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Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study
AIM: To determine the circadian rhythm alteration of cortisol excretion and the level of corticosteroids in children with different grades of autism severity. METHODS: The study included 45 children with different grades of autism severity (low [LFA], medium [MFA], and high functioning autism [HFA])...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Croatian Medical Schools
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583392/ https://www.ncbi.nlm.nih.gov/pubmed/23444244 http://dx.doi.org/10.3325/cmj.2013.54.33 |
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author | Lakshmi Priya, Malarveni Damodaran Geetha, Arumugam Suganya, Vijayashankar Sujatha, Sridharan |
author_facet | Lakshmi Priya, Malarveni Damodaran Geetha, Arumugam Suganya, Vijayashankar Sujatha, Sridharan |
author_sort | Lakshmi Priya, Malarveni Damodaran |
collection | PubMed |
description | AIM: To determine the circadian rhythm alteration of cortisol excretion and the level of corticosteroids in children with different grades of autism severity. METHODS: The study included 45 children with different grades of autism severity (low [LFA], medium [MFA], and high functioning autism [HFA]), 15 in each group, and 45 age/sex-matched children with typical development. The urinary levels of free cortisol (at three phases of 24-hour cycle), corticosteroids, vanilylmandelic acid, and 5-hydroxyindole acetic acid were determined. RESULTS: Alteration in the pattern of cortisol excretion (Phases I, II, and III) was observed in children with LFA (Phase I: 43.8 ± 4.43 vs 74.30±8.62, P = 0.000; Phase II: 21.1±2.87 vs 62±7.68, P < 0.001; Phase III: 9.9 ± 1.20 vs 40 ± 5.73, P < 0.001) and MFA (Phase I: 43.8 ± 4.43 vs 52.6±7.90, P < 0.001; Phase II: 21.1±2.87 vs 27.4±4.05, P < 0.001; Phase III: 9.9 ± 1.20 vs 19 ± 2.50, P < 0.001) compared to the control group. The corticosteroids excretion levels were higher in all the groups of children with autism than in the control group. The level of 5-hydroxyindole acetic acid was significantly higher in children with LFA (8.2±1.48 vs 6.8±0.85, P < 0.001) and MFA (8.2±1.48 vs 7.4± 0.89, P = 0.001) and not significantly higher in children with HFA than in the control group. The changes were correlated with degrees of severity of the disorder. CONCLUSION: These data suggest that altered cortisol excretion pattern and high level of corticosteroids in urine may probably be a consequence of altered hypothalamic-pituitary-adrenal axis function, which may contribute to the pathogenesis and affect the severity of autism. |
format | Online Article Text |
id | pubmed-3583392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Croatian Medical Schools |
record_format | MEDLINE/PubMed |
spelling | pubmed-35833922013-02-28 Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study Lakshmi Priya, Malarveni Damodaran Geetha, Arumugam Suganya, Vijayashankar Sujatha, Sridharan Croat Med J Clinical Science AIM: To determine the circadian rhythm alteration of cortisol excretion and the level of corticosteroids in children with different grades of autism severity. METHODS: The study included 45 children with different grades of autism severity (low [LFA], medium [MFA], and high functioning autism [HFA]), 15 in each group, and 45 age/sex-matched children with typical development. The urinary levels of free cortisol (at three phases of 24-hour cycle), corticosteroids, vanilylmandelic acid, and 5-hydroxyindole acetic acid were determined. RESULTS: Alteration in the pattern of cortisol excretion (Phases I, II, and III) was observed in children with LFA (Phase I: 43.8 ± 4.43 vs 74.30±8.62, P = 0.000; Phase II: 21.1±2.87 vs 62±7.68, P < 0.001; Phase III: 9.9 ± 1.20 vs 40 ± 5.73, P < 0.001) and MFA (Phase I: 43.8 ± 4.43 vs 52.6±7.90, P < 0.001; Phase II: 21.1±2.87 vs 27.4±4.05, P < 0.001; Phase III: 9.9 ± 1.20 vs 19 ± 2.50, P < 0.001) compared to the control group. The corticosteroids excretion levels were higher in all the groups of children with autism than in the control group. The level of 5-hydroxyindole acetic acid was significantly higher in children with LFA (8.2±1.48 vs 6.8±0.85, P < 0.001) and MFA (8.2±1.48 vs 7.4± 0.89, P = 0.001) and not significantly higher in children with HFA than in the control group. The changes were correlated with degrees of severity of the disorder. CONCLUSION: These data suggest that altered cortisol excretion pattern and high level of corticosteroids in urine may probably be a consequence of altered hypothalamic-pituitary-adrenal axis function, which may contribute to the pathogenesis and affect the severity of autism. Croatian Medical Schools 2013-02 /pmc/articles/PMC3583392/ /pubmed/23444244 http://dx.doi.org/10.3325/cmj.2013.54.33 Text en Copyright © 2013 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Lakshmi Priya, Malarveni Damodaran Geetha, Arumugam Suganya, Vijayashankar Sujatha, Sridharan Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study |
title | Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study |
title_full | Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study |
title_fullStr | Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study |
title_full_unstemmed | Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study |
title_short | Abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study |
title_sort | abnormal circadian rhythm and cortisol excretion in autistic children: a clinical study |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583392/ https://www.ncbi.nlm.nih.gov/pubmed/23444244 http://dx.doi.org/10.3325/cmj.2013.54.33 |
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