氨基丁酸代谢的神经递质紊乱——SSADH缺乏症的神经心理学特征

IF 3.5 2区 生物学 Q2 ENDOCRINOLOGY & METABOLISM Molecular genetics and metabolism Pub Date : 2025-03-01 Epub Date: 2025-02-04 DOI:10.1016/j.ymgme.2025.109051
Itay Tokatly Latzer , Ellen Hanson , Mariarita Bertoldi , Melissa L. DiBacco , Deniz Aygun , Onur Afacan , Àngeles García-Cazorla , Natalia Juliá-Palacios , Thomas Opladen , Oya Kuseyri Hübschmann , Kathrin Jeltsch , Petra Aden , Mari Oppebøen , Alexander Rotenberg , Melissa Tsuboyama , Jean-Baptiste Roullet , Phillip L. Pearl
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引用次数: 0

摘要

背景与目的琥珀半醛脱氢酶缺乏症(SSADHD)是一种遗传性代谢性疾病,导致神经递质γ-氨基丁酸(GABA)的高生理浓度。本研究旨在提供迄今为止最全面的SSADHD患者的神经心理特征描述,并评估皮质抑制的神经影像学、神经生理学和生化指标是否与标准化行为测试相关。方法入选SSADHD自然历史研究的参与者接受了医学和神经学检查、磁共振成像(MRI)和波谱学(MRS)、GABA及其相关代谢物生化测试、经颅磁刺激(TMS)、基因表达量化,以及完整的神经心理学评估,包括认知、适应技能、运动功能、接受和表达语言、自闭症谱系障碍、以及行为问题。结果该研究的65名受试者(54%为女性,中位年龄9.6(5.4-14.7))的神经心理学特征几乎普遍包括智力障碍、适应技能延迟和表达性语言缺陷(多于接受性语言)。自闭症谱系障碍约占50%,行为问题约占70%,主要是强迫行为和注意力问题,但也包括情感问题、焦虑,很少有攻击性和可能的精神病。相关分析显示,内在化、外在化和整体精神疾病发病率的增加与年龄的增加显著相关(R = 0.391, p = 0.033),以及与年龄无关的皮质抑制降低的指标,如mr衍生的GABA (R = - 0.530, p = 0.029)和tms衍生的静息运动阈值(R = - 0.418, p = 0.053)。SSADHD的自然史研究表明,智力障碍、适应技能延迟和表达性语言接受性缺陷几乎是普遍存在的,其中绝大多数是行为问题。SSADHD患者精神疾病发病率的增加与年龄无关的皮质抑制下降可能作为建立SSADHD和其他非综合征性精神疾病的行为和精神结局的疾病特异性生物标志物的基础。
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The neuropsychological profile of SSADH deficiency, a neurotransmitter disorder of GABA metabolism

Background and objectives

Succinic semialdehyde dehydrogenase deficiency (SSADHD) is an inherited metabolic disorder resulting in hyper-physiologic concentrations of the neurotransmitter γ-aminobutyrate (GABA). This study aims to provide the most comprehensive description, to date, of the neuropsychological profile of individuals with SSADHD and assess whether neuroimaging, neurophysiologic, and biochemical indices of cortical inhibition correlate with those of standardized behavioral tests.

Methods

Participants enrolled in the SSADHD Natural History Study underwent medical and neurological examinations, magnetic resonance imaging (MRI) and spectroscopy (MRS), biochemical tests of GABA and its related metabolites, transcranial magnetic stimulation (TMS), and gene expression quantification, as well as complete neuropsychological assessment including standardized measures for cognition, adaptive skills, motor function, receptive and expressive language, autism spectrum disorder, and behavior problems.

Results

The neuropsychological profile of the study's 65 enrollees [54 % females, median (interquartile range) age 9.6 (5.4–14.7)] consisted almost universally of intellectual disability, delays in adaptive skills, and deficits in expressive more than receptive language. Autism Spectrum Disorder was noted in ∼50 %, and behavioral problems in ∼70 %, predominated by obsessive-compulsive behaviors and attention problems but also including affective problems, anxiety, and, rarely, aggression and possible psychosis. Correlation analyses showed that increased internalizing, externalizing, and overall psychiatric morbidity significantly correlated with increasing age (R = 0.391, p = 0.033), as well as age-independent indices representing decreased cortical inhibition such as lower MRS-derived GABA (R = −0.530, p = 0.029) and TMS-derived resting motor threshold (R = −0.418, p = 0.053).

Discussion

The natural history study of SSADHD indicates that intellectual disability, delayed adaptive skills, and expressive>receptive language deficits are nearly universal, with behavior problems in the vast majority. Increased psychiatric morbidity in SSADHD with age-independent decreased cortical inhibition may serve as the basis for establishing disorder-specific biomarkers for behavioral and psychiatric outcomes in SSADHD and other non-syndromic psychiatric disorders.
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来源期刊
Molecular genetics and metabolism
Molecular genetics and metabolism 生物-生化与分子生物学
CiteScore
5.90
自引率
7.90%
发文量
621
审稿时长
34 days
期刊介绍: Molecular Genetics and Metabolism contributes to the understanding of the metabolic and molecular basis of disease. This peer reviewed journal publishes articles describing investigations that use the tools of biochemical genetics and molecular genetics for studies of normal and disease states in humans and animal models.
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