Evidence map›Paper›PMID 26894484›Full record

ArticlePsychoneuroendocrinology2016

PTSD is associated with an increase in aged T cell phenotypes in adults living in Detroit.

Allison E Aiello, Jennifer B Dowd, Bamini Jayabalasingham, Lydia Feinstein, Monica Uddin, Amanda M Simanek, Caroline K Cheng, Sandro Galea, Derek E Wildman, Karestan Koenen and 1 more

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
1.8field-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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

11 authors at 8 institutions in 3 countries.

Allison E AielloDepartment of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. Electronic address: aaiello@email.unc.edu.
Jennifer B DowdCUNY School of Public Health, Hunter College, City University of New York, NY, USA. Electronic address: jdowd@hunter.cuny.edu.
Bamini JayabalasinghamCUNY School of Public Health, Hunter College, City University of New York, NY, USA. Electronic address: baminij@gmail.com.
Lydia FeinsteinDepartment of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. Electronic address: lfeinst@email.unc.edu.
Monica UddinDepartment of Psychology, University of Illinois at Urbana-Champaign, Champaign, IL, USA. Electronic address: muddin@illinois.edu.
Amanda M SimanekJoseph J. Zilber School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, WI, USA. Electronic address: simaneka@uwm.edu.
Caroline K ChengSchool of Public Health, University of Michigan, Ann Arbor, MI, USA. Electronic address: kaiyi@med.umich.edu.
Sandro GaleaBoston University School of Public Health, Boston University, Boston, MA, USA. Electronic address: sgalea@bu.edu.
Derek E WildmanDepartment of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, IL, USA. Electronic address: wildmand@illinois.edu.
Karestan KoenenDepartment of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, MA, USA. Electronic address: kkoenen@hsph.harvard.edu.
Graham PawelecDepartment of Internal Medicine II, Centre for Medical Research, University of Tubingen, Tubingen, Germany. Electronic address: graham.pawelec@uni-tuebingen.de.
City University of New York · USUniversity of Illinois Urbana-Champaign · USUniversity of North Carolina at Chapel Hill · USBoston University · USHarvard University · USUniversity of Michigan · USUniversity of Tübingen · DEUniversity School of Milwaukee · US

Funding

POPULATION STUDIEST32HD007168 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ELIZABETH A FRANKENBERG · 1985 to 2026
$13.8M
Research Services CoreP2CHD050924 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KAREN B GUZZO · 2015 to 2026
$9.6M
Ecologic Stressors, PTSD, and Drug Use in DetroitR01DA022720 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI AIELLO, ALLISON E · 2007 to 2011
$4.7M
Epigenetic Mechanisms of T Cell Dysregulation in PTSDR01AI129788 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI · 2017 to 2021
$2.4M
Infectious Links Between Psychosocial Stress and AgingR01AG040115 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI AIELLO, ALLISON E · 2012 to 2014
$1.7M
Candidate Epigenetic Biomarkers For PTSD: Insights From DetroitRC1MH088283 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI AIELLO, ALLISON E · 2009 to 2010
$995k
NIAID NIH HHS R01 AI129788NIA NIH HHS R01 AG040115NICHD NIH HHS P2C HD050924NICHD NIH HHS T32 HD007168NIDA NIH HHS DA022720-S1NIDA NIH HHS DA22720NIDA NIH HHS R01 DA022720NIMHD NIH HHS L60 MD001300NIMH NIH HHS RC1 MH088283NIMH NIH HHS RC1MH088283
6 · The paper itself

Abstract

backgroundPsychosocial stress is thought to play a key role in the acceleration of immunological aging. This study investigated the relationship between lifetime and past-year history of post-traumatic stress disorder (PTSD) and the distribution of T cell phenotypes thought to be characteristic of immunological aging.

methodsData were from 85 individuals who participated in the community-based Detroit Neighborhood Health Study. Immune markers assessed included the CD4:CD8 ratio, the ratio of late-differentiated effector (CCR7-CD45RA+CD27-CD28-) to naïve (CCR7+CD45RA+CD27+CD28+) T cells, the percentage of KLRG1-expressing cells, and the percentage of CD57-expressing cells.

resultsIn models adjusted for age, gender, race/ethnicity, education, smoking status, and medication use, we found that past-year PTSD was associated with statistically significant differences in the CD8+ T cell population, including a higher ratio of late-differentiated effector to naïve T cells, a higher percentage of KLRG1+ cells, and a higher percentage of CD57+ cells. The percentage of CD57+ cells in the CD4 subset was also significantly higher and the CD4:CD8 ratio significantly lower among individuals who had experienced past-year PTSD. Lifetime PTSD was also associated with differences in several parameters of immune aging.

conclusionsPTSD is associated with an aged immune phenotype and should be evaluated as a potential catalyzer of accelerated immunological aging in future studies.

Indexed as

AdultAgedAged, 80 and overCellular SenescenceFemaleHumansImmunophenotypingMaleMiddle AgedPhenotypeStress Disorders, Post-TraumaticT-Lymphocyte SubsetsYoung AdultAgingDetroitImmunityImmunosenescencePost traumatic stress disorderT cells

Identifiers

PMID26894484
PMCPMC4826331
OpenAlexW2253484288

What OpenQuestion 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 OpenQuestion graph.