Single Subject Classification of Alzheimer's Disease and Behavioral Variant Frontotemporal Dementia Using Anatomical, Diffusion Tensor, and Resting-State Functional Magnetic Resonance Imaging
Overlapping clinical symptoms often complicate differential diagnosis between patients with Alzheimer's disease (AD) and behavioral variant frontotemporal dementia (bvFTD). Magnetic resonance imaging (MRI) reveals disease specific structural and functional differences that aid in differentiatin...
Saved in:
Published in | Journal of Alzheimer's disease Vol. 62; no. 4; p. 1827 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
01.01.2018
|
Subjects | |
Online Access | Get more information |
Cover
Loading…
Abstract | Overlapping clinical symptoms often complicate differential diagnosis between patients with Alzheimer's disease (AD) and behavioral variant frontotemporal dementia (bvFTD). Magnetic resonance imaging (MRI) reveals disease specific structural and functional differences that aid in differentiating AD from bvFTD patients. However, the benefit of combining structural and functional connectivity measures to-on a subject-basis-differentiate these dementia-types is not yet known.
Anatomical, diffusion tensor (DTI), and resting-state functional MRI (rs-fMRI) of 30 patients with early stage AD, 23 with bvFTD, and 35 control subjects were collected and used to calculate measures of structural and functional tissue status. All measures were used separately or selectively combined as predictors for training an elastic net regression classifier. Each classifier's ability to accurately distinguish dementia-types was quantified by calculating the area under the receiver operating characteristic curves (AUC).
Highest AUC values for AD and bvFTD discrimination were obtained when mean diffusivity, full correlations between rs-fMRI-derived independent components, and fractional anisotropy (FA) were combined (0.811). Similarly, combining gray matter density (GMD), FA, and rs-fMRI correlations resulted in highest AUC of 0.922 for control and bvFTD classifications. This, however, was not observed for control and AD differentiations. Classifications with GMD (0.940) and a GMD and DTI combination (0.941) resulted in similar AUC values (p = 0.41).
Combining functional and structural connectivity measures improve dementia-type differentiations and may contribute to more accurate and substantiated differential diagnosis of AD and bvFTD patients. Imaging protocols for differential diagnosis may benefit from also including DTI and rs-fMRI. |
---|---|
AbstractList | Overlapping clinical symptoms often complicate differential diagnosis between patients with Alzheimer's disease (AD) and behavioral variant frontotemporal dementia (bvFTD). Magnetic resonance imaging (MRI) reveals disease specific structural and functional differences that aid in differentiating AD from bvFTD patients. However, the benefit of combining structural and functional connectivity measures to-on a subject-basis-differentiate these dementia-types is not yet known.
Anatomical, diffusion tensor (DTI), and resting-state functional MRI (rs-fMRI) of 30 patients with early stage AD, 23 with bvFTD, and 35 control subjects were collected and used to calculate measures of structural and functional tissue status. All measures were used separately or selectively combined as predictors for training an elastic net regression classifier. Each classifier's ability to accurately distinguish dementia-types was quantified by calculating the area under the receiver operating characteristic curves (AUC).
Highest AUC values for AD and bvFTD discrimination were obtained when mean diffusivity, full correlations between rs-fMRI-derived independent components, and fractional anisotropy (FA) were combined (0.811). Similarly, combining gray matter density (GMD), FA, and rs-fMRI correlations resulted in highest AUC of 0.922 for control and bvFTD classifications. This, however, was not observed for control and AD differentiations. Classifications with GMD (0.940) and a GMD and DTI combination (0.941) resulted in similar AUC values (p = 0.41).
Combining functional and structural connectivity measures improve dementia-type differentiations and may contribute to more accurate and substantiated differential diagnosis of AD and bvFTD patients. Imaging protocols for differential diagnosis may benefit from also including DTI and rs-fMRI. |
Author | Bouts, Mark J R J Hafkemeijer, Anne Feis, Rogier A van der Grond, Jeroen Rombouts, Serge A R B van Swieten, John C Möller, Christiane de Rooij, Mark Wink, Alle Meije Schouten, Tijn M de Vos, Frank van der Flier, Wiesje M Pijnenburg, Yolande A L Vrenken, Hugo Barkhof, Frederik Dopper, Elise Scheltens, Philip |
Author_xml | – sequence: 1 givenname: Mark J R J surname: Bouts fullname: Bouts, Mark J R J organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands – sequence: 2 givenname: Christiane surname: Möller fullname: Möller, Christiane organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands – sequence: 3 givenname: Anne surname: Hafkemeijer fullname: Hafkemeijer, Anne organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands – sequence: 4 givenname: John C surname: van Swieten fullname: van Swieten, John C organization: Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands – sequence: 5 givenname: Elise surname: Dopper fullname: Dopper, Elise organization: Alzheimer Center and Department of Neurology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands – sequence: 6 givenname: Wiesje M surname: van der Flier fullname: van der Flier, Wiesje M organization: Department of Epidemiology and Biostatistics, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands – sequence: 7 givenname: Hugo surname: Vrenken fullname: Vrenken, Hugo organization: Department of Physics and Medical Technology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands – sequence: 8 givenname: Alle Meije surname: Wink fullname: Wink, Alle Meije organization: Department of Radiology and Nuclear Medicine, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands – sequence: 9 givenname: Yolande A L surname: Pijnenburg fullname: Pijnenburg, Yolande A L organization: Alzheimer Center and Department of Neurology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands – sequence: 10 givenname: Philip surname: Scheltens fullname: Scheltens, Philip organization: Alzheimer Center and Department of Neurology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands – sequence: 11 givenname: Frederik surname: Barkhof fullname: Barkhof, Frederik organization: Institute of Neurology and Healthcare Engineering, University College London, London, UK – sequence: 12 givenname: Tijn M surname: Schouten fullname: Schouten, Tijn M organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands – sequence: 13 givenname: Frank surname: de Vos fullname: de Vos, Frank organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands – sequence: 14 givenname: Rogier A surname: Feis fullname: Feis, Rogier A organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands – sequence: 15 givenname: Jeroen surname: van der Grond fullname: van der Grond, Jeroen organization: Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands – sequence: 16 givenname: Mark surname: de Rooij fullname: de Rooij, Mark organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands – sequence: 17 givenname: Serge A R B surname: Rombouts fullname: Rombouts, Serge A R B organization: Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29614652$$D View this record in MEDLINE/PubMed |
BookMark | eNo1kM1OwkAUhSdGIz-68QHM7NxQnZnblnaJIIrBmAi4JZfpLQxpp6QzmOjL-WoW1NVNTr585-Z02KmtLDF2JcUtKIC758EokH2RpHDC2jLpR0GSiqTFOs5thRAg0v45a6k0lmEcqTb7nhm7LojP9qstac-HBTpncqPRm8ryKueD4mtDpqT6xvGRcYSOONqM39MGP0xVY8HfsTZoPR_XlfWVp3J3jEdUkvUG-cI1JXxg0VdlYy56jSjP9-7QMCfrqrp3VL6R8w0ZzDx64uO91YcnGtMLri15ow9EE1hNfFLiumEv2FmOhaPLv9tli_HDfPgUTF8fJ8PBNNCQgA8UaJ2CSqMwFKEKM5GByHMZyyiSoWrmShOVCMAYdawSCCOICWQUAqxkJoFUl13_enf7VUnZclebEuvP5f-S6gdcU3aW |
CitedBy_id | crossref_primary_10_1080_14737175_2022_2048648 crossref_primary_10_1016_j_nicl_2022_102947 crossref_primary_10_1007_s11548_024_03197_w crossref_primary_10_3389_fncom_2019_00072 crossref_primary_10_1177_19714009251313511 crossref_primary_10_1097_RMR_0000000000000223 crossref_primary_10_3389_fnagi_2020_602510 crossref_primary_10_1002_alz_13441 crossref_primary_10_1016_j_nicl_2019_101718 crossref_primary_10_18632_aging_203984 crossref_primary_10_1111_jon_13063 crossref_primary_10_3233_JAD_181004 crossref_primary_10_1016_j_neurobiolaging_2024_08_008 crossref_primary_10_1002_ana_25547 crossref_primary_10_1016_j_clinph_2024_12_008 crossref_primary_10_1016_j_nicl_2018_07_014 crossref_primary_10_1002_hbm_24554 crossref_primary_10_1097_WCO_0000000000000838 crossref_primary_10_14336_AD_2018_1129 crossref_primary_10_1016_j_nicl_2019_101811 crossref_primary_10_1016_j_neurad_2020_04_004 crossref_primary_10_1016_j_nicl_2019_101711 crossref_primary_10_1007_s11357_022_00539_x crossref_primary_10_1016_j_heliyon_2022_e08901 crossref_primary_10_1136_jnnp_2019_320774 crossref_primary_10_1212_WNL_0000000000201292 crossref_primary_10_1093_braincomms_fcaa079 crossref_primary_10_1177_20584601211066467 |
ContentType | Journal Article |
DBID | NPM |
DOI | 10.3233/JAD-170893 |
DatabaseName | PubMed |
DatabaseTitle | PubMed |
DatabaseTitleList | PubMed |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | no_fulltext_linktorsrc |
EISSN | 1875-8908 |
ExternalDocumentID | 29614652 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GroupedDBID | --- 0R~ 0VX 29J 36B 4.4 53G 5GY AAFNC AAWTL ABDBF ABIVO ABJNI ABUBZ ABUJY ACGFS ACPQW ACPRK ACUHS ADZMO AELRD AENEX AFRAH AFRHK AGIAB AHDMH AIRSE AJNRN ALMA_UNASSIGNED_HOLDINGS CAG COF DU5 EAD EAP EBS EJD EMB EMK EMOBN ESX F5P HZ~ IL9 IOS MET MIO MV1 NGNOM NPM O9- P2P Q1R S70 SV3 TUS VUG |
ID | FETCH-LOGICAL-c383t-23cc93295440424d0d30ff16155142089982803a6ac62834536e315433b1d13e2 |
IngestDate | Thu Apr 03 07:04:41 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Keywords | behavioral variant frontotemporal dementia functional MRI differential diagnosis Alzheimer’s disease diffusion tensor imaging classification machine learning |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c383t-23cc93295440424d0d30ff16155142089982803a6ac62834536e315433b1d13e2 |
OpenAccessLink | http://hdl.handle.net/1887/73457 |
PMID | 29614652 |
ParticipantIDs | pubmed_primary_29614652 |
PublicationCentury | 2000 |
PublicationDate | 2018-01-01 |
PublicationDateYYYYMMDD | 2018-01-01 |
PublicationDate_xml | – month: 01 year: 2018 text: 2018-01-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | Netherlands |
PublicationPlace_xml | – name: Netherlands |
PublicationTitle | Journal of Alzheimer's disease |
PublicationTitleAlternate | J Alzheimers Dis |
PublicationYear | 2018 |
SSID | ssj0003097 |
Score | 2.4125187 |
Snippet | Overlapping clinical symptoms often complicate differential diagnosis between patients with Alzheimer's disease (AD) and behavioral variant frontotemporal... |
SourceID | pubmed |
SourceType | Index Database |
StartPage | 1827 |
Title | Single Subject Classification of Alzheimer's Disease and Behavioral Variant Frontotemporal Dementia Using Anatomical, Diffusion Tensor, and Resting-State Functional Magnetic Resonance Imaging |
URI | https://www.ncbi.nlm.nih.gov/pubmed/29614652 |
Volume | 62 |
hasFullText | |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF4auHCpiniWh-aAxME1eL3O2j4mQFQilUObot6qtb1uTVunUhIh9c_x1zqzu34kahFwsSKvbG08n2a_eTP2XhUceYXUfpCRtyrV3E8KFfgqVInUsUhzbbJ8v8v942h6MjzZGjzoZS2tltnH_ObOupL_kSreQ7lSlew_SLZ9Kd7A3yhfvKKE8fpXMj7Cc4dyAVcZeVPsgEtK_Wlp4Ojy5lxXZkBKvKBOmxSMMfGCcVee_wPNZfy-yGGpl4HrVYXK0DgOK-XZrIJRjea56S1g1FRVlitytHkztIPnbRLoITXtqM98w2G9CR6aztd4oM5qqpc08YLa1Cl8uzITku6jx2tb34gjjeer5aIpNfKm3mEX3Tqg0P9YthWO506LdQBW5QX-teqnm-Ndd0tUy3X0qyI7oklTdl5k5xfhSc8voq0uR1PMT9Ig6St7GfZAHfU0N9pZ8V1HigjJ5T2Zjr74PA4SO86xh63rKwOuMEWeI20z3j-vbrT3bpYGbICGDk1uJXeToxIiSGPbU5e28anbBPWwdg9u2EOGF8122LaTGIwsOp-wLV0_Zb8tMsEhE9aRCfMSWvF-WIDDJSCAoMMlOFzCOi6hwSUYXEKHyz1oUQkWlXvmlWuYhA6T0GASWkyCw-Qzdjz5Ovu877tRIX4uErH0Q5HnaImkQ2p3GUZFUIigLE3QnVMCSZomNIZNSZVLJNTRUEgt0HoQIuMFFzp8zh7W81q_ZBDhEzlHK7zIZKSyUCHj5TLMEiHKCJXZK_bCfu_Ta9sP5rSRxO69K6_Z4w6ib9ijEhWQfotsdpm9MxK_BRyho98 |
linkProvider | National Library of Medicine |
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=Single+Subject+Classification+of+Alzheimer%27s+Disease+and+Behavioral+Variant+Frontotemporal+Dementia+Using+Anatomical%2C+Diffusion+Tensor%2C+and+Resting-State+Functional+Magnetic+Resonance+Imaging&rft.jtitle=Journal+of+Alzheimer%27s+disease&rft.au=Bouts%2C+Mark+J+R+J&rft.au=M%C3%B6ller%2C+Christiane&rft.au=Hafkemeijer%2C+Anne&rft.au=van+Swieten%2C+John+C&rft.date=2018-01-01&rft.eissn=1875-8908&rft.volume=62&rft.issue=4&rft.spage=1827&rft_id=info:doi/10.3233%2FJAD-170893&rft_id=info%3Apmid%2F29614652&rft_id=info%3Apmid%2F29614652&rft.externalDocID=29614652 |