Department of Psychiatry, Weill Cornell Medical College, White Plains, New York, USA.
J Clin Psychiatry. 2010 Nov;71(11):1416-24. doi: 10.4088/JCP.10r06485gry.
The development of geriatric psychopharmacology was built on advances in geriatric psychiatry nosology and clinical pharmacology and on increased investment in aging research by the National Institute of Mental Health and by academic institutions. Application of the US Food and Drug Administration's geriatric labeling rule provided further impetus. Developments in the knowledge about 3 principal classes of medications (antidepressants, antipsychotics, and treatments for Alzheimer's disease) illustrate the trajectory of geriatric psychopharmacology research. Nonetheless, the loss of information about age effects that has resulted from applying age exclusion criteria in studies limited to either younger adults or geriatric patients is regrettable. Antidepressant trials have moved from studying younger and medically well "geriatric" samples to focusing on "older old" persons and those with significant medical comorbidity including coronary artery disease, cerebrovascular disease, and dementia. Increased specificity is reflected in studies of relationships between specific neuropsychological deficits, specific brain abnormalities, and antidepressant responsiveness. Clinical trials in older adults have demonstrated that the efficacy of antipsychotic medications continues across the lifespan, but that sensitivity to specific side effects changes in older age, with poor tolerability frequently mitigating the benefits of treatment. Treatments for Alzheimer's disease have fallen within the purview of geriatric psychopharmacology. The research focus is increasingly shifting from treatments to slow the course of cognitive decline to studies of early diagnosis and of interventions designed to prevent the development of deficits in vulnerable individuals. The importance of geriatric psychopharmacology will grow further as the average lifespan increases all over the world.
老年精神药理学的发展建立在老年精神病学分类学和临床药理学的进步以及国立精神卫生研究所和学术机构对衰老研究的投资增加的基础上。美国食品和药物管理局(FDA)老年标签规则的应用提供了进一步的动力。关于三类主要药物(抗抑郁药、抗精神病药和治疗阿尔茨海默病的药物)的知识发展说明了老年精神药理学研究的轨迹。尽管如此,由于将年龄排除标准应用于仅限于年轻成年人或老年患者的研究中,导致关于年龄影响的信息丢失,这令人遗憾。抗抑郁药试验已从研究年轻且身体状况良好的“老年”样本转向关注“年老”人群和那些患有重大合并症的人群,包括冠状动脉疾病、脑血管疾病和痴呆症。研究特定神经心理缺陷、特定大脑异常与抗抑郁药反应之间的关系的研究反映了更高的特异性。在老年人群中的临床试验表明,抗精神病药物的疗效在整个生命周期内持续存在,但在老年时对特定副作用的敏感性会发生变化,较差的耐受性经常减轻治疗的益处。治疗阿尔茨海默病属于老年精神药理学的范畴。研究重点正从减缓认知衰退的治疗方法逐渐转向早期诊断和针对脆弱个体的缺陷预防干预措施的研究。随着世界各地的平均寿命增加,老年精神药理学的重要性将进一步提高。