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Abstract Details

Unveiling Disparities in Âé¶¹´«Ã½Ó³»­HPI: A Comprehensive Analysis of Etiology, Presentation, and Treatment in Peripheral Neuropathy
Neuromuscular and Clinical Neurophysiology (EMG)
P9 - Poster Session 9 (11:45 AM-12:45 PM)
11-031
 This study aims to identify etiological trends, clinical presentations, management practices, and associated comorbidities among Âé¶¹´«Ã½Ó³»­HPI patients diagnosed with peripheral neuropathy.
Peripheral neuropathy is a complex condition with various causes and presentations. While its management remains inconsistent, research on its clinical manifestation and treatment among Asian American, Native Hawaiian, and Pacific Islander (Âé¶¹´«Ã½Ó³»­HPI) populations is particularly limited. This study aims to explore etiological patterns, clinical characteristics, comorbidities, and treatment practices in Âé¶¹´«Ã½Ó³»­HPI patients diagnosed with peripheral neuropathy to better understand and address health disparities within this demographic.

A retrospective cohort study was conducted using data from Hawaii Pacific Neuroscience, an outpatient neurology clinic. Key variables collected included patient demographics, comorbidities, possible etiological factors, clinical symptoms, and treatment plans. Statistical analyses were performed to uncover disparities in diagnosing, presenting, and managing peripheral neuropathy across different demographic groups.


This study included 310 patients, with 70.7% identified as Âé¶¹´«Ã½Ó³»­HPI (39.4% NHPIs and 31.3% Asians). Diabetic neuropathy (n=283) was the most common cause, followed by idiopathic, toxic, and paraneoplastic neuropathy. Diabetic neuropathy was significantly more common among Âé¶¹´«Ã½Ó³»­HPI patients (p<0.001), who were diagnosed approximately five years earlier than non-Âé¶¹´«Ã½Ó³»­HPI patients (p<0.001). Furthermore, Âé¶¹´«Ã½Ó³»­HPI patients presented with higher rates of obesity (p<0.001) and multiple comorbidities (p=0.002), particularly hypertension, type II diabetes, and a strong family history of diabetes (all p<0.001). Clinically, Âé¶¹´«Ã½Ó³»­HPI patients reported more frequent muscle weakness (p=0.013) and numbness (p=0.018) and were more likely to receive physical therapy (p<0.001) and undergo multiple treatment modalities (p<0.001).


The study reveals significant health disparities in the Âé¶¹´«Ã½Ó³»­HPI population, with diabetic neuropathy as the leading cause of peripheral neuropathy. Âé¶¹´«Ã½Ó³»­HPI patients experience earlier onset, more severe symptoms, and a higher burden of comorbidities, requiring more aggressive, multidisciplinary care. These findings underscore the need for improved prevention, treatment, and management strategies to reduce complications in this population.


Authors/Disclosures
Anita Cheung, MPH
PRESENTER
Miss Cheung has nothing to disclose.
Lauren Kim Miss Kim has nothing to disclose.
Jiwoo Kim, medical student Miss Kim has nothing to disclose.
D-Dré Wright Ms. Wright has nothing to disclose.
Ryan Nakamura Mr. Nakamura has received personal compensation for serving as an employee of Hawaii Health & Harm Reduction Center.
Masako Matsunaga (University of Hawaii at Manoa) Masako Matsunaga has nothing to disclose.
Enrique Carrazana (Neurelis, Inc.) Enrique Carrazana has received personal compensation for serving as an employee of Neurelis. Enrique Carrazana has received personal compensation in the range of $10,000-$49,999 for serving as an officer or member of the Board of Directors for Hawaii-Biotech, CND Life Sciences, Apex Labs. Enrique Carrazana has stock in Neurelis, CND, Apex.
Kore K. Liow, MD, FACP (University of Hawaii, John Burns School of Medicine) The institution of Dr. Liow has received research support from UCB. The institution of Dr. Liow has received research support from Livanova. The institution of Dr. Liow has received research support from Biogen. The institution of Dr. Liow has received research support from Novartis. The institution of Dr. Liow has received research support from Eisai. The institution of Dr. Liow has received research support from Engage Therapeutics. The institution of Dr. Liow has received research support from SK Lifescience. The institution of Dr. Liow has received research support from Cerevel. The institution of Dr. Liow has received research support from Xenon. The institution of Dr. Liow has received research support from NeuroDerm. The institution of Dr. Liow has received research support from Avanir. The institution of Dr. Liow has received research support from Annovis. The institution of Dr. Liow has received research support from Acadia. The institution of Dr. Liow has received research support from Prothena. The institution of Dr. Liow has received research support from SAGE. The institution of Dr. Liow has received research support from Annovis. The institution of Dr. Liow has received research support from Cyclerion.