Evidence map›Paper›PMID 33685492›Full record

ArticleImmunity & ageing : I & A2021

Age-related differences in monocyte DNA methylation and immune function in healthy Kenyan adults and children.

Katherine R Dobbs, Paula Embury, Emmily Koech, Sidney Ogolla, Stephen Munga, James W Kazura, Arlene E Dent

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 16 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 2 countries.

Katherine R DobbsCenter for Global Health and Diseases, Case Western Reserve University, 10900 Euclid Avenue LC: 4983, Cleveland, OH, 44106, USA.
Paula EmburyCenter for Global Health and Diseases, Case Western Reserve University, 10900 Euclid Avenue LC: 4983, Cleveland, OH, 44106, USA.
Emmily KoechCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Sidney OgollaCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Stephen MungaCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
James W KazuraCenter for Global Health and Diseases, Case Western Reserve University, 10900 Euclid Avenue LC: 4983, Cleveland, OH, 44106, USA.
Arlene E DentCenter for Global Health and Diseases, Case Western Reserve University, 10900 Euclid Avenue LC: 4983, Cleveland, OH, 44106, USA. aed9@case.edu.
Case Western Reserve University · USKenya Medical Research Institute · KERainbow Babies & Children's Hospital · US

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Naturally Acquired Immunity to Malaria during the Epidemiologic Transition in KenR01AI095192 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 2011 to 2015
$3.2M
Epigenetic Reprogramming of Monocyte Functions during Acute Uncomplicated Malaria in Kenyan ChildrenK23AI132644 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI DOBBS, KATHERINE ROSE · 2018 to 2022
$948k
NCATS NIH HHS 4UL1TR000439NCATS NIH HHS UL1 TR000439NIAID NIH HHS K23 AI132644NIAID NIH HHS L40 AI113800NIAID NIH HHS R01 AI095192
6 · The paper itself

Abstract

backgroundAge-related changes in adaptive and innate immune cells have been associated with a decline in effective immunity and chronic, low-grade inflammation. Epigenetic, transcriptional, and functional changes in monocytes occur with aging, though most studies to date have focused on differences between young adults and the elderly in populations with European ancestry; few data exist regarding changes that occur in circulating monocytes during the first few decades of life or in African populations. We analyzed DNA methylation profiles, cytokine production, and inflammatory gene expression profiles in monocytes from young adults and children from western Kenya.

resultsWe identified several hypo- and hyper-methylated CpG sites in monocytes from Kenyan young adults vs. children that replicated findings in the current literature of differential DNA methylation in monocytes from elderly persons vs. young adults across diverse populations. Differentially methylated CpG sites were also noted in gene regions important to inflammation and innate immune responses. Monocytes from Kenyan young adults vs. children displayed increased production of IL-8, IL-10, and IL-12p70 in response to TLR4 and TLR2/1 stimulation as well as distinct inflammatory gene expression profiles.

conclusionsThese findings complement previous reports of age-related methylation changes in isolated monocytes and provide novel insights into the role of age-associated changes in innate immune functions.

Indexed as

AgeingAgingDNA methylationEpigeneticInnate immuneMonocyte

Identifiers

PMID33685492
PMCPMC7938546
OpenAlexW3134269281

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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.