Green Robert C, DeKosky Steven T
Department of Neurology, Boston University School of Medicine, Boston, MA 02118, USA.
Neurology. 2006 Nov 14;67(9 Suppl 3):S2-5. doi: 10.1212/wnl.67.9_suppl_3.s2.
Many new treatments under development for Alzheimer disease (AD) will be disease-modifying rather than symptomatic. Clinical evaluation of these treatments will require primary and secondary prevention trials. We describe some of the methodologic challenges in designing primary prevention trials for AD and illustrate these with examples from the ADAPT (Alzheimer Disease Anti-Inflammatory Prevention Trial) Study and GEM (Ginkgo in Evaluation of Memory) Study. Primary prevention trials for AD present many design challenges. In most situations, secondary prevention trials provide the most feasible first step toward primary prevention.
许多正在研发的治疗阿尔茨海默病(AD)的新疗法将具有疾病修饰作用而非仅仅缓解症状。对这些疗法的临床评估将需要进行一级和二级预防试验。我们描述了在设计AD一级预防试验时面临的一些方法学挑战,并以ADAPT(阿尔茨海默病抗炎预防试验)研究和GEM(银杏叶评估记忆)研究中的实例进行说明。AD的一级预防试验面临诸多设计挑战。在大多数情况下,二级预防试验是迈向一级预防最可行的第一步。