Evidence map›Paper›PMID 31219558›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2019

A Randomized Placebo-Controlled Trial of Low-Dose Testosterone Therapy in Women With Anorexia Nervosa.

Allison Kimball, Melanie Schorr, Erinne Meenaghan, Katherine N Bachmann, Kamryn T Eddy, Madhusmita Misra, Elizabeth A Lawson, Elana Kreiger-Benson, David B Herzog, Stuart Koman and 5 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Endocrine complications of anorexia nervosa.Journal of eating disorders · 2023
    Review
  9. Article
  10. Article
  11. Use of androgens at different stages of life: reproductive period.Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia · 2021
    Article
  12. Review
  13. 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

15 authors at 3 institutions in 1 country.

Allison KimballNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Melanie SchorrNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Erinne MeenaghanNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Katherine N BachmannNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Kamryn T EddyHarvard Medical School, Boston, Massachusetts.
Madhusmita MisraNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Elizabeth A LawsonNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Elana Kreiger-BensonNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
David B HerzogHarvard Medical School, Boston, Massachusetts.
Stuart KomanWalden Behavioral Care, Waltham, Massachusetts.
Robert J KeaneWalden Behavioral Care, Waltham, Massachusetts.
Seda EbrahimiCambridge Eating Disorder Center, Cambridge, Massachusetts.
David SchoenfeldHarvard Medical School, Boston, Massachusetts.
Anne KlibanskiNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Karen K MillerNeuroendocrine Unit, Massachusetts General Hospital, Boston, Massachusetts.
Harvard University · USMassachusetts General Hospital · USWalden University · US

Funding

Harvard Clinical and Translational Science CenterUL1TR001102 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2013 to 2017
$106.2M
HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI STEVEN K. GRINSPOON · 1994 to 2026
$31.6M
Harvard Clinical and Translational Science Center (UL1)UL1TR000170 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2012 to 2013
$31.4M
TRAINING PROGRAM IN ENDOCRINOLOGY AND DIABETEST32DK007028 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Karen K Miller · 1986 to 2026
$18.5M
Hormonal Factors in the Treatment of Anorexia NervosaR01MH083657 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI KLIBANSKI, ANNE · 2010 to 2014
$2.1M
Growth Hormone and Cardiovascular DiseaseK24HL092902 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MILLER, KAREN K · 2010 to 2019
$1.6M
Relative Sarcopenia and Cardiometabolic Risk in Young Adults with ObesityK23DK115903 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI HAINES, MELANIE SCHORR · 2017 to 2021
$1.1M
Appetite-regulating Hormones and Neurocircuitry in Anorexia NervosaK23MH092560 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI LAWSON, ELIZABETH AUSTEN · 2011 to 2015
$935k
NCATS NIH HHS UL1 TR000170NCATS NIH HHS UL1 TR001102NCRR NIH HHS UL1 RR025758NHLBI NIH HHS K24 HL092902NIDDK NIH HHS K23 DK115903NIDDK NIH HHS P30 DK040561NIDDK NIH HHS T32 DK007028NIMH NIH HHS K23 MH092560NIMH NIH HHS R01 MH083657
6 · The paper itself

Abstract

contextAnorexia nervosa (AN) is a psychiatric illness with considerable morbidity and no approved medical therapies. We have shown that relative androgen deficiency in AN is associated with greater depression and anxiety symptom severity.

objectiveTo determine whether low-dose testosterone therapy is an effective endocrine-targeted therapy for AN.

designDouble-blind, randomized, placebo-controlled trial.

settingClinical research center.

participantsNinety women, 18 to 45 years, with AN and free testosterone levels below the median for healthy women.

interventionTransdermal testosterone, 300 μg daily, or placebo patch for 24 weeks.

main outcome measuresPrimary end point: body mass index (BMI). Secondary end points: depression symptom severity [Hamilton Depression Rating Scale (HAM-D)], anxiety symptom severity [Hamilton Anxiety Rating Scale (HAM-A)], and eating disorder psychopathology and behaviors.

resultsMean BMI increased by 0.0 ± 1.0 kg/m2 in the testosterone group and 0.5 ± 1.1 kg/m2 in the placebo group (P = 0.03) over 24 weeks. At 4 weeks, there was a trend toward a greater decrease in HAM-D score (P = 0.09) in the testosterone vs placebo group. At 24 weeks, mean HAM-D and HAM-A scores decreased similarly in both groups [HAM-D: -2.9 ± 4.9 (testosterone) vs -3.0 ± 5.0 (placebo), P = 0.72; HAM-A: -4.5 ± 5.3 (testosterone) vs -4.3 ± 4.4 (placebo), P = 0.25]. There were no significant differences in eating disorder scores between groups. Testosterone therapy was safe and well tolerated with no increase in androgenic side effects compared with placebo.

conclusionLow-dose testosterone therapy for 24 weeks was associated with less weight gain-and did not lead to sustained improvements in depression, anxiety, or disordered eating symptoms-compared with placebo in women with AN.

Indexed as

Body Mass IndexAdministration, CutaneousAdolescentAdultAge FactorsAnorexia NervosaAnxietyDepressionDose-Response Relationship, DrugDouble-Blind MethodDrug Administration ScheduleFemaleFollow-Up StudiesHumansMiddle AgedPatient SelectionTestosterone

Identifiers

PMID31219558
PMCPMC6736210
OpenAlexW2944695313

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.