Evidence map›Paper›PMID 32438247›Full record

ArticlePsychoneuroendocrinology2020

PTSD and the klotho longevity gene: Evaluation of longitudinal effects on inflammation via DNA methylation.

Erika J Wolf, Mark W Logue, Xiang Zhao, Nikolaos P Daskalakis, Filomene G Morrison, Shaline Escarfulleri, Annjanette Stone, Steven A Schichman, Regina E McGlinchey, William P Milberg and 3 more

Open access · greenAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Role of Klotho Protein in Neuropsychiatric Disorders: A Narrative Review.Indian journal of clinical biochemistry : IJCB · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
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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

13 authors at 5 institutions in 1 country.

Erika J WolfNational Center for PTSD at VA Boston Healthcare System, United States; Department of Psychiatry, Boston University School of Medicine, United States. Electronic address: Erika.Wolf@va.gov.
Mark W LogueNational Center for PTSD at VA Boston Healthcare System, United States; Department of Psychiatry, Boston University School of Medicine, United States; Biomedical Genetics, Boston University School of Medicine, United States.
Xiang ZhaoNational Center for PTSD at VA Boston Healthcare System, United States; Department of Psychiatry, Boston University School of Medicine, United States.
Nikolaos P DaskalakisDepartment of Psychiatry, Harvard Medical School, McLean Hospital, United States.
Filomene G MorrisonNational Center for PTSD at VA Boston Healthcare System, United States; Department of Psychiatry, Boston University School of Medicine, United States.
Shaline EscarfulleriNational Center for PTSD at VA Boston Healthcare System, United States.
Annjanette StonePharmacogenomics Analysis Laboratory, Research Service, Central Arkansas Veterans Healthcare System, United States.
Steven A SchichmanPharmacogenomics Analysis Laboratory, Research Service, Central Arkansas Veterans Healthcare System, United States.
Regina E McGlincheyGeriatric Research Educational and Clinical Center and Translational Research Center for TBI and Stress Disorders, VA Boston Healthcare System, United States; Department of Psychiatry, Harvard Medical School, United States.
William P MilbergGeriatric Research Educational and Clinical Center and Translational Research Center for TBI and Stress Disorders, VA Boston Healthcare System, United States; Department of Psychiatry, Harvard Medical School, United States.
Cidi ChenDepartment of Biochemistry, Boston University School of Medicine, United States.
Carmela R AbrahamDepartment of Biochemistry, Boston University School of Medicine, United States; Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, United States.
Mark W MillerNational Center for PTSD at VA Boston Healthcare System, United States; Department of Psychiatry, Boston University School of Medicine, United States.
University School · USHarvard University · USBoston University · USCentral Arkansas Veterans Healthcare System · USNational Center for PTSD · US

Funding

Postdoctoral Training Program in Stress and TraumaT32MH019836 · NIMH · TUFTS UNIVERSITY BOSTON · PI DENISE M. SLOAN · 1996 to 2026
$4.7M
Neuroimaging Genetics of PTSDR21MH102834 · NIMH · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MILLER, MARK W · 2014 to 2015
$355k
Traumatic Stress and Accelerated Aging in DNA MethylationR03AG051877 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WOLF, ERIKA J · 2016 to 2017
$179k
PTSD-Related Accelerated Aging in DNA Methylation and Risk for Metabolic SyndromeI01CX001276 · VA · VA BOSTON HEALTH CARE SYSTEM · PI WOLF, ERIKA J · 2016 to 2021
–
Translational Research Center for Traumatic Brain Injury and Stress Disorders (TRACTS)I50RX003001 · VA · VA BOSTON HEALTH CARE SYSTEM · PI Ricardo E. Jorge, WILLIAM P MILBERG · 2018 to 2026
–
CSRD VA I01 CX001276NIA NIH HHS R03 AG051877NIMH NIH HHS R21 MH102834NIMH NIH HHS T32 MH019836RRD VA I50 RX003001
6 · The paper itself

Abstract

backgroundLongevity gene klotho (KL) is associated with age-related phenotypes including lifespan, cardiometabolic disorders, cognition, and brain morphology, in part, by conferring protection against inflammation. We hypothesized that the KL/inflammation association might be altered in the presence of psychiatric stress and operate via epigenetic pathways. We examined KL polymorphisms, and their interaction with posttraumatic stress disorder (PTSD) symptoms, in association with KL DNA methylation in blood. We further examined KL DNA methylation as a predictor of longitudinal changes in a peripheral biomarker of inflammation (C-reactive protein; CRP).

methodsThe sample comprised 309 white non-Hispanic military veterans (93.5 % male; mean age: 32 years, range: 19-65; 30 % PTSD per structured diagnostic interview); 111 were reassessed approximately two years later.

resultsAnalyses revealed a methylation quantitative trait locus at rs9527025 (C370S, previously implicated in numerous studies of aging) in association with a Cytosine-phosphate-Guanine site (cg00129557; B = -.65, p =  1.29 X 10

conclusionsResults contribute to our understanding of the epigenetic correlates of inflammation in PTSD and suggest that KL methylation may be a mechanism by which KL genotype confers risk vs. resilience to accelerated aging in those experiencing traumatic stress.

Indexed as

Aging, PrematureInflammationStress Disorders, Post-TraumaticAdultAgedBiomarkersC-Reactive ProteinDNA MethylationEpigenesis, GeneticFemaleGene-Environment InteractionGenetic Predisposition to DiseaseGlucuronidaseHumansKlotho ProteinsLongevityBiomarkersC-Reactive ProteinGlucuronidaseKlotho ProteinsAccelerated agingInflammationKlothoMethylationPTSD

Identifiers

PMID32438247
PMCPMC7293549
OpenAlexW3016890173

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.