Evidence map›Paper›PMID 38951900›Full record

ArticleAlzheimer's research & therapy2024

Subjective cognitive concerns, APOE ε4, PTSD symptoms, and risk for dementia among older veterans.

Zoe E Neale, Jennifer R Fonda, Mark W Miller, Erika J Wolf, Rui Zhang, Richard Sherva, Kelly M Harrington, Victoria Merritt, Matthew S Panizzon, Richard L Hauger and 3 more

Abstract read
In one paragraph

Article in Alzheimer's research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Review
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.

Zoe E NealeNational Center for PTSD, Behavioral Sciences Division, VA Boston Healthcare System, 150 South Huntington Ave (116B-2), Boston, MA, 02130, USA.
Jennifer R FondaDepartment of Psychiatry, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, 02130, USA.
Mark W MillerNational Center for PTSD, Behavioral Sciences Division, VA Boston Healthcare System, 150 South Huntington Ave (116B-2), Boston, MA, 02130, USA.
Erika J WolfNational Center for PTSD, Behavioral Sciences Division, VA Boston Healthcare System, 150 South Huntington Ave (116B-2), Boston, MA, 02130, USA.
Rui ZhangNational Center for PTSD, Behavioral Sciences Division, VA Boston Healthcare System, 150 South Huntington Ave (116B-2), Boston, MA, 02130, USA.
Richard ShervaBiomedical Genetics, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, 02130, USA.
Kelly M HarringtonDepartment of Psychiatry, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, 02130, USA.
Victoria MerrittCenter of Excellence for Stress and Mental Health, VA San Diego Healthcare System, San Diego, CA, USA.
Matthew S PanizzonDepartment of Psychiatry, University of California, La Jolla, San Diego, CA, USA.
Richard L HaugerCenter of Excellence for Stress and Mental Health, VA San Diego Healthcare System, San Diego, CA, USA.
J Michael GazianoMillion Veteran Program (MVP) Coordinating Center, VA Boston Healthcare System, Boston, MA, USA.
VA Million Veteran Program
Mark W LogueNational Center for PTSD, Behavioral Sciences Division, VA Boston Healthcare System, 150 South Huntington Ave (116B-2), Boston, MA, 02130, USA. loguem@bu.edu.

Funding

The VETSA Longitudinal Twin Study of Cognition and Aging (VETSA 4)R01AG050595 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELMAN, JEREMY A, FRANZ, CAROL ELAINE · 2015 to 2024
$28.0M
Postdoctoral Training Program in Stress and TraumaT32MH019836 · NIMH · TUFTS UNIVERSITY BOSTON · PI DENISE M. SLOAN · 1996 to 2026
$4.7M
Promotion of Angiogenesis in Lung Cancer by MIFR01CA094121 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ARENBERG, DOUGLAS · 2002 to 2010
$1.9M
Molecular regulation of muscle development by Smyd1R01AR072703 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI DU, SHAOJUN · 2018 to 2023
$1.7M
Detection/Dysplastic Epithelium/Gastrointestinal TractR33CA094304 · NCI · UNIVERSITY HOSPITALS OF CLEVELAND · PI SIVAK, MICHAEL V · 2002 to 2004
$1.5M
ROLE OF PROGESTERONE RECEPTOR RATIO IN BREAST CANCERF32CA090073 · NCI · UNIVERSITY OF COLORADO DENVER · PI JACOBSEN, BRITTA M · 2001 to 2003
$127k
BLRD VA I01 BX004192BLRD VA I01 BX005749CSRD VA I01 CX001727CSRD VA IK2 CX002192NCI NIH HHS F32 CA090073NCI NIH HHS R01 CA094121NCI NIH HHS R33 CA094304NIAMS NIH HHS R01 AR072703NIA NIH HHS AG050595NIA NIH HHS R01 AG050595NIMH NIH HHS T32 MH019836NIMH NIH HHS T32MH019836U.S. Department of Veterans Affairs BX004192U.S. Department of Veterans Affairs CX001727U.S. Department of Veterans Affairs IK2CX002192-01A2
6 · The paper itself

Abstract

backgroundPosttraumatic stress disorder (PTSD) and traumatic brain injury (TBI) are associated with self-reported problems with cognition as well as risk for Alzheimer's disease and related dementias (ADRD). Overlapping symptom profiles observed in cognitive disorders, psychiatric disorders, and environmental exposures (e.g., head injury) can complicate the detection of early signs of ADRD. The interplay between PTSD, head injury, subjective (self-reported) cognitive concerns and genetic risk for ADRD is also not well understood, particularly in diverse ancestry groups.

methodsUsing data from the U.S. Department of Veterans Affairs (VA) Million Veteran Program (MVP), we examined the relationship between dementia risk factors (APOE ε4, PTSD, TBI) and subjective cognitive concerns (SCC) measured in individuals of European (n = 140,921), African (n = 15,788), and Hispanic (n = 8,064) ancestry (EA, AA, and HA, respectively). We then used data from the VA electronic medical record to perform a retrospective survival analysis evaluating PTSD, TBI, APOE ε4, and SCC and their associations with risk of conversion to ADRD in Veterans aged 65 and older.

resultsPTSD symptoms (B = 0.50-0.52, p < 1E-250) and probable TBI (B = 0.05-0.19, p = 1.51E-07 - 0.002) were positively associated with SCC across all three ancestry groups. APOE ε4 was associated with greater SCC in EA Veterans aged 65 and older (B = 0.037, p = 1.88E-12). Results of Cox models indicated that PTSD symptoms (hazard ratio [HR] = 1.13-1.21), APOE ε4 (HR = 1.73-2.05) and SCC (HR = 1.18-1.37) were positively associated with risk for ADRD across all three ancestry groups. In the EA group, probable TBI also contributed to increased risk of ADRD (HR = 1.18).

conclusionsThe findings underscore the value of SCC as an indicator of ADRD risk in Veterans 65 and older when considered in conjunction with other influential genetic, clinical, and demographic risk factors.

Indexed as

Apolipoprotein E4DementiaStress Disorders, Post-TraumaticVeteransAgedAged, 80 and overApolipoproteins EBrain Injuries, TraumaticFemaleHumansMaleRetrospective StudiesRisk FactorsUnited StatesApoE protein, humanApolipoprotein E4Apolipoproteins EAPOE ε4DementiaPTSDSurvival analysisTBI

Identifiers

PMID38951900
PMCPMC11218206

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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.