Beijing Huilongguan Hospital, Peking University Huilongguan Clinical School of Medicine, Beijing, 100096, China.
Department of Psychiatry, Yale University School of Medicine, New Haven, CT, 06510, USA.
Transl Psychiatry. 2022 Jun 2;12(1):225. doi: 10.1038/s41398-022-02007-8.
Previous genome-wide association studies (GWAS) reported that the allele C of rs945270 of the kinectin 1 gene (KTN1) most significantly increased the gray matter volume (GMV) of the putamen and modestly regulated the risk for attention deficit hyperactivity disorder (ADHD). On the other hand, ADHD is known to be associated with a reduction in subcortical and cortical GMVs. Here, we examined the interrelationships of the GMVs, rs945270 alleles, and ADHD symptom scores in the same cohort of children. With data of rs945270 genotypes, GMVs of 118 brain regions, and ADHD symptom scores of 3372 boys and 3129 girls of the Adolescent Brain Cognition Development project, we employed linear regression analyses to examine the pairwise correlations adjusted for the third of the three traits and other relevant covariates, and examine their mediation effects. We found that the major allele C of rs945270 modestly increased risk for ADHD in males only when controlling for the confounding effects of the GMV of any one of the 118 cerebral regions (0.026 ≤ p ≤ 0.059: Top two: left and right putamen). This allele also significantly increased putamen GMV in males alone (left p = 2.8 × 10, and right p = 9.4 × 10; α = 2.1 × 10) and modestly increased other subcortical and cortical GMVs in both sexes (α < p < 0.05), whether or not adjusted for ADHD symptom scores. Both subcortical and cortical GMVs were significantly or suggestively reduced in ADHD when adjusted for rs945270 alleles, each more significantly in females (3.6 × 10 ≤ p < α; Top two: left pallidum and putamen) and males (3.5 × 10 ≤ p < α), respectively. Finally, the left and right putamen GMVs reduced 14.0% and 11.7% of the risk effects of allele C on ADHD, and allele C strengthened 4.5% (left) and 12.2% (right) of the protective effects of putamen GMVs on ADHD risk, respectively. We concluded that the rs945270-GMVs-ADHD relationships were sex-different. In males, the major allele C of rs945270 increased risk for ADHD, which was compromised by putamen GMVs; this allele also but only significantly increased putamen GMVs that then significantly protected against ADHD risk. In females, the top two GMVs significantly decreasing ADHD risk were left pallidum and putamen GMVs. Basal ganglia the left putamen in particular play the most critical role in the pathogenesis of ADHD.
先前的全基因组关联研究(GWAS)报道,kinetictin1 基因(KTN1)rs945270 等位基因 C 最显著增加了壳核的灰质体积(GMV),并适度调节了注意缺陷多动障碍(ADHD)的风险。另一方面,ADHD 与皮质下和皮质 GMV 的减少有关。在这里,我们在同一批儿童中检查了 GMV、rs945270 等位基因和 ADHD 症状评分之间的相互关系。使用来自青少年大脑认知发展项目的 3372 名男孩和 3129 名女孩的 rs945270 基因型、118 个脑区的 GMV 和 ADHD 症状评分的数据,我们采用线性回归分析来检查经过调整的三个特征中的第三个特征和其他相关协变量的两两相关性,并检查它们的中介效应。我们发现,当控制 118 个大脑区域中任意一个 GMV 的混杂效应时,rs945270 的主要等位基因 C 仅在男性中适度增加了 ADHD 的风险(0.026≤p≤0.059:前两个:左、右壳核)。该等位基因还单独显著增加了男性的壳核 GMV(左 p=2.8×10,右 p=9.4×10;α=2.1×10),并适度增加了两性的其他皮质下和皮质 GMV(α< p<0.05),无论是否调整 ADHD 症状评分。调整 rs945270 等位基因后,皮质下和皮质 GMV 均显著或提示性降低,女性(3.6×10≤p<α;前两个:左苍白球和壳核)和男性(3.5×10≤p<α)更显著。最后,左、右壳核 GMV 分别降低了等位基因 C 对 ADHD 的风险效应的 14.0%和 11.7%,而等位基因 C 增强了壳核 GMV 对 ADHD 风险的保护效应的 4.5%(左)和 12.2%(右)。我们得出结论,rs945270-GMV-ADHD 关系存在性别差异。在男性中,rs945270 的主要等位基因 C 增加了 ADHD 的风险,而壳核 GMV 则削弱了这种风险;该等位基因还单独但仅显著增加了壳核 GMV,然后显著降低了 ADHD 的风险。在女性中,降低 ADHD 风险的两个最重要的 GMV 是左苍白球和壳核 GMV。基底神经节,特别是左壳核,在 ADHD 的发病机制中起着最重要的作用。