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Copeptin Kinetics and Its Relationship to Osmolality During Rehydration for Diabetic Ketoacidosis in Children

Abstract Context Copeptin is a surrogate marker for arginine vasopressin (AVP) release in response to hyperosmolal stimuli such as diabetic ketoacidosis (DKA). Objective The objective of this work is to characterize kinetics of copeptin and osmolality, and their dynamic relationship during rehydrati...

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Published in:The journal of clinical endocrinology and metabolism 2020-11, Vol.105 (11), p.1-e4178
Main Authors: Burckhardt, Marie-Anne, Gotta, Verena, Beglinger, Svetlana, Renggli, Luzia, Bachmann, Sara, Hess, Melanie, Rentsch, Katharina, Pfister, Marc, Koch, Gilbert, Davis, Elizabeth A, Zumsteg, Urs, Jones, Timothy W, Szinnai, Gabor
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container_issue 11
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container_title The journal of clinical endocrinology and metabolism
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creator Burckhardt, Marie-Anne
Gotta, Verena
Beglinger, Svetlana
Renggli, Luzia
Bachmann, Sara
Hess, Melanie
Rentsch, Katharina
Pfister, Marc
Koch, Gilbert
Davis, Elizabeth A
Zumsteg, Urs
Jones, Timothy W
Szinnai, Gabor
description Abstract Context Copeptin is a surrogate marker for arginine vasopressin (AVP) release in response to hyperosmolal stimuli such as diabetic ketoacidosis (DKA). Objective The objective of this work is to characterize kinetics of copeptin and osmolality, and their dynamic relationship during rehydration and insulin therapy in children with type 1 diabetes (T1D) and DKA. Design and Setting A prospective, observational, multicenter study was conducted. Patients and Intervention Children with T1D admitted for DKA underwent serial serum copeptin and osmolality measurements from start of rehydration at 14 time points during 72 hours. Main Outcome Measures Measurements included temporal course of copeptin and osmolality (kinetics), relationship between both (dynamics), and association between-subject variability (BSV) (coefficient of variation, CV%). Results Twenty-eight children (20 newly diagnosed T1D) aged 1 to 16 years were included. Copeptin decreased from 95 pmol/L (95% CI, 55-136 pmol/L) (CV%, 158%) to 9.7 pmol/L (95% CI, 8.1-11.4 pmol/L) (CV%, 31%) with a 50% recovery time (t1/2) of 7.1 hours (range, 5.1-11.5 hours) (114%). Serum osmolality decreased from 321 mOsm/kg (range, 315-327 mOsm/kg) (4%) to 294 mOsm/kg (range, 292-296 mOsm/kg) (1%) with a t1/2 of 4.3 hours (range, 3.0-5.6 hours) (64%). Copeptin levels doubled with each osmolality increase by 15 mOsm/kg (range, 10-21 mOsm/kg) (59%), from 9.8 pmol/L (range, 7.3-12.3 pmol/L) (48%) to 280 mOsm/kg. Copeptin kinetics differed between newly diagnosed and known T1D patients (P = .001), and less between mild vs moderate-severe DKA (P = .04). Conclusions First, this study characterized for the first time copeptin kinetics and dynamics in the high hyperosmolar range in children with DKA. Second, it revealed significant differences in copeptin kinetics between newly diagnosed and known T1D patients that may be explained by changes at the osmoreceptor and renal AVP receptor level due to longstanding osmotic diuresis and DKA.
doi_str_mv 10.1210/clinem/dgaa568
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Objective The objective of this work is to characterize kinetics of copeptin and osmolality, and their dynamic relationship during rehydration and insulin therapy in children with type 1 diabetes (T1D) and DKA. Design and Setting A prospective, observational, multicenter study was conducted. Patients and Intervention Children with T1D admitted for DKA underwent serial serum copeptin and osmolality measurements from start of rehydration at 14 time points during 72 hours. Main Outcome Measures Measurements included temporal course of copeptin and osmolality (kinetics), relationship between both (dynamics), and association between-subject variability (BSV) (coefficient of variation, CV%). Results Twenty-eight children (20 newly diagnosed T1D) aged 1 to 16 years were included. Copeptin decreased from 95 pmol/L (95% CI, 55-136 pmol/L) (CV%, 158%) to 9.7 pmol/L (95% CI, 8.1-11.4 pmol/L) (CV%, 31%) with a 50% recovery time (t1/2) of 7.1 hours (range, 5.1-11.5 hours) (114%). Serum osmolality decreased from 321 mOsm/kg (range, 315-327 mOsm/kg) (4%) to 294 mOsm/kg (range, 292-296 mOsm/kg) (1%) with a t1/2 of 4.3 hours (range, 3.0-5.6 hours) (64%). Copeptin levels doubled with each osmolality increase by 15 mOsm/kg (range, 10-21 mOsm/kg) (59%), from 9.8 pmol/L (range, 7.3-12.3 pmol/L) (48%) to 280 mOsm/kg. Copeptin kinetics differed between newly diagnosed and known T1D patients (P = .001), and less between mild vs moderate-severe DKA (P = .04). Conclusions First, this study characterized for the first time copeptin kinetics and dynamics in the high hyperosmolar range in children with DKA. Second, it revealed significant differences in copeptin kinetics between newly diagnosed and known T1D patients that may be explained by changes at the osmoreceptor and renal AVP receptor level due to longstanding osmotic diuresis and DKA.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/clinem/dgaa568</identifier><identifier>PMID: 32835363</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adolescent ; Arginine Vasopressin - blood ; Argipressin ; Biomarkers - blood ; Child ; Child, Preschool ; Children ; Diabetes ; Diabetes mellitus (insulin dependent) ; Diabetes therapy ; Diabetic acidosis ; Diabetic ketoacidosis ; Diabetic Ketoacidosis - blood ; Diabetic Ketoacidosis - therapy ; Diabetics ; Diuresis ; Female ; Fluid Therapy ; Glycopeptides - blood ; Humans ; Infant ; Insulin ; Ketoacidosis ; Male ; Osmolar Concentration ; Osmotic pressure ; Prospective Studies ; Rehydration ; Type 1 diabetes ; Vasopressin</subject><ispartof>The journal of clinical endocrinology and metabolism, 2020-11, Vol.105 (11), p.1-e4178</ispartof><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020</rights><rights>Copyright © Oxford University Press 2015</rights><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5078-a95e5cfbee1bceaeaa797bae4ac4329e7fe8aaf55f59b315b02f784d63625e3</citedby><cites>FETCH-LOGICAL-c5078-a95e5cfbee1bceaeaa797bae4ac4329e7fe8aaf55f59b315b02f784d63625e3</cites><orcidid>0000-0002-7989-1998 ; 0000-0003-2597-1228 ; 0000-0001-6254-5207 ; 0000-0002-6585-9778 ; 0000-0002-9386-0506 ; 0000-0003-0559-2597 ; 0000-0002-6274-5900</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32835363$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burckhardt, Marie-Anne</creatorcontrib><creatorcontrib>Gotta, Verena</creatorcontrib><creatorcontrib>Beglinger, Svetlana</creatorcontrib><creatorcontrib>Renggli, Luzia</creatorcontrib><creatorcontrib>Bachmann, Sara</creatorcontrib><creatorcontrib>Hess, Melanie</creatorcontrib><creatorcontrib>Rentsch, Katharina</creatorcontrib><creatorcontrib>Pfister, Marc</creatorcontrib><creatorcontrib>Koch, Gilbert</creatorcontrib><creatorcontrib>Davis, Elizabeth A</creatorcontrib><creatorcontrib>Zumsteg, Urs</creatorcontrib><creatorcontrib>Jones, Timothy W</creatorcontrib><creatorcontrib>Szinnai, Gabor</creatorcontrib><title>Copeptin Kinetics and Its Relationship to Osmolality During Rehydration for Diabetic Ketoacidosis in Children</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>Abstract Context Copeptin is a surrogate marker for arginine vasopressin (AVP) release in response to hyperosmolal stimuli such as diabetic ketoacidosis (DKA). Objective The objective of this work is to characterize kinetics of copeptin and osmolality, and their dynamic relationship during rehydration and insulin therapy in children with type 1 diabetes (T1D) and DKA. Design and Setting A prospective, observational, multicenter study was conducted. Patients and Intervention Children with T1D admitted for DKA underwent serial serum copeptin and osmolality measurements from start of rehydration at 14 time points during 72 hours. Main Outcome Measures Measurements included temporal course of copeptin and osmolality (kinetics), relationship between both (dynamics), and association between-subject variability (BSV) (coefficient of variation, CV%). Results Twenty-eight children (20 newly diagnosed T1D) aged 1 to 16 years were included. Copeptin decreased from 95 pmol/L (95% CI, 55-136 pmol/L) (CV%, 158%) to 9.7 pmol/L (95% CI, 8.1-11.4 pmol/L) (CV%, 31%) with a 50% recovery time (t1/2) of 7.1 hours (range, 5.1-11.5 hours) (114%). Serum osmolality decreased from 321 mOsm/kg (range, 315-327 mOsm/kg) (4%) to 294 mOsm/kg (range, 292-296 mOsm/kg) (1%) with a t1/2 of 4.3 hours (range, 3.0-5.6 hours) (64%). Copeptin levels doubled with each osmolality increase by 15 mOsm/kg (range, 10-21 mOsm/kg) (59%), from 9.8 pmol/L (range, 7.3-12.3 pmol/L) (48%) to 280 mOsm/kg. Copeptin kinetics differed between newly diagnosed and known T1D patients (P = .001), and less between mild vs moderate-severe DKA (P = .04). Conclusions First, this study characterized for the first time copeptin kinetics and dynamics in the high hyperosmolar range in children with DKA. 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Objective The objective of this work is to characterize kinetics of copeptin and osmolality, and their dynamic relationship during rehydration and insulin therapy in children with type 1 diabetes (T1D) and DKA. Design and Setting A prospective, observational, multicenter study was conducted. Patients and Intervention Children with T1D admitted for DKA underwent serial serum copeptin and osmolality measurements from start of rehydration at 14 time points during 72 hours. Main Outcome Measures Measurements included temporal course of copeptin and osmolality (kinetics), relationship between both (dynamics), and association between-subject variability (BSV) (coefficient of variation, CV%). Results Twenty-eight children (20 newly diagnosed T1D) aged 1 to 16 years were included. Copeptin decreased from 95 pmol/L (95% CI, 55-136 pmol/L) (CV%, 158%) to 9.7 pmol/L (95% CI, 8.1-11.4 pmol/L) (CV%, 31%) with a 50% recovery time (t1/2) of 7.1 hours (range, 5.1-11.5 hours) (114%). Serum osmolality decreased from 321 mOsm/kg (range, 315-327 mOsm/kg) (4%) to 294 mOsm/kg (range, 292-296 mOsm/kg) (1%) with a t1/2 of 4.3 hours (range, 3.0-5.6 hours) (64%). Copeptin levels doubled with each osmolality increase by 15 mOsm/kg (range, 10-21 mOsm/kg) (59%), from 9.8 pmol/L (range, 7.3-12.3 pmol/L) (48%) to 280 mOsm/kg. Copeptin kinetics differed between newly diagnosed and known T1D patients (P = .001), and less between mild vs moderate-severe DKA (P = .04). Conclusions First, this study characterized for the first time copeptin kinetics and dynamics in the high hyperosmolar range in children with DKA. Second, it revealed significant differences in copeptin kinetics between newly diagnosed and known T1D patients that may be explained by changes at the osmoreceptor and renal AVP receptor level due to longstanding osmotic diuresis and DKA.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>32835363</pmid><doi>10.1210/clinem/dgaa568</doi><orcidid>https://orcid.org/0000-0002-7989-1998</orcidid><orcidid>https://orcid.org/0000-0003-2597-1228</orcidid><orcidid>https://orcid.org/0000-0001-6254-5207</orcidid><orcidid>https://orcid.org/0000-0002-6585-9778</orcidid><orcidid>https://orcid.org/0000-0002-9386-0506</orcidid><orcidid>https://orcid.org/0000-0003-0559-2597</orcidid><orcidid>https://orcid.org/0000-0002-6274-5900</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0021-972X
ispartof The journal of clinical endocrinology and metabolism, 2020-11, Vol.105 (11), p.1-e4178
issn 0021-972X
1945-7197
language eng
recordid cdi_proquest_miscellaneous_2437124366
source Oxford Journals Online
subjects Adolescent
Arginine Vasopressin - blood
Argipressin
Biomarkers - blood
Child
Child, Preschool
Children
Diabetes
Diabetes mellitus (insulin dependent)
Diabetes therapy
Diabetic acidosis
Diabetic ketoacidosis
Diabetic Ketoacidosis - blood
Diabetic Ketoacidosis - therapy
Diabetics
Diuresis
Female
Fluid Therapy
Glycopeptides - blood
Humans
Infant
Insulin
Ketoacidosis
Male
Osmolar Concentration
Osmotic pressure
Prospective Studies
Rehydration
Type 1 diabetes
Vasopressin
title Copeptin Kinetics and Its Relationship to Osmolality During Rehydration for Diabetic Ketoacidosis in Children
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