Schumacher Martin M, Santambrogio Jacopo
Independent Researcher, Linsenackerweg 4, 4450 Sissach, Switzerland.
Adele Bonolis AS.FRA. Onlus Foundation, 20854 Vedano al Lambro, Italy.
J Pers Med. 2023 May 16;13(5):837. doi: 10.3390/jpm13050837.
The dexamethasone suppression test (DST) assesses the functionality of the HPA axis and can be regarded as the first potential biomarker in psychiatry. In 1981, a group of researchers at the University of Michigan published a groundbreaking paper regarding its use for diagnosing melancholic depression, reporting a diagnostic sensitivity of 67% and a specificity of 95%. While this study generated much enthusiasm and high expectations in the field of biological psychiatry, subsequent studies produced equivocal results, leading to the test being rejected by the American Psychiatric Association. The scientific reasons leading to the rise and fall of the DST are assessed in this review, suggestions are provided as to how the original test can be improved, and its potential applications in clinical psychiatry are discussed. An improved, standardized, and validated version of the DST would be a biologically meaningful and useful biomarker in psychiatry, providing a tool for clinicians caring for depressed patients in the areas of diagnosis, treatment, and prognosis, and predicting the risk of suicide. Additionally, such a test could be a crucial part in the generation of biologically homogenous patient cohorts, necessary for the successful development of new psychotropic medications.
地塞米松抑制试验(DST)评估下丘脑-垂体-肾上腺(HPA)轴的功能,可被视为精神病学中的首个潜在生物标志物。1981年,密歇根大学的一组研究人员发表了一篇关于其用于诊断忧郁症抑郁症的开创性论文,报告其诊断敏感性为67%,特异性为95%。虽然这项研究在生物精神病学领域引发了极大的热情和高度期望,但随后的研究结果却模棱两可,导致该测试被美国精神病学协会拒绝。本综述评估了导致DST兴衰的科学原因,就如何改进原始测试提出了建议,并讨论了其在临床精神病学中的潜在应用。改进的、标准化的和经过验证的DST版本将是精神病学中具有生物学意义且有用的生物标志物,为临床医生在抑郁症患者的诊断、治疗和预后方面提供工具,并预测自杀风险。此外,这样的测试可能是生成生物学上同质的患者队列的关键部分,这对于新型精神药物的成功研发是必要的。