33 results on '"Safarpour, Delaram"'
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2. Changes in Anticholinergic Burden in Parkinson’s Disease After Deep Brain Stimulation
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Jiao, Jocelyn, Brumbach, Barbara H., Hantke, Nathan, Wilhelmi, Morgan, Bonilla, Christian, and Safarpour, Delaram
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- 2024
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3. Gastrointestinal Dysfunction in Parkinson’s Disease
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Safarpour, Delaram, Sharzehi, Kaveh, and Pfeiffer, Ronald F.
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- 2022
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4. Telemedicine and Deep brain stimulation - Current practices and recommendations
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Sharma, Vibhash D., Safarpour, Delaram, Mehta, Shyamal H., Vanegas-Arroyave, Nora, Weiss, Daniel, Cooney, Jeffrey W., Mari, Zoltan, and Fasano, Alfonso
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- 2021
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5. The Potential Therapeutic Effects of Botulinum Neurotoxins on Neoplastic Cells: A Comprehensive Review of In Vitro and In Vivo Studies.
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Safarpour, Delaram, Tavassoli, Fattaneh A., and Jabbari, Bahman
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NEUROTOXIC agents , *TREATMENT effectiveness , *PROTEIN receptors , *CLOSTRIDIOIDES difficile , *CELL membranes - Abstract
A systematic review of the literature found fifteen articles on the effect of a botulinum toxin on neoplastic cell lines and eight articles on in vivo neoplasms. The reported in vitro effects rely on high doses or the mechanical disruption of cell membranes to introduce the botulinum neurotoxin into the cell cytoplasm. The potency of the botulinum neurotoxin to intoxicate non-neuronal cells (even cell lines expressing an appropriate protein receptor) is several orders of magnitude lower compared to that to intoxicate the primary neurons. The data suggest that the botulinum toxin disrupts the progression of cancer cells, with some studies reporting apoptotic effects. A majority of the data in the in vivo studies also showed similar results. No safety issues were disclosed in the in vivo studies. Limited studies have suggested similar anti-neoplastic potential for the clostridium difficile. New modes of delivery have been tested to enhance the in vivo delivery of the botulinum toxin to neoplastic cells. Careful controlled studies are necessary to demonstrate the efficacy and safety of this mode of anti-neoplastic treatment in humans. [ABSTRACT FROM AUTHOR]
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- 2024
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6. Standing Balance Conditions and Digital Sway Measures for Clinical Trials of Friedreich's Ataxia.
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Casey, Hannah L., Shah, Vrutangkumar V., Muzyka, Daniel, McNames, James, El‐Gohary, Mahmoud, Sowalsky, Kristen, Safarpour, Delaram, Carlson‐Kuhta, Patricia, Schmahmann, Jeremy D., Rosenthal, Liana S., Perlman, Susan, Rummey, Christian, Horak, Fay B., and Gomez, Christopher M.
- Abstract
Background: Progressive loss of standing balance is a feature of Friedreich's ataxia (FRDA). Objectives: This study aimed to identify standing balance conditions and digital postural sway measures that best discriminate between FRDA and healthy controls (HC). We assessed test–retest reliability and correlations between sway measures and clinical scores. Methods: Twenty‐eight subjects with FRDA and 20 HC completed six standing conditions: feet apart, feet together, and feet tandem, both with eyes opened (EO) and eyes closed. Sway was measured using a wearable sensor on the lumbar spine for 30 seconds. Test completion rate, test–retest reliability with intraclass correlation coefficients, and areas under the receiver operating characteristic curves (AUCs) for each measure were compared to identify distinguishable FRDA sway characteristics from HC. Pearson correlations were used to evaluate the relationships between discriminative measures and clinical scores. Results: Three of the six standing conditions had completion rates over 70%. Of these three conditions, natural stance and feet together with EO showed the greatest completion rates. All six of the sway measures' mean values were significantly different between FRDA and HC. Four of these six measures discriminated between groups with >0.9 AUC in all three conditions. The Friedreich Ataxia Rating Scale Upright Stability and Total scores correlated with sway measures with P‐values <0.05 and r‐values (0.63–0.86) and (0.65–0.81), respectively. Conclusion: Digital postural sway measures using wearable sensors are discriminative and reliable for assessing standing balance in individuals with FRDA. Natural stance and feet together stance with EO conditions suggest use in clinical trials for FRDA. © 2024 International Parkinson and Movement Disorder Society. [ABSTRACT FROM AUTHOR]
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- 2024
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7. Measuring freezing of gait during daily-life: an open-source, wearable sensors approach
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Mancini, Martina, Shah, Vrutangkumar V., Stuart, Samuel, Curtze, Carolin, Horak, Fay B., Safarpour, Delaram, and Nutt, John G.
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- 2021
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8. Digital Measures of Postural Sway Quantify Balance Deficits in Spinocerebellar Ataxia.
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Shah, Vrutangkumar V., Muzyka, Daniel, Jagodinsky, Adam, McNames, James, Casey, Hannah, El-Gohary, Mahmoud, Sowalsky, Kristen, Safarpour, Delaram, Carlson-Kuhta, Patricia, Schmahmann, Jeremy D., Rosenthal, Liana S., Perlman, Susan, Horak, Fay B., and Gomez, Christopher M.
- Abstract
Background: Maintaining balance is crucial for independence and quality of life. Loss of balance is a hallmark of spinocerebellar ataxia (SCA). Objective: The aim of this study was to identify which standing balance conditions and digital measures of body sway were most discriminative, reliable, and valid for quantifying balance in SCA. Methods: Fifty-three people with SCA (13 SCA1, 13 SCA2, 14 SCA3, and 13 SCA6) and Scale for Assessment and Rating of Ataxia (SARA) scores 9.28 ( 4.36 and 31 healthy controls were recruited. Subjects stood in six test conditions (natural stance, feet together and tandem, each with eyes open [EO] and eyes closed [EC]) with an inertial sensor on their lower back for 30 seconds (2). We compared test completion rate, test–retest reliability, and areas under the receiver operating characteristic curve (AUC) for seven digital sway measures. Pearson’s correlations related sway with the SARA and the Patient-Reported Outcome Measure of Ataxia (PROM ataxia). Results: Most individuals with SCA (85%–100%) could stand for 30 seconds with natural stance EO or EC, and with feet together EO. The most discriminative digital sway measures (path length, range, area, and root mean square) from the two most reliable and discriminative conditions (natural stance EC and feet together EO) showed intraclass correlation coefficients from 0.70 to 0.91 and AUCs from 0.83 to 0.93. Correlations of sway with SARA were significant (maximum r = 0.65 and 0.73). Correlations with PROM ataxia were mild to moderate (maximum r = 0.56 and 0.34). Conclusion: Inertial sensor measures of extent of postural sway in conditions of natural stance EC and feet together stance EO were discriminative, reliable, and valid for monitoring SCA. © 2024 International Parkinson and Movement Disorder Society [ABSTRACT FROM AUTHOR]
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- 2024
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9. Botulinum Toxin Treatment for Cancer-Related Disorders: A Systematic Review.
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Safarpour, Delaram and Jabbari, Bahman
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BOTULINUM A toxins , *BOTULINUM toxin , *PYLORUS , *MASSETER muscle , *PAROTID gland surgery , *SALINE injections , *PAROTID glands , *ESOPHAGEAL cancer - Abstract
This systematic review investigates the effect of botulinum neurotoxin (BoNT) therapy on cancer-related disorders. A major bulk of the literature is focused on BoNT's effect on pain at the site of surgery or radiation. All 13 published studies on this issue indicated reduction or cessation of pain at these sites after local injection of BoNTs. Twelve studies addressed the effect of BoNT injection into the pylorus (sphincter between the stomach and the first part of the gut) for the prevention of gastroparesis after local resection of esophageal cancer. In eight studies, BoNT injection was superior to no intervention; three studies found no difference between the two approaches. One study compared the result of intra-pyloric BoNT injection with preventive pyloromyotomy (resection of pyloric muscle fibers). Both approaches reduced gastroparesis, but the surgical approach had more serious side effects. BoNT injection was superior to saline injection in the prevention of esophageal stricture after surgery (34% versus 6%, respectively, p = 0.02) and produced better results (30% versus 40% stricture) compared to steroid (triamcinolone) injection close to the surgical region. All 12 reported studies on the effect of BoNT injection into the parotid region for the reduction in facial sweating during eating (gustatory hyperhidrosis) found that BoNT injections stopped or significantly reduced facial sweating that developed after parotid gland surgery. Six studies showed that BoNT injection into the parotid region prevented the development of or healed the fistulas that developed after parotid gland resection—parotidectomy gustatory hyperhidrosis (Frey syndrome), post-surgical parotid fistula, and sialocele. Eight studies suggested that BoNT injection into masseter muscle reduced or stopped severe jaw pain after the first bite (first bite syndrome) that may develop as a complication of parotidectomy. [ABSTRACT FROM AUTHOR]
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- 2023
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10. Adjusting for Underrepresentation Reveals Widespread Underestimation of Parkinson's Disease Symptom Burden.
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Hamedani, Ali G., Auinger, Peggy, Willis, Allison W., Safarpour, Delaram, Shprecher, David, Stover, Natividad, Subramanian, Thyagarajan, and Cloud, Leslie
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Background: Clinical research is limited by underrepresentation, but the impact of underrepresentation on patient‐reported outcomes in Parkinson's disease (PD) is unknown. Objectives: To produce nationwide estimates of non‐motor symptom (NMS) prevalence and PD‐related quality of life (QOL) limitations while accounting for underrepresentation. Methods: We performed a cross‐sectional analysis of data from the Fox Insight (FI) study, an ongoing prospective longitudinal study of persons with self‐reported PD. Using epidemiologic literature and United States (US) Census Bureau, Medicare, and National Health and Aging Trends Study data, we simulated a "virtual census" of the PD population. To compare the PD census to the FI cohort, we used logistic regression to model the odds of study participation and calculate predicted probabilities of participation for inverse probability weighting. Results: There are an estimated 849,488 persons living with PD in the US. Compared to 22,465 eligible FI participants, non‐participants are more likely to be older, female, and non‐White; live in rural regions; have more severe PD; and have lower levels of education. When these predictors were incorporated into a multivariable regression model, predicted probability of participation was much higher for FI participants than non‐participants, indicating a significant difference in the underlying populations (propensity score distance 2.62). Estimates of NMS prevalence and QOL limitation were greater when analyzed using inverse probability of participation weighting compared to unweighted means and frequencies. Conclusions: PD‐related morbidity may be underestimated because of underrepresentation, and inverse probability of participation weighting can be used to give greater weight to underrepresented groups and produce more generalizable estimates. © 2023 International Parkinson and Movement Disorder Society. [ABSTRACT FROM AUTHOR]
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- 2023
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11. Chapter 27 - Botulinum toxin for motor disorders
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Safarpour, Delaram and Jabbari, Bahman
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- 2023
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12. An Overview of Gastrointestinal Dysfunction in Parkinsonian Syndromes.
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Talman, Lauren and Safarpour, Delaram
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PARKINSONIAN disorders , *PARKINSON'S disease , *ENTERIC nervous system , *GASTROINTESTINAL system , *CENTRAL nervous system , *MOVEMENT disorders - Abstract
Gastrointestinal (GI) dysfunction is a common nonmotor symptom in Parkinson's disease (PD) as well as other parkinsonian syndromes and may precede the onset of motor symptoms by decades. Involvement of all segments of the GI tract can lead to altered responses to medications and worsened quality of life for patients. While some GI symptoms occur in isolation, others overlap. Therefore, understanding the changes in different segments of the GI tract and how they relate to altered responses to PD treatment can guide both diagnostic and pharmacological interventions. Gut microbiota plays a critical role in immune activity and modulation of the enteric and central nervous systems. Understanding this bidirectional relationship helps to elucidate the pathogenesis of neurodegeneration. This review will describe the current understanding of how GI dysfunction develops in parkinsonian syndromes, common symptoms in PD and related disorders, and available treatments. [ABSTRACT FROM AUTHOR]
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- 2023
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13. Therapies for Parkinson's disease and the gut microbiome: evidence for bidirectional connection.
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Hey, Grace, Nair, Navya, Klann, Emily, Gurrala, Anjela, Safarpour, Delaram, Mai, Volker, Ramirez-Zamora, Adolfo, and Vedam-Mai, Vinata
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DRUG therapy for Parkinson's disease ,BRAIN ,GASTROINTESTINAL system ,RECTAL medication ,GUT microbiome ,ANTIPARKINSONIAN agents ,TREATMENT effectiveness ,PARKINSON'S disease ,PHARMACEUTICAL gels ,EVALUATION - Abstract
The gut brain axis (GBA), a bidirectional communication pathway has often been linked to health and disease, and gut microbiota (GM), a key component of this pathway shown to be altered in Parkinson's disease (PD), are suggested to contribute to the pathogenesis of PD. There are few studies that report the impact of oral medication therapy on GM, however, there are even fewer studies that discuss the impact of other treatments such as device assisted therapies (DAT) including deep brain stimulation (DBS), levodopa-carbidopa intestinal gel infusion (LCIG) and photobiomodulation (PBM) and how these might impact GM. Here, we review the literature and summarize findings of the potential contributions of GM to the heterogenous clinical response to pharmaceutical therapies among individuals with PD. We also discuss the potential interactions between the GM and DATs such as DBS and LCIG and present evidence for alterations in GM in response to DATs. Given the complexity and highly individual nature of the GM of patients with PD and the potential influence that other external factors such as diet, lifestyle, medications, stage of the disease and other comorbidities, further investigations into the response of GM to therapies are worthy of future study in prospective, controlled trials as well as medication naïve individuals. Such detailed studies will help us further comprehend the relationship between GM in PD patients, and will help investigate the potential of targeting GM associated changes as a treatment avenue for PD. [ABSTRACT FROM AUTHOR]
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- 2023
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14. 15 - Neurogenic Dysphagia
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Safarpour, Delaram, Sharzehi, Kaveh, and Pfeiffer, Ronald F.
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- 2022
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15. Botulinum Toxin Treatment of Neuropathic Pain
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Mittal, Shivam Om, Safarpour, Delaram, and Jabbari, Bahman
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- 2016
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16. Identifying the therapeutic zone in globus pallidus deep brain stimulation for Parkinson’s disease.
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Holland, Marshall T., Jiao, Jocelyn, Mantovani, Alessandra, Anderson, Shannon, Mitchell, Katherine A., Safarpour, Delaram, and Burchiel, Kim J.
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- 2023
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17. Chapter 13 - Other Neurologic Disorders Associated with Gastrointestinal Disease
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Safarpour, Delaram, Sharzehi, Kaveh, and Pfeiffer, Ronald F.
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- 2021
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18. Gastrointestinal Motility and Response to Levodopa in Parkinson's Disease: A Proof‐of‐Concept Study.
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Safarpour, Delaram, Brumbach, Barbara H., Arena, Monica, Quinn, Joseph, Diamond, Sarah, Nutt, Jay G., and Pfeiffer, RonaldF.
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Background: Simultaneous measurement of gastrointestinal transit time (GITT) and plasma levodopa concentration (PLC) is crucial to understanding the effect of dysfunctional motility on levodopa response in patients with Parkinson's disease (PwPD). Objective: The aim is to determine if altered segmental GITT correlates with clinical response and PLC variability in PwPD. Methods: Ten typical and 10 erratic responders ingested the SmartPill (SP) wireless motility capsule. Serial PLC and finger tapping, obtained every 30 minutes for 3 hours after SP/levodopa ingestion, evaluated the correlation between GITT, clinical response, and PLC. Glucose breath testing assessed small intestinal bacterial overgrowth (SIBO). Results: GITT was not significantly different in "typical" and "erratic" responders. SIBO was positive in half of the erratic and negative in most typical responders. Conclusion: SP is a feasible technology for assessing GITT in PwPD. A larger study may be able to significantly differentiate/correlate GITT in different segments of the GI tract with response to levodopa. © 2022 International Parkinson and Movement Disorder Society. [ABSTRACT FROM AUTHOR]
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- 2022
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19. Botulinum Toxin A for Treatment of Allodynia of Complex Regional Pain Syndrome: A Pilot Study
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Safarpour, Delaram, Salardini, Arash, Richardson, Diana, and Jabbari, Bahman
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- 2010
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20. Botulinum Toxin A (Botox) for Treatment of Proximal Myofascial Pain in Complex Regional Pain Syndrome: Two Cases
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Safarpour, Delaram and Jabbari, Bahman
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- 2010
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21. Case Report: Yellow Fever Vaccine-Associated Neurotropic Disease and Associated MRI, EEG, and CSF Findings.
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Cohen, Michelle, Nguyen, Madeline, Nix, Chad D., Case, Brendan, Nickerson, Joshua P., Bernard, Jacqueline, Durrant, Julia, Safarpour, Delaram, Tucker, Tarvez, Vagnerova, Kamila, and Messer, William B.
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YELLOW fever ,POLYNEUROPATHIES ,POSTVACCINAL encephalitis ,VACCINATION complications ,ELECTROENCEPHALOGRAPHY ,MAGNETIC resonance imaging - Abstract
Yellow fever vaccine-associated neurotropic disease (YEL-AND) is a rare and serious complication following vaccination with the 17D live attenuated yellow fever vaccine. Cases of YEL-AND have presented as acute inflammatory demyelinating polyneuropathy, acute disseminated encephalomyelitis, and meningoencephalitis. To date, intracranial imaging of the progression and resolution of this disease has been minimally depicted in the literature. We present the case of a 67-year-old woman who developed YEL-AND following vaccination. Her diagnosis was complicated by imaging findings consistent with variant Creutzfeldt Jakob Disease. Her clinical history and the progression of her intracranial imaging is discussed in this case report. [ABSTRACT FROM AUTHOR]
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- 2022
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22. Surrogates for rigidity and PIGD MDS-UPDRS subscores using wearable sensors.
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Safarpour, Delaram, Dale, Marian L., Shah, Vrutangkumar V., Talman, Lauren, Carlson-Kuhta, Patricia, Horak, Fay B., and Mancini, Martina
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PARKINSON'S disease , *POSTURE disorders , *ACCIDENTAL falls , *WEARABLE technology , *WALKING , *FERRANS & Powers Quality of Life Index , *NEUROLOGICAL disorders , *POSTURAL balance , *GAIT in humans , *GAIT disorders , *RESEARCH funding - Abstract
Background: Telemedicine has the advantage of expanding access to care for patients with Parkinson's Disease (PD). However, rigidity and postural instability in PD are difficult to measure remotely, and are important measures of functional impairment and fall risk.Research Question: Can measures from wearable sensors be used as future surrogates for the MDS-UPDRS rigidity and Postural Instability and Gait Difficulty (PIGD) subscores?Methods: Thirty-one individuals with mild to moderate PD wore 3 inertial sensors at home for one week to measure quantity and quality of gait and turning in daily life. Separately, we performed a clinical assessment and balance characterization of postural sway with the same wearable sensors in the laboratory (On medication). We then first performed a traditional correlation analysis between clinical scores and objective measures of gait and balance followed by multivariable linear regression employing a best subset selection strategy.Results: The number of walking bouts and turns correlated significantly with the rigidity subscore, while the number of turns, foot pitch angle, and sway area while standing correlated significantly with the PIGD subscore (p < 0.05). The multivariable linear regression showed that rigidity subscore was best predicted by the number of walking bouts while the PIGD subscore was best predicted by a combination of number of walking bouts, gait speed, and postural sway.Significance: The correlation between objective sensor data and MDS-UPDRS rigidity and PIGD scores paves the way for future larger studies that evaluate use of objective sensor data to supplement remote MDS-UPDRS assessment. [ABSTRACT FROM AUTHOR]- Published
- 2022
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23. List of Contributors
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Abou-Khalil, Bassel W., Adamczyk, Peter, Ajtai, Bela, Allen, Jeffrey C., Ally, Brandon, Almeida, Andrea A., Amato, Anthony A., Aminoff, Michael J., Anderson, Nicolaas C., Ashizawa, Tetsuo, Attar, Hatim, Avidan, Alon Y., Baehring, Joachim M., Bag, Asim K., Balcer, Laura J., Ballester, Leomar Y., Baloh, Robert W., Barkoudah, Elizabeth, Barker, Roger A., Barmore, Ryan, Bartleson, J.D., Batla, Amit, Beckham, John David, Beglinger, Leigh, Benninger, David H., Berger, Joseph R., Biller, José, Black, David F., Boulis, Nicholas, Bowley, Michael P., Braksick, Sherri A., Bramlett, Helen M., Bromley, Steven M., Bruni, Joseph, Brust, John C.M., Burnette, W. Bryan, Camfield, Carol, Camfield, Peter, Carson, Alan, Cassimatis, Dimitri, Cavaliere, Robert, Chad, David A., Chandran, Vijay, Chelimsky, Gisela, Chelimsky, Thomas, Chitnis, Tanuja, Chokroverty, Sudhansu, Chukwueke, Ugonma N., Cooper, Paul E., Cordeau, Dany, Courtois, Frédérique, Creutzfeldt, Claire J., Dalmau, Josep, Daroff, Robert B., DasGupta, Ranan, Deutsch, Mariel B., Devereaux, Michael W., DiBacco, Melissa, Dietrich, W. Dalton, Dinakar, Pradeep, Dobkin, Bruce H., Doty, Richard L., Duckwiler, Gary R., Emerson, Ronald G., Fabian, Michelle T., Faridar, Alireza, Fearon, Conor, Felker, Marcia V., Fessler, Richard D., Fessler, Richard G., Fitzgerald, Kathryn C., Flores-Sarnat, Laura, Fogel, Brent L., Forester, Brent P., Fugate, Jennifer E., Gallagher, Martin J., Gardner, Sharon L., Garfinkle, Jarred, Garza, Ivan, Melo de Gusmao, Claudio, Gehl, Carissa, Geiger, Christopher D., Geldmacher, David S., Gerard, Carter, Geschwind, Daniel H., Geschwind, Michael D., Gifford, Katherine A., Gibson, K. Michael, Golomb, Meredith R., Goode, Rachel, Graff-Radford, Jonathan, Groover, Olivia, Guptill, Jeffrey T., Hahn, Cecil D., Hall, Christine, Hallett, Mark, Hamati, Aline I., Hart, David, Hellwig, Sabine, Herholz, Karl, Hill, Alan, Hill, Benjamin D., Hochberg, Fred H., Huntoon, Kristin, Huse, Jason T., Islam, Monica P., Iv, Michael, Jehan, Reza, Jankovic, Joseph, Josephson, S. Andrew, Jovin, Tudor G., Kang, Min K., Karajannis, Matthias A., Kase, Carlos S., Katirji, Bashar, Kerber, Kevin A., Kerchner, Geoffrey A., Khanna, Ryan, Khoury, Samia J., Kirshner, Howard S., Klöppel, Stefan, Koshy, Anita A., Krieger, Stephen C., Kumar, Abhay, Kurtzke, John F., Kutcher, Jeffrey S., Kuo, Sheng-Han, Lang, Anthony E., Lavin, Patrick J.M., Lawrence, Alice, Lazzaro, Marc A., Langner, Sönke, Liebeskind, David S., Lin, Chih-Chun, Lindzen, Eric, Lockwood, Alan H., Lopate, Glenn, Lublin, Fred D., Lyerly, Michael J., Macdonald, Robert L., Mackay, Devin D., Mallery, Robert, Masdeu, Joseph C., Mazziotta, John C., Mendez, Mario F., Meyer, Philipp T., Michaud, Dominique S., Miller, Amanda, Misulis, Karl E., Mitsumoto, Hiroshi, Murray, Brian, Murray, E. Lee, Murray, Evan D., Nahab, Fadi, Nass, Ruth, Nayak, Lakshmi, Newman, Nancy J., Nguyen, Thanh N., Nogueira, Raul G., Nutt, John G., Nuwer, Marc R., O’Banion, D. David, Okun, Michael S., O’Rourke, Justin J.F., Padilla, Claudia R., Panicker, Jalesh N., Parand, Leila, Paulsen, Jane S., Pearl, Phillip L., Peng-Chen, Zhongxing, Perez, David L., Petersen, Ronald C., Pfeiffer, Ronald F., Pitceathly, Robert D.S., Pomeroy, Scott L., Prasad, Sashank, Price, Bruce H., Price, Raymond S., Ptáček, Louis J., Rabinstein, Alejandro A., Ramaswamy, Vijay, Reimschisel, Tyler, Remler, Bernd F., Rijntjes, Michel, Roach, E. Steve, Robertson, Carrie E., Robinson, Maisha T., Ronthal, Michael, Roos, Karen L., Roque, Ashley M., Rosenberg, Gary A., Rosenfeld, Myrna R., Rucker, Janet C., Ruland, Sean D., Safarpour, Delaram, Sanders, Donald B., Sarnat, Harvey B., Saver, Jeffrey L., Sawlani, Komal T., Schapira, Anthony H.V., Schiff, David, Schneck, Michael J., Scott, Kirsten M., Seay, Meagan D., Shaner, D. Malcolm, Sharzehi, Kaveh, Shoamanesh, Ashkan, Sidhu, Reet, Smith, Jonathan H., Snyder, Laura A., So, Yuen T., Solbrig, Marylou V., Srivastava, Siddharth, Stippler, Martina, Stone, Jon, Swanson, Jerry W., Szeder, Viktor, Tan, Lee A., Tateshima, Satoshi, Tee, Boon Lead, Teipel, Stefan J., Thomas, Reena P., Thompson, Philip D., Thurtell, Matthew J., Tomsak, Robert L., Tsao, Bryan, Turner, Chris, Tyler, Kenneth L., Van Uum, Stan H.M., Verma, Ashok, Wall, Michael, Wallin, Mitchell T., Wang, Leo H., Weissenborn, Karin, Weiller, Cornelius, Whealy, Mark A., Wen, Patrick Y., Wijdicks, Eelco F.M., Wilson, Stephen M., Winkel, Daniel, Yerstein, Oleg Y., and Zaidat, Osama O.
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- 2022
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24. Good Response to Deep Brain Stimulation in Two Forms of Inherited Chorea Related to GNAO1 and Neuroacanthocystosis with Illustrative Videos.
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Yamamoto, Erin A., Berry, Megan, Harris, William, Shahin, Maryam N., Wilson, Jenny L., Safarpour, Delaram, and Raslan, Ahmed M.
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MOVEMENT disorders ,DEEP brain stimulation ,CHOREA - Abstract
Keywords: deep brain stimulation; chorea; inherited movement disorder; globus pallidus interna EN deep brain stimulation chorea inherited movement disorder globus pallidus interna 401 403 3 04/05/22 20220401 NES 220401 Chorea is a hyperkinetic movement disorder characterized by involuntary brief, random, and irregular muscle contractions conveying a feeling of restlessness.1 Inherited choreas constitute a significant portion of choreas, including neuroacanthocytosis (NA), I GNAO1 i -associated movement disorder (GNAO1), Huntington's disease, dentatorubral-pallidoluysian atrophy, Wilson's disease, familial paroxysmal kinesigenic choreoathetosis, and intracerebral calcifications. Currently, chorea is not an approved indication for DBS; however, reports of off-label globus pallidus interna (GPi) DBS for genetic choreas demonstrate generally satisfactory outcomes. [Extracted from the article]
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- 2022
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25. Role of Directional Configuration in Deep Brain Stimulation for Essential Tremor: A Single Center Experience.
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VEERAPPAN, VENKA, ANDERSON, SHANNON, SAFARPOUR, DELARAM, and HILLER, AMIE L.
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BRAIN stimulation ,ESSENTIAL tremor ,PARKINSON'S disease ,GAIT disorders ,CELL nuclei - Abstract
Background: Traditionally, the standard of care for medication refractory essential tremor has been to utilize omnidirectional deep brain stimulation of the ventral intermediate nucleus. The advent of directional stimulation allows for spatial restriction of the stimulation on selected targets without involving the neighboring structures, thereby limiting off-target side effects and improving clinical utility. Methods: We performed a retrospective review of patients between February 2017 and September 2019 who had received ventral intermediate nucleus deep brain stimulation that allowed for directional programming (specifically Abbott/St. Jude). Initial and final major programming sessions post-operatively (approximately 30- and 90-days postsurgery) were examined to determine frequency and reason for use of directional programming. Results: A total of 33 total patients were identified. A little over half were males (58%, N = 19), with an average age of 68 years old (SD 9.3) at the time of surgery, and a disease duration of almost 30 years (27.2, SD 19) with a wide range from 2-62 years. After initial programming, over 50% (17 of 33) of patients were using directional configurations. This increased to 85% (28 of 33) at the 90-day programming. Reasons for conversion to directional configuration included avoidance of side effects (specifically, muscle contractions (9/33), paresthesia (5/33), dysarthria (1/33) and gait ataxia (1/33)) or improved tremor control (12/33). Discussion: Our single-center experience suggests that in the large majority of cases, directional leads were utilized and offered advantages in tremor control or side effect avoidance. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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26. Contributors
- Author
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Abrams, Gary M., Albers, Gregory W., Amans, Matthew R., Aminoff, Michael J., Batla, Amit, Betjemann, John P., Camilleri, Michael, Chen, Robert, Christine, Chadwick W., Coleman, Kyle J., Davies-Jones, G.A.B., DeAngelis, Lisa M., Dhand, Amar, Dillon, William P., Douglas, Vanja C., Fox, Christine, Furman, Joseph M., Gelb, Douglas J., Gladstone, David J., Glynn, Simon M., Goodin, Douglas S., Goodman, Brent P., Greenlee, John E., Guterman, Elan, Halabi, Cathra, Hallett, Mark, Halperin, John J., Harris, Shelby, Hemphill, J. Claude, III, Hurko, Orest, Irani, Sarosh R., Jo, Jasmin, Josephson, S. Andrew, Kaley, Thomas J., Kim, Anthony S., Ko, Nerissa U., Koshy, Anita A., Kraler, Lironn, Krumholz, Allan, Leonard, John M., Levin, Morris, Manno, Edward M., Mastaglia, Frank L., Maurer, Carine W., McCall, Andrew A., Messing, Robert O., Miravalle, Augusto, Monderer, Renee, Morren, John A., Muccilli, Alexandra D., Muir, Ryan T., Murphy, Olwen C., Nash, Kendall, Ooi, Winnie W., Pal, Pramod K., Panicker, Jalesh N., Parent, Jack M., Peluso, Michael J., Perfect, John R., Peyvandi, Shabnam, Pfeiffer, Ronald F., Phillips, Steven M., Poncelet, Ann Noelle, Prasad, Sashank, Prasad, Shweta, Probasco, John C., Purdy, Kaylynn, Rabinstein, Alejandro A., Ralph, Jeffrey W., Ramachandran, Prashanth S., Roos, Karen L., Rose-Innes, Andrew P., Safarpour, Delaram, Schiff, David, Schipper, Hyman M., Shah, Maulik P., Sharzehi, Kaveh, Shaw, Pamela J., Spudich, Serena, Srinivasan, Jayashri, Stern, Barney J., Sun, Chung-Huan Johnny, Sussman, Jon D., Thorpy, Michael, Verber, Nick S., VoduŠek, David B., Weissenborn, Karin, Williams, Linda S., Wilson, Michael R., and Zochodne, Douglas W.
- Published
- 2021
- Full Text
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27. Neurogastroenterology.
- Author
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Safarpour, Delaram and Pfeiffer, Ronald F.
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- *
ENTERIC nervous system , *SPINAL cord - Published
- 2023
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28. Clinical Epidemiology, Evaluation, and Management of Dementia in Parkinson Disease.
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Safarpour, Delaram and Willis, Allison W.
- Abstract
The prevalence of neurodegenerative diseases such as Parkinson disease (PD) will increase substantially, due to the aging of the population and improved treatments leading to better disease-related outcomes. Dementia is the most common nonmotor symptom in PD, and most patients with PD will have cognitive dysfunction and cognitive decline in the course of their disease. The development of cognitive dysfunction in PD greatly limits the ability to participate in activities of daily living and can be a tipping point for nursing home placement or major caregiver stress. Understanding the different causes of dementia and how to reduce the incidence and impact of secondary cognitive dysfunction in PD are necessary skills for primary care physicians and neurologists. In this review, we discuss the clinical epidemiology of dementia in PD with an emphasis on preventable cognitive dysfunction, present tools for outpatient evaluation of cognitive dysfunction, and describe current pharmacological treatments for dementia in PD. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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29. Nursing home and end-of-life care in Parkinson disease.
- Author
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Safarpour, Delaram, Thibault, Dylan P, DeSanto, Cori L, Boyd, Cynthia M, Dorsey, E Ray, Racette, Brad A, and Willis, Allison W
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- 2015
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30. End of Life in Neurodegenerative Diseases: An Unrecognized Opportunity for Better Care.
- Author
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Jiao JM and Safarpour D
- Subjects
- Humans, Neurodegenerative Diseases therapy, Terminal Care
- Published
- 2024
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31. Botulinum toxin for motor disorders.
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Safarpour D and Jabbari B
- Subjects
- Humans, Botulinum Toxins therapeutic use, Motor Disorders, Dystonia drug therapy, Dystonic Disorders, Movement Disorders drug therapy
- Abstract
Botulinum neurotoxins are a group of biological toxins produced by the gram-negative bacteria Clostridium botulinum. After intramuscular injection, they produce dose-related muscle relaxation, which has proven useful in the treatment of a large number of motor and movement disorders. In this chapter, we discuss the utility of botulinum toxin treatment in three major and common medical conditions related to the dysfunction of the motor system, namely dystonia, tremor, and spasticity. A summary of the existing literature is provided along with different techniques of injection including those recommended by the authors., (Copyright © 2023 Elsevier B.V. All rights reserved.)
- Published
- 2023
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32. Identifying the therapeutic zone in globus pallidus deep brain stimulation for Parkinson's disease.
- Author
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Holland MT, Jiao J, Mantovani A, Anderson S, Mitchell KA, Safarpour D, and Burchiel KJ
- Subjects
- Humans, Globus Pallidus surgery, Levodopa therapeutic use, Treatment Outcome, Electrodes, Implanted, Parkinson Disease drug therapy, Subthalamic Nucleus surgery, Deep Brain Stimulation, Dyskinesias drug therapy
- Abstract
Objective: The globus pallidus internus (GPI) has been demonstrated to be an effective surgical target for deep brain stimulation (DBS) treatment in patients with medication-refractory Parkinson's disease (PD). The ability of neurosurgeons to define the area of greatest therapeutic benefit within the globus pallidus (GP) may improve clinical outcomes in these patients. The objective of this study was to determine the best DBS therapeutic implantation site within the GP for effective treatment in PD patients., Methods: The authors performed a retrospective review of 56 patients who underwent bilateral GP DBS implantation at their institution during the period from January 2015 to January 2020. Each implanted contact was anatomically localized. Patients were followed for stimulation programming for at least 6 months. The authors reviewed preoperative and 6-month postsurgery clinical outcomes based on data from the Unified Parkinson's Disease Rating Scale Part III (UPDRS III), dyskinesia scores, and levodopa equivalent daily dose (LEDD)., Results: Of the 112 leads implanted, the therapeutic cathode was most frequently located in the lamina between the GPI external segment (GPIe) and the GP externus (GPE) (n = 40). Other common locations included the GPE (n = 24), the GPIe (n = 15), and the lamina between the GPI internal segment (GPIi) and the GPIe (n = 14). In the majority of patients (73%) a monopolar programming configuration was used. At 6 months postsurgery, UPDRS III off medications (OFF) and on stimulation (ON) scores significantly improved (z = -4.02, p < 0.001), as did postsurgery dyskinesia ON scores (z = -4.08, p < 0.001) and postsurgery LEDD (z = -4.7, p < 0.001)., Conclusions: Though the ventral GP (pallidotomy target) has been a commonly used target for GP DBS, a more dorsolateral target may be more effective for neuromodulation strategies. The assessment of therapeutic contact locations performed in this study showed that the lamina between GPI and GPE used in most patients is the optimal central stimulation target. This information should improve preoperative GP targeting.
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- 2022
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33. Good Response to Deep Brain Stimulation in Two Forms of Inherited Chorea Related to GNAO1 and Neuroacanthocystosis with Illustrative Videos.
- Author
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Yamamoto EA, Berry M, Harris W, Shahin MN, Wilson JL, Safarpour D, and Raslan AM
- Abstract
Competing Interests: No specific funding was received for this work. The authors have no conflicts of interest to declare.
- Published
- 2021
- Full Text
- View/download PDF
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