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Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults
Purpose: African American individuals are more prone to salt-sensitive hypertension than Caucasian individuals. Small changes in serum sodium (Na(+)) result in increased blood pressure (BP). However, it remains unclear if there are racial differences in BP responsiveness to increases in serum Na(+)....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174209/ https://www.ncbi.nlm.nih.gov/pubmed/30327611 http://dx.doi.org/10.3389/fphys.2018.01354 |
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author | Wenner, Megan M. Paul, Erin P. Robinson, Austin T. Rose, William C. Farquhar, William B. |
author_facet | Wenner, Megan M. Paul, Erin P. Robinson, Austin T. Rose, William C. Farquhar, William B. |
author_sort | Wenner, Megan M. |
collection | PubMed |
description | Purpose: African American individuals are more prone to salt-sensitive hypertension than Caucasian individuals. Small changes in serum sodium (Na(+)) result in increased blood pressure (BP). However, it remains unclear if there are racial differences in BP responsiveness to increases in serum Na(+). Therefore, the purpose of this investigation was to determine if African American adults have altered BP responsiveness to acute changes in serum Na(+) compared to Caucasian adults. Methods: We measured beat-by-beat BP, serum Na(+), plasma renin activity (PRA), angiotensin II (Ang II), and aldosterone (Aldo) during a 60-min 3% NaCl infusion (hypertonic saline infusion, HSI) in 39 participants (19 African Americans, age: 23 ± 1, 20 Caucasians, age: 25 ± 1). Data reported as African American vs. Caucasian cohort, mean ± SEM. Results: Baseline BP and serum Na(+) were similar between groups and increased during HSI in both African American and Caucasian participants (p < 0.01). However, the peak change in serum Na(+) was greater in African American participants (Δ5.8 ± 0.34 vs. Δ4.85 ± 0.38 mmol/L, p = 0.03). There was a significant group effect (p = 0.02) and an interaction between race and serum Na(+) on systolic BP (p = 0.02). Larger categorical changes in serum Na(+) corresponded to changes in systolic BP (p < 0.01) and African American participants demonstrated greater systolic BP responses for a given categorical serum Na(+) increase (p < 0.01). Baseline Aldo was lower in African American adults (7.2 ± 0.6 vs. 12.0 ± 1.9 ng/dL, p = 0.03), there was a trend for lower baseline PRA (0.59 ± 0.9 vs. 1.28 ± 0.34 ng/mL/h, p = 0.07), and baseline Ang II was not different (14.2 ± 1.8 vs. 18.5 ± 1.4 pg/mL, p = 0.17). PRA and Aldo decreased during the HSI (p ≤ 0.01), with a greater decline in PRA (Δ–0.31 ± 0.07 vs. Δ–0.85 ± 0.25 ng/mL/h, p < 0.01) and Aldo (Δ–2.5 ± 0.5 vs. Δ–5.0 ± 1.1 ng/dL, p < 0.01) in Caucasian participants. However, the racial difference in PRA (p = 0.57) and Aldo (p = 0.59) reduction were no longer significant following baseline covariate analysis. Conclusion: African American individuals demonstrate augmented serum Na(+) to an acute hypertonic saline load and greater systolic BP responsiveness to a given serum Na(+). The altered BP response may be attributable to lower basal PRA and Aldo and a subsequently blunted RAAS response during the HSI. |
format | Online Article Text |
id | pubmed-6174209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61742092018-10-16 Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults Wenner, Megan M. Paul, Erin P. Robinson, Austin T. Rose, William C. Farquhar, William B. Front Physiol Physiology Purpose: African American individuals are more prone to salt-sensitive hypertension than Caucasian individuals. Small changes in serum sodium (Na(+)) result in increased blood pressure (BP). However, it remains unclear if there are racial differences in BP responsiveness to increases in serum Na(+). Therefore, the purpose of this investigation was to determine if African American adults have altered BP responsiveness to acute changes in serum Na(+) compared to Caucasian adults. Methods: We measured beat-by-beat BP, serum Na(+), plasma renin activity (PRA), angiotensin II (Ang II), and aldosterone (Aldo) during a 60-min 3% NaCl infusion (hypertonic saline infusion, HSI) in 39 participants (19 African Americans, age: 23 ± 1, 20 Caucasians, age: 25 ± 1). Data reported as African American vs. Caucasian cohort, mean ± SEM. Results: Baseline BP and serum Na(+) were similar between groups and increased during HSI in both African American and Caucasian participants (p < 0.01). However, the peak change in serum Na(+) was greater in African American participants (Δ5.8 ± 0.34 vs. Δ4.85 ± 0.38 mmol/L, p = 0.03). There was a significant group effect (p = 0.02) and an interaction between race and serum Na(+) on systolic BP (p = 0.02). Larger categorical changes in serum Na(+) corresponded to changes in systolic BP (p < 0.01) and African American participants demonstrated greater systolic BP responses for a given categorical serum Na(+) increase (p < 0.01). Baseline Aldo was lower in African American adults (7.2 ± 0.6 vs. 12.0 ± 1.9 ng/dL, p = 0.03), there was a trend for lower baseline PRA (0.59 ± 0.9 vs. 1.28 ± 0.34 ng/mL/h, p = 0.07), and baseline Ang II was not different (14.2 ± 1.8 vs. 18.5 ± 1.4 pg/mL, p = 0.17). PRA and Aldo decreased during the HSI (p ≤ 0.01), with a greater decline in PRA (Δ–0.31 ± 0.07 vs. Δ–0.85 ± 0.25 ng/mL/h, p < 0.01) and Aldo (Δ–2.5 ± 0.5 vs. Δ–5.0 ± 1.1 ng/dL, p < 0.01) in Caucasian participants. However, the racial difference in PRA (p = 0.57) and Aldo (p = 0.59) reduction were no longer significant following baseline covariate analysis. Conclusion: African American individuals demonstrate augmented serum Na(+) to an acute hypertonic saline load and greater systolic BP responsiveness to a given serum Na(+). The altered BP response may be attributable to lower basal PRA and Aldo and a subsequently blunted RAAS response during the HSI. Frontiers Media S.A. 2018-10-01 /pmc/articles/PMC6174209/ /pubmed/30327611 http://dx.doi.org/10.3389/fphys.2018.01354 Text en Copyright © 2018 Wenner, Paul, Robinson, Rose and Farquhar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Wenner, Megan M. Paul, Erin P. Robinson, Austin T. Rose, William C. Farquhar, William B. Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults |
title | Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults |
title_full | Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults |
title_fullStr | Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults |
title_full_unstemmed | Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults |
title_short | Acute NaCl Loading Reveals a Higher Blood Pressure for a Given Serum Sodium Level in African American Compared to Caucasian Adults |
title_sort | acute nacl loading reveals a higher blood pressure for a given serum sodium level in african american compared to caucasian adults |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174209/ https://www.ncbi.nlm.nih.gov/pubmed/30327611 http://dx.doi.org/10.3389/fphys.2018.01354 |
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