Laboratory of Experimental Psychology and Neuroscience (LPEN), Institute of Cognitive and Translational Neuroscience (INCYT), INECO Foundation, Favaloro University, Buenos Aires, Argentina.
National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.
J Neuropsychol. 2018 Sep;12(3):389-408. doi: 10.1111/jnp.12120. Epub 2017 Mar 11.
Frontostriatal networks play critical roles in grounding action semantics and syntactic skills. Indeed, their atrophy distinctively disrupts both domains, as observed in patients with Huntington's disease (HD) and Parkinson's disease, even during early disease stages. However, frontostriatal degeneration in these conditions may begin up to 15 years before the onset of clinical symptoms, opening avenues for pre-clinical detection via sensitive tasks. Such a mission is particularly critical in HD, given that patients' children have 50% chances of inheriting the disease. Against this background, we assessed whether deficits in the above-mentioned domains emerge in subjects at risk to develop HD. We administered tasks tapping action semantics, object semantics, and two forms of syntactic processing to 18 patients with HD, 19 asymptomatic first-degree relatives, and sociodemographically matched controls for each group. The patients evinced significant deficits in all tasks, but only those in the two target domains were independent of overall cognitive state. More crucially, relative to controls, the asymptomatic relatives were selectively impaired in action semantics and in the more complex syntactic task, with both patterns emerging irrespective of the subjects' overall cognitive state. Our findings highlight the relevance of these dysfunctions as potential prodromal biomarkers of HD. Moreover, they offer theoretical insights into the differential contributions of frontostriatal hubs to both domains while paving the way for innovations in diagnostic procedures.
额眶部-纹状体网络在使动作语义和句法技能具象化方面发挥着关键作用。事实上,正如亨廷顿病(HD)和帕金森病患者所观察到的那样,即使在疾病早期阶段,这些网络的萎缩也会明显破坏这两个领域。然而,在这些情况下,额眶部-纹状体的退化可能在出现临床症状前 15 年就开始了,为通过敏感任务进行临床前检测开辟了途径。鉴于 HD 患者的子女有 50%的机会遗传该病,因此在这种情况下,这样的任务尤为关键。在此背景下,我们评估了是否有发展为 HD 风险的受试者在上述领域出现缺陷。我们对 18 名 HD 患者、19 名无症状一级亲属和每组年龄、性别相匹配的对照组进行了动作语义、物体语义以及两种句法处理形式的任务测试。患者在所有任务中都表现出明显的缺陷,但只有在两个目标领域的缺陷才与整体认知状态无关。更重要的是,与对照组相比,无症状亲属在动作语义和更复杂的句法任务中表现出选择性损伤,而这些模式的出现与受试者的整体认知状态无关。我们的研究结果强调了这些功能障碍作为 HD 潜在前驱生物标志物的重要性。此外,它们为额眶部-纹状体枢纽对这两个领域的不同贡献提供了理论上的见解,同时为诊断程序的创新铺平了道路。