Does Serotonin Augmentation Have Any Effect on Cognition and Activities of Daily Living in Alzheimer's Dementia?: A Double-Blind, Placebo-Controlled Clinical Trial

Objective: Recent studies suggest that cholinergic dysfunction does not provide a complete account of age-related cognitive deficits, and other neuronal systems like monoaminergic hypofunction are involved. In several studies, selective serotonin reuptake inhibitors demonstrated promotion in neurogenesis in the hippocampus and enhanced memory and cognition. The aim of this study is to survey the effect of serotonin augmentation on cognition and activities of daily living in patients with Alzheimer's disease. Method: The trial was designed as a 12-week randomized, placebo-controlled, double-blind study. One hundred twenty-two patients aged 55 to 85 years with mild-to-moderate Alzheimer's dementia were randomly allocated in 1 of the 3 treatment groups: fluoxetine plus rivastigmine, rivastigmine alone, or placebo group. Efficacy measures comprised assessments of cognition, activities of daily living, and global functioning. Hamilton Depression Scale also was used to assess changes in mood throughout the study. Result: Fluoxetine plus rivastigmine and rivastigmine groups demonstrated improvement on measures of cognitive and memory without any significant difference; however, the former group did better in their activities of daily living and global functioning. Patients taking placebo had significant deterioration in all the efficacy measures. Patients taking rivastigmine or rivastigmine plus fluoxetine had improvements in Hamilton Depression Scale without significant differences. Conclusions: Concomitant use of selective serotonin-enhancing agents and acetyl cholinesterase inhibitors can provide greater benefit in activities of daily living and global functioning in patients with cognitive impairment. Because our study is preliminary, larger double-blind studies are needed to confirm the results.

[1]  M. Hamilton,et al.  Development of a rating scale for primary depressive illness. , 1967, The British journal of social and clinical psychology.

[2]  D. Price,et al.  Age-related changes in multiple neurotransmitter systems in the monkey brain , 1989, Neurobiology of Aging.

[3]  P. Delgado,et al.  Alzheimer disease, serotonin systems, and tryptophan depletion. , 2002, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

[4]  M. D. O'Brien,et al.  Cerebral blood flow in dementia , 1986, Neurology.

[5]  H. Manev,et al.  Fluoxetine increases the content of neurotrophic protein S100beta in the rat hippocampus. , 2001, European journal of pharmacology.

[6]  B. Reisberg,et al.  Brief Cognitive Rating Scale (BCRS). , 1988, Psychopharmacology bulletin.

[7]  P. Cowen,et al.  Low-dose tryptophan depletion in recovered depressed patients induces changes in cognitive processing without depressive symptoms , 2005, Biological Psychiatry.

[8]  Eric J. Nestler,et al.  Chronic Antidepressant Treatment Increases Neurogenesis in Adult Rat Hippocampus , 2000, The Journal of Neuroscience.

[9]  J L Mack,et al.  Assessment of Functional Ability in Alzheimer Disease: A Review and a Preliminary Report on the Cleveland Scale for Activities of Daily Living , 1992, Alzheimer disease and associated disorders.

[10]  H Merskey,et al.  Temporal lobe atrophy on magnetic resonance imaging in the diagnosis of early Alzheimer's disease. , 1993, Archives of neurology.

[11]  Eric Vermetten,et al.  Hippocampal volume, memory, and cortisol status in major depressive disorder: effects of treatment , 2004, Biological Psychiatry.

[12]  M. Lawton,et al.  Assessment of older people: self-maintaining and instrumental activities of daily living. , 1969, The Gerontologist.

[13]  D. Kupfer,et al.  Serotonin in Aging, Late-Life Depression, and Alzheimer's Disease: The Emerging Role of Functional Imaging , 1998, Neuropsychopharmacology.

[14]  L. Iversen,et al.  Non-cholinergic neurotransmitter abnormalities in Alzheimer's disease. , 1986, British medical bulletin.

[15]  M. Esiri,et al.  Postmortem serotoninergic correlates of cognitive decline in Alzheimer's disease , 2002, Neuroreport.

[16]  S. DeKosky,et al.  Monoamine neurons in aging and Alzheimer's disease , 2005, Journal of Neural Transmission / General Section JNT.

[17]  S. Marumoto,et al.  Pharmacological characterization of RS-1259, an orally active dual inhibitor of acetylcholinesterase and serotonin transporter, in rodents: possible treatment of Alzheimer's disease. , 2003, Journal of pharmacological sciences.

[18]  B. Jacobs,et al.  Adult brain neurogenesis and psychiatry: a novel theory of depression , 2000, Molecular Psychiatry.

[19]  David Wechsler,et al.  Wechsler Memory scale. , 2005 .

[20]  E. Gould,et al.  Neurogenesis in the Dentate Gyrus of the Adult Tree Shrew Is Regulated by Psychosocial Stress and NMDA Receptor Activation , 1997, The Journal of Neuroscience.

[21]  J L McGaugh,et al.  The role of interactions between the cholinergic system and other neuromodulatory systems in learing and memory , 1991, Synapse.

[22]  P. Riekkinen,et al.  Interaction between 5-HT1A and nicotinic cholinergic receptors in the regulation of water maze navigation behavior , 1994, Brain Research.

[23]  S. Folstein,et al.  "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. , 1975, Journal of psychiatric research.

[24]  W J Riedel,et al.  Serotonin and human cognitive performance. , 2006, Current pharmaceutical design.

[25]  Rita Moretti,et al.  Depression and Alzheimer's disease: Symptom or comorbidity? , 2002, American journal of Alzheimer's disease and other dementias.

[26]  Steven M. Southwick,et al.  Long-term treatment with paroxetine increases verbal declarative memory and hippocampal volume in posttraumatic stress disorder , 2003, Biological Psychiatry.

[27]  G. Grossberg,et al.  Behavioral and Psychological Symptoms of Dementia as a Risk Factor for Nursing Home Placement , 2000, International Psychogeriatrics.

[28]  G. Iverson Interpreting change on the WAIS-III/WMS-III in clinical samples. , 2001, Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists.

[29]  P. Francis,et al.  Serotonergic pathology is not widespread in Alzheimer patients without prominent aggressive symptoms , 1992, Neurochemical Research.