Evidence map›Paper›PMID 12438645›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Progesterone receptor knockout mice have an improved glucose homeostasis secondary to beta -cell proliferation.

Frédéric Picard, Mitsuhiro Wanatabe, Kristina Schoonjans, John Lydon, Bert W O'Malley, Johan Auwerx

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

67 citing papers in PubMed, 1 synthesis or guideline pooled it, 165 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. bioRxiv : the preprint server for biology · 2025
    Article
  6. Mechanistic Insights IntoDiabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Article
  7. Article
  8. Article
  9. Emerging Perspectives on the Impact of Diabetes Mellitus and Anti-Diabetic Drugs on Premenstrual Syndrome. A Narrative Review.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2024
    Review
  10. Article
  11. Mapping novel QTL and fine mapping of previously identified QTL associated with glucose tolerance using the collaborative cross mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Combined Effects ofNutrients · 2023
    Article
  16. Type 1 Diabetes and the Menstrual Cycle: Where/How Does Exercise Fit in?International journal of environmental research and public health · 2023
    Review
  17. Article
  18. Review
  19. Observational
  20. Review

7 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Frédéric PicardInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Centre National de la Recherche ScientifiqueInstitut National de la Santé et de la Recherche MédicalUniversité Louis Pasteur, 67404 Illkirch, France.
Mitsuhiro Wanatabe
Kristina Schoonjans
John Lydon
Bert W O'Malley
Johan Auwerx
Baylor College of Medicine · USInstitut Clinique de la Souris · FR

Funding

TISSUE COACTIVATOR AND RECEPTOR EXPRESSION FINGERPRINTSP01DK059820 · NIDDK · INSTITUT DE GENETIQUE ET BIOLOGIE MOLECU · PI O'MALLEY, BERT W · 2001 to 2016
$23.1M
SEX HORMONE RECEPTOR COMPONENTS AND THE CELL GENOMER01HD007857 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI DAVID M LONARD, JOHN P LYDON · 1985 to 2026
$14.6M
SEX HORMONE RECEPTOR COMPONENTS &THE CELL GENOMER37HD007857 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MC KEOWN, MICHAEL B · 1987 to 1996
–
NICHD NIH HHS HD07857NICHD NIH HHS R01 HD007857NIDDK NIH HHS 1-P01-DK59820-01NIDDK NIH HHS P01 DK059820
6 · The paper itself

Abstract

Gestational diabetes coincides with elevated circulating progesterone levels. We show that progesterone accelerates the progression of diabetes in female dbdb mice. In contrast, RU486, an antagonist of the progesterone receptor (PR), reduces blood glucose levels in both female WT and dbdb mice. Furthermore, female, but not male, PR-- mice had lower fasting glycemia than PR++ mice and showed higher insulin levels on glucose injection. Pancreatic islets from female PR-- mice were larger and secreted more insulin consequent to an increase in beta-cell mass due to an increase in beta-cell proliferation. These findings demonstrate an important role of progesterone signaling in insulin release and pancreatic function and suggest that it affects the susceptibility to diabetes.

Indexed as

AnimalsBlood GlucoseCell CountCell DivisionCell SizeDiabetes, GestationalDiabetes Mellitus, ExperimentalFemaleGlucoseGlucose Tolerance TestHomeostasisHormone AntagonistsHyperglycemiaInsulinInsulin ResistanceInsulin SecretionBlood GlucoseGlucoseHormone AntagonistsInsulinMifepristoneProgesteroneReceptors, ProgesteroneNon-programmatic

Identifiers

PMID12438645
PMCPMC137770
OpenAlexW1627267625

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.