Evidence map›Paper›PMID 38260683›Full record

ArticlebioRxiv : the preprint server for biology2024

Late-life dietary folate restriction reduces biosynthetic processes without compromising healthspan in mice.

Heidi M Blank, Staci E Hammer, Laurel Boatright, Courtney Roberts, Katarina E Heyden, Aravindh Nagarajan, Mitsuhiro Tsuchiya, Marcel Brun, Charles D Johnson, Patrick J Stover and 8 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 2 countries.

Heidi M BlankDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0002-2251-5246
Staci E HammerDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0001-5874-5521
Laurel BoatrightDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.
Courtney RobertsDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.
Katarina E HeydenDivision of Nutritional Sciences, Cornell University, Ithaca, United States.
Aravindh NagarajanDepartment of Microbial Pathogenesis and Immunology, School of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID 0000-0001-9613-3729
Mitsuhiro TsuchiyaDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, United States.
Marcel BrunTexas A&M Agrilife Research, Genomics and Bioinformatics Service, College Station, United States.ORCID 0000-0002-6452-5856
Charles D JohnsonTexas A&M Agrilife Research, Genomics and Bioinformatics Service, College Station, United States.
Patrick J StoverDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0002-7546-3814
Raquel SitcheranDepartment of Cell Biology and Genetics, School of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID 0000-0001-8916-9707
Brian K KennedyDepartments of Biochemistry and Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID 0000-0002-5754-1874
L Garry AdamsDepartment of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M, College Station, Texas, USA.ORCID 0000-0002-7246-1602
Matt KaeberleinDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, United States.ORCID 0000-0002-1311-3421
Martha S FieldDivision of Nutritional Sciences, Cornell University, Ithaca, United States.ORCID 0000-0001-7547-5180
David W ThreadgillDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0003-3538-1635
Helene L Andrews-PolymenisDepartment of Microbial Pathogenesis and Immunology, School of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID 0000-0002-1818-1335
Michael PolymenisDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, United States.ORCID 0000-0003-1507-0936
Texas A&M Health Science Center · USTexas A&M University · USCenter for Advancing Health · USCornell University · USUniversity of Washington · USNational University of Singapore · SG

Funding

Coupling Of Protein Synthesis With Cell DivisionR01GM123139 · NIGMS · TEXAS A&M AGRILIFE RESEARCH · PI POLYMENIS, MICHAEL S · 2017 to 2024
$2.9M
Type I Interferon Responses in the Pathobiology of Anthracycline-induced CardiotoxicityR01HL148153 · NHLBI · TEXAS A&M UNIVERSITY · PI John Travis Hinson, Andrew Phillip West · 2020 to 2026
$2.8M
Elucidating the Bacterial and Host Mechanisms Governing B. burgdorferi-Related Type I Interferon ResponsesR21AI153879 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI HYDE, JENNY A. · 2021 to 2022
$409k
NHLBI NIH HHS R01 HL148153NIAID NIH HHS R21 AI153879NIGMS NIH HHS R01 GM123139
6 · The paper itself

Abstract

Folate is a vitamin required for cell growth and is present in fortified foods in the form of folic acid to prevent congenital abnormalities. The impact of low folate status on life-long health is poorly understood. We found that limiting folate levels with the folate antagonist methotrexate increased the lifespan of yeast and worms. We then restricted folate intake in aged mice and measured various health metrics, metabolites, and gene expression signatures. Limiting folate intake decreased anabolic biosynthetic processes in mice and enhanced metabolic plasticity. Despite reduced serum folate levels in mice with limited folic acid intake, these animals maintained their weight and adiposity late in life, and we did not observe adverse health outcomes. These results argue that the effectiveness of folate dietary interventions may vary depending on an individual's age and sex. A higher folate intake is advantageous during the early stages of life to support cell divisions needed for proper development. However, a lower folate intake later in life may result in healthier aging.

Identifiers

PMID38260683
PMCPMC10802571
OpenAlexW4390813055

What OpenQuestion holds

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LicenceCC BY-ND
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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.