Searched for: school:SOM
Department/Unit:Neurology
Deep brain stimulation in Parkinson's disease: A multicentric, long-term, observational pilot study
Scelzo, Emma; Beghi, Ettore; Rosa, Manuela; Angrisano, Serena; Antonini, Angelo; Bagella, Caterina; Bianchi, Elisa; Caputo, Elena; Lena, Francesco; Lopiano, Leonardo; Marcante, Andrea; Marceglia, Sara; Massaro, Francesco; Modugno, Nicola; Pacchetti, Claudio; Pilleri, Manuela; Pozzi, Nicolo Gabriele; Romito, Luigi Michele; Santilli, Marco; Tamma, Filippo; Weis, Luca; Zibetti, Maurizio; Priori, Alberto
BACKGROUND:The impact of deep brain stimulation (DBS) on cognitive and urinary disorders, falls, and eventually hospitalizations and mortality in Parkinson's disease (PD) is still debated. OBJECTIVE:We compared the rates of dementia, mild cognitive impairment (MCI), urinary incontinence, nocturia, falls, hospitalizations, and mortality in a cohort of PD patients undergoing DBS with a cohort of medically-treated patients chosen as controls. METHODS:We conducted a retrospective pilot study in six Italian DBS centers. 91 PD patients receiving DBS and 91 age- and gender-matched controls receiving the best medical treatment alone with a minimum follow-up of one year were enrolled. Clinical data were collected from baseline to the last follow-up visit using an ad-hoc developed web-based system. RESULTS:The risk of dementia was similar in the two groups while patients in the surgical cohort had lower rates of MCI, urinary incontinence, nocturia, and falls. In contrast, the risk of hospital admissions related to PD was higher in the surgical cohort. However, when excluding hospitalizations related to DBS surgery, the difference between the two cohorts was not significant. The surgical cohort had a lower number of hospitalizations not related to PD. The risk of death was similar in the two groups. CONCLUSION/CONCLUSIONS:Despite a higher risk of hospitalization, patients receiving DBS had a lower rate of MCI, urinary incontinence, nocturia and falls, without evidence of an increased risk of dementia and mortality. Although these findings need to be confirmed in prospective studies, they seem to suggest that DBS may play a significant role in the management of non-motor symptoms and common complications of advanced PD.
PMID: 31476620
ISSN: 1878-5883
CID: 4066992
Hospital distance, socioeconomic status, and timely treatment of ischemic stroke
Ader, Jeremy; Wu, Jingjing; Fonarow, Gregg C; Smith, Eric E; Shah, Shreyansh; Xian, Ying; Bhatt, Deepak L; Schwamm, Lee H; Reeves, Mathew J; Matsouaka, Roland A; Sheth, Kevin N
OBJECTIVE:To determine whether lower socioeconomic status (SES) and longer home to hospital driving time are associated with reductions in tissue plasminogen activator (tPA) administration and timeliness of the treatment. METHODS:We conducted a retrospective observational study using data from the Get With The Guidelines-Stroke Registry (GWTG-Stroke) between January 2015 and March 2017. The study included 118,683 ischemic stroke patients age ≥18 who were transported by emergency medical services to one of 1,489 US hospitals. We defined each patient's SES based on zip code median household income. We calculated the driving time between each patient's home zip code and the hospital where he or she was treated using the Google Maps Directions Application Programing Interface. The primary outcomes were tPA administration and onset-to-arrival time (OTA). Outcomes were analyzed using hierarchical multivariable logistic regression models. RESULTS:= 0.6103). CONCLUSIONS:Longer driving times were associated with lower odds of tPA administration and longer OTA; however, SES did not modify these associations.
PMCID:6711658
PMID: 31320472
ISSN: 1526-632x
CID: 5675232
Editors' note: Teaching Video NeuroImages: Vestibulo-ocular reflex defect in cerebellar stroke
Lewis, Ariane; Galetta, Steven
ORIGINAL:0014546
ISSN: 1526-632x
CID: 4354252
Image processing and analysis methods for the Adolescent Brain Cognitive Development Study
Hagler, Donald J; Hatton, SeanN; Cornejo, M Daniela; Makowski, Carolina; Fair, Damien A; Dick, Anthony Steven; Sutherland, Matthew T; Casey, B J; Barch, Deanna M; Harms, Michael P; Watts, Richard; Bjork, James M; Garavan, Hugh P; Hilmer, Laura; Pung, Christopher J; Sicat, Chelsea S; Kuperman, Joshua; Bartsch, Hauke; Xue, Feng; Heitzeg, Mary M; Laird, Angela R; Trinh, Thanh T; Gonzalez, Raul; Tapert, Susan F; Riedel, Michael C; Squeglia, Lindsay M; Hyde, Luke W; Rosenberg, Monica D; Earl, Eric A; Howlett, Katia D; Baker, Fiona C; Soules, Mary; Diaz, Jazmin; de Leon, Octavio Ruiz; Thompson, Wesley K; Neale, Michael C; Herting, Megan; Sowell, Elizabeth R; Alvarez, Ruben P; Hawes, Samuel W; Sanchez, Mariana; Bodurka, Jerzy; Breslin, Florence J; Morris, Amanda Sheffield; Paulus, Martin P; Simmons, W Kyle; Polimeni, Jonathan R; van der Kouwe, Andre; Nencka, Andrew S; Gray, Kevin M; Pierpaoli, Carlo; Matochik, John A; Noronha, Antonio; Aklin, Will M; Conway, Kevin; Glantz, Meyer; Hoffman, Elizabeth; Little, Roger; Lopez, Marsha; Pariyadath, Vani; Weiss, Susan Rb; Wolff-Hughes, Dana L; DelCarmen-Wiggins, Rebecca; Feldstein Ewing, Sarah W; Miranda-Dominguez, Oscar; Nagel, Bonnie J; Perrone, Anders J; Sturgeon, Darrick T; Goldstone, Aimee; Pfefferbaum, Adolf; Pohl, Kilian M; Prouty, Devin; Uban, Kristina; Bookheimer, Susan Y; Dapretto, Mirella; Galvan, Adriana; Bagot, Kara; Giedd, Jay; Infante, M Alejandra; Jacobus, Joanna; Patrick, Kevin; Shilling, Paul D; Desikan, Rahul; Li, Yi; Sugrue, Leo; Banich, Marie T; Friedman, Naomi; Hewitt, John K; Hopfer, Christian; Sakai, Joseph; Tanabe, Jody; Cottler, Linda B; Nixon, Sara Jo; Chang, Linda; Cloak, Christine; Ernst, Thomas; Reeves, Gloria; Kennedy, David N; Heeringa, Steve; Peltier, Scott; Schulenberg, John; Sripada, Chandra; Zucker, Robert A; Iacono, William G; Luciana, Monica; Calabro, Finnegan J; Clark, Duncan B; Lewis, David A; Luna, Beatriz; Schirda, Claudiu; Brima, Tufikameni; Foxe, John J; Freedman, Edward G; Mruzek, Daniel W; Mason, Michael J; Huber, Rebekah; McGlade, Erin; Prescot, Andrew; Renshaw, Perry F; Yurgelun-Todd, Deborah A; Allgaier, Nicholas A; Dumas, Julie A; Ivanova, Masha; Potter, Alexandra; Florsheim, Paul; Larson, Christine; Lisdahl, Krista; Charness, Michael E; Fuemmeler, Bernard; Hettema, John M; Maes, Hermine H; Steinberg, Joel; Anokhin, Andrey P; Glaser, Paul; Heath, Andrew C; Madden, Pamela A; Baskin-Sommers, Arielle; Constable, R Todd; Grant, Steven J; Dowling, Gayathri J; Brown, Sandra A; Jernigan, Terry L; Dale, Anders M
The Adolescent Brain Cognitive Development (ABCD) Study is an ongoing, nationwide study of the effects of environmental influences on behavioral and brain development in adolescents. The main objective of the study is to recruit and assess over eleven thousand 9-10-year-olds and follow them over the course of 10 years to characterize normative brain and cognitive development, the many factors that influence brain development, and the effects of those factors on mental health and other outcomes. The study employs state-of-the-art multimodal brain imaging, cognitive and clinical assessments, bioassays, and careful assessment of substance use, environment, psychopathological symptoms, and social functioning. The data is a resource of unprecedented scale and depth for studying typical and atypical development. The aim of this manuscript is to describe the baseline neuroimaging processing and subject-level analysis methods used by ABCD. Processing and analyses include modality-specific corrections for distortions and motion, brain segmentation and cortical surface reconstruction derived from structural magnetic resonance imaging (sMRI), analysis of brain microstructure using diffusion MRI (dMRI), task-related analysis of functional MRI (fMRI), and functional connectivity analysis of resting-state fMRI. This manuscript serves as a methodological reference for users of publicly shared neuroimaging data from the ABCD Study.
PMID: 31415884
ISSN: 1095-9572
CID: 4042682
Mineralocorticoid receptor antagonist use after hospitalization of patients with heart failure and post-discharge outcomes: a single-center retrospective cohort study
Durstenfeld, Matthew S; Katz, Stuart D; Park, Hannah; Blecker, Saul
BACKGROUND:Mineralocorticoid receptor antagonists (MRA) are an underutilized therapy for heart failure with a reduced ejection fraction (HFrEF), but the current impact of hospitalization on MRA use is not well characterized. The objective of this study was to describe contemporary MRA prescription for heart failure patients before and after the full scope of hospitalizations and the association between MRA discharge prescription and post-hospitalization outcomes. METHODS:We conducted a retrospective cohort study at an academic hospital system in 2013-2016. Among 1500 included hospitalizations of 1009 unique patients with HFrEF and without MRA contraindication, the mean age was 71.9 ± 13.6 years and 443 (29.5%) were female. We compared MRA prescription before and after hospitalizations with McNemar's test and between patients with principal and secondary diagnoses of HFrEF with the chi-square test, and association of MRA discharge prescription with 30-day and 180-day mortality and readmissions using generalized estimating equations. RESULTS:MRA prescriptions increased from 303 (20.2%) to 375 (25.0%) at discharge (+4.8%, p < 0.0001). More patients with principal diagnosis of HFrEF compared to those hospitalized for other reasons received MRA (34.9% versus 21.3%, p < 0.0001) and had them initiated (21.8% versus 9.7%, p < 0.0001). MRA prescription at discharge was not associated with mortality or readmission at 30 and 180 days, and there was no interaction with principal/secondary diagnosis. CONCLUSIONS:Among hospitalized HFrEF patients, 75% did not receive MRA before or after hospitalization, and nearly 90% of eligible patients did not have MRA initiated. As we found no signal for short-term harm after discharge, hospitalization may represent an opportunity to initiate guideline-directed heart failure therapy.
PMID: 31399059
ISSN: 1471-2261
CID: 4034482
Patients with dorsolateral prefrontal cortex lesions are capable of discriminatory threat learning but appear impaired in cognitive regulation of subjective fear
Kroes, Marijn C W; Dunsmoor, Joseph E; Hakimi, Mathew; Oosterwaal, Sofie; Meager, Michael R; Phelps, Elizabeth A
Humans are able to cognitively regulate emotions by changing their thoughts. Neuroimaging studies show correlations between dorsolateral prefrontal cortex (dlPFC) activity and cognitive regulation of emotions. Here our objective was to investigate whether dlPFC damage is associated with impaired cognitive regulation of emotion. We therefore tested the ability of patients with dlPFC lesions (N = 6) and matched control participants (N = 19) to utilize a laboratory version of cognitive regulation training (CRT) to regulate subjective fear and autonomic threat responses following Pavlovian threat conditioning. We found that patients with dlPFC lesions were able to acquire conditioned threat but seemed impaired in their ability to utilize CRT to cognitively regulate subjective fear to a threatening stimulus. Despite inclusion of a limited number of lesion patients, our results suggest that the dlPFC is important for the cognitive regulation of subjective fear.
PMID: 31119295
ISSN: 1749-5024
CID: 3920792
Suppression of the photoparoxysmal response in photosensitive epilepsy with cenobamate (YKP3089)
Kasteleijn-Nolst Trenite, Dorothee G A; DiVentura, Bree D; Pollard, John R; Krauss, Gregory L; Mizne, Sarah; French, Jacqueline A
OBJECTIVE:To evaluate the effect of cenobamate in patients with photoparoxysmal-EEG response (PPR) to intermittent photic stimulation (IPS) as proof of principle of efficacy in patients with epilepsy. METHODS:In this multicenter, single-blind study, adults with photosensitive epilepsy, with/without concomitant antiepileptic drug therapy, underwent IPS under 3 eye conditions after a single dose of placebo (day -1, day 2) or cenobamate (day 1; 100, 250, or 400 mg). Complete suppression was a standardized photosensitivity range reduction to 0 over ≥1 time points for all eye conditions. Partial suppression was a ≥3-point reduction over ≥3 testing times vs the same time points on day -1 in ≥1 eye condition. Pharmacokinetics and safety were assessed. RESULTS:Of 6 evaluable patients, 5 reentered to receive higher doses. Cenobamate 100 mg produced partial suppression in 1 of 3 patients; 250 mg produced complete suppression in 1 of 4 and partial suppression in 4 of 4 patients; and 400 mg produced complete suppression in 1 of 4 and partial suppression in 2 of 4 patients. PPR was consistently reduced on days 1 and 2 (>24 hours after cenobamate) vs day -1 (placebo) with the 250- and 400-mg doses. Area under the plasma concentration-time curve (before dose to last measurable concentration) values between 201 and 400 μg/h/mL resulted in partial suppression in 4 of 6 (66%) patients. Most common adverse events were dizziness and somnolence. CONCLUSIONS:This proof-of-principle study demonstrated that cenobamate is a potentially effective product for epilepsy. CLINICALTRIALSGOV IDENTIFIER/UNASSIGNED:NCT00616148. CLASSIFICATION OF EVIDENCE/METHODS:This study provides Class III evidence that, for patients with photosensitive epilepsy, cenobamate suppresses IPS-induced PPR.
PMID: 31292226
ISSN: 1526-632x
CID: 3976662
Haploinsufficiency in the ANKS1B gene encoding AIDA-1 leads to a neurodevelopmental syndrome
Carbonell, Abigail U; Cho, Chang Hoon; Tindi, Jaafar O; Counts, Pamela A; Bates, Juliana C; Erdjument-Bromage, Hediye; Cvejic, Svetlana; Iaboni, Alana; Kvint, Ifat; Rosensaft, Jenny; Banne, Ehud; Anagnostou, Evdokia; Neubert, Thomas A; Scherer, Stephen W; Molholm, Sophie; Jordan, Bryen A
Neurodevelopmental disorders, including autism spectrum disorder, have complex polygenic etiologies. Single-gene mutations in patients can help define genetic factors and molecular mechanisms underlying neurodevelopmental disorders. Here we describe individuals with monogenic heterozygous microdeletions in ANKS1B, a predicted risk gene for autism and neuropsychiatric diseases. Affected individuals present with a spectrum of neurodevelopmental phenotypes, including autism, attention-deficit hyperactivity disorder, and speech and motor deficits. Neurons generated from patient-derived induced pluripotent stem cells demonstrate loss of the ANKS1B-encoded protein AIDA-1, a brain-specific protein highly enriched at neuronal synapses. A transgenic mouse model of Anks1b haploinsufficiency recapitulates a range of patient phenotypes, including social deficits, hyperactivity, and sensorimotor dysfunction. Identification of the AIDA-1 interactome using quantitative proteomics reveals protein networks involved in synaptic function and the etiology of neurodevelopmental disorders. Our findings formalize a link between the synaptic protein AIDA-1 and a rare, previously undefined genetic disease we term ANKS1B haploinsufficiency syndrome.
PMCID:6684583
PMID: 31388001
ISSN: 2041-1723
CID: 4033212
Anhedonia following mild traumatic brain injury in rats: A behavioral economic analysis of positive and negative reinforcement
Avcu, Pelin; Fortress, Ashley M; Fragale, Jennifer E; Spiegler, Kevin M; Pang, Kevin C H
Psychiatric disorders affect nearly 50% of individuals who have experienced a traumatic brain injury (TBI). Anhedonia is a major symptom of numerous psychiatric disorders and is a diagnostic criterion for depression. It has recently been appreciated that reinforcement may be separated into consummatory (hedonic), motivational and decisional components, all of which may be affected differently in disease. Although anhedonia is typically assessed using positive reinforcement, the importance of stress in psychopathology suggests the study of negative reinforcement (removal or avoidance of aversive events) may be equally important. The present study investigated positive and negative reinforcement following a rat model of mild TBI (mTBI) using lateral fluid percussion. Hedonic value and motivation for reinforcement was determined by behavioral economic analyses. Following mTBI, the hedonic value of avoiding foot shock was reduced. In contrast, the hedonic value of escaping foot shock or obtaining a sucrose pellet was not altered by mTBI. Moreover, motivation to avoid or escape foot shock or to acquire sucrose was not altered by mTBI. Our results suggest that individuals experiencing mTBI find avoidance of aversive events less reinforcing, and therefore are less apt to utilize proactive control of stress.
PMID: 30998994
ISSN: 1872-7549
CID: 5865642
Correlation of Tumor Treating Fields Dosimetry to Survival Outcomes in Newly Diagnosed Glioblastoma: A Large-Scale Numerical Simulation-Based Analysis of Data from the Phase 3 EF-14 Randomized Trial
Ballo, Matthew T; Urman, Noa; Lavy-Shahaf, Gitit; Grewal, Jai; Bomzon, Ze'ev; Toms, Steven
INTRODUCTION/BACKGROUND:Tumor Treating Fields (TTFields) are approved for glioblastoma based on improved overall survival (OS) and progression-free survival (PFS) in the phase 3 EF-14 trial of newly diagnosed glioblastoma. To test the hypothesis that increasing TTFields dose at the tumor site improves patient outcomes, we performed a simulation-based study investigating the association between TTFields dose and survival (OS and PFS) in patients treated with TTFields in EF-14. METHODS AND MATERIALS/METHODS:EF-14 patient cases (NÂ =Â 340) were included. Realistic head models were derived from T1-contrast images captured at baseline. The transducer array layout on each patient was obtained from EF-14 records; average compliance (fraction of time patient was on active treatment) and average electrical current delivered to the patient were derived from log files of the TTFields devices used by patients. TTFields intensity distributions and power densities were calculated using the finite element method. Local minimum dose density (LMiDD) was defined as the product of TTFields intensity, tissue-specific conductivities, and patient compliance. The average LMiDD within a tumor bed comprising the gross tumor volume and the 3-mm-wide peritumoral boundary zone was calculated. RESULTS:: OS was 25.2 versus 20.4Â months (PÂ =Â .003, hazard ratio [HR]Â =Â 0.611) and PFS was 8.5 versus 6.7Â months (PÂ =Â .02, HRÂ =Â 0.699). The median OS and PFS were longer when the average TTFields intensity was >1.06Â V/cm: OS was 24.3 versus 21.6Â months (PÂ =Â .03, HRÂ =Â 0.705) and PFS was 8.1 versus 7.9Â months (PÂ =Â .03, HRÂ =Â 0.721). CONCLUSIONS:In this study we present the first reported analysis demonstrating patient-level dose responses to TTFields. We provide a rigorous definition for TTFields dose and set a conceptual framework for future work on TTFields dosimetry and treatment planning.
PMID: 31026557
ISSN: 1879-355x
CID: 4096982