Evidence map›Paper›PMID 38753229›Full record

ArticleGeroScience2024

Clinical biomarker-based biological age predicts deaths in Brazilian adults: the ELSA-Brasil study.

Amanda Viana Machado, Juliana Freitas de Mello E Silva, Enrico Antônio Colosimo, Belinda L Needham, Chams Bicalho Maluf, Luana Giatti, Lidyane V Camelo, Sandhi Maria Barreto

Abstract read
In one paragraph

Article in GeroScience, 2024. 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. Article
  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.

Amanda Viana MachadoPostgraduate Program in Public Health, School of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0001-5879-9466
Juliana Freitas de Mello E SilvaCenter of Data Integration and Knowledge for Healthcare, Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.ORCID 0000-0002-9020-8811
Enrico Antônio ColosimoDepartment of Statistics, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0001-8705-4674
Belinda L NeedhamDepartment of Epidemiology and Center for Social Epidemiology and Population Health, University of Michigan, Ann Arbor, USA.ORCID 0000-0001-5939-2027
Chams Bicalho MalufDepartment of Clinic Pathology, School of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0002-3690-2554
Luana GiattiSchool of Medicine & Clinical Hospital, Universidade Federal de Minas Gerais, Avenida Professor, Alfredo Balena, 190, Belo Horizonte, Minas Gerais, CEP, 30130-100, Brazil.ORCID 0000-0001-5454-2460
Lidyane V CameloSchool of Medicine & Clinical Hospital, Universidade Federal de Minas Gerais, Avenida Professor, Alfredo Balena, 190, Belo Horizonte, Minas Gerais, CEP, 30130-100, Brazil.ORCID 0000-0001-7471-7547
Sandhi Maria BarretoSchool of Medicine & Clinical Hospital, Universidade Federal de Minas Gerais, Avenida Professor, Alfredo Balena, 190, Belo Horizonte, Minas Gerais, CEP, 30130-100, Brazil. sandhi.barreto@gmail.com.ORCID 0000-0001-7383-7811

Funding

Brazilian Ministry of Health (Department of Science and Technology) and the Brazilian Ministry of Science, Technology and Innovation (FINEP, Financiadora de Estudos e Projetos and CNPq, National Research Council) 01 06 0071.00Brazilian Ministry of Health (Department of Science and Technology) and the Brazilian Ministry of Science, Technology and Innovation (FINEP, Financiadora de Estudos e Projetos and CNPq, National Research Council) 01 06 0115.00Brazilian Ministry of Health (Department of Science and Technology) and the Brazilian Ministry of Science, Technology and Innovation (FINEP, Financiadora de Estudos e Projetos and CNPq, National Research Council) 01 06 0212.00Brazilian Ministry of Health (Department of Science and Technology) and the Brazilian Ministry of Science, Technology and Innovation (FINEP, Financiadora de Estudos e Projetos and CNPq, National Research Council) 01 06 0278.00Brazilian Ministry of Health (Department of Science and Technology) and the Brazilian Ministry of Science, Technology and Innovation (FINEP, Financiadora de Estudos e Projetos and CNPq, National Research Council) 01 06 0300.00Brazilian Ministry of Health (Department of Science and Technology) and the Brazilian Ministry of Science, Technology and Innovation (FINEP, Financiadora de Estudos e Projetos and CNPq, National Research Council) Grant No 01 06 0010.00Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001
6 · The paper itself

Abstract

Biological age is a construct that seeks to evaluate the biological wear and tear process of the organism that cannot be observed by chronological age. We estimate individuals' biological age based on biomarkers from multiple systems and validate it through its association with mortality from natural causes. Biological age was estimated in 12,109 participants (6621 women and 5488 men) from the first visit of the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil) who had valid data for the biomarkers used in the analyses. Biological age was estimated using the Klemera and Doubal method. The difference between chronological age and biological age (Δage) was computed. Cox proportional hazard models stratified by sex were used to assess whether Δage was associated with mortality risk after a median follow-up of 9.1 years. The accuracy of the models was estimated by the area under the curve (AUC). Δage had equal mean for men and women, with greater variability for men. Cox models showed that every 1-year increase in Δage was associated with increased mortality in men (HR (95% CI) 1.21; 1.17-1.25) and women (HR (95% CI) 1.24; 1.15-1.34), independently of chronological age. Results of the AUC demonstrated that the predictive power of models that only included chronological age (AUC chronological age = 0.7396) or Δage (AUC Δage = 0.6842) was lower than those that included both, chronological age and Δage (AUC chronological age + Δage = 0.802), in men. This difference was not observed in women. We demonstrate that biological age is strongly related to mortality in both genders and is a valid predictor of death in Brazilian adults, especially among men.

Indexed as

AgingBiomarkersProportional Hazards ModelsAdultAgedBrazilFemaleHumansLongitudinal StudiesMaleMiddle AgedMortalityBiomarkersAgingBiological ageKlemera and Doubal methodMortality

Identifiers

PMID38753229
PMCPMC11494676

What OpenQuestion holds

Textmetadata
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.