制定治疗主要精神疾病:算法针对主要影响的脑细胞类型

Jeffrey Fessel
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引用次数: 3

摘要

背景:大多数精神疾病的药物治疗都是从偶然发现的因不同原因开具的药物的益处中发展起来的。提出了一种制定药物治疗的算法方法,基于该方法,脑细胞类型的活动变化组合在任何特定情况下都是主导性的,因为这些细胞类型包含并替代了影响其功能的遗传、代谢和环境信息。该算法之所以有效,是因为一些或所有受影响细胞类型的功能都受益于几种可用的药物:克莱门汀、丹特罗林、红细胞生成素、芬戈莫德、氟西汀、锂、美金刚、米诺环素、吡格列酮、吡拉西坦和利鲁唑程序/发现:双相情感障碍、重度抑郁障碍、精神分裂症、阿尔茨海默病和创伤后应激障碍,对算法进行了说明;对他们来说,文献综述表明,没有一种细胞类型改变的单一组合可以解释所有病例;但是,对于每种情况,与其他可能的组合相比,它们确定哪种组合发生得最频繁,即占主导地位。知道在特定条件下改变的细胞类型的主要组合,就可以用上述列表中的药物组合进行治疗。可能从该疗法中受益的患者百分比取决于该特定疾病患者出现显性组合的频率。结论:了解精神疾病中细胞类型变化的主要组合,可以通过算法制定合理的治疗方案。对同一条件的不同研究往往产生不同的结果;所有这些都可能是正确的,因为相同的临床表型来自受损细胞类型的不同组合,从而产生不同的结果。临床试验将验证拟议的药物概念和选择。
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Formulating treatment of major psychiatric disorders: algorithm targets the dominantly affected brain cell-types.

Background: Pharmacotherapy for most psychiatric conditions was developed from serendipitous observations of benefit from drugs prescribed for different reasons. An algorithmic approach to formulating pharmacotherapy is proposed, based upon which combination of changed activities by brain cell-types is dominant for any particular condition, because those cell-types contain and surrogate for genetic, metabolic and environmental information, that has affected their function. The algorithm performs because functions of some or all the affected cell-types benefit from several available drugs: clemastine, dantrolene, erythropoietin, fingolimod, fluoxetine, lithium, memantine, minocycline, pioglitazone, piracetam, and riluzole PROCEDURES/FINDINGS: Bipolar disorder, major depressive disorder, schizophrenia, Alzheimer's disease, and post-traumatic stress disorder, illustrate the algorithm; for them, literature reviews show that no single combination of altered cell-types accounts for all cases; but they identify, for each condition, which combination occurs most frequently, i.e., dominates, as compared with other possible combinations. Knowing the dominant combination of altered cell-types in a particular condition, permits formulation of therapy with combinations of drugs taken from the above list. The percentage of patients who might benefit from that therapy, depends upon the frequency with which the dominant combination occurs in patients with that particular condition.

Conclusions: Knowing the dominant combination of changed cell types in psychiatric conditions, permits an algorithmically formulated, rationally-based treatment. Different studies of the same condition often produce discrepant results; all might be correct, because identical clinical phenotypes result from different combinations of impaired cell-types, thus producing different results. Clinical trials would validate both the proposed concept and choice of drugs.

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