Literature DB >> 32507371

Pharmacological treatment strategies for lowering prolactin in people with a psychotic disorder and hyperprolactinaemia: A systematic review and meta-analysis.

Javier Labad1, Itziar Montalvo2, Alexandre González-Rodríguez3, Clemente García-Rizo4, Benedicto Crespo-Facorro5, José Antonio Monreal6, Diego Palao6.   

Abstract

Different therapeutic strategies are used for lowering prolactin concentrations in patients with psychotic disorders with antipsychotic-induced hyperprolactinaemia. We aimed to examine the evidence from open-label studies and randomized clinical trials (RCTs) that studied four prolactin-lowering therapeutic strategies in people with psychotic disorders and hyperprolactinaemia: 1) switching to prolactin-sparing antipsychotics; 2) adding aripiprazole; 3) adding dopamine agonists; and 4) adding metformin. RCTs were included in a meta-analysis. Effect sizes (Hedges' g) of prolactin reductions with each strategy were calculated. Withdrawal rates were also considered. We identified 26 studies. Nine studies explored switching antipsychotic treatment to aripiprazole (n = 4), olanzapine (n = 1), quetiapine (n = 2), paliperidone palmitate (n = 1) or blonanserin (n = 1). Twelve studies tested the addition of aripiprazole. Six studies explored the addition of cabergoline (n = 3), bromocriptine (n = 2) or terguride (n = 1). We also found one meta-analysis testing the addition of metformin to antipsychotic treatment but no other individual studies. A meta-analysis could only be performed for the addition of aripiprazole, the strategy with the best level of evidence. Five RCTs testing the addition of aripiprazole yielded a significant reduction in prolactin concentration compared to placebo (N = 3) or maintaining antipsychotic treatment (N = 2): Hedges' g was -1.35 (CI 95%: -1.93 to -0.76, p < 0.001). The three placebo-controlled RCTs for aripiprazole addition showed similar withdrawal rates for aripiprazole (10.1%) and placebo (11.5%), without significant differences in the meta-analysis. Our study suggests that, in terms of levels of evidence, adding aripiprazole is the first option to be considered for lowering prolactin concentrations in patients with schizophrenia and hyperprolactinaemia.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Antipsychotics; Aripiprazole; Dopamine agonists; Hyperprolactinaemia; Schizophrenia; Switching

Mesh:

Substances:

Year:  2020        PMID: 32507371     DOI: 10.1016/j.schres.2020.04.031

Source DB:  PubMed          Journal:  Schizophr Res        ISSN: 0920-9964            Impact factor:   4.939


  6 in total

1.  Pharmacological treatment strategies for antipsychotic-induced hyperprolactinemia: a systematic review and network meta-analysis.

Authors:  Zhe Lu; Yaoyao Sun; Yuyanan Zhang; Yu Chen; Liangkun Guo; Yundan Liao; Zhewei Kang; Xiaoyang Feng; Weihua Yue
Journal:  Transl Psychiatry       Date:  2022-07-05       Impact factor: 7.989

Review 2.  Is Adjunct Aripiprazole Effective in Treating Hyperprolactinemia Induced by Psychotropic Medication? A Narrative Review.

Authors:  Frank M C Besag; Michael J Vasey; Iffah Salim
Journal:  CNS Drugs       Date:  2021-04-20       Impact factor: 5.749

3.  The More, the Merrier…? Antipsychotic Polypharmacy Treatment Strategies in Schizophrenia From a Pharmacology Perspective.

Authors:  Stephan Hjorth
Journal:  Front Psychiatry       Date:  2021-11-24       Impact factor: 4.157

4.  Influence of antipsychotics on metabolic syndrome risk in patients with schizophrenia.

Authors:  Aleksandra Koricanac; Aleksandra Tomic Lucic; Mirjana Veselinovic; Danijela Bazic Sretenovic; Gorica Bucic; Anja Azanjac; Olivera Radmanovic; Mirjana Matovic; Marijana Stanojevic; Aleksandra Jurisic Skevin; Bojana Simovic Markovic; Jelena Pantic; Nebojša Arsenijevic; Gordana D Radosavljevic; Maja Nikolic; Nenad Zornic; Jelena Nesic; Nemanja Muric; Branimir Radmanovic
Journal:  Front Psychiatry       Date:  2022-07-25       Impact factor: 5.435

5.  Plasma microRNA Array Analysis Identifies Overexpressed miR-19b-3p as a Biomarker of Bipolar Depression Distinguishing From Unipolar Depression.

Authors:  Yu Chen; Jiabo Shi; Haiyan Liu; Qiang Wang; Xiangxiang Chen; Hao Tang; Rui Yan; Zhijian Yao; Qing Lu
Journal:  Front Psychiatry       Date:  2020-08-11       Impact factor: 4.157

6.  Pharmacological treatment algorithms for the acute phase, agitation, and maintenance phase of first-episode schizophrenia: Japanese Society of Clinical Neuropsychopharmacology treatment algorithms.

Authors:  Hiroyoshi Takeuchi; Yoshiteru Takekita; Hikaru Hori; Kazuto Oya; Itaru Miura; Naoki Hashimoto; Norio Yasui-Furukori
Journal:  Hum Psychopharmacol       Date:  2021-07-09       Impact factor: 1.672

  6 in total

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