Cargando…
Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank
BACKGROUND: X-linked ichthyosis (XLI) is an uncommon dermatological condition resulting from a deficiency of the enzyme steroid sulfatase (STS), often caused by X-linked deletions spanning STS. Some medical comorbidities have been identified in XLI cases, but small samples of relatively young patien...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525778/ https://www.ncbi.nlm.nih.gov/pubmed/32139392 http://dx.doi.org/10.1136/jmedgenet-2019-106676 |
_version_ | 1783588765536616448 |
---|---|
author | Brcic, Lucija Underwood, Jack FG Kendall, Kimberley M Caseras, Xavier Kirov, George Davies, William |
author_facet | Brcic, Lucija Underwood, Jack FG Kendall, Kimberley M Caseras, Xavier Kirov, George Davies, William |
author_sort | Brcic, Lucija |
collection | PubMed |
description | BACKGROUND: X-linked ichthyosis (XLI) is an uncommon dermatological condition resulting from a deficiency of the enzyme steroid sulfatase (STS), often caused by X-linked deletions spanning STS. Some medical comorbidities have been identified in XLI cases, but small samples of relatively young patients has limited this. STS is highly expressed in subcortical brain structures, and males with XLI and female deletion carriers appear at increased risk of developmental/mood disorders and associated traits; the neurocognitive basis of these findings has not been examined. METHODS: Using the UK Biobank resource, comprising participants aged 40–69 years recruited from the general UK population, we compared multiple medical/neurobehavioural phenotypes in males (n=86) and females (n=312) carrying genetic deletions spanning STS (0.8–2.5 Mb) (cases) to male (n=190 577) and female (n=227 862) non-carrier controls. RESULTS: We identified an elevated rate of atrial fibrillation/flutter in male deletion carriers (10.5% vs 2.7% in male controls, Benjamini-Hochberg corrected p=0.009), and increased rates of mental distress (p=0.003), irritability (p<0.001) and depressive-anxiety traits (p<0.05) in male deletion carriers relative to male controls completing the Mental Health Questionnaire. While academic attainment was unaffected, male and female deletion carriers exhibited impaired performance on the Fluid Intelligence Test (Cohen’s d≤0.05, corrected p<0.1). Neuroanatomical analysis in female deletion carriers indicated reduced right putamen and left nucleus accumbens volumes (Cohen’s d≤0.26, corrected p<0.1). CONCLUSION: Adult males with XLI disease-causing deletions are apparently at increased risk of cardiac arrhythmias and self-reported mood problems; altered basal ganglia structure may underlie altered function and XLI-associated psychiatric/behavioural phenotypes. These results provide information for genetic counselling of deletion-carrying individuals and reinforce the need for multidisciplinary medical care. |
format | Online Article Text |
id | pubmed-7525778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-75257782020-10-19 Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank Brcic, Lucija Underwood, Jack FG Kendall, Kimberley M Caseras, Xavier Kirov, George Davies, William J Med Genet Genotype-Phenotype Correlations BACKGROUND: X-linked ichthyosis (XLI) is an uncommon dermatological condition resulting from a deficiency of the enzyme steroid sulfatase (STS), often caused by X-linked deletions spanning STS. Some medical comorbidities have been identified in XLI cases, but small samples of relatively young patients has limited this. STS is highly expressed in subcortical brain structures, and males with XLI and female deletion carriers appear at increased risk of developmental/mood disorders and associated traits; the neurocognitive basis of these findings has not been examined. METHODS: Using the UK Biobank resource, comprising participants aged 40–69 years recruited from the general UK population, we compared multiple medical/neurobehavioural phenotypes in males (n=86) and females (n=312) carrying genetic deletions spanning STS (0.8–2.5 Mb) (cases) to male (n=190 577) and female (n=227 862) non-carrier controls. RESULTS: We identified an elevated rate of atrial fibrillation/flutter in male deletion carriers (10.5% vs 2.7% in male controls, Benjamini-Hochberg corrected p=0.009), and increased rates of mental distress (p=0.003), irritability (p<0.001) and depressive-anxiety traits (p<0.05) in male deletion carriers relative to male controls completing the Mental Health Questionnaire. While academic attainment was unaffected, male and female deletion carriers exhibited impaired performance on the Fluid Intelligence Test (Cohen’s d≤0.05, corrected p<0.1). Neuroanatomical analysis in female deletion carriers indicated reduced right putamen and left nucleus accumbens volumes (Cohen’s d≤0.26, corrected p<0.1). CONCLUSION: Adult males with XLI disease-causing deletions are apparently at increased risk of cardiac arrhythmias and self-reported mood problems; altered basal ganglia structure may underlie altered function and XLI-associated psychiatric/behavioural phenotypes. These results provide information for genetic counselling of deletion-carrying individuals and reinforce the need for multidisciplinary medical care. BMJ Publishing Group 2020-10 2020-03-05 /pmc/articles/PMC7525778/ /pubmed/32139392 http://dx.doi.org/10.1136/jmedgenet-2019-106676 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Genotype-Phenotype Correlations Brcic, Lucija Underwood, Jack FG Kendall, Kimberley M Caseras, Xavier Kirov, George Davies, William Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank |
title | Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank |
title_full | Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank |
title_fullStr | Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank |
title_full_unstemmed | Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank |
title_short | Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank |
title_sort | medical and neurobehavioural phenotypes in carriers of x-linked ichthyosis-associated genetic deletions in the uk biobank |
topic | Genotype-Phenotype Correlations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525778/ https://www.ncbi.nlm.nih.gov/pubmed/32139392 http://dx.doi.org/10.1136/jmedgenet-2019-106676 |
work_keys_str_mv | AT brciclucija medicalandneurobehaviouralphenotypesincarriersofxlinkedichthyosisassociatedgeneticdeletionsintheukbiobank AT underwoodjackfg medicalandneurobehaviouralphenotypesincarriersofxlinkedichthyosisassociatedgeneticdeletionsintheukbiobank AT kendallkimberleym medicalandneurobehaviouralphenotypesincarriersofxlinkedichthyosisassociatedgeneticdeletionsintheukbiobank AT caserasxavier medicalandneurobehaviouralphenotypesincarriersofxlinkedichthyosisassociatedgeneticdeletionsintheukbiobank AT kirovgeorge medicalandneurobehaviouralphenotypesincarriersofxlinkedichthyosisassociatedgeneticdeletionsintheukbiobank AT davieswilliam medicalandneurobehaviouralphenotypesincarriersofxlinkedichthyosisassociatedgeneticdeletionsintheukbiobank |