Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2009 Dec;66(12):1545-51.
doi: 10.1001/archneurol.2009.288.

Quantitative template for subtyping primary progressive aphasia

Affiliations
Comparative Study

Quantitative template for subtyping primary progressive aphasia

Marsel Mesulam et al. Arch Neurol. 2009 Dec.

Abstract

Background: The syndrome of primary progressive aphasia (PPA) is diagnosed when a gradual failure of word usage or comprehension emerges as the principal feature of a neurodegenerative disease.

Objective: To provide a quantitative algorithm for classifying PPA into agrammatic (PPA-G), semantic (PPA-S), and logopenic (PPA-L) variants, each of which is known to have a different probability of association with Alzheimer disease vs frontotemporal lobar degeneration.

Design: Prospective study.

Setting: University medical center.

Patients: Sixteen consecutively enrolled patients with PPA who underwent neuropsychological testing and magnetic resonance imaging recruited nationally in the United States as part of a longitudinal study.

Results: A 2-dimensional template that reflects performance on tests of syntax (Northwestern Anagram Test) and lexical semantics (Peabody Picture Vocabulary Test-Fourth Edition) classified all 16 patients in concordance with a clinical diagnosis that had been made before the administration of quantitative tests. All 3 PPA subtypes had distinctly asymmetrical atrophy of the left perisylvian language network. Each subtype also had distinctive peak atrophy sites: PPA-G in the inferior frontal gyrus (Broca area), PPA-S in the anterior temporal lobe, and PPA-L in Brodmann area 37.

Conclusions: Once an accurate root diagnosis of PPA is made, subtyping can be quantitatively guided using a 2-dimensional template based on orthogonal tasks of grammatical competence and word comprehension. Although the choice of tasks and the precise cutoff levels may need to be adjusted to fit linguistic and educational backgrounds, these 16 patients demonstrate the feasibility of using a simple algorithm for clinicoanatomical classification in PPA. Prospective studies will show whether this subtyping can improve clinical prediction of the underlying neuropathologic condition.

PubMed Disclaimer

Figures

Figures 1–3
Figures 1–3
Performance of the 16 patients in the 5 language tests. The height of the bars represents performance as a percentage, where 100% reflects a perfect score for that task. PPVT- Peabody Picture Vocabulary Test. NAT- Northwestern Anagram Test. BNT- Boston Naming Test. F- Fluency. R- Repetition.
Figures 1–3
Figures 1–3
Performance of the 16 patients in the 5 language tests. The height of the bars represents performance as a percentage, where 100% reflects a perfect score for that task. PPVT- Peabody Picture Vocabulary Test. NAT- Northwestern Anagram Test. BNT- Boston Naming Test. F- Fluency. R- Repetition.
Figures 1–3
Figures 1–3
Performance of the 16 patients in the 5 language tests. The height of the bars represents performance as a percentage, where 100% reflects a perfect score for that task. PPVT- Peabody Picture Vocabulary Test. NAT- Northwestern Anagram Test. BNT- Boston Naming Test. F- Fluency. R- Repetition.
Figure 4
Figure 4
A 2-dimensional template based on single word comprehension and grammatical structure of sentences. The 60% performance level divides the template into four quadrants, one for each subtype. In this group of cases, the PPVT was used to assess word comprehension, and the NAT to assess grammar. The values in the x and y axes reflect the performance percentages shown in Figures 1–3.
Figure 5
Figure 5
Distribution of cortical thinning. Red shading indicates a significance level of p<0.01, and the yellow p<0.001. Abbreviations: DF, Dorsolateral prefrontal cortex; IFG, Inferior frontal gyrus; ITG, Inferior temporal gyrus; MTG, Middle temporal gyrus; PM, Premotor cortex; STG, Superior temporal gyrus; TPJ, Temporoparietal junction; 37, Area 37 of Broadmann;

Similar articles

Cited by

References

    1. Rabinovici GD, Jagust WJ, Furst AJ, et al. Aβ amyloid and glucose metabolism in three variants of primary progressive aphasia. Annals of Neurology. 2008;64:388–401. - PMC - PubMed
    1. Mesulam M, Wicklund A, Johnson N, et al. Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia. Annals of Neurology. 2008;63:709–719. - PMC - PubMed
    1. Knibb JA, Xuereb JH, Patterson K, Hodges JR. Clinical and pathological characterization of progressive aphasia. Annals of Neurology. 2006;59:156–165. - PubMed
    1. Mesulam M–M, Weintraub S. Primary progressive aphasia and kindred disorders. In: Duyckaerts C, Litvan I, editors. Handbook of Clinical Neurology. New York: Elsevier; 2008. pp. 573–587. - PubMed
    1. Mesulam M-M. Primary progressive aphasia: A language-based dementia. New England Journal of Medicine. 2003;348:1535–1542. - PubMed

Publication types