Ian Storey, Matthew A. Lambon Ralph, Eleonora Catricalà, Stefano F. Cappa, A. Halai, Nikil Patel, Peter Garrard, James B. Rowe, Karalyn Patterson, Ruth Ingram, Katie A. Peterson, Patel, Nikil [0000-0003-2888-9668], Storey, Ian [0000-0002-0952-0673], Halai, Ajay [0000-0003-1725-7948], Patterson, Karalyn E [0000-0003-1927-7424], Lambon Ralph, Matthew A [0000-0001-5907-2488], Garrard, Peter [0000-0001-8268-9718], Apollo - University of Cambridge Repository, Patterson, Karalyn [0000-0003-1927-7424], Lambon Ralph, Matthew [0000-0001-5907-2488], and Rowe, James [0000-0001-7216-8679]
Background: There are few available methods for qualitatively evaluating patients with primary progressive aphasia (PPA). Commonly adopted approaches are time-consuming, of limited accuracy, or designed to assess different patient populations. This paper introduces a new clinical test - the Mini Linguistic State Examination (MLSE) - which was designed uniquely to enable a clinician to assess and subclassify both classical and mixed presentations of PPA. The adoption of a novel assessment method (error classification) greatly amplifies the clinical information that can be derived from a set of standard linguistic tasks and allows a five-dimensional profile to be defined. Methods: Fifty-four patients and 30 matched controls were recruited. Five domains of language competence (motor speech, phonology, semantics, syntax, and working memory) were assessed using a sequence of 11 distinct linguistic assays. A random forest classification was used to assess the diagnostic accuracy for predicting PPA subtypes and create a decision tree as a guide to clinical classification. Findings: The random forest prediction model was 96% accurate overall (92% for logopenic variant, 93% for semantic variant, and 98% for non-fluent variant PPA). The derived decision tree produced a correct classification of 91% of participants whose data were not included in the training set. Interpretation: The MLSE is a new cognitive test incorporating a novel and powerful, yet straightforward, approach to scoring. Rigorous assessment of its diagnostic accuracy confirmed excellent matching of PPA syndromes to clinical gold standard diagnoses. Adoption of the MLSE by clinicians will have a decisive impact on the consistency and uniformity with which patients can be described clinically. It will also facilitate screening for cohort-based research, including future therapeutic trials, and is suitable for describing, quantifying and monitoring language deficits in other brain disorders. Funding Information: The research was funded by a Medical Research Council Research Grant award (Ref MR/N025881/1) to PG, MLR JR, KP and SC. Additional support was provided through grants from the MRC (UAG051 and G101400), Wellcome Trust (103838) and ERC (GAP: 670428), and through funding awarded to the National Institute for Health Research Cambridge Biomedical Research Centre and to the MRC CBU (MC_UU_00005/18). Declaration of Interests: JBR reports consultancy unrelated to the work with Biogen, UCB, Asceneuron and Althira; and receipt of research grants, unrelated to this work, from Janssen, AZ-Medimmune, and Lilly. The other authors declare no conflicts of interest. Ethics Approval Statement: Written informed consent was provided by all participants. The study protocol was reviewed and approved by the London (Chelsea) Research Ethics Committee [Ref. 16/LO/1735].