Souvenaid Reduces Behavioral Deficits and Improves Social Cognition Skills in Frontotemporal Dementia: A Proof-of-Concept Study
Background: Souvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the poten...
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Published in | Neuro-degenerative diseases Vol. 15; no. 1; pp. 58 - 62 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Basel, Switzerland
S. Karger AG
01.02.2015
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Subjects | |
Online Access | Get full text |
ISSN | 1660-2854 1660-2862 1660-2862 |
DOI | 10.1159/000369811 |
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Abstract | Background: Souvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid™ to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored. Objective: To evaluate the impact of Souvenaid™ on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD). Methods: Twenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid™ (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks. Results: Treatment with Souvenaid™ was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid™ was discontinued. Souvenaid™ did not have an effect on executive functions. Conclusions: Our results provide evidence of the potential of Souvenaid™ therapy for the treatment of behavioral disturbances and social cognition skills in FTD. |
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AbstractList | Background: Souvenaid[TM] is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid[TM] has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid[TM] to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored. Objective: To evaluate the impact of Souvenaid[TM] on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD). Methods: Twenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid[TM] (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks. Results: Treatment with Souvenaid[TM] was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid[TM] was discontinued. Souvenaid[TM] did not have an effect on executive functions. Conclusions: Our results provide evidence of the potential of Souvenaid[TM] therapy for the treatment of behavioral disturbances and social cognition skills in FTD. Keywords: Behavioral deficits, Fronto-temporal dementia, Medical foods Background: Souvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid™ to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored. Objective: To evaluate the impact of Souvenaid™ on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD). Methods: Twenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid™ (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks. Results: Treatment with Souvenaid™ was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid™ was discontinued. Souvenaid™ did not have an effect on executive functions. Conclusions: Our results provide evidence of the potential of Souvenaid™ therapy for the treatment of behavioral disturbances and social cognition skills in FTD. Background: Souvenaid(TM) is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid(TM) has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid(TM) to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored. Objective: To evaluate the impact of Souvenaid(TM) on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD). Methods: Twenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid(TM) (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks. Results: Treatment with Souvenaid(TM) was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid(TM) was discontinued. Souvenaid(TM) did not have an effect on executive functions. Conclusions: Our results provide evidence of the potential of Souvenaid(TM) therapy for the treatment of behavioral disturbances and social cognition skills in FTD. © 2015 S. Karger AG, Basel Souvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid™ to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored.BACKGROUNDSouvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid™ to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored.To evaluate the impact of Souvenaid™ on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD).OBJECTIVETo evaluate the impact of Souvenaid™ on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD).Twenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid™ (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks.METHODSTwenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid™ (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks.Treatment with Souvenaid™ was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid™ was discontinued. Souvenaid™ did not have an effect on executive functions.RESULTSTreatment with Souvenaid™ was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid™ was discontinued. Souvenaid™ did not have an effect on executive functions.Our results provide evidence of the potential of Souvenaid™ therapy for the treatment of behavioral disturbances and social cognition skills in FTD.CONCLUSIONSOur results provide evidence of the potential of Souvenaid™ therapy for the treatment of behavioral disturbances and social cognition skills in FTD. Background: Souvenaid(TM) is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid(TM) has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid(TM) to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored. Objective: To evaluate the impact of Souvenaid(TM) on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD). Methods: Twenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid(TM) (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks. Results: Treatment with Souvenaid(TM) was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid(TM) was discontinued. Souvenaid(TM) did not have an effect on executive functions. Conclusions: Our results provide evidence of the potential of Souvenaid(TM) therapy for the treatment of behavioral disturbances and social cognition skills in FTD. copyright 2015 S. Karger AG, Basel Souvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been shown to improve cognitive function in subjects with mild Alzheimer's disease in randomized clinical trials. To date, however, the potential of Souvenaid™ to improve cognitive functioning in subjects with other neurodegenerative conditions also characterized by synaptic loss has not been explored. To evaluate the impact of Souvenaid™ on executive functions, social cognition and behavioral disturbances in subjects with the behavioral variant of frontotemporal dementia (bv-FTD). Twenty-six subjects with bv-FTD were enrolled in the study and randomized to Souvenaid™ (125 ml/day) or placebo groups. After 12 weeks, subjects were switched between the two groups. All subjects, blinded to treatment, underwent clinical and cognitive evaluations at enrollment, after 12 weeks and after 24 weeks. Treatment with Souvenaid™ was associated with a significant reduction of behavioral symptoms and an increase in Theory of Mind skills compared to placebo, which both returned to baseline when Souvenaid™ was discontinued. Souvenaid™ did not have an effect on executive functions. Our results provide evidence of the potential of Souvenaid™ therapy for the treatment of behavioral disturbances and social cognition skills in FTD. |
Audience | Academic |
Author | Pardini, Matteo Amore, Mario Massucco, Davide Serrati, Carlo Sassos, Davide Emberti Gialloreti, Leonardo Mattei, Chiara Cocito, Leonardo Abate, Lucia Krueger, Frank Guida, Silvia |
Author_xml | – sequence: 1 givenname: Matteo surname: Pardini fullname: Pardini, Matteo email: matteo.pardini@gmail.com – sequence: 2 givenname: Carlo surname: Serrati fullname: Serrati, Carlo – sequence: 3 givenname: Silvia surname: Guida fullname: Guida, Silvia – sequence: 4 givenname: Chiara surname: Mattei fullname: Mattei, Chiara – sequence: 5 givenname: Lucia surname: Abate fullname: Abate, Lucia – sequence: 6 givenname: Davide surname: Massucco fullname: Massucco, Davide – sequence: 7 givenname: Davide surname: Sassos fullname: Sassos, Davide – sequence: 8 givenname: Mario surname: Amore fullname: Amore, Mario – sequence: 9 givenname: Frank surname: Krueger fullname: Krueger, Frank – sequence: 10 givenname: Leonardo surname: Cocito fullname: Cocito, Leonardo – sequence: 11 givenname: Leonardo surname: Emberti Gialloreti fullname: Emberti Gialloreti, Leonardo |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25592742$$D View this record in MEDLINE/PubMed |
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Keywords | Medical foods Behavioral deficits Fronto-temporal dementia |
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References | Guy W: ECDEU Assessment Manual for Psychopharmacology - Revised, 1976. Rockville, MD, US Department of Health, Education, and Welfare, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, NIMH Psychopharmacology Research Branch, Division of Extramural Research Programs. Baloyannis SJ, Mauroudis I, Manolides SL, Manolides LS: The acoustic cortex in frontotemporal dementia: a Golgi and electron microscope study. Acta Otolaryngol 2011;131:359-361.2118905110.3109/00016489.2010.539267 Clare R, King VG, Wirenfeldt M, Vinters HV: Synapse loss in dementias. J Neurosci Res 2010;88:2083-2090.2053337710.1002/jnr.22392 Terry RD, Masliah E, Salmon DP, Butters N, DeTeresa R, Hill R, Hansen LA, Katzman R: Physical basis of cognitive alterations in Alzheimer's disease: synapse loss is the major correlate of cognitive impairment. Ann Neurol 1991;30:572-580.178968410.1002/ana.410300410 Wisniewski SR, Rush AJ, Balasubramani GK, Trivedi MH, Nierenberg AA, STARD Investigators: Self-rated global measure of the frequency, intensity, and burden of side effects. J Psychiatr Pract 2006;12:71-79.1672890310.1097/00131746-200603000-00002 Rascovsky K, Hodges JR, Knopman D, Mendez MF, Kramer JH, Neuhaus J, van Swieten JC, Seelaar H, Dopper EG, Onyike CU, Hillis AE, Josephs KA, Boeve BF, Kertesz A, Seeley WW, Rankin KP, Johnson JK, Gorno-Tempini ML, Rosen H, Prioleau-Latham CE, Lee A, Kipps CM, Lillo P, Piguet O, Rohrer JD, Rossor MN, Warren JD, Fox NC, Galasko D, Salmon DP, Black SE, Mesulam M, Weintraub S, Dickerson BC, Diehl-Schmid J, Pasquier F, Deramecourt V, Lebert F, Pijnenburg Y, Chow TW, Manes F, Grafman J, Cappa SF, Freedman M, Grossman M, Miller BL: Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 2011;134:2456-2477.2181089010.1093/brain/awr179 Dubois B, Slachevsky A, Litvan I, Pillon B: The FAB: a Frontal Assessment Battery at bedside. Neurology 2000;55:1621-1626.1111321410.1212/WNL.55.11.1621 Scheltens P, Twisk JW, Blesa R, Scarpini E, von Arnim CA, Bongers A, Harrison J, Swinkels SH, Stam CJ, de Waal H, Wurtman RJ, Wieggers RL, Vellas B, Kamphuis PJ: Efficacy of Souvenaid™ in mild Alzheimer's disease: results from a randomized, controlled trial. J Alzheimers Dis 2012;31:225-236.2276677010.3233/JAD-2012-121189 Pardini M, Emberti Gialloreti L, Mascolo M, Benassi F, Abate L, Guida S, Viani E, Dal Monte O, Schintu S, Krueger F, Cocito L: Isolated theory of mind deficits and risk for frontotemporal dementia: a longitudinal pilot study. J Neurol Neurosurg Psychiatry 2013;84:818-821.2311748710.1136/jnnp-2012-303684 van Wijk N, Broersen LM, de Wilde MC, Hageman RJ, Groenendijk M, Sijben JW, Kamphuis PJ: Targeting synaptic dysfunction in Alzheimer's disease by administering a specific nutrient combination. J Alzheimers Dis 2014;38:459-479.2398542010.3233/JAD-130998 Davies CA, Mann DM, Sumpter PQ, Yates PO: A quantitative morphometric analysis of the neuronal and synaptic content of the frontal and temporal cortex in patients with Alzheimer's disease. J Neurol Sci 1987;78:151-164.357245410.1016/0022-510X(87)90057-8 Cummings JL, Mega M, Gray K, Rosenberg-Thompson S, Carusi DA, Gornbein J: The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology 1994;44:2308-2314.799111710.1212/WNL.44.12.2308 Baron-Cohen S, Wheelwright S, Hill J, Raste Y, Plumb I: The ‘Reading the Mind in the Eyes' Test revised version: a study with normal adults, and adults with Asperger syndrome or high-functioning autism. J Child Psychol Psychiatry 2001;42:241-251.1128042010.1017/S0021963001006643 Brun A, Liu X, Erikson C: Synapse loss and gliosis in the molecular layer of the cerebral cortex in Alzheimer's disease and in frontal lobe degeneration. Neurodegeneration 1995;4:171-177.758368110.1006/neur.1995.0021 Sakamoto T, Cansev M, Wurtman RJ: Oral supplementation with docosahexaenoic acid and uridine-5′-monophosphate increases dendritic spine density in adult gerbil hippocampus. Brain Res 2007;1182:50-59.1795071010.1016/j.brainres.2007.08.089 de Waal H, Stam CJ, Lansbergen MM, Wieggers RL, Kamphuis PJ, Scheltens P, Maestú F, van Straaten EC: The effect of Souvenaid™ on functional brain network organisation in patients with mild Alzheimer's disease: a randomised controlled study. PLoS One 2014;9:e86558.2447514410.1371/journal.pone.0086558 Richardson UI, Watkins CJ, Pierre C, Ulus IH, Wurtman RJ: Stimulation of CDP-choline synthesis by uridine or cytidine in PC12 rat pheochromocytoma cells. Brain Res 2003;971:161-167.1270623210.1016/S0006-8993(03)02333-3 ref13 ref12 ref15 ref14 ref11 ref10 ref2 ref1 ref16 ref8 ref7 ref9 ref4 ref3 ref6 ref5 |
References_xml | – reference: Clare R, King VG, Wirenfeldt M, Vinters HV: Synapse loss in dementias. J Neurosci Res 2010;88:2083-2090.2053337710.1002/jnr.22392 – reference: Guy W: ECDEU Assessment Manual for Psychopharmacology - Revised, 1976. Rockville, MD, US Department of Health, Education, and Welfare, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, NIMH Psychopharmacology Research Branch, Division of Extramural Research Programs. – reference: Rascovsky K, Hodges JR, Knopman D, Mendez MF, Kramer JH, Neuhaus J, van Swieten JC, Seelaar H, Dopper EG, Onyike CU, Hillis AE, Josephs KA, Boeve BF, Kertesz A, Seeley WW, Rankin KP, Johnson JK, Gorno-Tempini ML, Rosen H, Prioleau-Latham CE, Lee A, Kipps CM, Lillo P, Piguet O, Rohrer JD, Rossor MN, Warren JD, Fox NC, Galasko D, Salmon DP, Black SE, Mesulam M, Weintraub S, Dickerson BC, Diehl-Schmid J, Pasquier F, Deramecourt V, Lebert F, Pijnenburg Y, Chow TW, Manes F, Grafman J, Cappa SF, Freedman M, Grossman M, Miller BL: Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 2011;134:2456-2477.2181089010.1093/brain/awr179 – reference: Cummings JL, Mega M, Gray K, Rosenberg-Thompson S, Carusi DA, Gornbein J: The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology 1994;44:2308-2314.799111710.1212/WNL.44.12.2308 – reference: Dubois B, Slachevsky A, Litvan I, Pillon B: The FAB: a Frontal Assessment Battery at bedside. Neurology 2000;55:1621-1626.1111321410.1212/WNL.55.11.1621 – reference: van Wijk N, Broersen LM, de Wilde MC, Hageman RJ, Groenendijk M, Sijben JW, Kamphuis PJ: Targeting synaptic dysfunction in Alzheimer's disease by administering a specific nutrient combination. J Alzheimers Dis 2014;38:459-479.2398542010.3233/JAD-130998 – reference: Baron-Cohen S, Wheelwright S, Hill J, Raste Y, Plumb I: The ‘Reading the Mind in the Eyes' Test revised version: a study with normal adults, and adults with Asperger syndrome or high-functioning autism. J Child Psychol Psychiatry 2001;42:241-251.1128042010.1017/S0021963001006643 – reference: Sakamoto T, Cansev M, Wurtman RJ: Oral supplementation with docosahexaenoic acid and uridine-5′-monophosphate increases dendritic spine density in adult gerbil hippocampus. Brain Res 2007;1182:50-59.1795071010.1016/j.brainres.2007.08.089 – reference: Brun A, Liu X, Erikson C: Synapse loss and gliosis in the molecular layer of the cerebral cortex in Alzheimer's disease and in frontal lobe degeneration. Neurodegeneration 1995;4:171-177.758368110.1006/neur.1995.0021 – reference: de Waal H, Stam CJ, Lansbergen MM, Wieggers RL, Kamphuis PJ, Scheltens P, Maestú F, van Straaten EC: The effect of Souvenaid™ on functional brain network organisation in patients with mild Alzheimer's disease: a randomised controlled study. PLoS One 2014;9:e86558.2447514410.1371/journal.pone.0086558 – reference: Scheltens P, Twisk JW, Blesa R, Scarpini E, von Arnim CA, Bongers A, Harrison J, Swinkels SH, Stam CJ, de Waal H, Wurtman RJ, Wieggers RL, Vellas B, Kamphuis PJ: Efficacy of Souvenaid™ in mild Alzheimer's disease: results from a randomized, controlled trial. J Alzheimers Dis 2012;31:225-236.2276677010.3233/JAD-2012-121189 – reference: Wisniewski SR, Rush AJ, Balasubramani GK, Trivedi MH, Nierenberg AA, STARD Investigators: Self-rated global measure of the frequency, intensity, and burden of side effects. J Psychiatr Pract 2006;12:71-79.1672890310.1097/00131746-200603000-00002 – reference: Pardini M, Emberti Gialloreti L, Mascolo M, Benassi F, Abate L, Guida S, Viani E, Dal Monte O, Schintu S, Krueger F, Cocito L: Isolated theory of mind deficits and risk for frontotemporal dementia: a longitudinal pilot study. J Neurol Neurosurg Psychiatry 2013;84:818-821.2311748710.1136/jnnp-2012-303684 – reference: Richardson UI, Watkins CJ, Pierre C, Ulus IH, Wurtman RJ: Stimulation of CDP-choline synthesis by uridine or cytidine in PC12 rat pheochromocytoma cells. Brain Res 2003;971:161-167.1270623210.1016/S0006-8993(03)02333-3 – reference: Baloyannis SJ, Mauroudis I, Manolides SL, Manolides LS: The acoustic cortex in frontotemporal dementia: a Golgi and electron microscope study. Acta Otolaryngol 2011;131:359-361.2118905110.3109/00016489.2010.539267 – reference: Terry RD, Masliah E, Salmon DP, Butters N, DeTeresa R, Hill R, Hansen LA, Katzman R: Physical basis of cognitive alterations in Alzheimer's disease: synapse loss is the major correlate of cognitive impairment. Ann Neurol 1991;30:572-580.178968410.1002/ana.410300410 – reference: Davies CA, Mann DM, Sumpter PQ, Yates PO: A quantitative morphometric analysis of the neuronal and synaptic content of the frontal and temporal cortex in patients with Alzheimer's disease. J Neurol Sci 1987;78:151-164.357245410.1016/0022-510X(87)90057-8 – ident: ref8 doi: 10.1016/0022-510X(87)90057-8 – ident: ref14 doi: 10.1002/ana.410300410 – ident: ref15 doi: 10.1371/journal.pone.0086558 – ident: ref11 doi: 10.1212/WNL.55.11.1621 – ident: ref2 doi: 10.3233/JAD-130998 – ident: ref4 doi: 10.1016/j.brainres.2007.08.089 – ident: ref9 doi: 10.1093/brain/awr179 – ident: ref6 doi: 10.3109/00016489.2010.539267 – ident: ref13 doi: 10.1097/00131746-200603000-00002 – ident: ref16 doi: 10.1136/jnnp-2012-303684 – ident: ref10 doi: 10.1212/WNL.44.12.2308 – ident: ref12 doi: 10.1017/S0021963001006643 – ident: ref1 doi: 10.1002/jnr.22392 – ident: ref5 doi: 10.3233/JAD-2012-121189 – ident: ref3 doi: 10.1016/S0006-8993(03)02333-3 – ident: ref7 doi: 10.1006/neur.1995.0021 |
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Snippet | Background: Souvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been... Souvenaid™ is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid™ has been shown to... Background: Souvenaid[TM] is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid[TM] has... Background: Souvenaid(TM) is a nutraceutical compound thought to positively enhance synaptic function. In line with this mechanism of action, Souvenaid(TM) has... |
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Title | Souvenaid Reduces Behavioral Deficits and Improves Social Cognition Skills in Frontotemporal Dementia: A Proof-of-Concept Study |
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