Max Planck Institute of Psychiatry, Munich, Germany.
HMNC Holding GmbH, Munich, Germany.
Pharmacopsychiatry. 2024 Nov;57(6):263-274. doi: 10.1055/a-2372-3549. Epub 2024 Aug 19.
The future of depression pharmacotherapy lies in a precision medicine approach that recognizes that depression is a disease where different causalities drive symptoms. That approach calls for a departure from current diagnostic categories, which are broad enough to allow adherence to the "one-size-fits-all" paradigm, which is complementary to the routine use of "broad-spectrum" mono-amine antidepressants. Similar to oncology, narrowing the overinclusive diagnostic window by implementing laboratory tests, which guide specifically targeted treatments, will be a major step forward in overcoming the present drug discovery crisis.A substantial subgroup of patients presents with signs and symptoms of hypothalamic-pituitary-adrenocortical (HPA) overactivity. Therefore, this stress hormone system was considered to offer worthwhile targets. Some promising results emerged, but in sum, the results achieved by targeting corticosteroid receptors were mixed.More specific are non-peptidergic drugs that block stress-responsive neuropeptides, corticotropin-releasing hormone (CRH), and arginine vasopressin (AVP) in the brain by antagonizing their cognate CRHR1-and V1b-receptors. If a patient's depressive symptomatology is driven by overactive V1b-signaling then a V1b-receptor antagonist should be first-line treatment. To identify the patient having this V1b-receptor overactivity, a neuroendocrine test, the so-called dex/CRH-test, was developed, which indicates central AVP release but is too complicated to be routinely used. Therefore, this test was transformed into a gene-based "near-patient" test that allows immediate identification if a depressed patient's symptomatology is driven by overactive V1b-receptor signaling. We believe that this precision medicine approach will be the next major innovation in the pharmacotherapy of depression.
抑郁症药物治疗的未来在于一种精准医学方法,该方法认识到抑郁症是一种病因不同导致症状不同的疾病。这种方法需要摒弃当前的诊断类别,这些类别足够宽泛,可以允许遵循“一刀切”的范式,这与常规使用“广谱”单胺类抗抑郁药是互补的。与肿瘤学类似,通过实施实验室测试来缩小过于宽泛的诊断窗口,这些测试可以指导具体的靶向治疗,这将是克服当前药物发现危机的重要一步。相当一部分患者表现出下丘脑-垂体-肾上腺皮质(HPA)过度活跃的迹象和症状。因此,这个应激激素系统被认为是一个有价值的靶点。出现了一些有希望的结果,但总的来说,靶向皮质激素受体的结果好坏参半。更具体的是一些非肽类药物,它们通过拮抗其同源 CRHR1 和 V1b 受体,阻断大脑中应激反应性神经肽、促肾上腺皮质释放激素(CRH)和精氨酸加压素(AVP),从而提供有价值的靶点。如果患者的抑郁症状是由过度活跃的 V1b 信号驱动的,那么 V1b 受体拮抗剂应该是一线治疗药物。为了确定具有这种 V1b 受体过度活跃的患者,开发了一种神经内分泌测试,即所谓的 dex/CRH 测试,该测试表明中枢 AVP 释放,但过于复杂,无法常规使用。因此,该测试被转化为基于基因的“近患者”测试,如果抑郁患者的症状是由过度活跃的 V1b 受体信号驱动的,可以立即识别。我们相信,这种精准医学方法将成为抑郁症药物治疗的下一个重大创新。