Evidence map›Paper›PMID 37269981›Full record

ArticleCanadian journal of diabetes2023

Age-related Differences in T-cell Subsets and Markers of Subclinical Inflammation in Aging Are Independently Associated With Type 2 Diabetes in the Health and Retirement Study.

Sithara Vivek, Eileen M Crimmins, Anna E Prizment, Helen C S Meier, Ramya Ramasubramanian, Helene Barcelo, Jessica Faul, Bharat Thyagarajan

Abstract read
In one paragraph

Article in Canadian journal of diabetes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. 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

8 authors.

Sithara VivekDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, United States.
Eileen M CrimminsDavis School of Gerontology, University of Southern California, Los Angeles, California, United States.
Anna E PrizmentDivision of Hematology, Oncology and Transplantation, Medical School, University of Minnesota, Minneapolis, Minnesota, United States.
Helen C S MeierInstitute for Social Research, Survey Research Center, University of Michigan, Ann Arbor, Michigan, United States.
Ramya RamasubramanianDivision of Epidemiology and Community Health, University of Minnesota School of Public Health, Minneapolis, Minnesota, United States.
Helene BarceloDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, United States.
Jessica FaulInstitute for Social Research, Survey Research Center, University of Michigan, Ann Arbor, Michigan, United States.
Bharat ThyagarajanDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, United States. Electronic address: thya0003@umn.edu.

Funding

HRS Yrs29-34: Y33 SSA CoFundingU01AG009740 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jessica Faul, KENNETH M LANGA · 1990 to 2026
$555.8M
USC/UCLA Center on Biodemography &Population HealthP30AG017265 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JENNIFER A AILSHIRE, HIRAM BELTRAN-SANCHEZ · 1999 to 2026
$17.9M
Biological Underpinnings of Socioeconomic Differentials in Health and MortalityR01AG060110 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CRIMMINS, EILEEN M · 2018 to 2022
$2.6M
NIA NIH HHS P30 AG017265NIA NIH HHS R01 AG060110NIA NIH HHS U01 AG009740
6 · The paper itself

Abstract

objectivesAge-related changes in adaptive immunity and subclinical inflammation are both important risk factors for diabetes in older adults. We evaluated the independent association between T-cell subsets, subclinical inflammation, and diabetes risk in the Health and Retirement Study (HRS).

methodsWe measured 11 T-cell subsets, 5 pro-inflammatory markers, and 2 anti-inflammatory markers from the 2016 wave of the HRS (baseline). Diabetes/prediabetes status was estimated at the 2016, 2018, and 2020 waves of HRS, based on levels of blood glucose/glycated hemoglobin in plasma or self-reported status. We used survey generalized logit models to evaluate the cross-sectional associations and Cox proportional hazard models to evaluate longitudinal associations.

resultsAmong 8,540 participants (56 to 107 years of age), 27.6% had prevalent type 2 diabetes and 31.1% had prediabetes in the 2016 survey. After adjusting for age, sex, race/ethnicity, education, obesity, smoking, comorbidity index, and cytomegalovirus seropositivity, individuals with type 2 diabetes had lower naive T cells and higher memory and terminal effector T cells as compared with normoglycemic individuals. Among 3,230 normoglycemic participants in the 2016 survey, the incidence of diabetes was 1.8% over 4 years of follow-up. The baseline percentage of CD4

conclusionsThis study showed that the baseline percentage of CD4

Indexed as

Diabetes Mellitus, Type 2Prediabetic StateAgedAgingCross-Sectional StudiesHumansInflammationInterleukin-6RetirementT-Lymphocyte SubsetsInterleukin-6age-related immune phenotypecellules T à mémoirecellules T naïvesCMV seropositivitydiabètediabetesinflammationmemory T cellsnaive T cellsphénotype immunitaire lié à l’âgeséropositivité au CMV

Identifiers

PMID37269981
PMCPMC10592537

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.