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Leveraging relatedness-based measures in people with language disorders: A scoping review 在语言障碍患者中利用基于亲缘关系的测量方法:范围综述。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-12-16 DOI: 10.1111/jnp.12405
Logan A. Gaudet, Lena Rybka, Emmanuel Mandonnet, Emmanuelle Volle, Marion Barberis, Roel Jonkers, Adrià Rofes

Understanding lexico-semantic processing is crucial for dissecting the complexities of language and its disorders. Relatedness-based measures, or those which investigate the degree of relatedness in meaning between either task items or items produced by participants, offer the opportunity to harness novel computational and analytical techniques from cognitive network science. Recognizing the need to deepen our understanding of lexico-semantic deficits through diverse experimental and analytical approaches, this review explores the use of such measures in research into language disorders. A comprehensive search of four electronic databases covering publications from the last 11 years (October 2013–September 2024) identified 38 original experimental studies employing relatedness-based measures in populations with language disorders or other neurological conditions. Articles were examined for the types of tasks used, populations studied, item selection methods and analytical approaches. The predominant use of category fluency tasks emerged across studies, with a notable absence of relatedness judgement tasks or comparable paradigms. Commonly discussed populations included individuals with post-stroke aphasia, mild cognitive impairment and schizophrenia. Analytical methods varied significantly, ranging from more traditional approaches of clustering and switching to more sophisticated computational techniques. Despite the evident utility of category fluency tasks in research and clinical settings, the review underscores a critical need to diversify experimental paradigms and probe lexico-semantic processing in a more multifaceted manner. A broadened approach in future language disorder research should incorporate innovative analytical techniques, investigations of neural correlates and a wider array of tasks employing relatedness-based measures already present in healthy populations.

理解词汇语义加工对于剖析语言的复杂性及其障碍是至关重要的。基于相关性的测量,或那些调查任务项目或参与者产生的项目之间意义的相关性程度的测量,提供了利用认知网络科学的新计算和分析技术的机会。认识到需要通过不同的实验和分析方法来加深我们对词汇语义缺陷的理解,本综述探讨了这些方法在语言障碍研究中的应用。通过对过去11年(2013年10月- 2024年9月)出版物的四个电子数据库进行全面检索,确定了38项原始实验研究,这些研究采用基于亲缘关系的方法对语言障碍或其他神经系统疾病人群进行了测量。文章审查了使用的任务类型、研究的人口、项目选择方法和分析方法。类别流畅性任务的主要使用出现在研究中,明显缺乏相关性判断任务或可比范式。通常讨论的人群包括中风后失语症、轻度认知障碍和精神分裂症患者。分析方法变化很大,从更传统的聚类和转换到更复杂的计算技术。尽管类别流畅性任务在研究和临床环境中具有明显的效用,但该综述强调了多样化实验范式和以更多方面的方式探索词汇-语义处理的迫切需要。在未来的语言障碍研究中,一个更广泛的方法应该包括创新的分析技术,神经相关性的调查,以及采用健康人群中已经存在的基于相关性的测量方法的更广泛的任务。
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引用次数: 0
The efficacy and feasibility of an immersive virtual reality game to train spatial attention orientation after stroke: A stage 2 report 沉浸式虚拟现实游戏训练中风后空间注意力定向的有效性和可行性:第二阶段报告。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-12-12 DOI: 10.1111/jnp.12403
Hanne Huygelier, Nora Tuts, Karla Michiels, Eline Note, Fabienne Schillebeeckx, Jos Tournoy, Vero Vanden Abeele, Raymond van Ee, Céline R. Gillebert

Spatial neglect is a post-stroke attention deficit for which there is no evidence-based intervention. Immersive virtual reality (IVR) may increase treatment efficacy, as it allows to train spatial attention in a rich environment. This study evaluated the efficacy and feasibility of an IVR patient-tailored training (HEMIRehApp). Using a cross-over design, an active (spatially biased) and placebo (spatially unbiased) IVR intervention were compared. We aimed to recruit 8 per-protocol left-sided neglect patients. The primary outcome was response times on the Posner cueing task. To evaluate feasibility, we documented the number of recruited patients, cybersickness and patients' experience with HEMIRehApp. After 2 years of recruitment, we were able to enrol 6 patients, of whom 2 completed the full protocol. The target sample size was not feasible due to a lower than expected prevalence of left-sided neglect and a higher than expected drop-out rate. The planned group-level analysis was therefore replaced by a single-case analysis. The results in the 2 per-protocol cases suggest a superior effect of spatially biased IVR training than unbiased IVR training inside IVR. IVR training was feasible as all 6 enrolled patients were able to complete 10 IVR training sessions, but the cross-over protocol itself was unfeasible. While the low sample size prevented us from conclusively evaluating the efficacy of HEMIRehApp, our preliminary single-case results suggest that neglect patients were able to improve attentional orientation towards eccentric target locations in IVR. Follow-up studies are needed to further validate these findings.

空间忽略是中风后的一种注意力缺陷,目前尚无循证干预措施。沉浸式虚拟现实(IVR)可以在丰富的环境中训练空间注意力,从而提高治疗效果。本研究评估了 IVR 患者定制训练(HEMIRehApp)的有效性和可行性。采用交叉设计,比较了积极(空间偏差)和安慰剂(空间无偏差)的 IVR 干预。我们的目标是按协议招募 8 名左侧忽视患者。主要结果是对波斯纳提示任务的反应时间。为了评估可行性,我们记录了招募患者的数量、晕机情况以及患者使用 HEMIRehApp 的体验。经过 2 年的招募,我们招募了 6 名患者,其中 2 人完成了全部方案。由于左侧疏忽的发病率低于预期,且辍学率高于预期,因此无法达到目标样本量。因此,计划中的群体分析被单例分析所取代。2 个按方案进行的病例结果表明,在 IVR 内部进行有空间偏差的 IVR 训练比无空间偏差的 IVR 训练效果更好。IVR 训练是可行的,因为所有 6 名入选患者都能完成 10 次 IVR 训练,但交叉方案本身并不可行。由于样本量较少,我们无法对 HEMIRehApp 的疗效进行最终评估,但我们的初步单例结果表明,忽视患者能够在 IVR 中改善对偏心目标位置的注意定向。要进一步验证这些发现,还需要进行后续研究。
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引用次数: 0
‘I still remember’: Increased categoric autobiographical memories in behavioural variant of frontotemporal dementia “我还记得”:额颞叶痴呆行为变异患者类别自传式记忆增加。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-12-10 DOI: 10.1111/jnp.12404
Mohamad El Haj, Dimitrios Kapogiannis, Claire Boutoleau-Bretonnière

Autobiographical memory is diminished in patients with behavioural variant of frontotemporal dementia (bvFTD), and research has focused on the hampered ability of patients to retrieve specific memories. In this study, we implemented a methodology seeking to provide a qualitative analysis of autobiographical specificity. We invited patients with bvFTD and control participants to retrieve autobiographical memories and we distinguished between specific, categoric, extended and semantic autobiographical retrieval. The analysis demonstrated that patients with bvFTD produced more categoric than specific, extended or semantic memories. Thus, despite the decreased ability to retrieve specific memories, an increased ability to produce categoric memories can be observed in patients with bvFTD. These results support a positive view according to which autobiographical retrieval in bvFTD is not solely characterized by over-generality, but also by increased retrieval of categoric memories. Categoric memories, albeit lacking uniqueness, nevertheless, involve retrieval of similar or related events upon which patients may draw knowledge related to their self-image and life story.

行为变异额颞叶痴呆(bvFTD)患者的自传体记忆减弱,研究重点是患者恢复特定记忆的能力受到阻碍。在这项研究中,我们实施了一种方法,旨在提供自传特异性的定性分析。我们邀请bvFTD患者和对照组进行自传体记忆检索,并区分了特定自传体记忆、类别自传体记忆、扩展自传体记忆和语义自传体记忆。分析表明,bvFTD患者产生的分类记忆多于特定记忆、扩展记忆或语义记忆。因此,尽管恢复特定记忆的能力下降,但在bvFTD患者中可以观察到产生分类记忆的能力增加。这些结果支持了一个积极的观点,根据该观点,bvFTD的自传体检索不仅具有过度概括的特征,而且还具有分类记忆检索的增加。范畴记忆虽然缺乏独特性,但涉及到相似或相关事件的检索,患者可以从中提取与他们的自我形象和生活故事相关的知识。
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引用次数: 0
Non-optimal cognitive offloading in schizophrenia in a prospective memory task: Influence of both metacognitive beliefs and cognitive effort avoidance 精神分裂症患者在前瞻性记忆任务中的非最佳认知卸载:元认知信念和认知努力回避的影响。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-11-18 DOI: 10.1111/jnp.12399
Amandine Décombe, Chiara Scarampi, Elora Malleville, Delphine Capdevielle, Sam J. Gilbert, Stéphane Raffard

Cognitive offloading refers to the use of physical action and the external environment to simplify mental demand. One form of this—intention offloading—involves the use of external reminders to support delayed intentions. Both beliefs of poor memory ability and a preference to avoid cognitive effort lead to offloading intentions rather than using internal memory. Schizophrenia is a population with deficits in prospective memory and to overcome this difficulty, neuropsychological interventions can propose external aids such as reminders. However, it is unknown what motivates individuals with schizophrenia to spontaneously use reminders. Twenty-seven individuals with schizophrenia and twenty-seven non-clinical individuals were recruited to perform a prospective memory task, with two levels of difficulty, by deciding whether to use reminders or their internal memory. The proportion of reminder use, performance (hits and errors), subjective effort and metacognitive beliefs were recorded. The results show a non-optimal use of reminders in the schizophrenia group: this group used more reminders than the non-clinical group when the task was easy but did not increase reminder usage when the task became more difficult. Individuals with schizophrenia perceived the task to be more effortful than the non-clinical individuals in the easy task, but also had a high estimation of their memory ability. Reminder usage in schizophrenia is atypical and non-optimal. This may relate to effort and metacognition but the direct influence of these factors remains to be demonstrated. The overall results open perspectives on the neuropsychological treatment of prospective memory in this population.

认知卸载指的是利用实际行动和外部环境来简化心理需求。其中一种形式--意向卸载--涉及使用外部提醒来支持延迟的意向。记忆能力差的信念和避免认知努力的偏好都会导致意向卸载,而不是使用内部记忆。精神分裂症患者在前瞻性记忆方面存在缺陷,为了克服这一困难,神经心理学干预措施可以提供外部帮助,如提醒。然而,精神分裂症患者自发使用提醒器的动机是什么尚不得而知。研究人员招募了27名精神分裂症患者和27名非临床患者,让他们通过决定使用提醒器还是内部记忆来完成一项有两种难度的前瞻性记忆任务。研究人员记录了使用提醒器的比例、表现(命中和错误)、主观努力和元认知信念。结果表明,精神分裂症组对提醒器的使用并不理想:当任务简单时,该组比非临床组使用更多的提醒器,但当任务变得更加困难时,提醒器的使用并没有增加。在完成简单任务时,精神分裂症患者认为比非临床患者更费力,但他们对自己的记忆能力也有很高的评价。精神分裂症患者对提醒的使用是非典型和非最佳的。这可能与努力和元认知有关,但这些因素的直接影响仍有待证实。总体结果为该人群前瞻性记忆的神经心理学治疗提供了新的视角。
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引用次数: 0
Alzheimer's disease—Biomarkers, clinical evaluation or both? 阿尔茨海默病--生物标志物、临床评估还是两者兼而有之?
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-11-14 DOI: 10.1111/jnp.12401
Joel Simrén, Nicholas J. Ashton, Marc Suárez-Calvet, Henrik Zetterberg
<p>Recent developments in fluid and imaging biomarkers that reflect the key pathological hallmarks of Alzheimer's disease (AD)—deposits of extracellular amyloid-β (Aβ) and intracellular tau proteins—have transformed the perception of the disease in living individuals from a clinical syndrome to a biological continuum that begins prior to the onset of symptoms (Scheltens et al., <span>2021</span>). Over the past two decades, biomarker research has revealed that Aβ deposition and abnormal tau metabolism begin years before symptoms appear, following a predictable sequence of biological changes (Bateman et al., <span>2012</span>; Villemagne et al., <span>2013</span>). This suggests a prolonged preclinical phase of the disease. Biomarkers, which have greatly expanded our understanding of disease progression, are now routinely applied in clinical settings. These include Food and Drug Administration (FDA)-approved positron emission tomography (PET) imaging agents of Aβ plaques and tau aggregates, cerebrospinal fluid (CSF) measures of Aβ and phosphorylated tau (p-tau), and soon, plasma measures of tau forms phosphorylated at amino acid 217 (p-tau217).</p><p>As AD neuropathology is the defining hallmark of the disease (Hyman et al., <span>2012</span>), as well as being the target of emerging treatments, recently approved in some countries (Cummings et al., <span>2023</span>), it is reasoned that biomarkers that directly reflect these changes should be the defining features of the disease. This view was formally articulated in the recent publication of novel Alzheimer's Association diagnostic and staging criteria for AD, which suggest that the disease can be diagnosed when a so-called ‘Core 1’ biomarker of Aβ proteinopathy or phosphorylated and secreted tau is abnormal, resulting in a purely biological definition of the disease (Jack et al., <span>2024</span>). In prior years, studies have shown that PET detect Aβ (Clark et al., <span>2012</span>) and tau (Fleisher et al., <span>2020</span>) neuropathology with high (~90%) accuracy. CSF tests of Aβ42/40 and Aβ42/p-tau (Janelidze et al., <span>2017</span>) have been validated against amyloid PET with similar accuracy, and subsequently also neuropathology (Mattsson-Carlgren et al., <span>2022</span>). Over the past 5 years, an expanding body of research indicates that plasma p-tau217 can detect Aβ pathology with high accuracy (Ashton et al., <span>2023</span>, <span>2024</span>; Schindler et al., <span>2024</span>), which will improve the access to biological AD diagnoses in clinical settings beyond what health care systems are currently scaled to accommodate.</p><p>The recently published diagnostic and staging criteria (Jack et al., <span>2024</span>) are a development of the criteria published by the National Institute of Aging and Alzheimer's Association (NIA-AA) in 2018, which aimed to establish a common language for further research in the biological evolution of AD and its relation to resulting symptom
反映阿尔茨海默病(AD)关键病理特征的流体和成像生物标志物(细胞外淀粉样蛋白-β (a β)和细胞内tau蛋白沉积)的最新进展,已将活个体对该疾病的认知从临床综合征转变为在症状发作之前开始的生物连续体(Scheltens等人,2021)。在过去的二十年中,生物标志物研究表明,a β沉积和异常tau代谢在症状出现前几年就开始了,遵循可预测的生物学变化序列(Bateman等,2012;Villemagne et al., 2013)。这表明该疾病的临床前阶段较长。生物标志物,极大地扩展了我们对疾病进展的理解,现在被常规地应用于临床环境。这些包括美国食品和药物管理局(FDA)批准的Aβ斑块和tau聚集体的正电子发射断层扫描(PET)显像剂,脑脊液(CSF)测量Aβ和磷酸化tau (p-tau),以及很快,血浆测量氨基酸217磷酸化的tau形式(p-tau217)。由于阿尔茨海默病的神经病理学是该疾病的决定性标志(Hyman et al., 2012),也是一些国家最近批准的新兴治疗方法的目标(Cummings et al., 2023),因此有理由认为直接反映这些变化的生物标志物应该是该疾病的决定性特征。这一观点在最近发表的阿尔茨海默病协会的新AD诊断和分期标准中得到了正式阐述,该标准表明,当a β蛋白病或磷酸化和分泌的tau蛋白的所谓“Core 1”生物标志物异常时,可以诊断出该疾病,从而导致该疾病的纯生物学定义(Jack等人,2024)。前几年的研究表明,PET检测Aβ (Clark et al., 2012)和tau (Fleisher et al., 2020)神经病理学具有很高(~90%)的准确性。a - β42/40和a - β42/p-tau的脑脊液测试(Janelidze等人,2017)已经在淀粉样PET上得到了类似的准确性验证,随后也得到了神经病理学的验证(Mattsson-Carlgren等人,2022)。在过去的5年中,越来越多的研究表明血浆p-tau217可以高精度地检测Aβ病理(Ashton et al., 2023,2024;Schindler等人,2024),这将改善临床环境中生物AD诊断的可及性,超出目前卫生保健系统的规模。最近发表的诊断和分期标准(Jack et al., 2024)是对美国国家衰老与阿尔茨海默病协会(NIA-AA)于2018年发布的标准的发展,旨在为进一步研究阿尔茨海默病的生物进化及其与由此产生的症状学的关系建立一种共同语言(Jack et al., 2018)。与该文件一样,在最近的标准中,临床分期方案作为疾病定义的补充(Jack et al., 2024)。最近的标准还增加了一个生物学分期方案,表明tau PET(“Core 2生物标志物”;包括有前途的尽管是探索性的tau聚集体流体生物标志物;Horie等人,2023)与Aβ PET结合使用,用于对疾病进行生物学分期,因为tau聚集物与症状有更密切的关系(Ossenkoppele等人,2018)。在这些标准之前的另一个关键发展是,最近FDA全面批准了lecanemab (van Dyck等人,2023年)和donanemab (Sims等人,2023年),现在世界其他地区的其他几个监管机构也批准了这两种药物。这些试验依赖于谨慎使用基于生物标志物的纳入,确保个体具有治疗所针对的病理(即Aβ病理)。在一些早期失败的试验中,情况并非如此,在这些试验中,阿尔茨海默氏症是临床定义的,这意味着诊断与生物标志物状态无关。在其中一项试验中,相当大比例的研究参与者被发现为a β阴性(Salloway et al., 2014),因此可能被误诊。换句话说,为了成功地治疗疾病的生物学,疾病的定义必须基于其潜在的生物学。此外,血浆p-tau217和胶质纤维酸性蛋白(GFAP;一种反映胶质细胞激活的星形胶质蛋白)在临床试验中显示出对抗a β药物的反应,这表明它们可以用作靶标参与生物标志物(Pontecorvo等人,2022;Sims et al., 2023)。进一步支持这一点的是,脑脊液和成像生物标志物以及分子神经病理学的最新进展,使该领域能够获得更多关于神经心理学测量、症状学和生物标志物/神经病理学发现之间关系的知识。这些研究发现,通常与AD病理相关的经典遗忘综合征可能是由于边缘显性年龄相关性TDP-43脑病(LATE)所致(Nelson等)。 (2019)在很大比例的病例中,特别是在最年长的老年患者中。相反,原发性进行性失语(Bergeron等人,2018)、行为/执行障碍综合征(Ossenkoppele等人,2015)、皮质基底综合征(Lee等人,2011)和后皮质萎缩(Alladi等人,2007)等综合征也可能与AD的潜在病理有关。众所周知,个体可能表现为多种病理(Robinson et al., 2018),对病理有不同的认知恢复力(Stern, 2012),有疾病进展的遗传修饰因子(Van Cauwenberghe et al., 2016),或者具有与阿尔茨海默氏症不典型相关的症状(例如认知症状的波动,在路易体痴呆中很常见),这可以反映在临床阶段和生物学阶段的分离(Jack et al., 2024)。然而,再一次,如果阳性生物标志物与临床表现不一致,这并不意味着疾病不存在。另一方面,需要仔细的临床判断来确定哪种病理最可能解释症状。阿尔茨海默病生物学定义的批评者表示,这些新标准将能够检测出患有阿尔茨海默病的无症状个体,尽管尚不确定他们最终是否会因该疾病而出现症状。然而,阿尔茨海默病协会的标准强调,目前AD可以但不应该在没有认知症状(临床阶段1)的个体中被诊断出来(Jack et al., 2024),同样的推理也适用于大多数有主观认知症状的个体(即没有客观损害;临床阶段2),因为没有批准的治疗方法用于这一群体,并且这些病例的疾病患病率较低,因此阳性预测值较低,导致更高的假阳性结果和不必要的调查和焦虑(Hansson &amp;杰克,2024)。如果正在进行的临床前AD试验取得成功,这种情况可能会改变(Rafii等人,2023),导致与心血管疾病(例如治疗高血压或降脂)或2型糖尿病(治疗无症状高血糖)相当的情况。在缺乏此类治疗方法的情况下,我们认为目前应仅在有症状的个体中使用生物标志物诊断AD,同时进行仔细的临床评估,因为这种疾病的检测前概率较高,并且后果可行(例如,有症状的治疗和在一些国家的疾病改善治疗)。正在制定关于如何以及何时诊断AD的具体工作流程和基于场景的指南。未来的研究非常重要,以增加对AD是某一患者症状的原因的信心,包括验证反映tau聚集体的液体生物标志物(即提供与tau PET相似的信息)。脑脊液测量微管结合区(MTBR) tau已显示出可喜的结果(Horie等人,2023;Salvado等,2024)和脑脊液或血浆中氨基酸205处的p-tau (p-tau205) (Gobom等,2022;Lantero-Rodriguez et al., 2024;Montoliu-Gaya, Alosco等,2023;Montoliu-Gaya, Benedet等,2023),它比反映
{"title":"Alzheimer's disease—Biomarkers, clinical evaluation or both?","authors":"Joel Simrén,&nbsp;Nicholas J. Ashton,&nbsp;Marc Suárez-Calvet,&nbsp;Henrik Zetterberg","doi":"10.1111/jnp.12401","DOIUrl":"10.1111/jnp.12401","url":null,"abstract":"&lt;p&gt;Recent developments in fluid and imaging biomarkers that reflect the key pathological hallmarks of Alzheimer's disease (AD)—deposits of extracellular amyloid-β (Aβ) and intracellular tau proteins—have transformed the perception of the disease in living individuals from a clinical syndrome to a biological continuum that begins prior to the onset of symptoms (Scheltens et al., &lt;span&gt;2021&lt;/span&gt;). Over the past two decades, biomarker research has revealed that Aβ deposition and abnormal tau metabolism begin years before symptoms appear, following a predictable sequence of biological changes (Bateman et al., &lt;span&gt;2012&lt;/span&gt;; Villemagne et al., &lt;span&gt;2013&lt;/span&gt;). This suggests a prolonged preclinical phase of the disease. Biomarkers, which have greatly expanded our understanding of disease progression, are now routinely applied in clinical settings. These include Food and Drug Administration (FDA)-approved positron emission tomography (PET) imaging agents of Aβ plaques and tau aggregates, cerebrospinal fluid (CSF) measures of Aβ and phosphorylated tau (p-tau), and soon, plasma measures of tau forms phosphorylated at amino acid 217 (p-tau217).&lt;/p&gt;&lt;p&gt;As AD neuropathology is the defining hallmark of the disease (Hyman et al., &lt;span&gt;2012&lt;/span&gt;), as well as being the target of emerging treatments, recently approved in some countries (Cummings et al., &lt;span&gt;2023&lt;/span&gt;), it is reasoned that biomarkers that directly reflect these changes should be the defining features of the disease. This view was formally articulated in the recent publication of novel Alzheimer's Association diagnostic and staging criteria for AD, which suggest that the disease can be diagnosed when a so-called ‘Core 1’ biomarker of Aβ proteinopathy or phosphorylated and secreted tau is abnormal, resulting in a purely biological definition of the disease (Jack et al., &lt;span&gt;2024&lt;/span&gt;). In prior years, studies have shown that PET detect Aβ (Clark et al., &lt;span&gt;2012&lt;/span&gt;) and tau (Fleisher et al., &lt;span&gt;2020&lt;/span&gt;) neuropathology with high (~90%) accuracy. CSF tests of Aβ42/40 and Aβ42/p-tau (Janelidze et al., &lt;span&gt;2017&lt;/span&gt;) have been validated against amyloid PET with similar accuracy, and subsequently also neuropathology (Mattsson-Carlgren et al., &lt;span&gt;2022&lt;/span&gt;). Over the past 5 years, an expanding body of research indicates that plasma p-tau217 can detect Aβ pathology with high accuracy (Ashton et al., &lt;span&gt;2023&lt;/span&gt;, &lt;span&gt;2024&lt;/span&gt;; Schindler et al., &lt;span&gt;2024&lt;/span&gt;), which will improve the access to biological AD diagnoses in clinical settings beyond what health care systems are currently scaled to accommodate.&lt;/p&gt;&lt;p&gt;The recently published diagnostic and staging criteria (Jack et al., &lt;span&gt;2024&lt;/span&gt;) are a development of the criteria published by the National Institute of Aging and Alzheimer's Association (NIA-AA) in 2018, which aimed to establish a common language for further research in the biological evolution of AD and its relation to resulting symptom","PeriodicalId":197,"journal":{"name":"Journal of Neuropsychology","volume":"19 2","pages":"165-171"},"PeriodicalIF":1.8,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jnp.12401","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142613232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Resolving the problem of surface dyslexia in Italian through inflection of irregular verbs 通过不规则动词的变位解决意大利语表层阅读障碍问题。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-11-14 DOI: 10.1111/jnp.12400
Daniele Licciardo, Valeria Isella, Elisa Canu, Marta Forestiero, Veronica Castelnovo, Stefania Valsecchi, Federica Agosta, Massimo Filippi, Ildebrando Appollonio, Peter J Nestor

Surface dyslexia and dysgraphia are considered diagnostic features of semantic variant primary progressive aphasia (svPPA) and are useful signs in English, a language whose attributes afford numerous opportunities to observe these phenomena. This, however, is not the case in many languages, including Italian, that have high transparency between orthography and phonology, making surface reading and spelling errors scarce. This creates a problem in applying the diagnostic recommendations for svPPA in such languages. Surface dyslexia and dysgraphia are examples of ‘regularization’ errors in which semantic knowledge loss leads to a failure to recognize exceptions that do not follow standard rules of pronunciation. Another form of regularization involves the incorrect inflection of irregular verbs using the rules that govern regular verbs. Unlike irregularly pronounced words, Italian, as with many languages, has numerous irregular verbs. The Italian Verb Inflection Test (IVIT) was developed to test the hypothesis that svPPA would regularize irregular verbs when inflecting them into two Italian past tenses. Results confirmed that people with svPPA made a significantly greater proportion of regularization errors compared to people with typical Alzheimer's disease or logopenic variant PPA. Without recourse to the other diagnostic features of PPA subgroups, the IVIT on its own could separate svPPA from these other two groups with 70% sensitivity and ~ 80% specificity. Regularization of irregular verb inflection offers a solution to the problem of applying the surface dyslexia/dysgraphia criterion for svPPA diagnosis in Italian.

表面阅读障碍和书写障碍被认为是语义变异型原发性进行性失语症(svPPA)的诊断特征,在英语中是有用的标志,因为英语的特性为观察这些现象提供了大量机会。然而,包括意大利语在内的许多语言却并非如此,因为意大利语的正字法和语音学之间的透明度很高,表面阅读和拼写错误很少。这就给在这类语言中应用 svPPA 诊断建议带来了问题。表面阅读障碍和书写障碍是 "正则化 "错误的例子,其中语义知识的缺失导致无法识别不遵循标准发音规则的例外情况。另一种 "规则化 "错误是使用规则动词的规则对不规则动词进行错误的变形。与不规则发音的单词不同,意大利语和许多语言一样,有许多不规则动词。我们开发了意大利语动词变位测试(IVIT),以检验 svPPA 在将不规则动词变位为两种意大利语过去式时,是否会将其规则化的假设。结果证实,与典型阿尔茨海默病或对数变异型 PPA 患者相比,svPPA 患者的规则化错误比例明显更高。在不考虑 PPA 亚群的其他诊断特征的情况下,IVIT 本身就能将 svPPA 与其他两类患者区分开来,灵敏度为 70%,特异度约为 80%。不规则动词变音的正规化为应用表面阅读障碍/书写障碍标准进行意大利语 svPPA 诊断提供了一个解决方案。
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引用次数: 0
Reducing confusion surrounding expert conceptions of Alzheimer's and dementia: A practical analysis 减少专家对阿尔茨海默氏症和痴呆症概念的混淆:实用分析。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-10-25 DOI: 10.1111/jnp.12398
Timothy Daly, Ignacio Mastroleo

Biological, clinicobiological and clinical conceptions of Alzheimer's disease and related dementias are being promoted simultaneously to different practical ends. The co-existence of contemporary conceptions and the ‘scary label’ associated with older diagnostic criteria create the possibility of misunderstanding and harm. In this comment, we argue in favour of socio-ethical interventions targeted to health workers and the general public so as to lower the uncertainties introduced by contemporary diagnostic criteria and to articulate how they relate to established criteria.

为了不同的实际目的,阿尔茨海默病和相关痴呆症的生物学、临床生物学和临床概念正在同时得到推广。现代概念和与旧诊断标准相关的 "可怕标签 "并存,有可能造成误解和伤害。在这篇评论中,我们主张针对医务工作者和公众采取社会伦理干预措施,以降低当代诊断标准带来的不确定性,并阐明这些标准与既定标准的关系。
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引用次数: 0
Translation and validation of the abbreviated Prefrontal Symptoms Inventory (PSI-20): A tool for assessing prefrontal symptoms in English-speaking populations 前额叶症状调查表(PSI-20)缩写本的翻译和验证:用于评估英语国家人群前额叶症状的工具。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-10-10 DOI: 10.1111/jnp.12397
María A. Sosa, Eduardo J. Pedrero-Pérez, José M. Ruiz-Sánchez de León

This study introduces the translation and validation of the Prefrontal Symptoms Inventory (PSI) into English, aiming to provide an ecologically valid tool for assessing prefrontal symptoms in English-speaking populations in the United States. The prefrontal cortex (PFC) plays a crucial role in executive functions and other higher-order cognitive processes, with dysfunctions in this area associated with various cognitive, emotional and behavioural changes. Despite the existence of established tools like the Dysexecutive Questionnaire (DEX), the PSI addresses limitations found in the literature, presenting a novel ecologically valid tool for assessing prefrontal symptoms. The current study, involving 226 English-speaking participants, lays a foundational step for validating the PSI for use in a new population. Semi-confirmatory factorial analysis revealed a unidimensional structure, mirroring the Spanish version with robust fit indicators. Additionally, in assessing convergent validity, the abbreviated version (PSI-20) exhibited high correlations with DEX scores and moderate correlations with Psychological Stress Scale and General Health Questionnaire-12 scores. These findings align with previous reports, supporting the PSI-20's measurement of similar constructs related to prefrontal cortex activity and mental health components. The results of this study overall highlight the PSI's potential contribution to advancing prefrontal symptom evaluation in clinical and non-clinical settings.

本研究介绍了前额叶症状量表(PSI)的英语翻译和验证,旨在为美国的英语人群提供一种生态学上有效的前额叶症状评估工具。前额叶皮层(PFC)在执行功能和其他高阶认知过程中起着至关重要的作用,该区域的功能障碍与各种认知、情绪和行为变化有关。尽管有执行障碍问卷(DEX)等成熟的工具,但 PSI 解决了文献中发现的局限性,为评估前额叶症状提供了一种新的生态学上有效的工具。本研究涉及 226 名英语参与者,为验证 PSI 在新人群中的使用奠定了基础。半确认性因子分析显示了一个单维度结构,与西班牙语版本一致,并具有稳健的拟合指标。此外,在评估收敛效度时,缩略版(PSI-20)与 DEX 分数呈高度相关,与心理压力量表和一般健康问卷-12 分数呈中度相关。这些结果与之前的报告一致,支持 PSI-20 测量与前额叶皮层活动和心理健康成分相关的类似构念。这项研究的结果从总体上强调了 PSI 在临床和非临床环境中推进前额叶症状评估的潜在贡献。
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引用次数: 0
Cognitive assessment: More important than ever 认知评估:比以往任何时候都更重要。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-10-02 DOI: 10.1111/jnp.12396
Stefano F. Cappa
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引用次数: 0
From neuropsychology to embodied neuroscience: Introduction to the special issue on body representation and body transformations 从神经心理学到具身神经科学:身体表征与身体转换特刊导言。
IF 1.8 4区 心理学 Q2 PSYCHOLOGY Pub Date : 2024-09-23 DOI: 10.1111/jnp.12395
Paul M. Jenkinson, Valentina Moro
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引用次数: 0
期刊
Journal of Neuropsychology
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