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Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion

BACKGROUND: Lysyl oxidase-like 2 (LOXL2) belongs to a family of the LOX secretory enzyme, which involves the cross-linkage of extracellular matrix (ECM) proteins. Here, we aimed to analyze the correlation between serum LOXL2 and pelvic adhesion in chronic pelvic inflammatory disease (PID). METHODS:...

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Autores principales: Xie, Chan, Tang, Bixin, Wu, Kunlun, Meng, Qingyi, Wang, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896148/
https://www.ncbi.nlm.nih.gov/pubmed/35246120
http://dx.doi.org/10.1186/s12905-022-01640-1
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author Xie, Chan
Tang, Bixin
Wu, Kunlun
Meng, Qingyi
Wang, Fang
author_facet Xie, Chan
Tang, Bixin
Wu, Kunlun
Meng, Qingyi
Wang, Fang
author_sort Xie, Chan
collection PubMed
description BACKGROUND: Lysyl oxidase-like 2 (LOXL2) belongs to a family of the LOX secretory enzyme, which involves the cross-linkage of extracellular matrix (ECM) proteins. Here, we aimed to analyze the correlation between serum LOXL2 and pelvic adhesion in chronic pelvic inflammatory disease (PID). METHODS: A total of 143 patients with PID and 130 healthy controls were included in this study. The serum levels of LOXL2 were measured using enzyme-linked immunosorbent assay (ELISA) kits. The patients were divided into non-adhesion group (102 cases) and adhesion group (41 cases). RESULTS: It was found that the serum level of LOXL2 expression was elevated in PID patients compared with healthy controls, and was elevated in PID patients with pelvic adhesion compared to patients without adhesion. In all PID patients, serum LOXL2 level was positively correlated with matrix metalloproteinases-9 (MMP-9), transforming growth factor-β (TGF-β1), whole blood viscosity (WBV) at low shear rate (LSR), WBV at high shear rate (HSR), and hematocrit (HcT). Multivariate logistic regression analysis showed that serum LOXL2 level was an independent risk factor for pelvic adhesion in PID patients (OR = 1.058; 95% CI = 1.030–1.086, P < 0.001). CONCLUSIONS: Serum LOXL2 level not only predicts the presence of PID, but serum LOXL2 concentration is also associated with the presence of pelvic adhesions.
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spelling pubmed-88961482022-03-10 Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion Xie, Chan Tang, Bixin Wu, Kunlun Meng, Qingyi Wang, Fang BMC Womens Health Original Research BACKGROUND: Lysyl oxidase-like 2 (LOXL2) belongs to a family of the LOX secretory enzyme, which involves the cross-linkage of extracellular matrix (ECM) proteins. Here, we aimed to analyze the correlation between serum LOXL2 and pelvic adhesion in chronic pelvic inflammatory disease (PID). METHODS: A total of 143 patients with PID and 130 healthy controls were included in this study. The serum levels of LOXL2 were measured using enzyme-linked immunosorbent assay (ELISA) kits. The patients were divided into non-adhesion group (102 cases) and adhesion group (41 cases). RESULTS: It was found that the serum level of LOXL2 expression was elevated in PID patients compared with healthy controls, and was elevated in PID patients with pelvic adhesion compared to patients without adhesion. In all PID patients, serum LOXL2 level was positively correlated with matrix metalloproteinases-9 (MMP-9), transforming growth factor-β (TGF-β1), whole blood viscosity (WBV) at low shear rate (LSR), WBV at high shear rate (HSR), and hematocrit (HcT). Multivariate logistic regression analysis showed that serum LOXL2 level was an independent risk factor for pelvic adhesion in PID patients (OR = 1.058; 95% CI = 1.030–1.086, P < 0.001). CONCLUSIONS: Serum LOXL2 level not only predicts the presence of PID, but serum LOXL2 concentration is also associated with the presence of pelvic adhesions. BioMed Central 2022-03-04 /pmc/articles/PMC8896148/ /pubmed/35246120 http://dx.doi.org/10.1186/s12905-022-01640-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Original Research
Xie, Chan
Tang, Bixin
Wu, Kunlun
Meng, Qingyi
Wang, Fang
Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion
title Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion
title_full Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion
title_fullStr Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion
title_full_unstemmed Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion
title_short Increased serum LOXL2 concentration in pelvic inflammatory disease with pelvic adhesion
title_sort increased serum loxl2 concentration in pelvic inflammatory disease with pelvic adhesion
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896148/
https://www.ncbi.nlm.nih.gov/pubmed/35246120
http://dx.doi.org/10.1186/s12905-022-01640-1
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