Evidence map›Paper›PMID 21683476›Full record

ArticleNeurobiology of aging2012

Perimenopausal regulation of steroidogenesis in the nonhuman primate.

Krystina G Sorwell, Steven G Kohama, Henryk F Urbanski

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% of its field
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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Brain-derived estrogen and neural function.Neuroscience and biobehavioral reviews · 2022
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

3 authors at 2 institutions in 1 country.

Krystina G SorwellDivision of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, USA.
Steven G Kohama
Henryk F Urbanski
Oregon National Primate Research Center · USOregon Health & Science University · US

Funding

YR 50 PROJ- ROBERTS PRIMATE ISLETP51RR000163 · NCRR · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI PICKER, LOUIS J. · 1985 to 2011
$140.8M
VASOACTIVE FACTORS IN ART CYCLES AND OVARIAN HYPERSTIMULATION SYNDROMEU54HD018185 · NICHD · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI STOUFFER, RICHARD L · 1999 to 2010
$13.8M
Cognition in Rhesus Macaques in Relation to Age and Endocrine StatusR01AG036670 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI URBANSKI, HENRYK F · 2011 to 2015
$3.2M
Interacting Impact of Adrenal and Ovarian Aging on the CNSR01AG029612 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI URBANSKI, HENRYK F · 2007 to 2011
$2.4M
Neuroscience of AgingT32AG023477 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI URBANSKI, HENRYK F · 2005 to 2015
$2.4M
Postnatal Development of Ionotropic Glutamate ReceptorsR01HD029186 · NICHD · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI URBANSKI, HENRYK F · 1993 to 2006
$1.2M
Interacting Impact of Adrenal and Ovarian Aging on the CNSR56AG029612 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI URBANSKI, HENRYK F · 2018 to 2018
$700k
REPRODUCTIVE STEROIDS AND EXPERIMENTAL STROKEK01RR000163 · NCRR · OREGON HEALTH AND SCIENCE UNIVERSITY · PI MURPHY, STEPHANIE J · 2000 to 2004
$479k
REPRODUCTIVE BIOLOGY IN PRIMATES: CENTER FACILITIESP30HD018185 · NICHD · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI SPINDEL, ELIOT R · 1985 to 1998
–
NCRR NIH HHS K01 RR000163NCRR NIH HHS P51 RR000163NCRR NIH HHS RR000163NIA NIH HHS AG023477NIA NIH HHS AG029612NIA NIH HHS AG036670NIA NIH HHS R01 AG029612NIA NIH HHS R01 AG036670NIA NIH HHS R56 AG029612NIA NIH HHS T32 AG023477NICHD NIH HHS HD018185NICHD NIH HHS HD029186NICHD NIH HHS P30 HD018185NICHD NIH HHS R01 HD029186NICHD NIH HHS U54 HD018185
6 · The paper itself

Abstract

Human aging is characterized by a marked decrease in circulating levels of dehydroepiandrosterone (DHEA) and DHEA-sulfate (DHEAS), hormonal changes associated with cognitive decline. Despite beneficial effects of DHEA supplementation in rodents, studies in elderly humans have generally failed to show cognitive improvement after treatment. In the present study we evaluate the effects of age and estradiol supplementation on expression of genes involved in the de novo synthesis of DHEA and its conversion to estradiol in the rhesus macaque hippocampus. Using reverse transcription polymerase chain reaction (RT-PCR) we demonstrate the expression of genes associated with this synthesis in several areas of the rhesus brain. Furthermore, real-time PCR reveals an age-related attenuation of hippocampal expression level of the genes CYP17A1, STS, and 3BHSD1/2. Additionally, short-term administration of estradiol is associated with decreased expression of CYP17A1, STS, SULT2B1, and AROMATASE, consistent with a downregulation not only of estrogen synthesis from circulating DHEA, but also of de novo DHEA synthesis within the hippocampus. These findings suggest a decline in neurosteroidogenesis may account for the inefficacy of DHEA supplementation in elderly humans, and that central steroidogenesis may be a function of circulating hormones and menopausal status.

Indexed as

AgingAnimalsBiomarkersDehydroepiandrosteroneEstradiolFemaleHippocampusHydrocortisoneMacaca mulattaMalePerimenopausePrimatesBiomarkersDehydroepiandrosteroneEstradiolHydrocortisone

Identifiers

PMID21683476
PMCPMC3196783
OpenAlexW1979230846

What OpenQuestion holds

Textmetadata
LicenceTDM
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.