Evidence map›Paper›PMID 23921139›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2013

Androgens influence microvascular dilation in PCOS through ET-A and ET-B receptors.

Megan M Wenner, Hugh S Taylor, Nina S Stachenfeld

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 66 citations in OpenAlex.

  1. Trial
  2. ETAmerican journal of physiology. Heart and circulatory physiology · 2021
    Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. A new link between low testosterone and cardiovascular disease risk.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  8. Review
  9. Endothelial dysfunction in middle-aged and older men with low testosterone is associated with elevated circulating endothelin-1.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  10. Article
  11. Guidelines on the use of sex and gender in cardiovascular research.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Obesity and cardiovascular disease in women.International journal of obesity (2005) · 2020
    Review
  19. Racial disparities in cardiovascular disease risk: mechanisms of vascular dysfunction.American journal of physiology. Heart and circulatory physiology · 2019
    Review
  20. 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

3 authors at 2 institutions in 1 country.

Megan M WennerJohn B. Pierce Laboratory, New Haven, Connecticut;
Hugh S Taylor
Nina S Stachenfeld
Yale University · USUniversity of Delaware · US

Funding

Compromised microcirculation in women with Polycystic Ovary SyndromeR21HL093450 · NHLBI · JOHN B. PIERCE LABORATORY, INC. · PI STACHENFELD, NINA · 2009 to 2010
$479k
NHLBI NIH HHS R21-HL-093450
6 · The paper itself

Abstract

Hyperandrogenism and vascular dysfunction often coexist in women with polycystic ovary syndrome (PCOS). We hypothesized that testosterone compromises cutaneous microvascular dilation in women with PCOS via the endothelin-1 ET-B subtype receptor. To control and isolate testosterone's effects on microvascular dilation, we administered a gonadotropin-releasing hormone antagonist (GnRHant) for 11 days in obese, otherwise healthy women [controls, 22.0 (4) yr, 36.0 (3.2) kg/m(2)] or women with PCOS [23 (4) yr, 35.4 (1.3) kg/m(2)], adding testosterone (T; 2.5 mg/day) on days 8-11. Using laser Doppler flowmetry and cutaneous microdialysis, we measured changes in skin microcirculatory responsiveness (ΔCVC) to local heating while perfusing ET-A (BQ-123) and ET-B (BQ-788) receptor antagonists under three experimental conditions: baseline (BL; prehormone intervention), GnRHant (day 4 of administration), and T administration. At BL, ET-A receptor inhibition enhanced heat-induced vasodilation in both groups [ΔCVC control 2.03 (0.65), PCOS 2.10 (0.25), AU/mmHg, P < 0.05]; ET-B receptor inhibition reduced vasodilation in controls only [ΔCVC 0.98 (0.39), 1.41 (0.45) AU/mmHg for controls, PCOS] compared with saline [ΔCVC controls 1.27 (0.48), PCOS 1.31 (0.13) AU/mmHg]. GnRHant enhanced vasodilation in PCOS [saline ΔCVC 1.69 (0.23) AU/mmHg vs. BL, P < 0.05] and abolished the ET-A effect in both groups, a response reasserted with T in controls. ET-B receptor inhibition reduced heat-induced vasodilation in both groups during GnRHant and T [ΔCVC, controls: 0.95 (0.21) vs. 0.51 (13); PCOS: 1.27 (0.23) vs. 0.84 (0.27); for GnRHant vs. T, P < 0.05]. These data demonstrate that androgen suppression improves microvascular dilation in PCOS via ET-A and ET-B receptors.

Indexed as

AdultAndrogensEndothelium, VascularFemaleGlucose Tolerance TestGonadotropin-Releasing HormoneHormone AntagonistsHumansInsulin ResistanceMicrovesselsObesityPolycystic Ovary SyndromeReceptor, Endothelin AReceptor, Endothelin BTestosteroneVasodilationAndrogensganirelixGonadotropin-Releasing HormoneHormone AntagonistsReceptor, Endothelin AReceptor, Endothelin BTestosteronealdosteroneendothelinpolycystic ovary syndrometestosteronevasoconstrictionvasodilation

Identifiers

PMID23921139
PMCPMC3798701
OpenAlexW1989335478

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.