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Dive into the research topics where Michèle Houde is active.

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Featured researches published by Michèle Houde.


American Journal of Alzheimers Disease and Other Dementias | 2010

The Value of PET in Mild Cognitive Impairment, Typical and Atypical/Unclear Dementias: A Retrospective Memory Clinic Study

Robert Laforce; James P. Buteau; Nancy Paquet; Louis Verret; Michèle Houde; Rémi W. Bouchard

This retrospective study examined the role of [18F]fluorodeoxyglucose positron emission tomography (FDG-PET) in the diagnosis of atypical/unclear dementias in a memory clinic setting. A total of 94 patients with a diagnosis of mild cognitive impairment (MCI) or dementia, who had a PET study within 2 months of their diagnosis, were reevaluated at 5 and 18 months. Results showed that PET was associated with a change in diagnosis in 29% of patients and a 64% increase in the use of cholinesterase inhibitors (ChEIs). PET significantly lowered the number of atypical/unclear diagnoses from 39.4% to 16% and nearly 30% of these were found to have a typical Alzheimer’s disease (AD) pattern of hypometabolism. In conclusion, the addition of PET to the investigation of atypical/unclear cases of dementia helped generating a more accurate diagnosis and initiating earlier treatment. PET was of limited contribution to typical AD and frontotemporal dementia (FTD) cases. This study provides guiding evidence about the true value of PET imaging in the day-to-day challenge of dementia diagnosis.


Neurocase | 2015

Improving verb anomia in the semantic variant of primary progressive aphasia: the effectiveness of a semantic-phonological cueing treatment

Joël Macoir; M. Leroy; Sonia Routhier; Noémie Auclair-Ouellet; Michèle Houde; Robert Laforce

The semantic variant of primary progressive aphasia (svPPA) is known to affect the comprehension and production of all content words, including verbs. However, studies of the treatment of anomia in this disorder focused on relearning object names only. This study reports treatment of verb anomia in an individual with svPPA. The semantic-phonological cueing therapy resulted in significant improvement in naming abilities, for treated verbs only. This case study demonstrates that improvement in verb-naming abilities may be possible in svPPA. The almost complete maintenance of the treatment’s effects in the patient 4 weeks after the end of the therapy also suggests improvements may be durable, at least in the short term, for some individuals with svPPA.


Journal of Alzheimer's Disease | 2015

Clinical Impact of a Second FDG-PET in Atypical/Unclear Dementia Syndromes.

David Bergeron; Jean-Mathieu Beauregard; Jean Guimond; Marie-Pierre Fortin; Michèle Houde; Stéphane Poulin; Louis Verret; Rémi W. Bouchard; Robert Laforce

Diagnosis of atypical/unclear dementia is often difficult and this delays treatment initiation. Several authors have shown that beyond standard dementia workup, 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) reduces the number of unclear diagnoses, leads to earlier treatment, and has a beneficial impact on families. However, it is not uncommon that the FDG-PET findings are equivocal in this setting. For those cases, a repeat FDG-PET may clarify the diagnosis and prevent treatment delay. We retrospectively assessed the clinical impact of a repeat FDG-PET in 59 patients with atypical/unclear dementia syndromes and inconclusive initial FDG-PET. Changes in primary diagnosis, diagnostic confidence, and management following the second FDG-PET were examined. Conducting a second FDG-PET reduced the number of unclear diagnoses from 80% to 34% , led to diagnostic change in 24% of cases, and treatment modification in 22% of patients. Overall, the clinical impact was higher when initial diagnostic confidence was low and the second FDG-PET repeated ≥12 months after the first one. In tertiary care memory clinic settings, when diagnostic incertitude persists despite extensive evaluation and an equivocal FDG-PET, repeating the FDG-PET 12 months later can greatly clarify the diagnosis and improve management.


Neurocase | 2016

Production of morphologically derived words in the semantic variant of primary progressive aphasia: preserved decomposition and composition but impaired validation

Noémie Auclair-Ouellet; Marion Fossard; Michèle Houde; Robert Laforce; Joël Macoir

Abstract Although there is growing interest in inflectional morphology in semantic variant primary progressive aphasia (svPPA), derivational morphology has rarely been studied in this population. This study reports the performance of N.G., a 72-year-old-woman with svPPA in a verb production task designed to entail morphological processing (composition, decomposition) and self-appraisal of her productions. N.G. demonstrated an over-reliance on morphological processing and failures in her appraisal of root/affix combinations that resulted in the production of morphological paraphasias and neologisms. Her performance in lexical decision of verbs and pseudo-verbs points to the involvement of semantic impairment in these difficulties.


Archives of Clinical Neuropsychology | 2018

Validation of the Dépistage Cognitif de Québec: A New Cognitive Screening Tool for Atypical Dementias

Robert Laforce; Leila Sellami; David Bergeron; Louis Verret; Marie-Pierre Fortin; Michèle Houde; Martin Roy; Stéphane Poulin; Joël Macoir; Carol Hudon; Rémi W. Bouchard

Objective This study aimed to validate and provide normative data for the Dépistage Cognitif de Québec (DCQ; www.dcqtest.org), a new cognitive screening tool for atypical dementias. Method The DCQ was developed by expert behavioral neurologists and clinical neuropsychologists based on updated criteria for Alzheimers disease, primary progressive aphasia, and behavioral variant frontotemporal dementia. It targets five relevant domains: Memory, Visuospatial, Executive, Language, and Behavior. Validation was performed in a population-based sample of 410 healthy French-speaking Canadians aged between 50 and 89 years old. Normative data were derived from a subsample of 285 participants. Results Mean DCQ total score (out of 100) was 89.17 (SD = 7.36). Pearsons correlation coefficient showed a strong and significant correlation (r = .71, p < .001) with the Montreal Cognitive Assessment. Internal consistency for the cognitive domains assessed by Cronbachs alpha was satisfactory (.74). Test-retest reliability was adequate (Pearsons coefficient = . 70, p < .001) and interrater reliability, excellent (intraclass correlation = .99, p < .001). Normative data shown in percentiles were stratified by age and education. Conclusions This study suggests that the DCQ is a valid and reliable cognitive screening test. Application of the DCQ on populations with atypical dementias is underway to derive sensitivity and specificity values for various dementias.


Alzheimers & Dementia | 2017

DÉ́PISTAGE COGNITIF DE QUÉBÉC (DCQ): VALIDATION AND NORMATIVE DATA FOR A NOVEL COGNITIVE SCREENING TOOL FOR ATYPICAL DEMENTIAS

David Bergeron; Leila Sellami; Louis Verret; Marie-Pierre Fortin; Michèle Houde; Carol Hudon; Stéphane Poulin; Martin Roy; Rémi W. Bouchard; Robert Laforce

Mental State Examination, the original version of the MoCA, and the quality of life scale CASP-19. A multiple regression analysis was performed to verify the influence of age and education and the predictive capacity of the original version of the test on its alternative version. Results: Cronbach’s alpha coefficient was .76. Elimination of any of the items of the 2 version of MoCA never reduces the reliability to below .73. Convergent validity was .65 (p<.001), and divergent validity was .03 (p1⁄40.79). Correlation between the 1 and the 2 version of MoCA was significant and high (r1⁄40.86). There was a negative effect of age (b 1⁄4–0.141, p < 0.01) and a positive effect of education (b 1⁄4–0.549, p < 0.001), but these two effects did not remained significant when the total score of the original form of MoCA was included in the regression model (b1⁄4–0.691, p < 0.001) (Figure1). Conclusions: Our preliminary results showed good psychometrical properties for the 2nd alternative form of the Spanish version and strong relations between forms. Further analyses are required in order to guarantee the use of the alternate Spanish version of the MoCA test in clinical follow-ups and longitudinal studies.


Alzheimers & Dementia | 2015

Clinical utility of amyloid PET in the differential diagnosis of atypical dementias and its impact on caregivers

Robert Laforce; Mohamed Reda Bensaïdane; Rémi W. Bouchard; Marie-Pierre Fortin; Michèle Houde; Pedro Rosa-Neto; Stéphane Poulin; Louis Verret; Jean-Paul Soucy; Jean-Mathieu Beauregard

not available. PL-04-02 BIOCHEMICALLY BASED QUANTITATIVE NEUROPATHOLOGY IN CLINICAL


Alzheimers & Dementia | 2015

Clinical utility of amyloid imaging in the differential diagnosis of atypical/unclear dementias and its impact on caregivers

Mohamed Reda Bensaïdane; Rémi W. Bouchard; Marie-Pierre Fortin; Michèle Houde; Pedro Rosa Neto; Stéphane Poulin; Louis Verret; Jean-Paul Soucy; Jean-Mathieu Beauregard; Robert Laforce

Recent studies have supported a role for amyloid positron emission tomography (PET) imaging in distinguishing Alzheimer’s disease (AD) pathology from other pathological protein accumulations leading to dementia. We investigated the clinical utility of amyloid PET in the differential diagnosis of atypical dementia cases and its impact on caregivers. Using the amyloid tracer 18F-NAV4694, we prospectively scanned 28 patients (mean age 59.3 y, s.d. 5.8; mean MMSE 21.4, s.d. 6.0) with an atypical dementia syndrome. Following a comprehensive diagnostic workup (i.e., history taking, neurological examination, blood tests, neuropsychological evaluation, MRI, and FDG-PET), no certain diagnosis could be arrived at. Amyloid PET was then conducted and classified as positive or negative. Attending physicians were asked to evaluate whether this result led to a change in diagnosis or altered management. They also reported their degree of confidence in the diagnosis. Caregivers were met after disclosure of amyloid PET results and completed a questionnaire/interview to assess the impact of the scan. Our cohort was evenly divided between positive (14/28) and negative (14/28) 18F-NAV4694 cases. Amyloid PET resulted in a diagnostic change in 9/28 cases (32.1%: 17.8% changed from AD to non-AD, 14.3% from non-AD to AD). There was a 44% increase in diagnostic confidence. Altered management occurred in 71.4% (20/28) of cases. Knowledge of amyloid status improved caregivers’ outcomes in all domains (anxiety, depression, disease perception, future anticipation, and quality of life). This study suggests a useful additive role for amyloid PET in atypical cases with an unclear diagnosis beyond the extensive workup of a tertiary memory clinic. Amyloid PET increased diagnostic confidence and led to clinically significant alterations in management. The information gained from that test was well received by caregivers and encouraged spending quality time with their loved ones.


Journal of Alzheimer's Disease | 2016

Clinical Utility of Amyloid PET Imaging in the Differential Diagnosis of Atypical Dementias and Its Impact on Caregivers.

Mohamed Reda Bensaïdane; Jean-Mathieu Beauregard; Stéphane Poulin; François-Alexandre Buteau; Jean Guimond; David Bergeron; Louis Verret; Marie-Pierre Fortin; Michèle Houde; Rémi W. Bouchard; Jean-Paul Soucy; Robert Laforce


Alzheimers & Dementia | 2013

Months backward test as a reliable predictor of cognitive decline in mild Alzheimer's disease

Marissa Tardif; Martin Roy; Bouchard Remi; Robert Laforce; Louis Verret; Marie-Pierre Fortin; Michèle Houde; Stéphane Poulin

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Jean-Paul Soucy

Montreal Neurological Institute and Hospital

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