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Regulation of urinary calcium excretion by vasopressin
BACKGROUND: The antidiuretic hormone (ADH) or arginine vasopressin (AVP) regulates the body's water balance. Recently, modifications in AVP levels have been related to osteoporosis during ageing and microgravity/bed rest. Therefore the present study was devised to assess whether the absence of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577769/ https://www.ncbi.nlm.nih.gov/pubmed/33123363 http://dx.doi.org/10.1093/ckj/sfaa134 |
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author | Anastasio, Pietro Trepiccione, Francesco De Santo, Natale Gaspare Capasso, Giovambattista Viggiano, Davide Capolongo, Giovanna |
author_facet | Anastasio, Pietro Trepiccione, Francesco De Santo, Natale Gaspare Capasso, Giovambattista Viggiano, Davide Capolongo, Giovanna |
author_sort | Anastasio, Pietro |
collection | PubMed |
description | BACKGROUND: The antidiuretic hormone (ADH) or arginine vasopressin (AVP) regulates the body's water balance. Recently, modifications in AVP levels have been related to osteoporosis during ageing and microgravity/bed rest. Therefore the present study was devised to assess whether the absence of AVP, as in patients with central diabetes insipidus (CDI), modulates renal calcium excretion. METHODS: We retrospectively analysed data from 12 patients with CDI with measured 24-h urinary excretion levels of calcium. Data were available at the moment of the diagnosis when patients were drug-free and after therapy with dDAVP, an analog of AVP. Hypercalciuria was defined as 24-h urinary Ca(2+) >275 mg/day in males and >250 mg/day in females and a urinary calcium (Ca):creatinine (Cr) ratio >0.20 mg/mg. RESULTS: Untreated CDI patients had a daily urinary Ca(2+) excretion of 383 ± 47 mg/day and a urinary Ca:Cr ratio of 0.26 ± 0.38 mg/mg. The urine osmolarity significantly increased after the administration of dDAVP by 210% and the urinary flow decreased by 72%. Furthermore, the estimated glomerular filtration rate (eGFR) increased by 7%, which did not reach statistical significance. dDAVP treatment did not significantly modify the urinary Ca(2+) concentration; however, the daily calcium excretion and the urinary Ca:Cr ratio were significantly decreased (160 ± 27 mg/day and 0.11 ± 0.02 mg/mg, respectively). CONCLUSIONS: Patients with CDI show hypercalciuria even though urine is more diluted than normal controls, and dDAVP reverses this effect. These data support the intriguing relationship between AVP and osteoporosis in ageing and microgravity/bed rest. |
format | Online Article Text |
id | pubmed-7577769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75777692020-10-28 Regulation of urinary calcium excretion by vasopressin Anastasio, Pietro Trepiccione, Francesco De Santo, Natale Gaspare Capasso, Giovambattista Viggiano, Davide Capolongo, Giovanna Clin Kidney J Original Articles BACKGROUND: The antidiuretic hormone (ADH) or arginine vasopressin (AVP) regulates the body's water balance. Recently, modifications in AVP levels have been related to osteoporosis during ageing and microgravity/bed rest. Therefore the present study was devised to assess whether the absence of AVP, as in patients with central diabetes insipidus (CDI), modulates renal calcium excretion. METHODS: We retrospectively analysed data from 12 patients with CDI with measured 24-h urinary excretion levels of calcium. Data were available at the moment of the diagnosis when patients were drug-free and after therapy with dDAVP, an analog of AVP. Hypercalciuria was defined as 24-h urinary Ca(2+) >275 mg/day in males and >250 mg/day in females and a urinary calcium (Ca):creatinine (Cr) ratio >0.20 mg/mg. RESULTS: Untreated CDI patients had a daily urinary Ca(2+) excretion of 383 ± 47 mg/day and a urinary Ca:Cr ratio of 0.26 ± 0.38 mg/mg. The urine osmolarity significantly increased after the administration of dDAVP by 210% and the urinary flow decreased by 72%. Furthermore, the estimated glomerular filtration rate (eGFR) increased by 7%, which did not reach statistical significance. dDAVP treatment did not significantly modify the urinary Ca(2+) concentration; however, the daily calcium excretion and the urinary Ca:Cr ratio were significantly decreased (160 ± 27 mg/day and 0.11 ± 0.02 mg/mg, respectively). CONCLUSIONS: Patients with CDI show hypercalciuria even though urine is more diluted than normal controls, and dDAVP reverses this effect. These data support the intriguing relationship between AVP and osteoporosis in ageing and microgravity/bed rest. Oxford University Press 2020-09-16 /pmc/articles/PMC7577769/ /pubmed/33123363 http://dx.doi.org/10.1093/ckj/sfaa134 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. 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 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 | Original Articles Anastasio, Pietro Trepiccione, Francesco De Santo, Natale Gaspare Capasso, Giovambattista Viggiano, Davide Capolongo, Giovanna Regulation of urinary calcium excretion by vasopressin |
title | Regulation of urinary calcium excretion by vasopressin |
title_full | Regulation of urinary calcium excretion by vasopressin |
title_fullStr | Regulation of urinary calcium excretion by vasopressin |
title_full_unstemmed | Regulation of urinary calcium excretion by vasopressin |
title_short | Regulation of urinary calcium excretion by vasopressin |
title_sort | regulation of urinary calcium excretion by vasopressin |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577769/ https://www.ncbi.nlm.nih.gov/pubmed/33123363 http://dx.doi.org/10.1093/ckj/sfaa134 |
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