Genetic determinants of longitudinal behavioural trajectories in rare conditions: The case of fragile X syndrome

IF 2.3 3区 心理学 Q2 BEHAVIORAL SCIENCES Behavioural Brain Research Pub Date : 2025-05-08 Epub Date: 2025-03-05 DOI:10.1016/j.bbr.2025.115527
Lydia Cartwright , Gaia Scerif , Chris Oliver , Andrew Beggs , Joanne Stockton , Lucy Wilde , Hayley Crawford
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Abstract

Despite being a monogenic condition, individual variability in the phenotypic profile of fragile X syndrome (FXS) is substantial, with behavioural outcomes differing in severity and frequency. Existing studies have revealed that common variation in 5-HTTLPR (serotonin) and COMT (dopamine) single nucleotide polymorphisms (SNPs) is associated with behavioural variation in FXS when measured cross-sectionally. However, the associations between SNPs and longitudinal behavioural trajectories in FXS remain unknown. This study explored relationships between three SNPs, selected a priori (5-HTTLPR, COMT and monoamine oxidase A (MAOA)), and trajectories of clinically relevant behaviours in 42 males with FXS. Autistic characteristics, property destruction, aggression, stereotyped behaviour, self-injury, repetitive behaviour, and mood/interest and pleasure were measured at two time points across three years via a series of standardised informant questionnaires. DNA was extracted from saliva samples and a combination of PCR and TaqMan genotyping was performed for genetic confirmation of FXS, and COMT, 5-HTTLPR and MAOA analyses. Results revealed that males with FXS with AA COMT genotype were less likely to display persistent stereotyped behaviour compared to AG or GG genotypes. Participants with the S/S 5-HTTLPR genotype displayed a steeper decline in repetitive and stereotyped behaviours compared to the L/S or L/L genotypes. Participants with the three-repeat MAOA genotype demonstrated a steeper decline in communication skills over three years compared to those with four repeats. This study documents the association between common genetic variation and behavioural trajectories in males with FXS. Results suggest specific SNPs play an important role in longitudinal behavioural patterns in FXS. This work may facilitate an understanding of individual trajectories for people with FXS, and, therefore, support future tailored interventions.
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在罕见情况下纵向行为轨迹的遗传决定因素:脆性X综合征的情况
尽管脆性X综合征(FXS)是一种单基因疾病,但其表型特征的个体差异很大,其行为结果在严重程度和频率上存在差异。现有研究表明,5-HTTLPR(5-羟色胺)和COMT(多巴胺)单核苷酸多态性(snp)的常见变异与FXS的行为变异有关。然而,snp与FXS纵向行为轨迹之间的关系尚不清楚。本研究探讨了42例男性FXS患者的三个先验snp (5-HTTLPR、COMT和单胺氧化酶a (MAOA))与临床相关行为轨迹之间的关系。自闭症特征、财产破坏、攻击性、刻板行为、自残、重复行为、情绪/兴趣和快乐在三年内的两个时间点通过一系列标准化的信息调查者问卷进行测量。从唾液样本中提取DNA,结合PCR和TaqMan基因分型对FXS进行遗传确证,并进行COMT、5-HTTLPR和MAOA分析。结果显示,与AG或GG基因型相比,携带AA COMT基因型FXS的雄性更不可能表现出持久的刻板行为。与L/S或L/L基因型相比,S/S 5-HTTLPR基因型的参与者在重复和刻板行为方面表现出更大的下降。与具有四个重复基因型的参与者相比,具有三个重复MAOA基因型的参与者在三年内表现出更大的沟通技巧下降。本研究记录了FXS雄性常见遗传变异与行为轨迹之间的关系。结果表明,特定的snp在FXS的纵向行为模式中起重要作用。这项工作可能有助于了解FXS患者的个体轨迹,从而支持未来量身定制的干预措施。
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来源期刊
Behavioural Brain Research
Behavioural Brain Research 医学-行为科学
CiteScore
5.60
自引率
0.00%
发文量
383
审稿时长
61 days
期刊介绍: Behavioural Brain Research is an international, interdisciplinary journal dedicated to the publication of articles in the field of behavioural neuroscience, broadly defined. Contributions from the entire range of disciplines that comprise the neurosciences, behavioural sciences or cognitive sciences are appropriate, as long as the goal is to delineate the neural mechanisms underlying behaviour. Thus, studies may range from neurophysiological, neuroanatomical, neurochemical or neuropharmacological analysis of brain-behaviour relations, including the use of molecular genetic or behavioural genetic approaches, to studies that involve the use of brain imaging techniques, to neuroethological studies. Reports of original research, of major methodological advances, or of novel conceptual approaches are all encouraged. The journal will also consider critical reviews on selected topics.
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