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      Assessment of cerebral microbleeds by susceptibility-weighted imaging in Alzheimer’s disease patients: A neuroimaging biomarker of the disease

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          Abstract

          <div class="section"> <a class="named-anchor" id="d6396697e146"> <!-- named anchor --> </a> <h5 class="section-title" id="d6396697e147">Purpose</h5> <p id="d6396697e149">The objective of this study was to correlate the presence and distribution of cerebral microbleeds in Alzheimer’s disease patients with cerebrospinal fluid biomarkers (amyloid-beta and phosphorylated tau 181 protein levels) and cognitive decline by using susceptibility-weighted imaging magnetic resonance sequences at 1.5 T. </p> </div><div class="section"> <a class="named-anchor" id="d6396697e151"> <!-- named anchor --> </a> <h5 class="section-title" id="d6396697e152">Material and methods</h5> <p id="d6396697e154">Fifty-four consecutive Alzheimer’s disease patients underwent brain magnetic resonance imaging at 1.5 T to assess the presence and distribution of cerebral microbleeds on susceptibility-weighted imaging images. The images were analyzed in consensus by two neuroradiologists, each with at least 10 years’ experience. Dementia severity was assessed with the Mini-Mental State Examination score. </p> <p id="d6396697e156">A multiple regression analysis was performed to assess the associations between the number and location of cerebral microbleed lesions with the age, sex, duration of the disease, cerebrospinal fluid amyloid-beta and phosphorylated tau 181 protein levels, and cognitive functions. </p> </div><div class="section"> <a class="named-anchor" id="d6396697e158"> <!-- named anchor --> </a> <h5 class="section-title" id="d6396697e159">Results</h5> <p id="d6396697e161">A total of 296 microbleeds were observed in 54 patients; 38 patients (70.4%) had lobar distribution, 13 patients (24.1%) had non-lobar distribution, and the remaining three patients (5.6%) had mixed distribution, demonstrating that Alzheimer’s disease patients present mainly a lobar distribution of cerebral microbleeds. </p> <p id="d6396697e163">The age and the duration of the disease were correlated with the number of lobar cerebral microbleeds ( <i>P</i> &lt; 0.001). </p> <p id="d6396697e168">Cerebrospinal fluid amyloid-beta, phosphorylated tau 181 protein levels, and cognitive decline were correlated with the number of lobar cerebral microbleeds in Alzheimer’s disease patients ( <i>P</i> &lt; 0.001). </p> </div><div class="section"> <a class="named-anchor" id="d6396697e173"> <!-- named anchor --> </a> <h5 class="section-title" id="d6396697e174">Conclusion</h5> <p id="d6396697e176">Lobar distribution of cerebral microbleeds is associated with Alzheimer’s disease and the number of lobar cerebral microbleeds directly correlates with cerebrospinal fluid amyloid-beta and phosphorylated tau 181 protein levels and with the cognitive decline of Alzheimer’s disease patients. </p> </div>

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          Most cited references19

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          Alzheimer's disease.

          Alzheimer's disease is the most common cause of dementia. Research advances have enabled detailed understanding of the molecular pathogenesis of the hallmarks of the disease--ie, plaques, composed of amyloid beta (Abeta), and tangles, composed of hyperphosphorylated tau. However, as our knowledge increases so does our appreciation for the pathogenic complexity of the disorder. Familial Alzheimer's disease is a very rare autosomal dominant disease with early onset, caused by mutations in the amyloid precursor protein and presenilin genes, both linked to Abeta metabolism. By contrast with familial disease, sporadic Alzheimer's disease is very common with more than 15 million people affected worldwide. The cause of the sporadic form of the disease is unknown, probably because the disease is heterogeneous, caused by ageing in concert with a complex interaction of both genetic and environmental risk factors. This seminar reviews the key aspects of the disease, including epidemiology, genetics, pathogenesis, diagnosis, and treatment, as well as recent developments and controversies.
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            Alzheimer disease in the US population: prevalence estimates using the 2000 census.

            Current and future estimates of Alzheimer disease (AD) are essential for public health planning. To provide prevalence estimates of AD for the US population from 2000 through 2050. Alzheimer disease incidence estimates from a population-based, biracial, urban study, using a stratified random sampling design, were converted to prevalence estimates and applied to US Census Bureau estimates of US population growth. A geographically defined community of 3 adjacent neighborhoods in Chicago, Ill, applied to the US population. Alzheimer disease incidence was measured in 3838 persons free of AD at baseline; 835 persons were evaluated for disease incidence. Main Outcome Measure Current and future estimates of prevalence of clinically diagnosed AD in the US population. In 2000, there were 4.5 million persons with AD in the US population. By 2050, this number will increase by almost 3-fold, to 13.2 million. Owing to the rapid growth of the oldest age groups of the US population, the number who are 85 years and older will more than quadruple to 8.0 million. The number who are 75 to 84 years old will double to 4.8 million, while the number who are 65 to 74 years old will remain fairly constant at 0.3 to 0.5 million. The number of persons with AD in the US population will continue to increase unless new discoveries facilitate prevention of the disease.
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              Susceptibility-weighted imaging: technical aspects and clinical applications, part 2.

              Susceptibility-weighted imaging (SWI) has continued to develop into a powerful clinical tool to visualize venous structures and iron in the brain and to study diverse pathologic conditions. SWI offers a unique contrast, different from spin attenuation, T1, T2, and T2* (see Susceptibility-Weighted Imaging: Technical Aspects and Clinical Applications, Part 1). In this clinical review (Part 2), we present a variety of neurovascular and neurodegenerative disease applications for SWI, covering trauma, stroke, cerebral amyloid angiopathy, venous anomalies, multiple sclerosis, and tumors. We conclude that SWI often offers complementary information valuable in the diagnosis and potential treatment of patients with neurologic disorders.
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                Author and article information

                Journal
                The Neuroradiology Journal
                Neuroradiol J
                SAGE Publications
                1971-4009
                2385-1996
                June 20 2017
                August 2017
                May 02 2017
                August 2017
                : 30
                : 4
                : 330-335
                Affiliations
                [1 ]DIBIMED – Sezione di Scienze Radiologiche, Università degli Studi di Palermo, Italy
                [2 ]Neuroradiology Section, Christiana Care Health System, USA
                [3 ]PROSAMI, Università degli Studi di Palermo, Italy
                Article
                10.1177/1971400916689483
                5524273
                28463092
                9497630b-515a-4bd3-a234-13bfa85fe429
                © 2017

                http://journals.sagepub.com/page/policies/text-and-data-mining-license

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