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The Effect of the APOE Genotype on Individual BrainAGE in Normal Aging, Mild Cognitive Impairment, and Alzheimer's Disease.
PLoS One 2016; 11(7):e0157514Plos

Abstract

In our aging society, diseases in the elderly come more and more into focus. An important issue in research is Mild Cognitive Impairment (MCI) and Alzheimer's Disease (AD) with their causes, diagnosis, treatment, and disease prediction. We applied the Brain Age Gap Estimation (BrainAGE) method to examine the impact of the Apolipoprotein E (APOE) genotype on structural brain aging, utilizing longitudinal magnetic resonance image (MRI) data of 405 subjects from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. We tested for differences in neuroanatomical aging between carrier and non-carrier of APOE ε4 within the diagnostic groups and for longitudinal changes in individual brain aging during about three years follow-up. We further examined whether a combination of BrainAGE and APOE status could improve prediction accuracy of conversion to AD in MCI patients. The influence of the APOE status on conversion from MCI to AD was analyzed within all allelic subgroups as well as for ε4 carriers and non-carriers. The BrainAGE scores differed significantly between normal controls, stable MCI (sMCI) and progressive MCI (pMCI) as well as AD patients. Differences in BrainAGE changing rates over time were observed for APOE ε4 carrier status as well as in the pMCI and AD groups. At baseline and during follow-up, BrainAGE scores correlated significantly with neuropsychological test scores in APOE ε4 carriers and non-carriers, especially in pMCI and AD patients. Prediction of conversion was most accurate using the BrainAGE score as compared to neuropsychological test scores, even when the patient's APOE status was unknown. For assessing the individual risk of coming down with AD as well as predicting conversion from MCI to AD, the BrainAGE method proves to be a useful and accurate tool even if the information of the patient's APOE status is missing.

Authors+Show Affiliations

Medical Faculty, University of Jena, Jena, Germany.Structural Brain Mapping Group, Department of Neurology, University Hospital Jena, Jena, Germany. Department of Psychiatry, University Hospital Jena, Jena, Germany.Structural Brain Mapping Group, Department of Neurology, University Hospital Jena, Jena, Germany.No affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

27410431

Citation

Löwe, Luise Christine, et al. "The Effect of the APOE Genotype On Individual BrainAGE in Normal Aging, Mild Cognitive Impairment, and Alzheimer's Disease." PloS One, vol. 11, no. 7, 2016, pp. e0157514.
Löwe LC, Gaser C, Franke K, et al. The Effect of the APOE Genotype on Individual BrainAGE in Normal Aging, Mild Cognitive Impairment, and Alzheimer's Disease. PLoS ONE. 2016;11(7):e0157514.
Löwe, L. C., Gaser, C., & Franke, K. (2016). The Effect of the APOE Genotype on Individual BrainAGE in Normal Aging, Mild Cognitive Impairment, and Alzheimer's Disease. PloS One, 11(7), pp. e0157514. doi:10.1371/journal.pone.0157514.
Löwe LC, et al. The Effect of the APOE Genotype On Individual BrainAGE in Normal Aging, Mild Cognitive Impairment, and Alzheimer's Disease. PLoS ONE. 2016;11(7):e0157514. PubMed PMID: 27410431.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The Effect of the APOE Genotype on Individual BrainAGE in Normal Aging, Mild Cognitive Impairment, and Alzheimer's Disease. AU - Löwe,Luise Christine, AU - Gaser,Christian, AU - Franke,Katja, AU - ,, Y1 - 2016/07/13/ PY - 2015/12/28/received PY - 2016/05/30/accepted PY - 2016/7/14/entrez PY - 2016/7/15/pubmed PY - 2017/7/25/medline SP - e0157514 EP - e0157514 JF - PloS one JO - PLoS ONE VL - 11 IS - 7 N2 - In our aging society, diseases in the elderly come more and more into focus. An important issue in research is Mild Cognitive Impairment (MCI) and Alzheimer's Disease (AD) with their causes, diagnosis, treatment, and disease prediction. We applied the Brain Age Gap Estimation (BrainAGE) method to examine the impact of the Apolipoprotein E (APOE) genotype on structural brain aging, utilizing longitudinal magnetic resonance image (MRI) data of 405 subjects from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. We tested for differences in neuroanatomical aging between carrier and non-carrier of APOE ε4 within the diagnostic groups and for longitudinal changes in individual brain aging during about three years follow-up. We further examined whether a combination of BrainAGE and APOE status could improve prediction accuracy of conversion to AD in MCI patients. The influence of the APOE status on conversion from MCI to AD was analyzed within all allelic subgroups as well as for ε4 carriers and non-carriers. The BrainAGE scores differed significantly between normal controls, stable MCI (sMCI) and progressive MCI (pMCI) as well as AD patients. Differences in BrainAGE changing rates over time were observed for APOE ε4 carrier status as well as in the pMCI and AD groups. At baseline and during follow-up, BrainAGE scores correlated significantly with neuropsychological test scores in APOE ε4 carriers and non-carriers, especially in pMCI and AD patients. Prediction of conversion was most accurate using the BrainAGE score as compared to neuropsychological test scores, even when the patient's APOE status was unknown. For assessing the individual risk of coming down with AD as well as predicting conversion from MCI to AD, the BrainAGE method proves to be a useful and accurate tool even if the information of the patient's APOE status is missing. SN - 1932-6203 UR - http://www.unboundmedicine.com/medline/citation/27410431/The_Effect_of_the_APOE_Genotype_on_Individual_BrainAGE_in_Normal_Aging_Mild_Cognitive_Impairment_and_Alzheimer's_Disease_ L2 - http://dx.plos.org/10.1371/journal.pone.0157514 DB - PRIME DP - Unbound Medicine ER -