David Shprecher

ORCID: 0000-0002-4217-0097
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About
Contact & Profiles
Research Areas
  • Parkinson's Disease Mechanisms and Treatments
  • Obsessive-Compulsive Spectrum Disorders
  • Neurological disorders and treatments
  • Autism Spectrum Disorder Research
  • Ginkgo biloba and Cashew Applications
  • Restless Legs Syndrome Research
  • Dementia and Cognitive Impairment Research
  • Botulinum Toxin and Related Neurological Disorders
  • Sleep and Wakefulness Research
  • Attention Deficit Hyperactivity Disorder
  • Genetic Neurodegenerative Diseases
  • Alzheimer's disease research and treatments
  • Nuclear Receptors and Signaling
  • Chemical Reactions and Isotopes
  • Olfactory and Sensory Function Studies
  • RNA regulation and disease
  • Pharmacological Effects and Toxicity Studies
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Sleep and related disorders
  • Balance, Gait, and Falls Prevention
  • Cerebral Palsy and Movement Disorders
  • Long-Term Effects of COVID-19
  • Neurological Disease Mechanisms and Treatments
  • Pharmaceutical studies and practices
  • Health Systems, Economic Evaluations, Quality of Life

Banner Sun Health Research Institute
2016-2025

University of Arizona
2017-2025

Banner Health
2021-2025

Banner - University Medical Center Tucson
2024

Centre National de la Recherche Scientifique
2024

Banner - University Medical Center Phoenix
2024

Université Clermont Auvergne
2024

Institut Pascal
2024

University of Rochester
2008-2022

University of Utah
2012-2021

<h3>Importance</h3> Deutetrabenazine is a novel molecule containing deuterium, which attenuates CYP2D6 metabolism and increases active metabolite half-lives may therefore lead to stable systemic exposure while preserving key pharmacological activity. <h3>Objective</h3> To evaluate efficacy safety of deutetrabenazine treatment control chorea associated with Huntington disease. <h3>Design, Setting, Participants</h3> Ninety ambulatory adults diagnosed manifest disease baseline total maximal...

10.1001/jama.2016.8655 article EN JAMA 2016-07-05

To determine the efficacy and safety of deutetrabenazine as a treatment for tardive dyskinesia (TD).One hundred seventeen patients with moderate to severe TD received or placebo in this randomized, double-blind, multicenter trial. Eligibility criteria included an Abnormal Involuntary Movement Scale (AIMS) score ≥6 assessed by blinded central video rating, stable psychiatric illness, psychoactive medication treatment. Primary endpoint was change AIMS from baseline week 12. Secondary endpoints...

10.1212/wnl.0000000000003960 article EN cc-by-nc-nd Neurology 2017-04-27
Brent Bluett Daniel M. Togasaki Dragos Mihaila Marian L. Evatt Michael Rezak and 95 more Samay Jain Michael A. Schwarzschild Alberto Ascherio Cindy Casaceli Gary C. Curhan Rebecca C. Fitzgerald Cornelia Kamp Codrin Lungu Eric A. Macklin Kenneth Marek Dariush Mozaffarian David Oakes Alice Rudolph Ira Shoulson Aleksandar Videnović B.L. Scott Lisa Gauger Jason Aldred Melissa Bixby Jill Ciccarello Steven A. Gunzler Claire Henchcliffe Matthew Brodsky Kellie Keith Robert A. Hauser Christopher G. Goetz Mark S. LeDoux Vanessa K. Hinson Rajeev Kumar Alberto J. Espay Joohi Jimenez‐Shahed Christine Hunter Chadwick W. Christine Aaron Daley Maureen A. Leehey Joy Antonelle de Marcaida Joseph H. Friedman Albert Y. Hung Grace Bwala Irene Litvan David K. Simon Tanya Simuni Cynthia Poon Mya C. Schiess Kelvin L. Chou Ariane Park Danish Bhatti Carolyn Peterson Susan R. Criswell Liana S. Rosenthal Jennifer Durphy Holly A. Shill Shyamal H. Mehta Anwar Ahmed Andres Deik John Y. Fang Natividad Stover Lin Zhang Richard B. Dewey Ashley Gerald James T. Boyd Emily Houston Valerie Suski Sherri Mosovsky Leslie Cloud Binit Shah Marie Saint‐Hilaire Raymond James S. Elizabeth Zauber Stephen G. Reich David Shprecher Rajesh Pahwa April Langhammer Kathrin LaFaver Peter A. LeWitt Patricia L. Kaminski John L. Goudreau Doozie Russell David Houghton Ashley LaRoche Karen Thomas Martha McGraw Zoltan Mari Carmen Serrano Karen Blindauer Marcie Rabin Roger Kurlan John C. Morgan Michael J. Soileau Melissa Ainslie Iván Bódis-Wollner Ruth B. Schneider Cheryl Waters Amber Servi Ratel Christopher A. Beck

Urate elevation, despite associations with crystallopathic, cardiovascular, and metabolic disorders, has been pursued as a potential disease-modifying strategy for Parkinson disease (PD) based on convergent biological, epidemiological, clinical data.To determine whether sustained urate-elevating treatment the urate precursor inosine slows early PD progression.Randomized, double-blind, placebo-controlled, phase 3 trial of oral in PD. A total 587 individuals consented, 298 not yet requiring...

10.1001/jama.2021.10207 article EN JAMA 2021-09-14

Abstract Digital health technologies can provide continuous monitoring and objective, real-world measures of Parkinson’s disease (PD), but have primarily been evaluated in small, single-site studies. In this 12-month, multicenter observational study, we whether a smartwatch smartphone application could measure features early PD. 82 individuals with early, untreated PD 50 age-matched controls wore research-grade sensors, smartwatch, while performing standardized assessments the clinic. At...

10.1038/s41531-023-00497-x article EN cc-by npj Parkinson s Disease 2023-04-17

Delayed post-hypoxic leukoencephalopathy (DPHL) is a demyelinating syndrome characterized by acute onset of neuropsychiatric symptoms days to weeks following apparent recovery from coma after period prolonged cerebral hypo-oxygenation. It dia

10.3233/nre-2010-0536 article EN Neurorehabilitation 2010-01-28
Scott Schobel Giuseppe Palermo Peggy Auinger Jeffrey D. Long Shiyang Ma and 95 more Omar Khwaja Dylan Trundell Merit Cudkowicz Steven M. Hersch Cristina Sampaio E. Ray Dorsey Blair R. Leavitt Karl Kieburtz Jeffrey Sevigny Douglas R. Langbehn Sarah J. Tabrizi John Adams Mandar Jog Christopher Hyson Sarah Furtado Andrew P. Duker Melissa J. Armstrong Christian Lachner Hubert H. Fernandez Michael S. Okun David Shprecher Michael S. Cartwright Clement T. Loy Joohi Jiminez-Shahed B. Robottom Gregory Suter Theresa HM Moore Jane Forsyth Andrea Hurt Joann Belden Katie Price Diane Erickson Breanna Nickels Misty M Thompson Linda Cole Julie Megens Emilija Makaji Sara-Lynn Masse Keith Malarick Louisa Mook Susan Maya Alex Bender Jessica Meyer Puja Turakhia Katherine Harwood Kathryn Duderstadt S. Lenarz Judy Hamerlinck Patricia Edern Charlyne Hickey Ashley Owens Clare Gibbons Carolyn Steele Gray Jean A. Jaglin Kimberly Janko Holly Lawrence B. Estes Brigid Hayward Allison E. Johnson Amit Gode Giselle Huet Beverly Romero-Kersh K. Wernette Elizabeth Sullivan Jamie Guyot Julie Konkle Christine J. O’Neill Pamela King Amanda Martin John Bautista Nicole Mans Jane Griffith Erica Surles Sharon Halton Alicia Palao Nathalie Padron Kolleen Elliott Lynn Elizabeth Oelke London Butterfield Peggy Perry-Trice Sarah Wyne Carol Pantella Lorelei Tainsh Elaine Sperin Sharon Evans Maureen Gartner Amy Duffy Pamela Kristof Lisa Niles Steven Rainone Angie Wernle Ronda Clouse Michelle Cines Kelly Dustin Maura Deeley

<h3>Objective:</h3> To identify an improved measure of clinical progression in early Huntington disease (HD) using data from prospective observational cohort studies and placebo group randomized double-blind trials. <h3>Methods:</h3> We studied Unified Disease Rating Scale (UHDRS) non-UHDRS measures brain progressive atrophy 1,668 individuals with HD followed up prospectively for to 30 36 months longitudinal follow-up. <h3>Results:</h3> The results demonstrated that a composite motor,...

10.1212/wnl.0000000000004743 article EN Neurology 2017-11-15
Andrew McGarry Michael McDermott Karl Kieburtz Elisabeth A. de Blieck F Béal and 95 more Karen Marder Christopher A. Ross Ira Shoulson Peter R. Gilbert William Mallonee Mark Guttman Joanne Wojcieszek Rajeev Kumar Mark S. LeDoux Mary Jenkins H. Diana Rosas Martha Nance Kevin Biglan Peter G. Como Richard Dubinsky Kathleen M. Shannon Padraig O’Suilleabhain Kelvin L. Chou Francis O. Walker W. R. Wayne Martin Vicki Wheelock Elizabeth McCusker Joseph Jankovic Carlos Singer Juan Sanchez‐Ramos B.L. Scott Oksana Suchowersky Stewart A. Factor Donald S. Higgins Eric Molho Fredy J. Revilla John N. Caviness Joseph H. Friedman Joel S. Perlmutter Andrew Feigin Karen E. Anderson Ramon L. Rodriguez Nikolaus R. McFarland Russell L. Margolis Eric S. Farbman Lynn A. Raymond Valerie Suski Sandra K. Kostyk Amy Colcher Lauren Seeberger Eric A. Epping Sherali Esmail Nancy Díaz Wai Lun Alan Fung Alan Diamond Samuel Frank Philip Hanna Neal Hermanowicz Leon Dure Merit Cudkowicz John Adams Mandar Jog Christopher Hyson Sarah Furtado Andrew P. Duker Melissa J. Armstrong Christian Lachner Hubert Fernandez Michael S. Okun David Shprecher Michael S. Cartwright Clement T. Loy Joohi Jiminez-Shahed B. Robottom Gregory Suter Theresa HM Moore Jane Forsyth Andrea Hurt Joann Belden Katie Price Diane Erickson Breanna Nickels Misty M Thompson Linda Cole Julie Megens Emilija Makaji Sara-Lynn Masse Keith Malarick Louisa Mook Susan Maya Alex Bender Jessica Meyer Puja Turakhia Katherine Harwood Kathryn Duderstadt S. Lenarz Judy Hamerlinck Patricia Edern Charlyne Hickey Ashley Owens

To test the hypothesis that chronic treatment of early-stage Huntington disease (HD) with high-dose coenzyme Q10 (CoQ) will slow progressive functional decline HD.We performed a multicenter randomized, double-blind, placebo-controlled trial. Patients HD (n = 609) were enrolled at 48 sites in United States, Canada, and Australia from 2008 to 2012. randomized receive either CoQ 2,400 mg/d or matching placebo, then followed for 60 months. The primary outcome variable was change baseline month...

10.1212/wnl.0000000000003478 article EN Neurology 2016-12-03
Tanya Simuni Liz Uribe Hyunkeun Ryan Cho Chelsea Caspell-Garcia Christopher S. Coffey and 95 more Andrew Siderowf John Q. Trojanowski Leslie M. Shaw John Seibyl Andrew Singleton Arthur W. Toga Doug Galasko Tatiana Foroud Duygu Tosun Kathleen L. Poston Daniel Weintraub Brit Mollenhauer Caroline M. Tanner Karl Kieburtz Lana M. Chahine Alyssa Reimer Samantha J. Hutten Susan Bressman Kenneth Marek Vanessa Arnedo Adrienne Clark Mark Fraiser Catherine Kopil Sohini Chowdhury Todd Sherer Nichole Daegele Cynthia Casaceli Ray Dorsey Renée Wilson Sugi Mahes Christina M. Salerno Karen Crawford Paola Casalin Giulia Malferrari Mali Gani Weisz Avi Orr‐Urtreger Thomas J. Montine Chris Baglieri Amanda Christini David Russell Nabila Dahodwala Nir Giladi Stewart A. Factor Penelope Hogarth David G. Standaert Robert A. Hauser Joseph Jankovic Marie Saint‐Hilaire Irene Hegeman Richard David Shprecher Hubert Fernandez Katrina Brockmann Liana S. Rosenthal Paolo Barone Alberto J. Espay Dominic B. Rowe Karen Marder A. Parra Santiago Shu‐Ching Hu Stuart Isaacson Jean‐Christophe Corvol Javiar Ruiz Martinez Eduardo Tolosa Yen Tai Marios Politis Debra Smejdir Linda Rees Karen Williams Farah Kausar Karen Williams Whitney Richardson Diana Willeke Shawnees Peacock Barbara Sommerfeld Alison Freed Katrina Wakeman Courtney Blair Stephanie Guthrie Leigh Harrell Christine Hunter Cathi-Ann Thomas Raymond James Grace Zimmerman Victoria Brown Jennifer Mule Ella Hilt Kori Ribb Susan Ainscough Misty Wethington Madelaine Ranola Helen Mejia Santana J.M. Moreno Deborah Raymond Krista Speketer Lisbeth Carvajal

10.1016/s1474-4422(19)30319-9 article EN The Lancet Neurology 2019-11-03

To identify the causal gene in a multi-incident U.S. kindred with Parkinson's disease (PD). We characterized family classical PD phenotype which 7 individuals (5 males and 2 females) were affected mean age at onset of 46.1 years (range, 29-57 years). performed whole exome sequencing on 4 1 unaffected members. Sanger-sequencing was then used to verify genotype all candidate variants remainder pedigree. Cultured cells transfected wild-type or mutant constructs characterize proteins interest....

10.1186/s13024-015-0045-4 article EN cc-by Molecular Neurodegeneration 2015-09-24
Ralf Reilmann Andrew McGarry Igor D. Grachev Juha‐Matti Savola Beth Borowsky and 95 more Eli Eyal Nicholas J. Gross Douglas R. Langbehn Robin Schubert Anna Teige Wickenberg Spyros Papapetropoulos Michael R. Hayden Ferdinando Squitieri Karl Kieburtz G. Bernhard Landwehrmeyer Pinky Agarwal Karen E. Anderson N. Ahmad Aziz J.P. Azulay Anne‐Catherine Bachoud‐Lévi Roger A. Barker Agnieszka Bebak Markus Beuth Kevin Biglan Stéphanie Blin Stefan Bohlen Raphael M. Bonelli Sue Caldwell Fabienne Calvas Jonielyn Carlos Simona Castagliuolo Terrence Chong Phyllis Chua Allison Coleman Jody Corey‐Bloom Rebecca Cousins David Craufurd Jill Davison E Decorte Giuseppe De Michele Laura Dornhege Andrew Feigin Stephanie Gallehawk Pascale Gauteul Carey Gonzales Jane Griffith А.В. Густов Mark Guttman Beatrix Heim Hope Heller Lena E. Hjermind С. Н. Иллариошкин Larry Ivanko Jessica Jaynes Mollie W. Jenckes Barbara Kaminski Anne Kampstra Agnieszka Konkel S V Kopishinskaya Pierre Krystkowiak Suresh K Komati Alexander Kwako Stefan Lakoning Guzal Latipova Blair R. Leavitt Clement T. Loy Cheryl MacFarlane Louise Madsen Karen Marder Sarah L. Mason Neila Mendis Tilak Mendis Andrea H. Németh Louise Nevitt Virginia Norris Christine J. O’Neill Audrey Olivier Michael Orth Ashley Owens Peter K. Panegyres Susan Perlman J. Samuel Preston Josef Priller Alicja Puch Oliver Quarrell Domenica Ragosta Amandine Rialland Hugh Rickards Anna Maria Romoli Christopher A. Ross Anne Rosser Monika Rudzińska Cinzina V Russo Carsten Saft Victoria Segro Klaus Seppi Barbara Shannon David Shprecher C. Simonin Zara Skitt

10.1016/s1474-4422(18)30391-0 article EN The Lancet Neurology 2018-12-15

The coronavirus SARS-CoV-2 (SCV2) causes acute respiratory distress, termed COVID-19 disease, with substantial morbidity and mortality. As SCV2 is related to previously-studied coronaviruses that have been shown the capability for brain invasion, it seems likely may be able do so as well. To date, although there many clinical autopsy-based reports describe a broad range of SCV2-associated neurological conditions, unclear what fraction these due direct CNS invasion versus indirect effects...

10.1101/2021.02.15.21251511 preprint EN cc-by-nd medRxiv (Cold Spring Harbor Laboratory) 2021-02-18

Rapid eye movement (REM) sleep behavior disorder (RBD) is widely considered a prodromal synucleinopathy, as most with RBD develop overt synucleinopathy within ~10 years. Accordingly, offers an opportunity to test potential treatments at the earliest stages of synucleinopathy. The North American Prodromal Synucleinopathy (NAPS) Consortium has created multisite participant, primarily clinic-based cohort better understand characteristics diagnosis, and in future work, identify predictors...

10.1002/acn3.51738 article EN cc-by Annals of Clinical and Translational Neurology 2023-02-08

Digital measures may provide objective, sensitive, real-world of disease progression in Parkinson's (PD). However, multicenter longitudinal assessments such are few. We recently demonstrated that baseline gait, tremor, finger tapping, and speech from a commercially available smartwatch, smartphone, research-grade wearable sensors differed significantly between 82 individuals with early, untreated PD 50 age-matched controls. Here, we evaluated the change these over 12 months observational...

10.1038/s41531-024-00721-2 article EN cc-by npj Parkinson s Disease 2024-06-12

This study was designed to correlate clinical findings with the extent of pathologic a-synuclein (aSyn) in brain using Unified Staging System for Lewy Body disorders (USSLB). Data from 280 cases Arizona Study Aging and Neurodegenerative Disorders are presented. Each case had a complete USSLB staging at least 1 full research assessment, including subspecialty neurologist-administered movement cognitive evaluation. Of 280, 25.7% were cognitively normal, 8.6% mild impairment, 65.7% dementia....

10.1093/jnen/nlz080 article EN Journal of Neuropathology & Experimental Neurology 2019-09-05

The cause of progressive supranuclear palsy (PSP) is largely unknown. Based on evidence for impaired mitochondrial activity in PSP, we hypothesized that the disease may be related to exposure environmental toxins, some which are inhibitors.This multicenter case-control study included 284 incident PSP cases 350 and age-, sex-, race-matched controls primarily from same geographical areas. All subjects were administered standardized interviews obtain data demographics, residential history,...

10.1002/mds.26512 article EN Movement Disorders 2016-02-08

<strong>Background:</strong> Deutetrabenazine, an inhibitor of vesicular monoamine transporter type 2 (VMAT2) depletes presynaptic dopamine and is useful in the treatment hyperkinetic movement disorders. This study explored safety, tolerability, preliminary efficacy deutetrabenazine adolescents with moderate-to-severe tics associated Tourette syndrome (TS). <strong>Methods:</strong> In this open-label 12–18-year-old patients TS-related tics, was titrated up to 36 mg/day over 6 weeks...

10.5334/tohm.287 article EN cc-by Tremor and Other Hyperkinetic Movements 2016-11-07

Brains of 42 COVID-19 decedents and 107 non-COVID-19 controls were studied. RT-PCR screening 16 regions from 20 autopsies found SARS-CoV-2 E gene viral sequences in 7 (2.5% 320 samples), concentrated 4/20 subjects (20%). Additional olfactory bulb (OB), amygdala (AMY) entorhinal area for E, N1, N2, RNA-dependent RNA polymerase, S detected one or more these OB 8/21 (38%). It is uncertain whether represent viable virus. Significant histopathology was limited to 2/42 cases (4.8%), with a large...

10.1093/jnen/nlac056 article EN Journal of Neuropathology & Experimental Neurology 2022-07-11

Parkinson disease (PD) is associated with α-synuclein (αS) aggregation within enteric neurons. ENT-01 inhibits the formation of αS aggregates and improved constipation in an open-label study patients PD.To evaluate safety efficacy oral for neurologic symptoms PD constipation.Randomized, placebo-controlled phase 2b study. (ClinicalTrials.gov: NCT03781791).Outpatient.150 constipation.ENT-01 or placebo daily up to 25 days. After baseline assessment severity, dosing was escalated prokinetic...

10.7326/m22-1438 article EN Annals of Internal Medicine 2022-11-07

REM sleep behavior disorder (RBD) is a parasomnia characterized by dream enactment. The International RBD Study Group developed the Symptom Severity Scale (RBDSSS) to assess symptom severity for clinical or research use. We assessed psychometric and clinimetric properties of RBDSSS in participants enrolled North American Prodromal Synucleinopathy (NAPS) Consortium RBD. NAPS participants, who have polysomnogram-confirmed RBD, their bedpartners completed (participant bedpartner versions)....

10.1212/wnl.0000000000208008 article EN Neurology 2024-01-05

Neuropathology has demonstrated a high rate of comorbid pathology in dementia due to Alzheimer's disease (ADD). The most common major comorbidity is Lewy body (LBD), either as with bodies (AD-DLB) or (AD-LB), the latter representing subjects ADD and LBD not meeting neuropathological distribution density thresholds for DLB. Although it been established that undifferentiated have more rapid cognitive decline than those alone, still unknown whether AD-LB subjects, who represent majority...

10.1371/journal.pone.0217566 article EN cc-by PLoS ONE 2019-06-25
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