Sarah Benisty
University of Paris
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Neurology | 2009
Sonia Reyes; Anand Viswanathan; Ophélia Godin; Carole Dufouil; Sarah Benisty; K. Hernandez; Annie Kurtz; Eric Jouvent; Michael O'Sullivan; V. Czernecki; Marie-Germaine Bousser; Martin Dichgans; Hugues Chabriat
Objective: The frequency and impact of apathy in subcortical ischemic vascular dementia (SIVD) remain undetermined. The frequency, clinical, neuropsychological, and imaging correlates of apathy were assessed in a large cohort of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, a genetic model of SIVD. Methods: Apathy was diagnosed based on Neuropsychiatric Inventory assessment. Degree of disability was assessed by modified Rankin scale, cognitive impairment by Mattis Dementia Rating Scale (MDRS) and Mini-Mental State Examination (MMSE), autonomy by the Instrumental Activities of Daily Living (IADL) scale, and quality of life by SEP-59 self-questionnaire. Validated imaging methods were used to determine the total burden of cerebral lesions. Results: Among 132 patients, 54 (41%) were apathetic. Apathetic patients were older than nonapathetic subjects, had a lower MMSE and MDRS score, had more global disability, and were more limited in IADL. Apathetic patients were more frequently depressed compared to nonapathetic patients and more frequently presented additional neuropsychiatric symptoms. Multiple regression modeling showed a significant and independent association between apathy and a lower score of overall quality of life and between apathy and a higher load of white matter and lacunar lesions. Conclusions: The results suggest that apathy is common in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), appears in association with cognitive impairment, global functional disability, and severe neuropsychiatric symptoms during the course of the disease, and can occur separately from depression. Apathy has an independent impact on the overall quality of life in CADASIL. CADASIL = cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; DSM-IV = Diagnostic and Statistical Manual of Mental Disorders, 4th edition; IADL = Instrumental Activities of Daily Living; ICC = intracranial cavity; LL = lacunar lesions; MDRS = Mattis Dementia Rating Scale; MMSE = Mini-Mental State Examination; mRS = modified Rankin scale; NA = not applicable because of insufficient observations; nCM = number of cerebral microhemorrhages; nLL = normalized volume of lacunar lesions; NPI = Neuropsychiatric Inventory; nWMH = normalized volume of white matter hyperintensities; QOL = quality of life; SIVD = subcortical ischemic vascular dementia; TIA = transient ischemic attack; WMH = white matter hyperintensities.Objective:The frequency and impact of apathy in subcortical ischemic vascular dementia (SIVD) remain undetermined. The frequency, clinical, neuropsychological, and imaging correlates of apathy were assessed in a large cohort of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, a genetic model of SIVD. Methods:Apathy was diagnosed based on Neuropsychiatric Inventory assessment. Degree of disability was assessed by modified Rankin scale, cognitive impairment by Mattis Dementia Rating Scale (MDRS) and Mini-Mental State Examination (MMSE), autonomy by the Instrumental Activities of Daily Living (IADL) scale, and quality of life by SEP-59 self-questionnaire. Validated imaging methods were used to determine the total burden of cerebral lesions. Results:Among 132 patients, 54 (41%) were apathetic. Apathetic patients were older than nonapathetic subjects, had a lower MMSE and MDRS score, had more global disability, and were more limited in IADL. Apathetic patients were more frequently depressed compared to nonapathetic patients and more frequently presented additional neuropsychiatric symptoms. Multiple regression modeling showed a significant and independent association between apathy and a lower score of overall quality of life and between apathy and a higher load of white matter and lacunar lesions. Conclusions:The results suggest that apathy is common in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), appears in association with cognitive impairment, global functional disability, and severe neuropsychiatric symptoms during the course of the disease, and can occur separately from depression. Apathy has an independent impact on the overall quality of life in CADASIL. GLOSSARYCADASIL = cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; DSM-IV = Diagnostic and Statistical Manual of Mental Disorders, 4th edition; IADL = Instrumental Activities of Daily Living; ICC = intracranial cavity; LL = lacunar lesions; MDRS = Mattis Dementia Rating Scale; MMSE = Mini-Mental State Examination; mRS = modified Rankin scale; NA = not applicable because of insufficient observations; nCM = number of cerebral microhemorrhages; nLL = normalized volume of lacunar lesions; NPI = Neuropsychiatric Inventory; nWMH = normalized volume of white matter hyperintensities; QOL = quality of life; SIVD = subcortical ischemic vascular dementia; TIA = transient ischemic attack; WMH = white matter hyperintensities.
Neurobiology of Disease | 2010
Julien Dumurgier; Claire Paquet; Sarah Benisty; Claire Kiffel; Claude Lidy; François Mouton-Liger; Hugues Chabriat; Jean-Louis Laplanche; Jacques Hugon
In Alzheimers disease (AD), the cognitive reserve theory predicts that at any level of assessed clinical severity, the underlying brain pathology is more advanced in patients with more cognitive reserve. Recent evidences suggest that cerebrospinal fluid (CSF) biomarkers may reflect the brain pathology in AD. We investigated the relationship between education level and CSF concentrations of β-amyloid, total tau and phosphorylated tau (ptau-181) in a cohort of 70 subjects newly diagnosed with AD. We report that CSF concentration of β-amyloid was inversely associated with years of education, after adjustment for age, sex, and severity of the disease. We further demonstrate in stratified analysis that this relation was mainly present in mild form of the disease (CDR1), and was attenuated in more advanced forms of the disease. These results are consistent with the cognitive reserve theory, and suggest that cognitive reserve may be protective against amyloid related cognitive impairment at the onset of the clinical dementia.
Stroke | 2008
Sarah Benisty; Karen Hernandez; Anand Viswanathan; Sonia Reyes; Annie Kurtz; Michael O'Sullivan; Marie-Germaine Bousser; Martin Dichgans; Hugues Chabriat
Background and Purpose— Subcortical ischemic vascular dementia (SIVD) is a major subtype of vascular dementia (VaD). Recently, the diagnostic criteria of VaD have been modified to encompass this entity. Application of these criteria in CADASIL, a genetic model of SIVD, may help to better assess their significance. The aim of this study was to compare different sets of diagnostic criteria of VaD in a population of CADASIL patients. Methods— Different sets of diagnostic criteria of VaD (DSMIV, ICD10, standard NINDS-AIREN, modified NINDS-AIREN for SIVD) were applied to 115 CADASIL patients. Diagnosis of VaD was made through 2 steps: (1) diagnosis of dementia and (2) association of dementia to lesions of vascular origin. The percentage of patients satisfying the different sets and the concordance between these criteria was analyzed. Results— At least 1 set of criteria was satisfied for diagnosis in 29 subjects with dementia. In this group of patients, the sensitivity of the DSM IV, ICD 10, and standard NINDS-AIREN criteria for VaD was, respectively, 79%, 72%, and 45%. In contrast, the sensitivity of the NINDS-AIREN criteria for SIVD was 90%. The incomplete sensitivity of these last criteria was related to the absence of focal signs in some patients. The neuroimaging criteria were satisfied in all patients with dementia. Conclusions— The modified NINDS-AIREN criteria of SIVD are the most sensitive VaD criteria in CADASIL. Among these criteria, the neuroimaging criteria, although poorly specific to dementia, have a complete sensitivity. In contrast, focal signs were inconstant in CADASIL patients with dementia.
Neurobiology of Aging | 2011
S. Epelbaum; Sarah Benisty; Sonia Reyes; Michael O'Sullivan; Eric Jouvent; Marco Düring; D. Hervé; Christian Opherk; K. Hernandez; Annie Kurtz; Anand Viswanathan; M. G. Bousser; Martin Dichgans; Hugues Chabriat
In the elderly, the high prevalence of Alzheimers disease neuropathology presents a major challenge to the investigation of memory decline in common diseases such as small vessel disease. CADASIL represents a unique clinical model to determine the spectrum of memory impairment in subcortical ischemic vascular dementia (SIVD). One hundred and forty CADASIL patients underwent detailed clinical, neuropsychological and imaging analyses. The Free and Cued Selective Reminding Test was used as a measure of verbal memory. Forty-four out of 140 CADASIL patients (31.4%) presented with memory impairment according to this test. Eight out of 44 (18.2%) subjects with memory impairment matched the definition of the amnestic syndrome of hippocampal type. While alterations in spontaneous recall were related to the severity of subcortical ischemic lesions, the profile of memory impairment, particularly the sensitivity to cueing was found related to other factors such as hippocampal atrophy.
Journal of Alzheimer's Disease | 2012
Sarah Benisty; Sonia Reyes; Ophélia Godin; Dominique Hervé; Nikola Zieren; Eric Jouvent; Yi-Cheng Zhu; Marco Düring; Martin Dichgans; Hugues Chabriat
To better characterize the clinical spectrum related to white-matter hyperintensities (WMH) in small vessel disease, 66 patients with WMH but without any lacunar infarct were selected out of a cohort of 248 CADASIL individuals. Characteristics of these patients were compared to those of patients with lacunar infarcts. Relationships between the normalized volume of WMH (nWMH), presence of microhemorrhages, brain parenchymal fraction (BPF). and cognitive performances were assessed. The Trail Making Test (TMT) A and B times, Mattis Dementia Rating Scale (MDRS) total score, attention subscore, verbal fluency score and delayed memory recall were significantly correlated with nWMH but not with BPF. Presence of microhemorrhages was associated with worse TMT B time and attention MDRS subscore after adjustment for WMH. All subjects had Mini-Mental Status Examination scores ≥24 and presented with no or only mild disability. These results suggest that CADASIL patients with isolated WMH can present with executive and attention deficit but not with severe disability and that additional lesions are needed to cause significant disability and/or dementia.
Journal of Alzheimer's Disease | 2011
Julien Dumurgier; Claire Paquet; Katell Peoc'h; Pauline Lapalus; François Mouton-Liger; Sarah Benisty; Stéphanie Chasseigneaux; Hughes Chabriat; Jacques Hugon
Glucose dysmetabolism has been consistently associated with an increased risk of cognitive disorders, and brain insulin resistance could play a role in Alzheimers disease (AD) pathogenesis. Recent evidence suggests that cerebrospinal fluid (CSF) biomarkers may reflect the brain pathology in AD. We have investigated the relationship between CSF concentrations of amyloid-β peptide 1-42 (Aβ₁₋₄₂), total tau, and phosphorylated tau (ptau-181) and plasma and CSF glucose levels in a cohort of 94 newly diagnosed non-diabetics AD patients. We report that CSF Aβ₁₋₄₂ level was inversely associated with CSF to plasma glucose ratio (Spearmans coefficient = -0.27, p = 0.008). This relationship remained after adjustment for age, gender, body mass index, hypertension, and MMSE score (β [SE] of linear regression = -0.93 [0.37], p = 0.01). In stratified analysis, this relationship was observed only in patients who did not carry the apolipoprotein E4 allele. No significant relationship was found between glucose levels and total tau or phosphorylated tau 181. These results support the idea that a link between glucose dysmetabolism and the amyloid pathway may exist in the pathogenesis of AD.
Alzheimers & Dementia | 2011
Sarah Benisty; Marc Verny; Catherine Thomas-Antérion; Christine Perret-Guillaume; Marion Paulin; Farid El Massioui; Laurence Salomon; Isabelle Mahé
Span Backwards plus Attention and Calculation, Color Trails 1 plus 2, ADAS-Cog, Attention and Calculation, Letter Fluency plus Category Fluency, and Color Trails 2. Several neuropsychological tests’ score distributions did not overlap completely (examples: Category Fluency, Digit Span Backwards, Color Trails 1), with worst and best scores uniquely associated with fast decliners and improvers respectively. Measures with restricted or narrow ranges did not have unique values, examples: MMSE and Attention and Calculation. Conclusions: Consistent with the known relationship between severity and rate of decline in AD, in the blinded data fast decliners and improvers were different at screening on verbal fluency, working memory, and complex information processing speed. Further analyses will focus on the smaller placebo group. These measures have potential use in strategic subject selection to fulfill the NINCDS-ADRDA requirement of supplementing theMMSE for confirming cognitive impairment, documenting progressivity (another NINCDS-ADRDA diagnostic criterion neglected in trials), and identifying improvers at screening for exclusion, and should be considered in protocol design.
Alzheimers & Dementia | 2010
Julien Dumurgier; Claire Paquet; Sarah Benisty; Claire Kiffel; Claude Lidy; François Mouton-Liger; Hughues Chabriat; Jean-Louis Laplanche; Jacques Hugon
O4-06-08 EDUCATION LEVEL AND CSF BIOMARKERS IN ALZHEIMER’S DISEASE: THE COGNITIVE RESERVE THEORY Julien Dumurgier, Claire Paquet, Sarah Benisty, Claire Kiffel, Claude Lidy, François Mouton-Liger, Hughues Chabriat, Jean-Louis Laplanche, Jacques Hugon, CMRR Paris Nord, Lariboisière Fernand Widal Hospital, Paris, France; Department of Geriatrics, Lariboisière Fernand Widal Hospital, Paris, France; Department of Histology and Biology of Aging, Lariboisière Fernand Widal Hospital, Paris, France; Department of Neurology, Lariboisière Fernand Widal Hospital, Paris, France; Department of Biochemistry, Lariboisière Fernand Widal Hospital, Paris, France. Contact e-mail: [email protected]
Alzheimers & Dementia | 2012
Julien Dumurgier; Claire Paquet; Katell Peoc'h; Pauline Lapalus; François Mouton-Liger; Sarah Benisty; Hugues Chabriat; Jacques Hugon
Alzheimers & Dementia | 2011
Sarah Benisty; Sonia Reyes; Ophélia Godin; Dominique Hervé; Yi-Cheng Zhu; Nikola Zieren; Marco Duering; Martin Dichgans; Hugues Chabriat