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Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis
BACKGROUND: High rates of adverse mood/neurodevelopmental traits are seen in multiple dermatological conditions, and can significantly affect patient quality of life. Understanding the sex‐specific nature, magnitude, impact and basis of such traits in lesser‐studied conditions like ichthyosis, is im...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314151/ https://www.ncbi.nlm.nih.gov/pubmed/35104372 http://dx.doi.org/10.1111/ced.15116 |
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author | Wren, Georgina H. Humby, Trevor Thompson, Andrew R. Davies, William |
author_facet | Wren, Georgina H. Humby, Trevor Thompson, Andrew R. Davies, William |
author_sort | Wren, Georgina H. |
collection | PubMed |
description | BACKGROUND: High rates of adverse mood/neurodevelopmental traits are seen in multiple dermatological conditions, and can significantly affect patient quality of life. Understanding the sex‐specific nature, magnitude, impact and basis of such traits in lesser‐studied conditions like ichthyosis, is important for developing effective interventions. AIM: To quantify and compare relevant psychological traits in men with X‐linked ichthyosis (XLI, n = 54) or in XLI carrier women (n = 83) and in patients with ichthyosis vulgaris (IV, men n = 23, women n = 59) or psoriasis (men n = 30, women n = 122), and to identify factors self‐reported to contribute most towards depressive, anxious and irritable phenotypes. METHODS: Participants recruited via relevant charities or social media completed an online survey of established questionnaires. Data were analysed by sex and skin condition, and compared with general population data. RESULTS: Compared with the general population, there was a higher rate of lifetime prevalence of mood disorder diagnoses across all groups and of neurodevelopmental disorder diagnoses in the XLI groups. The groups exhibited similarly significant elevations in recent mood symptoms (Cohen d statistic 0.95–1.28, P < 0.001) and neurodevelopmental traits (d = 0.31–0.91, P < 0.05) compared with general population controls, and self‐reported moderate effects on quality of life and stigmatization. There were strong positive associations between neurodevelopmental traits and recent mood symptoms (r > 0.47, P < 0.01), and between feelings of stigmatization and quality of life, particularly in men. Numerous factors were identified as contributing significantly to mood symptoms in a condition or sex‐specific, or condition or sex‐independent, manner. CONCLUSION: We found that individuals with XLI, IV or psoriasis show higher levels of mood disorder diagnoses and symptoms than matched general population controls, and that the prevalence and severity of these is similar across conditions. We also identified a number of factors potentially conferring either general or condition‐specific risk of adverse mood symptoms in the three skin conditions, which could be targeted clinically and/or through education programmes. In clinical practice, recognizing mood/neurodevelopmental problems in ichthyosis and psoriasis, and addressing the predisposing factors identified by this study should benefit the mental health of affected individuals. |
format | Online Article Text |
id | pubmed-9314151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93141512022-07-30 Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis Wren, Georgina H. Humby, Trevor Thompson, Andrew R. Davies, William Clin Exp Dermatol Original Articles BACKGROUND: High rates of adverse mood/neurodevelopmental traits are seen in multiple dermatological conditions, and can significantly affect patient quality of life. Understanding the sex‐specific nature, magnitude, impact and basis of such traits in lesser‐studied conditions like ichthyosis, is important for developing effective interventions. AIM: To quantify and compare relevant psychological traits in men with X‐linked ichthyosis (XLI, n = 54) or in XLI carrier women (n = 83) and in patients with ichthyosis vulgaris (IV, men n = 23, women n = 59) or psoriasis (men n = 30, women n = 122), and to identify factors self‐reported to contribute most towards depressive, anxious and irritable phenotypes. METHODS: Participants recruited via relevant charities or social media completed an online survey of established questionnaires. Data were analysed by sex and skin condition, and compared with general population data. RESULTS: Compared with the general population, there was a higher rate of lifetime prevalence of mood disorder diagnoses across all groups and of neurodevelopmental disorder diagnoses in the XLI groups. The groups exhibited similarly significant elevations in recent mood symptoms (Cohen d statistic 0.95–1.28, P < 0.001) and neurodevelopmental traits (d = 0.31–0.91, P < 0.05) compared with general population controls, and self‐reported moderate effects on quality of life and stigmatization. There were strong positive associations between neurodevelopmental traits and recent mood symptoms (r > 0.47, P < 0.01), and between feelings of stigmatization and quality of life, particularly in men. Numerous factors were identified as contributing significantly to mood symptoms in a condition or sex‐specific, or condition or sex‐independent, manner. CONCLUSION: We found that individuals with XLI, IV or psoriasis show higher levels of mood disorder diagnoses and symptoms than matched general population controls, and that the prevalence and severity of these is similar across conditions. We also identified a number of factors potentially conferring either general or condition‐specific risk of adverse mood symptoms in the three skin conditions, which could be targeted clinically and/or through education programmes. In clinical practice, recognizing mood/neurodevelopmental problems in ichthyosis and psoriasis, and addressing the predisposing factors identified by this study should benefit the mental health of affected individuals. John Wiley and Sons Inc. 2022-03-04 2022-06 /pmc/articles/PMC9314151/ /pubmed/35104372 http://dx.doi.org/10.1111/ced.15116 Text en © 2022 The Authors. Clinical and Experimental Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Wren, Georgina H. Humby, Trevor Thompson, Andrew R. Davies, William Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis |
title | Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis |
title_full | Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis |
title_fullStr | Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis |
title_full_unstemmed | Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis |
title_short | Mood symptoms, neurodevelopmental traits, and their contributory factors in X‐linked ichthyosis, ichthyosis vulgaris and psoriasis |
title_sort | mood symptoms, neurodevelopmental traits, and their contributory factors in x‐linked ichthyosis, ichthyosis vulgaris and psoriasis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314151/ https://www.ncbi.nlm.nih.gov/pubmed/35104372 http://dx.doi.org/10.1111/ced.15116 |
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