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...

Full description

Saved in:
Bibliographic Details
Published inAnnals of neurology Vol. 83; no. 5; pp. 994 - 1002
Main Authors Kotagal, Vikas, Spino, Cathie, Bohnen, Nicolaas I., Koeppe, Robert, Albin, Roger L.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.05.2018
Subjects
Online AccessGet full text

Cover

Loading…
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
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
BookMark eNp1kd9KHDEUxoMoutpe9AXKQG8sOHrydxIKwiK1CtIWWq9DJpOxsbOJTWaVvesj9Fl8kD5En6TRXaWV9uoQzu_7-HK-bbQeYnAIvcCwjwHIgQlmn3BCxRqaYE5xLQlT62gCVLCaY8q20HbOlwCgBIZNtEWUEByEmKA3n1yKYww-7FU_b399_2FmiyH6bq8yoatsvAh-9DFUPlQfTfrqQy6PzmdnsnuGNnozZPd8NXfQ-fHbz0cn9dmHd6dH07PaMkZFbZ1tqeoJ432HiWwaYpXjQlLbgIEGeIcZgCCi562SLZWtoR3QRvVNa6xgdAcdLn2v5u3MddaFMZlBXyU_M2mho_H6703wX_RFvNYCCCZAi8HuyiDFb3OXRz3z2bphMMHFedYESANCgWwK-uoJehnnKZTvFYorJimXslAv_0z0GOXhrgU4WAI2xZyT67X1o7m7ZAnoB41B3zWnS3P6vrmieP1E8WD6L3blfuMHt_g_qKfvp0vFbzW0p6E
CitedBy_id crossref_primary_10_3390_ijms22168525
crossref_primary_10_3390_ijms231911418
crossref_primary_10_1007_s00702_019_01979_0
crossref_primary_10_1038_s41398_021_01539_9
crossref_primary_10_1002_mdc3_14191
crossref_primary_10_1016_j_apsb_2023_08_009
crossref_primary_10_1007_s12035_021_02375_0
crossref_primary_10_1016_j_inoche_2021_108582
crossref_primary_10_1016_j_neurobiolaging_2023_07_011
crossref_primary_10_3389_frsle_2023_1298854
crossref_primary_10_1016_j_molstruc_2024_140746
crossref_primary_10_1007_s13311_020_00963_x
crossref_primary_10_1093_brain_awad265
crossref_primary_10_1016_j_mhpa_2024_100582
crossref_primary_10_1007_s00415_019_09538_z
crossref_primary_10_1002_mds_29220
crossref_primary_10_3389_fnagi_2022_832768
crossref_primary_10_3233_JPD_230051
crossref_primary_10_3389_fcimb_2023_1296713
crossref_primary_10_1016_j_cpet_2020_12_002
crossref_primary_10_1007_s10517_019_04485_1
crossref_primary_10_1016_j_arr_2022_101759
crossref_primary_10_1016_j_jhazmat_2024_136793
crossref_primary_10_1111_ene_16158
crossref_primary_10_1038_s41572_021_00280_3
crossref_primary_10_1007_s00018_019_03298_9
crossref_primary_10_1016_j_nbd_2023_106254
crossref_primary_10_1111_cns_14655
crossref_primary_10_1038_s41598_023_37644_6
crossref_primary_10_1007_s10571_023_01320_0
crossref_primary_10_1016_j_biopha_2018_12_140
crossref_primary_10_1080_13813455_2018_1484771
crossref_primary_10_1016_j_ejphar_2025_177419
crossref_primary_10_1016_j_jagp_2019_03_002
crossref_primary_10_1016_j_yfrne_2020_100861
crossref_primary_10_1021_acs_jmedchem_8b00760
crossref_primary_10_1186_s41983_024_00813_z
crossref_primary_10_1053_j_semnuclmed_2018_07_006
crossref_primary_10_3233_JPD_181472
crossref_primary_10_1016_j_nbas_2023_100071
crossref_primary_10_1093_brain_awab156
Cites_doi 10.1001/archneurol.2012.764
10.1016/S1474-4422(16)30328-3
10.1007/s00213-002-1073-7
10.1126/scitranslmed.3007901
10.1002/ana.24859
10.1016/j.expneurol.2007.02.001
10.1212/WNL.42.9.1702
10.1212/WNL.0b013e3182698d4a
10.1016/S0165-1781(02)00136-1
10.1002/da.22584
10.1212/WNL.0000000000003840
10.1002/mds.25213
10.1016/bs.irn.2016.12.001
10.1517/13543784.7.10.1691
10.1097/00004647-199609000-00008
10.1212/WNL.0000000000004705
10.1038/s41598-017-04144-3
10.1016/j.neuropharm.2016.09.021
10.1016/j.jpsychires.2015.07.024
10.1016/j.jad.2008.11.020
10.1002/mds.26191
10.1002/acn3.246
10.1111/bpa.12069
10.1111/ane.12365
10.1126/scitranslmed.3008169
10.1007/s12031-015-0647-x
10.1074/jbc.M114.589069
10.1074/jbc.271.8.4188
10.1212/01.wnl.0000336340.89821.b3
10.1016/j.parkreldis.2016.04.015
10.1212/WNL.0b013e3182516244
10.1186/s13195-014-0052-7
10.1002/mds.26369
10.1016/j.nbd.2010.10.005
10.1038/nrneurol.2017.27
10.1073/pnas.1107411108
10.1534/genetics.104.032540
10.1038/sj.jcbfm.9600599
10.1176/appi.neuropsych.22.2.188
10.1016/j.pneurobio.2011.09.005
10.1016/j.nbd.2010.05.028
10.1002/ana.24969
10.1136/jnnp.55.3.181
10.1097/YIC.0b013e32834ace0f
10.3233/JAD-161135
10.1176/appi.ajp.2017.17040404
10.1212/WNL.0b013e3181c34b47
10.1111/j.1471-4159.2011.07459.x
ContentType Journal Article
Copyright 2018 American Neurological Association
2018 American Neurological Association.
Copyright_xml – notice: 2018 American Neurological Association
– notice: 2018 American Neurological Association.
DBID AAYXX
CITATION
NPM
7TK
7U7
C1K
K9.
7X8
5PM
DOI 10.1002/ana.25236
DatabaseName CrossRef
PubMed
Neurosciences Abstracts
Toxicology Abstracts
Environmental Sciences and Pollution Management
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
ProQuest Health & Medical Complete (Alumni)
Toxicology Abstracts
Neurosciences Abstracts
Environmental Sciences and Pollution Management
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
ProQuest Health & Medical Complete (Alumni)
PubMed

Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1531-8249
EndPage 1002
ExternalDocumentID PMC6021203
29665066
10_1002_ana_25236
ANA25236
Genre article
Journal Article
GrantInformation_xml – fundername: NINDS NIH HHS
  grantid: R56 NS082941
– fundername: CSRD VA
  grantid: IK2 CX001186
– fundername: NIA NIH HHS
  grantid: P30 AG053760
GroupedDBID ---
.3N
.55
.GA
.GJ
.Y3
05W
0R~
10A
1CY
1L6
1OB
1OC
1ZS
23M
2QL
31~
33P
3O-
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5VS
66C
6J9
6P2
6PF
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
AAEJM
AAESR
AAEVG
AAHHS
AAHQN
AAIPD
AAMNL
AANHP
AANLZ
AAONW
AAQQT
AASGY
AAWTL
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABIVO
ABJNI
ABLJU
ABOCM
ABPVW
ABQWH
ABXGK
ACAHQ
ACBMB
ACBWZ
ACCFJ
ACCZN
ACGFO
ACGFS
ACGOF
ACMXC
ACPOU
ACPRK
ACRPL
ACRZS
ACSCC
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEGXH
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFAZI
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFWVQ
AFZJQ
AHBTC
AHMBA
AI.
AIACR
AIAGR
AITYG
AIURR
AIWBW
AJBDE
AJJEV
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BY8
C45
CS3
D-6
D-7
D-E
D-F
DCZOG
DPXWK
DR1
DR2
DRFUL
DRMAN
DRSTM
EBS
EJD
EMOBN
F00
F01
F04
F5P
F8P
FEDTE
FUBAC
FYBCS
G-S
G.N
GNP
GODZA
GOZPB
GRPMH
H.X
HBH
HF~
HGLYW
HHY
HHZ
HVGLF
HZ~
IX1
J0M
J5H
JPC
KBYEO
KD1
KQQ
L7B
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LXL
LXN
LXY
LYRES
M6M
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N4W
N9A
NF~
NNB
O66
O9-
OHT
OIG
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
PQQKQ
Q.-
Q.N
Q11
QB0
QRW
R.K
RIWAO
RJQFR
ROL
RWD
RWI
RX1
SAMSI
SJN
SUPJJ
TEORI
UB1
V2E
V8K
V9Y
VH1
W8V
W99
WBKPD
WH7
WHWMO
WIB
WIH
WIJ
WIK
WJL
WOHZO
WQJ
WRC
WUP
WVDHM
WXI
WXSBR
X7M
XG1
XJT
XPP
XSW
XV2
YOC
YQJ
ZGI
ZRF
ZRR
ZXP
ZZTAW
~IA
~WT
~X8
AAYXX
AEYWJ
AGHNM
AGQPQ
AGYGG
CITATION
NPM
7TK
7U7
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
C1K
K9.
7X8
5PM
ID FETCH-LOGICAL-c4436-cecb39f245fd128772c9e5683c70a0705d1400626f5b98b38ba3d0379f7bac643
IEDL.DBID DR2
ISSN 0364-5134
1531-8249
IngestDate Thu Aug 21 18:19:47 EDT 2025
Fri Jul 11 04:45:10 EDT 2025
Fri Jul 25 12:24:05 EDT 2025
Thu Apr 03 07:02:00 EDT 2025
Tue Jul 01 02:24:10 EDT 2025
Thu Apr 24 23:04:16 EDT 2025
Wed Jan 22 17:02:04 EST 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Language English
License 2018 American Neurological Association.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4436-cecb39f245fd128772c9e5683c70a0705d1400626f5b98b38ba3d0379f7bac643
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.25236
PMID 29665066
PQID 2059483588
PQPubID 946345
PageCount 9
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_6021203
proquest_miscellaneous_2027069087
proquest_journals_2059483588
pubmed_primary_29665066
crossref_citationtrail_10_1002_ana_25236
crossref_primary_10_1002_ana_25236
wiley_primary_10_1002_ana_25236_ANA25236
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate May 2018
2018-05-00
20180501
PublicationDateYYYYMMDD 2018-05-01
PublicationDate_xml – month: 05
  year: 2018
  text: May 2018
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Minneapolis
PublicationTitle Annals of neurology
PublicationTitleAlternate Ann Neurol
PublicationYear 2018
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 2015; 2
2017; 7
2012; 120
2013; 28
2017; 82
2011; 2
2017; 81
2007; 205
2017; 88
2015; 30
2002; 111
2017; 89
2016; 31
2014; 24
2013; 70
2017; 132
2012; 79
1992; 55
1996; 16
2017; 113
2012; 78
2016; 58
2010; 40
2009; 117
2018; 175
2010; 22
2015; 69
2011; 108
2009; 73
2017; 59
2002; 162
2009; 72
2017; 16
2005; 169
2017; 13
2011; 95
2015; 131
2008; 28
2017; 34
1996; 271
2011; 41
2011; 26
2012; 69
1998; 7
1992; 42
2016; 27
2014; 6
2014; 289
e_1_2_8_28_1
e_1_2_8_24_1
e_1_2_8_47_1
e_1_2_8_26_1
e_1_2_8_49_1
e_1_2_8_3_1
e_1_2_8_5_1
e_1_2_8_7_1
e_1_2_8_9_1
Kang JH (e_1_2_8_27_1) 2013; 70
e_1_2_8_20_1
e_1_2_8_43_1
e_1_2_8_22_1
e_1_2_8_45_1
e_1_2_8_41_1
e_1_2_8_17_1
e_1_2_8_19_1
e_1_2_8_13_1
e_1_2_8_36_1
e_1_2_8_15_1
e_1_2_8_38_1
e_1_2_8_32_1
e_1_2_8_11_1
e_1_2_8_34_1
e_1_2_8_51_1
e_1_2_8_30_1
e_1_2_8_29_1
e_1_2_8_25_1
e_1_2_8_48_1
e_1_2_8_2_1
e_1_2_8_4_1
e_1_2_8_6_1
e_1_2_8_8_1
e_1_2_8_21_1
e_1_2_8_42_1
e_1_2_8_23_1
e_1_2_8_44_1
e_1_2_8_40_1
e_1_2_8_18_1
e_1_2_8_39_1
Hajian‐Tilaki K (e_1_2_8_46_1) 2011; 2
e_1_2_8_14_1
e_1_2_8_35_1
e_1_2_8_16_1
e_1_2_8_37_1
e_1_2_8_10_1
e_1_2_8_31_1
e_1_2_8_12_1
e_1_2_8_33_1
e_1_2_8_50_1
References_xml – volume: 16
  start-page: 834
  year: 1996
  end-page: 840
  article-title: Distribution volume ratios without blood sampling from graphical analysis of PET data
  publication-title: J Cereb Blood Flow Metab
– volume: 2
  start-page: 949
  year: 2015
  end-page: 959
  article-title: Dopaminergic, serotonergic, and noradrenergic deficits in Parkinson disease
  publication-title: Ann Clin Transl Neurol
– volume: 7
  start-page: 4983
  year: 2017
  article-title: A tricyclic antidepressant, amoxapine, reduces amyloid‐β generation through multiple serotonin receptor 6‐mediated targets
  publication-title: Sci Rep
– volume: 81
  start-page: 171
  year: 2017
  end-page: 180
  article-title: Serotonin transporter in Parkinson's disease: a meta‐analysis of positron emission tomography studies
  publication-title: Ann Neurol
– volume: 6
  start-page: 226ra30
  year: 2014
  article-title: Longitudinal change in CSF biomarkers in autosomal‐dominant Alzheimer's disease
  publication-title: Sci Transl Med
– volume: 31
  start-page: 111
  year: 2016
  end-page: 117
  article-title: Striatal and cortical β‐amyloidopathy and cognition in Parkinson's disease
  publication-title: Mov Disord
– volume: 82
  start-page: 128
  year: 2017
  end-page: 132
  article-title: Decreased plasma β‐amyloid in the Alzheimer's disease APP A673T variant carriers
  publication-title: Ann Neurol
– volume: 6
  start-page: 236re4
  year: 2014
  article-title: An antidepressant decreases CSF Aβ production in healthy individuals and in transgenic AD mice
  publication-title: Sci Transl Med
– volume: 113
  start-page: 89
  issue: pt A
  year: 2017
  end-page: 99
  article-title: The antidepressant bupropion is a negative allosteric modulator of serotonin type 3A receptors
  publication-title: Neuropharmacology
– volume: 69
  start-page: 35
  year: 2015
  end-page: 41
  article-title: Plasma and cerebrospinal fluid amyloid‐β levels in late‐life depression: a systematic review and meta‐analysis
  publication-title: J Psychiatr Res
– volume: 205
  start-page: 325
  year: 2007
  end-page: 329
  article-title: 5‐HT4 receptor and Alzheimer's disease: the amyloid connection
  publication-title: Exp Neurol
– volume: 59
  start-page: 1439
  year: 2017
  end-page: 1448
  article-title: Severity of depression impacts imminent conversion from mild cognitive impairment to Alzheimer's disease
  publication-title: J Alzheimers Dis
– volume: 24
  start-page: 18
  year: 2014
  end-page: 24
  article-title: St. John's wort reduces beta‐amyloid accumulation in a double transgenic Alzheimer's disease mouse model‐role of P‐glycoprotein
  publication-title: Brain Pathol
– volume: 22
  start-page: 188
  year: 2010
  end-page: 195
  article-title: The impact of antidepressant treatment on cognitive functioning in depressed patients with Parkinson's disease
  publication-title: J Neuropsychiatry Clin Neurosci
– volume: 79
  start-page: 1161
  year: 2012
  end-page: 1167
  article-title: Aβ‐amyloid deposition in patients with Parkinson disease at risk for development of dementia
  publication-title: Neurology
– volume: 27
  start-page: 85
  year: 2016
  end-page: 88
  article-title: Use of antidepressants in Parkinson's disease: a Swedish register‐based study of over 1.5 million older people
  publication-title: Parkinsonism Relat Disord
– volume: 28
  start-page: 296
  year: 2013
  end-page: 301
  article-title: β‐Amyloid and postural instability and gait difficulty in Parkinson's disease at risk for dementia
  publication-title: Mov Disord
– volume: 13
  start-page: 217
  year: 2017
  end-page: 231
  article-title: Cognitive decline in Parkinson disease
  publication-title: Nat Rev Neurol
– volume: 6
  start-page: 52
  year: 2014
  article-title: Striatal and extrastriatal dopamine transporter levels relate to cognition in Lewy body diseases: an (11)C altropane positron emission tomography study
  publication-title: Alzheimers Res Ther
– volume: 41
  start-page: 377
  year: 2011
  end-page: 384
  article-title: Striatal Aβ peptide deposition mirrors dementia and differentiates DLB and PDD from other parkinsonian syndromes
  publication-title: Neurobiol Dis
– volume: 120
  start-page: 46
  issue: suppl 1
  year: 2012
  end-page: 54
  article-title: Activation of α‐secretase cleavage
  publication-title: J Neurochem
– volume: 132
  start-page: 275
  year: 2017
  end-page: 294
  article-title: Cerebrospinal fluid biomarkers of cognitive decline in Parkinson's disease
  publication-title: Int Rev Neurobiol
– volume: 28
  start-page: 441
  year: 2008
  end-page: 444
  article-title: Spared caudal brainstem SERT binding in early Parkinson's disease
  publication-title: J Cereb Blood Flow Metab
– volume: 89
  start-page: 2335
  year: 2017
  end-page: 2340
  article-title: SNPs in Aβ clearance proteins: lower CSF Aβ levels and earlier onset of dementia in PD
  publication-title: Neurology
– volume: 131
  start-page: 275
  year: 2015
  end-page: 281
  article-title: Cognitive performances and DAT imaging in early Parkinson's disease with mild cognitive impairment: a preliminary study
  publication-title: Acta Neurol Scand
– volume: 169
  start-page: 1425
  year: 2005
  end-page: 1436
  article-title: Serotonin (5HT), fluoxetine, imipramine and dopamine target distinct 5HT receptor signaling to modulate Caenorhabditis elegans egg‐laying behavior
  publication-title: Genetics
– volume: 40
  start-page: 216
  year: 2010
  end-page: 221
  article-title: Staging of serotonergic dysfunction in Parkinson's disease: an in vivo 11C‐DASB PET study
  publication-title: Neurobiol Dis
– volume: 162
  start-page: 193
  year: 2002
  end-page: 202
  article-title: In vitro receptor screening of pure constituents of St. John's wort reveals novel interactions with a number of GPCRs
  publication-title: Psychopharmacology
– volume: 42
  start-page: 1702
  year: 1992
  end-page: 1706
  article-title: Kynurenine pathway abnormalities in Parkinson's disease
  publication-title: Neurology
– volume: 70
  start-page: 1277
  year: 2013
  end-page: 1287
  article-title: Association of cerebrospinal fluid β‐amyloid 1‐42, T‐tau, P‐tau181, and α‐synuclein levels with clinical features of drug‐naive patients with early Parkinson disease
  publication-title: JAMA Neurol
– volume: 175
  start-page: 232
  year: 2018
  end-page: 241
  article-title: Impact of SSRI therapy on risk of conversion from mild cognitive impairment to Alzheimer's dementia in individuals with previous depression
  publication-title: Am J Psychiatry
– volume: 34
  start-page: 217
  year: 2017
  end-page: 226
  article-title: The association of antidepressant drug usage with cognitive impairment or dementia, including Alzheimer disease: a systematic review and meta‐analysis
  publication-title: Depress Anxiety
– volume: 108
  start-page: 14968
  year: 2011
  end-page: 14973
  article-title: Serotonin signaling is associated with lower amyloid‐β levels and plaques in transgenic mice and humans
  publication-title: Proc Natl Acad Sci U S A
– volume: 16
  start-page: 66
  year: 2017
  end-page: 75
  article-title: Clinical variables and biomarkers in prediction of cognitive impairment in patients with newly diagnosed Parkinson's disease: a cohort study
  publication-title: Lancet Neurol
– volume: 69
  start-page: 1628
  year: 2012
  end-page: 1631
  article-title: Cerebral amyloid deposition and serotoninergic innervation in Parkinson disease
  publication-title: Arch Neurol
– volume: 7
  start-page: 1691
  year: 1998
  end-page: 1699
  article-title: Duloxetine (LY 248686): an inhibitor of serotonin and noradrenaline uptake and an antidepressant drug candidate
  publication-title: Expert Opin Investig Drugs
– volume: 95
  start-page: 629
  year: 2011
  end-page: 635
  article-title: The Parkinson Progression Marker Initiative (PPMI)
  publication-title: Prog Neurobiol
– volume: 72
  start-page: 886
  year: 2009
  end-page: 892
  article-title: A controlled trial of antidepressants in patients with Parkinson disease and depression
  publication-title: Neurology
– volume: 88
  start-page: 1501
  year: 2017
  end-page: 1511
  article-title: Decrease in Aβ42 predicts dopa‐resistant gait progression in early Parkinson disease
  publication-title: Neurology
– volume: 58
  start-page: 88
  year: 2016
  end-page: 92
  article-title: CSF β‐amyloid 1‐42 predicts progression to cognitive impairment in newly diagnosed parkinson disease
  publication-title: J Mol Neurosci
– volume: 111
  start-page: 117
  year: 2002
  end-page: 124
  article-title: Interaction of lithium with 5‐HT(1B) receptors in depressed unipolar patients treated with clomipramine and lithium versus clomipramine and placebo: preliminary results
  publication-title: Psychiatry Res
– volume: 289
  start-page: 30990
  year: 2014
  end-page: 31000
  article-title: Molecular mechanisms of Alzheimer disease protection by the A673T allele of amyloid precursor protein
  publication-title: J Biol Chem
– volume: 55
  start-page: 181
  year: 1992
  end-page: 184
  article-title: Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico‐pathological study of 100 cases
  publication-title: J Neurol Neurosurg Psychiatry
– volume: 26
  start-page: 316
  year: 2011
  end-page: 322
  article-title: Do continued antidepressants protect against dementia in patients with severe depressive disorder?
  publication-title: Int Clin Psychopharmacol
– volume: 117
  start-page: 24
  year: 2009
  end-page: 29
  article-title: Antidepressants and dementia
  publication-title: J Affect Disord
– volume: 78
  start-page: 1229
  year: 2012
  end-page: 1236
  article-title: A randomized, double‐blind, placebo‐controlled trial of antidepressants in Parkinson disease
  publication-title: Neurology
– volume: 2
  start-page: 289
  year: 2011
  end-page: 298
  article-title: Sample size estimation in epidemiologic studies
  publication-title: Caspian J Intern Med
– volume: 30
  start-page: 928
  year: 2015
  end-page: 935
  article-title: Amyloid deposition in Parkinson's disease and cognitive impairment: a systematic review
  publication-title: Mov Disord
– volume: 73
  start-page: 1738
  year: 2009
  end-page: 1745
  article-title: Validity of the MoCA and MMSE in the detection of MCI and dementia in Parkinson disease
  publication-title: Neurology
– volume: 271
  start-page: 4188
  year: 1996
  end-page: 4194
  article-title: Serotonin 5‐HT2a and 5‐HT2c receptors stimulate amyloid precursor protein ectodomain secretion
  publication-title: J Biol Chem
– ident: e_1_2_8_19_1
  doi: 10.1001/archneurol.2012.764
– ident: e_1_2_8_34_1
  doi: 10.1016/S1474-4422(16)30328-3
– ident: e_1_2_8_26_1
  doi: 10.1007/s00213-002-1073-7
– ident: e_1_2_8_42_1
  doi: 10.1126/scitranslmed.3007901
– ident: e_1_2_8_11_1
  doi: 10.1002/ana.24859
– ident: e_1_2_8_17_1
  doi: 10.1016/j.expneurol.2007.02.001
– ident: e_1_2_8_36_1
  doi: 10.1212/WNL.42.9.1702
– ident: e_1_2_8_3_1
  doi: 10.1212/WNL.0b013e3182698d4a
– ident: e_1_2_8_25_1
  doi: 10.1016/S0165-1781(02)00136-1
– ident: e_1_2_8_51_1
  doi: 10.1002/da.22584
– ident: e_1_2_8_4_1
  doi: 10.1212/WNL.0000000000003840
– ident: e_1_2_8_5_1
  doi: 10.1002/mds.25213
– ident: e_1_2_8_9_1
  doi: 10.1016/bs.irn.2016.12.001
– ident: e_1_2_8_23_1
  doi: 10.1517/13543784.7.10.1691
– ident: e_1_2_8_21_1
  doi: 10.1097/00004647-199609000-00008
– ident: e_1_2_8_8_1
  doi: 10.1212/WNL.0000000000004705
– ident: e_1_2_8_18_1
  doi: 10.1038/s41598-017-04144-3
– volume: 2
  start-page: 289
  year: 2011
  ident: e_1_2_8_46_1
  article-title: Sample size estimation in epidemiologic studies
  publication-title: Caspian J Intern Med
– ident: e_1_2_8_24_1
  doi: 10.1016/j.neuropharm.2016.09.021
– ident: e_1_2_8_29_1
  doi: 10.1016/j.jpsychires.2015.07.024
– ident: e_1_2_8_45_1
  doi: 10.1016/j.jad.2008.11.020
– ident: e_1_2_8_6_1
  doi: 10.1002/mds.26191
– ident: e_1_2_8_35_1
  doi: 10.1002/acn3.246
– ident: e_1_2_8_14_1
  doi: 10.1111/bpa.12069
– ident: e_1_2_8_32_1
  doi: 10.1111/ane.12365
– ident: e_1_2_8_13_1
  doi: 10.1126/scitranslmed.3008169
– ident: e_1_2_8_7_1
  doi: 10.1007/s12031-015-0647-x
– ident: e_1_2_8_40_1
  doi: 10.1074/jbc.M114.589069
– ident: e_1_2_8_15_1
  doi: 10.1074/jbc.271.8.4188
– ident: e_1_2_8_48_1
  doi: 10.1212/01.wnl.0000336340.89821.b3
– ident: e_1_2_8_47_1
  doi: 10.1016/j.parkreldis.2016.04.015
– ident: e_1_2_8_49_1
  doi: 10.1212/WNL.0b013e3182516244
– ident: e_1_2_8_33_1
  doi: 10.1186/s13195-014-0052-7
– ident: e_1_2_8_39_1
  doi: 10.1002/mds.26369
– ident: e_1_2_8_38_1
  doi: 10.1016/j.nbd.2010.10.005
– volume: 70
  start-page: 1277
  year: 2013
  ident: e_1_2_8_27_1
  article-title: Association of cerebrospinal fluid β‐amyloid 1‐42, T‐tau, P‐tau181, and α‐synuclein levels with clinical features of drug‐naive patients with early Parkinson disease
  publication-title: JAMA Neurol
– ident: e_1_2_8_2_1
  doi: 10.1038/nrneurol.2017.27
– ident: e_1_2_8_12_1
  doi: 10.1073/pnas.1107411108
– ident: e_1_2_8_22_1
  doi: 10.1534/genetics.104.032540
– ident: e_1_2_8_10_1
  doi: 10.1038/sj.jcbfm.9600599
– ident: e_1_2_8_50_1
  doi: 10.1176/appi.neuropsych.22.2.188
– ident: e_1_2_8_31_1
  doi: 10.1016/j.pneurobio.2011.09.005
– ident: e_1_2_8_37_1
  doi: 10.1016/j.nbd.2010.05.028
– ident: e_1_2_8_41_1
  doi: 10.1002/ana.24969
– ident: e_1_2_8_20_1
  doi: 10.1136/jnnp.55.3.181
– ident: e_1_2_8_44_1
  doi: 10.1097/YIC.0b013e32834ace0f
– ident: e_1_2_8_28_1
  doi: 10.3233/JAD-161135
– ident: e_1_2_8_43_1
  doi: 10.1176/appi.ajp.2017.17040404
– ident: e_1_2_8_30_1
  doi: 10.1212/WNL.0b013e3181c34b47
– ident: e_1_2_8_16_1
  doi: 10.1111/j.1471-4159.2011.07459.x
SSID ssj0009610
Score 2.4696841
Snippet Objective 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)...
SourceID pubmedcentral
proquest
pubmed
crossref
wiley
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 994
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fana.25236
https://www.ncbi.nlm.nih.gov/pubmed/29665066
https://www.proquest.com/docview/2059483588
https://www.proquest.com/docview/2027069087
https://pubmed.ncbi.nlm.nih.gov/PMC6021203
Volume 83
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NTtwwEB4hDohLy09pw58C6qEHsmTtOHbEaYVACAkOqEgckCL_RV3Requye-mpj8Cz8CA8BE_C2PmBBSohbpE8URyPx_7GM_MZ4CtlNk-JJIk2lUkynYpE4j6QCJtJgfihMsIXOJ-c5kfn2fEFu5iBvbYWpuaH6A7cvGWE9dobuFTXu4-kodLJHkE3ytNt-1wtD4jOHqmjijwwEfgwW8L6NGtZhVKy2705vRe9AJgv8ySf4tewAR1-hMu263XeyVVvMlY9_fcZq-M7_20BPjTANB7UM2kRZqxbgrmTJvS-DHu4qozG_vB2J767vf93I3-hrz80O7F0Jm6ykEYuHrrYV1KHorK4Cf98gvPDg-_7R0lz80Kis4zmibZa0aIiGasMbmCIwHVhWS6o5qnERYIZ9MtS9IUqpgqhqFCSmpTyouJKagQ5KzDrRs5-gbifc44okplcoTNGpSBKUS6lVhaxmUgj-NbqoNQNLbm_HeNnWRMqkxIHowyDEcF2J_q75uJ4TWi9VWTZmON1SQIrDWVCRLDVNaMh-eiIdHY08TKEe9pmwSP4XOu9-wpBp5AhOIuAT82ITsCTdE-3uOGPQNadew79lOJvBoX_v-Pl4HQQHlbfLroG8wjgRJ2AuQ6z4z8Tu4Egaaw2gzU8APa5DYE
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NbtQwEB61RaJcoAUKgZYGxIFDs03t-CeCywqoFujuAbVSLyjyX9QV4EWwe-HEI_AsPAgPwZMwdn7KUpAQt0ieKI7HY3_jmfkM8JAyx3OiSGZsbbPC5DJTuA9k0hVKIn6orQwFzuMJH50UL0_Z6Qo86WphGn6I_sAtWEZcr4OBhwPp_XPWUOXVgKAfxVfhUrjROzDnP3t9Th5V8shFEAJtGTugRccrlJP9_tXl3egCxLyYKfkrgo1b0OE1eNN1vsk8eTtYzPXAfP6N1_F__24DrrbYNB02k2kTVpy_DpfHbfT9BjzGhWU2D-e3e-n3bz--fFXv0d2f2r1UeZu2iUgzn059GoqpY11Z2kaAbsLJ4fPjp6OsvXwhM0VBeWac0bSsScFqi3sYgnBTOsYlNSJXuE4wi65Zju5QzXQpNZVaUZtTUdZCK4M4ZwvW_My725AecCEQSDLLNfpjVEmiNRVKGe0Qnsk8gUedEirTMpOHCzLeVQ2nMqlwMKo4GAk86EU_NHQcfxLa7jRZtRb5qSKRmIYyKRO43zejLYUAifJutggyRATmZikSuNUovv8KQb-QIT5LQCxNiV4g8HQvt_jpWeTr5oFGP6f4m1Hjf-94NZwM48OdfxfdhfXR8fioOnoxeXUXriCek00-5jaszT8u3A5iprm-F03jJ72fEZ0
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3JbhQxEC2FIEVc2AkNARrEgUN64tjtpZXTiDAKS0YIESkHpJa3FiPAE8HMhROfwLfwIXwEX0LZvYQhICFuLbla7Xa57FeuqmeAh4x7QaimhXWNK0pLVKFxHyiUL7VC_NA4FQucD6fi4Kh8dsyP12Cvr4Vp-SGGA7doGWm9jgZ-4pqdU9JQHfSIohslzsH5UpAq3tuw_-qUO6oSiYogxtkKvsvKnlaI0J3h1dXN6AzCPJso-SuATTvQ5BK86fveJp68Gy0XZmQ__0br-J8_dxkudsg0H7dT6Qqs-XAVNg672Ps12MNlZb6Ip7fb-fdvP7581R_Q2Z-57VwHl3dpSPOQz0IeS6lTVVnexX-uw9HkyevHB0V39UJhy5KJwnprWNXQkjcOdzCE4LbyXChmJdG4SnCHjhlBZ6jhplKGKaOZI0xWjTTaIsq5AethHvxNyHeFlAgjuRMGvTGmFTWGSa2t8QjOFMngUa-D2na85PF6jPd1y6hMaxyMOg1GBg8G0ZOWjONPQlu9IuvOHj_VNNHSMK5UBveHZrSkGB7Rwc-XUYbKyNusZAabrd6Hr1D0CjmiswzkyowYBCJL92pLmL1NbN0ikugThr-ZFP73jtfj6Tg93Pp30Xuw8XJ_Ur94On1-Gy4gmFNtMuYWrC8-Lv0dBEwLczcZxk-CGBBM
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Serotonin%2C+beta-amyloid%2C+and+cognition+in+Parkinson+disease&rft.jtitle=Annals+of+neurology&rft.au=Kotagal%2C+Vikas&rft.au=Spino%2C+Cathie&rft.au=Bohnen%2C+Nicolaas+I&rft.au=Koeppe%2C+Robert+A.&rft.date=2018-05-01&rft.issn=0364-5134&rft.eissn=1531-8249&rft.volume=83&rft.issue=5&rft.spage=994&rft.epage=1002&rft_id=info:doi/10.1002%2Fana.25236&rft_id=info%3Apmid%2F29665066&rft.externalDocID=PMC6021203
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0364-5134&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0364-5134&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0364-5134&client=summon