Department of Pathology, School of Basic Medicine, Weifang Medical University, Weifang 261053, China; School of Mental Health, Jining Medical University, Jining 272013, China.
Psychiatry Department, Shandong Daizhuang Hospital, Jining 272051, China.
J Affect Disord. 2022 Mar 1;300:505-510. doi: 10.1016/j.jad.2021.12.138. Epub 2022 Jan 4.
The gene-gene interaction is known to be the genetic cause of major depressive disorder (MDD). Several genes have been found to be related to MDD. The objectives of this study were to verify the susceptibility genes of MDD in a sample of university students in China, and to investigate possible gene-gene interactions in relation to the risk of MDD.
7,627 Chinese Han freshmen were enrolled at baseline survey in 2018. After a 2-year follow-up, 170 new onset MDD cases and 680 controls with DNA samples reserved were sequenced and genotyped for 4 selected Single Nucleotide Polymorphisms (SNPs) in a nested case-control study (ratio of 1:4). Chi-square test was used to identify the relationships between SNPs and risk of MDD. Generalized multifactor dimensionality reduction (GMDR) was used to analyze the gene-gene interactions.
The 2-year incidence of MDD in Chinese college students was 3.75% (95% CI: 3.24%, 4.34%). There was no statistical difference in MDD incidences between males (3.74%, 95% CI: 3.12%, 4.49%) and females (3.77%, 95% CI: 2.97%, 4.78%) (p>0.05). TMEM161B (rs768705) was positively associated with new onset MDD (χ = 0.75, p = 0.023). The AG genotype of rs768705 was significant (OR=1.640, 95%CI:1.414-2.358). The gene-gene interaction between TMEM161B (rs768705) and LHPP (rs35936514) was statistically significant in this nested case-control study (p = 0.011). The CV consistency was 9/10 and the testing accuracy was 0.5274.
The results could not be inferred to other ethnics.
This study provided evidence that combined rs768705 (TMEM161B) and rs35936514 (LHPP) may modulate the risk of MDD.
基因-基因相互作用被认为是导致重度抑郁症(MDD)的遗传原因。已经发现了一些与 MDD 相关的基因。本研究的目的是在中国大学生样本中验证 MDD 的易感基因,并研究与 MDD 风险相关的可能的基因-基因相互作用。
2018 年基线调查时纳入了 7627 名中国汉族大一新生。经过 2 年的随访,有 170 例新发 MDD 病例和 680 例保留 DNA 样本的对照被纳入嵌套病例对照研究进行测序和基因分型(1:4 的比例)。卡方检验用于识别 SNP 与 MDD 风险之间的关系。广义多因素维度缩减(GMDR)用于分析基因-基因相互作用。
中国大学生 MDD 的 2 年发病率为 3.75%(95%CI:3.24%,4.34%)。男女生 MDD 发病率无统计学差异(男性 3.74%,95%CI:3.12%,4.49%;女性 3.77%,95%CI:2.97%,4.78%)(p>0.05)。TMEM161B(rs768705)与新发 MDD 呈正相关(χ=0.75,p=0.023)。rs768705 的 AG 基因型具有显著性(OR=1.640,95%CI:1.414-2.358)。在该嵌套病例对照研究中,TMEM161B(rs768705)和 LHPP(rs35936514)之间的基因-基因相互作用具有统计学意义(p=0.011)。CV 一致性为 9/10,检验准确率为 0.5274。
结果不能推断为其他种族。
本研究提供了证据表明,联合 rs768705(TMEM161B)和 rs35936514(LHPP)可能调节 MDD 的风险。