Evidence map›Paper›PMID 29529168›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2018

Elevated Total Homocysteine in All Participants and Plasma Vitamin B12 Concentrations in Women Are Associated With All-Cause and Cardiovascular Mortality in the Very Old: The Newcastle 85+ Study.

Nuno Mendonça, Carol Jagger, Antoneta Granic, Carmen Martin-Ruiz, John C Mathers, Chris J Seal, Tom R Hill

Open access · hybridAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Excessive vitamin BJournal of eating disorders · 2025
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  4. Article
  5. Article
  6. Emerging Roles of Vitamin BInternational journal of molecular sciences · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Nonlinear associations of serum cobalamin with risk of all-cause and cardiovascular mortality in hypertensive adults.Hypertension research : official journal of the Japanese Society of Hypertension · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Plasma Vitamin BNutrients · 2021
    Article
  20. 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 3 institutions in 1 country.

Nuno MendonçaInstitute of Cellular Medicine, Newcastle upon Tyne, UK.
Carol JaggerNewcastle University Institute for Ageing, Newcastle University, Newcastle upon Tyne, UK.
Antoneta GranicAGE Research Group, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.
Carmen Martin-RuizNewcastle University Institute for Ageing, Newcastle University, Newcastle upon Tyne, UK.
John C MathersInstitute of Cellular Medicine, Newcastle upon Tyne, UK.
Chris J SealInstitute of Cellular Medicine, Newcastle upon Tyne, UK.
Tom R HillInstitute of Cellular Medicine, Newcastle upon Tyne, UK.
Cellular Therapeutics (United Kingdom) · GBNewcastle University · GBNIHR Newcastle Biomedical Research Centre · GB

Funding

Biotechnology and Biological Sciences Research Council G0500997Medical Research Council G0500997Medical Research Council MR/J50001X/1Medical Research Council MR/L016354/1Medical Research Council MR/P020941/1
6 · The paper itself

Abstract

Background: Folate and vitamin B12 are keys to the correct functioning of one-carbon (1-C) metabolism. The current evidence on associations between 1-C metabolism biomarkers and mortality is inconclusive and generally based on younger or institutionalized populations. This study aimed to determine the associations between biomarkers of 1-C metabolism and all-cause and cardiovascular (CVD) mortality in the very old. Methods: The Newcastle 85+ Study is a prospective longitudinal study of participants aged 85 at recruitment living in Northeast England. Baseline red blood cell folate (RBC folate), plasma vitamin B12, and total homocysteine (tHcy) concentrations were available for 752-766 participants. Associations between biomarkers of 1-C metabolism and all-cause and CVD mortality for up to 9 years were assessed by Cox proportional hazard models and confirmed by restricted cubic splines. Results: Participants with higher tHcy concentrations had higher risk of death from any cause (hazard ratio [HR] [×10 μmol/L]: 1.24, 95% confidence interval [CI]: 1.10-1.41) and cardiovascular diseases (HR [×10 μmol/L]: 1.23, 95% CI: 1.04-1.45) than those with lower concentrations; and women with higher plasma vitamin B12 concentrations had increased risk of all-cause and cardiovascular mortality (HR [×100 pmol/L]: 1.10, 95% CI: 1.04-1.16) after adjustment for key sociodemographic, lifestyle, and health confounders. Conclusion: Higher concentrations of tHcy in all participants and plasma vitamin B12 in women were associated with increased risk of all-cause and CVD mortality in the very old. This confirms findings for tHcy in younger populations but the adverse relationships between elevated plasma vitamin B12 concentrations and mortality in this setting are novel and require further investigation.

Indexed as

Cardiovascular DiseasesHomocysteineRisk AssessmentAged, 80 and overAgingBiomarkersCorrelation of DataDemographyErythrocytesFemaleFolic AcidHealth Status DisparitiesHumansMaleRisk FactorsSex FactorsBiomarkersFolic AcidHomocysteineVitamin B 12

Identifiers

PMID29529168
PMCPMC6093381
OpenAlexW2792161139

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.