22q11.2和16p11.2缺失和重复的神经认知概况。

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-07-24 DOI:10.1038/s41380-024-02661-y
Ruben C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne van den Bree, Jacob Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne S Bassett, Donna M McDonald-McGinn, Raquel E Gur
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引用次数: 0

摘要

染色体位点 22q11.2 和 16p11.2 上的罕见复发性拷贝数变异(CNVs)是一种遗传疾病,具有导致神经精神疾病的终生风险。微缺失和重复与神经认知缺陷有关,但很少有研究使用相同的测量方法对这些群体进行比较,以解决测量差异带来的混淆。我们报告了一项前瞻性国际合作研究,该研究采用了相同的计算机化神经认知评估方法--宾夕法尼亚大学计算机化神经认知电池(CNB),在一项关于罕见基因组疾病的多站点研究中进行:22q11.2缺失(n = 492);22q11.2重复(n = 106);16p11.2缺失(n = 117);16p11.2重复(n = 46)。检查的领域包括执行功能、外显记忆、复杂认知、社会认知和精神运动速度。每个领域的准确性和速度作为因变量被纳入混合模型重复测量分析。病灶(22q11.2、16p11.2)和拷贝数(缺失/重复)是分组因素,测量(准确性、速度)和神经认知领域是重复测量因素,性别和地点是协变量。我们还研究了与智商的相关性。我们发现,基因座 × 拷贝数 × 领域 × 测量存在明显的交互作用(p = 0.0004)。与 22q11.2 缺失相比,22q11.2 缺失与更大的表现准确性缺陷有关,而与 16p11.2 缺失相比,16p11.2 缺失与更大的特异性缺陷有关。与缺失相比,这两个位点的重复与速度降低有关。22q11.2缺失组的记忆能力特别差,而16p11.2重复组在复杂认知方面的缺陷最大。CNB 的平均准确率与全面智商(Full Scale IQ)呈中度相关。22q11.2和16p11.2的缺失和重复对神经认知的准确性和速度有不同的影响,这表明表现特征具有位点特异性。这些表现特征的差异有助于了解导致表现和结果异质性的机理基础,只有在使用相同神经认知评估的大规模国际联盟中才能确定。未来的研究可以将表现特征与临床特征和大脑功能联系起来。
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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.

Rare recurrent copy number variants (CNVs) at chromosomal loci 22q11.2 and 16p11.2 are genetic disorders with lifespan risk for neuropsychiatric disorders. Microdeletions and duplications are associated with neurocognitive deficits, yet few studies compared these groups using the same measures to address confounding measurement differences. We report a prospective international collaboration applying the same computerized neurocognitive assessment, the Penn Computerized Neurocognitive Battery (CNB), administered in a multi-site study on rare genomic disorders: 22q11.2 deletions (n = 492); 22q11.2 duplications (n = 106); 16p11.2 deletion (n = 117); and 16p11.2 duplications (n = 46). Domains examined include executive functions, episodic memory, complex cognition, social cognition, and psychomotor speed. Accuracy and speed for each domain were included as dependent measures in a mixed-model repeated measures analysis. Locus (22q11.2, 16p11.2) and Copy number (deletion/duplication) were grouping factors and Measure (accuracy, speed) and neurocognitive domain were repeated measures factors, with Sex and Site as covariates. We also examined correlation with IQ. We found a significant Locus × Copy number × Domain × Measure interaction (p = 0.0004). 22q11.2 deletions were associated with greater performance accuracy deficits than 22q11.2 duplications, while 16p11.2 duplications were associated with greater specific deficits than 16p11.2 deletions. Duplications at both loci were associated with reduced speed compared to deletions. Performance profiles differed among the groups with particularly poor memory performance of the 22q11.2 deletion group while the 16p11.2 duplication group had greatest deficits in complex cognition. Average accuracy on the CNB was moderately correlated with Full Scale IQ. Deletions and duplications of 22q11.2 and 16p11.2 have differential effects on accuracy and speed of neurocognition indicating locus specificity of performance profiles. These profile differences can help inform mechanistic substrates to heterogeneity in presentation and outcome, and can only be established in large-scale international consortia using the same neurocognitive assessment. Future studies could aim to link performance profiles to clinical features and brain function.

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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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