Memory, mood and associated neuroanatomy in individuals with steroid sulphatase deficiency (X-linked ichthyosis)

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-05-05 DOI:10.1111/gbb.12893
Georgina H. Wren, Jessica Flanagan, Jack F. G. Underwood, Andrew R. Thompson, Trevor Humby, William Davies
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Abstract

Steroid sulphatase (STS) cleaves sulphate groups from steroid hormones, and steroid (sulphate) levels correlate with mood and age-related cognitive decline. In animals, STS inhibition or deletion of the associated gene, enhances memory/neuroprotection and alters hippocampal neurochemistry. Little is known about the consequences of constitutive STS deficiency on memory-related processes in humans. We investigated self-reported memory performance (Multifactorial Memory Questionnaire), word-picture recall and recent mood (Kessler Psychological Distress Scale, K10) in adult males with STS deficiency diagnosed with the dermatological condition X-linked ichthyosis (XLI; n = 41) and in adult female carriers of XLI-associated genetic variants (n = 79); we compared results to those obtained from matched control subjects [diagnosed with ichthyosis vulgaris (IV, n = 98) or recruited from the general population (n = 250)]. Using the UK Biobank, we compared mood/memory-related neuroanatomy in carriers of genetic deletions encompassing STS (n = 28) and non-carriers (n = 34,522). We found poorer word-picture recall and lower perceived memory abilities in males with XLI and female carriers compared with control groups. XLI-associated variant carriers and individuals with IV reported more adverse mood symptoms, reduced memory contentment and greater use of memory aids, compared with general population controls. Mood and memory findings appeared largely independent. Neuroanatomical analysis only indicated a nominally-significantly larger molecular layer in the right hippocampal body of deletion carriers relative to non-carriers. In humans, constitutive STS deficiency appears associated with mood-independent impairments in memory but not with large effects on underlying brain structure; the mediating psychobiological mechanisms might be explored further in individuals with XLI and in new mammalian models lacking STS developmentally.

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类固醇硫酸酯酶缺乏症(X-连锁鱼鳞病)患者的记忆力、情绪和相关神经解剖学特征
类固醇硫酸酯酶(STS)能分解类固醇激素中的硫酸酯基团,而类固醇(硫酸酯)水平与情绪和年龄相关的认知能力衰退有关。在动物体内,抑制 STS 或删除相关基因可增强记忆/神经保护并改变海马神经化学。关于 STS 构成性缺乏对人类记忆相关过程的影响,人们知之甚少。我们调查了被诊断患有皮肤病 X 连锁鱼鳞病(XLI)的 STS 缺乏症成年男性和成年女性的自我报告记忆表现(多因素记忆问卷)、单词-图片回忆和近期情绪(凯斯勒心理压力量表,K10);n = 41)和 XLI 相关基因变异的成年女性携带者(n = 79);我们将结果与匹配对照组(诊断为寻常型鱼鳞病(IV,n = 98)或从普通人群中招募(n = 250))的结果进行了比较。通过英国生物数据库,我们比较了STS基因缺失携带者(n = 28)和非携带者(n = 34 522)的情绪/记忆相关神经解剖学。我们发现,与对照组相比,XLI男性携带者和女性携带者的单词-图片回忆能力较差,感知记忆能力较低。与普通人群对照组相比,XLI 相关变异携带者和 IV 型患者报告的不良情绪症状更多,记忆满足感降低,记忆辅助工具的使用率更高。情绪和记忆结果似乎在很大程度上是独立的。神经解剖学分析表明,与非基因缺失携带者相比,基因缺失携带者右侧海马体的分子层明显增大。在人类中,STS的构成性缺失似乎与情绪无关的记忆障碍有关,但对潜在的大脑结构没有很大影响;可以在XLI患者和发育过程中缺乏STS的新哺乳动物模型中进一步探索心理生物学的中介机制。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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