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No Racial Differences Found in Access to Biologics: A Population-Based Study of Psoriasis Patients in the United States

August 2023 | Volume 22 | Issue 8 | 835 | Copyright © August 2023


Published online July 31, 2023

doi:10.36849/JDD.7134

Reddy R, Khan S, Yee D, et al. No racial differences found in access to biologics: a population-based study of psoriasis patients in the United States. 

Rasika Reddy MDa, Sabrina Khan MDb, Danielle Yee MDb, Nicole Maynard MDb, Manan Mehta MDb, Caterina Zagona-Prizio MDc, Samiya Khan MDd, Vipawee Chat MDb, Kevin Wu MDb, April W. Armstrong MD MPHb

aUniversity of Texas Southwestern Medical Center, Dallas, TX
bKeck School of Medicine, University of Southern California, Los Angeles, CA
cUniversity of Colorado School of Medicine, Denver, CO
dLong School of Medicine, University of Texas at San Antonio, San Antonio, TX

Abstract
Background: Conflicting evidence exists regarding the role of race in access to biologics for patients with psoriasis. Objective: To compare biologic use among adult and pediatric United States psoriasis patients of different racial backgrounds.
Methods: Population-based study of US psoriasis patients using the 2003 to 2018 Medical Expenditure Panel Survey (MEPS).
Results: Among 31,525,500 adults and children with psoriasis (weighted), 3,026,578 (9.6%) were on biologics. Among psoriasis patients, 27,464,864 (87.1%) self-identified as white, 2,033,802 (6.5%) self-identified as Black, 1,173,435 (3.7%) self-identified as Asian or Pacific Islander, and 853,399 (2.7%) self-identified as other races. Among those on biologics, 2,778,239 (91.8%) self-identified as white, 84,971 (2.8%) identified as Black, 89,452 (3.0%) self-identified as Asian or Pacific Islander, and 73,917 (2.4%) self-identified as other races. Multivariate logistic regression revealed no significant differences in biologic access between whites and non-whites after adjusting for sociodemographic factors including insurance status (OR for Blacks: 0.347 [0.118, 1.021], P=0.055; OR for Asians: 0.616 [0.240, 1.579], P=0.311; OR for other races: 0.850 [0.216, 3.336], P=0.814.
Conclusion: The results of this study suggest that race alone is not independently associated with access to biologics among adult US psoriasis patients. Additional studies are necessary to evaluate factors independently associated with biologics access among adults and children with psoriasis in the US.

J Drugs Dermatol. 2023;22(8):835-837. doi:10.36849/JDD.7134

Reddy R, Khan S, Yee D, et al. No racial differences found in access to biologics: a population-based study of psoriasis patients in the United States. 

INTRODUCTION

Psoriasis is a chronic inflammatory disease that affects more than 7.5 million people in the United States.1 Although psoriasis is most prevalent in whites (3.2%), African Americans often exhibit more extensive skin involvement, present with more severe variants of psoriasis, and experience greater psychological burden and impaired quality-of-life than whites.2-6 Since 2003, biologics have become increasingly popular for the treatment of moderate-to-severe psoriasis, and have resulted in higher patient satisfaction and compliance rates compared with oral, photo, or topical therapies.7,8 However, multiple studies have shown that African Americans have less access to biologics than whites.9,10 A 2015 study on the US Medicare population demonstrated that African American patients were 69% less likely to use biologics compared with white patients.11 However, the association between race and biologics has not been evaluated in a nationally representative psoriasis population. This population-based study aims to evaluate the impact of race on access to biologics among adult and pediatric psoriasis patients in the US. We hypothesized that our analysis would demonstrate racial differences in biologics access similar to previous studies.

We conducted a cross-sectional, population-based study using the Medical Expenditure Panel Survey (MEPS) national database from 2003-2018. We identified adults and children (mean age 49.36 years) with a reported diagnosis of psoriasis by the ICD-9 diagnosis code "696" or ICD-10 code "L40". Race was categorized based on the MEPS classification: white, Black, Asian or Pacific Islander, Alaska Native or American Indian, or multiple races; the latter two groups were later grouped together due to insufficient sample size. Access to an approved biologic medication for psoriasis was identified by the household-reported receipt of a prescription biologic. Multivariate logistic regression was used to investigate the association between race and access to biologics, adjusting for potential confounders including age, sex, ethnicity, insurance status, education level, poverty level, personal income, employment status, number of outpatient visits, region of care, and the Charlson Comorbidity Index. 

A weighted total of 31,525,500 adult and child patients with psoriasis in the US were identified from 2003 to 2018. 87.1% self-identified as white, 6.5% self-identified as Black, 3.7% self-identified as Asian, and 2.7% self-identified as other races,