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MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia

Background: Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common cause of primary adrenal insufficiency during childhood and patients are at risk for life-threatening adrenal crisis. In a recent study from our group, we reported gastrointestinal and upper...

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Autores principales: Mallappa, Ashwini, Sinaii, Ninet, El-Maouche, Diala, Veeraraghavan, Padmasree, Joyal, Elizabeth, Hargreaves, Courtney J, Merke, Deborah P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207682/
http://dx.doi.org/10.1210/jendso/bvaa046.1156
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author Mallappa, Ashwini
Sinaii, Ninet
El-Maouche, Diala
Veeraraghavan, Padmasree
Joyal, Elizabeth
Hargreaves, Courtney J
Merke, Deborah P
author_facet Mallappa, Ashwini
Sinaii, Ninet
El-Maouche, Diala
Veeraraghavan, Padmasree
Joyal, Elizabeth
Hargreaves, Courtney J
Merke, Deborah P
author_sort Mallappa, Ashwini
collection PubMed
description Background: Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common cause of primary adrenal insufficiency during childhood and patients are at risk for life-threatening adrenal crisis. In a recent study from our group, we reported gastrointestinal and upper respiratory tract infections as the two most common precipitating events for adrenal crises and hospitalizations across all ages. We also reported 11 incidents of life-threatening hypoglycemic events in children, sometimes accompanied by seizures. Objective: To evaluate the annual rates of illnesses in patients with CAH. Methods: We retrospectively reviewed longitudinally collected data over 23 years from 156 CAH patients enrolled in our CAH natural history study (www.clinicaltrials.gov #NCT00250159). Incidence of illnesses and occurrence of stress-dose days were computed per person-years. Incidence rate ratio (IRR) with 95% confidence intervals (CI) were calculated for comparisons. Results: A total of 2298 visits (1909 for children and 389 for adults) were available for evaluation among the 156 patients (21-OHD: 97.4%). A total of 1870 illness events (1664 in children) were observed in 143 patients (121 children) and 2710 stress-dose days (2460 in children) were observed in 141 patients (120 children) during the study period. The incidence rate of illnesses was higher in children than adults (1.5 vs. 0.5 illnesses/person-years, IRR = 3.1, 95% CI 2.7 - 3.6; P<.0001) with incidence highest in young patients: 2.5 illnesses/person-years in <3 year olds. Similarly, the stress-dose days were higher in children than adults (2.2 vs. 0.6 days/person-years, IRR = 3.8, 95% CI 3.3 - 4.3; P<.0001). Conclusions: Patients with CAH do not appear to have higher rates of infectious illnesses than expected, but remain at risk for life-threatening adrenal crises. As expected, illness rates are higher during childhood than adulthood. Prevention of adrenal crisis is crucial and is best accomplished through repeated age-specific education of patients and caregivers. Acknowledgement: This research was supported by the Intramural Research Program at the National Institutes of Health (NIH), Bethesda, Maryland.
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spelling pubmed-72076822020-05-13 MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia Mallappa, Ashwini Sinaii, Ninet El-Maouche, Diala Veeraraghavan, Padmasree Joyal, Elizabeth Hargreaves, Courtney J Merke, Deborah P J Endocr Soc Adrenal Background: Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common cause of primary adrenal insufficiency during childhood and patients are at risk for life-threatening adrenal crisis. In a recent study from our group, we reported gastrointestinal and upper respiratory tract infections as the two most common precipitating events for adrenal crises and hospitalizations across all ages. We also reported 11 incidents of life-threatening hypoglycemic events in children, sometimes accompanied by seizures. Objective: To evaluate the annual rates of illnesses in patients with CAH. Methods: We retrospectively reviewed longitudinally collected data over 23 years from 156 CAH patients enrolled in our CAH natural history study (www.clinicaltrials.gov #NCT00250159). Incidence of illnesses and occurrence of stress-dose days were computed per person-years. Incidence rate ratio (IRR) with 95% confidence intervals (CI) were calculated for comparisons. Results: A total of 2298 visits (1909 for children and 389 for adults) were available for evaluation among the 156 patients (21-OHD: 97.4%). A total of 1870 illness events (1664 in children) were observed in 143 patients (121 children) and 2710 stress-dose days (2460 in children) were observed in 141 patients (120 children) during the study period. The incidence rate of illnesses was higher in children than adults (1.5 vs. 0.5 illnesses/person-years, IRR = 3.1, 95% CI 2.7 - 3.6; P<.0001) with incidence highest in young patients: 2.5 illnesses/person-years in <3 year olds. Similarly, the stress-dose days were higher in children than adults (2.2 vs. 0.6 days/person-years, IRR = 3.8, 95% CI 3.3 - 4.3; P<.0001). Conclusions: Patients with CAH do not appear to have higher rates of infectious illnesses than expected, but remain at risk for life-threatening adrenal crises. As expected, illness rates are higher during childhood than adulthood. Prevention of adrenal crisis is crucial and is best accomplished through repeated age-specific education of patients and caregivers. Acknowledgement: This research was supported by the Intramural Research Program at the National Institutes of Health (NIH), Bethesda, Maryland. Oxford University Press 2020-05-08 /pmc/articles/PMC7207682/ http://dx.doi.org/10.1210/jendso/bvaa046.1156 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Adrenal
Mallappa, Ashwini
Sinaii, Ninet
El-Maouche, Diala
Veeraraghavan, Padmasree
Joyal, Elizabeth
Hargreaves, Courtney J
Merke, Deborah P
MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia
title MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia
title_full MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia
title_fullStr MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia
title_full_unstemmed MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia
title_short MON-158 Rates of Illnesses in Patients with Congenital Adrenal Hyperplasia
title_sort mon-158 rates of illnesses in patients with congenital adrenal hyperplasia
topic Adrenal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207682/
http://dx.doi.org/10.1210/jendso/bvaa046.1156
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