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Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men

Components of the renin–angiotensin–aldosterone system (RAAS) are present on bone cells. One measure of RAAS activity, the aldosterone-renin-ratio (ARR), is used to screen for primary aldosteronism. Associations between ARR and bone mineral density are conflicting. This study investigated associatio...

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Autores principales: Holloway-Kew, Kara L., Anderson, Kara B., Rufus-Membere, Pamela, Tembo, Monica C., Sui, Sophia X., Hyde, Natalie K., Kotowicz, Mark A., Gwini, Stella M., Yang, Jun, Diez-Perez, Adolfo, Henneberg, Maciej, Liao, Wan-Hui, Pasco, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618308/
https://www.ncbi.nlm.nih.gov/pubmed/37690031
http://dx.doi.org/10.1007/s00223-023-01131-x
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author Holloway-Kew, Kara L.
Anderson, Kara B.
Rufus-Membere, Pamela
Tembo, Monica C.
Sui, Sophia X.
Hyde, Natalie K.
Kotowicz, Mark A.
Gwini, Stella M.
Yang, Jun
Diez-Perez, Adolfo
Henneberg, Maciej
Liao, Wan-Hui
Pasco, Julie A.
author_facet Holloway-Kew, Kara L.
Anderson, Kara B.
Rufus-Membere, Pamela
Tembo, Monica C.
Sui, Sophia X.
Hyde, Natalie K.
Kotowicz, Mark A.
Gwini, Stella M.
Yang, Jun
Diez-Perez, Adolfo
Henneberg, Maciej
Liao, Wan-Hui
Pasco, Julie A.
author_sort Holloway-Kew, Kara L.
collection PubMed
description Components of the renin–angiotensin–aldosterone system (RAAS) are present on bone cells. One measure of RAAS activity, the aldosterone-renin-ratio (ARR), is used to screen for primary aldosteronism. Associations between ARR and bone mineral density are conflicting. This study investigated associations between ARR and peripheral quantitative computed tomography (pQCT) and impact microindentation (IMI). Male participants (n = 431) were from the Geelong Osteoporosis Study. “Likely” primary aldosteronism was defined as ARR ≥ 70 pmol/mIU. Another group, “possible” primary aldosteronism, was defined as either ARR ≥ 70 pmol/mIU or taking a medication that affects the RAAS, but not a beta blocker, and renin < 15 mU/L. Using pQCT, images at 4% and 66% of radial (n = 365) and tibial (n = 356) length were obtained. Using IMI measurements, bone material strength index (BMSi; n = 332) was determined. Associations between ARR or likely/possible primary aldosteronism and IMI or pQCT-derived bone parameters were tested using median regression. ARR and aldosterone values were not associated with any of the pQCT-derived bone variables in either unadjusted or adjusted analyses. Men with likely primary aldosteronism (n = 16), had lower adjusted total bone area (radial 66% site, − 12.5%). No associations were observed for men with possible primary aldosteronism (unadjusted or adjusted). No associations with BMSi were observed (p > 0.05). There were no associations between ARR or aldosterone and pQCT-derived bone parameters. Men with likely primary aldosteronism had lower bone area, suggesting clinically high levels of ARR may have a negative impact on bone health. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00223-023-01131-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-106183082023-11-02 Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men Holloway-Kew, Kara L. Anderson, Kara B. Rufus-Membere, Pamela Tembo, Monica C. Sui, Sophia X. Hyde, Natalie K. Kotowicz, Mark A. Gwini, Stella M. Yang, Jun Diez-Perez, Adolfo Henneberg, Maciej Liao, Wan-Hui Pasco, Julie A. Calcif Tissue Int Original Research Components of the renin–angiotensin–aldosterone system (RAAS) are present on bone cells. One measure of RAAS activity, the aldosterone-renin-ratio (ARR), is used to screen for primary aldosteronism. Associations between ARR and bone mineral density are conflicting. This study investigated associations between ARR and peripheral quantitative computed tomography (pQCT) and impact microindentation (IMI). Male participants (n = 431) were from the Geelong Osteoporosis Study. “Likely” primary aldosteronism was defined as ARR ≥ 70 pmol/mIU. Another group, “possible” primary aldosteronism, was defined as either ARR ≥ 70 pmol/mIU or taking a medication that affects the RAAS, but not a beta blocker, and renin < 15 mU/L. Using pQCT, images at 4% and 66% of radial (n = 365) and tibial (n = 356) length were obtained. Using IMI measurements, bone material strength index (BMSi; n = 332) was determined. Associations between ARR or likely/possible primary aldosteronism and IMI or pQCT-derived bone parameters were tested using median regression. ARR and aldosterone values were not associated with any of the pQCT-derived bone variables in either unadjusted or adjusted analyses. Men with likely primary aldosteronism (n = 16), had lower adjusted total bone area (radial 66% site, − 12.5%). No associations were observed for men with possible primary aldosteronism (unadjusted or adjusted). No associations with BMSi were observed (p > 0.05). There were no associations between ARR or aldosterone and pQCT-derived bone parameters. Men with likely primary aldosteronism had lower bone area, suggesting clinically high levels of ARR may have a negative impact on bone health. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00223-023-01131-x) contains supplementary material, which is available to authorized users. Springer US 2023-09-10 2023 /pmc/articles/PMC10618308/ /pubmed/37690031 http://dx.doi.org/10.1007/s00223-023-01131-x Text en © The Author(s) 2023 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 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/) .
spellingShingle Original Research
Holloway-Kew, Kara L.
Anderson, Kara B.
Rufus-Membere, Pamela
Tembo, Monica C.
Sui, Sophia X.
Hyde, Natalie K.
Kotowicz, Mark A.
Gwini, Stella M.
Yang, Jun
Diez-Perez, Adolfo
Henneberg, Maciej
Liao, Wan-Hui
Pasco, Julie A.
Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men
title Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men
title_full Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men
title_fullStr Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men
title_full_unstemmed Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men
title_short Associations Between Aldosterone-Renin-Ratio and Bone Parameters Derived from Peripheral Quantitative Computed Tomography and Impact Microindentation in Men
title_sort associations between aldosterone-renin-ratio and bone parameters derived from peripheral quantitative computed tomography and impact microindentation in men
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618308/
https://www.ncbi.nlm.nih.gov/pubmed/37690031
http://dx.doi.org/10.1007/s00223-023-01131-x
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