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Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis

BACKGROUND: Prolactin (PRL), an inflammatory hormone with cytokine properties, has long been considered to play a crucial role in the pathogenesis of autoimmune diseases, including systemic sclerosis (SSc). However, the plasma/serum levels of PRL in SSc were inconsistent in published studies. The ai...

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Autores principales: Wu, Yang, Li, Meng-Lei, Han, Hua-Jing, Huang, Li-Jun, He, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505334/
https://www.ncbi.nlm.nih.gov/pubmed/32957368
http://dx.doi.org/10.1097/MD.0000000000022239
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author Wu, Yang
Li, Meng-Lei
Han, Hua-Jing
Huang, Li-Jun
He, Yong
author_facet Wu, Yang
Li, Meng-Lei
Han, Hua-Jing
Huang, Li-Jun
He, Yong
author_sort Wu, Yang
collection PubMed
description BACKGROUND: Prolactin (PRL), an inflammatory hormone with cytokine properties, has long been considered to play a crucial role in the pathogenesis of autoimmune diseases, including systemic sclerosis (SSc). However, the plasma/serum levels of PRL in SSc were inconsistent in published studies. The aim of this study was to evaluate the plasma/serum levels of PRL in patients with SSc accurately. METHODS: Electronic databases, including PubMed, EMBASE, Cochrane Library, CNKI, VIP and WANFANG databases, were searched up to October 15, 2019. Pooled standard mean difference (SMD) with 95% confidence interval (CI) was calculated by fixed-effect or random-effects model analysis. All statistical analyses were conducted with STATA 12.0. RESULTS: Fifty three articles were obtained after searching databases, and 9 studies with 293 SSc patients and 282 controls were finally included. The meta-analysis showed that the plasma/serum PRL level in SSC patients was significantly increased compared with the healthy controls, with the SMD of 1.00 and 95% CI (0.56, 1.43). Subgroup analysis showed that female patients had higher plasma/serum PRL levels. However, no significant change in plasma/serum PRL levels was observed in male patients (P = .318). In subgroup analysis by detection type, electrochemiluminescence immunoassay (ECLIA) group and enzyme-linked immunosorbent assay (ELISA) group showed higher PRL levels among SSc patients. CONCLUSIONS: In summary, our meta-analysis showed a significantly higher plasma/serum PRL level in SSc patients than healthy controls, and it was associated with gender and detection method.
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spelling pubmed-75053342020-09-24 Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis Wu, Yang Li, Meng-Lei Han, Hua-Jing Huang, Li-Jun He, Yong Medicine (Baltimore) 6900 BACKGROUND: Prolactin (PRL), an inflammatory hormone with cytokine properties, has long been considered to play a crucial role in the pathogenesis of autoimmune diseases, including systemic sclerosis (SSc). However, the plasma/serum levels of PRL in SSc were inconsistent in published studies. The aim of this study was to evaluate the plasma/serum levels of PRL in patients with SSc accurately. METHODS: Electronic databases, including PubMed, EMBASE, Cochrane Library, CNKI, VIP and WANFANG databases, were searched up to October 15, 2019. Pooled standard mean difference (SMD) with 95% confidence interval (CI) was calculated by fixed-effect or random-effects model analysis. All statistical analyses were conducted with STATA 12.0. RESULTS: Fifty three articles were obtained after searching databases, and 9 studies with 293 SSc patients and 282 controls were finally included. The meta-analysis showed that the plasma/serum PRL level in SSC patients was significantly increased compared with the healthy controls, with the SMD of 1.00 and 95% CI (0.56, 1.43). Subgroup analysis showed that female patients had higher plasma/serum PRL levels. However, no significant change in plasma/serum PRL levels was observed in male patients (P = .318). In subgroup analysis by detection type, electrochemiluminescence immunoassay (ECLIA) group and enzyme-linked immunosorbent assay (ELISA) group showed higher PRL levels among SSc patients. CONCLUSIONS: In summary, our meta-analysis showed a significantly higher plasma/serum PRL level in SSc patients than healthy controls, and it was associated with gender and detection method. Lippincott Williams & Wilkins 2020-09-18 /pmc/articles/PMC7505334/ /pubmed/32957368 http://dx.doi.org/10.1097/MD.0000000000022239 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle 6900
Wu, Yang
Li, Meng-Lei
Han, Hua-Jing
Huang, Li-Jun
He, Yong
Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis
title Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis
title_full Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis
title_fullStr Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis
title_full_unstemmed Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis
title_short Elevated plasma/serum levels of prolactin in patients with systemic sclerosis: A systematic review and meta-analysis
title_sort elevated plasma/serum levels of prolactin in patients with systemic sclerosis: a systematic review and meta-analysis
topic 6900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505334/
https://www.ncbi.nlm.nih.gov/pubmed/32957368
http://dx.doi.org/10.1097/MD.0000000000022239
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