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Cardiometabolic profile of young women with hypoprolactinemia
PURPOSE: Unlike hyperprolactinemia, clinical significance of prolactin deficiency remains poorly understood. The aim of this study was to assess the cardiometabolic profile of patients with low prolactin levels. METHODS: The study population consisted of three groups of young women. Two groups were...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474346/ https://www.ncbi.nlm.nih.gov/pubmed/35906342 http://dx.doi.org/10.1007/s12020-022-03145-1 |
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author | Krysiak, Robert Kowalcze, Karolina Okopień, Bogusław |
author_facet | Krysiak, Robert Kowalcze, Karolina Okopień, Bogusław |
author_sort | Krysiak, Robert |
collection | PubMed |
description | PURPOSE: Unlike hyperprolactinemia, clinical significance of prolactin deficiency remains poorly understood. The aim of this study was to assess the cardiometabolic profile of patients with low prolactin levels. METHODS: The study population consisted of three groups of young women. Two groups were chronically treated with cabergoline but differed in prolactin levels, which were either abnormally low (group A; n = 16) or within the reference range (group B, n = 23). Group C, serving as a control group, included 28 drug-naïve women with normal prolactin levels. The dose of cabergoline in group A was then tapered down. Glucose homeostasis markers, plasma lipids and circulating levels of hormones, uric acid, high-sensitivity C-reactive protein (hsCRP), fibrinogen and homocysteine, as well as the carotid intima-media thickness were assessed at baseline and 6 months later. RESULTS: Compared with subjects with normal prolactin levels, women with hypoprolactinemia had higher levels of 2-h postchallenge glucose, glycated hemoglobin, triglycerides, uric acid, hsCRP and fibrinogen, lower values of HDL-cholesterol, total testosterone and free androgen index, as well as reduced insulin sensitivity. No differences in these variables were observed between groups B and C. Apart from prolactin normalization, cabergoline dose reduction reversed all laboratory disturbances reported in group A. CONCLUSION: The obtained results suggest that hypoprolactinemia in women of reproductive age may increase cardiometabolic risk. |
format | Online Article Text |
id | pubmed-9474346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-94743462022-09-16 Cardiometabolic profile of young women with hypoprolactinemia Krysiak, Robert Kowalcze, Karolina Okopień, Bogusław Endocrine Original Article PURPOSE: Unlike hyperprolactinemia, clinical significance of prolactin deficiency remains poorly understood. The aim of this study was to assess the cardiometabolic profile of patients with low prolactin levels. METHODS: The study population consisted of three groups of young women. Two groups were chronically treated with cabergoline but differed in prolactin levels, which were either abnormally low (group A; n = 16) or within the reference range (group B, n = 23). Group C, serving as a control group, included 28 drug-naïve women with normal prolactin levels. The dose of cabergoline in group A was then tapered down. Glucose homeostasis markers, plasma lipids and circulating levels of hormones, uric acid, high-sensitivity C-reactive protein (hsCRP), fibrinogen and homocysteine, as well as the carotid intima-media thickness were assessed at baseline and 6 months later. RESULTS: Compared with subjects with normal prolactin levels, women with hypoprolactinemia had higher levels of 2-h postchallenge glucose, glycated hemoglobin, triglycerides, uric acid, hsCRP and fibrinogen, lower values of HDL-cholesterol, total testosterone and free androgen index, as well as reduced insulin sensitivity. No differences in these variables were observed between groups B and C. Apart from prolactin normalization, cabergoline dose reduction reversed all laboratory disturbances reported in group A. CONCLUSION: The obtained results suggest that hypoprolactinemia in women of reproductive age may increase cardiometabolic risk. Springer US 2022-07-29 2022 /pmc/articles/PMC9474346/ /pubmed/35906342 http://dx.doi.org/10.1007/s12020-022-03145-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Krysiak, Robert Kowalcze, Karolina Okopień, Bogusław Cardiometabolic profile of young women with hypoprolactinemia |
title | Cardiometabolic profile of young women with hypoprolactinemia |
title_full | Cardiometabolic profile of young women with hypoprolactinemia |
title_fullStr | Cardiometabolic profile of young women with hypoprolactinemia |
title_full_unstemmed | Cardiometabolic profile of young women with hypoprolactinemia |
title_short | Cardiometabolic profile of young women with hypoprolactinemia |
title_sort | cardiometabolic profile of young women with hypoprolactinemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474346/ https://www.ncbi.nlm.nih.gov/pubmed/35906342 http://dx.doi.org/10.1007/s12020-022-03145-1 |
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