Evidence map›Paper›PMID 41432232›Full record

ArticleAging cell2026

Preliminary Evidence for Increased Histone Succinylation as a Potential Epigenetic Marker for Longevity.

Stephanie Stransky, Sarah Graff, Kai Mao, Derek M Huffman, Sofiya Milman, Nir Barzilai, Simone Sidoli

Abstract read
In one paragraph

Article in Aging cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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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.

Stephanie StranskyDepartment of Biochemistry, Albert Einstein College of Medicine, New York, New York, USA.
Sarah GraffDepartment of Biochemistry, Albert Einstein College of Medicine, New York, New York, USA.
Kai MaoDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, New York, New York, USA.
Derek M HuffmanDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, New York, New York, USA.
Sofiya MilmanInstitute for Aging Research, Department of Medicine, Albert Einstein College of Medicine, New York, New York, USA.
Nir BarzilaiInstitute for Aging Research, Department of Medicine, Albert Einstein College of Medicine, New York, New York, USA.
Simone SidoliDepartment of Biochemistry, Albert Einstein College of Medicine, New York, New York, USA.

Funding

Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VIJG, JAN · 2010 to 2024
$10.8M
Somatotropic Signaling and Resilience to Aging and Alzheimer's DiseaseR01AG061155 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI MILMAN, SOFIYA · 2019 to 2023
$4.3M
Orbitrap Exploris 480 Basic SystemS10OD030286 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SIDOLI, SIMONE · 2021 to 2021
$600k
Hevolution Foundation (AFAR)National Institutes of Health (NIH) P30AG038072National Institutes of Health (NIH) R01AG061155NIA NIH HHS P30 AG038072NIA NIH HHS R01 AG061155NIH HHS S10 OD030286NIH Office of the Director S10OD030286
6 · The paper itself

Abstract

Histone post-translational modifications (PTMs) are critical regulators of chromatin structure and gene expression, with broad implications for development, metabolism, and aging. While canonical modifications such as methylation and acetylation are well characterized, the role of histone succinylation remains poorly understood. Here, we investigated histone succinylation in the context of aging and exceptional longevity. Using mass spectrometry-based proteomics, we quantified histone succinylation in B-cells from four groups: young individuals, older individuals without parental longevity (OPUS), long-lived individuals, and offspring of long-lived individuals (OPEL). We found that histone succinylation was significantly elevated in the OPEL group compared to both young and OPUS cohorts. Nuclear proteomics further revealed enrichment of succinylated proteins in OPEL samples, supporting a role for succinylation in chromatin organization. To test whether succinate availability impacts healthspan, we supplemented middle-aged mice with succinic acid. While body weight, frailty index, and cognition were unaffected, succinic acid improved motor coordination and muscle strength. Together, our findings provide preliminary evidence that enhanced histone succinylation may serve as a protective epigenetic mechanism in individuals predisposed to exceptional longevity, and that succinate supplementation can selectively improve aspects of physical performance during aging.

Indexed as

Epigenesis, GeneticHistonesLongevitySuccinic AcidAgedAnimalsBiomarkersFemaleHumansMaleMiceMice, Inbred C57BLProtein Processing, Post-TranslationalBiomarkersHistonesSuccinic Acidagingchromatin modificationsepigeneticshealthspanhistone succinylationlongevityprogeny of long‐lived individuals

Identifiers

PMID41432232
PMCPMC12723716

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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.