Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Mol Psychiatry. 2021 Jul;26(7):3363-3373. doi: 10.1038/s41380-021-01062-9. Epub 2021 Mar 22.
Treatment-resistant depression (TRD) is a major contributor to the disability caused by major depressive disorder (MDD). Primary care electronic health records provide an easily accessible approach to investigate TRD clinical and genetic characteristics. MDD defined from primary care records in UK Biobank (UKB) and EXCEED studies was compared with other measures of depression and tested for association with MDD polygenic risk score (PRS). Using prescribing records, TRD was defined from at least two switches between antidepressant drugs, each prescribed for at least 6 weeks. Clinical-demographic characteristics, SNP-based heritability (h) and genetic overlap with psychiatric and non-psychiatric traits were compared in TRD and non-TRD MDD cases. In 230,096 and 8926 UKB and EXCEED participants with primary care data, respectively, the prevalence of MDD was 8.7% and 14.2%, of which 13.2% and 13.5% was TRD, respectively. In both cohorts, MDD defined from primary care records was strongly associated with MDD PRS, and in UKB it showed overlap of 71-88% with other MDD definitions. In UKB, TRD vs healthy controls and non-TRD vs healthy controls h was comparable (0.25 [SE = 0.04] and 0.19 [SE = 0.02], respectively). TRD vs non-TRD was positively associated with the PRS of attention deficit hyperactivity disorder, with lower socio-economic status, obesity, higher neuroticism and other unfavourable clinical characteristics. This study demonstrated that MDD and TRD can be reliably defined using primary care records and provides the first large scale population assessment of the genetic, clinical and demographic characteristics of TRD.
治疗抵抗性抑郁症(TRD)是导致重度抑郁症(MDD)致残的主要原因。初级保健电子健康记录为研究 TRD 的临床和遗传特征提供了一种易于获取的方法。在 UK Biobank(UKB)和 EXCEED 研究中,从初级保健记录中定义的 MDD 与其他抑郁测量方法进行了比较,并测试了与 MDD 多基因风险评分(PRS)的关联。使用处方记录,通过至少两次抗抑郁药物转换来定义 TRD,每种药物的处方至少为 6 周。在 TRD 和非 TRD MDD 病例中比较了临床人口统计学特征、基于 SNP 的遗传率(h)以及与精神和非精神特征的遗传重叠。在分别具有初级保健数据的 230096 和 8926 名 UKB 和 EXCEED 参与者中,MDD 的患病率分别为 8.7%和 14.2%,其中分别有 13.2%和 13.5%为 TRD。在两个队列中,从初级保健记录中定义的 MDD 与 MDD PRS 密切相关,在 UKB 中,它与其他 MDD 定义的重叠率为 71-88%。在 UKB 中,TRD 与健康对照组和非 TRD 与健康对照组的 h 相当(0.25 [SE = 0.04]和 0.19 [SE = 0.02])。TRD 与非 TRD 与注意力缺陷多动障碍的 PRS 呈正相关,与社会经济地位较低、肥胖、神经质较高以及其他不利的临床特征相关。这项研究表明,使用初级保健记录可以可靠地定义 MDD 和 TRD,并首次对 TRD 的遗传、临床和人口统计学特征进行了大规模的人群评估。