Evidence map›Paper›PMID 36189794›Full record

Trial reportThe Journal of clinical investigation2022

Melanocortin 4 receptor agonism enhances sexual brain processing in women with hypoactive sexual desire disorder.

Layla Thurston, Tia Hunjan, Edouard G Mills, Matthew B Wall, Natalie Ertl, Maria Phylactou, Beatrice Muzi, Bijal Patel, Emma C Alexander, Sofiya Suladze and 7 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04179734 (Physiological Study to Determine the Role of the Melanocortin-4 Receptor in Brain Activity in Women With Hypoactive Sexual Desire Disorder), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-weighted citation impact, top 9% 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.

NCT04179734 phase4completednot on this map

Physiological Study to Determine the Role of the Melanocortin-4 Receptor in Brain Activity in Women With Hypoactive Sexual Desire Disorder

TypeinterventionalSponsorImperial College Healthcare NHS TrustRan2019 to 2020Enrolled40ConditionsHypoactive Sexual Desire DisorderArmsBremelanotide, Placebo
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 20 citations in OpenAlex.

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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

17 authors at 4 institutions in 3 countries.

Layla ThurstonSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Tia HunjanSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Edouard G MillsSection 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.
Natalie ErtlSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Maria PhylactouSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Beatrice MuziSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Bijal PatelSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Emma C AlexanderSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Sofiya SuladzeSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Manish ModiSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Pei C EngSection of Endocrinology and Investigative Medicine, Imperial College London, London, United Kingdom.
Paul A BassettStatsconsultancy Ltd., Amersham, Bucks, 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 and.
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 · GBImperial College Healthcare NHS Trust · GBInvicro (United Kingdom) · GBSt. Mary’s Hospital · ZA

Funding

Medical Research Council MR/T006242/1
6 · The paper itself

Abstract

BACKGROUNDHypoactive sexual desire disorder (HSDD) is characterized by a persistent deficiency of sexual fantasies and desire for sexual activity, causing marked distress and interpersonal difficulty. It is the most prevalent female sexual health problem globally, affecting approximately 10% of women, but has limited treatment options. Melanocortin 4 receptor (MC4R) agonists have emerged as a promising therapy for women with HSDD, through unknown mechanisms. Studying the pathways involved is crucial for our understanding of normal and abnormal sexual behavior.METHODSUsing psychometric, functional neuroimaging, and hormonal analyses, we conducted a randomized, double-blinded, placebo-controlled, crossover clinical study to assess the effects of MC4R agonism compared with placebo on sexual brain processing in 31 premenopausal heterosexual women with HSDD.RESULTSMC4R agonism significantly increased sexual desire for up to 24 hours after administration compared with placebo. During functional neuroimaging, MC4R agonism enhanced cerebellar and supplementary motor area activity and deactivated the secondary somatosensory cortex, specifically in response to visual erotic stimuli, compared with placebo. In addition, MC4R agonism enhanced functional connectivity between the amygdala and the insula during visual erotic stimuli compared with placebo.CONCLUSIONThese data suggest that MC4R agonism enhanced sexual brain processing by reducing self-consciousness, increasing sexual imagery, and sensitizing women with HSDD to erotic stimuli. These findings provide mechanistic insight into the action of MC4R agonism in sexual behavior and are relevant to the ongoing development of HSDD therapies and MC4R agonist development more widely.TRIAL REGISTRATIONClinicalTrials.gov NCT04179734.FUNDINGThis is an investigator-sponsored study funded by AMAG Pharmaceuticals Inc., the Medical Research Council (MRC) (MR/T006242/1), and the National Institute for Health Research (NIHR) (CS-2018-18-ST2-002 and RP-2014-05-001).

Indexed as

Receptor, Melanocortin, Type 4Sexual Dysfunctions, PsychologicalBrainFemaleHumansInterleukin-1 Receptor-Like 1 ProteinSexual BehaviorInterleukin-1 Receptor-Like 1 ProteinReceptor, Melanocortin, Type 4EndocrinologyMelanocortinNeuroimaging

Identifiers

PMID36189794
PMCPMC9525110
OpenAlexW4300003869

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.