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2966 citation(s) found for "Go, Ronald S".

MRS in Mild Cognitive Impairment: Early Differentiation of Dementia with Lewy Bodies and Alzheimer's Disease
Ferman, Tanis J. , Smith, Glenn E. , Maroney‐Smith, Mandie, Spychalla, Anthony J., Jack, Clifford R. , Petersen, Ronald C. , Kantarci, Kejal , Maroney-Smith, Mandie, Zhang, Bing , Boeve, Bradley F. , Knopman, David S. , Jack, Clifford R , Kantarci, Kejal , Ferman, Tanis J

Mayo Clinic

Journal of Neuroimaging | July 16, 2014 | Volume: 25 | Issue: 2 | Pages: 269-274

10.1111/jon.12138 | PMID 25039916 Get It

ABSTRACTBACKGROUND AND PURPOSEMild cognitive impairment (MCI) precedes both Alzheimer's disease (AD) dementia and with Lewy bodies (DLB). We investigated proton magnetic resonance spectroscopy (MRS) characteristics of MCI patients who progressed to DLB compared to those who progressed to AD dementia or remained stable.METHODSConsecutive MCI patients who underwent single voxel MRS at baseline and progressed to DLB (n = 10) were identified during a median follow‐up period of 18 months. From the same cohort, we identified age‐ and sex‐matched MCI patients who progressed to AD dementia (n = 27) or remained stable (n = 20) during a similar follow‐up period. This study was approved by the Institutional Review Board and informed consent was from every subject.RESULTSMCI patients who progressed to AD dementia were characterized by lower N‐acetylaspartate (NAA)/Cr ratio in the posterior cingulate voxel compared to those who progressed to DLB (P = .001). Decreased NAA/Cr in the posterior cingulate voxel differentiated MCI patients who progressed to DLB from those who progressed to AD with an area under the receiver operating characteristic curve of .85 (P < .001) on logistic regression analysis.CONCLUSIONSMRS may be useful in differentiating MCI patients with prodromal AD dementia from those with prodromal DLB for early disease‐specific interventions.
Comparison of manual and semiautomated techniques for analyzing gastric volumes with MRI in humans
Bharucha, Adil E. , Karwoski, Ronald A., Fidler, Jeff L. , Holmes, David R. , Robb, Richard A., Riederer, Stephen J. , Zinsmeister, Alan R., Fidler, Jeff, Fidler, Jeff L.

Mayo Clinic

American Journal of Physiology-Gastrointestinal and Liver Physiology | July 11, 2014 | Volume: 307 | Issue: 5 | Pages: G582-G587

10.1152/ajpgi.00048.2014 | PMID 25012844 Get It

Gastric emptying, accommodation, and motility can be quantified with magnetic resonance imaging (MRI). The first step in image analysis entails segmenting the stomach from surrounding structures, usually by a time-consuming manual process. We have developed a semiautomated process to segment and measure gastric volumes with MRI. Gastric images were acquired with a three-dimensional gradient echo MRI sequence at 5, 10, 20, and 30 min after ingestion of a liquid nutrient (Ensure, 296 ml) labeled with gadolinium in 20 healthy volunteers and 29 patients with dyspeptic symptoms. The agreement between gastric volumes measured by manual segmentation and our new semiautomated algorithm was assessed with Lin's concordance correlation coefficient (CCC) and the Bland Altman test. At 5 min after a meal, food volumes measured by manual (352 ± 4 ml) and semiautomated (346 ± 4 ml) techniques were correlated {CCC[95% confidence interval (CI)] 0.70 (0.52, 0.81)}; air volumes measured by manual (88 ± 6 ml) and semiautomated (84 ± 6 ml) techniques were also correlated [CCC (95% CI) 0.89 (0.82, 0.94)]. Findings were similar at subsequent time points. The Bland Altman test was not significant. The time required for semiautomated segmentation ranged from an average of 204 s for the 5-min images to 233 s for the 20-min images. These times were appreciably smaller than the typical times of many tens of minutes, even hours, required for manual segmentation. To conclude, a semiautomated process can measure gastric food and air volume using MRI with comparable accuracy and far better efficiency than a manual process.
At the interface of sensory and motor dysfunctions and Alzheimer's disease
Gilmore, Grover C. , Kaye, Jeffrey , Murphy, Claire , Wingfield, Arthur , Bennett, David A. , Boxer, Adam L. , Buchman, Aron S. , Cruickshanks, Karen J., Devanand, Davangere P. , Duffy, Charles J., Gates, George A., Holtzer, Roee , Lin, Frank R. , McKee, Ann C. , Morris, John C. , Petersen, Ronald C. , Silbert, Lisa C. , Struble, Robert G., Trojanowski, John Q. , Verghese, Joe , Xu, Shunbin , Albers, Mark W. , Gall, Christine M. , Granholm, Ann‐Charlotte , Hensch, Takao K. , Hyman, Bradley T. , Wilson, Donald A. , Zhang, Li I. , Bennett, David A. , Morris, John C

Mayo Clinic

Alzheimer's & Dementia | July 8, 2014 | Volume: 11 | Issue: 1 | Pages: 70-98

10.1016/j.jalz.2014.04.514 | PMID 25022540 Get It

Abstract Recent evidence indicates that sensory and motor changes may precede the cognitive symptoms of Alzheimer's disease (AD) by several years and may signify increased risk of developing AD. Traditionally, sensory and motor dysfunctions in aging and AD have been studied separately. To ascertain the evidence supporting the relationship between age‐related changes in sensory and motor systems and the development of AD and to facilitate communication between several disciplines, the National Institute on Aging held an exploratory workshop titled “Sensory and Motor Dysfunctions in Aging and AD.” The scientific sessions of the workshop focused on age‐related and neuropathologic changes in the olfactory, visual, auditory, and motor systems, followed by extensive discussion and hypothesis generation related to the possible links among sensory, cognitive, and motor domains in aging and AD. Based on the data presented and discussed at this workshop, it is clear that sensory and motor regions of the central nervous system are affected by AD pathology and that interventions targeting amelioration of sensory‐motor deficits in AD may enhance patient function as AD progresses.
Trends in survival of patients with primary plasma cell leukemia: a population-based analysis
Rajkumar, S. Vincent , Dispenzieri, Angela , Lacy, Martha Q. , Kapoor, Prashant , Dingli, David , Lust, John A., Zeldenrust, Steven R., Hayman, Suzanne R. , Kyle, Robert A. , Kumar, Shaji , Rajkumar, S Vincent , Gonsalves, Wilson I. , Go, Ronald S. , Gupta, Vinay Kumar , Singh, Preet Paul , Buadi, Francis K. , Gertz, Morie A. , Dispenzieri, Angela , Dingli, David

Mayo Clinic

Blood | June 24, 2014 | Volume: 124 | Issue: 6 | Pages: 907-912

10.1182/blood-2014-03-565051 | PMID 24957143 Get It

Key Points Survival of patients with primary plasma cell leukemia has improved in recent years, but is still inferior to those patients with multiple myeloma. This survival benefit appears to be mainly in patients older than 65 years of age.
Association of Lifetime Intellectual Enrichment With Cognitive Decline in the Older Population
Vemuri, Prashanthi , Lesnick, Timothy G. , Przybelski, Scott A. , Mielke, Michelle M. , Roberts, Rosebud O., Geda, Yonas E. , Rocca, Walter A. , Petersen, Ronald C. , Machulda, Mary M. , Knopman, David S. , Jack, Clifford R. , Mielke, Michelle M , Vemuri, Prashanthi , Geda, Yonas E

Mayo Clinic

JAMA Neurology | June 23, 2014 | Volume: 71 | Issue: 8 | Pages: 1017

10.1001/jamaneurol.2014.963 | PMID 25054282 Get It

Effects of traumatic brain injury and posttraumatic stress disorder on Alzheimer's disease in veterans, using the Alzheimer's Disease Neuroimaging Initiative
Weiner, Michael W. , Veitch, Dallas P. , Aisen, Paul, Petersen, Ronald C. , Jagust, William, Trojanowski, John Q. , Shaw, Leslie M. , Saykin, Andrew J. , Harvey, Danielle , Pacifico, Anthony, Sheline, Yvette I. , Yaffe, Kristine , Mohlenoff, Brian, Hayes, Jacqueline , Neylan, Thomas C. , Grafman, Jordan Henry , Jack, Clifford R. , Green, Robert C. , Toga, Arthur W. , Friedl, Karl E. , Saykin, Andrew J , Harvey, Danielle J

Mayo Clinic

Alzheimer's & Dementia | June 9, 2014 | Volume: 10 | Issue: 3S | Pages: No page available

10.1016/j.jalz.2014.04.005 | PMID 24924673 Get It

AbstractBoth traumatic brain injury (TBI) and posttraumatic stress disorder (PTSD) are common problems resulting from military service, and both have been associated with increased risk of cognitive decline and dementia resulting from Alzheimer's disease (AD) or other causes. This study aims to use imaging techniques and biomarker analysis to determine whether traumatic brain injury (TBI) and/or PTSD resulting from combat or other traumas increase the risk for AD and decrease cognitive reserve in Veteran subjects, after accounting for age. Using military and Department of Veterans Affairs records, 65 Vietnam War veterans with a history of moderate or severe TBI with or without PTSD, 65 with ongoing PTSD without TBI, and 65 control subjects are being enrolled in this study at 19 sites. The study aims to select subject groups that are comparable in age, gender, ethnicity, and education. Subjects with mild cognitive impairment (MCI) or dementia are being excluded. However, a new study just beginning, and similar in size, will study subjects with TBI, subjects with PTSD, and control subjects with MCI. Baseline measurements of cognition, function, blood, and cerebrospinal fluid biomarkers; magnetic resonance images (structural, diffusion tensor, and resting state blood‐level oxygen dependent (BOLD) functional magnetic resonance imaging); and amyloid positron emission tomographic (PET) images with florbetapir are being obtained. One‐year follow‐up measurements will be collected for most of the baseline procedures, with the exception of the lumbar puncture, the PET imaging, and apolipoprotein E genotyping. To date, 19 subjects with TBI only, 46 with PTSD only, and 15 with TBI and PTSD have been recruited and referred to 13 clinics to undergo the study protocol. It is expected that cohorts will be fully recruited by October 2014. This study is a first step toward the design and statistical powering of an AD prevention trial using at‐risk veterans as subjects, and provides the basis for a larger, more comprehensive study of dementia risk factors in veterans.
Mean upper cervical cord area (MUCCA) measurement in long-standing multiple sclerosis: Relation to brain findings and clinical disability
Daams, Marita , Weiler, Florian , Steenwijk, Martijn D. , Hahn, Horst K. , Geurts, Jeroen J.G. , Schijndel, Ronald A. van , Balk, Lisanne J. , Tewarie, Prejaas , Tillema, Jan‐Mendelt , Killestein, Joep , Uitdehaag, Bernard M.J. , Barkhof, Frederik , Vrenken, Hugo , Barkhof, Frederik

Mayo Clinic

Multiple Sclerosis Journal | May 9, 2014 | Volume: 20 | Issue: 14 | Pages: 1860-1865

10.1177/1352458514533399 | PMID 24812042 Get It

Background: The majority of patients with multiple sclerosis (MS) present with spinal cord pathology. Spinal cord atrophy is thought to be a marker of disease severity, but in long-disease duration its relation to brain pathology and clinical disability is largely unknown. Objective: Our aim was to investigate mean upper cervical cord area (MUCCA) in patients with long-standing MS and assess its relation to brain magnetic resonance imaging (MRI) measures and clinical disability. Methods: MUCCA was measured in 196 MS patients and 55 healthy controls using 3DT1-weighted cervical images obtained at 3T MRI. Clinical disability was measured using the Expanded Disability Status Scale (EDSS), Nine-Hole-Peg test (9-HPT), and 25 feet Timed Walk Test (TWT). Stepwise linear regression was performed to assess the association between MUCCA and MRI measures, and between MUCCA and clinical disability. Results: MUCCA was smaller (mean 11.7%) in MS patients compared with healthy controls (72.56±9.82 and 82.24±7.80 mm 2 respectively; p<0.001), most prominently in male patients. MUCCA was associated with normalized brain volume, and number of cervical cord lesions. MUCCA was independently associated with EDSS, TWT, and 9-HPT. Conclusion: MUCCA was reduced in MS patients compared with healthy controls. It provides a relevant marker for clinical disability in long-standing disease, independent of other MRI measures.
Use of autologous hematopoietic cell transplantation as initial therapy in multiple myeloma and the impact of socio‐geo‐demographic factors in the era of novel agents
Al‐Hamadani, Mohammed , Hashmi, Shahrukh K. , Go, Ronald S. , Go, Ronald S

Mayo Clinic

American Journal of Hematology | May 3, 2014 | Volume: 89 | Issue: 8 | Pages: 825-830

10.1002/ajh.23753 | PMID 24799343 Get It

Very effective combination chemotherapy using novel agents has become available in multiple myeloma (MM). Its impact on the use of high‐dose chemotherapy and autologous hematopoietic stem cell transplantation (AHCT) as part of initial therapy is unknown. Using the National Cancer Data Base, we studied the rate of upfront AHCT use among 137,409 newly diagnosed MM patients from 1998 to 2010 in the United States and determined whether disparity exists among various sociodemographic as well as geographic subgroups. Overall, 12,378 (9.0%) patients received AHCT as part of initial treatment. The use of upfront AHCT increased steadily from 5.2% in 1998 to 12.1% in 2010 (trend test, P < 0.001), with no sign of plateau. This was seen across all socio‐geo‐demographic subgroups except among patients treated in the Northeast where the rate fell from 8.7% in 1998 to 6.6% in 2010. In multivariable analysis, patients with the following characteristics were the least likely to receive AHCT (odds ratio): year of diagnosis from 1998 to 2003 before the era of novel agents (0.67), older age (0.35), Black race (0.58), Hispanic ethnicity (0.78), low level of education or annual household income (0.55), residence in a metro area (0.66), no or unknown medical insurance (0.30), treatment at a community cancer center (0.16), and treatment facility located in the Northeast region (0.54). Even after the introduction of novel agents, the rate of upfront AHCT in MM continues to increase annually. Significant disparities exist dependent on demographic, social, and geographic factors. Am. J. Hematol. 89:825–830, 2014. © 2014 Wiley Periodicals, Inc.
Association of hypometabolism and amyloid levels in aging, normal subjects
Lowe, Val J. , Weigand, Stephen D. , Senjem, Matthew L. , Vemuri, Prashanthi , Jordan, Lennon, Kantarci, Kejal , Petersen, Ronald C. , Boeve, Bradley F. , Jack, Clifford R. , Knopman, David S. , Vemuri, Prashanthi , Senjem, Matthew L , Kantarci, Kejal

Mayo Clinic

Neurology | May 3, 2014 | Volume: 82 | Issue: 22 | Pages: 1959-1967

10.1212/wnl.0000000000000467 | PMID 24793183 Get It