Reduced cerebrospinal fluid concentration of interleukin-12/23 subunit p40 in patients with cognitive impairment

The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples. Consecutive patients with AD (n = 30), stable mild cognitive impai...

Full description

Saved in:
Bibliographic Details
Published inPloS one Vol. 12; no. 5; p. e0176760
Main Authors Johansson, Per, Almqvist, Erik G., Wallin, Anders, Johansson, Jan-Ove, Andreasson, Ulf, Blennow, Kaj, Zetterberg, Henrik, Svensson, Johan
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 02.05.2017
Public Library of Science (PLoS)
Subjects
Hip
Online AccessGet full text

Cover

Loading…
Abstract The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples. Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel. After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid1-42 (Aβ1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01). Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
AbstractList The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples.BACKGROUNDThe role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples.Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel.METHODSConsecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel.After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid1-42 (Aβ1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01).RESULTSAfter correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid1-42 (Aβ1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01).Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.CONCLUSIONSMost cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples. Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel. After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of [beta]-amyloid.sub.1-42 (A[beta].sub.1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01). Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
Background The role of inflammation in Alzheimer’s disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples. Methods Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel. Results After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid 1-42 (Aβ 1–42 ) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01). Conclusions Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
Background The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples. Methods Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel. Results After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of [beta]-amyloid.sub.1-42 (A[beta].sub.1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01). Conclusions Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
BackgroundThe role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples.MethodsConsecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel.ResultsAfter correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid1-42 (Aβ1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01).ConclusionsMost cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
Background The role of inflammation in Alzheimer’s disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples. Methods Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel. Results After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid1-42 (Aβ1–42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01). Conclusions Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples. Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel. After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid1-42 (Aβ1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01). Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines and chemokines in paired serum and cerebrospinal fluid (CSF) samples.Consecutive patients with AD (n = 30), stable mild cognitive impairment (SMCI, n = 11), other dementias (n = 11), and healthy controls (n = 18) were included. None of the subjects was treated with glucocorticoids, cholinesterase inhibitors, or non-steroidal anti-inflammatory drugs. Serum and CSF concentrations of interleukin-6 (IL-6), IL-8, IL-12/23 p40, IL-15, IL-16, vascular endothelial growth factor-A (VEGF-A), and three chemokines were measured using a multiplex panel.After correction for multiple comparisons, only CSF IL-12/23 p40 concentration differed significantly between the total patient group (n = 52) and controls (n = 18; p = 0.002). Further analyses showed that CSF IL-12/23 p40 concentration was decreased in all patient subgroups (AD, other dementias, and SMCI) compared to healthy controls (p < 0.01, p < 0.05, and p < 0.05, respectively). In the total study population (n = 70), CSF IL-12/23 p40 concentrations correlated positively with CSF concentrations of β-amyloid1-42 (Aβ1-42) and phosphorylated tau protein (P-tau) whereas in AD patients (n = 30), CSF IL-12/23 p40 only correlated positively with CSF P-Tau (r = 0.46, p = 0.01).Most cytokines and chemokines were similar in patients and controls, but CSF IL-12/23 subunit p40 concentration was decreased in patients with cognitive impairment, and correlated with markers of AD disease status. Further studies are needed to evaluate the role of CSF IL-12/23 p40 in other dementias and SMCI.
Audience Academic
Author Johansson, Jan-Ove
Andreasson, Ulf
Svensson, Johan
Blennow, Kaj
Zetterberg, Henrik
Almqvist, Erik G.
Johansson, Per
Wallin, Anders
AuthorAffiliation 1 Department of Neuropsychiatry, Skaraborg Central Hospital, Falköping, Sweden
Nathan S Kline Institute, UNITED STATES
2 Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
3 Department of Endocrinology, Skaraborg Central Hospital, Skövde, Sweden
5 UCL Institute of Neurology, Queen Square, London, United Kingdom
4 Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden
AuthorAffiliation_xml – name: 1 Department of Neuropsychiatry, Skaraborg Central Hospital, Falköping, Sweden
– name: Nathan S Kline Institute, UNITED STATES
– name: 2 Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
– name: 4 Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden
– name: 5 UCL Institute of Neurology, Queen Square, London, United Kingdom
– name: 3 Department of Endocrinology, Skaraborg Central Hospital, Skövde, Sweden
Author_xml – sequence: 1
  givenname: Per
  surname: Johansson
  fullname: Johansson, Per
– sequence: 2
  givenname: Erik G.
  surname: Almqvist
  fullname: Almqvist, Erik G.
– sequence: 3
  givenname: Anders
  surname: Wallin
  fullname: Wallin, Anders
– sequence: 4
  givenname: Jan-Ove
  surname: Johansson
  fullname: Johansson, Jan-Ove
– sequence: 5
  givenname: Ulf
  surname: Andreasson
  fullname: Andreasson, Ulf
– sequence: 6
  givenname: Kaj
  surname: Blennow
  fullname: Blennow, Kaj
– sequence: 7
  givenname: Henrik
  surname: Zetterberg
  fullname: Zetterberg, Henrik
– sequence: 8
  givenname: Johan
  orcidid: 0000-0002-4487-6405
  surname: Svensson
  fullname: Svensson, Johan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28464009$$D View this record in MEDLINE/PubMed
https://gup.ub.gu.se/publication/253387$$DView record from Swedish Publication Index
BookMark eNqNk1tr3DAQhU1JaS7tPyitoVDaB29kS_KlD4UQelkIBNLQVyHLY69Sr-VIVtL--45jJ6xDKMUPNjPfOZIPM4fBXmc6CILXMVnFNIuPr4y3nWxXPZZXJM7SLCXPgoO4oEmUJoTu7XzvB4fOXRHCaZ6mL4L9JGcpI6Q4CPoLqLyCKlRgobTG9RpNw7r1GmumU9ANVg7adKGpQ90NYFvwv3QXxclxQkPnS9_pIewZwW7YI4oKF97qYYP6Bnv6BkK97aW2W2y9DJ7XsnXwan4fBZdfv1yefo_Ozr-tT0_OIpVRMkSclTRLS04TRmrFE8gqnleQJSVhRcEzorK8rCte5CpnPOY8y6EoUFEwlgKhR8HbybZvjRNzVk7EecHyGAUjsZ6Iysgr0Vu9lfaPMFKLu4KxjZB20KoFEZOCECJVkuac8TFExhSlNSSUlKUs0CuavNwt9L5cuDW-F1hqvHAgEk5pniH_eb6dL7dQTSG3C9my0-mNaMyN4CymhI-X_zAbWHPtwQ1iq52CtpUdGD_9Z4Ezwcez3j1Cn05jphqJP6y72uC5ajQVJ-iE80VIitTqCQqfCrYapwVqjfWF4ONCgMwAv4dGeufE-sfF_7PnP5fs-x12A7IdNs60fhxUtwTf7Cb9EPH9BiDAJkDh8DsL9QMSEzEu2n1cYlw0MS8ayj49kik93O0JJqLbf4v_AqhXLRQ
CitedBy_id crossref_primary_10_1016_j_bbih_2020_100077
crossref_primary_10_1186_s12951_023_01793_7
crossref_primary_10_1016_j_exger_2022_111933
crossref_primary_10_3233_JAD_170887
crossref_primary_10_3389_fninf_2024_1348113
crossref_primary_10_1590_1980_5764_dn_2023_0027
crossref_primary_10_1038_s44400_024_00001_z
crossref_primary_10_1212_WNL_0000000000006082
crossref_primary_10_1002_alz_12342
crossref_primary_10_1002_alz_12651
crossref_primary_10_3389_fneur_2021_639353
crossref_primary_10_1038_s41598_017_14020_9
crossref_primary_10_1016_j_arr_2023_102037
crossref_primary_10_3389_fimmu_2018_00586
crossref_primary_10_3389_fneur_2018_01123
crossref_primary_10_3389_fnins_2018_00694
Cites_doi 10.1177/1533317514542644
10.1016/j.jns.2006.05.063
10.1007/BF02815140
10.1016/j.jalz.2016.02.010
10.1212/01.wnl.0000311269.57716.63
10.3233/JAD-2011-101878
10.1038/nri1001
10.1093/gerona/gls187
10.1001/archneur.63.4.538
10.1523/JNEUROSCI.4361-12.2013
10.1016/S0197-0186(99)00031-5
10.1096/fj.09-141754
10.1017/S1041610211000810
10.1159/000089137
10.1016/S0304-3940(00)01036-3
10.1016/S0197-4580(01)00285-8
10.1016/j.imlet.2007.09.002
10.1016/j.jneuroim.2014.03.013
10.1007/s11910-015-0531-7
10.1016/j.neulet.2013.06.031
10.1016/S0165-5728(00)00285-X
10.1212/WNL.34.7.939
10.1186/1471-2318-5-2
10.1007/s10072-006-0562-6
10.1038/nm.2965
10.1016/j.neulet.2005.03.051
10.1002/eji.200737772
10.1007/s00415-008-0737-6
10.1159/000329568
10.1212/WNL.43.2.250
10.1177/1533317512467680
10.1016/j.jneuroim.2014.06.026
10.1159/000161560
10.3109/13506120009146438
10.1159/000322092
10.1523/JNEUROSCI.23-20-07504.2003
10.1016/j.jneuroim.2013.01.002
10.1111/j.1468-1331.2006.01637.x
10.1016/j.biopsych.2010.06.012
10.1016/j.cytogfr.2014.07.017
10.1021/acschemneuro.5b00265
10.1371/journal.pone.0062679
10.1371/journal.pone.0030525
10.3233/JAD-141506
10.1016/j.neurobiolaging.2015.10.021
10.1177/0891988706286226
10.1111/j.1365-2796.2004.01388.x
10.1186/1471-2377-11-51
10.3233/JAD-131148
10.1016/j.jneuroim.2007.10.020
ContentType Journal Article
Copyright COPYRIGHT 2017 Public Library of Science
2017 Johansson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2017 Johansson et al 2017 Johansson et al
Copyright_xml – notice: COPYRIGHT 2017 Public Library of Science
– notice: 2017 Johansson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2017 Johansson et al 2017 Johansson et al
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
IOV
ISR
3V.
7QG
7QL
7QO
7RV
7SN
7SS
7T5
7TG
7TM
7U9
7X2
7X7
7XB
88E
8AO
8C1
8FD
8FE
8FG
8FH
8FI
8FJ
8FK
ABJCF
ABUWG
AEUYN
AFKRA
ARAPS
ATCPS
AZQEC
BBNVY
BENPR
BGLVJ
BHPHI
C1K
CCPQU
D1I
DWQXO
FR3
FYUFA
GHDGH
GNUQQ
H94
HCIFZ
K9.
KB.
KB0
KL.
L6V
LK8
M0K
M0S
M1P
M7N
M7P
M7S
NAPCQ
P5Z
P62
P64
PATMY
PDBOC
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
PTHSS
PYCSY
RC3
7X8
5PM
ADTPV
AOWAS
F1U
DOA
DOI 10.1371/journal.pone.0176760
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Gale In Context: Opposing Viewpoints
Gale In Context: Science
ProQuest Central (Corporate)
Animal Behavior Abstracts
Bacteriology Abstracts (Microbiology B)
Biotechnology Research Abstracts
Nursing & Allied Health Database
Ecology Abstracts
Entomology Abstracts (Full archive)
Immunology Abstracts
Meteorological & Geoastrophysical Abstracts
Nucleic Acids Abstracts
Virology and AIDS Abstracts
Agricultural Science Collection
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
ProQuest Pharma Collection
Public Health Database
Technology Research Database
ProQuest SciTech Collection
ProQuest Technology Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
Materials Science & Engineering Collection
ProQuest Central (Alumni)
ProQuest One Sustainability
ProQuest Central UK/Ireland
Advanced Technologies & Aerospace Collection
Agricultural & Environmental Science Collection
ProQuest Central Essentials
Biological Science Collection
ProQuest Central (New)
Technology Collection
Natural Science Collection
Environmental Sciences and Pollution Management
ProQuest One Community College
ProQuest Materials Science Collection
ProQuest Central
Engineering Research Database
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
AIDS and Cancer Research Abstracts
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
Materials Science Database
Nursing & Allied Health Database (Alumni Edition)
Meteorological & Geoastrophysical Abstracts - Academic
ProQuest Engineering Collection
ProQuest Biological Science Collection
Agricultural Science Database
ProQuest Health & Medical Collection
PML(ProQuest Medical Library)
Algology Mycology and Protozoology Abstracts (Microbiology C)
Biological Science Database
Engineering Database
Nursing & Allied Health Premium
ProQuest advanced technologies & aerospace journals
ProQuest Advanced Technologies & Aerospace Collection
Biotechnology and BioEngineering Abstracts
Environmental Science Database
Materials Science Collection
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
Engineering collection
Environmental Science Collection
Genetics Abstracts
MEDLINE - Academic
PubMed Central (Full Participant titles)
SwePub
SwePub Articles
SWEPUB Göteborgs universitet
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Agricultural Science Database
Publicly Available Content Database
ProQuest Central Student
ProQuest Advanced Technologies & Aerospace Collection
ProQuest Central Essentials
Nucleic Acids Abstracts
SciTech Premium Collection
ProQuest Central China
Environmental Sciences and Pollution Management
ProQuest One Applied & Life Sciences
ProQuest One Sustainability
Health Research Premium Collection
Meteorological & Geoastrophysical Abstracts
Natural Science Collection
Health & Medical Research Collection
Biological Science Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
Engineering Collection
Advanced Technologies & Aerospace Collection
Engineering Database
Virology and AIDS Abstracts
ProQuest Biological Science Collection
ProQuest One Academic Eastern Edition
Agricultural Science Collection
ProQuest Hospital Collection
ProQuest Technology Collection
Health Research Premium Collection (Alumni)
Biological Science Database
Ecology Abstracts
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
Environmental Science Collection
Entomology Abstracts
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
Environmental Science Database
ProQuest Nursing & Allied Health Source (Alumni)
Engineering Research Database
ProQuest One Academic
Meteorological & Geoastrophysical Abstracts - Academic
ProQuest One Academic (New)
Technology Collection
Technology Research Database
ProQuest One Academic Middle East (New)
Materials Science Collection
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Central
ProQuest Health & Medical Research Collection
Genetics Abstracts
ProQuest Engineering Collection
Biotechnology Research Abstracts
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Bacteriology Abstracts (Microbiology B)
Algology Mycology and Protozoology Abstracts (Microbiology C)
Agricultural & Environmental Science Collection
AIDS and Cancer Research Abstracts
Materials Science Database
ProQuest Materials Science Collection
ProQuest Public Health
ProQuest Nursing & Allied Health Source
ProQuest SciTech Collection
Advanced Technologies & Aerospace Database
ProQuest Medical Library
Animal Behavior Abstracts
Materials Science & Engineering Collection
Immunology Abstracts
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic






Agricultural Science Database
MEDLINE


Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  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
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: 8FG
  name: ProQuest Technology Collection
  url: https://search.proquest.com/technologycollection1
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Sciences (General)
Medicine
DocumentTitleAlternate CSF IL-12/23 p40 in cognitive impairment
EISSN 1932-6203
ExternalDocumentID 1894814510
oai_doaj_org_article_109000ac268545538644c33fe230bba9
oai_gup_ub_gu_se_253387
PMC5413050
A491017006
28464009
10_1371_journal_pone_0176760
Genre Journal Article
GeographicLocations Sweden
GeographicLocations_xml – name: Sweden
GrantInformation_xml – fundername: European Research Council
  grantid: 681712
– fundername: ;
  grantid: 2013-2546
– fundername: ;
  grantid: ALFGBG-139671
– fundername: ;
  grantid: 523-2007-7111
– fundername: ;
  grantid: ALFGBG-441051
– fundername: ;
  grantid: 14003
– fundername: ;
  grantid: 521-2013-2572
– fundername: ;
  grantid: 681712
– fundername: ;
  grantid: ALFGBG-146841
– fundername: ;
  grantid: ALFGBG-73040
GroupedDBID ---
123
29O
2WC
53G
5VS
7RV
7X2
7X7
7XC
88E
8AO
8C1
8CJ
8FE
8FG
8FH
8FI
8FJ
A8Z
AAFWJ
AAUCC
AAWOE
AAYXX
ABDBF
ABIVO
ABJCF
ABUWG
ACGFO
ACIHN
ACIWK
ACPRK
ACUHS
ADBBV
ADRAZ
AEAQA
AENEX
AEUYN
AFKRA
AFPKN
AFRAH
AHMBA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
APEBS
ARAPS
ATCPS
BAWUL
BBNVY
BCNDV
BENPR
BGLVJ
BHPHI
BKEYQ
BPHCQ
BVXVI
BWKFM
CCPQU
CITATION
CS3
D1I
D1J
D1K
DIK
DU5
E3Z
EAP
EAS
EBD
EMOBN
ESX
EX3
F5P
FPL
FYUFA
GROUPED_DOAJ
GX1
HCIFZ
HH5
HMCUK
HYE
IAO
IEA
IGS
IHR
IHW
INH
INR
IOV
IPY
ISE
ISR
ITC
K6-
KB.
KQ8
L6V
LK5
LK8
M0K
M1P
M48
M7P
M7R
M7S
M~E
NAPCQ
O5R
O5S
OK1
OVT
P2P
P62
PATMY
PDBOC
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
PTHSS
PV9
PYCSY
RNS
RPM
RZL
SV3
TR2
UKHRP
WOQ
WOW
~02
~KM
CGR
CUY
CVF
ECM
EIF
IPNFZ
NPM
PJZUB
PPXIY
PQGLB
RIG
BBORY
PMFND
3V.
7QG
7QL
7QO
7SN
7SS
7T5
7TG
7TM
7U9
7XB
8FD
8FK
AZQEC
C1K
DWQXO
FR3
GNUQQ
H94
K9.
KL.
M7N
P64
PKEHL
PQEST
PQUKI
PRINS
RC3
7X8
5PM
ADTPV
AOWAS
F1U
PUEGO
AAPBV
ABPTK
ESTFP
ID FETCH-LOGICAL-c730t-54b376b53240fc52e7d58de72b0499570c78bfd598c84515578e9976b9446e03
IEDL.DBID M48
ISSN 1932-6203
IngestDate Sun Nov 05 00:20:52 EDT 2023
Wed Aug 27 01:31:15 EDT 2025
Thu Aug 21 07:04:05 EDT 2025
Thu Aug 21 18:13:41 EDT 2025
Fri Jul 11 11:28:08 EDT 2025
Fri Jul 25 10:29:16 EDT 2025
Tue Jun 17 21:02:54 EDT 2025
Tue Jun 10 20:44:34 EDT 2025
Fri Jun 27 04:19:13 EDT 2025
Fri Jun 27 03:45:51 EDT 2025
Thu May 22 21:18:52 EDT 2025
Mon Jul 21 05:50:17 EDT 2025
Thu Apr 24 23:06:17 EDT 2025
Tue Jul 01 02:09:45 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Language English
License This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Creative Commons Attribution License
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c730t-54b376b53240fc52e7d58de72b0499570c78bfd598c84515578e9976b9446e03
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
Conceptualization: PJ EA AW J-OJ UA KB HZ JS.Data curation: PJ EA AW J-OJ UA KB HZ JS.Formal analysis: PJ EA AW J-OJ UA KB HZ JS.Funding acquisition: AW KB HZ JS.Investigation: PJ EA AW J-OJ UA KB HZ JS.Methodology: PJ EA AW J-OJ UA KB HZ JS.Project administration: PJ JS.Resources: PJ EA AW J-OJ UA KB HZ JS.Software: PJ EA AW J-OJ UA KB HZ JS.Supervision: AW KB HZ JS.Validation: PJ EA AW J-OJ UA KB HZ JS.Visualization: PJ EA JS.Writing – original draft: PJ EA JS.Writing – review & editing: PJ EA AW J-OJ UA KB HZ JS.
Competing Interests: The authors have declared that no competing interests exist.
ORCID 0000-0002-4487-6405
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1371/journal.pone.0176760
PMID 28464009
PQID 1894814510
PQPubID 1436336
PageCount e0176760
ParticipantIDs plos_journals_1894814510
doaj_primary_oai_doaj_org_article_109000ac268545538644c33fe230bba9
swepub_primary_oai_gup_ub_gu_se_253387
pubmedcentral_primary_oai_pubmedcentral_nih_gov_5413050
proquest_miscellaneous_1894917657
proquest_journals_1894814510
gale_infotracmisc_A491017006
gale_infotracacademiconefile_A491017006
gale_incontextgauss_ISR_A491017006
gale_incontextgauss_IOV_A491017006
gale_healthsolutions_A491017006
pubmed_primary_28464009
crossref_primary_10_1371_journal_pone_0176760
crossref_citationtrail_10_1371_journal_pone_0176760
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2017-05-02
PublicationDateYYYYMMDD 2017-05-02
PublicationDate_xml – month: 05
  year: 2017
  text: 2017-05-02
  day: 02
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: San Francisco
– name: San Francisco, CA USA
PublicationTitle PloS one
PublicationTitleAlternate PLoS One
PublicationYear 2017
Publisher Public Library of Science
Public Library of Science (PLoS)
Publisher_xml – name: Public Library of Science
– name: Public Library of Science (PLoS)
References S Kim (ref31) 2011; 11
P Gupta (ref10) 2015; 30
Y Liu (ref47) 2014; 271
J Wang (ref11) 2015; 44
M Rentzos (ref50) 2006; 249
A Chen (ref14) 2016; 38
E Vanmechelen (ref25) 2000; 285
A Yip (ref8) 2005; 5
A Helmy (ref28) 2012; 9
G McKhann (ref18) 1984; 34
M Motta (ref34) 2007; 114
S Rasmuson (ref27) 2011; 23
G Román (ref19) 1993; 43
I Blasko (ref33) 2006; 21
C Dinarello (ref1) 2007; 37
D Galimberti (ref37) 2006; 63
E Tarkowski (ref36) 2002; 23
G Kovacs (ref16) 2008; 26
M Xia (ref43) 2000; 108
J Trollor (ref52) 2010; 30
R Zhang (ref42) 2013; 256
M Tan (ref6) 2014; 38
H Vanderstichele (ref23) 2000; 7
G Trinchieri (ref44) 2003; 3
M Folstein (ref22) 1975; 12
P Chakrabarty (ref3) 2010; 24
A Kalb (ref26) 2013; 8
M Alsadany (ref39) 2013; 28
W Swardfager (ref12) 2010; 68
J Vom Berg (ref5) 2012; 18
I Horvath (ref51) 2016; 7
T Erkinjuntti (ref20) 2000; 59
P Johansson (ref17) 2011; 24
D Galimberti (ref41) 2007; 14
L Huang (ref32) 2013; 550
J Jia (ref30) 2005; 383
X Zhu (ref46) 2014; 274
A Koyama (ref15) 2013; 68
V Calsolaro (ref2) 2016; 12
G Pasqualetti (ref13) 2015; 15
Q Yan (ref7) 2003; 23
R Petersen (ref21) 2004; 256
S Ghosh (ref4) 2013; 33
K Blennow (ref24) 1995; 26
D Galimberti (ref29) 2008; 255
K Westin (ref40) 2012; 7
M Rentzos (ref38) 2006; 19
A Croxford (ref45) 2014; 25
S Engelborghs (ref49) 1999; 34
E Rota (ref48) 2006; 27
S Vlad (ref9) 2008; 70
K Bonotis (ref35) 2008; 193
References_xml – volume: 30
  start-page: 178
  year: 2015
  ident: ref10
  article-title: Role of traditional nonsteroidal anti-inflammatory drugs in Alzheimer's disease: a meta-analysis of randomized clinical trials
  publication-title: Am J Alzheimers Dis Other Demen
  doi: 10.1177/1533317514542644
– volume: 249
  start-page: 110
  year: 2006
  ident: ref50
  article-title: Interleukin-12 is reduced in cerebrospinal fluid of patients with Alzheimer's disease and frontotemporal dementia
  publication-title: J Neurol Sci
  doi: 10.1016/j.jns.2006.05.063
– volume: 26
  start-page: 231
  year: 1995
  ident: ref24
  article-title: Tau protein in cerebrospinal fluid: a biochemical marker for axonal degeneration in Alzheimer disease?
  publication-title: Mol Chem Neuropathol
  doi: 10.1007/BF02815140
– volume: 12
  start-page: 719
  year: 2016
  ident: ref2
  article-title: Neuroinflammation in Alzheimer's disease: Current evidence and future directions
  publication-title: Alzheimers Dement
  doi: 10.1016/j.jalz.2016.02.010
– volume: 70
  start-page: 1672
  year: 2008
  ident: ref9
  article-title: Protective effects of NSAIDs on the development of Alzheimer disease
  publication-title: Neurology
  doi: 10.1212/01.wnl.0000311269.57716.63
– volume: 24
  start-page: 537
  year: 2011
  ident: ref17
  article-title: Cerebrospinal fluid biomarkers for Alzheimer’s disease: diagnostic performance in a homogeneous mono-center population
  publication-title: J Alzheimers Dis
  doi: 10.3233/JAD-2011-101878
– volume: 3
  start-page: 133
  year: 2003
  ident: ref44
  article-title: Interleukin-12 and the regulation of innate resistance and adaptive immunity
  publication-title: Nat Rev Immunol
  doi: 10.1038/nri1001
– volume: 68
  start-page: 433
  year: 2013
  ident: ref15
  article-title: The role of peripheral inflammatory markers in dementia and Alzheimer's disease: a meta-analysis
  publication-title: J Gerontol A Biol Sci Med Sci
  doi: 10.1093/gerona/gls187
– volume: 63
  start-page: 538
  year: 2006
  ident: ref37
  article-title: Intrathecal chemokine synthesis in mild cognitive impairment and Alzheimer disease
  publication-title: Arch Neurol
  doi: 10.1001/archneur.63.4.538
– volume: 33
  start-page: 5053
  year: 2013
  ident: ref4
  article-title: Sustained interleukin-1β overexpression exacerbates tau pathology despite reduced amyloid burden in an Alzheimer's mouse model
  publication-title: J Neurosci
  doi: 10.1523/JNEUROSCI.4361-12.2013
– volume: 34
  start-page: 523
  year: 1999
  ident: ref49
  article-title: Unchanged levels of interleukins, neopterin, interferon-gamma and tumor necrosis factor-alpha in cerebrospinal fluid of patients with dementia of the Alzheimer type
  publication-title: Neurochem Int
  doi: 10.1016/S0197-0186(99)00031-5
– volume: 24
  start-page: 548
  year: 2010
  ident: ref3
  article-title: Massive gliosis induced by interleukin-6 suppresses Abeta deposition in vivo: evidence against inflammation as a driving force for amyloid deposition
  publication-title: FASEB J
  doi: 10.1096/fj.09-141754
– volume: 23
  start-page: 1386
  year: 2011
  ident: ref27
  article-title: Increased serum levels of dehydroepiandrosterone (DHEA) and interleukin-6 (IL-6) in women with mild to moderate Alzheimer's disease
  publication-title: Int Psychogeriatr
  doi: 10.1017/S1041610211000810
– volume: 21
  start-page: 9
  year: 2006
  ident: ref33
  article-title: Measurement of thirteen biological markers in CSF of patients with Alzheimer's disease and other dementias
  publication-title: Dement Geriatr Cogn Disord
  doi: 10.1159/000089137
– volume: 285
  start-page: 49
  year: 2000
  ident: ref25
  article-title: Quantification of tau phosphorylated at threonine 181 in human cerebrospinal fluid: a sandwich ELISA with a synthetic phosphopeptide for standardization
  publication-title: Neurosci Lett
  doi: 10.1016/S0304-3940(00)01036-3
– volume: 23
  start-page: 237
  year: 2002
  ident: ref36
  article-title: Increased intrathecal levels of the angiogenic factors VEGF and TGF-beta in Alzheimer's disease and vascular dementia
  publication-title: Neurobiol Aging
  doi: 10.1016/S0197-4580(01)00285-8
– volume: 114
  start-page: 46
  year: 2007
  ident: ref34
  article-title: Altered plasma cytokine levels in Alzheimer's disease: correlation with the disease progression
  publication-title: Immunol Lett
  doi: 10.1016/j.imlet.2007.09.002
– volume: 271
  start-page: 43
  year: 2014
  ident: ref47
  article-title: Interleukin-23 receptor polymorphisms are associated with Alzheimer's disease in Han Chinese
  publication-title: J Neuroimmunol
  doi: 10.1016/j.jneuroim.2014.03.013
– volume: 15
  start-page: 17
  year: 2015
  ident: ref13
  article-title: The role of neuroinflammation in dementias
  publication-title: Curr Neurol Neurosci Rep
  doi: 10.1007/s11910-015-0531-7
– volume: 550
  start-page: 60
  year: 2013
  ident: ref32
  article-title: Decreased serum levels of the angiogenic factors VEGF and TGF-β1 in Alzheimer's disease and amnestic mild cognitive impairment
  publication-title: Neurosci Lett
  doi: 10.1016/j.neulet.2013.06.031
– volume: 108
  start-page: 227
  year: 2000
  ident: ref43
  article-title: Expression of the chemokine receptor CXCR3 on neurons and the elevated expression of its ligand IP-10 in reactive astrocytes: in vitro ERK1/2 activation and role in Alzheimer's disease
  publication-title: J Neuroimmunol
  doi: 10.1016/S0165-5728(00)00285-X
– volume: 34
  start-page: 939
  year: 1984
  ident: ref18
  article-title: Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
  publication-title: Neurology
  doi: 10.1212/WNL.34.7.939
– volume: 5
  start-page: 2
  year: 2005
  ident: ref8
  article-title: Nonsteroidal anti-inflammatory drug use and Alzheimer's disease risk: the MIRAGE Study
  publication-title: BMC Geriatr
  doi: 10.1186/1471-2318-5-2
– volume: 27
  start-page: 33
  year: 2006
  ident: ref48
  article-title: Increased intrathecal TGF-beta1, but not IL-12, IFN-gamma and IL-10 levels in Alzheimer's disease patients
  publication-title: Neurol Sci
  doi: 10.1007/s10072-006-0562-6
– volume: 12
  start-page: 189
  year: 1975
  ident: ref22
  article-title: "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician
  publication-title: J Psychiatr Res
– volume: 59
  start-page: 23
  year: 2000
  ident: ref20
  article-title: Research criteria for subcortical vascular dementia in clinical trials
  publication-title: Neural Transm Suppl
– volume: 18
  start-page: 1812
  year: 2012
  ident: ref5
  article-title: Inhibition of IL-12/IL-23 signaling reduces Alzheimer's disease-like pathology and cognitive decline
  publication-title: Nat Med
  doi: 10.1038/nm.2965
– volume: 383
  start-page: 12
  year: 2005
  ident: ref30
  article-title: Cerebrospinal fluid tau, Abeta1-42 and inflammatory cytokines in patients with Alzheimer's disease and vascular dementia
  publication-title: Neurosci Lett
  doi: 10.1016/j.neulet.2005.03.051
– volume: 37
  start-page: S34
  issue: Suppl 1
  year: 2007
  ident: ref1
  article-title: Historical insights into cytokines
  publication-title: Eur J Immunol
  doi: 10.1002/eji.200737772
– volume: 255
  start-page: 539
  year: 2008
  ident: ref29
  article-title: Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration
  publication-title: J Neurol
  doi: 10.1007/s00415-008-0737-6
– volume: 9
  start-page: 81
  year: 2012
  ident: ref28
  article-title: Role of interleukin 6 and alpha-globulins in differentiating Alzheimer and vascular dementias
  publication-title: Neurodegener Dis
  doi: 10.1159/000329568
– volume: 43
  start-page: 250
  year: 1993
  ident: ref19
  article-title: Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop
  publication-title: Neurology
  doi: 10.1212/WNL.43.2.250
– volume: 28
  start-page: 54
  year: 2013
  ident: ref39
  article-title: Histone deacetylases enzyme, copper, and IL-8 levels in patients with Alzheimer's disease
  publication-title: Am J Alzheimers Dis Other Demen
  doi: 10.1177/1533317512467680
– volume: 274
  start-page: 180
  year: 2014
  ident: ref46
  article-title: Association of IL-12A and IL-12B polymorphisms with Alzheimer's disease susceptibility in a Han Chinese population
  publication-title: J Neuroimmunol
  doi: 10.1016/j.jneuroim.2014.06.026
– volume: 26
  start-page: 343
  year: 2008
  ident: ref16
  article-title: Mixed brain pathologies in dementia: the BrainNet Europe consortium experience
  publication-title: Dement Geriatr Cogn Disord
  doi: 10.1159/000161560
– volume: 7
  start-page: 245
  year: 2000
  ident: ref23
  article-title: Standardization of measurement of beta-amyloid(1–42) in cerebrospinal fluid and plasma
  publication-title: Amyloid
  doi: 10.3109/13506120009146438
– volume: 30
  start-page: 569
  year: 2010
  ident: ref52
  article-title: Systemic inflammation is associated with MCI and its subtypes: the Sydney Memory and Aging Study
  publication-title: Dement Geriatr Cogn Disord
  doi: 10.1159/000322092
– volume: 23
  start-page: 7504
  year: 2003
  ident: ref7
  article-title: Anti-inflammatory drug therapy alters beta-amyloid processing and deposition in an animal model of Alzheimer's disease
  publication-title: J Neurosci
  doi: 10.1523/JNEUROSCI.23-20-07504.2003
– volume: 256
  start-page: 38
  year: 2013
  ident: ref42
  article-title: Systemic immune system alterations in early stages of Alzheimer's disease
  publication-title: J Neuroimmunol
  doi: 10.1016/j.jneuroim.2013.01.002
– volume: 14
  start-page: e3
  year: 2007
  ident: ref41
  article-title: IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease
  publication-title: Eur J Neurol
  doi: 10.1111/j.1468-1331.2006.01637.x
– volume: 68
  start-page: 930
  year: 2010
  ident: ref12
  article-title: A meta-analysis of cytokines in Alzheimer's disease
  publication-title: Biol Psychiatry
  doi: 10.1016/j.biopsych.2010.06.012
– volume: 25
  start-page: 415
  year: 2014
  ident: ref45
  article-title: IL-12-and IL-23 in health and disease
  publication-title: Cytokine Growth Factor Rev
  doi: 10.1016/j.cytogfr.2014.07.017
– volume: 7
  start-page: 34
  year: 2016
  ident: ref51
  article-title: Pro-inflammatory S100A9 protein as a robust biomarker differentiating early stages of cognitive impairment in Alzheimer's disease
  publication-title: ACS Chem Neurosci
  doi: 10.1021/acschemneuro.5b00265
– volume: 8
  start-page: e62679
  year: 2013
  ident: ref26
  article-title: Acetylcholinesterase inhibitors reduce neuroinflammation and -degeneration in the cortex and hippocampus of a surgery stress rat model
  publication-title: PloS One
  doi: 10.1371/journal.pone.0062679
– volume: 7
  start-page: e30525
  year: 2012
  ident: ref40
  article-title: CCL2 is associated with a faster rate of cognitive decline during early stages of Alzheimer's disease
  publication-title: PloS One
  doi: 10.1371/journal.pone.0030525
– volume: 44
  start-page: 385
  year: 2015
  ident: ref11
  article-title: Anti-inflammatory drugs and risk of Alzheimer's disease: an updated systematic review and meta-analysis
  publication-title: J Alzheimers Dis
  doi: 10.3233/JAD-141506
– volume: 38
  start-page: 56
  year: 2016
  ident: ref14
  article-title: Multiplex analyte assays to characterize different dementias: brain inflammatory cytokines in poststroke and other dementias
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2015.10.021
– volume: 19
  start-page: 114
  year: 2006
  ident: ref38
  article-title: IL-15 is elevated in cerebrospinal fluid of patients with Alzheimer's disease and frontotemporal dementia
  publication-title: J Geriatr Psychiatry Neurol
  doi: 10.1177/0891988706286226
– volume: 256
  start-page: 183
  year: 2004
  ident: ref21
  article-title: Mild cognitive impairment as a diagnostic entity
  publication-title: J Intern Med
  doi: 10.1111/j.1365-2796.2004.01388.x
– volume: 11
  start-page: 51
  year: 2011
  ident: ref31
  article-title: Identification of peripheral inflammatory markers between normal control and Alzheimer's disease
  publication-title: BMC Neurol
  doi: 10.1186/1471-2377-11-51
– volume: 38
  start-page: 633
  year: 2014
  ident: ref6
  article-title: IL12/23 p40 inhibition ameliorates Alzheimer's disease-associated neuropathology and spatial memory in SAMP8 mice
  publication-title: J Alzheimers Dis
  doi: 10.3233/JAD-131148
– volume: 193
  start-page: 183
  year: 2008
  ident: ref35
  article-title: Systemic immune aberrations in Alzheimer's disease patients
  publication-title: J Neuroimmunol
  doi: 10.1016/j.jneuroim.2007.10.020
SSID ssj0053866
Score 2.3033397
Snippet The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured cytokines...
Background The role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured...
Background The role of inflammation in Alzheimer’s disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured...
BackgroundThe role of inflammation in Alzheimer's disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured...
Background The role of inflammation in Alzheimer’s disease (AD) and other cognitive disorders is unclear. In a well-defined mono-center population, we measured...
SourceID plos
doaj
swepub
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage e0176760
SubjectTerms Abuse
Activation
Activation analysis
Advertisements
Aged
Aged, 80 and over
Aging
Aging (artificial)
Alcohols
Alzheimer Disease - blood
Alzheimer Disease - cerebrospinal fluid
Alzheimer Disease - immunology
Alzheimer Inflammation Cognitive impairment Cerebrospinal fluid Interleukin Cytokine Chemokin Steroid homone
Alzheimer's disease
Amyloid beta-Peptides - cerebrospinal fluid
Analysis
Animal models
Annan klinisk medicin
Annan medicin och hälsovetenskap
Anti-inflammatory agents
Arches
Astrocytes
Attitude control
Autocrine signalling
Biology and Life Sciences
Biomarkers
Biomarkers - blood
Biomarkers - cerebrospinal fluid
Blood
Blood circulation
Body mass
Body Mass Index
Brain
Cerebrospinal fluid
Chemokines
Cholinesterase
Cholinesterase inhibitors
Clinical Medicine
Cognitive ability
Cognitive disorders
Cognitive Dysfunction - blood
Cognitive Dysfunction - cerebrospinal fluid
Cognitive Dysfunction - immunology
Cohort Studies
Cytokines
Dementia
Dementia disorders
Diabetes mellitus
Drug abuse
Drugs
Dura mater
Endocrinology
Evaluation
Family physicians
Female
Glucocorticoids
Growth factors
Health aspects
Hip
Hospitals
Humans
Immune system
Inactivation
Inflammation
Inhibitors
Interferon
Interleukin 1
Interleukin 6
Interleukin-12 Subunit p40 - blood
Interleukin-12 Subunit p40 - cerebrospinal fluid
Klinisk medicin
Male
Markers
Mathematical models
Medicine
Medicine and Health Sciences
Mental disorders
Mental Status Schedule
Mice
Microglia
Migration
Multiplexing
Myocardial infarction
Necrosis
Nervous system
Neurochemistry
Neurodegenerative diseases
Neurologi
Neurology
Neurons
Neurosciences
Nonsteroidal anti-inflammatory drugs
Other Clinical Medicine
Other Medical and Health Sciences
Pathogenesis
Peptide Fragments - cerebrospinal fluid
Phosphorylation
Physiology
Proteins
Psychiatry
Psykiatri
Risk
Sweden
tau Proteins - cerebrospinal fluid
Tumor necrosis factor-TNF
White People
Womens health
β-Amyloid
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3Nb9MwFLdQT1wQ42uFMgxCfByyuk4cp8eBmAYHkMZAu1mx43QVVRI1zf-_92w3YDFpHLj6PbfK-37J88-EvOaW59KWeSI5XmGW1QtwKcMTLavCYEdSWTcg-zU_-5F9uRSXf1z1hTNhHh7YC26Og4OMlYbnBSR7cE9I4CZNawu1s9alO7oHOW_fTPkYjGx5OCiXysU86OW4axt7DDaYSwdJ-TsRObz-MSpPuk3b31Ry_j05GeGLupx0ep_cC8UkPfEPcUDu2OYBOQju2tN3AVP6_UPSnSNEq62osVvogvGyENxZb4Y1rOHRxSbg59K2poghsd3Y4de6SRZ8zlPaD3oA56ddxoBKAxprT_E1Lh1HkCieuVxv8YXjI3Jx-uni41kSLltIDDj5LhGZhlijBQL01UZwKytRVFZyjU2RkMzIQteVWIIKM7wXRhZ2CbWMXkJDaVn6mEwakO4hoYVlQpuM2RxIzLCyzkohTFaLEmolLack3QtemQBEjvdhbJT7uiahIfHiU6guFdQ1Jcm4q_NAHLfwf0CdjrwIo-0WwLhUMC51m3FNyQu0COXPpI7BQJ1kSwxlELGm5JXjQCiNBmd1VuXQ9-rzt5__wPT9PGJ6G5jqFsRhynA-Ap4JIboizlnECQHBRORDtN-9VHq1KBCSB5QGQpntbfpm8suRjD-K83eNbQfPA419LkB7T7wLjJKFAieHTADCkpFzRKKPKc36yiGZCyyhBPzvG-9G0ZbV0ClYWg2qt4pDW1LIp_9Dqc_IXY61GU6t8hmZ7LaDfQ6V5U4fuSByDbIfdIo
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3db9MwELegSIgXxMbHCgMMQnw8ZE0df6RPaCCmgQRIY6C-WbHjdBVVEpLm_-fOcTNFTMBrfE6b-_Kdff4dIS-YY1K5TEaKYQszXszBpCyLjMpTixlJ7nyB7Bd5-p1_Wopl2HBrQ1nlzid6R51XFvfIZ_MUcUU4qNDb-leEXaPwdDW00LhObiB0GZZ0qeWQcIEtSxmuyyVqPgvSOaqr0h2BJkrlgSkvlyOP2j_45km9qdqrAs8_6ydHKKN-ZTq5Q26HkJIe9zqwR665cp_c_BwOzffJXrDflr4OINNv7pL6DDFbXU6tayAtxu4h-JJi063hGd5lLAOgLq0KiqASzcZ1P9dlNGczltC2Mx14A1rzGEZpgGdtKe7r0qEmieIlzHWDO5D3yPnJh_P3p1HovhBZsPptJLgB52MEIvYVVjCncpHmTjGDWZJQsVWpKXKxAJlybBSjUreA4MYsIMN0cXKfTEpg9AGhqYuFsTx2EoZiG2cFz4SwvBAZBE9GTUmyk4G2AZkcG2RstD9uU5Ch9JzUKDkdJDcl0TCr7pE5_kH_DsU70CKutn9QNSsdzBTP42GNyCyTKYSWqECc2yQpHGRqxmSLKXmKyqH7S6qDd9DHfIG-DVzYlDz3FIitUWLxzirr2lZ__PrjP4i-nY2IXgWiogJ22CxcmIBvQsyuEeXhiBI8hB0NH6Aq77jS6ktbgpk79b56-NkwjC_FgrzSVV1PA5m-FCC9B701DJyFiEfC0gDMUiM7GbF-PFKuLzy0ucCYSsDvvuwtajRl1dUaHq063TrNIE9J1cO___9H5BbDMAwLVNkhmWybzj2GIHJrnnhP8RuKenDO
  priority: 102
  providerName: ProQuest
Title Reduced cerebrospinal fluid concentration of interleukin-12/23 subunit p40 in patients with cognitive impairment
URI https://www.ncbi.nlm.nih.gov/pubmed/28464009
https://www.proquest.com/docview/1894814510
https://www.proquest.com/docview/1894917657
https://pubmed.ncbi.nlm.nih.gov/PMC5413050
https://gup.ub.gu.se/publication/253387
https://doaj.org/article/109000ac268545538644c33fe230bba9
http://dx.doi.org/10.1371/journal.pone.0176760
Volume 12
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3db9MwELdGJyFeEBsfK5RiEOLjISV17Th9QGibVgbSBhrb1DcrdpxSUSUhaST477lL3EgRneAlD_Y5Ue585zv7_DtCXjLLAmmjwJMMS5jxZAwqZZinZRwajEhiWyfIngenV_zzXMx3yKZmq2NguTW0w3pSV8Vq9Ovn7w-g8O_rqg1yvBk0yrPUjmCGBTKAIH4X1iaJqnrG23MF0O4gcBfobhrZWaBqHP_WWvfyVVZuc0X_zqjs4I7Wa9XsHrnrnEx62MyKPbJj031y-8wdo--TPafRJX3jYKff3if5BaK42pgaW0CgjPVE8CXJqlpCG95uTB3ELs0SijATxcpWP5apN2bv2ISWla7APtCc-9BLHWBrSXGnl7ZZShSvZS4L3JN8QC5nJ5fHp56rx-AZsANrT3AN5kgLxPBLjGBWxiKMrWQa4yYhfSNDncRiClLmWDpGhnYK7o6eQsxp_clD0kuB0QeEhtYX2nDfBtDlGz9KeCSE4YmIwJ3Ssk8mGxko47DKsWTGStUHcBJiloaTCiWnnOT6xGtH5Q1Wxz_oj1C8LS0ibdcNWbFQTnHxhB5WjciwIARnEycQ52YySSzEblpH0z55hpNDNddWW3uhDvkUrR0YtT55UVMg2kaK6TyLqCpL9enL9X8QfbvoEL12REkG7DCRu0IB_4QoXh3KQYcSbIbpdB_gVN5wpVTjEFF7QGjAlMFmem_vft5240sxRS-1WdXQQOwfCJDeo0YbWs6CDxTAYgHMkh096bC-25Muv9dg5wK9LAHffdVoVGfIosoVNC0qVVrFIHIJ5eObf-0JucPQKcN0VTYgvXVR2afgUq71kNyScwnP8HiMz9nHIdk9Ojn_ejGsN2mGtRX5Ax_DegE
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEF6VIAEXRMujgUIXxPPgxtl4vfYBofKoEvpAagPKbeVdr0NEZJs4FuJH8R-ZsdeuLCrg0qt37DjzHu_sN4Q8ZYb5wkS-IxiOMPOSIZiUZo4ScaCxIolN1SB74o8_ex9nfLZBfjVnYbCtsvGJlaOOM43fyAfDAHFFPFChN_l3B6dG4e5qM0KjVotD8_MHlGzF68l7kO8zxg4-TN-NHTtVwNGgzWuHewqMSnFEoks0Z0bEPIiNYAqzfy5cLQKVxDyEd_VwAIoITAhBW4VQORl3BI-9Qq5C3HXRoMSsre_Adfi-PZ03EsOBVYa9PEvNHii-LyoczPPoVw0JaENBL19mxUV57p_tmh1Q0yoQHtwiN20GS_drldskGybdIteO7R79Ftm07qKgLy2m9avbJD9FiFgTU21WUIXjsBJ8SLIsF3ANj06mFr-XZglFDIvV0pTfFqkzZAM2okWpSnA-NPdcWKUWDbag-BmZti1QFM98Llb4wfMOmV6GWO6SXgqM3iY0MC5X2nOND0uudqPEizjXXsIjyNWU6JNRIwOpLRA6zuNYymp3T0BBVHNSouSklVyfOO1deQ0E8g_6tyjelhZhvKsL2WourVfA7X8ISZFmfgCZLCqQ5-nRKDFQGCoVhX2yi8oh6zOxrTOS-16IrhQ8Zp88qSgQyiPFXqF5VBaFnHz68h9EZ6cdoheWKMmAHTqy5zPgPyFEWIdyp0MJDkl3lrdRlRuuFPLcdOHORr0vXn7cLuNDsf8vNVlZ04TAWA7Su1dbQ8tZSLB8iETALNGxkw7ruyvp4muFpM4xhePwu89ri-rcMi9zCZfmpSyMZFAWBeL-399_l1wfT4-P5NHk5PABucEwA8TeWLZDeutVaR5C_rpWjyqvQYm8ZC_1G2zNqsE
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwELdGkSZeEBsfKwxmEJ8PWVPHjpMHhAZjWhkMtA3UNytxnFJRJaFphPjT-O-4S5xMERPwslf74qb35Tvn_DtCHjPDfGki35EMW5jxdAwmpZkTyyTQmJEkpi6QPfYPP_N3UzFdI7_auzBYVtn6xNpRJ7nGM_LROEBcEQ4qNEptWcSn_YNXxXcHO0jhl9a2nUajIkfm5w9I38qXk32Q9RPGDt6evTl0bIcBR4NmrxzBYzCwWCAqXaoFMzIRQWIkizETENLVMojTRITw3hybocjAhLCBxyFkUcb1YNkr5Kr0xBhNTE67XA_ciO_bm3qeHI-sYuwWeWZ2wQh8WWNinu-EdcOAblsYFIu8vCjm_bN0swdwWm-KBzfIdRvN0r1G_TbImsk2yfoH-71-k2xY11HS5xbf-sVNUpwgXKxJqDZLyMixcQkuki6qOYzhNcrMYvnSPKWIZ7FcmOrbPHPGbMQ8WlZxBY6IFtyFWWqRYUuKR8q0K4eieP9zvsTDz1vk7DLEcpsMMmD0FqGBcUWsuWt8mHK1G6U8EkLzVEQQt8VySLxWBkpbUHTszbFQ9Zc-CclRw0mFklNWckPidE8VDSjIP-hfo3g7WoT0rgfy5UxZD4GlALA9RZr5AUS1qECca89LDSSJcRyFQ7KDyqGa-7GdY1J7PES3Ct5zSB7VFAjrkaGBzKKqLNXk45f_IDo96RE9s0RpDuzQkb2rAf8J4cJ6lNs9SnBOuje9harccqVU52YMT7bqffH0w24aF8VawMzkVUMTAmMFSO9OYw0dZyHY8mFXAmbJnp30WN-fyeZfa1R1geGcgN992lhU75FZVSgYmlWqNIpBihTIu39__x2yDv5JvZ8cH90j1xgGg1gmy7bJYLWszH0IZVfxg9ppUKIu2Un9Bqbbrvc
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=Reduced+cerebrospinal+fluid+concentration+of+interleukin-12%2F23+subunit+p40+in+patients+with+cognitive+impairment&rft.jtitle=PloS+one&rft.au=Johansson%2C+Per&rft.au=Almqvist%2C+Erik&rft.au=Wallin%2C+Anders&rft.au=Johansson%2C+Jan-Ove&rft.date=2017-05-02&rft.pub=Public+Library+of+Science&rft.eissn=1932-6203&rft.volume=12&rft.issue=5&rft_id=info:doi/10.1371%2Fjournal.pone.0176760&rft.externalDocID=1894814510
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1932-6203&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1932-6203&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1932-6203&client=summon