Evidence map›Paper›PMID 27840811›Full record

ArticleFrontiers in public health2016

Classification for Longevity Potential: The Use of Novel Biomarkers.

Marian Beekman, Hae-Won Uh, Diana van Heemst, Manfred Wuhrer, L Renee Ruhaak, Vanessa Gonzalez-Covarrubias, Thomas Hankemeier, Jeanine J Houwing-Duistermaat, P Eline Slagboom

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Article in Frontiers in public health, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-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

6 citing papers in PubMed, 10 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

9 authors at 4 institutions in 4 countries.

Marian BeekmanMolecular Epidemiology, Leiden University Medical Center , Leiden , Netherlands.
Hae-Won UhMedical Statistics and Bioinformatics, Leiden University Medical Center , Leiden , Netherlands.
Diana van HeemstGerontology and Geriatrics, Leiden University Medical Center , Leiden , Netherlands.
Manfred WuhrerCenter for Proteomics and Metabolomics, Leiden University Medical Center , Leiden , Netherlands.
L Renee RuhaakCenter for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, Netherlands; Department of Translational Molecular Pathology, MD Anderson Cancer Center, Houston, TX, USA.
Vanessa Gonzalez-CovarrubiasAnalytical Biosciences, Leiden Academic Centre for Drug Research, Leiden, Netherlands; Instituto Nacional de Medicina Genomica (INMEGEN), Mexico City, Mexico.
Thomas HankemeierAnalytical Biosciences, Leiden Academic Centre for Drug Research, Leiden, Netherlands; Netherlands Metabolomics Centre, Leiden, Netherlands.
Jeanine J Houwing-DuistermaatMedical Statistics and Bioinformatics, Leiden University Medical Center , Leiden , Netherlands.
P Eline SlagboomMolecular Epidemiology, Leiden University Medical Center , Leiden , Netherlands.
Leiden University Medical Center · NLNational Institute of Genomic Medicine · MXNetherlands Metabolomics Centre · NLThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn older people, chronological age may not be the best predictor of residual lifespan and mortality, because with age the heterogeneity in health is increasing. Biomarkers for biological age and residual lifespan are being developed to predict disease and mortality better at an individual level than chronological age. In the current paper, we aim to classify a group of older people into those with longevity potential or controls.

methodsIn the Leiden Longevity Study participated 1671 offspring of nonagenarian siblings, as the group with longevity potential, and 744 similarly aged controls. Using known risk factors for cardiovascular disease, previously reported markers for human longevity and other physiological measures as predictors, classification models for longevity potential were constructed with multiple logistic regression of the offspring-control status.

resultsThe Framingham Risk Score (FRS) is predictive for longevity potential [area under the receiver operating characteristic curve (AUC) = 64.7]. Physiological parameters involved in immune responses and glucose, lipid and energy metabolism further improve the prediction performance for longevity potential (AUCmale = 71.4, AUCfemale = 68.7).

conclusionUsing the FRS, the classification of older people in groups with longevity potential and controls is moderate, but can be improved to a reasonably good classification in combination with markers of immune response, glucose, lipid, and energy metabolism. We show that individual classification of older people for longevity potential may be feasible using biomarkers from a wide variety of different biological processes.

Indexed as

biomarkerclassification and predictionFramingham Risk Scorehuman longevity potentialsex-specific analysis

Identifiers

PMID27840811
PMCPMC5083840
OpenAlexW2539844934

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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.