Department of Medical Genetics, Oslo University Hospital, Oslo, Norway; Norwegian Centre for Mental Disorders Research (NORMENT), Division of Mental Health and Addiction, Oslo University Hospital and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Norwegian Centre for Mental Disorders Research (NORMENT), Division of Mental Health and Addiction, Oslo University Hospital and Institute of Clinical Medicine, University of Oslo, Oslo, Norway; Department of Psychiatry and Psychotherapy, Tübingen Center for Mental Health, University of Tübingen, Germany; German Center for Mental Health (DZPG), partner site Tübingen, Tübingen, Germany.
Biol Psychiatry. 2024 Jan 15;95(2):147-160. doi: 10.1016/j.biopsych.2023.08.018. Epub 2023 Sep 3.
Carriers of the 1q21.1 distal and 15q11.2 BP1-BP2 copy number variants exhibit regional and global brain differences compared with noncarriers. However, interpreting regional differences is challenging if a global difference drives the regional brain differences. Intraindividual variability measures can be used to test for regional differences beyond global differences in brain structure.
Magnetic resonance imaging data were used to obtain regional brain values for 1q21.1 distal deletion (n = 30) and duplication (n = 27) and 15q11.2 BP1-BP2 deletion (n = 170) and duplication (n = 243) carriers and matched noncarriers (n = 2350). Regional intra-deviation scores, i.e., the standardized difference between an individual's regional difference and global difference, were used to test for regional differences that diverge from the global difference.
For the 1q21.1 distal deletion carriers, cortical surface area for regions in the medial visual cortex, posterior cingulate, and temporal pole differed less and regions in the prefrontal and superior temporal cortex differed more than the global difference in cortical surface area. For the 15q11.2 BP1-BP2 deletion carriers, cortical thickness in regions in the medial visual cortex, auditory cortex, and temporal pole differed less and the prefrontal and somatosensory cortex differed more than the global difference in cortical thickness.
We find evidence for regional effects beyond differences in global brain measures in 1q21.1 distal and 15q11.2 BP1-BP2 copy number variants. The results provide new insight into brain profiling of the 1q21.1 distal and 15q11.2 BP1-BP2 copy number variants, with the potential to increase understanding of the mechanisms involved in altered neurodevelopment.
与非携带者相比,1q21.1 远端和 15q11.2BP1-BP2 拷贝数变异的携带者表现出区域性和全脑性的大脑差异。然而,如果全脑差异驱动了区域性脑差异,那么解释区域性差异是具有挑战性的。个体内变异性测量可用于测试大脑结构的区域性差异是否超出了全脑差异。
利用磁共振成像数据,获得了 1q21.1 远端缺失(n=30)和重复(n=27)以及 15q11.2BP1-BP2 缺失(n=170)和重复(n=243)携带者和匹配的非携带者(n=2350)的区域性脑值。个体内偏差分数,即个体的区域性差异与全脑差异的标准化差异,用于测试与全脑差异不同的区域性差异。
对于 1q21.1 远端缺失的携带者,内侧视觉皮层、后扣带和颞极的皮质表面积差异较小,而前额叶和颞上回的皮质表面积差异较大,与皮质表面积的全脑差异不同。对于 15q11.2BP1-BP2 缺失的携带者,内侧视觉皮层、听觉皮层和颞极的皮质厚度差异较小,而前额叶和躯体感觉皮层的皮质厚度差异较大,与皮质厚度的全脑差异不同。
我们发现 1q21.1 远端和 15q11.2BP1-BP2 拷贝数变异中存在全脑测量差异之外的区域性效应。这些结果为 1q21.1 远端和 15q11.2BP1-BP2 拷贝数变异的大脑特征提供了新的见解,有可能增加对神经发育改变所涉及的机制的理解。