Evidence map›Paper›PMID 19482904›Full record

ArticleMolecular human reproduction2009

PDE8A genetic variation, polycystic ovary syndrome and androgen levels in women.

Chen Chen, Jessica Wickenheisser, Kathryn G Ewens, Wendy Ankener, Richard S Legro, Andrea Dunaif, Jan M McAllister, Richard S Spielman, Jerome F Strauss

Open access · bronzeAbstract read
In one paragraph

Article in Molecular human reproduction, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Mitochondrial ProteinFrontiers in pharmacology · 2022
    Article
  3. The Role of PDE8 in T Cell Recruitment and Function in Inflammation.Frontiers in cell and developmental biology · 2021
    Review
  4. Article
  5. Article
  6. Review
  7. A subpathway-based method of drug reposition for polycystic ovary syndrome.Reproductive sciences (Thousand Oaks, Calif.) · 2015
    Article
  8. Phosphodiesterases and adrenal Cushing in mice and humans.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2014
    Review
  9. Review
  10. Regulation of adrenal steroidogenesis by the high-affinity phosphodiesterase 8 family.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2012
    Review
  11. Review
  12. 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

9 authors at 4 institutions in 1 country.

Chen ChenDepartment of Obstetrics and Gynecology, Virginia Commonwealth University, School of Medicine, Richmond, VA 23298, USA.
Jessica Wickenheisser
Kathryn G Ewens
Wendy Ankener
Richard S Legro
Andrea Dunaif
Jan M McAllister
Richard S Spielman
Jerome F Strauss
Penn State Milton S. Hershey Medical Center · USUniversity of Pennsylvania · USVirginia Commonwealth University · USNorthwestern University · US

Funding

Role of Androgen Excess in Provoking Oxidative Stress in FemalesP50HD044405 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DUNAIF, ANDREA E · 2002 to 2017
$17.2M
Translational Research in Polycystic Ovary SyndromeU54HD034449 · NICHD · VIRGINIA COMMONWEALTH UNIVERSITY · PI NESTLER, JOHN E · 1997 to 2012
$15.0M
NICHD NIH HHS 2U54 HD034449NICHD NIH HHS P50 HD044405NICHD NIH HHS U54 HD034449
6 · The paper itself

Abstract

Polycystic ovary syndrome (PCOS) is characterized by excessive theca cell androgen secretion, dependent upon LH, which acts through the intermediacy of 3',5'-cyclic adenosine monophosphate (cAMP). cAMP signaling pathways are controlled through regulation of its synthesis by adenylyl cyclases, and cAMP degradation by phosphodiesterases (PDEs). PDE8A, a high-affinity cAMP-specific PDE is expressed in the ovary and testis. Leydig cells from mice with a targeted mutation in the Pde8a gene are sensitized to the action of LH in terms of testosterone production. These observations led us to evaluate the human PDE8A gene as a PCOS candidate gene, and the hypothesis that reduced PDE8A activity or expression would contribute to excessive ovarian androgen production. We identified a rare variant (R136Q; NM_002605.2 c.407G > A) and studied another known single nucleotide polymorphism (SNP) (rs62019510, N401S) in the PDE8A coding sequence causing non-synonymous amino acid substitutions, and a new SNP in the promoter region (NT_010274.16:g.490155G > A). Although PDE8A kinetics were consistent with reduced activity in theca cell lysates, study of the expressed variants did not confirm reduced activity in cell-free assays. Sub-cellular localization of the enzyme was also not different among the coding sequence variants. The PDE8A promoter SNP and a previously described promoter SNP did not affect promoter activity in in vitro assays. The more common coding sequence SNP (N401S), and the promoter SNPs were not associated with PCOS in our transmission/disequilibrium test-based analysis, nor where they associated with total testosterone or dehydroepiandrosterone sulfate levels. These findings exclude a significant role for PDE8A as a PCOS candidate gene, and as a Las major determinant of androgen levels in women.

Indexed as

Genetic Variation3',5'-Cyclic-AMP PhosphodiesterasesAmino Acid SequenceAndrogensAnimalsCells, CulturedChlorocebus aethiopsCOS CellsDehydroepiandrosterone SulfateFemaleGenotypeHumansMolecular Sequence DataPolycystic Ovary SyndromePolymorphism, Single NucleotidePromoter Regions, Genetic3',5'-Cyclic-AMP PhosphodiesterasesAndrogensDehydroepiandrosterone SulfatePDE8A protein, humanTestosterone

Identifiers

PMID19482904
PMCPMC2709315
OpenAlexW2160321546

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.