Analysis of individual alpha frequency in a large cohort from a tertiary memory center
Background and Purpose Precise and timely diagnosis is crucial for the optimal use of emerging disease‐modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG), which is noninvasive and cost‐effective, can capture neural abnormalities linked to various dementias. This study expl...
Saved in:
Published in | European journal of neurology Vol. 31; no. 10; pp. e16424 - n/a |
---|---|
Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.10.2024
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Background and Purpose
Precise and timely diagnosis is crucial for the optimal use of emerging disease‐modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG), which is noninvasive and cost‐effective, can capture neural abnormalities linked to various dementias. This study explores the use of individual alpha frequency (IAF) derived from EEG as a diagnostic and prognostic tool in cognitively impaired patients.
Methods
This retrospective study included 375 patients from the tertiary Memory Clinic of IRCCS San Raffaele Hospital, Milan, Italy. Participants underwent clinical and neuropsychological assessments, brain imaging, cerebrospinal fluid biomarker analysis, and resting‐state EEG. Patients were categorized by amyloid status, the AT(N) classification system, clinical diagnosis, and mild cognitive impairment (MCI) progression to AD dementia. IAF was calculated and compared among study groups. Receiver operating characteristic (ROC) analysis was used to calculate its discriminative performance.
Results
IAF was higher in amyloid‐negative subjects and varied significantly across AT(N) groups. ROC analysis confirmed IAF's ability to distinguish A–T–N– from the A+T+N+ and A+T–N+ groups. IAF was lower in AD and Lewy body dementia patients compared to MCI and other dementia types, with moderate discriminatory capability. Among A+ MCI patients, IAF was significantly lower in those who converted to AD within 2 years compared to stable MCI patients and predicted time to conversion (p < 0.001, R = 0.38).
Conclusions
IAF is a valuable tool for dementia diagnosis and prognosis, correlating with amyloid status and neurodegeneration. It effectively predicts MCI progression to AD, supporting its use in early, targeted interventions in the context of disease‐modifying treatments. |
---|---|
AbstractList | Background and Purpose
Precise and timely diagnosis is crucial for the optimal use of emerging disease‐modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG), which is noninvasive and cost‐effective, can capture neural abnormalities linked to various dementias. This study explores the use of individual alpha frequency (IAF) derived from EEG as a diagnostic and prognostic tool in cognitively impaired patients.
Methods
This retrospective study included 375 patients from the tertiary Memory Clinic of IRCCS San Raffaele Hospital, Milan, Italy. Participants underwent clinical and neuropsychological assessments, brain imaging, cerebrospinal fluid biomarker analysis, and resting‐state EEG. Patients were categorized by amyloid status, the AT(N) classification system, clinical diagnosis, and mild cognitive impairment (MCI) progression to AD dementia. IAF was calculated and compared among study groups. Receiver operating characteristic (ROC) analysis was used to calculate its discriminative performance.
Results
IAF was higher in amyloid‐negative subjects and varied significantly across AT(N) groups. ROC analysis confirmed IAF's ability to distinguish A–T–N– from the A+T+N+ and A+T–N+ groups. IAF was lower in AD and Lewy body dementia patients compared to MCI and other dementia types, with moderate discriminatory capability. Among A+ MCI patients, IAF was significantly lower in those who converted to AD within 2 years compared to stable MCI patients and predicted time to conversion (p < 0.001, R = 0.38).
Conclusions
IAF is a valuable tool for dementia diagnosis and prognosis, correlating with amyloid status and neurodegeneration. It effectively predicts MCI progression to AD, supporting its use in early, targeted interventions in the context of disease‐modifying treatments. Precise and timely diagnosis is crucial for the optimal use of emerging disease-modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG), which is noninvasive and cost-effective, can capture neural abnormalities linked to various dementias. This study explores the use of individual alpha frequency (IAF) derived from EEG as a diagnostic and prognostic tool in cognitively impaired patients.BACKGROUND AND PURPOSEPrecise and timely diagnosis is crucial for the optimal use of emerging disease-modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG), which is noninvasive and cost-effective, can capture neural abnormalities linked to various dementias. This study explores the use of individual alpha frequency (IAF) derived from EEG as a diagnostic and prognostic tool in cognitively impaired patients.This retrospective study included 375 patients from the tertiary Memory Clinic of IRCCS San Raffaele Hospital, Milan, Italy. Participants underwent clinical and neuropsychological assessments, brain imaging, cerebrospinal fluid biomarker analysis, and resting-state EEG. Patients were categorized by amyloid status, the AT(N) classification system, clinical diagnosis, and mild cognitive impairment (MCI) progression to AD dementia. IAF was calculated and compared among study groups. Receiver operating characteristic (ROC) analysis was used to calculate its discriminative performance.METHODSThis retrospective study included 375 patients from the tertiary Memory Clinic of IRCCS San Raffaele Hospital, Milan, Italy. Participants underwent clinical and neuropsychological assessments, brain imaging, cerebrospinal fluid biomarker analysis, and resting-state EEG. Patients were categorized by amyloid status, the AT(N) classification system, clinical diagnosis, and mild cognitive impairment (MCI) progression to AD dementia. IAF was calculated and compared among study groups. Receiver operating characteristic (ROC) analysis was used to calculate its discriminative performance.IAF was higher in amyloid-negative subjects and varied significantly across AT(N) groups. ROC analysis confirmed IAF's ability to distinguish A-T-N- from the A+T+N+ and A+T-N+ groups. IAF was lower in AD and Lewy body dementia patients compared to MCI and other dementia types, with moderate discriminatory capability. Among A+ MCI patients, IAF was significantly lower in those who converted to AD within 2 years compared to stable MCI patients and predicted time to conversion (p < 0.001, R = 0.38).RESULTSIAF was higher in amyloid-negative subjects and varied significantly across AT(N) groups. ROC analysis confirmed IAF's ability to distinguish A-T-N- from the A+T+N+ and A+T-N+ groups. IAF was lower in AD and Lewy body dementia patients compared to MCI and other dementia types, with moderate discriminatory capability. Among A+ MCI patients, IAF was significantly lower in those who converted to AD within 2 years compared to stable MCI patients and predicted time to conversion (p < 0.001, R = 0.38).IAF is a valuable tool for dementia diagnosis and prognosis, correlating with amyloid status and neurodegeneration. It effectively predicts MCI progression to AD, supporting its use in early, targeted interventions in the context of disease-modifying treatments.CONCLUSIONSIAF is a valuable tool for dementia diagnosis and prognosis, correlating with amyloid status and neurodegeneration. It effectively predicts MCI progression to AD, supporting its use in early, targeted interventions in the context of disease-modifying treatments. Precise and timely diagnosis is crucial for the optimal use of emerging disease-modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG), which is noninvasive and cost-effective, can capture neural abnormalities linked to various dementias. This study explores the use of individual alpha frequency (IAF) derived from EEG as a diagnostic and prognostic tool in cognitively impaired patients. This retrospective study included 375 patients from the tertiary Memory Clinic of IRCCS San Raffaele Hospital, Milan, Italy. Participants underwent clinical and neuropsychological assessments, brain imaging, cerebrospinal fluid biomarker analysis, and resting-state EEG. Patients were categorized by amyloid status, the AT(N) classification system, clinical diagnosis, and mild cognitive impairment (MCI) progression to AD dementia. IAF was calculated and compared among study groups. Receiver operating characteristic (ROC) analysis was used to calculate its discriminative performance. IAF was higher in amyloid-negative subjects and varied significantly across AT(N) groups. ROC analysis confirmed IAF's ability to distinguish A-T-N- from the A+T+N+ and A+T-N+ groups. IAF was lower in AD and Lewy body dementia patients compared to MCI and other dementia types, with moderate discriminatory capability. Among A+ MCI patients, IAF was significantly lower in those who converted to AD within 2 years compared to stable MCI patients and predicted time to conversion (p < 0.001, R = 0.38). IAF is a valuable tool for dementia diagnosis and prognosis, correlating with amyloid status and neurodegeneration. It effectively predicts MCI progression to AD, supporting its use in early, targeted interventions in the context of disease-modifying treatments. Background and PurposePrecise and timely diagnosis is crucial for the optimal use of emerging disease‐modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG), which is noninvasive and cost‐effective, can capture neural abnormalities linked to various dementias. This study explores the use of individual alpha frequency (IAF) derived from EEG as a diagnostic and prognostic tool in cognitively impaired patients.MethodsThis retrospective study included 375 patients from the tertiary Memory Clinic of IRCCS San Raffaele Hospital, Milan, Italy. Participants underwent clinical and neuropsychological assessments, brain imaging, cerebrospinal fluid biomarker analysis, and resting‐state EEG. Patients were categorized by amyloid status, the AT(N) classification system, clinical diagnosis, and mild cognitive impairment (MCI) progression to AD dementia. IAF was calculated and compared among study groups. Receiver operating characteristic (ROC) analysis was used to calculate its discriminative performance.ResultsIAF was higher in amyloid‐negative subjects and varied significantly across AT(N) groups. ROC analysis confirmed IAF's ability to distinguish A–T–N– from the A+T+N+ and A+T–N+ groups. IAF was lower in AD and Lewy body dementia patients compared to MCI and other dementia types, with moderate discriminatory capability. Among A+ MCI patients, IAF was significantly lower in those who converted to AD within 2 years compared to stable MCI patients and predicted time to conversion (p < 0.001, R = 0.38).ConclusionsIAF is a valuable tool for dementia diagnosis and prognosis, correlating with amyloid status and neurodegeneration. It effectively predicts MCI progression to AD, supporting its use in early, targeted interventions in the context of disease‐modifying treatments. |
Author | Curti, Davide G. Rugarli, Giulia Santangelo, Roberto Magnani, Giuseppe Cursi, Marco Caso, Francesca Filippi, Massimo Spinelli, Edoardo G. Fanelli, Giovanna Franca Canu, Elisa Agosta, Federica Basaia, Silvia Coraglia, Federico Cecchetti, Giordano |
AuthorAffiliation | 5 Neurorehabilitation Unit IRCCS San Raffaele Scientific Institute Milan Italy 3 Neuroimaging Research Unit, Division of Neuroscience IRCCS San Raffaele Scientific Institute Milan Italy 1 Neurology Unit IRCCS San Raffaele Scientific Institute Milan Italy 4 Vita‐Salute San Raffaele University Milan Italy 2 Neurophysiology Service IRCCS San Raffaele Scientific Institute Milan Italy |
AuthorAffiliation_xml | – name: 5 Neurorehabilitation Unit IRCCS San Raffaele Scientific Institute Milan Italy – name: 2 Neurophysiology Service IRCCS San Raffaele Scientific Institute Milan Italy – name: 1 Neurology Unit IRCCS San Raffaele Scientific Institute Milan Italy – name: 4 Vita‐Salute San Raffaele University Milan Italy – name: 3 Neuroimaging Research Unit, Division of Neuroscience IRCCS San Raffaele Scientific Institute Milan Italy |
Author_xml | – sequence: 1 givenname: Giordano orcidid: 0000-0002-6544-410X surname: Cecchetti fullname: Cecchetti, Giordano organization: Vita‐Salute San Raffaele University – sequence: 2 givenname: Federica orcidid: 0000-0003-3121-4979 surname: Agosta fullname: Agosta, Federica organization: Vita‐Salute San Raffaele University – sequence: 3 givenname: Elisa orcidid: 0000-0001-5804-3378 surname: Canu fullname: Canu, Elisa organization: IRCCS San Raffaele Scientific Institute – sequence: 4 givenname: Silvia orcidid: 0000-0002-0722-6243 surname: Basaia fullname: Basaia, Silvia organization: IRCCS San Raffaele Scientific Institute – sequence: 5 givenname: Giulia surname: Rugarli fullname: Rugarli, Giulia organization: Vita‐Salute San Raffaele University – sequence: 6 givenname: Davide G. surname: Curti fullname: Curti, Davide G. organization: Vita‐Salute San Raffaele University – sequence: 7 givenname: Federico surname: Coraglia fullname: Coraglia, Federico organization: Vita‐Salute San Raffaele University – sequence: 8 givenname: Marco orcidid: 0000-0002-7928-0417 surname: Cursi fullname: Cursi, Marco organization: IRCCS San Raffaele Scientific Institute – sequence: 9 givenname: Edoardo G. orcidid: 0000-0003-1492-7221 surname: Spinelli fullname: Spinelli, Edoardo G. organization: Vita‐Salute San Raffaele University – sequence: 10 givenname: Roberto orcidid: 0000-0002-8760-2703 surname: Santangelo fullname: Santangelo, Roberto organization: IRCCS San Raffaele Scientific Institute – sequence: 11 givenname: Francesca surname: Caso fullname: Caso, Francesca organization: IRCCS San Raffaele Scientific Institute – sequence: 12 givenname: Giovanna Franca surname: Fanelli fullname: Fanelli, Giovanna Franca organization: IRCCS San Raffaele Scientific Institute – sequence: 13 givenname: Giuseppe surname: Magnani fullname: Magnani, Giuseppe organization: IRCCS San Raffaele Scientific Institute – sequence: 14 givenname: Massimo orcidid: 0000-0002-5485-0479 surname: Filippi fullname: Filippi, Massimo email: filippi.massimo@hsr.it organization: IRCCS San Raffaele Scientific Institute |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39087560$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kU1vEzEQhi1URD_gwB9AK3GBw7aetb3ZnFBVhYJUtRfgajn2uHHltYOdbZV_z4S0FSBhH8aa95nxfByzg5QTMvYW-CnQOcOEp9DLTr5gRyD7oQUh4IDeQkGrgMMhO671jnPezTr-ih2KOR9mqudH7Md5MnFbQ22yb0Jy4T64ycTGxPXKNL7gzwmT3ZLUmCaacouNzatcNqTlkXwbLJtgyrYZccxkLCZyvWYvvYkV3zzaE_b98-LbxZf26uby68X5VWsll7K1YLpu3s_mg3fKWYve2Y57h71wSy-NU9YOUsklQg_WLju6xnOlnJDCCiNO2Kd93vW0HNHtPi8m6nUJI9Wkswn6byWFlb7N9xpAghy4pAwfHjOUTL3WjR5DtRijSZinqgUf-rkicoe-_we9y1Oh-REFfAaKUzNEvfuzpOdanmZOwMc9YEuutaB_RoDr3T417VP_3iexZ3v2IUTc_h_Ui-vFPuIXO1iiWQ |
Cites_doi | 10.1016/j.neurobiolaging.2021.11.009 10.1016/0013-4694(87)90206-9 10.1097/WAD.0000000000000034 10.1016/S1474-4422(21)00066-1 10.1016/j.nicl.2021.102711 10.1159/000117270 10.1016/j.jalz.2018.02.018 10.1016/j.neurobiolaging.2011.12.011 10.1212/WNL.0b013e318224af8d 10.1017/S1041610221001083 10.1038/s41598-022-21951-5 10.1212/WNL.0000000000004058 10.1016/j.jalz.2011.03.008 10.1093/brain/awr179 10.1007/s00259-020-04853-4 |
ContentType | Journal Article |
Copyright | 2024 The Author(s). published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. 2024 The Author(s). European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. 2024. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
Copyright_xml | – notice: 2024 The Author(s). published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. – notice: 2024 The Author(s). European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. – notice: 2024. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
DBID | 24P AAYXX CITATION NPM 7TK 7U7 C1K K9. 7X8 5PM |
DOI | 10.1111/ene.16424 |
DatabaseName | Wiley Online Library Open Access 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 PubMed ProQuest Health & Medical Complete (Alumni) |
Database_xml | – sequence: 1 dbid: 24P name: Wiley Online Library Open Access url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html sourceTypes: Publisher – 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 |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
DocumentTitleAlternate | EEG alpha frequency in dementia |
EISSN | 1468-1331 |
EndPage | n/a |
ExternalDocumentID | PMC11414804 39087560 10_1111_ene_16424 ENE16424 |
Genre | shortCommunication Journal Article |
GroupedDBID | --- .3N .GA .Y3 05W 0R~ 10A 169 1OB 1OC 24P 29G 31~ 33P 36B 3SF 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5GY 5HH 5LA 5VS 66C 702 7PT 7X7 8-0 8-1 8-3 8-4 8-5 8FI 8FJ 8UM 930 A01 A03 AAESR AAEVG AAHHS AANHP AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABIVO ABJNI ABPVW ABUWG ABXGK ACAHQ ACBWZ ACCFJ ACCMX ACCZN ACGFS ACGOF ACMXC ACPOU ACPRK ACRPL ACSCC ACXBN ACXQS ACYXJ ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADNMO ADOZA ADPDF ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFEBI AFGKR AFKRA AFPWT AFRAH AFWVQ AFZJQ AHMBA AIACR AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ASPBG ATUGU AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BENPR BFHJK BHBCM BMXJE BROTX BRXPI BY8 C45 CAG CCPQU COF CS3 D-6 D-7 D-E D-F DCZOG DPXWK DR2 DRFUL DRMAN DRSTM DU5 EBS EJD EMOBN ESX EX3 F00 F5P FEDTE FUBAC FYBCS FYUFA G-S G.N GODZA H.X HF~ HMCUK HVGLF HZI HZ~ IHE IX1 J0M K48 KBYEO LATKE LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ O66 O9- OIG OVD OVEED P2P P2W P2X P2Z P4B P4D PALCI PQQKQ Q.N Q11 QB0 R.K RIG RIWAO RJQFR ROL RPM RX1 SAMSI SUPJJ TEORI UB1 UKHRP W8V W99 WBKPD WHWMO WIH WIJ WIK WOHZO WOW WQJ WVDHM WXI WXSBR XG1 YFH ZZTAW ~IA ~WT AAYXX AGQPQ CITATION AAMMB AEFGJ AGXDD AIDQK AIDYY NPM 7TK 7U7 C1K K9. 7X8 WIN 5PM |
ID | FETCH-LOGICAL-c4044-c1a2296798fd5dccefdc20fde63dbf4ad5cc8454be161ccb2b2baf055d343c3a3 |
IEDL.DBID | DR2 |
ISSN | 1351-5101 1468-1331 |
IngestDate | Thu Aug 21 18:34:15 EDT 2025 Tue Aug 05 10:07:18 EDT 2025 Sat Jul 26 02:06:43 EDT 2025 Mon Jul 21 06:03:45 EDT 2025 Tue Jul 01 03:16:03 EDT 2025 Wed Jan 22 17:14:28 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Keywords | differential diagnosis Alzheimer disease individual alpha frequency EEG biomarkers |
Language | English |
License | Attribution 2024 The Author(s). European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c4044-c1a2296798fd5dccefdc20fde63dbf4ad5cc8454be161ccb2b2baf055d343c3a3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-6544-410X 0000-0002-0722-6243 0000-0003-3121-4979 0000-0003-1492-7221 0000-0002-7928-0417 0000-0002-8760-2703 0000-0002-5485-0479 0000-0001-5804-3378 |
OpenAccessLink | https://proxy.k.utb.cz/login?url=https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fene.16424 |
PMID | 39087560 |
PQID | 3107150229 |
PQPubID | 1066358 |
PageCount | 6 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_11414804 proquest_miscellaneous_3086958044 proquest_journals_3107150229 pubmed_primary_39087560 crossref_primary_10_1111_ene_16424 wiley_primary_10_1111_ene_16424_ENE16424 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | October 2024 |
PublicationDateYYYYMMDD | 2024-10-01 |
PublicationDate_xml | – month: 10 year: 2024 text: October 2024 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: Oxford – name: Hoboken |
PublicationTitle | European journal of neurology |
PublicationTitleAlternate | Eur J Neurol |
PublicationYear | 2024 |
Publisher | John Wiley & Sons, Inc John Wiley and Sons Inc |
Publisher_xml | – name: John Wiley & Sons, Inc – name: John Wiley and Sons Inc |
References | 2022; 112 1987; 66 2021; 31 2021; 20 2021; 33 2017; 89 2022; 12 2011; 77 2020; 47 2014; 28 1996; 36 2012; 33 2011; 134 2011; 7 2018; 14 e_1_2_8_13_1 e_1_2_8_14_1 e_1_2_8_15_1 e_1_2_8_16_1 e_1_2_8_3_1 e_1_2_8_2_1 e_1_2_8_5_1 e_1_2_8_4_1 e_1_2_8_7_1 e_1_2_8_6_1 e_1_2_8_9_1 e_1_2_8_8_1 e_1_2_8_10_1 e_1_2_8_11_1 e_1_2_8_12_1 |
References_xml | – volume: 33 start-page: 2343 year: 2012 end-page: 2356 article-title: Quantitative EEG and LORETA: valuable tools in discerning FTD from AD? publication-title: Neurobiol Aging – volume: 47 start-page: 3152 year: 2020 end-page: 3164 article-title: CSF p‐tau/Abeta(42) ratio and brain FDG‐PET may reliably detect MCI "imminent" converters to AD publication-title: Eur J Nucl Med Mol Imaging – volume: 89 start-page: 88 year: 2017 end-page: 100 article-title: Diagnosis and management of dementia with Lewy bodies: fourth consensus report of the DLB consortium publication-title: Neurology – volume: 20 start-page: 484 year: 2021 end-page: 496 article-title: Clinical diagnosis of Alzheimer's disease: recommendations of the international working group publication-title: Lancet Neurol – volume: 112 start-page: 87 year: 2022 end-page: 101 article-title: Alpha desynchronization during Stroop test unmasks cognitively healthy individuals with abnormal CSF amyloid/tau publication-title: Neurobiol Aging – volume: 28 start-page: 206 year: 2014 end-page: 218 article-title: Diagnostic criteria for vascular cognitive disorders: a VASCOG statement publication-title: Alzheimer Dis Assoc Disord – volume: 66 start-page: 376 year: 1987 end-page: 382 article-title: Cerebral location of international 10‐20 system electrode placement publication-title: Electroencephalogr Clin Neurophysiol – volume: 33 start-page: 1321 year: 2021 end-page: 1325 article-title: Slowing on quantitative EEG is associated with transition to dementia in mild cognitive impairment publication-title: Int Psychogeriatr – volume: 14 start-page: 535 year: 2018 end-page: 562 article-title: NIA‐AA research framework: toward a biological definition of Alzheimer's disease publication-title: Alzheimers Dement – volume: 36 start-page: 268 year: 1996 end-page: 272 article-title: Inter‐ and intraobserver reproducibility of cerebral atrophy assessment on MRI scans with hemispheric infarcts publication-title: Eur Neurol – volume: 12 start-page: 18706 year: 2022 article-title: Implication of EEG theta/alpha and theta/beta ratio in Alzheimer's and Lewy body disease publication-title: Sci Rep – volume: 7 start-page: 270 year: 2011 end-page: 279 article-title: The diagnosis of mild cognitive impairment due to Alzheimer's disease: recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease publication-title: Alzheimers Dement – volume: 134 start-page: 2456 year: 2011 end-page: 2477 article-title: Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia publication-title: Brain – volume: 77 start-page: 118 year: 2011 end-page: 124 article-title: Quantitative EEG as a predictive biomarker for Parkinson disease dementia publication-title: Neurology – volume: 31 year: 2021 article-title: Resting‐state electroencephalographic biomarkers of Alzheimer's disease publication-title: Neuroimage Clin – ident: e_1_2_8_15_1 doi: 10.1016/j.neurobiolaging.2021.11.009 – ident: e_1_2_8_13_1 doi: 10.1016/0013-4694(87)90206-9 – ident: e_1_2_8_12_1 doi: 10.1097/WAD.0000000000000034 – ident: e_1_2_8_9_1 doi: 10.1016/S1474-4422(21)00066-1 – ident: e_1_2_8_2_1 doi: 10.1016/j.nicl.2021.102711 – ident: e_1_2_8_7_1 doi: 10.1159/000117270 – ident: e_1_2_8_6_1 doi: 10.1016/j.jalz.2018.02.018 – ident: e_1_2_8_3_1 doi: 10.1016/j.neurobiolaging.2011.12.011 – ident: e_1_2_8_4_1 doi: 10.1212/WNL.0b013e318224af8d – ident: e_1_2_8_5_1 doi: 10.1017/S1041610221001083 – ident: e_1_2_8_14_1 doi: 10.1038/s41598-022-21951-5 – ident: e_1_2_8_11_1 doi: 10.1212/WNL.0000000000004058 – ident: e_1_2_8_8_1 doi: 10.1016/j.jalz.2011.03.008 – ident: e_1_2_8_10_1 doi: 10.1093/brain/awr179 – ident: e_1_2_8_16_1 doi: 10.1007/s00259-020-04853-4 |
SSID | ssj0002720 |
Score | 2.4357407 |
Snippet | Background and Purpose
Precise and timely diagnosis is crucial for the optimal use of emerging disease‐modifying treatments for Alzheimer disease (AD).... Precise and timely diagnosis is crucial for the optimal use of emerging disease-modifying treatments for Alzheimer disease (AD). Electroencephalography (EEG),... Background and PurposePrecise and timely diagnosis is crucial for the optimal use of emerging disease‐modifying treatments for Alzheimer disease (AD).... |
SourceID | pubmedcentral proquest pubmed crossref wiley |
SourceType | Open Access Repository Aggregation Database Index Database Publisher |
StartPage | e16424 |
SubjectTerms | Abnormalities Alzheimer disease Alzheimer's disease Biomarkers Cerebrospinal fluid Cognitive ability Cost analysis Dementia Dementia and Cognitive Disorders Dementia disorders Diagnosis differential diagnosis EEG Electroencephalography individual alpha frequency Lewy bodies Memory Neurodegenerative diseases Neuroimaging Patients Short Communication |
Title | Analysis of individual alpha frequency in a large cohort from a tertiary memory center |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fene.16424 https://www.ncbi.nlm.nih.gov/pubmed/39087560 https://www.proquest.com/docview/3107150229 https://www.proquest.com/docview/3086958044 https://pubmed.ncbi.nlm.nih.gov/PMC11414804 |
Volume | 31 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Na9wwEB3SBEovTT9TN-milhx68eKVJVsmp7RsCIEsITRhDwUjyRJZ0nrLZveQ_vrOyB_NNgRCMRhjybZkaeQ3nqcngH0jMu9yNYpVJopYcO1iVegiJtdCG-GF9xTRPZ1kxxfiZCqnG3DQzYVp9CH6H25kGWG8JgPX5uaOkeNQMESsz0kLlLhaBIjO_0pHUXwxOFtyFFO_a1WFiMXTX7n-LboHMO_zJO_i1_ABOtqG713RG97J9XC1NEP7-x9Vx_-s2wt43gJTdtj0pJew4epX8PS0Db2_hstOvoTNPZv107hYmKzL_KKhZN9iEtPsB_HLGS2-u1gymsGC54h8MMMisZ9E7r1lVF23eAMXR-NvX4_jdlGG2IpEiNiONOcFxW58JStrna8sT3zlsrQyXuhKWquEFMYhlrTWcNy0T6SsUpHaVKdvYbOe1-4dMCW0G_FcG6sMLc-uhPJSKoOIJde5sBF86pqn_NVob5Sdz4JvqAxvKIK9ruHK1vxuSsSsOSJdLGgEH_tkNByKhujazVeYB525QiqsUwQ7TTv3T0kLEvrPkgjUWg_oM5Ao93pKPbsK4tzoX6KHmeBNP4cWfrjk5XgyDgfvH591F55xRFUNm3APNpeLlfuAqGhpBvCEizPc59N8AFtfxpOz80EwiUH4hfUHF74OMQ |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB6VIgGX8oZAAYM4cMkqm4wTR-KC0FYLdPeAWtQLimzHFquWLFp2D-2vZ8Z50KVCQiiXKHaS8WPsbzzjzwCvDebeFWocqxzLGFPtYlXqMmbTQhv06D17dGfzfHqMH0_kyQ687ffCtPwQw4Iba0YYr1nBeUH6kpbTWDAisJ_iNbjOJ3oHg-rzb_Io9jAGc0uOY-55Ha8Qx_EMr27PRlcg5tVIycsINkxBB7fhay98G3lyOtqszche_MHr-L-luwN7HTYV79rOdBd2XHMPbsw67_t9-NIzmIilF4thJ5cI-3WFX7VR2eeUJLQ44xBzwefvrtaCN7HQM44_WJBM4jvH954LLq9bPYDjg8nR-2ncncsQW0wQYzvWaVqy-8bXsrbW-dqmia9dntXGo66ltQolGkdw0lqT0qV9ImWdYWYznT2E3WbZuMcgFGo3TgttrDJ8QrtC5aVUhkBLoQu0Ebzq26f60dJvVL3ZQjVUhRqKYL9vuarTwJ8VwdaCwC4JGsHLIZl0hx0iunHLDeUhe66UisoUwaO2oYe_ZCVz_edJBGqrCwwZmJd7O6VZfAv83GRikpGZ0EffhCb-u-TVZD4JN0_-PesLuDk9mh1Whx_mn57CrZRAVhtcuA-769XGPSOQtDbPgy78Ami7DeQ |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB6VIlVcoDwbKGAQBy5ZZZNx4ohTRXdVHl0hRFEPSJHt2GJVyFbL7qH8emacB10qJIRyiWInsT0z8TeZ8WeAFwZz7wo1jlWOZYypdrEqdRmza6ENevSeI7rHs_zoBN-eytMteNWvhWn5IYYfbmwZ4XvNBn5e-0tGTp-CEWH9FK_BdcwTxSp9-PE3dxQHGIO3JccxK15HK8RpPMOtm5PRFYR5NVHyMoANM9D0Fnzp294mnpyN1iszsj__oHX8z87tws0OmYqDVpVuw5Zr7sDOcRd7vwufe_4SsfBiPqzjEmG1rvDLNif7goqEFt84wVzw7rvLleAlLHSNsw_m1CTxnbN7LwR31y3vwcl08un1UdztyhBbTBBjO9ZpWnLwxteyttb52qaJr12e1cajrqW1CiUaR2DSWpPSoX0iZZ1hZjOd3YftZtG4PRAKtRunhTZWGd6fXaHyUipDkKXQBdoInvfiqc5b8o2qd1pohKowQhHs94KrOvv7URFoLQjqUkMjeDYUk-VwOEQ3brGmOuTNlVJRnyJ40Mp5eEtWMtN_nkSgNjRgqMCs3JslzfxrYOcmB5NczIQe-jJI-O8tryazSTh5-O9Vn8LOh8Np9f7N7N0juJESwmozC_dhe7Vcu8eEkFbmSbCEX1t6DJw |
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=Analysis+of+individual+alpha+frequency+in+a+large+cohort+from+a+tertiary+memory+center&rft.jtitle=European+journal+of+neurology&rft.au=Cecchetti%2C+Giordano&rft.au=Agosta%2C+Federica&rft.au=Canu%2C+Elisa&rft.au=Basaia%2C+Silvia&rft.date=2024-10-01&rft.issn=1351-5101&rft.eissn=1468-1331&rft.volume=31&rft.issue=10&rft_id=info:doi/10.1111%2Fene.16424&rft.externalDBID=n%2Fa&rft.externalDocID=10_1111_ene_16424 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1351-5101&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1351-5101&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1351-5101&client=summon |