Evidence map›Paper›PMID 33037434›Full record

ReviewThe journals of gerontology. Series A, Biological sciences and medical sciences2021

The Interconnections Between Somatic and Ovarian Aging in Murine Models.

Augusto Schneider, Tatiana D Saccon, Driele N Garcia, Bianka M Zanini, José V V Isola, Jéssica D Hense, Joao A Alvarado-Rincón, Marcelo B Cavalcante, Jeffrey B Mason, Michael B Stout and 2 more

Abstract readReview
In one paragraph

Review in The journals of gerontology. Series A, Biological sciences and medical sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Somatotropic Axis, Pace of Life and Aging.Frontiers in endocrinology · 2022
    Review
  14. Benefits of Living Without Growth Hormone.The journals of gerontology. Series A, Biological sciences and medical sciences · 2021
    Article
  15. Geroscience Approaches to Women's Health in an Aging World.The journals of gerontology. Series A, Biological sciences and medical sciences · 2021
    Article
  16. Growth Hormone and Aging: New Findings.The world journal of men's health · 2021
    Review
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

12 authors.

Augusto SchneiderDepartamento de Nutrição, Faculdade de Nutrição, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.ORCID 0000-0002-3410-2860
Tatiana D SacconDepartamento de Nutrição, Faculdade de Nutrição, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.ORCID 0000-0001-5328-4922
Driele N GarciaDepartamento de Nutrição, Faculdade de Nutrição, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.
Bianka M ZaniniDepartamento de Nutrição, Faculdade de Nutrição, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.
José V V IsolaDepartamento de Nutrição, Faculdade de Nutrição, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.
Jéssica D HenseDepartamento de Nutrição, Faculdade de Nutrição, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.
Joao A Alvarado-RincónDepartamento de Nutrição, Faculdade de Nutrição, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.
Marcelo B CavalcanteFaculdade de Medicina, Universidade de Fortaleza, Ceará, Brazil.ORCID 0000-0001-9943-9731
Jeffrey B MasonDepartment of Animal, Dairy and Veterinary Sciences, Center for Integrated BioSystems, School of Veterinary Medicine, Utah State University, Logan.ORCID 0000-0003-2459-1186
Michael B StoutDepartment of Nutritional Sciences, University of Oklahoma Health Sciences Center.ORCID 0000-0002-9996-9123
Andrzej BartkeDepartments of Internal Medicine and Physiology, Southern Illinois, University School of Medicine, Springfield.
Michal M MasternakCollege of Medicine, Burnett School of Biomedical Sciences, University of Central Florida, Orlando.

Funding

Cellular senescence and epigenomic remodeling in ovarian agingR01AG069742 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI STOUT, MICHAEL B · 2020 to 2024
$2.0M
Mechanisms of metabolic, inflammatory and healthspan enhancement by 17a-estradiolR00AG051661 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI STOUT, MICHAEL B · 2018 to 2020
$746k
Role of adipose tissue cellular composition on healthy metabolismR15AG059190 · NIA · UNIVERSITY OF CENTRAL FLORIDA · PI MASTERNAK, MICHAL MATEUSZ · 2018 to 2020
$444k
Identification of the mechanisms responsible for the ovary-dependent extension of longevity and health spanR15AG061795 · NIA · UTAH STATE UNIVERSITY · PI MASON, JEFFREY B. · 2019 to 2019
$435k
Senescence cells as a source of pro-aging miR-146aR56AG061414 · NIA · UNIVERSITY OF CENTRAL FLORIDA · PI KIRKLAND, JAMES L., MASTERNAK, MICHAL MATEUSZ · 2019 to 2019
$406k
Role of GH/IGF1 signaling pathway on pro-longevity miRNAsR03AG059846 · NIA · UNIVERSITY OF CENTRAL FLORIDA · PI MASTERNAK, MICHAL MATEUSZ · 2018 to 2019
$298k
NIA NIH HHS R00 AG051661NIA NIH HHS R01 AG069742NIA NIH HHS R03 AG059846NIA NIH HHS R15 AG059190NIA NIH HHS R15 AG061795NIA NIH HHS R56 AG061414NIH HHS R01 AG069742
6 · The paper itself

Abstract

The mammalian female is born with a limited ovarian reserve of primordial follicles. These primordial follicles are slowly activated throughout the reproductive lifecycle, thereby determining lifecycle length. Once primordial follicles are exhausted, women undergo menopause, which is associated with several metabolic perturbations and a higher mortality risk. Long before exhaustion of the reserve, females experience severe declines in fertility and health. As such, significant efforts have been made to unravel the mechanisms that promote ovarian aging and insufficiency. In this review, we explain how long-living murine models can provide insights in the regulation of ovarian aging. There is now overwhelming evidence that most life-span-extending strategies, and long-living mutant models simultaneously delay ovarian aging. Therefore, it appears that the same mechanisms that regulate somatic aging may also be modulating ovarian aging and germ cell exhaustion. We explore several potential contributing mechanisms including insulin resistance, inflammation, and DNA damage-all of which are hallmarks of cellular aging throughout the body including the ovary. These findings are in alignment with the disposable soma theory of aging, which dictates a trade-off between growth, reproduction, and DNA repair. Therefore, delaying ovarian aging will not only increase the fertility window of middle age females, but may also actively prevent menopausal-related decline in systemic health parameters, compressing the period of morbidity in mid-to-late life in females.

Indexed as

AgingAnimalsCaloric RestrictionFemaleFertilityMenopauseMiceModels, AnimalOvarian FollicleOvarian ReserveCalorie restrictionFertilityFollicleIGFMenopause

Identifiers

PMID33037434
PMCPMC8361364

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.