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FRI302 Umar Durrani

Disclosure: U.S. Durrani: None. A. Paracha: None. S. Vasireddy: None. F. Waheed: None. M. Thomure: None. Prolactinomas are tumors of the pituitary gland that induce hyperprolactinemia. Symptoms at presentation can include growth delay, infertility, neurologic deficits and bothersome galactorrhea. Do...

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Autores principales: Durrani, Umar Safwaan, Paracha, Awais, Vasireddy, Satvik, Waheed, Fatima, Thomure, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553930/
http://dx.doi.org/10.1210/jendso/bvad114.1237
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author Durrani, Umar Safwaan
Paracha, Awais
Vasireddy, Satvik
Waheed, Fatima
Thomure, Michael
author_facet Durrani, Umar Safwaan
Paracha, Awais
Vasireddy, Satvik
Waheed, Fatima
Thomure, Michael
author_sort Durrani, Umar Safwaan
collection PubMed
description Disclosure: U.S. Durrani: None. A. Paracha: None. S. Vasireddy: None. F. Waheed: None. M. Thomure: None. Prolactinomas are tumors of the pituitary gland that induce hyperprolactinemia. Symptoms at presentation can include growth delay, infertility, neurologic deficits and bothersome galactorrhea. Dopamine suppresses prolactin production; therefore, dopamine agonists are first-line treatment for prolactinomas. However, hyperdopaminergia is also associated with psychiatric disorders. The dopamine hypothesis states that cerebral hyperdopaminergia can contribute to symptoms of schizophrenia. Thus, psychiatric disorders are commonly treated with dopamine antagonists. Almost 1 in 8 people in the world have a psychiatric condition. It is almost inevitable that the medical system will have to treat patients with both a psychiatric condition and a prolactinoma; thus, it is essential to identify treatment regimens for these patients. In order to identify potential treatments, we conducted a PubMed literature search focusing on patients with prolactinomas and co-existing psychiatric diagnoses. Our inclusion criteria helped us focus on patients who presented with concurrent prolactinoma and psychiatric condition which were confirmed by brain imaging, serologic prolactin levels, and reports of psychiatric conditions/episodes in their medical history (or chart). Our search yielded 30 studies representing a total of 54 patients with both conditions. We found that four key themes emerged from the literature: 1) discontinuing risperidone in exchange for other atypical antipsychotics such as aripiprazole, olanzapine or ziprasidone, 2) discontinuing thioridazine, thiothixene and remoxipride in exchange for clozapine, 3) dopamine agonist therapy cessation to abate psychiatric symptoms, and 4) surgery and/or radiation after pharmacotherapy. In conclusion, we would recommend focusing on specific antipsychotics (aripiprazole, olanzapine, ziprasidone, or clozapine) while shying away from (risperidone, thioridazine, thiothixene, and remoxipride). We would also recommend ceasing dopamine agonist therapy at least until symptoms improve. If these two methods are not yielding sufficient results, then pursuing surgical options or radiation therapy may be considered. Presentation: Friday, June 16, 2023
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spelling pubmed-105539302023-10-06 FRI302 Umar Durrani Durrani, Umar Safwaan Paracha, Awais Vasireddy, Satvik Waheed, Fatima Thomure, Michael J Endocr Soc Neuroendocrinology & Pituitary Disclosure: U.S. Durrani: None. A. Paracha: None. S. Vasireddy: None. F. Waheed: None. M. Thomure: None. Prolactinomas are tumors of the pituitary gland that induce hyperprolactinemia. Symptoms at presentation can include growth delay, infertility, neurologic deficits and bothersome galactorrhea. Dopamine suppresses prolactin production; therefore, dopamine agonists are first-line treatment for prolactinomas. However, hyperdopaminergia is also associated with psychiatric disorders. The dopamine hypothesis states that cerebral hyperdopaminergia can contribute to symptoms of schizophrenia. Thus, psychiatric disorders are commonly treated with dopamine antagonists. Almost 1 in 8 people in the world have a psychiatric condition. It is almost inevitable that the medical system will have to treat patients with both a psychiatric condition and a prolactinoma; thus, it is essential to identify treatment regimens for these patients. In order to identify potential treatments, we conducted a PubMed literature search focusing on patients with prolactinomas and co-existing psychiatric diagnoses. Our inclusion criteria helped us focus on patients who presented with concurrent prolactinoma and psychiatric condition which were confirmed by brain imaging, serologic prolactin levels, and reports of psychiatric conditions/episodes in their medical history (or chart). Our search yielded 30 studies representing a total of 54 patients with both conditions. We found that four key themes emerged from the literature: 1) discontinuing risperidone in exchange for other atypical antipsychotics such as aripiprazole, olanzapine or ziprasidone, 2) discontinuing thioridazine, thiothixene and remoxipride in exchange for clozapine, 3) dopamine agonist therapy cessation to abate psychiatric symptoms, and 4) surgery and/or radiation after pharmacotherapy. In conclusion, we would recommend focusing on specific antipsychotics (aripiprazole, olanzapine, ziprasidone, or clozapine) while shying away from (risperidone, thioridazine, thiothixene, and remoxipride). We would also recommend ceasing dopamine agonist therapy at least until symptoms improve. If these two methods are not yielding sufficient results, then pursuing surgical options or radiation therapy may be considered. Presentation: Friday, June 16, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10553930/ http://dx.doi.org/10.1210/jendso/bvad114.1237 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neuroendocrinology & Pituitary
Durrani, Umar Safwaan
Paracha, Awais
Vasireddy, Satvik
Waheed, Fatima
Thomure, Michael
FRI302 Umar Durrani
title FRI302 Umar Durrani
title_full FRI302 Umar Durrani
title_fullStr FRI302 Umar Durrani
title_full_unstemmed FRI302 Umar Durrani
title_short FRI302 Umar Durrani
title_sort fri302 umar durrani
topic Neuroendocrinology & Pituitary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553930/
http://dx.doi.org/10.1210/jendso/bvad114.1237
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