Research Article - Journal of Gastroenterology and Digestive Diseases (2017) Volume 2, Issue 3
Effects of race on treatment and outcomes of inflammatory bowel disease.
Christie L. Mannino, Jessica L. Sterling, Andrew R. Conn, Thomas A. Judge, Yize R. Wang*
Division of Gastroenterology and Liver Diseases, Cooper Medical School of Rowan University, Camden, NJ, USA
- *Corresponding Author:
- Yize R. Wang, MD, PhD
Division of Gastroenterology and Liver Diseases Cooper Digestive Health Institute 501 Fellowship Road, Suite 101 Mount Laurel, NJ 08054 USA
Tel: (856) 642-2133
Fax: (856) 642-2134
E-mail: wang-yize@cooperhealth.edu
Accepted on December 26, 2017
Citation: Mannino CL, Sterling JL, Conn AR, et al. Effects of race on treatment and outcomes of inflammatory bowel disease. J Gastroenterol Dig Dis. 2017;2(3):17-19.
Abstract
Objectives: Prior studies suggested that African American (AA) patients with inflammatory bowel disease (IBD) have worse outcomes compared to non-Hispanic white (NHW) patients. We aimed to compare racial differences in IBD treatment, medication compliance, and clinical remission at our institution. Methods: Chart review was performed on all gastroenterologist visits with the diagnosis of IBD between 01/2011 and 10/2012. Patient characteristics, IBD medical treatment, medication compliance, and clinical remission status were obtained at the last visit. The chi-square (or Fisher’s exact) test and multivariate logistic regression were used in statistical analysis. Results: There was no significant difference in IBD medical treatment between the 87 AA (49 Crohn’s, 38 UC) and 404 NHW patients (182 Crohn’s, 222 UC). Compared to NHW patients, AAs were more likely to use narcotics (16.1% vs 8.4%, p<0.05) and less likely to be compliant with medical treatment (83.9% vs 92.8%) and in clinical remission (12.6% vs 29.2%) (both p<0.05). In multivariate logistic regressions, AA race (odds ratio [OR] 0.40, 95% confidence interval [CI] 0.20-0.80) were negative associated with medication compliance; AA race (OR 0.33, 95% CI 0.17-0.65) and family history of IBD (OR 0.30, 95% CI 0.13-0.73) were negatively associated with clinical remission. Conclusion: Compared with NHW patients, AAs had similar IBD medical treatment, were more likely to use narcotics, and were less likely to be compliant with medical treatment and achieve clinical remission.
Keywords
IBD treatment, Clinical remission, Inflammatory bowel disease.
Introduction
Inflammatory Bowel Disease (IBD), i.e., Crohn’s disease and ulcerative colitis (UC), is characterized by chronic inflammation of the gastrointestinal tract. Previous studies showed an increase in the incidence of IBD including those in African American (AA) and Hispanic patients [1,2].
Previous literature on racial differences in IBD phenotype, treatment pattern, and outcomes yielded mixed results [3-14]. While some studies showed similar disease presentation, including age of onset and severity, and medical treatment, others showed more aggressive disease course, less use of immunomodulator and biological treatment, lower compliance with medical treatment, and more need for surgical resection in AA patients.
In this retrospective study, we compared AA and NHW IBD patients in disease characteristics, medical treatment, medication compliance and clinical remission at our tertiary IBD center. We hypothesized that AAs are similar to NHW patients in disease characteristics and medical treatment but due to socioeconomic factors, are less compliant with medical treatment and less likely in clinical remission.
Data and Methods
After IRB approval, a complete list of gastroenterologist visits of patients 18 years or older with the ICD-9 diagnosis codes 555.x for Crohn’s disease and 556.x for UC at Cooper University Health Care was obtained for the 22-month study period between January 1, 2011 and October 31, 2012. Indepth chart review was performed using the EPIC electronic medical record system to verify IBD diagnosis and obtain patient demographics, race/ethnicity, presence of primary sclerosing cholangitis (PSC), family history of IBD, current smoking status, use of various medications (NSAIDs except for aspirin, narcotics, steroids including budesonide, 5-ASA products, immunomodulators (azathioprine, 6-mercaptopurine, or methotrexate), and biological products (anti-TNF agents and natalizumab)), compliance with IBD treatment, and clinical remission status at the last visit with a gastroenterologist during the study period. Both medication compliance and clinical remission status were ascertained based on clinical documentation of the gastroenterologist at the last visit. Patients of other race/ethnicity (not AA or NHW) were excluded from the study sample. We also conducted subgroup analysis of patients with either Crohn’s disease or UC.
The Student’s t-test for a continuous variable (age), the chisquare test for a binary variable (or the Fisher’s exact test if one cell had an expected count<5), and the multivariate logistic regression with stepwise selection to identify significant variables with p<0.05 were used in statistical analysis.
Results
There were 491 IBD patients in our study sample, including 87 AA and 404 NHW patients (Table 1). Compared to NHW patients, AA patients were about 3 years younger (p<0.001) and similar in percentages of female, Crohn’s disease, PSC, family history of IBD, and current smoker.
Variables | Non-Hispanic White | African American |
---|---|---|
N | 404 | 87 |
Age, mean (SD), years | 47.3 (17.0) | 44.7 (16.3) *** |
Female, % | 57.2 | 60.9 |
Crohn’s disease, % | 45.0 | 56.3 |
PSC, % | 1.5 | 2.3 |
Family history of IBD, % | 11.6 | 6.9 |
Current smoker, % | 13.5 | 16.5% Z |
SD=Standard Deviation; PSC=Primary Sclerosing Cholangitis.
***p<0.001.
Table 1: Racial differences in patients with inflammatory bowel disease (IBD).
Narcotic use almost doubled in AA patients compared to NHW patients (16.1% vs 8.4%, p<0.05), due to more narcotic use in AA patients with Crohn’s disease (24.5% vs. 13.2%, p=0.05) but not in AA patients with UC (5.3% vs. 4.5%, p=0.69) (Table 2). AA patients were similar to NHW patients in the use of various IBD medications including 5-ASA, steroids, immunomodulators, and biologicals.
Variables | Non-Hispanic White | African American |
---|---|---|
N | 404 | 87 |
Medication use, % | ||
NSAIDs | 4.0 | 6.9 |
Narcotics | 8.4 | 16.1* |
5-ASA | 70.8 | 67.8 |
Steroids | 17.1 | 21.8 |
Immunomodulators | 19.1 | 24.1 |
Biologicals | 22.3 | 26.4 |
Medication compliance , % | 92.8 | 83.9** |
Clinical remission, % | 29.2 | 12.6** |
NSAID=Non-Steroidal Anti-Inflammatory Drugs; 5-ASA=5-Aminosalicylic Acid.
*p<0.05; **p<0.01.
Table 2: Racial differences in inflammatory bowel disease treatment, medication compliance and clinical remission.
Medication compliance was lower in AA patients (83.9% vs 92.8% for NHW patients, p<0.01), similar for AA patients with Crohn’s disease (81.6% vs. 92.9%, p<0.05) and AA patients with UC (86.8% vs. 92.8%, p=0.21). AA patients was much less likely in clinical remission compared to their NHW counterparts (12.6% vs. 29.2%, p<0.01), similar for AA patients with Crohn’s disease (12.2% vs. 24.2%, p=0.07) and AA patients with UC (13.2% vs. 33.3%, p<0.05) (Table 2).
In multivariate logistic regression, AA race (vs NHW) was negatively associated with compliance with IBD medication(s) (odds ratio [OR]: 0.40, 95% confidence interval [CI]: 0.20-0.80) (Table 3); none of the other patient characteristics from Table 1 were significant. Both AA race (vs NHW) (OR 0.33, 95% CI 0.17-0.65) and family history of IBD (OR 0.30, 95% CI 0.13-0.73) were negatively associated with achieving clinical remission in multivariate logistic regression; the other patient characteristics were not significant. Subgroup analyses of Crohn’s disease and UC confirmed the robustness of the above findings on differences between AA and NHW patients.
Variables | Odds Ratio (95% Confidence Interval) |
---|---|
Medication compliance | |
African American (vs Non-Hispanic White) | 0.40 (0.20,0.80) |
Clinical remission | |
African American (vs Non-Hispanic White) | 0.33 (0.17,0.65) |
Family history of IBD | 0.30 (0.13,0.73) |
Table 3: Logistic regression results on predictors of inflammatory bowel disease (IBD) medication compliance and clinical remission.
Discussion
In this retrospective study, we found that AA patients were similar to NHW patients in IBD characteristics and medical treatment but were more likely to use narcotics and less likely to comply with medical treatment and achieve clinical remission.
Considering that both AA and NHW patients were treated by the sample group of gastroenterologists at our tertiary IBD center, including three IBD subspecialists, it is not surprising that there was no racial difference in medical treatment. The finding of more narcotic use by AA patients is concerning, as narcotic use is associated with worse long-term outcomes [15]. In this retrospective study, we could not ascertain the clinical rationale for narcotics, its prescriber (gastroenterologist, primary care physician, emergency room physician, or others), and the length of usage, which are important questions for future research.
Our finding of less compliance with IBD medical treatment by AA patients is consistent with several previous studies [6,9,11,13] and likely contributed to their lower rate of clinical remission. AA patients are more likely of low socioeconomic status (education, income, etc) and consequently less likely to understand the risk/benefit tradeoffs of IBD therapy, afford often expensive medications, and have timely access to subspecialists. In addition, AA race-specific cultural and genetic factors may also contribute to racial differences in IBD outcomes [4,10,16]. To separate out the effects of socioeconomic factors from those of AA race-specific factors has important health policy and treatment implications but is not possible in our retrospective study. Use of AA care navigators in an IBD medical home setting may help, considering the lack of AA gastroenterologists (let along IBD subspecialists) in the United States.
One limitation of our study is the reliance on physician clinical documentation to measure medication compliance and clinical remission. Real compliance rate may be much lower than that reported by patients. This likely led to overestimation of medication compliance (as compliant patients are more likely to visit their gastroenterologists) and underestimation of clinical remission (due to the higher chance of sick visits for IBD flares) as shown by the high compliance and low remission rates in our study. Secondly, for AA patients, there may be socioeconomic, insurance, culture and communication barriers that bias physician assessment of medication compliance and clinical remission. Use of pill counts and endoscopic remission measures in a prospective study can mitigate such biases and provide accurate measures of medication compliance and clinical remission respectively. Thirdly, we did not have detailed information on Crohn’s disease surgical history and complications (bowel obstruction, fistula, etc) that affects narcotics use, medication compliance, and clinical remission..
Conclusion
In summary, despite similar medical treatment at our tertiary IBD center, AA patients were more likely to be on narcotics, less compliant with medical therapy, and less likely to achieve clinical remission. Whether socioeconomic, cultural, or other race related factors lead to these differences is an important question for future research.
Compared with NHW patients, AAs had similar IBD medical treatment, were more likely to use narcotics, and were less likely to be compliant with medical treatment and achieve clinical remission.
References
- Loftus EV Jr. Clinical epidemiology of inflammatory bowel disease: Incidence, prevalence, and environmental influences. Gastroenterology. 2004;126:1504-17.
- Hou JK, El-Serag H, Thirumurthi S. Distribution and manifestations of inflammatory bowel disease in Asians, Hispanics, and African Americans: A systematic review. Am J Gastroenterol 2009;104:2100-9.
- Goldman CD, Kodner IJ, Fry RD, et al. Clinical and operative experience with non-Caucasian patients with Crohn’s disease. Dis Colon Rectum. 1986;29:317-21.
- Straus WL, Eisen GM, Sandler RS, et al. Crohn’s disease: Does race matter? Am J Gastroenterol 2000;95:479-83.
- Deveaux PG, Kimberling J, Galandiuk S, et al. Crohn’s disease: Presentation and severity compared between black patients and white patients. Dis Colon Rectum. 2005;48:1404-409.
- Basu S, Lopez I, Kulkarni A, et al. Impact of race and ethnicity on inflammatory bowel disease. Am J Gastroenterol. 2005;100:2254-261.
- Nguyen GC, Torres EA, Rugueiro M, et al. Inflammatory bowel disease characteristics among African Americans, Hispanics, and non-Hispanic Whites: Characterization of a large North American cohort. Am J Gastroenterol. 2006;101:1012-23.
- Cross RK, Jung C, Wasan S, et al. Racial differences in disease phenotype in patients with Crohn’s disease. Inflamm Bowel Dis. 2006;12:192-98.
- Nguyen GC, Bayless TM, Powe NR, et al. Race and health insurance are predictors of hospitalized Crohn’s disease patients in undergoing bowel resection. Inflamm Bowel Dis. 2007;13:1408-416.
- Mahid SS, Aaron MM, Gholson RD, et al. Inflammatory bowel disease and African Americans: A systematic review. Inflamm Bowel Dis. 2008;14:960-67.
- Flasar MH, Johnson T, Roghmann M, et al. Disparities in the use of immunodulators and biologics for the treatment of inflammatory bowel disease: A retrospective cohort study. Inflamm Bowel Dis. 2008;14:13-19.
- Flasar MH, Quezada S, Bijpuria P, et al. Racial differences in disease extent and severity in patients with ulcerative colitis: A retrospective cohort study. Dig Dis Sci. 2008;53:2754-760.
- Sewell JL, Yee HF, Inadomi JM. Hospitalizations are increasing among minority patients with Crohn’s disease and ulcerative colitis. Inflamm Bowel Dis. 2010;16:204-07.
- Damas OM, Jahann DA, Reznik R, et al. Phenotypic manifestations of inflammatory bowel disease differ between Hispanics and non-Hispanic Whites: Results of a large cohort study. Am J Gastroenterol. 2013;108:231-9.
- Lichtenstein GR1, Feagan BG, Cohen RD, et al. Serious infection and mortality in patients with Crohn's disease: More than 5 years of follow-up in the TREAT registry. Am J Gastroenterol. 2012;107:1409-22.
- Kugathasan S, Loizides A, Babusukumar U, et al. Comparative phenotypic and CARD15 mutational analysis among African American, Hispanic, and White children with Crohn's disease. Inflamm Bowel Dis. 2005;11:631-8.