Evidence map›Paper›PMID 26990942›Full record

ArticleThe Journal of clinical endocrinology and metabolism2016

Evidence for Increased 5α-Reductase Activity During Early Childhood in Daughters of Women With Polycystic Ovary Syndrome.

Laura C Torchen, Jan Idkowiak, Naomi R Fogel, Donna M O'Neil, Cedric H L Shackleton, Wiebke Arlt, Andrea Dunaif

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
8.4field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Polycystic Ovary Syndrome: Ontogeny in Adolescence.Endocrinology and metabolism clinics of North America · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Implicating androgen excess in propagating metabolic disease in polycystic ovary syndrome.Therapeutic advances in endocrinology and metabolism · 2020
    Review
  15. Review
  16. Article
  17. Article
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  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

7 authors at 4 institutions in 2 countries.

Laura C TorchenDivision of Endocrinology, Metabolism, and Molecular Medicine (A.D.), Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Division of Pediatric Endocrinology (L.C.T., N.R.F.), Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Institute of Metabolism and Systems Research (J.I., D.M.O., C.H.L.S., W.A.), University of Birmingham, Birmingham B15 2TT, UK; Centre for Endocrinology, Diabetes and Metabolism (J.I., W.A.), Birmingham Health Partners, Birmingham B15 2TT, UK.
Jan IdkowiakDivision of Endocrinology, Metabolism, and Molecular Medicine (A.D.), Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Division of Pediatric Endocrinology (L.C.T., N.R.F.), Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Institute of Metabolism and Systems Research (J.I., D.M.O., C.H.L.S., W.A.), University of Birmingham, Birmingham B15 2TT, UK; Centre for Endocrinology, Diabetes and Metabolism (J.I., W.A.), Birmingham Health Partners, Birmingham B15 2TT, UK.
Naomi R FogelDivision of Endocrinology, Metabolism, and Molecular Medicine (A.D.), Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Division of Pediatric Endocrinology (L.C.T., N.R.F.), Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Institute of Metabolism and Systems Research (J.I., D.M.O., C.H.L.S., W.A.), University of Birmingham, Birmingham B15 2TT, UK; Centre for Endocrinology, Diabetes and Metabolism (J.I., W.A.), Birmingham Health Partners, Birmingham B15 2TT, UK.
Donna M O'NeilDivision of Endocrinology, Metabolism, and Molecular Medicine (A.D.), Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Division of Pediatric Endocrinology (L.C.T., N.R.F.), Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Institute of Metabolism and Systems Research (J.I., D.M.O., C.H.L.S., W.A.), University of Birmingham, Birmingham B15 2TT, UK; Centre for Endocrinology, Diabetes and Metabolism (J.I., W.A.), Birmingham Health Partners, Birmingham B15 2TT, UK.
Cedric H L ShackletonDivision of Endocrinology, Metabolism, and Molecular Medicine (A.D.), Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Division of Pediatric Endocrinology (L.C.T., N.R.F.), Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Institute of Metabolism and Systems Research (J.I., D.M.O., C.H.L.S., W.A.), University of Birmingham, Birmingham B15 2TT, UK; Centre for Endocrinology, Diabetes and Metabolism (J.I., W.A.), Birmingham Health Partners, Birmingham B15 2TT, UK.
Wiebke ArltDivision of Endocrinology, Metabolism, and Molecular Medicine (A.D.), Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Division of Pediatric Endocrinology (L.C.T., N.R.F.), Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Institute of Metabolism and Systems Research (J.I., D.M.O., C.H.L.S., W.A.), University of Birmingham, Birmingham B15 2TT, UK; Centre for Endocrinology, Diabetes and Metabolism (J.I., W.A.), Birmingham Health Partners, Birmingham B15 2TT, UK.
Andrea DunaifDivision of Endocrinology, Metabolism, and Molecular Medicine (A.D.), Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Division of Pediatric Endocrinology (L.C.T., N.R.F.), Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611; Institute of Metabolism and Systems Research (J.I., D.M.O., C.H.L.S., W.A.), University of Birmingham, Birmingham B15 2TT, UK; Centre for Endocrinology, Diabetes and Metabolism (J.I., W.A.), Birmingham Health Partners, Birmingham B15 2TT, UK.
University of Birmingham · GBNorthwestern University · USHealthPartners · USLurie Children's Hospital · 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
Testosterone-GnRH Frequency and the Evolution of PCOS in AdolescenceP50HD028934 · NICHD · UNIVERSITY OF VIRGINIA · PI HAISENLEDER, DANIEL J. · 2014 to 2018
$8.6M
Career Development in Women's Health (CDWH)K12HD055884 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DUNAIF, ANDREA E · 2007 to 2016
$4.2M
Medical Research Council G1001964Medical Research Council G116/172NICHD NIH HHS K12 HD055884NICHD NIH HHS P50 HD028934NICHD NIH HHS P50 HD044405Wellcome TrustWellcome Trust 092283
6 · The paper itself

Abstract

contextPolycystic ovary syndrome (PCOS) is a heritable, complex genetic disease. Animal models suggest that androgen exposure at critical developmental stages contributes to disease pathogenesis. We hypothesized that genetic variation resulting in increased androgen production produces the phenotypic features of PCOS by programming during critical developmental periods. Although we have not found evidence for increased in utero androgen levels in cord blood in the daughters of women with PCOS (PCOS-d), target tissue androgen production may be amplified by increased 5α-reductase activity analogous to findings in adult affected women. It is possible to noninvasively test this hypothesis by examining urinary steroid metabolites.

objectiveWe performed this study to investigate whether PCOS-d have altered androgen metabolism during early childhood. DESIGN, SETTING, AND

participantsTwenty-one PCOS-d, 1-3 years old, and 36 control girls of comparable age were studied at an academic medical center.

main outcome measuresUrinary steroid metabolites were measured by gas chromatography/mass spectrometry. Twenty-four hour steroid excretion rates and precursor to product ratios suggestive of 5α-reductase and 11β-hydroxysteroid dehydrogenase activities were calculated.

resultsAge did not differ but weight for length Z-scores were higher in PCOS-d compared to control girls (P = .02). PCOS-d had increased 5α-tetrahydrocortisol:tetrahydrocortisol ratios (P = .04), suggesting increased global 5α-reductase activity. There was no evidence for differences in 11β-hydroxysteroid dehydrogenase activity. Steroid metabolite excretion was not correlated with weight.

conclusionsOur findings suggest that differences in androgen metabolism are present in early childhood in PCOS-d. Increased 5α-reductase activity could contribute to the development of PCOS by amplifying target tissue androgen action.

Indexed as

Child of Impaired ParentsNuclear FamilyPolycystic Ovary SyndromeAdultChild, PreschoolCholestenone 5 alpha-ReductaseFemaleHumansInfantTetrahydrocortisolYoung AdultCholestenone 5 alpha-ReductaseTetrahydrocortisol

Identifiers

PMID26990942
PMCPMC4870855
OpenAlexW2302527435

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.