The Association of Blood-Based Inflammatory Factors IL-1β, TGF-β and CRP with Cognitive Function in Alzheimer’s Disease and Mild Cognitive Impairment

Objective Many patients suffer from dementia in its most common form, Alzheimer’s disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in the inflammatory response in Alzheimer’s disease and its mild cognitive impairment (MCI), were measured and analyzed.Methods Sevent...

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Published inPsychiatry investigation Vol. 18; no. 1; pp. 11 - 18
Main Authors Park, Jun Kyung, Lee, Kang Joon, Kim, Ji Yeon, Kim, Hyun
Format Journal Article
LanguageEnglish
Published Korea (South) Korean Neuropsychiatric Association 01.01.2021
대한신경정신의학회
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Abstract Objective Many patients suffer from dementia in its most common form, Alzheimer’s disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in the inflammatory response in Alzheimer’s disease and its mild cognitive impairment (MCI), were measured and analyzed.Methods Seventy nine subjects participated in this study (mean age: 75.56 years, female: 54.3%, AD: 26, MCI: 28, normal: 25). The overall cognitive function of the subjects and the severity of the disease stage were assessed using the Mini-Mental State Examination (MMSE-K), the Clinical Dementia Rating (CDR), the Global Deterioration Scale (GDS) and the Geriatric Depression Scale-Korean (GDS-K).Results It was observed that patients with AD had significantly higher levels of IL-1β and TGF-β than the patients with MCI and normal controls. In addition, the MCI group showed a statistically significantly higher TGF-β concentration than the normal group.Conclusion These results suggest that IL-1β and TGF-β may be useful biological markers for patients with Alzheimer’s disease.
AbstractList Many patients suffer from dementia in its most common form, Alzheimer's disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in the inflammatory response in Alzheimer's disease and its mild cognitive impairment (MCI), were measured and analyzed.OBJECTIVEMany patients suffer from dementia in its most common form, Alzheimer's disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in the inflammatory response in Alzheimer's disease and its mild cognitive impairment (MCI), were measured and analyzed.Seventy nine subjects participated in this study (mean age: 75.56 years, female: 54.3%, AD: 26, MCI: 28, normal: 25). The overall cognitive function of the subjects and the severity of the disease stage were assessed using the Mini-Mental State Examination (MMSE-K), the Clinical Dementia Rating (CDR), the Global Deterioration Scale (GDS) and the Geriatric Depression Scale-Korean (GDS-K).METHODSSeventy nine subjects participated in this study (mean age: 75.56 years, female: 54.3%, AD: 26, MCI: 28, normal: 25). The overall cognitive function of the subjects and the severity of the disease stage were assessed using the Mini-Mental State Examination (MMSE-K), the Clinical Dementia Rating (CDR), the Global Deterioration Scale (GDS) and the Geriatric Depression Scale-Korean (GDS-K).It was observed that patients with AD had significantly higher levels of IL-1β and TGF-β than the patients with MCI and normal controls. In addition, the MCI group showed a statistically significantly higher TGF-β concentration than the normal group.RESULTSIt was observed that patients with AD had significantly higher levels of IL-1β and TGF-β than the patients with MCI and normal controls. In addition, the MCI group showed a statistically significantly higher TGF-β concentration than the normal group.These results suggest that IL-1β and TGF-β may be useful biological markers for patients with Alzheimer's disease.CONCLUSIONThese results suggest that IL-1β and TGF-β may be useful biological markers for patients with Alzheimer's disease.
Objective Many patients suffer from dementia in its most common form, Alzheimer’s disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in the inflammatory response in Alzheimer’s disease and its mild cognitive impairment (MCI), were measured and analyzed.Methods Seventy nine subjects participated in this study (mean age: 75.56 years, female: 54.3%, AD: 26, MCI: 28, normal: 25). The overall cognitive function of the subjects and the severity of the disease stage were assessed using the Mini-Mental State Examination (MMSE-K), the Clinical Dementia Rating (CDR), the Global Deterioration Scale (GDS) and the Geriatric Depression Scale-Korean (GDS-K).Results It was observed that patients with AD had significantly higher levels of IL-1β and TGF-β than the patients with MCI and normal controls. In addition, the MCI group showed a statistically significantly higher TGF-β concentration than the normal group.Conclusion These results suggest that IL-1β and TGF-β may be useful biological markers for patients with Alzheimer’s disease. KCI Citation Count: 0
Objective Many patients suffer from dementia in its most common form, Alzheimer’s disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in the inflammatory response in Alzheimer’s disease and its mild cognitive impairment (MCI), were measured and analyzed.Methods Seventy nine subjects participated in this study (mean age: 75.56 years, female: 54.3%, AD: 26, MCI: 28, normal: 25). The overall cognitive function of the subjects and the severity of the disease stage were assessed using the Mini-Mental State Examination (MMSE-K), the Clinical Dementia Rating (CDR), the Global Deterioration Scale (GDS) and the Geriatric Depression Scale-Korean (GDS-K).Results It was observed that patients with AD had significantly higher levels of IL-1β and TGF-β than the patients with MCI and normal controls. In addition, the MCI group showed a statistically significantly higher TGF-β concentration than the normal group.Conclusion These results suggest that IL-1β and TGF-β may be useful biological markers for patients with Alzheimer’s disease.
Many patients suffer from dementia in its most common form, Alzheimer's disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in the inflammatory response in Alzheimer's disease and its mild cognitive impairment (MCI), were measured and analyzed. Seventy nine subjects participated in this study (mean age: 75.56 years, female: 54.3%, AD: 26, MCI: 28, normal: 25). The overall cognitive function of the subjects and the severity of the disease stage were assessed using the Mini-Mental State Examination (MMSE-K), the Clinical Dementia Rating (CDR), the Global Deterioration Scale (GDS) and the Geriatric Depression Scale-Korean (GDS-K). It was observed that patients with AD had significantly higher levels of IL-1β and TGF-β than the patients with MCI and normal controls. In addition, the MCI group showed a statistically significantly higher TGF-β concentration than the normal group. These results suggest that IL-1β and TGF-β may be useful biological markers for patients with Alzheimer's disease.
Author Park, Jun Kyung
Lee, Kang Joon
Kim, Ji Yeon
Kim, Hyun
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Cites_doi 10.1016/s0361-9230(03)00088-1
10.1371/journal.pone.0006344
10.1111/j.1365-2990.2005.00655.x
10.1038/39321
10.1006/neur.1995.0051
10.1159/000474940
10.1038/nrn1032
10.1016/j.cca.2005.06.013
10.1016/j.jpsychores.2004.01.004
10.1016/j.jneuroim.2003.11.003
10.1097/00001756-199301000-00018
10.1016/0014-5793(94)01142-7
10.1083/jcb.115.2.473
10.1523/jneurosci.23-30-09796.2003
10.1017/s1041610291000480
10.1056/nejm199902113400607
10.1016/0169-328x(92)90202-m
10.3758/brm.41.4.1149
10.1111/j.1471-4159.1991.tb03460.x
10.1002/glia.10161
10.2174/1567205013666151116130301
10.1016/s0165-5728(99)00226-x
10.1016/s0197-4580(00)00124-x
10.1128/cdli.1.4.433-436.1994
10.1016/j.exger.2004.07.007
10.1016/j.tins.2006.07.006
10.1007/s12031-014-0356-x
10.1038/nri1664
10.1097/00002093-199205000-00003
10.1007/bf02815005
10.1016/j.pneurobio.2011.11.008
10.1111/j.1440-1789.2006.00701.x
10.1016/j.archger.2009.09.028
10.1016/s0006-8993(96)01359-5
10.1016/0304-3940(94)90589-4
10.1007/s007020050029
10.1016/j.bbi.2017.01.020
10.1128/cdli.1.1.109-110.1994
10.1038/nm1781
10.2174/1389450043345308
10.1016/0006-291x(90)91229-l
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Keywords CRP
TGF-β
Alzheimer’s disease
IL-1β
Mild cognitive impairment
Language English
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References ref13
ref57
ref12
Reisberg (ref35) 1988
ref56
ref15
ref59
ref58
ref53
ref52
ref55
ref54
ref17
ref16
Park (ref33) 2012
ref51
Kaduszkiewicz (ref9) 2005
Hu (ref26) 2012
ref46
ref45
ref48
ref47
ref42
ref41
ref44
ref43
ref49
ref8
ref7
ref4
Morris (ref34) 1993
ref40
ref37
ref36
ref31
ref30
Boraschi (ref14) 1995
(ref3) 2013
ref2
ref1
ref39
Sperber (ref50) 1991
ref38
Wyss-Coray (ref10) 2006
Petersen (ref32) 1999
Norgaard (ref19) 1995
ref24
Dubois (ref5) 2013
ref23
Jose Miguel (ref6) 2012
ref25
ref20
Kumar (ref11) 2007
ref21
Zhang (ref22) 2016
ref28
ref27
Yasutake (ref18) 2006
de Almeids (ref29) 2011
References_xml – ident: ref46
  doi: 10.1016/s0361-9230(03)00088-1
– start-page: 1548
  volume-title: Standardization of Korean Version of the Mini-Mental State Examination (MMSE-K) for use in the elderly
  year: 2012
  ident: ref33
– start-page: 1757
  volume-title: Cholinesterase inhibitors for patients with Alzheimer’s disease: systematic revie of randomized clinical trials
  year: 2005
  ident: ref9
– ident: ref54
  doi: 10.1371/journal.pone.0006344
– ident: ref53
  doi: 10.1111/j.1365-2990.2005.00655.x
– ident: ref21
  doi: 10.1038/39321
– ident: ref20
  doi: 10.1006/neur.1995.0051
– ident: ref28
  doi: 10.1159/000474940
– ident: ref49
  doi: 10.1038/nrn1032
– ident: ref51
  doi: 10.1016/j.cca.2005.06.013
– ident: ref37
  doi: 10.1016/j.jpsychores.2004.01.004
– ident: ref41
  doi: 10.1016/j.jneuroim.2003.11.003
– start-page: 1005
  volume-title: Inflammation in Alzheimer’s disease: driving force, bystanderor beneficial response?
  year: 2006
  ident: ref10
– ident: ref56
  doi: 10.1097/00001756-199301000-00018
– ident: ref38
  doi: 10.1016/0014-5793(94)01142-7
– ident: ref57
  doi: 10.1083/jcb.115.2.473
– ident: ref16
  doi: 10.1523/jneurosci.23-30-09796.2003
– ident: ref36
  doi: 10.1017/s1041610291000480
– ident: ref24
  doi: 10.1056/nejm199902113400607
– ident: ref39
  doi: 10.1016/0169-328x(92)90202-m
– ident: ref31
  doi: 10.3758/brm.41.4.1149
– ident: ref52
  doi: 10.1111/j.1471-4159.1991.tb03460.x
– ident: ref48
  doi: 10.1002/glia.10161
– ident: ref4
  doi: 10.2174/1567205013666151116130301
– start-page: 897
  volume-title: Plasma multi analyze profiling in mild cognitive impairment and Alzheimer disease
  year: 2012
  ident: ref26
– ident: ref40
  doi: 10.1016/s0165-5728(99)00226-x
– ident: ref12
  doi: 10.1016/s0197-4580(00)00124-x
– ident: ref17
  doi: 10.1016/s0165-5728(99)00226-x
– ident: ref23
  doi: 10.1128/cdli.1.4.433-436.1994
– ident: ref44
  doi: 10.1016/j.exger.2004.07.007
– start-page: 75637
  volume-title: A review: inflammatory process in Alzheimer’s disease, role of cytokines
  year: 2012
  ident: ref6
– ident: ref47
  doi: 10.1016/j.tins.2006.07.006
– ident: ref2
  doi: 10.1007/s12031-014-0356-x
– ident: ref15
  doi: 10.1038/nri1664
– start-page: 2412
  volume-title: The Clinical Dementia Rating Scale (CDR): current version and scoring rules
  year: 1993
  ident: ref34
– ident: ref7
  doi: 10.1097/00002093-199205000-00003
– start-page: 303
  volume-title: Mild cognitive impairment: clinical characterization and outcome
  year: 1999
  ident: ref32
– ident: ref30
  doi: 10.1007/bf02815005
– ident: ref1
  doi: 10.1016/j.pneurobio.2011.11.008
– start-page: 481
  volume-title: Cytokines in Alzheiemer’s disease
  year: 1991
  ident: ref50
– start-page: 661
  volume-title: Global Deterioration Scale (GDS)
  year: 1988
  ident: ref35
– ident: ref43
  doi: 10.1111/j.1440-1789.2006.00701.x
– ident: ref45
  doi: 10.1016/j.archger.2009.09.028
– ident: ref25
  doi: 10.1016/s0006-8993(96)01359-5
– start-page: 31
  year: 2007
  ident: ref11
– ident: ref8
  doi: 10.1016/0304-3940(94)90589-4
– start-page: 208
  volume-title: 2013 Alzheimer’s disease facts and figures
  year: 2013
  ident: ref3
– ident: ref55
  doi: 10.1007/s007020050029
– ident: ref27
  doi: 10.1016/j.bbi.2017.01.020
– ident: ref42
  doi: 10.1128/cdli.1.1.109-110.1994
– ident: ref59
  doi: 10.1038/nm1781
– ident: ref13
  doi: 10.2174/1389450043345308
– start-page: 744
  volume-title: Alzheimer’s disease: from biomarkers to diagnosis
  year: 2013
  ident: ref5
– start-page: 402
  volume-title: Serum BDNF, TNF-alpha and IL-1 beta levels in dementia patients: comparison between Alzheimer’s disease and vascular dementia
  year: 2006
  ident: ref18
– start-page: 1503
  volume-title: Incidence of post dural puncutre headahce in research volunteers
  year: 2011
  ident: ref29
– ident: ref58
  doi: 10.1016/0006-291x(90)91229-l
– start-page: 5178
  volume-title: TGF-beta 1 factor in the cerebrovascular diseases of Alzheimer’s disease
  year: 2016
  ident: ref22
– start-page: 367
  volume-title: Transforming growth factor beta and cancer
  year: 1995
  ident: ref19
– start-page: 4719
  volume-title: Mapping of receptor biding sites on IL-1 beta by reconstruction of IL-1ra like domains
  year: 1995
  ident: ref14
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Snippet Objective Many patients suffer from dementia in its most common form, Alzheimer’s disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are...
Many patients suffer from dementia in its most common form, Alzheimer's disease (AD). In this study, the levels of IL-1β, TGF-β and CRP, which are involved in...
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Title The Association of Blood-Based Inflammatory Factors IL-1β, TGF-β and CRP with Cognitive Function in Alzheimer’s Disease and Mild Cognitive Impairment
URI https://www.ncbi.nlm.nih.gov/pubmed/33561929
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