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Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows

Sow mortality, as the result of pelvic organ prolapse (POP), has been increasing in the last decade in the U.S. swine industry. The objective of this study was to identify potential biological markers associated with risk of POP in sows. We hypothesized that sows differing in perineal score (PS) fro...

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Autores principales: Kiefer, Zoë E, Studer, Jamie M, Chipman, Amanda L, Adur, Malavika K, Mainquist-Whigham, Christine, Gabler, Nicholas K, Keating, Aileen F, Ross, Jason W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378218/
https://www.ncbi.nlm.nih.gov/pubmed/34228800
http://dx.doi.org/10.1093/jas/skab207
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author Kiefer, Zoë E
Studer, Jamie M
Chipman, Amanda L
Adur, Malavika K
Mainquist-Whigham, Christine
Gabler, Nicholas K
Keating, Aileen F
Ross, Jason W
author_facet Kiefer, Zoë E
Studer, Jamie M
Chipman, Amanda L
Adur, Malavika K
Mainquist-Whigham, Christine
Gabler, Nicholas K
Keating, Aileen F
Ross, Jason W
author_sort Kiefer, Zoë E
collection PubMed
description Sow mortality, as the result of pelvic organ prolapse (POP), has been increasing in the last decade in the U.S. swine industry. The objective of this study was to identify potential biological markers associated with risk of POP in sows. We hypothesized that sows differing in perineal score (PS) from PS1–PS3 (PS1—a presumed low POP risk; PS2—a presumed moderate POP risk; and PS3—a presumed high POP risk) would differ in circulatory biomarkers of inflammation and hormonal profiles. On gestation week 15, 2,864 individual sows were assigned a PS, and subsequently, 1.0%, 2.7%, and 23.4% of PS1, PS2, or PS3 sows, respectively, experienced POP. During PS assignment at days 107–116 of gestation, blood samples were collected from sows on two farms of similar genetics, feed sources, and health status. Whole blood was subjected to complete blood count (CBC) analysis (n = 212) and steroid hormones were measured in serum from a subset (n = 110) of animals assigned PS3 parity matched to PS1. Lipopolysaccharide-binding protein (LBP), tumor necrosis factor-alpha (TNF-α), haptoglobin, C-reactive protein (CRP), and creatine kinase (CK) levels were also evaluated. Complete blood count analysis revealed decreased (P ≤ 0.05) mean platelet volume (3.9%), lymphocytes (6.5%), and monocytes (7.5%) in PS3 compared to PS1 sows. Increased (P ≤ 0.02) abundance of androstenedione (13.4%), androsterone (18.2%), estrone (24.8%), and 17β-estradiol (26.2%) was observed in PS3 compared to PS1 sows. Additionally, a 25.8% increase (P = 0.04) in LBP in PS3 compared to PS1 sows was observed. Many dynamic physiological changes occur in sows during late gestation as they approach farrowing. The data presented herein demonstrate that distinct differences in concentrations of circulating biomarkers exist between late gestation sows at high or low risk for POP and may serve as a useful tool for understanding the etiology of POP and evaluation of mitigation strategies.
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spelling pubmed-83782182021-08-23 Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows Kiefer, Zoë E Studer, Jamie M Chipman, Amanda L Adur, Malavika K Mainquist-Whigham, Christine Gabler, Nicholas K Keating, Aileen F Ross, Jason W J Anim Sci Endocrinology and Physiology Sow mortality, as the result of pelvic organ prolapse (POP), has been increasing in the last decade in the U.S. swine industry. The objective of this study was to identify potential biological markers associated with risk of POP in sows. We hypothesized that sows differing in perineal score (PS) from PS1–PS3 (PS1—a presumed low POP risk; PS2—a presumed moderate POP risk; and PS3—a presumed high POP risk) would differ in circulatory biomarkers of inflammation and hormonal profiles. On gestation week 15, 2,864 individual sows were assigned a PS, and subsequently, 1.0%, 2.7%, and 23.4% of PS1, PS2, or PS3 sows, respectively, experienced POP. During PS assignment at days 107–116 of gestation, blood samples were collected from sows on two farms of similar genetics, feed sources, and health status. Whole blood was subjected to complete blood count (CBC) analysis (n = 212) and steroid hormones were measured in serum from a subset (n = 110) of animals assigned PS3 parity matched to PS1. Lipopolysaccharide-binding protein (LBP), tumor necrosis factor-alpha (TNF-α), haptoglobin, C-reactive protein (CRP), and creatine kinase (CK) levels were also evaluated. Complete blood count analysis revealed decreased (P ≤ 0.05) mean platelet volume (3.9%), lymphocytes (6.5%), and monocytes (7.5%) in PS3 compared to PS1 sows. Increased (P ≤ 0.02) abundance of androstenedione (13.4%), androsterone (18.2%), estrone (24.8%), and 17β-estradiol (26.2%) was observed in PS3 compared to PS1 sows. Additionally, a 25.8% increase (P = 0.04) in LBP in PS3 compared to PS1 sows was observed. Many dynamic physiological changes occur in sows during late gestation as they approach farrowing. The data presented herein demonstrate that distinct differences in concentrations of circulating biomarkers exist between late gestation sows at high or low risk for POP and may serve as a useful tool for understanding the etiology of POP and evaluation of mitigation strategies. Oxford University Press 2021-07-06 /pmc/articles/PMC8378218/ /pubmed/34228800 http://dx.doi.org/10.1093/jas/skab207 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the American Society of Animal Science. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Endocrinology and Physiology
Kiefer, Zoë E
Studer, Jamie M
Chipman, Amanda L
Adur, Malavika K
Mainquist-Whigham, Christine
Gabler, Nicholas K
Keating, Aileen F
Ross, Jason W
Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows
title Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows
title_full Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows
title_fullStr Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows
title_full_unstemmed Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows
title_short Circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows
title_sort circulating biomarkers associated with pelvic organ prolapse risk in late gestation sows
topic Endocrinology and Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378218/
https://www.ncbi.nlm.nih.gov/pubmed/34228800
http://dx.doi.org/10.1093/jas/skab207
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