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The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students

Our aim was to establish if the secretion of contactin 1 (CNTN-1), a widely researched pain biomarker correlates with the severity of dysmenorrhea and circulating levels of vascular cell adhesion molecule 1 (VCAM-1) and angiotensin II (ANG-II). This study was a longitudinal randomized clinical study...

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Autores principales: Njoku, Uche Chinedu, Amadi, Peter Uchenna, Agomuo, Emmanuel Nnabugwu, Bhebhe, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chonnam National University Medical School 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520371/
https://www.ncbi.nlm.nih.gov/pubmed/33014757
http://dx.doi.org/10.4068/cmj.2020.56.3.186
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author Njoku, Uche Chinedu
Amadi, Peter Uchenna
Agomuo, Emmanuel Nnabugwu
Bhebhe, Michael
author_facet Njoku, Uche Chinedu
Amadi, Peter Uchenna
Agomuo, Emmanuel Nnabugwu
Bhebhe, Michael
author_sort Njoku, Uche Chinedu
collection PubMed
description Our aim was to establish if the secretion of contactin 1 (CNTN-1), a widely researched pain biomarker correlates with the severity of dysmenorrhea and circulating levels of vascular cell adhesion molecule 1 (VCAM-1) and angiotensin II (ANG-II). This study was a longitudinal randomized clinical study that involved 95 female students between 17–25 years. The control participant group were students who, without medications, had not experienced dysmenorrhea, while the inclusion criteria were primary dysmenorrhea without medications. Data was collected using demographic questionnaires that also contained the Numeric Rating Scale (NRS-11), while blood samples were collected for analysis of CNTN-1, VCAM-1 and ANG-II by ELISA. The participants' mean BMI's across the four pain strata were between 16.60–38.43 kg/m(2) and in addition to age and menarche, showed no correlation to either the NRS-11 scale (r=−0.01214) or their CNTN-1 levels (r=0.009622). The severe dysmenorrhea group showed statistically higher (p<0.0001) and positive correlation to systolic (r=0.7304) and diastolic (0.6588) blood pressures. The contactin 1 levels (7.00-55.70 ng/mL) increased with higher menstrual pain and as the pain increased, so did the mean VCAM-1 and ANG-II levels (p<0.0001). A positive linear correlation (r=0.9691) was observed between the NRS-11 scale of the participants and their CNTN-1 activities while the CNTN-1 levels positively correlated with their VCAM-1 (r=0.9334) and ANG-II (r=0.8746) secretion. In summary, the severity of dysmenorrheal pain elevates the contactin 1 levels which affects their vascular health and blood pressure.
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spelling pubmed-75203712020-10-02 The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students Njoku, Uche Chinedu Amadi, Peter Uchenna Agomuo, Emmanuel Nnabugwu Bhebhe, Michael Chonnam Med J Original Article Our aim was to establish if the secretion of contactin 1 (CNTN-1), a widely researched pain biomarker correlates with the severity of dysmenorrhea and circulating levels of vascular cell adhesion molecule 1 (VCAM-1) and angiotensin II (ANG-II). This study was a longitudinal randomized clinical study that involved 95 female students between 17–25 years. The control participant group were students who, without medications, had not experienced dysmenorrhea, while the inclusion criteria were primary dysmenorrhea without medications. Data was collected using demographic questionnaires that also contained the Numeric Rating Scale (NRS-11), while blood samples were collected for analysis of CNTN-1, VCAM-1 and ANG-II by ELISA. The participants' mean BMI's across the four pain strata were between 16.60–38.43 kg/m(2) and in addition to age and menarche, showed no correlation to either the NRS-11 scale (r=−0.01214) or their CNTN-1 levels (r=0.009622). The severe dysmenorrhea group showed statistically higher (p<0.0001) and positive correlation to systolic (r=0.7304) and diastolic (0.6588) blood pressures. The contactin 1 levels (7.00-55.70 ng/mL) increased with higher menstrual pain and as the pain increased, so did the mean VCAM-1 and ANG-II levels (p<0.0001). A positive linear correlation (r=0.9691) was observed between the NRS-11 scale of the participants and their CNTN-1 activities while the CNTN-1 levels positively correlated with their VCAM-1 (r=0.9334) and ANG-II (r=0.8746) secretion. In summary, the severity of dysmenorrheal pain elevates the contactin 1 levels which affects their vascular health and blood pressure. Chonnam National University Medical School 2020-09 2020-09-24 /pmc/articles/PMC7520371/ /pubmed/33014757 http://dx.doi.org/10.4068/cmj.2020.56.3.186 Text en © Chonnam Medical Journal, 2020 http://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 (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Njoku, Uche Chinedu
Amadi, Peter Uchenna
Agomuo, Emmanuel Nnabugwu
Bhebhe, Michael
The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students
title The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students
title_full The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students
title_fullStr The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students
title_full_unstemmed The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students
title_short The Relationship between Pain and Vascular Function Biomarkers in Dysmenorrheal University Students
title_sort relationship between pain and vascular function biomarkers in dysmenorrheal university students
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520371/
https://www.ncbi.nlm.nih.gov/pubmed/33014757
http://dx.doi.org/10.4068/cmj.2020.56.3.186
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