A null mutation in SERPINE1 protects against biological aging in humans
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Humans with a rare gene mutation in SERPINE1 live longer and show evidence of protection from aging-related morbidity.
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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.
- ORCID
- Venue
- Science Advances
- Published
- 2017-11-03
- Volume
- 3
- Issue
- 11
- Pages
- eaao1617-eaao1617
- ISSN
- 2375-2548 (ISSN-L)
- PMC
- PMC5687852
- 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
- gold
- doi.org
- 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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