Evidence map›Paper›PMID 31603943›Full record

ArticlePloS one2019

Correlates of longitudinal leukocyte telomere length in the Costa Rican Longevity Study of Healthy Aging (CRELES): On the importance of DNA collection and storage procedures.

Luis Rosero-Bixby, David H Rehkopf, William H Dow, Jue Lin, Elissa S Epel, Jorge Azofeifa, Alejandro Leal

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

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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

7 authors at 4 institutions in 2 countries.

Luis Rosero-BixbyCentro Centroamericano de Población, Universidad de Costa Rica, San Jose, Costa Rica.ORCID 0000-0002-3063-3111
David H RehkopfSchool of Medicine, Division of Primary Care and Population Health, Stanford University, Stanford, CA, United States of America.
William H DowHealth Policy and Management, University of California Berkeley, Berkeley, CA, United States of America.
Jue LinBiochemistry and Biophysics, University of California San Francisco, San Francisco, CA, United States of America.
Elissa S EpelPsychiatry, University of California San Francisco, San Francisco, CA, United States of America.
Jorge AzofeifaEscuela de Biología, Universidad de Costa Rica, San Jose, Costa Rica.
Alejandro LealEscuela de Biología, Universidad de Costa Rica, San Jose, Costa Rica.
Universidad de Costa Rica · CRUniversity of California, San Francisco · USStanford University · USUniversity of California, Berkeley · US

Funding

Program Development (Pilot)P30AG012839 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI William H Dow · 1999 to 2026
$18.6M
Costa Rican Health and Retirement SurveyR01AG031716 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI DOW, WILLIAM H. · 2008 to 2012
$1.6M
Life course contexts and work - quantifying impacts on aging and chronic diseaseK01AG047280 · NIA · STANFORD UNIVERSITY · PI REHKOPF, DAVID H · 2014 to 2018
$632k
NIA NIH HHS K01 AG047280NIA NIH HHS P30 AG012839NIA NIH HHS R01 AG031716Wellcome TrustWellcome Trust 072406/Z/03/Z
6 · The paper itself

Abstract

The objective is to identify cofactors of leukocyte telomere length (LTL) in a Latin American population, specifically the association of LTL with 36 socio-demographic, early childhood, and health characteristics, as well as with DNA sample collection and storage procedures. The analysis is based on longitudinal information from a subsample of 1,261 individuals aged 60+ years at baseline from the Costa Rican Study of Longevity and Healthy Aging (CRELES): a nationally representative sample of elderly population. Random effects regression models for panel data were used to estimate the associations with LTL and its longitudinal changes. Sample collection procedures and DNA refrigerator storage time were strongly associated with LTL: telomeres are longer in blood collected in October-December, in DNA extracted from <1-year-old blood cells, and in DNA stored at 4°C for longer periods of time up to five years. The data confirmed that telomeres are shorter at older ages, as well as among males, and diabetic individuals, whereas telomeres are longer in the high-longevity Nicoya region. Most health, biomarkers, and early childhood indicators did not show significant associations with LTL. Longitudinal LTL variation over approximately two years was mainly associated with baseline LTL levels, as found in other studies. Our findings suggest that if there is unavoidable variability in season of sample collection and DNA storage time, these factors should be controlled for in all demographic and epidemiologic studies of LTL. However, due to unobserved components of measurement variation, statistical control may be inadequate as compared to standardization of data collection procedures.

Indexed as

LongevityAgedBlood Specimen CollectionCosta RicaDNAFemaleHealthy AgingHumansLeukocytesLongitudinal StudiesMaleMiddle AgedRegression AnalysisTelomereTelomere HomeostasisTime FactorsDNA

Identifiers

PMID31603943
PMCPMC6788698
OpenAlexW2979602627

What OpenQuestion holds

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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.