Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank

被引:32
作者
Brcic, Lucija [1 ]
Underwood, Jack F. G. [2 ,3 ,4 ]
Kendall, Kimberley M. [2 ,3 ]
Caseras, Xavier [2 ,3 ]
Kirov, George [2 ,3 ]
Davies, William [1 ,2 ,3 ,4 ]
机构
[1] Cardiff Univ, Sch Psychol, Tower Bldg,70,Pk Pl, Cardiff CF10 3AT, Wales
[2] Cardiff Univ, MRC Ctr Neuropsychiat Genet & Genom, Cardiff, Wales
[3] Cardiff Univ, Div Psychol Med & Clin Neurosci, Sch Med, Cardiff, Wales
[4] Cardiff Univ, Neurosci & Mental Hlth Res Inst, Cardiff, Wales
基金
英国惠康基金; 英国医学研究理事会;
关键词
arrhythmias; copy-number; dermatology; psychiatry; neurosciences; STEROID SULFATASE DEFICIENCY; DEHYDROEPIANDROSTERONE-SULFATE; ATRIAL-FIBRILLATION; HYPERACTIVITY DISORDER; RESPONSE CONTROL; MOUSE MODEL; RISK; ENDOPHENOTYPES; PARTICIPANTS; MODULATION;
D O I
10.1136/jmedgenet-2019-106676
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 spanningSTS. Some medical comorbidities have been identified in XLI cases, but small samples of relatively young patients has limited this.STSis 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 spanningSTS(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.
引用
收藏
页码:692 / 698
页数:7
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