Evidence map›Paper›PMID 37715962›Full record

ArticleThe Journal of clinical endocrinology and metabolism2024

Ropinirole for the Treatment of Hyperprolactinemia: A Dose-Escalation Study of Efficacy and Tolerability.

Liam J Heneghan, Amanda Tsang, Cara Dimino, Alexander G Khandji, Sunil K Panigrahi, Gabrielle Page-Wilson

Open access · bronzeAbstract readClinical Trial, Phase I
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

6 authors at 2 institutions in 1 country.

Liam J HeneghanDepartment of Medicine, Columbia University, Vagelos College of P&S, New York, NY 10032, USA.
Amanda TsangDepartment of Medicine, Columbia University, Vagelos College of P&S, New York, NY 10032, USA.
Cara DiminoDepartment of Medicine, Columbia University, Vagelos College of P&S, New York, NY 10032, USA.
Alexander G KhandjiDepartment of Radiology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Sunil K PanigrahiDepartment of Medicine, Columbia University, Vagelos College of P&S, New York, NY 10032, USA.
Gabrielle Page-WilsonDepartment of Medicine, Columbia University, Vagelos College of P&S, New York, NY 10032, USA.ORCID 0000-0002-4064-1211
Columbia University · USColumbia University Irving Medical Center · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024156 · NCRR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2006 to 2011
$53.0M
Clinical and Translational Science AwardUL1TR000040 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2012 to 2015
$26.2M
A New Therapeutic Option for the Treatment of ProlactinomasR21DK112093 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PAGEWILSON, GABRIELLE · 2016 to 2018
$600k
NCATS NIH HHSNCRR NIH HHS UL1 RR024156NIDDK NIH HHS R21 DK112093NIH HHS UL1-TR-000040
6 · The paper itself

Abstract

contextTreatment of hyperprolactinemia with ergoline dopamine agonists (DAs) can be complicated by intolerance and resistance.

objectiveThis study examines the efficacy and tolerability of the nonergot DA ropinirole for the long-term treatment of hyperprolactinemia.

methodsTwelve hyperprolactinemic women were treated with ropinirole in a 6-month, open-label, dose-escalation trial; 7 of the 12 continued treatment in an extension study for up to 17 months. Ropinirole doses were uptitrated to achieve normal prolactin (PRL) levels, restore menses, and eliminate galactorrhea.

resultsTwo of the 12 participants were DA naive; 6 of 12 were ergot DA intolerant; and 1 of 12 had known ergot DA resistance. Baseline PRL levels were 126.2 ± 41.4 ng/mL (SEM). Ropinirole was uptitrated from 0.125 to 0.25 mg/h to a median total daily dose (TDD) of 2 mg/d (1-4 mg/d [interquartile range]). PRL normalization was achieved in 50% of the participants (5 with microadenomas and 1 with idiopathic hyperprolactinemia) at a median effective TDD of 1 mg/d. Of the patients achieving PRL normalization, 83% were ergot DA intolerant. A persistent partial biochemical response (PRL reduction >50% from baseline) was achieved in 17% of the participants. During treatment, menses resumed in 67% of amenorrheic patients; galactorrhea resolved in 67%. Mild adverse effects were reported in 92% of participants; however, ropinirole was not discontinued because of intolerance even among the 50% of individuals with a prior history of ergot DA intolerance and resultant medication discontinuation.

conclusionThese data demonstrate the efficacy and tolerability of ropinirole for the treatment of hyperprolactinemia in patients with microprolactinomas and idiopathic hyperprolactinemia and suggest ropinirole may represent a novel therapeutic alternative for treating hyperprolactinemic disorders in patients with ergot DA intolerance.

Indexed as

AmenorrheaGalactorrheaHyperprolactinemiaIndolesPituitary NeoplasmsProlactinomaDopamine AgonistsFemaleHumansPregnancyProlactinDopamine AgonistsIndolesProlactinropiniroleclinical trialdopamine agonisthyperprolactinemiaprolactinomaropinirole

Identifiers

PMID37715962
PMCPMC10795899
OpenAlexW4386808408

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.