of recurrent circadian disruption and sleep curtailment on immune function.

Indexed as

AdultChemokine CCL2Circadian RhythmFemaleGranulocyte-Macrophage Colony-Stimulating FactorHumansInterleukin-8LipopolysaccharidesMaleTumor Necrosis Factor-alphaYoung AdultChemokine CCL2Granulocyte-Macrophage Colony-Stimulating FactorInterleukin-8LipopolysaccharidesTumor Necrosis Factor-alphaChemokineCircadianCytokineHumanImmune responseLipopolysaccharideMelatoninSleep

Identifiers

PMID25452149
PMCPMC4430446
OpenAlexW2060074281

What OpenQuestion holds

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LicenceCC BY-NC
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.