Knemometry is more sensitive to systemic effects of inhaled corticosteroids in children with asthma than 24-hour urine cortisol excretion
Background Pharmacodynamic assessment of the systemic effect of inhaled corticosteroids (ICSs) is often done by measuring 24-hour urine free cortisol (UFC) excretion. Knemometry assessing short-term lower-leg growth rate (LLGR) is a more rarely used alternative. Objective The primary aim of this stu...
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description | Background Pharmacodynamic assessment of the systemic effect of inhaled corticosteroids (ICSs) is often done by measuring 24-hour urine free cortisol (UFC) excretion. Knemometry assessing short-term lower-leg growth rate (LLGR) is a more rarely used alternative. Objective The primary aim of this study was to compare the sensitivity of LLGR and 24-hour UFC excretion for evaluating systemic exposure to ICSs in prepubertal children with asthma. The secondary aim was to evaluate factors influencing the precision of LLGR calculated by the traditional 1 leg nonparametric method versus a new 2 leg parametric method. Methods The study evaluated 60 children with mild asthma aged 5 to 12 years participating in a randomized controlled trial of ICSs with longitudinal concomitant assessments of LLGR and 24-hour UFC excretion. The sensitivity of the safety assessments was analyzed by comparing LLGR and 24-hour UFC in the placebo run-in period with values in the ICS treatment period by using paired t tests. Factors with a potential influence on LLGR were analyzed by means of ANOVA and the Levene test of homogeneity. Results The mean LLGR was significantly reduced during the ICS versus placebo run-in periods: 0.18 mm/wk (SD, 0.55 mm/wk) versus 0.45 mm/wk (SD, 0.39 mm/wk), with a mean difference of 0.27 mm/wk (95% CI, 0.05-0.48 mm/wk; P = .02). In contrast, there was no difference in 24-hour UFC excretion: 6.91 nmol/mmol (SD, 4.67 nmol/mmol) versus 7.58 nmol/mmol (SD, 6.17 nmol/mmol), with a mean difference of 0.67 nmol/mmol (95% CI, −1.13 to 2.48 nmol/mmol; P = .46). We observed no significant difference in parametric determined LLGR caused by the child's age or sex, investigator, or season of measurement, whereas some differences were observed for the nonparametric LLGR. Conclusion These findings suggest that knemometry is a more sensitive pharmacodynamic measure of systemic effects of ICSs than 24-hour UFC excretion and that a parametric determination of LLGR increases the sensitivity of the method. These findings should be considered by legislative authorities in the future. |
doi_str_mv | 10.1016/j.jaci.2016.09.041 |
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Knemometry assessing short-term lower-leg growth rate (LLGR) is a more rarely used alternative. Objective The primary aim of this study was to compare the sensitivity of LLGR and 24-hour UFC excretion for evaluating systemic exposure to ICSs in prepubertal children with asthma. The secondary aim was to evaluate factors influencing the precision of LLGR calculated by the traditional 1 leg nonparametric method versus a new 2 leg parametric method. Methods The study evaluated 60 children with mild asthma aged 5 to 12 years participating in a randomized controlled trial of ICSs with longitudinal concomitant assessments of LLGR and 24-hour UFC excretion. The sensitivity of the safety assessments was analyzed by comparing LLGR and 24-hour UFC in the placebo run-in period with values in the ICS treatment period by using paired t tests. Factors with a potential influence on LLGR were analyzed by means of ANOVA and the Levene test of homogeneity. Results The mean LLGR was significantly reduced during the ICS versus placebo run-in periods: 0.18 mm/wk (SD, 0.55 mm/wk) versus 0.45 mm/wk (SD, 0.39 mm/wk), with a mean difference of 0.27 mm/wk (95% CI, 0.05-0.48 mm/wk; P = .02). In contrast, there was no difference in 24-hour UFC excretion: 6.91 nmol/mmol (SD, 4.67 nmol/mmol) versus 7.58 nmol/mmol (SD, 6.17 nmol/mmol), with a mean difference of 0.67 nmol/mmol (95% CI, −1.13 to 2.48 nmol/mmol; P = .46). We observed no significant difference in parametric determined LLGR caused by the child's age or sex, investigator, or season of measurement, whereas some differences were observed for the nonparametric LLGR. Conclusion These findings suggest that knemometry is a more sensitive pharmacodynamic measure of systemic effects of ICSs than 24-hour UFC excretion and that a parametric determination of LLGR increases the sensitivity of the method. These findings should be considered by legislative authorities in the future.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2016.09.041</identifier><identifier>PMID: 28012663</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Administration, Inhalation ; Adrenal Cortex Hormones - pharmacology ; Allergy and Immunology ; Anti-Asthmatic Agents - pharmacology ; Asthma ; Asthma - urine ; Beclomethasone - pharmacology ; Child ; Child Development - drug effects ; Child, Preschool ; Children ; Children & youth ; Corticoids ; Corticosteroids ; Drug dosages ; Excretion ; Female ; Growth rate ; Homogeneity ; Hormones ; Humans ; Hydrocortisone - urine ; Immunomodulators ; inhaled corticosteroids ; knemometry ; Leg ; Leg - growth & development ; Legs ; Male ; Pharmacodynamics ; Respiratory therapy ; Sensitivity ; Short term ; Urine ; urine cortisol excretion ; Variance analysis</subject><ispartof>Journal of allergy and clinical immunology, 2017-08, Vol.140 (2), p.431-436</ispartof><rights>American Academy of Allergy, Asthma & Immunology</rights><rights>2016 American Academy of Allergy, Asthma & Immunology</rights><rights>Copyright © 2016 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Aug 1, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-b9ef5b58cb549f99b9b103a296e90a80dde49e0c6809233f50fa2cadfcf8cf53</citedby><cites>FETCH-LOGICAL-c483t-b9ef5b58cb549f99b9b103a296e90a80dde49e0c6809233f50fa2cadfcf8cf53</cites><orcidid>0000-0003-4131-7592</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0091674916312908$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28012663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chawes, Bo, MD, PhD, DMSc</creatorcontrib><creatorcontrib>Nilsson, Erik, MD</creatorcontrib><creatorcontrib>Nørgaard, Sarah, MSc</creatorcontrib><creatorcontrib>Dossing, Anna, MD</creatorcontrib><creatorcontrib>Mortensen, Li, MD</creatorcontrib><creatorcontrib>Bisgaard, Hans, MD, DMSc</creatorcontrib><title>Knemometry is more sensitive to systemic effects of inhaled corticosteroids in children with asthma than 24-hour urine cortisol excretion</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Background Pharmacodynamic assessment of the systemic effect of inhaled corticosteroids (ICSs) is often done by measuring 24-hour urine free cortisol (UFC) excretion. Knemometry assessing short-term lower-leg growth rate (LLGR) is a more rarely used alternative. Objective The primary aim of this study was to compare the sensitivity of LLGR and 24-hour UFC excretion for evaluating systemic exposure to ICSs in prepubertal children with asthma. The secondary aim was to evaluate factors influencing the precision of LLGR calculated by the traditional 1 leg nonparametric method versus a new 2 leg parametric method. Methods The study evaluated 60 children with mild asthma aged 5 to 12 years participating in a randomized controlled trial of ICSs with longitudinal concomitant assessments of LLGR and 24-hour UFC excretion. The sensitivity of the safety assessments was analyzed by comparing LLGR and 24-hour UFC in the placebo run-in period with values in the ICS treatment period by using paired t tests. Factors with a potential influence on LLGR were analyzed by means of ANOVA and the Levene test of homogeneity. Results The mean LLGR was significantly reduced during the ICS versus placebo run-in periods: 0.18 mm/wk (SD, 0.55 mm/wk) versus 0.45 mm/wk (SD, 0.39 mm/wk), with a mean difference of 0.27 mm/wk (95% CI, 0.05-0.48 mm/wk; P = .02). In contrast, there was no difference in 24-hour UFC excretion: 6.91 nmol/mmol (SD, 4.67 nmol/mmol) versus 7.58 nmol/mmol (SD, 6.17 nmol/mmol), with a mean difference of 0.67 nmol/mmol (95% CI, −1.13 to 2.48 nmol/mmol; P = .46). We observed no significant difference in parametric determined LLGR caused by the child's age or sex, investigator, or season of measurement, whereas some differences were observed for the nonparametric LLGR. Conclusion These findings suggest that knemometry is a more sensitive pharmacodynamic measure of systemic effects of ICSs than 24-hour UFC excretion and that a parametric determination of LLGR increases the sensitivity of the method. These findings should be considered by legislative authorities in the future.</description><subject>Administration, Inhalation</subject><subject>Adrenal Cortex Hormones - pharmacology</subject><subject>Allergy and Immunology</subject><subject>Anti-Asthmatic Agents - pharmacology</subject><subject>Asthma</subject><subject>Asthma - urine</subject><subject>Beclomethasone - pharmacology</subject><subject>Child</subject><subject>Child Development - drug effects</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Children & youth</subject><subject>Corticoids</subject><subject>Corticosteroids</subject><subject>Drug dosages</subject><subject>Excretion</subject><subject>Female</subject><subject>Growth rate</subject><subject>Homogeneity</subject><subject>Hormones</subject><subject>Humans</subject><subject>Hydrocortisone - urine</subject><subject>Immunomodulators</subject><subject>inhaled corticosteroids</subject><subject>knemometry</subject><subject>Leg</subject><subject>Leg - growth & development</subject><subject>Legs</subject><subject>Male</subject><subject>Pharmacodynamics</subject><subject>Respiratory therapy</subject><subject>Sensitivity</subject><subject>Short term</subject><subject>Urine</subject><subject>urine cortisol excretion</subject><subject>Variance analysis</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kk2L1TAUhoMozvXqH3AhATduWvPR9iYgwjA4Kg64cPYhTU9oapuMSTp6f4L_elLuqDALV_ngeV_OOe9B6CUlNSW0ezvVkzauZuVeE1mThj5CO0rkoeoEax-jHSGSVt2hkWfoWUoTKW8u5FN0xgShrOv4Dv3-4mEJC-R4xC7hJUTACXxy2d0CzgGnY8qwOIPBWjA54WCx86OeYcAmxOxMKEAMbkjlH5vRzUMEj3-6PGKd8rhonEftMWuqMawRr9F5OElTmDH8MhGyC_45emL1nODF_blH15cfri8-VVdfP36-OL-qTCN4rnoJtu1bYfq2kVbKXvaUcM1kB5JoQYYBGgnEdIJIxrltidXM6MEaK4xt-R69OdnexPBjhZTV4pKBedYewpoUFa08tG3TNAV9_QCdSgO-FKeoZK0klJeB7hE7USaGlCJYdRPdouNRUaK2nNSktpzUlpMiUpWciujVvfXaLzD8lfwJpgDvTgCUUdw6iCoZB97A4GKJQQ3B_d___QO5mZ13Rs_f4QjpXx8qMUXUt21TtkWhHadMEsHvAOmwu6I</recordid><startdate>20170801</startdate><enddate>20170801</enddate><creator>Chawes, Bo, MD, PhD, DMSc</creator><creator>Nilsson, Erik, MD</creator><creator>Nørgaard, Sarah, MSc</creator><creator>Dossing, Anna, MD</creator><creator>Mortensen, Li, MD</creator><creator>Bisgaard, Hans, MD, DMSc</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4131-7592</orcidid></search><sort><creationdate>20170801</creationdate><title>Knemometry is more sensitive to systemic effects of inhaled corticosteroids in children with asthma than 24-hour urine cortisol excretion</title><author>Chawes, Bo, MD, PhD, DMSc ; Nilsson, Erik, MD ; Nørgaard, Sarah, MSc ; Dossing, Anna, MD ; Mortensen, Li, MD ; Bisgaard, Hans, MD, DMSc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-b9ef5b58cb549f99b9b103a296e90a80dde49e0c6809233f50fa2cadfcf8cf53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Administration, Inhalation</topic><topic>Adrenal Cortex Hormones - pharmacology</topic><topic>Allergy and Immunology</topic><topic>Anti-Asthmatic Agents - pharmacology</topic><topic>Asthma</topic><topic>Asthma - urine</topic><topic>Beclomethasone - pharmacology</topic><topic>Child</topic><topic>Child Development - drug effects</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Children & youth</topic><topic>Corticoids</topic><topic>Corticosteroids</topic><topic>Drug dosages</topic><topic>Excretion</topic><topic>Female</topic><topic>Growth rate</topic><topic>Homogeneity</topic><topic>Hormones</topic><topic>Humans</topic><topic>Hydrocortisone - urine</topic><topic>Immunomodulators</topic><topic>inhaled corticosteroids</topic><topic>knemometry</topic><topic>Leg</topic><topic>Leg - growth & development</topic><topic>Legs</topic><topic>Male</topic><topic>Pharmacodynamics</topic><topic>Respiratory therapy</topic><topic>Sensitivity</topic><topic>Short term</topic><topic>Urine</topic><topic>urine cortisol excretion</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chawes, Bo, MD, PhD, DMSc</creatorcontrib><creatorcontrib>Nilsson, Erik, MD</creatorcontrib><creatorcontrib>Nørgaard, Sarah, MSc</creatorcontrib><creatorcontrib>Dossing, Anna, MD</creatorcontrib><creatorcontrib>Mortensen, Li, MD</creatorcontrib><creatorcontrib>Bisgaard, Hans, MD, DMSc</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chawes, Bo, MD, PhD, DMSc</au><au>Nilsson, Erik, MD</au><au>Nørgaard, Sarah, MSc</au><au>Dossing, Anna, MD</au><au>Mortensen, Li, MD</au><au>Bisgaard, Hans, MD, DMSc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Knemometry is more sensitive to systemic effects of inhaled corticosteroids in children with asthma than 24-hour urine cortisol excretion</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2017-08-01</date><risdate>2017</risdate><volume>140</volume><issue>2</issue><spage>431</spage><epage>436</epage><pages>431-436</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><abstract>Background Pharmacodynamic assessment of the systemic effect of inhaled corticosteroids (ICSs) is often done by measuring 24-hour urine free cortisol (UFC) excretion. Knemometry assessing short-term lower-leg growth rate (LLGR) is a more rarely used alternative. Objective The primary aim of this study was to compare the sensitivity of LLGR and 24-hour UFC excretion for evaluating systemic exposure to ICSs in prepubertal children with asthma. The secondary aim was to evaluate factors influencing the precision of LLGR calculated by the traditional 1 leg nonparametric method versus a new 2 leg parametric method. Methods The study evaluated 60 children with mild asthma aged 5 to 12 years participating in a randomized controlled trial of ICSs with longitudinal concomitant assessments of LLGR and 24-hour UFC excretion. The sensitivity of the safety assessments was analyzed by comparing LLGR and 24-hour UFC in the placebo run-in period with values in the ICS treatment period by using paired t tests. Factors with a potential influence on LLGR were analyzed by means of ANOVA and the Levene test of homogeneity. Results The mean LLGR was significantly reduced during the ICS versus placebo run-in periods: 0.18 mm/wk (SD, 0.55 mm/wk) versus 0.45 mm/wk (SD, 0.39 mm/wk), with a mean difference of 0.27 mm/wk (95% CI, 0.05-0.48 mm/wk; P = .02). In contrast, there was no difference in 24-hour UFC excretion: 6.91 nmol/mmol (SD, 4.67 nmol/mmol) versus 7.58 nmol/mmol (SD, 6.17 nmol/mmol), with a mean difference of 0.67 nmol/mmol (95% CI, −1.13 to 2.48 nmol/mmol; P = .46). We observed no significant difference in parametric determined LLGR caused by the child's age or sex, investigator, or season of measurement, whereas some differences were observed for the nonparametric LLGR. Conclusion These findings suggest that knemometry is a more sensitive pharmacodynamic measure of systemic effects of ICSs than 24-hour UFC excretion and that a parametric determination of LLGR increases the sensitivity of the method. These findings should be considered by legislative authorities in the future.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28012663</pmid><doi>10.1016/j.jaci.2016.09.041</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-4131-7592</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Inhalation Adrenal Cortex Hormones - pharmacology Allergy and Immunology Anti-Asthmatic Agents - pharmacology Asthma Asthma - urine Beclomethasone - pharmacology Child Child Development - drug effects Child, Preschool Children Children & youth Corticoids Corticosteroids Drug dosages Excretion Female Growth rate Homogeneity Hormones Humans Hydrocortisone - urine Immunomodulators inhaled corticosteroids knemometry Leg Leg - growth & development Legs Male Pharmacodynamics Respiratory therapy Sensitivity Short term Urine urine cortisol excretion Variance analysis |
title | Knemometry is more sensitive to systemic effects of inhaled corticosteroids in children with asthma than 24-hour urine cortisol excretion |
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