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Wiste, Heather J.

0009-0002-8833-2693

Mayo Clinic

Mayo Clinic

Citations 135

IC‐03‐04: Network‐Based TAU Deposition Patterns are Related to Functional Network Failure Largely Via Beta‐Amyloid Across The Alzheimer’s Spectrum
Lowe, Val J. , Wiste, Heather J. , Radford, Jonathan Graff, Petersen, Ronald C. , Jones, David T. , Senjem, Matthew L. , Boeve, Bradley F. , Knopman, David S. , Jack, Clifford R.

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_1 | Pages: No page available

10.1016/j.jalz.2016.06.074 Get It

IC‐01‐01: Predictors of Regional TAU‐PET Uptake: Mayo Clinic Study of Aging
Lowe, Val J. , Wiste, Heather J. , Weigand, Stephen D. , Petersen, Ronald C. , Vemuri, Prashanthi , Senjem, Matthew L. , Knopman, David S. , Jack, Clifford R.

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_1 | Pages: No page available

10.1016/j.jalz.2016.06.061 Get It

Practice effects and longitudinal cognitive change in clinically normal older adults differ by Alzheimer imaging biomarker status
Hagen, Clint , Wiste, Heather J. , Mielke, Michelle M. , Roberts, Rosebud O., Vemuri, Prashanthi , Lowe, Val J. , Jack, Clifford R. , Petersen, Ronald C. , Machulda, Mary M. , Knopman, David S. , Jack, Clifford R , Mielke, Michelle M , Vemuri, Prashanthi

The Clinical Neuropsychologist | October 11, 2016 | Volume: 31 | Issue: 1 | Pages: 99-117

10.1080/13854046.2016.1241303 Get It

Defining imaging biomarker cut points for brain aging and Alzheimer's disease
Jack, Clifford R. , Wiste, Heather J. , Weigand, Stephen D. , Therneau, Terry M. , Lowe, Val J. , Gunter, Jeffrey L. , Senjem, Matthew L. , Kantarci, Kejal , Mielke, Michelle M. , Roberts, Rosebud O., Vemuri, Prashanthi , Reyes, Denise A., Petersen, Ronald C. , Knopman, David S. , Jones, David T. , Machulda, Mary M. , Jack, Clifford R , Mielke, Michelle M , Vemuri, Prashanthi , Senjem, Matthew L , Kantarci, Kejal

Alzheimer's & Dementia | October 5, 2016 | Volume: 13 | Issue: 3 | Pages: 205-216

10.1016/j.jalz.2016.08.005 Get It

Abstract Introduction Our goal was to develop cut points for amyloid positron emission tomography (PET), tau PET, flouro‐deoxyglucose (FDG) PET, and MRI cortical thickness. Methods We examined five methods for determining cut points. Results The reliable worsening method produced a cut point only for amyloid PET. The specificity, sensitivity, and accuracy of cognitively impaired versus young clinically normal (CN) methods labeled the most people abnormal and all gave similar cut points for tau PET, FDG PET, and cortical thickness. Cut points defined using the accuracy of cognitively impaired versus age‐matched CN method labeled fewer people abnormal. Discussion In the future, we will use a single cut point for amyloid PET (standardized uptake value ratio, 1.42; centiloid, 19) based on the reliable worsening cut point method. We will base lenient cut points for tau PET, FDG PET, and cortical thickness on the accuracy of cognitively impaired versus young CN method and base conservative cut points on the accuracy of cognitively impaired versus age‐matched CN method.
F3‐02‐01: The relationship of primary age‐related tauopathy (PART) to snap: Controversy or parallel?
Lowe, Val J. , Wiste, Heather J. , Parisi, Joseph E., Boeve, Bradley, Gunter, Jeffrey L. , Petersen, Ronald C. , Murray, Melissa E. , Knopman, David S. , Kantarci, Kejal , Senjem, Matthew L. , Dickson, Dennis W. , Vemuri, Prashanthi , Jack, Clifford R.

Alzheimer's & Dementia | December 15, 2015 | Volume: 11 | Issue: 7S_Part_4 | Pages: No page available

10.1016/j.jalz.2015.07.226 Get It

Association of Elevated Amyloid Levels With Cognition and Biomarkers in Cognitively Normal People From the Community
Petersen, Ronald C. , Wiste, Heather J. , Weigand, Stephen D. , Rocca, Walter A. , Roberts, Rosebud O., Lowe, Val J. , Geda, Yonas E. , Jack, Clifford R. , Mielke, Michelle M. , Knopman, David S. , Pankratz, V. Shane , Machulda, Mary M. , Jack, Clifford R , Geda, Yonas E

JAMA Neurology | November 23, 2015 | Volume: 73 | Issue: 1 | Pages: 85

10.1001/jamaneurol.2015.3098 Get It

Left ventricular hypertrophy after hypertensive pregnancy disorders
Scantlebury, Dawn C. , Kane, Garvan C. , Wiste, Heather J. , Bailey, Kent R. , Arnett, Donna K. , Devereux, Richard B. , Hunt, Steven C. , Weder, Alan B., Rodríguez, Beatriz L. , Boerwinkle, Eric , Weissgerber, Tracey L. , Garovic, Vesna D. , Turner, Stephen T. , Weissgerber, Tracey L , Mosley, Thomas H. , Garovic, Vesna D , Arnett, Donna K

Heart | August 4, 2015 | Volume: 101 | Issue: 19 | Pages: 1584-1590

10.1136/heartjnl-2015-308098 Get It

Objective Cardiac changes of hypertensive pregnancy include left ventricular hypertrophy (LVH) and diastolic dysfunction. These are thought to regress postpartum. We hypothesised that women with a history of hypertensive pregnancy would have altered LV geometry and function when compared with women with only normotensive pregnancies. Methods In this cohort study, we analysed echocardiograms of 2637 women who participated in the Family Blood Pressure Program. We compared LV mass and function in women with hypertensive pregnancies with those with normotensive pregnancies. Results Women were evaluated at a mean age of 56 years: 427 (16%) had at least one hypertensive pregnancy; 2210 (84%) had normotensive pregnancies. Compared with women with normotensive pregnancies, women with hypertensive pregnancy had a greater risk of LVH (OR: 1.42; 95% CI 1.01 to 1.99, p=0.05), after adjusting for age, race, research network of the Family Blood Pressure Program, education, parity, BMI, hypertension and diabetes. When duration of hypertension was taken into account, this relationship was no longer significant (OR: 1.19; CI 0.08 to 1.78, p=0.38). Women with hypertensive pregnancies also had greater left atrial size and lower mitral E/A ratio after adjusting for demographic variables. The prevalence of systolic dysfunction was similar between the groups. Conclusions A history of hypertensive pregnancy is associated with LVH after adjusting for risk factors; this might be explained by longer duration of hypertension. This finding supports current guidelines recommending surveillance of women following a hypertensive pregnancy, and sets the stage for longitudinal echocardiographic studies to further elucidate progression of LV geometry and function after pregnancy. Clinical trial registrations GENOA- NCT00005269; HyperGEN- NCT00005267; Sapphire- NCT00005270; GenNet- NCT00005268.
Clinical Outcomes of Cardiac Resynchronization with Epicardial Left Ventricular Lead
Chen, Lu , Fu, Hai‐Xia , Pretorius, Victor , Wiste, Heather J. , Yuan, Hongtao, Feld, Gregory K. , Cha, Yong‐Mei , Birgersdotter‐Green, Ulrika , Fu, Haixia, Yang, Dachun, YANG, DACHUN, Pretorius, Victor

Pacing and Clinical Electrophysiology | July 14, 2015 | Volume: 38 | Issue: 10 | Pages: 1201-1209

10.1111/pace.12687 Get It

BackgroundLeft ventricular (LV) pacing in cardiac resynchronization therapy (CRT) can be achieved via a transvenous or epicardial route. A surgically implanted epicardial LV (eLV) lead is used after a standard transvenous LV (tLV) lead implantation has failed. However, studies of clinical outcomes in patients with eLV leads and comparisons of outcome between tLV and eLV‐CRT are sparse. Therefore, the purpose of this study is to compare clinical response between tLV‐CRT and eLV‐CRT, as well as to understand the differences within the eLV‐CRT population.MethodsForty‐four patients received eLV‐CRT following unsuccessful attempts of tLV‐CRT implantation between 2002 and 2013 at the University of California, San Diego (UCSD) and Mayo Clinics. These patients were matched for age, gender, and etiology of cardiomyopathy in a 1:2 ratio with a cohort of patients who received tLV‐CRT during the same time period.ResultsDuring a mean follow‐up of 57 months, similar clinical outcomes and survival rate were noted between tLV and eLV‐CRT patients (all P > 0.05). Within the eLV‐CRT group, dilated cardiomyopathy patients had significant improvement in New York Heart Association class and ejection fraction (both P < 0.05), while ischemic cardiomyopathy patients did not (both P > 0.05). eLV‐CRT patients with nonanterior lead location had significantly improved survival (P < 0.001). There was also a trend for improved survival in those with nonapical lead location (P = 0.09).ConclusionIn this case‐matched two‐centered study, comparable improvements were noted in patients with tLV‐CRT and eLV‐CRT. Operators should target nonanterior and nonapical locations during eLV‐CRT implantation. Use of eLV‐CRT should be considered a viable alternative for CRT candidates.