Abstract
Effective biomarkers play important roles for accurate diagnosis of Alzheimer’s Disease (AD), including its intermediate stage (i.e. mild cognitive impairment, MCI). In this paper, a new feature selection scheme was proposed to improve the identification AD and MCI from healthy controls (HC) by a support vector machine (SVM) based-classifier with recursive feature addition. Our method can find the significant features automatically, and the experiments in this work demonstrates that our scheme can achieve better classification performance based on a dataset with 103 subjects where three biomarkers, i.e., structural MR imaging (MRI), functional imaging PET, and cerebrospinal fluid(CSF), had been used. Our proposed method demonstrated its effectiveness in identifying AD from HC with an accuracy of 95.0 %, while only 89.3 % for the classifier without the step of feature selection. In addition, some features selected in this work had shown strong relation with AD by other previous studies, which can provide the support for the significance of our results.
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Ramaroson, H., Helmer, C., Barberger-Gateau, P., Letenneur, L., Dartigues, J.F.: Prevalence of dementia and Alzheimer’s disease among subjects aged 75 years or over: updated results of the PAQUID cohort. Rev. Neurol. (Paris) 159, 405–411 (2003)
Brookmeyer, R., Johnson, E., Ziegler-Graham, K., Arrighi, H.M.: Forecasting the global burden of Alzheimer’s disease. Alzheimer’s Dement. 3, 186–191 (2007)
De Toledo-Morrell, L., Stoub, T.R., Bulgakova, M., Wilson, R.S., Bennett, D.A., Leurgans, S., et al.: MRI-derived entorhinal volume is a good predictor of conversion from MCI to AD. Neurobiol. Aging 25, 1197–1203 (2004)
Nestor, P.J., Scheltens, P., Hodges, J.R.: Advances in the early detection of Alzheimer’s disease. Nat. Med. 10(suppl.), S34–S41 (2004). (Review)
Jack Jr., C.R., Shiung, M.M., Weigand, S.D., O’Brien, P.C., Gunter, J.L., Boeve, B.F., et al.: Brain atrophy rates predict subsequent clinical conversion in normal elderly and amnestic MCI. Neurology 65, 1227–1231 (2005)
Ramírez, J., Górriz, J.M., Salas-Gonzalez, D., Romero, A., López, M., Álvarez, I., et al.: Computer-aided diagnosis of Alzheimer’s type dementia combining support vector machines and discriminant set of features. Inf. Sci. 237, 59–72 (2013)
Hoffman, J.M., Welsh-Bohmer, K.A., Hanson, M., Crain, B., Hulette, C., Earl, N., et al.: FDG PET imaging in patients with pathologically verified dementia. J. Nucl. Med. 41, 1920–1928 (2000)
Ishii, K., Sasaki, H., Kono, A.K., Miyamoto, N., Fukuda, T., Mori, E.: Comparison of gray matter and metabolic reduction in mild Alzheimer’s disease using FDG-PET and voxel-based morphometric MR studies. Eur. J. Nucl. Med. Mol. Imaging 32, 959–963 (2005)
McEvoy, L.K., Fennema-Notestine, C., Roddey, J.C., Hagler Jr., D.J., Holland, D., Karow, D.S., Pung, C.J., Brewer, J.B., Dale, A.M.: Alzheimer disease: quantitative structural neuroimaging for detection and prediction of clinical and structural changes in mild cognitive impairment. Radiology 251, 195–205 (2009)
Klunk, W.E., Engler, H., Nordberg, A., Wang, Y., Blomqvist, G., Holt, D.P., et al.: Imaging brain amyloid in Alzheimer’s disease with Pittsburgh Compound-B. Ann. Neurol. 55, 306–319 (2004)
Ji, Y., Permanne, B., Sigurdsson, E.M., Holtzman, D.M., Wisniewski, T.: Amyloid beta40/42 clearance across the blood-brain barrier following intra-ventricular injections in wild-type, apoE knock-out and human apoE3 or E4 expressing transgenic mice. J. Alzheimers Dis. 3, 23–30 (2001)
Bouwman, F.H., Schoonenboom, S.N., van der Flier, W.M., van Elk, E.J., Kok, A., Barkhof, F., et al.: CSF biomarkers and medial temporal lobe atrophy predict dementia in mild cognitive impairment. Neurobiol. Aging 28, 1070–1074 (2007)
Fjell, A.M., Walhovd, K.B., Fennema-Notestine, C., McEvoy, L.K., Hagler, D.J., Holland, D., et al.: CSF biomarkers in prediction of cerebral and clinical change in mild cognitive impairment and Alzheimer’s disease. J. Neurosci. 30, 2088–2101 (2010)
Orru, G., Pettersson-Yeo, W., Marquand, A.F., Sartori, G., Mechelli, A.: Using support vector machine to identify imaging biomarkers of neurological and psychiatric disease: a critical review. Neurosci. Biobehav. Rev. 36, 1140–1152 (2012)
Vemuri, P., Gunter, J.L., Senjem, M.L., Whitwell, J.L., Kantarci, K., Knopman, D.S., et al.: Alzheimer’s disease diagnosis in individual subjects using structural MR images: validation studies. Neuroimage 39, 1186–1197 (2008)
Magnin, B., Mesrob, L., Kinkingnehun, S., Pelegrini-Issac, M., Colliot, O., Sarazin, M., et al.: Support vector machine-based classification of Alzheimer’s disease from whole-brain anatomical MRI. Neuroradiology 51, 73–83 (2009)
Kohannim, O., Hua, X., Hibar, D.P., Lee, S., Chou, Y.Y., Toga, A.W., et al.: Boosting power for clinical trials using classifiers based on multiple biomarkers. Neurobiol. Aging 31, 1429–1442 (2010)
Westman, E., Muehlboeck, J.S., Simmons, A.: Combining MRI and CSF measures for classification of Alzheimer’s disease and prediction of mild cognitive impairment conversion. Neuroimage 62, 229–238 (2012)
Walhovd, K.B., Fjell, A.M., Brewer, J., McEvoy, L.K., Fennema-Notestine, C., Hagler Jr., D.J., et al.: Combining MR imaging, positron-emission tomography, and CSF biomarkers in the diagnosis and prognosis of Alzheimer disease. AJNR Am. J. Neuroradiol. 31, 347–354 (2010)
Zhang, D., Wang, Y., Zhou, L., Yuan, H., Shen, D.: Multimodal classification of Alzheimer’s disease and mild cognitive impairment. Neuroimage 55, 856–867 (2011)
Hinrichs, C., Singh, V., Xu, G., Johnson, S.C.: Predictive markers for AD in a multi-modality framework: an analysis of MCI progression in the ADNI population. Neuroimage 55, 574–589 (2011)
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D., Stadlan, E.M.: 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. Neurology 34, 939–944 (1984)
McKhann, G.M., Knopman, D.S., Chertkow, H., Hyman, B.T., Jack Jr., C.R., Kawas, C.H., et al.: The diagnosis of dementia due to Alzheimer’s disease: recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement. 7, 263–269 (2011)
Vapnik, V.: The Nature of Statistical Learning Theory. Springer, New York (1999)
Chang, C.-C., Lin, C.-J.: LIBSVM: a library for support vector machines. ACM Trans. Intell. Syst. Technol. 2, 27:27–27:27 (2011)
Chu, C., Hsu, A.L., Chou, K.H., Bandettini, P., Lin, C.: Does feature selection improve classification accuracy? Impact of sample size and feature selection on classification using anatomical magnetic resonance images. Neuroimage 60, 59–70 (2012)
Walhovd, K.B., Fjell, A.M., Dale, A.M., McEvoy, L.K., Brewer, J., Karow, D.S., et al.: Multi-modal imaging predicts memory performance in normal aging and cognitive decline. Neurobiol. Aging 31, 1107–1121 (2010)
Fan, Y., Resnick, S.M., Wu, X., Davatzikos, C.: Structural and functional biomarkers of prodromal Alzheimer’s disease: a high-dimensional pattern classification study. Neuroimage 41, 277–285 (2008)
Fan, Y., Rao, H., Hurt, H., Giannetta, J., Korczykowski, M., Shera, D., et al.: Multivariate examination of brain abnormality using both structural and functional MRI. Neuroimage 36, 1189–1199 (2007)
Costafreda, S.G., Chu, C., Ashburner, J., Fu, C.H.: Prognostic and diagnostic potential of the structural neuroanatomy of depression. PLoS ONE 4, e6353 (2009)
Chetelat, G., Desgranges, B., De La Sayette, V., Viader, F., Eustache, F., Baron, J.-C.: Mapping gray matter loss with voxel-based morphometry in mild cognitive impairment. NeuroReport 13, 1939–1943 (2002)
Misra, C., Fan, Y., Davatzikos, C.: Baseline and longitudinal patterns of brain atrophy in MCI patients, and their use in prediction of short-term conversion to AD: results from ADNI. Neuroimage 44, 1415–1422 (2009)
Hampel, H., Burger, K., Teipel, S.J., Bokde, A.L., Zetterberg, H., Blennow, K.: Core candidate neurochemical and imaging biomarkers of Alzheimer’s disease. Alzheimers Dement. 4, 38–48 (2008)
Jack Jr., C.R., Petersen, R.C., Xu, Y.C., O’Brien, P.C., Smith, G.E., Ivnik, R.J., et al.: Prediction of AD with MRI-based hippocampal volume in mild cognitive impairment. Neurology 52, 1397–1403 (1999)
Barnes, J., Scahill, R.I., Boyes, R.G., Frost, C., Lewis, E.B., Rossor, C.L., et al.: Differentiating AD from aging using semiautomated measurement of hippocampal atrophy rates. Neuroimage 23, 574–581 (2004)
Edward, E.S., Stephen, M.K.: Cognitive Psychology: Mind and Brain, pp. 21, 194–199, 349. Prentice Hall, New Jersey (2007)
Arnold, S.E., Hyman, B.T., Van Hoesen, G.W.: Neuropathologic changes of the temporal pole in Alzheimer’s disease and Pick’s disease. Arch. Neurol. 51, 145–150 (1994)
Yang, J., Pan, P., Song, W., Huang, R., Li, J., Chen, K., et al.: Voxelwise meta-analysis of gray matter anomalies in Alzheimer’s disease and mild cognitive impairment using anatomic likelihood estimation. J. Neurol. Sci. 316, 21–29 (2012)
Acknowledgments
This work was supported by the National Natural Science Foundation of China (Nos. 61300058, 61472282 and 61374181), Anhui Provincial Natural Science Foundation (No. 1508085MF129). The authors give special thanks to Professor D.Q. Zhang in Nanjing University of Aeronautics and Astronautics for his work in data preprocessing, and the data support from ADNI.
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Shen, H., Zhang, W., Chen, P., Zhang, J., Fang, A., Wang, B. (2016). A Feature Selection Scheme for Accurate Identification of Alzheimer’s Disease. In: Ortuño, F., Rojas, I. (eds) Bioinformatics and Biomedical Engineering. IWBBIO 2016. Lecture Notes in Computer Science(), vol 9656. Springer, Cham. https://doi.org/10.1007/978-3-319-31744-1_7
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DOI: https://doi.org/10.1007/978-3-319-31744-1_7
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