Serotonin, β‐amyloid, and cognition in Parkinson disease
Objective Serotoninergic neurotransmission may modulate β‐amyloid peptide (Aβ) metabolism through upregulation of α‐secretase. Early Parkinson disease (PD) shows variable serotoninergic denervation, which may impact Aβ deposition. Methods We conducted 3 analyses to explore associations between serot...
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Published in | Annals of neurology Vol. 83; no. 5; pp. 994 - 1002 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.05.2018
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Subjects | |
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Abstract | Objective
Serotoninergic neurotransmission may modulate β‐amyloid peptide (Aβ) metabolism through upregulation of α‐secretase. Early Parkinson disease (PD) shows variable serotoninergic denervation, which may impact Aβ deposition.
Methods
We conducted 3 analyses to explore associations between serotoninergic neurotransmission and cerebral Aβ burden in PD. The first was a cross‐sectional imaging study of PD subjects (n = 23) using the serotoninergic transporter positron emission tomography (PET) ligand [11C]3‐amino‐4‐(2‐dimethylaminomethyl‐phenylsulfaryl)‐benzonitrile (DASB) and amyloid PET Pittsburgh compound B ([11C]PiB). The second was a baseline study of Parkinson's Progression Markers Initiative (PPMI) subjects exploring the influence of serotoninergic medications on cerebrospinal fluid (CSF) Aβ‐42 levels (n = 389), controlling for age, sex, Geriatric Depression Scale, disease duration, and education. Third, we fit an interval censored proportional hazard model with longitudinal PPMI data (n = 367) to test whether serotoninergic medication use associates with reduced risk of PD cognitive decline, defined as time to reach a Montreal Cognitive Assessment score ≤ 20, adjusting for baseline caudate dopamine transporter [123I]ioflupane single photon emission computed tomography and CSF Aβ‐42 levels.
Results
Serotoninergic DASB distribution volume ratio (DVR) inversely associated with PiB DVR in the cerebral cortex (Pearson r = −0.478, p = 0.021) but not the striatum (r = −0.264, p = 0.224). In the baseline PPMI analysis, serotoninergic medication use for ≥6 months associated with a lower level of CSF Aβ‐42 (t = −2.20, p = 0.029). In the longitudinal PPMI model, baseline serotoninergic medication use associated with a reduced risk of cognitive decline (t = −2.03, p = 0.043) after controlling for covariates.
Interpretation
Cortical Aβ burden in PD associates inversely with serotoninergic innervation. Serotoninergic medications may alter Aβ metabolism and reduce the risk of PD cognitive decline. Ann Neurol 2018;83:994–1002 |
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AbstractList | Serotoninergic neurotransmission may modulate β-amyloid peptide (Aβ) metabolism through upregulation of α-secretase. Early Parkinson disease (PD) shows variable serotoninergic denervation, which may impact Aβ deposition.OBJECTIVESerotoninergic neurotransmission may modulate β-amyloid peptide (Aβ) metabolism through upregulation of α-secretase. Early Parkinson disease (PD) shows variable serotoninergic denervation, which may impact Aβ deposition.We conducted 3 analyses to explore associations between serotoninergic neurotransmission and cerebral Aβ burden in PD. The first was a cross-sectional imaging study of PD subjects (n = 23) using the serotoninergic transporter positron emission tomography (PET) ligand [11 C]3-amino-4-(2-dimethylaminomethyl-phenylsulfaryl)-benzonitrile (DASB) and amyloid PET Pittsburgh compound B ([11 C]PiB). The second was a baseline study of Parkinson's Progression Markers Initiative (PPMI) subjects exploring the influence of serotoninergic medications on cerebrospinal fluid (CSF) Aβ-42 levels (n = 389), controlling for age, sex, Geriatric Depression Scale, disease duration, and education. Third, we fit an interval censored proportional hazard model with longitudinal PPMI data (n = 367) to test whether serotoninergic medication use associates with reduced risk of PD cognitive decline, defined as time to reach a Montreal Cognitive Assessment score ≤ 20, adjusting for baseline caudate dopamine transporter [123 I]ioflupane single photon emission computed tomography and CSF Aβ-42 levels.METHODSWe conducted 3 analyses to explore associations between serotoninergic neurotransmission and cerebral Aβ burden in PD. The first was a cross-sectional imaging study of PD subjects (n = 23) using the serotoninergic transporter positron emission tomography (PET) ligand [11 C]3-amino-4-(2-dimethylaminomethyl-phenylsulfaryl)-benzonitrile (DASB) and amyloid PET Pittsburgh compound B ([11 C]PiB). The second was a baseline study of Parkinson's Progression Markers Initiative (PPMI) subjects exploring the influence of serotoninergic medications on cerebrospinal fluid (CSF) Aβ-42 levels (n = 389), controlling for age, sex, Geriatric Depression Scale, disease duration, and education. Third, we fit an interval censored proportional hazard model with longitudinal PPMI data (n = 367) to test whether serotoninergic medication use associates with reduced risk of PD cognitive decline, defined as time to reach a Montreal Cognitive Assessment score ≤ 20, adjusting for baseline caudate dopamine transporter [123 I]ioflupane single photon emission computed tomography and CSF Aβ-42 levels.Serotoninergic DASB distribution volume ratio (DVR) inversely associated with PiB DVR in the cerebral cortex (Pearson r = -0.478, p = 0.021) but not the striatum (r = -0.264, p = 0.224). In the baseline PPMI analysis, serotoninergic medication use for ≥6 months associated with a lower level of CSF Aβ-42 (t = -2.20, p = 0.029). In the longitudinal PPMI model, baseline serotoninergic medication use associated with a reduced risk of cognitive decline (t = -2.03, p = 0.043) after controlling for covariates.RESULTSSerotoninergic DASB distribution volume ratio (DVR) inversely associated with PiB DVR in the cerebral cortex (Pearson r = -0.478, p = 0.021) but not the striatum (r = -0.264, p = 0.224). In the baseline PPMI analysis, serotoninergic medication use for ≥6 months associated with a lower level of CSF Aβ-42 (t = -2.20, p = 0.029). In the longitudinal PPMI model, baseline serotoninergic medication use associated with a reduced risk of cognitive decline (t = -2.03, p = 0.043) after controlling for covariates.Cortical Aβ burden in PD associates inversely with serotoninergic innervation. Serotoninergic medications may alter Aβ metabolism and reduce the risk of PD cognitive decline. Ann Neurol 2018;83:994-1002.INTERPRETATIONCortical Aβ burden in PD associates inversely with serotoninergic innervation. Serotoninergic medications may alter Aβ metabolism and reduce the risk of PD cognitive decline. Ann Neurol 2018;83:994-1002. ObjectiveSerotoninergic neurotransmission may modulate β‐amyloid peptide (Aβ) metabolism through upregulation of α‐secretase. Early Parkinson disease (PD) shows variable serotoninergic denervation, which may impact Aβ deposition.MethodsWe conducted 3 analyses to explore associations between serotoninergic neurotransmission and cerebral Aβ burden in PD. The first was a cross‐sectional imaging study of PD subjects (n = 23) using the serotoninergic transporter positron emission tomography (PET) ligand [11C]3‐amino‐4‐(2‐dimethylaminomethyl‐phenylsulfaryl)‐benzonitrile (DASB) and amyloid PET Pittsburgh compound B ([11C]PiB). The second was a baseline study of Parkinson's Progression Markers Initiative (PPMI) subjects exploring the influence of serotoninergic medications on cerebrospinal fluid (CSF) Aβ‐42 levels (n = 389), controlling for age, sex, Geriatric Depression Scale, disease duration, and education. Third, we fit an interval censored proportional hazard model with longitudinal PPMI data (n = 367) to test whether serotoninergic medication use associates with reduced risk of PD cognitive decline, defined as time to reach a Montreal Cognitive Assessment score ≤ 20, adjusting for baseline caudate dopamine transporter [123I]ioflupane single photon emission computed tomography and CSF Aβ‐42 levels.ResultsSerotoninergic DASB distribution volume ratio (DVR) inversely associated with PiB DVR in the cerebral cortex (Pearson r = −0.478, p = 0.021) but not the striatum (r = −0.264, p = 0.224). In the baseline PPMI analysis, serotoninergic medication use for ≥6 months associated with a lower level of CSF Aβ‐42 (t = −2.20, p = 0.029). In the longitudinal PPMI model, baseline serotoninergic medication use associated with a reduced risk of cognitive decline (t = −2.03, p = 0.043) after controlling for covariates.InterpretationCortical Aβ burden in PD associates inversely with serotoninergic innervation. Serotoninergic medications may alter Aβ metabolism and reduce the risk of PD cognitive decline. Ann Neurol 2018;83:994–1002 Serotoninergic neurotransmission may modulate β-amyloid peptide (Aβ) metabolism through upregulation of α-secretase. Early Parkinson disease (PD) shows variable serotoninergic denervation, which may impact Aβ deposition. We conducted 3 analyses to explore associations between serotoninergic neurotransmission and cerebral Aβ burden in PD. The first was a cross-sectional imaging study of PD subjects (n = 23) using the serotoninergic transporter positron emission tomography (PET) ligand [ C]3-amino-4-(2-dimethylaminomethyl-phenylsulfaryl)-benzonitrile (DASB) and amyloid PET Pittsburgh compound B ([ C]PiB). The second was a baseline study of Parkinson's Progression Markers Initiative (PPMI) subjects exploring the influence of serotoninergic medications on cerebrospinal fluid (CSF) Aβ-42 levels (n = 389), controlling for age, sex, Geriatric Depression Scale, disease duration, and education. Third, we fit an interval censored proportional hazard model with longitudinal PPMI data (n = 367) to test whether serotoninergic medication use associates with reduced risk of PD cognitive decline, defined as time to reach a Montreal Cognitive Assessment score ≤ 20, adjusting for baseline caudate dopamine transporter [ I]ioflupane single photon emission computed tomography and CSF Aβ-42 levels. Serotoninergic DASB distribution volume ratio (DVR) inversely associated with PiB DVR in the cerebral cortex (Pearson r = -0.478, p = 0.021) but not the striatum (r = -0.264, p = 0.224). In the baseline PPMI analysis, serotoninergic medication use for ≥6 months associated with a lower level of CSF Aβ-42 (t = -2.20, p = 0.029). In the longitudinal PPMI model, baseline serotoninergic medication use associated with a reduced risk of cognitive decline (t = -2.03, p = 0.043) after controlling for covariates. Cortical Aβ burden in PD associates inversely with serotoninergic innervation. Serotoninergic medications may alter Aβ metabolism and reduce the risk of PD cognitive decline. Ann Neurol 2018;83:994-1002. Objective Serotoninergic neurotransmission may modulate β‐amyloid peptide (Aβ) metabolism through upregulation of α‐secretase. Early Parkinson disease (PD) shows variable serotoninergic denervation, which may impact Aβ deposition. Methods We conducted 3 analyses to explore associations between serotoninergic neurotransmission and cerebral Aβ burden in PD. The first was a cross‐sectional imaging study of PD subjects (n = 23) using the serotoninergic transporter positron emission tomography (PET) ligand [11C]3‐amino‐4‐(2‐dimethylaminomethyl‐phenylsulfaryl)‐benzonitrile (DASB) and amyloid PET Pittsburgh compound B ([11C]PiB). The second was a baseline study of Parkinson's Progression Markers Initiative (PPMI) subjects exploring the influence of serotoninergic medications on cerebrospinal fluid (CSF) Aβ‐42 levels (n = 389), controlling for age, sex, Geriatric Depression Scale, disease duration, and education. Third, we fit an interval censored proportional hazard model with longitudinal PPMI data (n = 367) to test whether serotoninergic medication use associates with reduced risk of PD cognitive decline, defined as time to reach a Montreal Cognitive Assessment score ≤ 20, adjusting for baseline caudate dopamine transporter [123I]ioflupane single photon emission computed tomography and CSF Aβ‐42 levels. Results Serotoninergic DASB distribution volume ratio (DVR) inversely associated with PiB DVR in the cerebral cortex (Pearson r = −0.478, p = 0.021) but not the striatum (r = −0.264, p = 0.224). In the baseline PPMI analysis, serotoninergic medication use for ≥6 months associated with a lower level of CSF Aβ‐42 (t = −2.20, p = 0.029). In the longitudinal PPMI model, baseline serotoninergic medication use associated with a reduced risk of cognitive decline (t = −2.03, p = 0.043) after controlling for covariates. Interpretation Cortical Aβ burden in PD associates inversely with serotoninergic innervation. Serotoninergic medications may alter Aβ metabolism and reduce the risk of PD cognitive decline. Ann Neurol 2018;83:994–1002 |
Author | Bohnen, Nicolaas I. Koeppe, Robert Kotagal, Vikas Albin, Roger L. Spino, Cathie |
AuthorAffiliation | 5 Department of Radiology, Division of Nuclear Medicine, University of Michigan, Ann Arbor, MI 1 Department of Neurology, University of Michigan, Ann Arbor, MI 4 Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, MI 2 Veterans Affairs Ann Arbor Health System (VAAAHS), Ann Arbor, Michigan 3 University of Michigan Morris K. Udall Center of Excellence for Parkinson’s Disease Research, Ann Arbor, MI |
AuthorAffiliation_xml | – name: 2 Veterans Affairs Ann Arbor Health System (VAAAHS), Ann Arbor, Michigan – name: 4 Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, MI – name: 3 University of Michigan Morris K. Udall Center of Excellence for Parkinson’s Disease Research, Ann Arbor, MI – name: 5 Department of Radiology, Division of Nuclear Medicine, University of Michigan, Ann Arbor, MI – name: 1 Department of Neurology, University of Michigan, Ann Arbor, MI |
Author_xml | – sequence: 1 givenname: Vikas surname: Kotagal fullname: Kotagal, Vikas email: vikaskot@med.umich.edu organization: Veterans Affairs Ann Arbor Health System – sequence: 2 givenname: Cathie surname: Spino fullname: Spino, Cathie organization: School of Public Health, University of Michigan – sequence: 3 givenname: Nicolaas I. surname: Bohnen fullname: Bohnen, Nicolaas I. organization: University of Michigan – sequence: 4 givenname: Robert surname: Koeppe fullname: Koeppe, Robert organization: University of Michigan – sequence: 5 givenname: Roger L. surname: Albin fullname: Albin, Roger L. organization: University of Michigan Morris K. Udall Center of Excellence for Parkinson's Disease Research |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29665066$$D View this record in MEDLINE/PubMed |
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Serotoninergic neurotransmission may modulate β‐amyloid peptide (Aβ) metabolism through upregulation of α‐secretase. Early Parkinson disease (PD)... Serotoninergic neurotransmission may modulate β-amyloid peptide (Aβ) metabolism through upregulation of α-secretase. Early Parkinson disease (PD) shows... ObjectiveSerotoninergic neurotransmission may modulate β‐amyloid peptide (Aβ) metabolism through upregulation of α‐secretase. Early Parkinson disease (PD)... |
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SubjectTerms | Baseline studies Benzonitrile Cerebral cortex Cerebrospinal fluid Cognition Cognitive ability Computed tomography Denervation Disease control Dopamine Dopamine transporter Drugs Innervation Mental depression Metabolism Movement disorders Neostriatum Neurodegenerative diseases Neuroimaging Neurotransmission Parkinson's disease Photon emission Positron emission Positron emission tomography Risk Secretase Serotonin Single photon emission computed tomography Statistical models Tomography β-Amyloid |
Title | Serotonin, β‐amyloid, and cognition in Parkinson disease |
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