Cited by 160Genetics, Aging, and Longevity in Model OrganismsTelomeres, Telomerase, and SenescenceGenetic Associations and Epidemiology

A null mutation in SERPINE1 protects against biological aging in humans

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Khan, Sadiya S., Shah, Sanjiv J., Klyachko, Ekaterina, Baldridge, Abigail S., Eren, Mesut, Place, Aaron T., Aviv, Abraham, Puterman, Eli +6 more·2017·Science Advances

Abstract

Humans with a rare gene mutation in SERPINE1 live longer and show evidence of protection from aging-related morbidity.

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Crossref · 10.1126/sciadv.aao1617

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  • Genes that regulate lifespan in animal models and human studies, and multiple experimental paradigms, have demonstrated that it is possible to manipulate ageing biology to rejuvenate physiological functioning in complex model organisms.

    “Genes that regulate lifespan in animal models6–9 and human studies10–14 as well as multiple experimental paradigms, such as caloric restriction, heterochronic parabiosis and partial epigenetic reprogramming, have demonstrated that it is possible to manipulate ageing biology to ‘rejuvenate’ physiological functioning in complex model organisms15–28.”

    From Measuring biological age using omics data (2022) · cites this paper as [13]

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Authors
Khan, S. S., Shah, S. J., Klyachko, E., Baldridge, A. S., Eren, M., Place, A. T., Aviv, A., Puterman, E., Lloyd-Jones, D. M., Heiman, M., Miyata, T., Gupta, S., Shapiro, A. D., & Vaughan, D. E.
Affiliations
  • Northwestern University (US)
  • Rutgers New Jersey Medical School (US)
  • University of British Columbia (CA)
  • Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
  • Indiana Hemophilia and Thrombosis Center (US)
  • Tohoku University (JP)
Corresponding author
  • Khan, Sadiya S.
  • Shah, Sanjiv J.
  • Vaughan, Douglas E.
Venue
Science Advances
Published
2017-11-03
Volume
3
Issue
11
Pages
eaao1617-eaao1617
ISSN
2375-2548 (ISSN-L)
OpenAlex
W2768485358
Cited by
157
References
65
Citations by year
2026: 17 · 2025: 22 · 2024: 18 · 2023: 16 · 2022: 11 · 2021: 24 · 2020: 21 · 2019: 15 · 2018: 12 · 2017: 1
FWCI
5.70
Type
journal article
Language
en
Open access
Licence
cc-by-nc
Locations
  • Science Advances (publishedVersion, cc-by-nc)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • Rutgers University Community Repository (Rutgers University) (submittedVersion)
Funders
  • National Institutes of Health (award336021, F32 HL129695, award351840, R01 HL107577, award351841, R01 HL127028, award352250, R01 HL051387, award353576, R01HD071180, award353577, R01HL116446, award353578, R01HL134840)
  • National Institute on Aging (award353156, (CARDIA) AG0005)
  • National Heart, Lung, and Blood Institute (award353150, (CARDIA) University of Alabama, Birmingham, HHSN268201300025C, award353151, (CARDIA) University of Alabama, Birmingham, HHSN268201300026C, award353152, (CARDIA) Northwestern University, HHSN268201300027C, award353153, (CARDIA) University of Minnesota, HHSN268201300028C, award353154, (CARDIA) Kaiser Foundation Research Institute, HHSN268201300029C, award353155, (CARDIA) Johns Hopkins University School of Medicine, HHSN268200900041C)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
Keywords
SERPINE1, plasminogen activator inhibitor-1, null mutations, loss-of-function mutations, biological aging, longevity, leukocyte telomere length, fasting insulin, diabetes mellitus, genetic isolation
MeSH terms
Adult, Aged, Alleles, Female, Genotype, Heterozygote, Humans, Insulin, Leukocytes, Longevity, Male, Middle Aged, Pedigree, Telomere, Plasminogen Activator Inhibitor 1, Amish

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