Evidence map›Paper›PMID 26406330›Full record

Trial reportPloS one2015

Increase in the Inflammatory Marker GlycA over 13 Years in Young Adults Is Associated with Poorer Cognitive Function in Midlife.

Irit Cohen-Manheim, Glen M Doniger, Ronit Sinnreich, Ely S Simon, Ronit Pinchas-Mizrachi, James D Otvos, Jeremy D Kark

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Title: Human Serum/Plasma Glycoprotein Analysis byJournal of clinical medicine · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. 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

7 authors at 4 institutions in 2 countries.

Irit Cohen-ManheimHebrew University-Hadassah Braun School of Public Health and Community Medicine, Ein Kerem, Jerusalem, 91120, Israel.
Glen M DonigerDepartment of Clinical Research, NeuroTrax Corporation, Modiin, 71711, Israel; Center for Medical Decision Making, Ono Academic College, Kiryat Ono, 55000, Israel.
Ronit SinnreichHebrew University-Hadassah Braun School of Public Health and Community Medicine, Ein Kerem, Jerusalem, 91120, Israel.
Ely S SimonDepartment of Clinical Research, NeuroTrax Corporation, Modiin, 71711, Israel; Department of Neurology, Albert Einstein College of Medicine, the Bronx, New York City, New York, 10461, United States of America.
Ronit Pinchas-MizrachiHebrew University-Hadassah Braun School of Public Health and Community Medicine, Ein Kerem, Jerusalem, 91120, Israel.
James D OtvosLabCorp, Raleigh, North Carolina, 27616, United States of America.
Jeremy D KarkHebrew University-Hadassah Braun School of Public Health and Community Medicine, Ein Kerem, Jerusalem, 91120, Israel.
Hebrew University of Jerusalem · ILAlbert Einstein College of Medicine · USLabCorp (United States) · USOno Academic College · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammatory markers are elevated in patients with dementia. Evidence for an association between inflammation and cognitive function in dementia-free individuals is sparse, inconsistent, and predominantly restricted to the elderly. Assessment of inflammatory markers in young adults as predictors of cognitive function in midlife, well before the onset of overt dementia, is lacking. Furthermore, rarely has the relation with longitudinal change in inflammatory markers been examined.

objectiveTo examine the association of the inflammatory markers C-reactive protein (CRP), fibrinogen, white blood cell count (WBC) and GlycA, a novel NMR-determined biomarker of systemic inflammation, measured in young adulthood and of GlycA change over 13 years follow-up with cognitive function in midlife.

methods507 participants of the Jerusalem Lipid Research Clinic (LRC) study were assessed at 3 time points over 18-22 years. First, the inflammatory variables GlycA, CRP, fibrinogen, and WBC were measured in blood samples drawn at ages 28-32. Then, in blood samples drawn a mean 13 years later (range, 12-16 years) at ages 41-46, GlycA was again measured (in 484 individuals). Subsequently at ages 48-52, on average 7 years later, global cognitive function and its five specific component domains were assessed with a NeuroTrax computerized test battery. Multiple regression and multivariable logistic models were applied.

resultsInverse unadjusted associations were shown for baseline levels and longitudinal change in inflammatory markers and measures of cognition. Multiple regression models were adjusted for age at cognitive assessment, sex, socio-demographic characteristics, baseline measures of leisure-time vigorous activity, smoking status and body mass index (BMI) at ages 28-32, change in smoking status and BMI between ages 28-32 and 41-46, and depression assessed at the time of cognitive testing. The highest quintile of GlycA change, but not the baseline inflammation measures, was inversely related to global cognition (standardized β = -.109, p = .011) as well as to the information processing speed and memory domains (standardized β = -.124, p = .008 and-.117, p = .014, respectively). The multivariable-adjusted odds ratio for low ranked global cognitive function (lowest fifth) comparing the extreme quintiles of GlycA change was 4.8 (95%CI, 1.7-13.5, p = .003; p for trend = .031).

conclusionsIn this longitudinal study of a novel systemic inflammatory marker in a population-based cohort of young adults, GlycA increase over 13 years, but not baseline measures of inflammation, was associated with poorer cognitive function in midlife.

Indexed as

CognitionMagnetic Resonance SpectroscopyModels, BiologicalAdolescentAdultBiomarkersFemaleFollow-Up StudiesHumansInflammation MediatorsMaleMiddle AgedBiomarkersInflammation Mediators

Identifiers

PMID26406330
PMCPMC4583455
OpenAlexW2180978184

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.