MRC Centre for Neuropsychiatric Genetics and Genomics and Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, United Kingdom.
School of Psychology, Cardiff University, Cardiff, United Kingdom.
PLoS One. 2019 Feb 15;14(2):e0212330. doi: 10.1371/journal.pone.0212330. eCollection 2019.
X-linked ichthyosis (XLI) is a rare X-linked dermatological condition arising from deficiency for the enzyme steroid sulfatase (STS). STS is normally expressed in the brain, and males with XLI exhibit personality differences from males in the general population, and are at increased risk of developmental and mood disorders. As the STS gene escapes X-inactivation, female carriers of XLI-associated genetic mutations have reduced STS expression/activity relative to non-carrier females, and could manifest similar behavioural phenotypes to males with XLI. Additionally, as STS activity normally increases in female tissues towards late pregnancy and into the puerperium, carrier females could theoretically present with increased rates of postpartum psychopathology. Using a worldwide online survey comprising custom-designed demographic questionnaires and multiple validated psychological questionnaires, we collected detailed self-reported information on non-postpartum and postpartum behaviour in confirmed adult (>16yrs) female carriers of genetic mutations associated with XLI (n = 94) for statistical comparison to demographically-matched previously-published normative data from female controls (seven independent studies, 98≤n≤2562), adult males with XLI (n = 58), and to newly-obtained online survey data from a general population sample of mothers from the United Kingdom and United States of America (n = 263). The pattern of results in carrier females relative to controls was remarkably similar to that previously observed in males with XLI, with evidence for increased rates of developmental and mood disorders, and elevated levels of inattention, impulsivity, autism-related traits and general psychological distress. Carrier females exhibited a significantly elevated rate of postpartum mental health conditions (notably mild depression) relative to controls which could not be accounted for by social factors. Our data confirm the psychological profile associated with XLI-associated mutations, and suggest that female carriers may be at increased risk of psychopathology, including in the postpartum period. These findings are relevant to families affected by XLI, to clinicians involved in the care of these families, and to genetic counsellors.
X 连锁鱼鳞病(XLI)是一种罕见的 X 连锁皮肤疾病,由类固醇硫酸酯酶(STS)缺乏引起。STS 通常在大脑中表达,XLI 男性与普通人群中的男性相比表现出不同的人格特征,并且患发育和情绪障碍的风险增加。由于 STS 基因逃避 X 染色体失活,XLI 相关基因突变的女性携带者的 STS 表达/活性相对非携带者女性降低,并且可能表现出与 XLI 男性相似的行为表型。此外,由于 STS 活性通常在女性组织中在妊娠后期和产褥期增加,携带者女性理论上可能表现出更高的产后精神病理学发病率。使用一项全球在线调查,包括定制的人口统计学问卷和多个经过验证的心理问卷,我们收集了已确认成年(>16 岁)XLI 相关基因突变女性携带者的非产后和产后行为的详细自我报告信息,用于与人口统计学匹配的以前发表的女性对照者的参考数据(七个独立研究,n=98-2562)、XLI 男性(n=58)和从英国和美国的一般人群样本中获得的新的在线调查数据(n=263)进行统计学比较。携带者女性相对于对照组的结果模式与之前在 XLI 男性中观察到的模式非常相似,有证据表明发育和情绪障碍的发生率增加,以及注意力不集中、冲动、自闭症相关特征和一般心理困扰程度升高。与对照组相比,携带者女性产后心理健康状况(尤其是轻度抑郁)的发生率显著升高,这不能用社会因素来解释。我们的数据证实了与 XLI 相关突变相关的心理特征,并表明女性携带者可能面临更高的精神病理学风险,包括在产后期间。这些发现与受 XLI 影响的家庭、参与这些家庭护理的临床医生以及遗传咨询师有关。