Stein Murray B, Choi Karmel W, Jain Sonia, Campbell-Sills Laura, Chen Chia-Yen, Gelernter Joel, He Feng, Heeringa Steven G, Maihofer Adam X, Nievergelt Caroline, Nock Matthew K, Ripke Stephan, Sun Xiaoying, Kessler Ronald C, Smoller Jordan W, Ursano Robert J
Department of Psychiatry, University of California San Diego, La Jolla, California.
Department of Family Medicine and Public Health, University of California San Diego, La Jolla, California.
Am J Med Genet B Neuropsychiatr Genet. 2019 Jul;180(5):310-319. doi: 10.1002/ajmg.b.32730. Epub 2019 May 13.
Though a growing body of preclinical and translational research is illuminating a biological basis for resilience to stress, little is known about the genetic basis of psychological resilience in humans. We conducted genome-wide association studies (GWASs) of self-assessed (by questionnaire) and outcome-based (incident mental disorders from predeployment to postdeployment) resilience among European (EUR) ancestry soldiers in the Army study to assess risk and resilience in servicemembers. Self-assessed resilience (N = 11,492) was found to have significant common-variant heritability (h = 0.162, se = 0.050, p = 5.37 × 10 ), and to be significantly negatively genetically correlated with neuroticism (r = -0.388, p = .0092). GWAS results from the EUR soldiers revealed a genome-wide significant locus on an intergenic region on Chr 4 upstream from doublecortin-like kinase 2 (DCLK2) (four single nucleotide polymorphisms (SNPs) in LD; top SNP: rs4260523 [p = 5.65 × 10 ] is an eQTL in frontal cortex), a member of the doublecortin family of kinases that promote survival and regeneration of injured neurons. A second gene, kelch-like family member 36 (KLHL36) was detected at gene-wise genome-wide significance [p = 1.89 × 10 ]. A polygenic risk score derived from the self-assessed resilience GWAS was not significantly associated with outcome-based resilience. In very preliminary results, genome-wide significant association with outcome-based resilience was found for one locus (top SNP: rs12580015 [p = 2.37 × 10 ]) on Chr 12 downstream from solute carrier family 15 member 5 (SLC15A5) in subjects (N = 581) exposed to the highest level of deployment stress. The further study of genetic determinants of resilience has the potential to illuminate the molecular bases of stress-related psychopathology and point to new avenues for therapeutic intervention.
尽管越来越多的临床前和转化研究正在揭示应激恢复力的生物学基础,但对于人类心理恢复力的遗传基础却知之甚少。在陆军研究中,我们对欧洲(EUR)血统士兵中通过问卷自我评估的和基于结果(从部署前到部署后发生的精神障碍)的恢复力进行了全基因组关联研究(GWAS),以评估军人的风险和恢复力。发现自我评估的恢复力(N = 11492)具有显著的常见变异遗传力(h = 0.162,标准误 = 0.050,p = 5.37×10 ),并且与神经质显著负遗传相关(r = -0.388,p = 0.0092)。EUR士兵的GWAS结果揭示了4号染色体上双皮质素样激酶2(DCLK2)上游基因间区域的一个全基因组显著位点(连锁不平衡中的四个单核苷酸多态性(SNP);顶级SNP:rs4260523 [p = 5.65×10 ]是额叶皮质中的一个表达定量性状位点),DCLK2是促进受损神经元存活和再生的双皮质素激酶家族成员。第二个基因,kelch样家族成员36(KLHL36)在基因水平全基因组显著性水平上被检测到 [p = 1.89×10 ]。从自我评估的恢复力GWAS得出的多基因风险评分与基于结果的恢复力没有显著关联。在非常初步的结果中,在暴露于最高水平部署压力的受试者(N = 581)中,发现12号染色体上溶质载体家族15成员5(SLC15A5)下游的一个位点(顶级SNP:rs12580015 [p = 2.37×10 ])与基于结果的恢复力存在全基因组显著关联。对应激恢复力的遗传决定因素的进一步研究有可能阐明应激相关精神病理学的分子基础,并指出治疗干预的新途径。