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Neuroimaging biomarkers are important in diagnosis and monitoring the effects of interventions. As memory impairments are among the first symptoms of AD, the relationship between imaging findings and memory deficits is important in biomarker research. The most established magnetic resonance imaging (MRI) finding is hippocampal atrophy, which is related to memory decline and currently used as a diagnostic criterion for AD. While the medial temporal lobes are impacted early by the spread of neurofibrillary tangles, other networks and regional changes can be found quite early in the progression. Atrophy in several frontal and parietal regions, cortical thinning, and white matter alterations correlate with memory deficits in early AD. Changes in activation and connectivity have been detected by functional MRI (fMRI). Task\u2010based fMRI studies have revealed medial temporal lobe hypoactivation, parietal hyperactivation, and frontal hyperactivation in AD during memory tasks, and activation patterns of these regions are also altered in preclinical and prodromal AD. Resting state fMRI has revealed alterations in default mode network activity related to memory in early AD. These studies are limited in part due to the historic inclusion of patients who had suspected AD but likely did not have the disorder. Modern biomarkers allow for more diagnostic certainty, allowing better understanding of neuroimaging markers in true AD, even in the preclinical stage. Larger patient cohorts, comparison of candidate imaging biomarkers to more established biomarkers, and inclusion of more detailed neuropsychological batteries to assess multiple aspects of memory are needed to better understand the memory deficit in AD and help develop new biomarkers. This article reviews MRI findings related to episodic memory impairments in AD and introduces a new study with multimodal imaging and comprehensive neuropsychiatric evaluation to overcome current limitations.<\/jats:p>","DOI":"10.1016\/j.trci.2018.04.007","type":"journal-article","created":{"date-parts":[[2018,6,14]],"date-time":"2018-06-14T00:47:08Z","timestamp":1528937228000},"page":"395-413","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":74,"title":["Current understanding of magnetic resonance imaging biomarkers and memory in Alzheimer's disease"],"prefix":"10.1002","volume":"4","author":[{"given":"Ece","family":"Bayram","sequence":"first","affiliation":[{"name":"Department of Neurology Cleveland Clinic Lou Ruvo Center for Brain Health Las Vegas NV USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica Z.K.","family":"Caldwell","sequence":"additional","affiliation":[{"name":"Department of Neurology Cleveland Clinic Lou Ruvo Center for Brain Health Las Vegas NV USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarah J.","family":"Banks","sequence":"additional","affiliation":[{"name":"Department of Neurology Cleveland Clinic Lou Ruvo Center for Brain Health Las Vegas NV USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2018,6,13]]},"reference":[{"key":"e_1_2_9_2_1","unstructured":"United States Food and Drug Administration.Guidance for Industry Alzheimer's Disease: Developing Drugs for the Treatment of Early Stage Disease (FDA\u20102013\u2010D\u20100077) DRAFT Available at:http:\/\/www.fda.gov\/downloads\/Drugs\/GuidanceComplianceRegulatoryInformation\/Guidances\/UCM338287.pdf2013. 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