15 results on '"Hamedani, Ali G"'
Search Results
2. Visual dysfunction in dementia with Lewy bodies
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Devenyi, Ryan A. and Hamedani, Ali G.
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- 2024
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3. Cataract surgery utilization in Parkinson’s disease: the english longitudinal survey on ageing
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Xu, Angela L. and Hamedani, Ali G.
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- 2024
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4. Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts
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Dratch, Laynie, Azage, Meron, Baldwin, Aaron, Johnson, Kelsey, Paul, Rachel A., Bardakjian, Tanya M., Michon, Sara-Claude, Amado, Defne A., Baer, Michael, Deik, Andres F., Elman, Lauren B., Gonzalez-Alegre, Pedro, Guo, Michael H., Hamedani, Ali G., Irwin, David J., Lasker, Aaron, Orthmann-Murphy, Jennifer, Quinn, Colin, Tropea, Thomas F., Scherer, Steven S., and Ellis, Colin A.
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- 2024
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5. Consensus practice recommendations for management of gastrointestinal dysfunction in Parkinson disease
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Safarpour, Delaram, Stover, Natividad, Shprecher, David R., Hamedani, Ali G., Pfeiffer, Ronald F., Parkman, Henry P., Quigley, Eamonn MM., and Cloud, Leslie J.
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- 2024
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6. Trends and Disparities in the Utilization of Thymectomy for Myasthenia Gravis in the United States
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Morganroth, Jennifer, primary, Zuroff, Leah, additional, Guidon, Amanda C., additional, Liu, Grant T., additional, Bird, Shawn J., additional, Singhal, Sunil, additional, Wolfe, Gil I., additional, and Hamedani, Ali G., additional
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- 2024
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7. Self-reported Visual Difficulty, Age-related Eye Disease, and Neuropsychiatric Outcomes in Older Adults
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Hamedani, Ali G., primary, Willis, Allison W., additional, and Ying, Gui-Shuang, additional
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- 2024
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8. Attitudes and beliefs towards medication burden and deprescribing in Parkinson disease.
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Pham Nguyen, Thanh Phuong, Thibault, Dylan, Hamedani, Ali G., and Willis, Allison W.
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PATIENTS' attitudes ,INAPPROPRIATE prescribing (Medicine) ,DEPRESCRIBING ,PARKINSON'S disease ,PATIENT satisfaction - Abstract
Background: Deprescribing of potentially inappropriate medications is recommended for older adults and may improve health outcomes and quality of life in persons living with Parkinson disease (PD). Patient attitudes, beliefs, and preferences play a crucial role in the success of deprescribing interventions. We aimed to examine the attitudes and beliefs about medication burden and deprescribing among persons living with PD. Methods: We administered a survey to participants of Fox Insight, a prospective longitudinal study of persons living with PD. The survey included the revised Patients' Attitudes Towards Deprescribing (rPATD) questionnaire and additional questions about adverse drug effects. We used logistic regression models to explore potential predictors of treatment dissatisfaction and willingness to deprescribe. Results: Of the 4945 rPATD respondents, 31.6% were dissatisfied with their current medications, and 87.1% would be willing to deprescribe medications. Male sex was associated with a greater willingness to deprescribe (adjusted odds ratio [aOR] 1.62, 95% confidence interval [CI] 1.37–1.93). A greater belief that the medication burden was high or that some medications were inappropriate was associated with treatment dissatisfaction (aORs 3.74, 95% CI 3.26–4.29 and 5.61, 95% CI 4.85–6.50), and more willingness to deprescribe (aORs 1.74, 95% CI 1.47–2.06 and 2.87, 95% CI 2.41–3.42). Cognitive impairment was the adverse drug effect participants were most concerned about when prescribed new medications to treat nonmotor symptoms. Conclusions: Persons with PD are often dissatisfied with their overall medication load and are open to deprescribing. Medications that are associated with cognitive impairment might be prioritized targets for deprescribing interventions in this population. [ABSTRACT FROM AUTHOR]
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- 2024
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9. Application of High-Dimensional Propensity Score Methods to the National Health and Aging Trends Study.
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Hamedani, Ali G, Nguyen, Thanh Phuong Pham, Willis, Allison W, and Tazare, John R
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PROPORTIONAL hazards models , *OLDER people , *HEALTH surveys , *VISION disorders , *DEMENTIA - Abstract
Background High-dimensional propensity scoring (HDPS) is a method for empirically identifying potential confounders within large healthcare databases such as administrative claims data. However, this method has not yet been applied to large national health surveys such as the National Health and Aging Trends Study (NHATS), an ongoing nationally representative survey of older adults in the United States and important resource in gerontology research. Methods In this Research Practice article, we present an overview of HDPS and describe the specific data transformation steps and analytic considerations needed to apply it to national health surveys. We applied HDPS within NHATS to investigate the association between self-reported visual difficulty and incident dementia, comparing HDPS to conventional confounder selection methods. Results Among 7 207 dementia-free NHATS Wave 1 respondents, 528 (7.3%) had self-reported visual difficulty. In an unadjusted discrete time proportional hazards model accounting for the complex survey design of NHATS, self-reported visual difficulty was strongly associated with incident dementia (odds ratio [OR] 2.34, 95% confidence interval [CI]: 1.95–2.81). After adjustment for standard investigator-selected covariates via inverse probability weighting, the magnitude of this association decreased, but evidence of an association remained (OR 1.44, 95% CI: 1.11–1.85). Adding 75 HDPS-prioritized variables to the investigator-selected propensity score model resulted in further attenuation of the association between visual impairment and dementia (OR 0.94, 95% CI: 0.70–1.23). Conclusions HDPS can be successfully applied to national health surveys such as NHATS and may improve confounder adjustment. We hope developing this framework will encourage future consideration of HDPS in this setting. [ABSTRACT FROM AUTHOR]
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- 2024
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10. Social Determinants of Health in Idiopathic Intracranial Hypertension.
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Markowitz, Daniel, Aamodt, Whitley W., and Hamedani, Ali G.
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Background: Idiopathic intracranial hypertension (IIH) disproportionately affects women from socioeconomically disadvantaged communities, but specific social determinants of health have not been examined. Methods: We used data from the National Institutes of Health's All of Us Research Program, an ongoing nationwide study of more than 300,000 diverse individuals in the United States. Height and weight were measured at baseline, and participants completed questionnaires about demographics, health care access, and quality of life. Women aged 18--50 years with IIH were identified through electronic health record data, excluding those with venous thrombosis, meningitis, hydrocephalus, or central nervous system neoplasms. We used logistic regression to compare questionnaire responses for IIH cases and controls, adjusting for age, race, ethnicity, annual income, and body mass index (BMI). Results: We included 416 women with IIH and 107,111 women without IIH. The mean age was 38 years, and 49.3% identified as non-White. After adjusting for age, race/ ethnicity, and BMI, women with IIH were more likely to be unemployed (odds ratio [OR] 1.40, 95% confidential interval [CI]: 1.14--1.71) and report delaying care because of diffi- culty affording copays (OR 1.47, 95% CI: 1.02--2.10) or specialist care (OR 1.52, 95% CI: 1.06--2.18). They also delayed care because of rural residence (OR 2.08, 95% CI: 1.25--3.47) and transportation limitations (OR 2.23, 95% CI: 1.55--3.20). Although women with IIH were more likely to be non-Hispanic Black (OR 1.66, 95% CI: 1.32-- 2.09), this association lost significance when controlling for BMI and income (OR 1.27, 95% CI: 0.96--1.68). Conclusions: Women with IIH experience adverse social determinants of health beyond those associated with obesity alone. [ABSTRACT FROM AUTHOR]
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- 2024
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11. Validity of Administrative Coding for Nonarteritic Ischemic Optic Neuropathy.
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Hamedani, Ali G., Kim, Dale S., Chaitanuwong, Pareena, Gonzalez, Lizbeth A., Moss, Heather E., and DeLott, Lindsey B.
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Background: Administrative claims have been used to study the incidence and outcomes of nonarteritic ischemic optic neuropathy (NAION), but the validity of International Classi- fication of Diseases (ICD)-10 codes for identifying NAION has not been examined. Methods: We identified patients at 3 academic centers who received $1 ICD-10 code for NAION in 2018. We abstracted the final diagnosis from clinical documentation and recorded the number of visits with an NAION diagnosis code. We calculated positive predictive value (PPV) for the overall sample and stratified by subspecialty and the number of diagnosis codes. For patients with ophthalmology or neuro-ophthalmology visit data, we recorded presenting symptoms, examination findings, and laboratory data and calculated PPV relative to case definitions of NAION that incorporated sudden onset of symptoms, optic disc edema, afferent pupillary defect, and other characteristics. Results: Among 161 patients, PPV for $1 ICD-10 code was 74.5% (95% CI: 67.2%--80.7%). PPV was similar when restricted to patients who had visited an ophthalmologist (75.8%, 95% CI: 68.4%--82.0%) but increased to 86.8% when restricted to those who had visited neuroophthalmologists (95% CI: 79.2%--91.9%). Of 113 patients with .1 ICD-10 code and complete examination data, 37 (32.7%) had documented sudden onset, optic disc swelling, and an afferent pupillary defect (95% CI: 24.7%--42.0%). Of the 76 patients who did not meet these criteria, 54 (71.0%) still received a final clinical diagnosis of NAION; for most (41/54, 75.9%), this discrepancy was due to lack of documented optic disc edema. Conclusions: The validity of ICD-10 codes for NAION in administrative claims data is high, particularly when combined with provider specialty. [ABSTRACT FROM AUTHOR]
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- 2024
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12. Disparities in Genetic Testing for Neurologic Disorders
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Baldwin, Aaron, primary, Copeland, Juliette, additional, Azage, Meron, additional, Dratch, Laynie, additional, Johnson, Kelsey, additional, Paul, Rachel A., additional, Amado, Defne A., additional, Baer, Michael, additional, Deik, Andres, additional, Elman, Lauren B., additional, Guo, Michael, additional, Hamedani, Ali G., additional, Irwin, David J., additional, Lasker, Aaron, additional, Orthmann-Murphy, Jennifer, additional, Quinn, Colin C., additional, Tropea, Thomas F., additional, Scherer, Steven S., additional, Shinohara, Russell T., additional, Hamilton, Roy H., additional, and Ellis, Colin A., additional
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- 2024
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13. Interaction between visual impairment and genetic risk of dementia and psychosis in older adults.
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Hamedani, Ali G, Ellis, Colin A, Ehrlich, Joshua R, and Willis, Allison W
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RISK assessment , *VISION disorders , *ALZHEIMER'S disease , *RESEARCH funding , *SCHIZOPHRENIA , *DESCRIPTIVE statistics , *GENETIC risk score , *HALLUCINATIONS , *ODDS ratio , *PSYCHOSES , *DEMENTIA , *CONFIDENCE intervals , *GENETIC testing , *COMORBIDITY , *EVALUATION , *MIDDLE age - Abstract
Background Visual impairment (VI) is associated with dementia and other neuropsychiatric outcomes, but previous studies have not considered genetic sources of confounding or effect modification. Methods We analysed data from the Health and Retirement Study, an ongoing nationally representative survey of older US adults, a subset of whom underwent genetic testing from 2006 to 2012 (n = 13 465). Using discrete time proportional hazards models and generalised estimating equations, we measured the association between VI and dementia, depression and hallucinations adjusting for demographics and comorbidities, ancestry-specific principal components and polygenic risk scores (PRS) for Alzheimer's disease, major depressive disorder or schizophrenia. Effect modification was assessed using VI–PRS interaction terms and stratified analyses. Results VI was associated with dementia, depression and hallucinations after adjusting polygenic risk and other confounders. There was no VI–PRS interaction for dementia or depression. However, the association between VI and hallucinations varied by genetic risk of schizophrenia. Within the bottom four quintiles of schizophrenia PRS, VI was not associated with hallucinations among White (OR 1.16, 95% CI: 0.87–1.55) or Black participants (OR 0.96, 95% CI: 0.49–1.89). In contrast, VI was strongly associated with hallucinations among White (OR 2.08, 95% CI: 1.17–3.71) and Black (OR 10.63, 95% CI: 1.74–65.03) participants in the top quintile of schizophrenia PRS. Conclusions The association between VI and neuropsychiatric outcomes is not explained by shared genetic risk factors, and there is a significant interaction between VI and polygenic risk of hallucinations in older adults. [ABSTRACT FROM AUTHOR]
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- 2024
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14. Association of Visual Impairment With Neuropsychiatric Symptoms of Dementia.
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Li M and Hamedani AG
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Background: Visual impairment is a risk factor for cognitive impairment and hallucinations in older adults, but associations with other neuropsychiatric symptoms (NPS) of dementia have not been examined., Methods: We analyzed cross-sectional data from the Aging, Demographics, and Memory Study (ADAMS), a nationally representative sample of the US population aged 70+ years. Vision was measured by self-report and using a near card. Dementia was ascertained through cognitive testing with expert consensus, and NPS were screened using the Neuropsychiatric Inventory. We used logistic regression to measure the association between visual impairment and prevalent NPS adjusting for sociodemographic factors and comorbidities. Analyses incorporated sample weights to account for the complex survey design of ADAMS., Results: Of 624 participants with dementia, 332 (53%) had self-reported visual impairment and 193 (31%) had best-corrected acuity of 20/40 or worse. In unadjusted models, self-reported visual impairment was significantly associated with hallucinations (OR 2.88; 95% CI 1.12-7.44), depression (OR 2.79; 95% CI 1.7-4.57), and agitation (OR 1.61; 95% CI 1.05-2.48). Reduced visual acuity was associated with hallucinations (OR 10.13; 95% CI 2.93-34.98), psychosis (OR 6.69, 95% CI 2.53-17.7), and mania (OR 5.92, 95% CI 1.77-19.82). However, these associations did not remain significant after covariate adjustment., Conclusions: Visual impairment was associated with hallucinations, depression, agitation, psychosis, and mania in patients with dementia, but at least some of this relationship is explained by age, comorbidities, and other factors., Competing Interests: The authors report no conflicts of interest., (Copyright © 2024 by North American Neuro-Ophthalmology Society.)
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- 2024
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15. Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias.
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Lai RY, Rummey C, Amlang CJ, Lin CR, Chen TX, Perlman S, Wilmot G, Gomez CM, Schmahmann JD, Paulson H, Ying SH, Onyike CU, Zesiewicz TA, Bushara KO, Geschwind MD, Figueroa KP, Pulst SM, Subramony SH, Burns MR, Opal P, Duquette A, Ashizawa T, Hamedani AG, Davis MY, Srinivasan SR, Moore LR, Shakkottai VG, Rosenthal LS, and Kuo SH
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- Humans, Male, Female, Middle Aged, Adult, Aged, Severity of Illness Index, Prevalence, Depression epidemiology, Depression psychology, Quality of Life psychology, Spinocerebellar Ataxias psychology, Spinocerebellar Ataxias complications, Spinocerebellar Ataxias genetics, Spinocerebellar Ataxias epidemiology, Fatigue psychology, Fatigue epidemiology
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Background: Fatigue is a prevalent and debilitating symptom in neurological disorders, including spinocerebellar ataxias (SCAs). However, the risk factors of fatigue in the SCAs as well as its impact have not been well investigated., Objectives: To study the prevalence of fatigue in SCAs, the factors contributing to fatigue, and the influence of fatigue on quality of life., Methods: Fatigue was assessed in 418 participants with SCA1, SCA2, SCA3, and SCA6 from the Clinical Research Consortium for the Study of Cerebellar Ataxia using the Fatigue Severity Scale. We conducted multi-variable linear regression models to examine the factors contributing to fatigue as well as the association between fatigue and quality of life., Results: Fatigue was most prevalent in SCA3 (52.6%), followed by SCA1 (36.7%), SCA6 (35.7%), and SCA2 (35.6%). SCA cases with fatigue had more severe ataxia and worse depressive symptoms. In SCA3, those with fatigue had a longer disease duration and longer pathological CAG repeat numbers. In multi-variable models, depressive symptoms, but not ataxia severity, were associated with more severe fatigue. Fatigue, independent of ataxia and depression, contributed to worse quality of life in SCA3 and SCA6 at baseline, and fatigue continued affecting quality of life throughout the disease course in all types of SCA., Conclusions: Fatigue is a common symptom in SCAs and is closely related to depression. Fatigue significantly impacts patients' quality of life. Therefore, screening for fatigue should be considered a part of standard clinical care for SCAs., (© 2024 International Parkinson and Movement Disorder Society.)
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- 2024
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