Evidence map›Paper›PMID 36735255›Full record

Trial reportJAMA network open2023

Effects of Kisspeptin on Sexual Brain Processing and Penile Tumescence in Men With Hypoactive Sexual Desire Disorder: A Randomized Clinical Trial.

Edouard G Mills, Natalie Ertl, Matthew B Wall, Layla Thurston, Lisa Yang, Sofiya Suladze, Tia Hunjan, Maria Phylactou, Bijal Patel, Beatrice Muzi and 9 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in JAMA network open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
7.1field-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

13 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

  • Commented on by
    2023
5 · Who and what money

Authors and funding

19 authors at 3 institutions in 1 country.

Edouard G MillsSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Natalie ErtlSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Matthew B WallSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Layla ThurstonSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Lisa YangSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Sofiya SuladzeSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Tia HunjanSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Maria PhylactouSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Bijal PatelSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Beatrice MuziSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Dena EttehadSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Paul A BassettStatsconsultancy Ltd, Amersham, United Kingdom.
Jonathan HowardInvicro LLC, Hammersmith Hospital Campus, London, United Kingdom.
Eugenii A RabinerInvicro LLC, Hammersmith Hospital Campus, London, United Kingdom.
Paul BechSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Ali AbbaraSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
David GoldmeierJane Wadsworth Sexual Function Clinic, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom.
Alexander N ComninosSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Waljit S DhilloSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Imperial College London · GBHammersmith Hospital · GBImperial College Healthcare NHS Trust · GB

Funding

Department of Health CS-2018-18-ST2–002Medical Research Council MR/R000484/1Medical Research Council MR/T006242/1
6 · The paper itself

Abstract

Importance: The human physiological sexual response is crucial for reward, satisfaction, and reproduction. Disruption of the associated neurophysiological pathways predisposes to low sexual desire; the most prevalent psychological form is hypoactive sexual desire disorder (HSDD), which affects 8% of men but currently has no effective pharmacological treatment options. The reproductive neuropeptide kisspeptin offers a putative therapeutic target, owing to emerging understanding of its role in reproductive behavior. Objective: To determine the physiological, behavioral, neural, and hormonal effects of kisspeptin administration in men with HSDD. Design, Setting, and Participants: This double-blind, 2-way crossover, placebo-controlled randomized clinical trial was performed at a single academic research center in the UK. Eligible participants were right-handed heterosexual men with HSDD. Physiological, behavioral, functional magnetic resonance imaging (fMRI), and hormonal analyses were used to investigate the clinical and mechanistic effects of kisspeptin administration in response to visual sexual stimuli (short and long video tasks). The trial was conducted between January 11 and September 15, 2021, and data analysis was performed between October and November 2021. Interventions: Participants attended 2 study visits at least 7 days apart, in balanced random order, for intravenous infusion of kisspeptin-54 (1 nmol/kg/h) for 75 minutes or for administration of a rate-matched placebo. Main Outcomes and Measures: Changes in (1) brain activity on whole-brain analysis, as determined by fMRI blood oxygen level-dependent activity in response to visual sexual stimuli during kisspeptin administration compared with placebo, (2) physiological sexual arousal (penile tumescence), and (3) behavioral measures of sexual desire and arousal. Results: Of the 37 men randomized, 32 completed the trial. Participants had a mean (SD) age of 37.9 (8.6) years and a mean (SD) body mass index of 24.9 (5.4). On viewing sexual videos, kisspeptin significantly modulated brain activity in key structures of the sexual-processing network on whole-brain analysis compared with placebo (mean absolute change [Cohen d] = 0.81 [95% CI, 0.41-1.21]; P =  .003). Furthermore, improvements in several secondary analyses were observed, including significant increases in penile tumescence in response to sexual stimuli (by up to 56% more than placebo; mean difference = 0.28 units [95% CI, 0.04-0.52 units]; P = .02) and behavioral measures of sexual desire-most notably, increased happiness about sex (mean difference = 0.63 points [95% CI, 0.10-1.15 points]; P = .02). Conclusions and Relevance: Collectively, this randomized clinical trial provides the first evidence to date showing that kisspeptin administration substantially modulates sexual brain processing in men with HSDD, with associated increases in penile tumescence and behavioral measures of sexual desire and arousal. These data suggest that kisspeptin has potential as the first pharmacological treatment for men with low sexual desire. Trial Registration: isrctn.org Identifier: ISRCTN17271094.

Indexed as

Penile ErectionSexual Dysfunctions, PsychologicalAdultBrainHumansKisspeptinsMaleSexual BehaviorKisspeptins

Identifiers

PMID36735255
PMCPMC9898824
OpenAlexW4319062595

What OpenQuestion holds

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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.